172 results on '"Zhang, Ning"'
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2. Multiomics analysis of canine myocardium after circumferential pulmonary vein ablation: Effect of neuropeptide Y on long-term reinduction of atrial fibrillation.
- Author
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Song Q, Zhang N, Zhang Y, Zhang A, Li H, Bai S, Shang L, Du J, and Hou Y
- Subjects
- Animals, Dogs, Disease Models, Animal, Fibrosis, Heart Atria metabolism, Heart Atria pathology, Multiomics, Myocytes, Cardiac metabolism, Myocytes, Cardiac drug effects, Myocytes, Cardiac pathology, Proteome metabolism, Proteomics methods, Proto-Oncogene Proteins c-akt metabolism, Transcriptome, Apoptosis drug effects, Atrial Fibrillation metabolism, Atrial Fibrillation surgery, Atrial Fibrillation pathology, Catheter Ablation methods, Myocardium metabolism, Myocardium pathology, Neuropeptide Y metabolism, Pulmonary Veins metabolism, Pulmonary Veins surgery
- Abstract
Catheter ablation (CA) is an essential method for the interventional treatment of atrial fibrillation (AF), and it is very important to reduce long-term recurrence after CA. The mechanism of recurrence after CA is still unclear. We established a long-term model of beagle canines after circumferential pulmonary vein ablation (CPVA). The transcriptome and proteome were obtained using high-throughput sequencing and TMT-tagged LC-MS/LC analysis, respectively. Differentially expressed genes and proteins were screened and enriched, and the effect of fibrosis was found and verified in tissues. A downregulated protein, neuropeptide Y (NPY), was selected for validation and the results suggest that NPY may play a role in the long-term reinduction of AF after CPVA. Then, the molecular mechanism of NPY was further investigated. The results showed that the atrial effective refractory period (AERP) was shortened and fibrosis was increased after CPVA. Atrial myocyte apoptosis was alleviated by NPY intervention, and Akt activation was inhibited in cardiac fibroblasts. These results suggest that long-term suppression of NPY after CPVA may lead to induction of AF through promoting cardiomyocyte apoptosis and activating the Akt pathway in cardiac fibroblasts, which may make AF more likely to reinduce., (© 2024 The Author(s). Journal of Cellular and Molecular Medicine published by Foundation for Cellular and Molecular Medicine and John Wiley & Sons Ltd.)
- Published
- 2024
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3. The mechanism of reactive oxygen species generation, DNA damage and apoptosis in hemocytes of Litopenaeus vannamei under ammonia nitrogen exposure.
- Author
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Tong R, Li Y, Yu X, Zhang N, Liao Q, and Pan L
- Subjects
- Animals, Autophagy drug effects, Endoplasmic Reticulum Stress drug effects, Hemocytes drug effects, Apoptosis drug effects, Reactive Oxygen Species metabolism, Penaeidae drug effects, Penaeidae genetics, DNA Damage drug effects, Water Pollutants, Chemical toxicity, Ammonia toxicity
- Abstract
Ammonia-N poses a significant threat to aquatic animals. However, the mechanism of ROS production leading to DNA damage in hemocytes of crustaceans is still unclear. Additionally, the mechanism that cells respond to DNA damage by activating complex signaling networks has not been well studied. Therefore, we exposed shrimp to 0, 2, 10, and 20 mg/L NH
4 Cl for 0, 3, 6, 12, 24, 48, and 72 h, and explored the alterations in endoplasmic reticulum stress and mitochondrial fission, DNA damage, repair, autophagy and apoptosis. The findings revealed that ammonia exposure led to an increase in plasma ammonia content and neurotransmitter content (DA, 5-HT, ACh), and significant changes in gene expression of PLC and Ca2+ levels. The expression of disulfide bond formation-related genes (PDI, ERO1) and mitochondrial fission-related genes (Drp1, FIS1) were significantly increased, and the unfolded protein response was initiated. Simultaneously, ammonia-N exposure leads to an increase in ROS levels in hemocytes, resulting in DNA damage. DNA repair and autophagy were considerably influenced by ammonia-N exposure, as evidenced by changes in DNA repair and autophagy-related genes in hemocytes. Subsequently, apoptosis was induced by ammonia-N exposure, and this activation was associated with a caspase-dependent pathway and caspase-independent pathway, ultimately leading to a decrease in total hemocytes count. Overall, we hypothesized that neurotransmitters in the plasma of shrimp after ammonia-N exposure bind to receptors on hemocytes membrane, causing endoplasmic reticulum stress through the PLC-IP3R-Ca2+ signaling pathway and leading to mitochondrial fission. Consequently, this process resulted in increased ROS levels, hindered DNA repair, suppressed autophagy, and activated apoptosis. These cascading effects ultimately led to a reduction in total hemocytes count. The present study provides a molecular support for the understanding of the detrimental toxicity of ammonia-N exposure to crustaceans., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier B.V. All rights reserved.)- Published
- 2024
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4. Structural characterization and in vitro anti-colon cancer activity of a homogeneous polysaccharide from Agaricus bisporus.
- Author
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Zhang N, Liu Y, Tang FY, Yang LY, and Wang JH
- Subjects
- Humans, HT29 Cells, Molecular Weight, Epithelial-Mesenchymal Transition drug effects, Polysaccharides pharmacology, Polysaccharides chemistry, Monosaccharides analysis, Agaricus chemistry, Colonic Neoplasms drug therapy, Colonic Neoplasms pathology, Colonic Neoplasms metabolism, Antineoplastic Agents pharmacology, Antineoplastic Agents chemistry, Fungal Polysaccharides pharmacology, Fungal Polysaccharides chemistry, Cell Proliferation drug effects, Apoptosis drug effects
- Abstract
Colon cancer is the third most prevalent cancer and the second most deadly cancer in the world. Anti-colon cancer activity of Agaricus bisporus polysaccharides has not been studied. In this paper, Agaricus bisporus polysaccharides were sequentially extracted by room temperature water, hot water, high pressure hot water, dilute alkaline solution and concentrated alkaline solution. A homogeneous polysaccharide (WAAP-1) was obtained using DEAE Cellulose-52 column. Physicochemical properties, structural characterization and anti-colon cancer activity of WAAP-1 were investigated. The results showed that WAAP-1 was a neutral polysaccharide with molecular weight of 10.1 kDa. The monosaccharide composition was glucose, mannose and galactose with a molar ratio of 84.95:8.97:4.50. The main chain was mainly composed of (1,4)-α-D-Glcp and (1,6)-β-D-Manp. In vitro anti-colon cancer results showed that WAAP-1 could significantly inhibit proliferation of colon cancer cell HT-29. It promoted apoptosis and inhibited epithelial mesenchymal transition of HT-29 by up-regulating the expression of Caspase-3, Bax and E-cadherin proteins and down-regulating the expression of Bcl-2 and Vimentin proteins. The results provided new potential possibilities for the development of novel functional foods or antitumor drugs., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023. Published by Elsevier B.V.)
- Published
- 2023
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5. Downregulation of MDM2 by small interference RNA induces apoptosis and sensitizes MCF-7 breast cells to resveratrol.
- Author
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Zhang NX, Ma JF, Li SQ, Yin Z, and Li L
- Subjects
- Humans, Animals, Mice, Female, MCF-7 Cells, Resveratrol pharmacology, Down-Regulation, RNA, Small Interfering metabolism, RNA Interference, Cell Line, Tumor, Cell Proliferation, Proto-Oncogene Proteins c-mdm2 genetics, Proto-Oncogene Proteins c-mdm2 metabolism, Apoptosis, Breast Neoplasms drug therapy
- Abstract
Recent studies have demonstrated the mouse double minute gene (MDM2), a main oncogene, as a novel and interesting therapeutic target for cancer therapy. The aim of this study was to investigate the involvement of MDM2 in antiproliferative and antimetastatic effects of resveratrol in breast cancer cells. MCF-7 cells were transfected with siRNA against MDM2 and resveratrol. Proliferation and apoptosis were evaluated by MTT assay and cell death ELISA assay, respectively. MDM2, p53, Bax, Bcl-2, caspase-3, MMP-2, and MMP9 expressions were determined by qRT-PCR and Western blotting. Transfection with si-MDM2 significantly suppressed the expression of MDM2 expression, resulting in MCF-7 cell growth inhibition and spontaneous apoptosis. Pretreatment with Si-MDM2 synergically increased antiproliferation and antimetatstatic effects of resveratrol. No significant anticancer effects were detected with negative control siRNA treatment. Our findings suggest that silencing of MDM2 by specific siRNA effectively induce apoptosis and also enhanced anticancer effects of resveratrol. Therefore, siMDM2 may be a potent combination in breast therapy., (© 2022 John Wiley & Sons Ltd.)
- Published
- 2023
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6. Development and experimental verification of a prognosis model for cuproptosis-related subtypes in HCC.
- Author
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Wang Y, Zhang Y, Wang L, Zhang N, Xu W, Zhou J, Zhao Y, Zhu W, Zhang T, and Wang L
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- Humans, Biomarkers, Tumor genetics, Gene Expression Regulation, Neoplastic, Prognosis, Tumor Microenvironment genetics, Copper, Carcinoma, Hepatocellular pathology, Liver Neoplasms pathology, Apoptosis
- Abstract
Background: Cuproptosis is a recently discovered mechanism of programmed cell death caused by intracellular aggregation of mitochondrial lipoylated proteins and destabilization of iron-sulfur proteins triggered by copper. Hepatocellular carcinoma (HCC) is a common malignant tumor with a poor prognosis. We aimed to predict the survival of patients with HCC using the cuproptosis-related gene (CRG) expression., Methods: We analyzed the expression, methylation, and mutation status of CRGs in 538 HCC patients and correlated the date with clinical prognosis. HCC patients were divided into two clusters based on their CRG expression. The relationship between CRGs, risk genes, and the immune microenvironment was analyzed using the CIBERSORT algorithm and the single-cell data analysis method. A cuproptosis risk model was constructed according to the five risk genes using the LASSO COX method. To facilitate the clinical applicability of the proposed risk model, we constructed a nomogram and conducted an antineoplastic drug sensitivity analysis., Results: Our results suggest that the expression levels of CRGs in HCC are regulated by methylation. The prognoses were significantly different between the patients of the two clusters. The prognostic risk score positively correlated with memory T cell activation and negatively correlated with natural killer (NK) and regulatory T cell activation., Conclusion: Our findings indicate the involvement of CRG regulation in HCC and provide new insights into prognosis assessment. Drug sensitivity analysis predicted drug candidates for the treatment of patients with different HCC subtypes., (© 2022. Asian Pacific Association for the Study of the Liver.)
- Published
- 2022
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7. Dual-Targeting Antiproliferation Hybrids Derived from 1-Deoxynojirimycin and Kaempferol Induce MCF-7 Cell Apoptosis through the Mitochondria-Mediated Pathway.
- Author
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Zhang R, Zhang Y, Xin X, Huang G, Zhang N, Zeng Q, Tang L, Attaribo T, Lee KS, Jin BR, and Gui Z
- Subjects
- Calcium metabolism, Cell Cycle Checkpoints drug effects, Humans, MCF-7 Cells, Membrane Potential, Mitochondrial drug effects, Proto-Oncogene Proteins c-bcl-2 metabolism, Reactive Oxygen Species metabolism, 1-Deoxynojirimycin pharmacology, Apoptosis drug effects, Kaempferols pharmacology, Mitochondria drug effects
- Abstract
1-Deoxynojirimycin, an α-glucosidase inhibitor, possesses various biological activities such as antitumor, antidiabetic, and antiviral effects. However, the application of 1-deoxynojirimycin is restricted by its poor lipophilicity and low bioavailability. In this study, three 1-deoxynojirimycin derivatives ( 8 - 10 ) comprising 1-deoxynojirimycin and kaempferol were designed and synthesized to modify their pharmacokinetics and improve their antitumor efficacy. Among them, compound 10 , a conjugate of 1-deoxynojirimycin and kaempferol linked through an undecane chain, exhibited excellent lipophilicity, antiproliferative effects, and α-glucosidase inhibitory activity. Compared with 1-deoxynojirimycin, kaempferol, and their combination, compound 10 downregulated cyclooxygenase-2 (COX-2) expression, arrested the cell cycle at the S phase, induced cellular apoptosis, and inhibited the migration of MCF-7 cells. Moreover, further investigation indicated that compound 10 induced MCF-7 cell apoptosis through a mitochondrial-mediated pathway via the loss of mitochondrial membrane potential. This led to increasing intracellular levels of reactive oxygen species (ROS) and Ca
2+ , the downregulation of Bcl-2 expression, and the upregulation of Bax levels.- Published
- 2021
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8. Role of Bm30kc6 gene in cell apoptosis and the silk gland degradation signaling pathway in Bombyx mori L.
- Author
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Xiao Y, Li LL, Bibi A, Zhang N, Chen T, Mo Y, Yue W, and Miao Y
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- Animals, Bombyx metabolism, Caspase 3 genetics, Caspase 3 metabolism, Caspase Inhibitors pharmacology, Dactinomycin pharmacology, Ecdysone pharmacology, Gene Expression Regulation, Developmental, Hemolymph metabolism, Insect Proteins genetics, Insect Proteins metabolism, RNA, Small Interfering, Signal Transduction, Ultraviolet Rays, Apoptosis genetics, Bombyx genetics, Bombyx growth & development
- Abstract
Apoptosis is a process of programmed cell death that is regulated by genes independently. The Bm30kc6 gene is a kind of small molecular lipoprotein about 30 kDa, expressed highly in the late stage of the silkworm hemolymph. Our study showed that overexpression of Bm30kc6 could decrease caspase-3 activation. Meanwhile, activation of caspase-3 increased when Bm30kc6 expression was disturbed by small interfering RNA (siRNA). Cell apoptosis was decreased when Bm30kc6 was overexpressed under UV treatment. The apoptosis rate induced by actinomycin D is similar to the trend by UV. It was inferred that Bm30kc6 has an inhibitory effect on the apoptosis of silkworm cells. The apoptosis-related genes, such as BmFadd, BmDredd, and BmDaxx were increased after overexpression of Bm30kc6 or decreased after interference of siRNA. It was speculated that there was an interactive relationship between Bm30kc6, BmDaxx, BmFadd, and BmDredd in the apoptosis signaling pathways. We investigated the transcription expression of the Bm30kc6 gene in different growth stages and tissues of the silkworm. The results showed that Bm30kc6 reached its peak in the hemolymph during the 6th to 7th days of the 5th instar, or in spinning post 24 h of the silk gland. In the silkworm BmN cells treated with caspase-3/7 inhibitor, the caspase-3 enzyme activity, and the expression levels of Bm30kc6, BmFadd, BmDredd, and BmDaxx were significantly reduced. The expression levels of Bm30kc6 increased sharply when silkworms were treated by molting hormone at Day 3 or 5 of the 5th instar. The results indicated that the expression of the Bm30kc6 gene was affected by the molting hormone and was likely to be its downstream target. In conclusion, the results suggest that the Bm30kc6 gene is involved in the regulation of the apoptotic signaling pathway and plays a role in the apoptotic process., (© 2020 Wiley Periodicals LLC.)
- Published
- 2020
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9. miR-410-3p regulates proliferation and apoptosis of fibroblast-like synoviocytes by targeting YY1 in rheumatoid arthritis.
- Author
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Wang Y, Jiao T, Fu W, Zhao S, Yang L, Xu N, and Zhang N
- Subjects
- Arthritis, Rheumatoid pathology, Base Sequence, Cell Cycle genetics, Cell Line, Cell Proliferation genetics, Fibroblasts metabolism, Humans, MicroRNAs genetics, Synoviocytes metabolism, Apoptosis genetics, Arthritis, Rheumatoid genetics, Fibroblasts pathology, MicroRNAs metabolism, Synoviocytes pathology, YY1 Transcription Factor metabolism
- Abstract
In our previous study, miR-410-3p had been confirmed to regulate inflammatory cytokine release in rheumatoid arthritis fibroblast-like synoviocytes (RA FLSs). However, other biological functions of miR-410-3p in RA FLSs still remain unexplored. In the present study, we focused on the effect of miR-410-3p on proliferation, apoptosis, and cell cycle of RA FLSs, and explored the potential underlying mechanism. miR-410-3p mRNA levels in the synovium and FLSs of patients with RA and of healthy controls were quantitated by RT-qPCR. The levels of miR-410-3p were reduced in both synovium and FLSs from patients with RA. Next, we focused on the roles of miR-410-3p in cell viability, apoptosis, and cell cycle, by transfecting miR-410-3p mimics and inhibitor into RA FLSs, and conducting CCK-8 assay, EdU staining and flow cytometry. Results showed that miR-410-3p up-regulation suppressed proliferation, promoted apoptosis and G1-S phase transition while miR-410-3p down-regulation had opposite effects. YY1 was verified as a direct target gene of miR-410-3p through the luciferase reporter system; YY1 up-regulation was able to rescue the effects of miR-410-3p in RA FLSs. Taken together, our current findings might provide a potential therapeutic target for RA., (Copyright © 2019 The Authors. Published by Elsevier Masson SAS.. All rights reserved.)
- Published
- 2019
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10. Protective effects of methane-rich saline on mice with allergic asthma by inhibiting inflammatory response, oxidative stress and apoptosis.
- Author
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Zhang N, Lu HT, Zhang RJ, and Sun XJ
- Subjects
- Animals, Asthma immunology, Asthma metabolism, Bronchial Hyperreactivity drug therapy, Cytokines analysis, Female, Mice, Mice, Inbred BALB C, Saline Solution, Apoptosis drug effects, Asthma drug therapy, Inflammation prevention & control, Methane pharmacology, Oxidative Stress drug effects
- Abstract
Background: Asthma is a common cause of breathing difficulty in children and adults, and is characterized by chronic airway inflammation that is poorly controlled by available treatments. This results in severe disability and applies a huge burden to the public health system. Methane has been demonstrated to function as a therapeutic agent in many diseases. The aim of the present study was to explore the effect of methane-rich saline (MRS) on the pathophysiology of a mouse model of asthma and its underlying mechanism., Methods: A murine model of ovalbumin (OVA)-induced allergic asthma was applied in this study. Mice were divided into three groups: a control group, an OVA group, and OVA-induced asthmatic mice treated with MRS as the third group. Lung resistance index (RI) and dynamic compliance (Cdyn) were measured to determine airway hyper-responsiveness (AHR). Haematoxylin and eosin (H&E) staining was performed and scored to show histopathological changes. Cell counts of bronchoalveolar lavage fluid (BALF) were recorded. Cytokines interleukin (IL)-4, IL-5, IL-13, tumor necrosis factor α (TNF-α), and C-X-C motif chemokine ligand 15 (CXCL15) from BALF and serum were measured by enzyme-linked immunosorbent assay (ELISA). The oxidative stress indexes, including malondialdehyde (MDA), superoxide dismutase (SOD), catalase (CAT), glutathione (GSH), myeloperoxidase (MPO), and 8-hydroxydeoxyguanosine (8-OHdG), were determined using commercial kits. Apoptosis was evaluated by western blot, quantitative real-time polymerase chain reaction (qRT-PCR), and biochemical examination., Results: MRS administration reversed the OVA-induced AHR, attenuated the pathological inflammatory infiltration, and decreased the cytokines IL-4, IL-5, IL-13, TNF-α, and CXCL15 in serum and BALF. Moreover, following MRS administration, the oxidative stress was alleviated as indicated by decreased MDA, MPO, and 8-OHdG, and elevated SOD and GSH. In addition, MRS exhibited an anti-apoptotic effect in this model, protecting epithelial cells from damage., Conclusions: Methane improves pulmonary function and decreases infiltrative inflammatory cells in the allergic asthmatic mouse model. This may be associated with its anti-inflammatory, antioxidative, and anti-apoptotic properties.
- Published
- 2019
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11. Dihydronicotinamide riboside is a potent NAD + concentration enhancer in vitro and in vivo .
- Author
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Yang Y, Mohammed FS, Zhang N, and Sauve AA
- Subjects
- Animals, Cell Line, Chromatography, High Pressure Liquid, Humans, Hydrogen Peroxide pharmacology, Injections, Intraperitoneal, Lactic Acid metabolism, Liver metabolism, Male, Methyl Methanesulfonate pharmacology, Mice, Mice, Inbred C57BL, NAD analysis, Neurons drug effects, Neurons metabolism, Niacinamide administration & dosage, Niacinamide chemical synthesis, Niacinamide pharmacology, Apoptosis drug effects, NAD metabolism, Niacinamide analogs & derivatives
- Abstract
Interest in pharmacological agents capable of increasing cellular NAD
+ concentrations has stimulated investigations of nicotinamide riboside (NR) and nicotinamide mononucleotide (NMN). NR and NMN require large dosages for effect. Herein, we describe synthesis of dihydronicotinamide riboside (NRH) and the discovery that NRH is a potent NAD+ concentration-enhancing agent, which acts within as little as 1 h after administration to mammalian cells to increase NAD+ concentrations by 2.5-10-fold over control values. Comparisons with NR and NMN show that in every instance, NRH provides greater NAD+ increases at equivalent concentrations. NRH also provides substantial NAD+ increases in tissues when administered by intraperitoneal injection to C57BL/6J mice. NRH substantially increases NAD+ /NADH ratio in cultured cells and in liver and no induction of apoptotic markers or significant increases in lactate levels in cells. Cells treated with NRH are resistant to cell death caused by NAD+ -depleting genotoxins such as hydrogen peroxide and methylmethane sulfonate. Studies to identify its biochemical mechanism of action showed that it does not inhibit NAD+ consumption, suggesting that it acts as a biochemical precursor to NAD+ Cell lysates possess an ATP-dependent kinase activity that efficiently converts NRH to the compound NMNH, but independent of Nrk1 or Nrk2. These studies identify a putative new metabolic pathway to NAD+ and a potent pharmacologic agent for NAD+ concentration enhancement in cells and tissues., (© 2019 Yang et al.)- Published
- 2019
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12. Long noncoding RNA FAL1 promotes proliferation and inhibits apoptosis of human colon cancer cells.
- Author
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Wu K, Zhang N, Ma J, Huang J, Chen J, Wang L, and Zhang J
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- Cell Movement, Colonic Neoplasms genetics, Colonic Neoplasms metabolism, Humans, Prognosis, Signal Transduction, Survival Rate, Tumor Cells, Cultured, Apoptosis, Cell Proliferation, Colonic Neoplasms pathology, Gene Expression Regulation, Neoplastic, RNA, Long Noncoding genetics
- Abstract
Aberrant expression of long non-coding RNAs (lncRNAs) has been associated with a variety of malignancies including colon cancer. In this study, we aimed to characterize the biological mechanisms of focally amplified lncRNA on chromosome 1 (FAL1) in colon cancers. Here, our results indicate that FAL1 expression was remarkably up-regulated in colon tumor tissues as compared to corresponding tumor-adjacent normal tissues. Importantly, the cumulative survival rate of patients with high levels of FAL1 in tumor tissues was considerably lower than those with low FAL1 levels in tumor tissues. Cox regression analysis showed that lncRNA FAL1 could act as an independent prognostic factor in CRC. Knockdown of FAL1 in HT29 cells attenuated cell proliferation and stimulated cell apoptosis. In contrast, overmetastasis-related molecules Bcl-2, TGF-β1, p65, and PCNA at the mRNA and protein levels. Mechanistically, FAL1 was found to interact with STAT3 at 200 to 400 bp and promote phosphorylation of STAT3. In addition, we found that knockdown of STAT3 in HT29 cells abolished the effects of FAL1 on cell proliferation as well as the expression of TGF-β1 and Bcl-2. Based on these findings, we concluded that FAL1 might be a potential oncogene for the progression of colon cancer. © 2018 IUBMB Life, 70(11):1093-1100, 2018., (© 2018 International Union of Biochemistry and Molecular Biology.)
- Published
- 2018
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13. A commercial Roundup® formulation induced male germ cell apoptosis by promoting the expression of XAF1 in adult mice.
- Author
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Jiang X, Zhang N, Yin L, Zhang WL, Han F, Liu WB, Chen HQ, Cao J, and Liu JY
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- Adaptor Proteins, Signal Transducing, Animals, Apoptosis Regulatory Proteins, Caspase 3 drug effects, Cell Survival drug effects, Glycine toxicity, Inhibitor of Apoptosis Proteins biosynthesis, Male, Mice, Organ Size drug effects, Poly (ADP-Ribose) Polymerase-1 drug effects, Sperm Count, Sperm Motility drug effects, Spermatogenesis drug effects, Spermatozoa drug effects, Spermatozoa ultrastructure, Glyphosate, Apoptosis drug effects, F-Box Proteins biosynthesis, Germ Cells drug effects, Glycine analogs & derivatives, Herbicides toxicity
- Abstract
Roundup® is extensively used for weed control worldwide. Residues of this compound may lead to side effects of the male reproductive system. However, the toxic effects and mechanisms of Roundup® of male germ cells remain unclear. We aimed to investigate the apoptosis-inducing effects of Roundup® on mouse male germ cells and explore the role of a novel tumor suppressor XAF1 (X-linked inhibitor of apoptosis-associated factor 1) involved in this process. We demonstrated that Roundup® can impair spermatogenesis, decrease sperm motility and concentration, and increase the sperm deformity rate in mice. In addition, excessive apoptosis of germ cells accompanied by the overexpression of XAF1 occurred after Roundup® exposure both in vitro and in vivo. Furthermore, the low expression of XIAP (X-linked inhibitor of apoptosis) induced by Roundup® was inversely correlated with XAF1. Moreover, the knockdown of XAF1 attenuated germ cell apoptosis, improved XIAP expression and inhibited the activation of its downstream target proteins, caspase-3 and PARP, after Roundup® exposure. Taken together, our data indicated that XAF1 plays an important role in Roundup®-induced male germ cell apoptosis. The present study suggested that Roundup® exposure has potential negative implications on male reproductive health in mammals., (Copyright © 2018 Elsevier B.V. All rights reserved.)
- Published
- 2018
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14. Bisphenol A induced male germ cell apoptosis via IFNβ-XAF1-XIAP pathway in adult mice.
- Author
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Jiang X, Yin L, Zhang N, Han F, Liu WB, Zhang X, Chen HQ, Cao J, and Liu JY
- Subjects
- Adaptor Proteins, Signal Transducing, Animals, Apoptosis Regulatory Proteins, Cell Line, F-Box Proteins genetics, Gene Expression drug effects, Gene Knockdown Techniques, Inhibitor of Apoptosis Proteins genetics, Interferon-beta genetics, Male, Mice, Spermatogenesis drug effects, Testis pathology, Up-Regulation drug effects, Apoptosis drug effects, Benzhydryl Compounds toxicity, F-Box Proteins drug effects, Germ Cells drug effects, Inhibitor of Apoptosis Proteins drug effects, Interferon-beta drug effects, Phenols toxicity, Signal Transduction drug effects
- Abstract
Bisphenol A (BPA) impairs male fertility by acting as an endocrine disruptor. However, the mechanisms by which BPA cause reproductive toxicity are not fully elucidated. Here, we explored the role of XAF1, a novel pro-apoptosis molecule, in BPA-induced abnormal spermatogenesis and the transcriptional regulation mechanism of BPA-induced XAF1. BPA exposure detrimentally impacted spermatogenesis by inducing excessive germ cell apoptosis. XAF1 was upregulated in germ cells after BPA exposure, which was involved in the apoptosis pathway. In addition, the expression levels of XIAP and XAF1 were inversely correlated after BPA exposure. Knockdown of XAF1 expression partially inhibited the apoptosis of GC-2 cells, suppressed the activation of caspase 3 and improved the BPA-induced XIAP expression. Moreover, IFNβ expression levels were significantly upregulated after BPA exposure both in vitro and in vivo, and these levels were positively related to the expression of XAF1. Furthermore, IFNβ knockdown reduced the expression of XAF1 and increased the expression of XIAP in BPA-treated GC-2 cells. Together, these data indicated that BPA triggers male germ cell apoptosis in mice via the IFNβ-XAF1-XIAP pathway, which may contribute to BPA-induced testis toxicity., (Copyright © 2018 Elsevier Inc. All rights reserved.)
- Published
- 2018
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15. Progesterone inhibited endoplasmic reticulum stress associated apoptosis induced by interleukin-1β via the GRP78/PERK/CHOP pathway in BeWo cells.
- Author
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Liu L, Zhang Y, Wang Y, Peng W, Zhang N, and Ye Y
- Subjects
- Adult, Cell Line, Endoplasmic Reticulum Chaperone BiP, Female, Humans, Placenta cytology, Pre-Eclampsia blood, Pregnancy, Apoptosis, Endoplasmic Reticulum Stress, Heat-Shock Proteins metabolism, Interleukin-1beta metabolism, Placenta metabolism, Pre-Eclampsia metabolism, Progesterone blood, Signal Transduction, Transcription Factor CHOP metabolism, eIF-2 Kinase metabolism
- Abstract
Aim: Pre-eclampsia (PE) is a pregnancy complication characterized by new onset maternal hypertension and proteinuria. Its underlying mechanisms are unclear. This study investigated the relationship between progesterone and endoplasmic reticulum stress (ERS) associated apoptosis induced by interleukin (IL)-1β via the glucose regulated protein 78 (GRP78)/protein kinase RNA-like endoplasmic reticulum kinase (PERK)/C/EBP-homologous protein (CHOP) pathway in BeWo cells., Methods: Venous blood and placental tissues were collected from PE patients, normal pregnancy and preterm delivery cases, respectively. Progesterone serum levels were detected by enzyme-linked immunosorbent assay and ERS-related protein expression in placentas was examined by immunohistochemistry, reverse transcriptase-polymerase chain reaction and Western blot. BeWo cells were stimulated by IL-1β to induce ERS associated apoptosis in vitro. The apoptotic rate was measured by flow cytometry. The mechanism of progesterone acting on IL-1β induced ERS associated apoptosis was investigated by reverse transcriptase-polymerase chain reaction, Western blot and PERK small interfering RNA, with RU486 used as a receptor inhibitor., Results: PE patients exhibited decreased serum levels of progesterone and activated ERS and increased ERS-related protein expression. IL-1β could induce ERS and associated cell apoptosis by activating the GRP78/PERK/CHOP signal pathway, which could be inhibited by progesterone. PERK could be upregulated and phosphorylation activated in ERS. The protective effects of progesterone could be attenuated by RU486., Conclusion: IL-1β could induce ERS associated cell apoptosis by activating the GRP78/PERK/CHOP signal pathway in BeWo cells and may play an important role in PE occurrence. Progesterone levels were decreased in patients with PE and seemed to have a protective effect by inhibiting ERS associated cell apoptosis., (© 2017 Japan Society of Obstetrics and Gynecology.)
- Published
- 2018
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16. Goserelin promotes the apoptosis of epithelial ovarian cancer cells by upregulating forkhead box O1 through the PI3K/AKT signaling pathway.
- Author
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Zhang N, Qiu J, Zheng T, Zhang X, Hua K, and Zhang Y
- Subjects
- Animals, Antineoplastic Agents, Hormonal pharmacology, Biomarkers, Tumor genetics, Carcinoma, Ovarian Epithelial, Cell Proliferation drug effects, Female, Forkhead Box Protein O1 genetics, Humans, Mice, Mice, Nude, Neoplasms, Glandular and Epithelial drug therapy, Neoplasms, Glandular and Epithelial metabolism, Ovarian Neoplasms drug therapy, Ovarian Neoplasms metabolism, Phosphatidylinositol 3-Kinase genetics, Phosphorylation, Proto-Oncogene Proteins c-akt genetics, Signal Transduction drug effects, Tumor Cells, Cultured, Up-Regulation, Xenograft Model Antitumor Assays, Apoptosis drug effects, Biomarkers, Tumor metabolism, Forkhead Box Protein O1 metabolism, Goserelin pharmacology, Neoplasms, Glandular and Epithelial pathology, Ovarian Neoplasms pathology, Phosphatidylinositol 3-Kinase metabolism, Proto-Oncogene Proteins c-akt metabolism
- Abstract
Gonadotropins, including luteinizing hormone (LH) and follicle stimulating hormone (FSH), are conducive to the growth of ovarian cancer based on the 'gonadotropin theory' and are regulated by gonadotropin-releasing hormone (GnRH). The present study was carried out to investigate the effect of goserelin, a GnRH agonist, on the apoptosis of epithelial ovarian cancer (EOC) cells and the underlying in vitro and in vivo mechanisms. Through flow cytometry, Hoechst staining and TUNEL staining, we demonstrated that goserelin promoted the apoptosis of EOC cells both in vitro and in vivo. Through human apoptosis gene PCR array, we verified that the promotion of EOC cell apoptosis by goserelin was linked to the upregulation of members of the tumor necrosis factor (TNF) and TNF receptor superfamilies, which have been identified as downstream targets of forkhead box O1 (FOXO1). Goserelin enhanced FOXO1 expression, and siRNA-mediated knockdown of FOXO1 abrogated the induction of apoptosis by goserelin. Moreover, goserelin decreased AKT activity, and FOXO1 upregulation by goserelin was dependent on the phosphatidylinositol 3-kinase (PI3K)/AKT pathway. In vivo, the expression of key factors in the PI3K/AKT/FOXO1 pathway was consistent with that observed in vitro. In conclusion, our data suggested that goserelin may promote EOC cell apoptosis by upregulating FOXO1 through the PI3K/AKT signaling pathway. We believe that GnRH agonists may be potential antitumor agents, and key factors in the PI3K/AKT-FOXO1 pathway may also be novel therapeutic targets for the treatment of EOC.
- Published
- 2018
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17. TNF-α induces autophagy through ERK1/2 pathway to regulate apoptosis in neonatal necrotizing enterocolitis model cells IEC-6.
- Author
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Yuan Y, Ding D, Zhang N, Xia Z, Wang J, Yang H, Guo F, and Li B
- Subjects
- Animals, Animals, Newborn, Cell Line, Cell Proliferation, Intestine, Small pathology, Phosphorylation, Rats, Sprague-Dawley, Apoptosis, Autophagy, Enterocolitis, Necrotizing enzymology, Enterocolitis, Necrotizing pathology, Extracellular Signal-Regulated MAP Kinases metabolism, MAP Kinase Signaling System drug effects, Models, Biological, Tumor Necrosis Factor-alpha metabolism
- Abstract
Necrotizing enterocolitis (NEC) is a potentially fatal illness in premature neonates. Tumor necrosis factor-α (TNF-α) and autophagy are associated with the pathogenesis of NEC. This study aimed to explore whether TNF-α might regulate apoptosis in neonatal NEC model cells IEC-6 via regulation of autophagy. NEC rat model was induced by hand feeding and exposure to asphyxia/cold-stress for histologic examination. The NEC in vitro model (IEC-6/NEC cells) was established by stimulating the intestinal epithelial cell line IEC-6 with lipopolysaccharide (LPS, 100 μg/mL) for 3 h to investigate the effects of TNF-α on IEC-6 proliferation and apoptosis. In this study, NEC rats showed decreased proliferating cell nuclear antigen (PCNA) expression, increased TUNEL-positive cells, higher expression of TNF-α, p-ERK1/2, and autophagy-related proteins in rat small intestine compared with their controls. Additionally, the LPS-stimulated IEC-6/NEC cells showed a significantly decreased proliferation and increased apoptosis compared with the control cells. Furthermore, the LPS-stimulated IEC-6/NEC cells exhibited enhanced autophagy level, as evidenced by a dose-dependent increase in Beclin-1 protein expression, LC3II/LC3I ratio and accumulation of MDC-positive autophagic vacuoles. Moreover, inhibition of autophagy by wortmannin or LY294002 significantly abolished the LPS-mediated decreased proliferation and increased apoptosis of IEC-6/NEC cells. Results also showed that inhibition of ERK1/2 pathway using U0126 significantly inhibited TNF-α-induced autophagy. Furthermore, the TNF-α-mediated inhibition of IEC-6 proliferation and promotion of IEC-6 apoptosis was abolished by U0126. Our findings demonstrated that TNF-α might induce autophagy through ERK1/2 pathway to regulate apoptosis in neonatal NEC cells IEC-6. Our study enhances our understanding of neonatal NEC pathogenesis.
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- 2018
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18. Autophagy inhibits high glucose induced cardiac microvascular endothelial cells apoptosis by mTOR signal pathway.
- Author
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Zhang Z, Zhang S, Wang Y, Yang M, Zhang N, Jin Z, Ding L, Jiang W, Yang J, Sun Z, Qiu C, and Hu T
- Subjects
- Adenine analogs & derivatives, Adenine pharmacology, Animals, Caspases metabolism, Cells, Cultured, Heart physiopathology, Male, Myocardium cytology, Phosphorylation drug effects, Proto-Oncogene Proteins c-akt metabolism, Rats, Rats, Sprague-Dawley, Sirolimus pharmacology, TOR Serine-Threonine Kinases antagonists & inhibitors, Apoptosis drug effects, Endothelial Cells drug effects, Glucose pharmacology, Heart drug effects, Signal Transduction drug effects, TOR Serine-Threonine Kinases metabolism
- Abstract
Cardiac microvascular endothelial cells (CMECs) dysfunction is an important pathophysiological event in the cardiovascular complications induced by diabetes. However, the underlying mechanism is not fully clarified. Autophagy is involved in programmed cell death. Here we investigated the potential role of autophagy on the CMECs injury induced by high glucose. CMECs were cultured in normal or high glucose medium for 6, 12 and 24 h respectively. The autophagy of CMECs was measured by green fluorescence protein (GFP)-LC3 plasmid transfection. Moreover, the apoptosis of CMEC was determined by flow cytometry. Furthermore, 3-Methyladenine (3MA), ATG7 siRNA and rapamycin were administrated to regulate the autophagy state. Moreover, Western blotting assay was performed to measure the expressions of Akt, mTOR, LC3 and p62. High glucose stress decreased the autophagy, whereas increased the apoptosis in CMECs time dependently. Meanwhile, high glucose stress activated the Akt/mTOR signal pathway. Furthermore, autophagy inhibitor, 3-MA and ATG7 siRNA impaired the autophagy and increased the apoptosis in CMECs induced by high glucose stress. Conversely, rapamycin up-regulated the autophagy and decreased the apoptosis in CMECs under high glucose condition. Our data provide evidence that high glucose directly inhibits autophagy, as a beneficial adaptive response to protect CMECs against apoptosis. Furthermore, the autophagy was mediated, at least in part, by mTOR signaling.
- Published
- 2017
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19. Bortezomib sensitizes human osteosarcoma cells to adriamycin-induced apoptosis through ROS-dependent activation of p-eIF2α/ATF4/CHOP axis.
- Author
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Xian M, Cao H, Cao J, Shao X, Zhu D, Zhang N, Huang P, Li W, Yang B, Ying M, and He Q
- Subjects
- Activating Transcription Factor 4 metabolism, Animals, Blotting, Western, Bortezomib pharmacology, Cell Line, Tumor, Cell Proliferation drug effects, Doxorubicin pharmacology, Eukaryotic Initiation Factor-2 metabolism, Flow Cytometry, Humans, Mice, Mice, Nude, Proteasome Inhibitors pharmacology, Reactive Oxygen Species metabolism, Reverse Transcriptase Polymerase Chain Reaction, Transcription Factor CHOP metabolism, Xenograft Model Antitumor Assays, Antineoplastic Combined Chemotherapy Protocols pharmacology, Apoptosis drug effects, Bone Neoplasms pathology, Osteosarcoma pathology, Signal Transduction drug effects
- Abstract
Osteosarcoma is the most common bone cancer, and chemotherapy is currently indispensable for its treatment. Adriamycin has been claimed to be the most effective agent for osteosarcoma, however, the outcome of adriamycin chemotherapy remains unsatisfactory. Here, we reported a potent combination therapy that bortezomib, a proteasome inhibitor, enhances adriamycin-induced apoptosis to eliminate osteosarcoma cells and we revealed that the activation of p-eIF2α/ATF4/CHOP axis is the underlying associated mechanisms. First, we observed that bortezomib enhances adriamycin-mediated inhibition of cell proliferation and enhances the apoptosis in osteosarcoma cell lines. Moreover, this drug combination produced more potent tumor-growth inhibitory effects in human osteosarcoma cell line KHOS/NP xenografts. Our study showed that reactive oxygen species (ROS) plays an important role in apoptosis induced by adriamycin plus bortezomib, whereas ROS scavenger NAC could almost completely block the apoptosis induced by the combination treatment. Meanwhile, p-eIF2α is remarkably elevated in the combination group. As a result, ATF4 exhibits strong activation which consequently induces the activation of CHOP and leads to the cell death. Finally, 13 primary osteosarcoma cells demonstrated potent response to the combination treatment. In a human osteosarcoma patient-derived xenograft (PDX) model, our finding suggests that when combined with bortezomib, a relatively low dose of adriamycin produced more potent tumor-growth inhibitory effects without increased toxicity. Thus, our findings not only provide a promising combination strategy to overcome osteosarcoma but also shed new light on the strategy of combining increased ROS and inhibited proteasome to open up new opportunities for the clinical development of chemotherapy regimens., (© 2017 UICC.)
- Published
- 2017
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20. Induction of Apoptosis by the Nonstructural Protein 4 and 10 of Porcine Reproductive and Respiratory Syndrome Virus.
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Yuan S, Zhang N, Xu L, Zhou L, Ge X, Guo X, and Yang H
- Subjects
- Animals, BH3 Interacting Domain Death Agonist Protein genetics, BH3 Interacting Domain Death Agonist Protein metabolism, Bcl-2-Like Protein 11 genetics, Bcl-2-Like Protein 11 metabolism, Caspase 8 genetics, Caspase 8 metabolism, Caspase 9 genetics, Caspase 9 metabolism, Cell Line, Chlorocebus aethiops, Endoplasmic Reticulum metabolism, Endoplasmic Reticulum virology, Epithelial Cells metabolism, Epithelial Cells virology, Gene Expression Regulation, Kidney Glomerulus metabolism, Kidney Glomerulus virology, Macrophages, Alveolar metabolism, Macrophages, Alveolar virology, Mitochondria metabolism, Mitochondria virology, Porcine Reproductive and Respiratory Syndrome metabolism, Porcine Reproductive and Respiratory Syndrome virology, Porcine respiratory and reproductive syndrome virus growth & development, Porcine respiratory and reproductive syndrome virus metabolism, Signal Transduction, Swine, Viral Nonstructural Proteins metabolism, Virus Replication, bcl-X Protein genetics, bcl-X Protein metabolism, Apoptosis genetics, Host-Pathogen Interactions, Porcine Reproductive and Respiratory Syndrome genetics, Porcine respiratory and reproductive syndrome virus genetics, Viral Nonstructural Proteins genetics
- Abstract
Infection by most viruses triggers apoptosis in host cells, and viruses manipulate this cell response to promote viral replication, virus spread, and cell killing. Porcine reproductive and respiratory syndrome virus (PRRSV) has been shown to induce apoptosis both in vitro and in vivo, while the regulatory roles of PRRSV-encoded products in apoptosis are not fully understood. In the present study, we first showed a biphasic apoptosis regulation by a highly pathogenic PRRSV strain JXwn06. It was indicated that PRRSV infection delays apoptosis at early infection but activates apoptosis at late infection in MARC-145 cells. In PRRSV-infected MARC-145 cells, procaspase-8, -9 and -12 were activated at late infection, demonstrating the involvements of death receptor pathway, mitochondrial pathway and endoplasmic reticulum (ER) stress pathway in inducing apoptosis. PRRSV was also shown to induce a similar apoptosis process in pulmonary alveolar macrophages (PAMs) with an early initiation. Next, the PRRSV-encoded apoptosis inducers were screened, indicating that the nonstructural protein (Nsp) 4 and Nsp10 of PRRSV are pro-apoptotic. In the presence of Nsp4, it was confirmed that procaspase-8, -9 and -12 were cleaved, and Nsp4 facilitates the cleavage of procaspase-9 by activating B-cell lymphoma 2 interacting mediator of cell death (Bim), a pro-apoptotic protein. In addition, Nsp4 was shown to induce the degradation of an anti-apoptotic protein, B-cell lymphoma-extra large (Bcl-xL). Nsp10 was shown to activate procaspase-8 and -9 but procaspase-12 and to upregulate the expression of BH3-only pro-apoptotic protein BH3 interacting-domain death agonist (Bid) and its active form, truncated Bid (tBid). Clearly, the participation of both activated caspase-8 and Bid is required for Nsp10-induced apoptosis, indicating a crosstalk between extrinsic- and mitochondria-dependent pathways. Together, our findings suggest that PRRSV infection regulates apoptosis in a two-phase manner and activates all three apoptotic pathways; the Nsp4 and Nsp10 of PRRSV function as apoptosis inducers with different molecular basis.
- Published
- 2016
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21. Apatinib inhibits VEGF signaling and promotes apoptosis in intrahepatic cholangiocarcinoma.
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Peng H, Zhang Q, Li J, Zhang N, Hua Y, Xu L, Deng Y, Lai J, Peng Z, Peng B, Chen M, Peng S, and Kuang M
- Subjects
- Animals, Bile Duct Neoplasms drug therapy, Bile Duct Neoplasms pathology, Cholangiocarcinoma drug therapy, Cholangiocarcinoma pathology, Humans, Mice, Mice, Inbred NOD, Mice, SCID, Signal Transduction drug effects, Vascular Endothelial Growth Factor A drug effects, Vascular Endothelial Growth Factor Receptor-2 drug effects, Xenograft Model Antitumor Assays, Antineoplastic Agents pharmacology, Apoptosis drug effects, Bile Duct Neoplasms metabolism, Cholangiocarcinoma metabolism, Pyridines pharmacology, Vascular Endothelial Growth Factor A metabolism, Vascular Endothelial Growth Factor Receptor-2 metabolism
- Abstract
Tumor cells co-express vascular endothelial growth factor (VEGF) and VEGF receptors (VEGFRs) that interact each other to support a self-sustainable cell growth. So far, this autocrine VEGF loop is not reported in human intrahepatic cholangiocarcinoma (ICC). Apatinib is a highly selective VEGFR2 inhibitor, but its effects on ICC have not been investigated. In this study, we reported that VEGF and phosphorylated VEGFR2 were expressed at a significantly high level in ICC patient tissues (P<0.05). In vitro, treating ICC cell lines RBE and SSP25 with recombinant human VEGF (rhVEGF) induced phosphorylation of VEGFR1 (pVEGFR1) and VEGFR2 (pVEGFR2); however, only the VEGFR2 played a role in the anti-apoptotic cell growth through activating a PI3K-AKT-mTOR anti-apoptotic signaling pathway which generated more VEGF to enter this autocrine loop. Apatinib inhibited the anti-apoptosis induced by VEGF signaling, and promoted cell death in vitro. In addition, Apatinib treatment delayed xenograft tumor growth in vivo. In conclusion, the autocrine VEGF/VEGFR2 signaling promotes ICC cell survival. Apatinib inhibits anti-apoptotic cell growth through suppressing the autocrine VEGF signaling, supporting a potential role for using Apatinib in the treatment of ICC.
- Published
- 2016
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22. Guggulsterone induces apoptosis of human hepatocellular carcinoma cells through intrinsic mitochondrial pathway.
- Author
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Shi JJ, Jia XL, Li M, Yang N, Li YP, Zhang X, Gao N, and Dang SS
- Subjects
- Carcinoma, Hepatocellular metabolism, Carcinoma, Hepatocellular pathology, Cell Cycle Checkpoints drug effects, Cell Proliferation drug effects, Dose-Response Relationship, Drug, Gene Expression Regulation, Neoplastic, Hep G2 Cells, Humans, Liver Neoplasms metabolism, Liver Neoplasms pathology, Mitochondria metabolism, Mitochondria pathology, Proto-Oncogene Proteins c-bcl-2 genetics, Proto-Oncogene Proteins c-bcl-2 metabolism, Signal Transduction drug effects, Time Factors, Transforming Growth Factor beta1 metabolism, Tumor Necrosis Factor-alpha metabolism, Vascular Endothelial Growth Factor A metabolism, bcl-2-Associated X Protein genetics, bcl-2-Associated X Protein metabolism, Antineoplastic Agents, Phytogenic pharmacology, Apoptosis drug effects, Carcinoma, Hepatocellular drug therapy, Liver Neoplasms drug therapy, Mitochondria drug effects, Pregnenediones pharmacology
- Abstract
Aim: To investigate the effects of guggulsterone on the proliferation and apoptosis of human hepatoma HepG2 cells in vitro and relevant mechanisms., Methods: Human hepatocellular carcinoma HepG2 cells and normal human liver L-02 cells were treated with different concentrations of guggulsterone (5-100 μmol/L) for 24-72 h. Cell proliferation was tested by MTT assay. Cell cycle and apoptosis were investigated using flow cytometry (FACS). Bcl-2 and Bax mRNA and protein expression was detected by real-time PCR and Western blot, respectively. TGF-β1, TNF-α, and VEGF contents were determined by ELISA., Results: Guggulsterone significantly inhibited HepG2 cell proliferation in a dose- and time-dependent manner. FACS showed that guggulsterone arrested HepG2 cell cycle at G0/G1 phase. Guggulsterone induced apoptosis was also observed in HepG2 cells, with 24.91% ± 2.41% and 53.03% ± 2.28% of apoptotic cells in response to the treatment with 50 μmol/L and 75 μmol/L guggulsterone, respectively. Bax mRNA and protein expression was significantly increased and Bcl-2 mRNA and protein expression was decreased. ELISA analysis showed that the concentrations of TGF-β1 and VEGF were significantly decreased and TNF-α concentration was increased., Conclusion: Guggulsterone exerts its anticancer effects by inhibiting cell proliferation and inducing apoptosis in HepG2 cells. Guggulsterone induces apoptosis by activation of the intrinsic mitochondrial pathway.
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- 2015
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23. Histone deacetylase inhibitor suberoyl bis-hydroxamic acid suppresses cell proliferation and induces apoptosis in breast cancer cells.
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Yang X, Zhang N, Shi Z, Yang Z, and Hu X
- Subjects
- Breast Neoplasms genetics, Breast Neoplasms metabolism, Cell Cycle Checkpoints drug effects, Cell Line, Tumor, Cell Proliferation drug effects, Female, Gene Expression, Humans, MCF-7 Cells, Proto-Oncogene Proteins c-bcl-2 genetics, Proto-Oncogene Proteins c-bcl-2 metabolism, bcl-2-Associated X Protein genetics, bcl-2-Associated X Protein metabolism, Apoptosis drug effects, Histone Deacetylase Inhibitors pharmacology, Hydroxamic Acids pharmacology
- Abstract
Suberoyl bis‑hydroxamic acid (SBHA) is a histone deacetylase inhibitor that has shown anticancer activity against numerous types of human cancer. The aim of the current study was to explore the effects of SBHA on the proliferation and apoptosis of breast cancer cells. MCF‑7 breast cancer cells were treated with different concentrations of SBHA and tested for cell viability, apoptosis and gene expression changes. The results showed that SBHA significantly inhibited the proliferation of MCF‑7 cells in a concentration‑dependent manner, as determined using a Cell Counting kit‑8 assay. SBHA‑treated MCF‑7 cells showed G0/G1 cell‑cycle arrest, coupled with elevated expression levels of p21 and p27 proteins. Hoechst 33258 staining revealed cell shrinkage, chromosomal condensation and nuclear fragmentation in MCF‑7 cells treated with SBHA. Flow cytometric analysis of Annexin V‑stained cells showed that SBHA treatment induced apoptotic cell death in a concentration‑dependent manner. Western blot analysis confirmed the upregulation of Bax and the downregulation of Bcl‑2 by SBHA. In conclusion, these results indicate that SBHA exerts cytotoxic effects against human breast cancer cells, which involves the modulation of p21, p27 and Bcl‑2 family proteins, consequently leading to cell‑cycle arrest and apoptosis.
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- 2015
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24. Nitidine chloride induces apoptosis, cell cycle arrest, and synergistic cytotoxicity with doxorubicin in breast cancer cells.
- Author
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Sun M, Zhang N, Wang X, Cai C, Cun J, Li Y, Lv S, and Yang Q
- Subjects
- Antineoplastic Combined Chemotherapy Protocols pharmacology, Blotting, Western, Doxorubicin administration & dosage, Drug Synergism, Flow Cytometry, Humans, In Situ Nick-End Labeling, MCF-7 Cells, Membrane Potential, Mitochondrial drug effects, Antineoplastic Agents, Phytogenic pharmacology, Apoptosis drug effects, Benzophenanthridines pharmacology, Breast Neoplasms pathology, Cell Cycle Checkpoints drug effects
- Abstract
Medicinal plant extracts have been widely used for cancer treatment. Nitidine chloride (NC) is a natural bioactive alkaloid that has recently been reported to have diverse anticancer properties. We aimed to investigate the cytotoxic effects of NC and the effectiveness of combinatorial treatment including NC and doxorubicin in breast cancer cells. Using MTT and flowcytometry assays, we found that NC induced cell growth inhibition and G2/M cell cycle arrest in a time- and dose-dependent manner both in MCF-7 and MDA-MB-231 breast cancer cell lines. Cancer cell growth inhibition was associated with increased levels of the p53 and p21 proteins. Apoptosis induction by NC treatment was confirmed by JC-1 mitochondrial membrane potential, annexin V-positive cell, and TUNEL staining. Using western blot analysis, we found that NC upregulated the pro-apoptotic proteins Bax, cleaved caspase-9 and -3 and cleaved PARP and that it downregulated the anti-apoptotic proteins Bcl-2 and PARP. By using the PI3K/Akt inhibitor LY294002, we further demonstrated that NC-induced apoptosis might be Akt-specific or dependent. In addition, NC exhibited a synergistic effect with doxorubicin on the growth inhibition of the human breast cancer cell lines MCF-7 and MDA-MB-231. Our study demonstrated the anticancer effect of NC on breast cancer and highlighted the potential clinical application of NC.
- Published
- 2014
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25. Preparation and characterization of monoclonal antibody against human B7-H4 molecule.
- Author
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Zhang N, Fang P, and Gu ZJ
- Subjects
- Antibodies, Monoclonal genetics, Antibodies, Monoclonal metabolism, Antibodies, Monoclonal pharmacology, Apoptosis drug effects, Cell Line, Epitopes genetics, Flow Cytometry, Humans, Hybridomas immunology, Jurkat Cells, V-Set Domain-Containing T-Cell Activation Inhibitor 1 metabolism, Antibodies, Monoclonal immunology, Apoptosis immunology, V-Set Domain-Containing T-Cell Activation Inhibitor 1 immunology
- Abstract
B7-H4, a member of B7 family, is widely expressed in tumor tissues and plays an important role in the negative regulation of T cell immunity. In this study, we report on the establishment and characterization of a functional anti-human B7-H4 monoclonal antibody (MAb) 5G3 through hybridoma method. Flow cytometry analysis showed that MAb 5G3 specifically bound to B7-H4 molecule. Functional experiments indicated that MAb 5G3 could block the inhibitory role of B7-H4 molecule on A549 cells in and reduce the apoptosis of Jurkat cells, suggesting that MAb 5G3 is an antagonistic antibody and a useful tool for further studies of B7-H4 functions in cancers.
- Published
- 2014
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26. Adiponectin promotes pancreatic cancer progression by inhibiting apoptosis via the activation of AMPK/Sirt1/PGC-1α signaling.
- Author
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Huang B, Cheng X, Wang D, Peng M, Xue Z, Da Y, Zhang N, Yao Z, Li M, Xu A, and Zhang R
- Subjects
- AMP-Activated Protein Kinases metabolism, Adiponectin metabolism, Animals, Caspase 3 genetics, Caspase 3 metabolism, Cell Line, Tumor, Cell Proliferation, Disease Progression, Female, Gene Expression Regulation, Neoplastic, HEK293 Cells, Hep G2 Cells, Humans, Immunoblotting, Mice, Inbred C57BL, Mice, Knockout, Mitochondria genetics, Mitochondria metabolism, Pancreatic Neoplasms metabolism, Pancreatic Neoplasms pathology, Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha, RNA Interference, Receptors, Adiponectin genetics, Receptors, Adiponectin metabolism, Reverse Transcriptase Polymerase Chain Reaction, Signal Transduction genetics, Sirtuin 1 metabolism, Transcription Factors metabolism, Tumor Burden genetics, AMP-Activated Protein Kinases genetics, Adiponectin genetics, Apoptosis genetics, Pancreatic Neoplasms genetics, Sirtuin 1 genetics, Transcription Factors genetics
- Abstract
Adiponectin is an adipocyte-secreted adipokine with pleiotropic actions. Clinical evidence has shown that serum adiponectin levels are increased and that adiponectin can protect pancreatic beta cells against apoptosis, which suggests that adiponectin may play an anti-apoptotic role in pancreatic cancer (PC). Here, we investigated the effects of adiponectin on PC development and elucidated the underlying molecular mechanisms. Adiponectin deficiency markedly attenuated pancreatic tumorigenesis in vivo. We found that adiponectin significantly inhibited the apoptosis of both human and mouse pancreatic cancer cells via adipoR1, but not adipoR2. Furthermore, adiponectin can increase AMP-activated protein kinase (AMPK) phosphorylation and NAD-dependent deacetylase sirtuin-1 (Sirt1) of PC cells. Knockdown of AMPK or Sirt1 can increase the apoptosis in PC cells. AMPK up-regulated Sirt1, and Sirt1 can inversely phosphorylate AMPK. Further studies have shown that Sirt1 can deacetylate peroxisome proliferator-activated receptor gamma coactivator 1-alpha (PGC1α), which can increase the expression levels of mitochondrial genes. Thus, adiponectin exerts potent anti-apoptotic effects on PC cells via the activation of AMPK/Sirt1/PGC1α signaling. Finally, adiponectin can elevate β-catenin levels. Taken together, these novel findings reveal an unconventional role of adiponectin in promoting pancreatic cancers, and suggest that the effects of adiponectin on tumorigenesis are highly tissue-dependent.
- Published
- 2014
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27. Edaravone protects against glutamate-induced PERK/EIF2α/ATF4 integrated stress response and activation of caspase-12.
- Author
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Fan J, Long H, Li Y, Liu Y, Zhou W, Li Q, Yin G, Zhang N, and Cai W
- Subjects
- Activating Transcription Factor 4, Animals, Annexin A5 metabolism, Antipyrine pharmacology, Cells, Cultured, Cerebral Cortex cytology, Edaravone, Embryo, Mammalian, Endoplasmic Reticulum drug effects, Endoplasmic Reticulum metabolism, Glutamic Acid toxicity, Microscopy, Electron, Transmission, Microtubule-Associated Proteins metabolism, Neurons ultrastructure, Rats, Rats, Wistar, Statistics, Nonparametric, Time Factors, Antipyrine analogs & derivatives, Apoptosis drug effects, Caspase 12 metabolism, Free Radical Scavengers pharmacology, Neurons drug effects, Signal Transduction drug effects
- Abstract
As a potent novel free radical scavenger, edaravone has been reported to have neuroprotective effects in both animals and humans, although the underlying mechanisms remain unclear. In our study, we generated a culture of almost pure neurons, which were either left untreated or prophylactically treated with edaravone, then exposed to 50 μM glutamate for 10 min. Flow Cytometry analysis was performed to quantify the percentage of apoptotic cells. Ultrastructural changes in the endoplasmic reticulum were observed by electron microscopy. Immunofluorescence and western blotting for activation of selected related molecules, including PERK (pancreatic ER stress kinase, PERK), eIF2α (eukaryotic initiation factor 2 alpha, eIF2α), activating ATF4 (transcription factor 4, ATF4), and caspase-12 were examined. In Glutamate-treated group, the sequential activation of PERK, eIF2α, ATF4 and caspase-12 could be observed at 2h, and peaked at 24h. However, treatment with edaravone was able to prevent these changes. In addition, the morphology of the endoplasmic reticulum was better preserved and the percentage of apoptotic cells was lower in cells treated with edaravone. In summary, our results indicate that ISR (PERK/eIF2/ATF4 integrated stress response, ISR) plays an important role in glutamate-induced nerve cells death, and that edaravone could protect neurons against glutamate-induced endoplasmic reticulum stress., (Copyright © 2013 Elsevier B.V. All rights reserved.)
- Published
- 2013
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28. Expression of bone morphogenetic protein-10 (BMP10) in human urothelial cancer of the bladder and its effects on the aggressiveness of bladder cancer cells in vitro.
- Author
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Zhang N, Ye L, Wu L, Deng X, Yang Y, and Jiang WG
- Subjects
- Blotting, Western, Bone Morphogenetic Proteins genetics, Cell Adhesion, Humans, Immunoenzyme Techniques, In Vitro Techniques, RNA, Messenger genetics, Real-Time Polymerase Chain Reaction, Reverse Transcriptase Polymerase Chain Reaction, Tumor Cells, Cultured, Urinary Bladder metabolism, Urinary Bladder Neoplasms genetics, Urinary Bladder Neoplasms metabolism, Apoptosis, Bone Morphogenetic Proteins metabolism, Cell Movement, Cell Proliferation, Urinary Bladder pathology, Urinary Bladder Neoplasms pathology
- Abstract
Background: Bone morphogenetic protein-10 (BMP10), a novel member of the bone morphogenetic protein (BMP) family, has been indicated as a possible tumour suppressor in prostate and breast cancer. However, its role in urothelial tumours remains unknown. In the present study, we examined the role of BMP10 in urothelial cancer cells and the expression of BMP10 in human urethelial cancer of the bladder., Materials and Methods: The expression of BMP10 was examined in human bladder tissues and in the T24 human bladder cancer cell line using immunochemical staining and reverse transcription polymerase chain reaction (RT-PCR), respectively. The biological impact of modifying BMP10 expression, through genetic manipulation, in urothelial cancer cells was evaluated using in vitro models., Results: mRNA for BMP10 and receptors of BMPs was expressed in T24 cell lines. BMP10 protein expression was observed in normal urothelial and stromal cells, but was found to be decreased in or absent from urothelial cancer cells. The frequency of positive staining in normal tissues (9/9) was significantly higher than that in urothelial cancer tissues (6/15) (p=0.007). T24 cells were transfected with BMP10 expression plasmid. It was further demonstrated that overexpression of BMP10 reduced the growth rate of T24 cells, and markedly reduced the motility, and adhesion of T24 cells in vitro. No significant effects were seen on in vitro invasiveness of T24 cells following BMP10 transfection., Conclusion: Expression of BMP10 protein is reduced in cancer cells of bladder tumours. Overexpression of BMP10 has an inhibitory effect on the growth, adhesion, and migration of bladder cancer cells in vitro. This would suggest a potential tumour suppressor role of BMP10 in bladder cancer.
- Published
- 2013
29. The oncogene metadherin modulates the apoptotic pathway based on the tumor necrosis factor superfamily member TRAIL (Tumor Necrosis Factor-related Apoptosis-inducing Ligand) in breast cancer.
- Author
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Zhang N, Wang X, Huo Q, Li X, Wang H, Schneider P, Hu G, and Yang Q
- Subjects
- Amino Acid Chloromethyl Ketones pharmacology, Animals, Caspase 8 metabolism, Cell Line, Tumor, Cell Survival, Female, Flow Cytometry methods, Humans, Mice, Mice, Nude, MicroRNAs metabolism, Proto-Oncogene Proteins c-bcl-2 metabolism, RNA-Binding Proteins, Recombinant Proteins metabolism, Apoptosis, Breast Neoplasms metabolism, Cell Adhesion Molecules metabolism, Gene Expression Regulation, Neoplastic, Membrane Proteins metabolism, TNF-Related Apoptosis-Inducing Ligand metabolism, Tumor Necrosis Factor-alpha metabolism
- Abstract
Metadherin (MTDH), the newly discovered gene, is overexpressed in more than 40% of breast cancers. Recent studies have revealed that MTDH favors an oncogenic course and chemoresistance. With a number of breast cancer cell lines and breast tumor samples, we found that the relative expression of MTDH correlated with tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) sensitivity in breast cancer. In this study, we found that knockdown of endogenous MTDH cells sensitized the MDA-MB-231 cells to TRAIL-induced apoptosis both in vitro and in vivo. Conversely, stable overexpression of MTDH in MCF-7 cells enhanced cell survival with TRAIL treatment. Mechanically, MTDH down-regulated caspase-8, decreased caspase-8 recruitment into the TRAIL death-inducing signaling complex, decreased caspase-3 and poly(ADP-ribose) polymerase-2 processing, increased Bcl-2 expression, and stimulated TRAIL-induced Akt phosphorylation, without altering death receptor status. In MDA-MB-231 breast cancer cells, sensitization to TRAIL upon MTDH down-regulation was inhibited by the caspase inhibitor Z-VAD-fmk (benzyloxycarbonyl-VAD-fluoromethyl ketone), suggesting that MTDH depletion stimulates activation of caspases. In MCF-7 breast cancer cells, resistance to TRAIL upon MTDH overexpression was abrogated by depletion of Bcl-2, suggesting that MTDH-induced Bcl-2 expression contributes to TRAIL resistance. We further confirmed that MTDH may control Bcl-2 expression partly by suppressing miR-16. Collectively, our results point to a protective function of MTDH against TRAIL-induced death, whereby it inhibits the intrinsic apoptosis pathway through miR-16-mediated Bcl-2 up-regulation and the extrinsic apoptosis pathway through caspase-8 down-regulation.
- Published
- 2013
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30. A selective inhibitor of Drp1, mdivi-1, acts against cerebral ischemia/reperfusion injury via an anti-apoptotic pathway in rats.
- Author
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Zhang N, Wang S, Li Y, Che L, and Zhao Q
- Subjects
- Animals, Brain drug effects, Brain metabolism, Brain pathology, Brain Ischemia drug therapy, Brain Ischemia etiology, Cytochromes c genetics, Cytochromes c metabolism, Dynamins genetics, Dynamins metabolism, Infarction, Middle Cerebral Artery complications, Male, Neurons drug effects, Neurons pathology, Neuroprotective Agents therapeutic use, Quinazolinones therapeutic use, RNA, Messenger metabolism, Rats, Rats, Wistar, Reperfusion Injury drug therapy, Reperfusion Injury etiology, Apoptosis drug effects, Brain Ischemia pathology, Dynamins antagonists & inhibitors, Neuroprotective Agents pharmacology, Quinazolinones pharmacology, Reperfusion Injury pathology
- Abstract
Mitochondrial division inhibitor (mdivi-1) is a derivative of quinazolinone that acts as a selective inhibitor of a mitochondrial fission protein Drp1. A previous study demonstrated that as a selective inhibitor of Drp1, mdivi-1 has a protective effect in an experimental model of heart ischemia/reperfusion injury. In this study, we investigated the protective effects of mdivi-1 on cerebral ischemia/reperfusion injury in a middle cerebral artery occlusion mouse model. We found that mdivi-1 (1.2mg/kg) significantly reduced cerebral damage induced by ischemia/reperfusion. This neuroprotective effect was dose-dependent. Mdivi-1 treatment blocked apoptotic cell death in cerebral ischemia/reperfusion injury, and significantly decreased the expression of Drp1 and Cytochrome C. These results suggest that mdivi-1 exerts neuroprotective effects against nerve injury after cerebral ischemia/reperfusion, and the underlying mechanism may be through the prevention of Cytochrome C release and suppression of the mitochondrial apoptosis pathway., (Crown Copyright © 2013. Published by Elsevier Ireland Ltd. All rights reserved.)
- Published
- 2013
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31. GRIM-19 inhibits the STAT3 signaling pathway and sensitizes gastric cancer cells to radiation.
- Author
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Bu X, Zhao C, Wang W, and Zhang N
- Subjects
- Aged, Apoptosis genetics, Apoptosis Regulatory Proteins genetics, Caspases biosynthesis, Caspases genetics, Cell Line, Tumor, Female, Gene Expression Regulation, Neoplastic genetics, Humans, Male, Middle Aged, NADH, NADPH Oxidoreductases genetics, Neoplasm Proteins genetics, Radiation Tolerance, STAT3 Transcription Factor genetics, Stomach Neoplasms genetics, X-Rays, Apoptosis radiation effects, Apoptosis Regulatory Proteins biosynthesis, Gene Expression Regulation, Neoplastic radiation effects, NADH, NADPH Oxidoreductases biosynthesis, Neoplasm Proteins metabolism, STAT3 Transcription Factor metabolism, Signal Transduction, Stomach Neoplasms metabolism, Stomach Neoplasms radiotherapy
- Abstract
Gastric cancer is one of the most common malignancies, and radiation resistance is one of the key obstacles in gastric cancer treatment. In this study, we demonstrate that "genes associated retinoid-IFN induced mortality-19" (GRIM-19) expression was lower in patients with radiotherapy-resistant tumors compared to patients with radiotherapy-sensitive tumors. In order to further investigate the effects of GRIM-19 expression on the radiation response in gastric cancer cells, we established BGC-803 clones stably expressing exogenous GRIM-19. We found that the percentage of apoptotic cells was higher in cells expressing GRIM-19 than untransfected cells post-radiation treatment. Furthermore, caspase-3, -8, and -9 activity was significantly increased in GRIM-19-expressing cells compared to untransfected cells after radiation. Finally, we demonstrate that expression of GRIM-19 in BGC-803 cells suppresses accumulation of STAT3. Collectively, these data show that GRIM-19 expression sensitizes BGC-803 cells to radiation, and this is likely due to suppression of STAT3 accumulation. In summary, our results indicate that GRIM-19 expression might be a useful therapy to enhance apoptosis in gastric cancer cells in response to radiation treatment., (Copyright © 2012 Elsevier B.V. All rights reserved.)
- Published
- 2013
- Full Text
- View/download PDF
32. Vitamin D analog EB1089 induces apoptosis in a subpopulation of SGC-7901 gastric cancer cells through a mitochondrial-dependent apoptotic pathway.
- Author
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Wang W, Zhao CH, Zhang N, and Wang J
- Subjects
- Calcitriol pharmacology, Caspase 3 genetics, Caspase 3 metabolism, Caspase 9 genetics, Caspase 9 metabolism, Cell Line, Tumor, Humans, Mitochondria pathology, Receptors, Calcitriol genetics, Receptors, Calcitriol metabolism, Reverse Transcriptase Polymerase Chain Reaction, Signal Transduction, Stomach Neoplasms metabolism, bcl-2-Associated X Protein genetics, bcl-2-Associated X Protein metabolism, Antineoplastic Agents pharmacology, Apoptosis drug effects, Calcitriol analogs & derivatives, Mitochondria drug effects, Vitamin D pharmacology
- Abstract
Gastric cancer is the second leading cause of cancer death worldwide. Cancer stem-like side population (SP) cells may be important factors that hinder efficacy of chemopreventative and chemotherapeutic approaches in gastric cancer. EB1089 is an antitumor agent that has been used in many cancers; however, no reports to date have determined the effects of EB1089 in gastric cancer. In our study, SP and main population (MP) cells were isolated from 4 gastric cancer cell lines in different stages of differentiation by flow cytometry (FCM) and confirmed by reverse transcription polymerase chain reaction (RT-PCR) and Western blot. EB1089 decreased the proliferation, increased apoptosis, and induced mitochondrial damage in the SP cells isolated from 1 cell type (SGC-7901), but not MP cells, through increased Bax and decreased Bcl-2 and Bcl-xL protein expression. This protein expression pattern induced the activation of caspase-3 and caspase-9. The effects of EB1089 on SGC-7901 SP cells were blocked by treating cells with vitamin D receceptor (VDR) siRNA or butin (an inhibitor of the mitochondrial apoptosis pathway). Our results suggest that EB1089 targets SGC-7901 SP cells through a mitochondrial apoptosis pathway. However, further studies are needed to elucidate the signal transduction between VDR and the mitochondrial apoptosis pathway.
- Published
- 2013
- Full Text
- View/download PDF
33. Disruption of growth factor receptor-binding protein 10 in the pancreas enhances β-cell proliferation and protects mice from streptozotocin-induced β-cell apoptosis.
- Author
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Zhang J, Zhang N, Liu M, Li X, Zhou L, Huang W, Xu Z, Liu J, Musi N, DeFronzo RA, Cunningham JM, Zhou Z, Lu XY, and Liu F
- Subjects
- Animals, Apoptosis genetics, Cell Proliferation drug effects, Female, GRB10 Adaptor Protein genetics, Immunohistochemistry, Insulin-Secreting Cells, Male, Mice, Mice, Inbred C57BL, Mice, Knockout, Apoptosis drug effects, GRB10 Adaptor Protein metabolism, Pancreas metabolism, Streptozocin pharmacology
- Abstract
Defects in insulin secretion and reduction in β-cell mass are associated with type 2 diabetes in humans, and understanding the basis for these dysfunctions may reveal strategies for diabetes therapy. In this study, we show that pancreas-specific knockout of growth factor receptor-binding protein 10 (Grb10), which is highly expressed in pancreas and islets, leads to elevated insulin/IGF-1 signaling in islets, enhanced β-cell mass and insulin content, and increased insulin secretion in mice. Pancreas-specific disruption of Grb10 expression also improved glucose tolerance in mice fed with a high-fat diet and protected mice from streptozotocin-induced β-cell apoptosis and body weight loss. Our study has identified Grb10 as an important regulator of β-cell proliferation and demonstrated that reducing the expression level of Grb10 could provide a novel means to increase β-cell mass and reduce β-cell apoptosis. This is critical for effective therapeutic treatment of both type 1 and 2 diabetes.
- Published
- 2012
- Full Text
- View/download PDF
34. Edaravone protects cortical neurons from apoptosis by inhibiting the translocation of BAX and Increasing the interaction between 14-3-3 and p-BAD.
- Author
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Fan J, Zhang N, Yin G, Zhang Z, Cheng G, Qian W, Long H, and Cai W
- Subjects
- Animals, Antipyrine pharmacology, Apoptosis physiology, Cell Survival drug effects, Cell Survival physiology, Cells, Cultured, Cerebral Cortex cytology, Edaravone, Female, Fetus cytology, Free Radical Scavengers pharmacology, Microscopy, Electron, Transmission, Mitochondria drug effects, Mitochondria physiology, Mitochondria ultrastructure, Neurons metabolism, Neurons ultrastructure, Neuroprotective Agents pharmacology, Pregnancy, Rats, Rats, Sprague-Dawley, 14-3-3 Proteins metabolism, Antipyrine analogs & derivatives, Apoptosis drug effects, Neurons drug effects, bcl-2-Associated X Protein metabolism, bcl-Associated Death Protein metabolism
- Abstract
Edaravone, a free radical scavenger, has shown neuroprotection properties in both animals and humans. To evaluate the mechanisms involved, we obtained a culture of almost pure neurons. The neurons, either untreated or prophylactically treated with edaravone, were exposed to 300 μM hydrogen peroxide. We examined alterations in mitochondria, the percent of apoptotic cells and the immunoblots of key regulatory proteins, and the protein-protein interactions and the cellular locations of cytochrome c. The levels of p-JNK (Thr183/Tyr185) and cytochrome c in cytosol and BAX in heavy membrane (HM), respectively, were increased at 0.5 h and reached the peak at 12 h after stimulation with hydrogen peroxide. The levels of p-BAD and BAX in the cytosol and the interaction between BAD and 14-3-3 were decreased in the untreated neurons. However, edaravone could prevent these changes. In addition, mitochondrial morphology was better preserved and the percentage of apoptosis was lower under the treatment with edaravone. In summary, the present study indicates that edaravone could protect neurons by inhibiting: (1) the activity of JNK, (2) the disassociation of BAD from 14-3-3, and (3) the translocation of BAX from cytosol to mitochondria.
- Published
- 2012
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- View/download PDF
35. Inflammation & apoptosis in spinal cord injury.
- Author
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Zhang N, Yin Y, Xu SJ, Wu YP, and Chen WS
- Subjects
- Anti-Inflammatory Agents therapeutic use, Antioxidants therapeutic use, Apoptosis drug effects, Humans, Inflammation drug therapy, Spinal Cord Injuries drug therapy, Apoptosis physiology, Inflammation pathology, Spinal Cord Injuries pathology
- Abstract
Spinal cord injury (SCI) consists of a two-steps process involving a primary mechanical injury followed by an inflammatory process and apoptosis. Secondary insult is characterized by further destruction of neuronal and glial cells, and leads to expansion of the damage, so that the paralysis can extend to higher segments. With the identification of mechanisms that either promote or prevent neuronal inflammation and apoptosis come new approaches for preventing and treating neurodegenerative disorders. From a clinical perspective, this article discusses novel targets for the development of therapeutic agents that have the potential to protect the spinal cord from irreversible damage and promote functional recovery.
- Published
- 2012
36. Fank1 interacts with Jab1 and regulates cell apoptosis via the AP-1 pathway.
- Author
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Wang H, Song W, Hu T, Zhang N, Miao S, Zong S, and Wang L
- Subjects
- Animals, B-Cell Lymphoma 3 Protein, COP9 Signalosome Complex, Cell Line, DNA-Binding Proteins physiology, Humans, Intracellular Signaling Peptides and Proteins physiology, Peptide Hydrolases physiology, Proto-Oncogene Proteins metabolism, Proto-Oncogene Proteins c-jun metabolism, Transcription Factor AP-1 metabolism, Transcription Factors physiology, Transfection, Apoptosis, DNA-Binding Proteins metabolism, Intracellular Signaling Peptides and Proteins metabolism, Peptide Hydrolases metabolism, Signal Transduction, Transcription Factors metabolism
- Abstract
Regulation of apoptosis at various stages of differentiation plays an important role in spermatogenesis. Therefore, the identification and characterisation of highly expressed genes in the testis that are involved in apoptosis is of great value to delineate the mechanism of spermatogenesis. Here, we reported that Fank1, a novel gene highly expressed in testis, functioned as an anti-apoptotic protein that activated the activator protein 1 (AP-1) pathway. We found that Jab1 (Jun activation domain-binding protein 1), a co-activator of AP-1, specifically interacted with Fank1. Reporter analyses showed that Fank1 activated AP-1 pathway in a Jab1-dependent manner. Fank1 overexpression also increased the expression and activation of endogenous c-Jun. Further study showed that Fank1 inhibited cell apoptosis by upregulating and activating endogenous c-Jun and its downstream target, Bcl-3. This process was shown to be Jab1 dependent. Taken together, our results indicated that by interacting with Jab1, Fank1 could suppress cell apoptosis by activating the AP-1-induced anti-apoptotic pathway.
- Published
- 2011
- Full Text
- View/download PDF
37. Huaier aqueous extract inhibits proliferation of breast cancer cells by inducing apoptosis.
- Author
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Zhang N, Kong X, Yan S, Yuan C, and Yang Q
- Subjects
- Antineoplastic Agents isolation & purification, Biological Factors isolation & purification, Biological Factors pharmacology, Blotting, Western, Breast Neoplasms metabolism, Breast Neoplasms pathology, Caspase 3 metabolism, Cell Cycle drug effects, Cell Line, Tumor, Cell Movement drug effects, Cell Shape drug effects, Cell Survival drug effects, Dose-Response Relationship, Drug, Female, Flow Cytometry, Humans, Membrane Potential, Mitochondrial drug effects, Proto-Oncogene Proteins c-bcl-2 metabolism, Tumor Suppressor Protein p53 metabolism, bcl-2-Associated X Protein metabolism, Antineoplastic Agents pharmacology, Apoptosis drug effects, Basidiomycota chemistry, Cell Proliferation drug effects
- Abstract
Aqueous extract of Trametes robiniophila murr (Huaier) has been commonly used in China for cancer complementary therapy in recent years; however, the mechanisms of its anticancer effects are largely unknown. In the present study, we aim to investigate its inhibitory effect on both MCF-7 and MDA-MB-231 cells, and explore the possible mechanisms of its anticancer effect. Cell viability and motility were measured by MTT and invasive assays, migration and scratch assays in vitro, respectively. The distribution of cell cycle, PI-Annexin-V staining and Rhodamine 123 assay were analyzed by flow cytometry, and western blot were used to test the apoptotic pathways. We found that Huaier extract could strongly inhibit cell viability of MCF-7 and MDA-MB-231 cells in a time- and dose-dependent manner; however, MDA-MB-231 cells showed more susceptibility to the treatment. Furthermore, cell invasiveness and migration were also suppressed with exposure to Huaier extract. We also indicated that Huaier could induce G0/G1 cell-cycle arrest, p53 accumulation and activation selectively in MCF-7 cells. Inspiringly, the PI-Annexin-V staining assay and western blot analysis confirmed cell apoptosis executed by caspase-3. Decreased mitochondrial membrane potential by Rhodamine 123 assay and down-regulation of Bcl-2 and up-regulation of BCL2-associated X protein (BAX) indicated that Huaier induced apoptosis through the mitochondrial pathway. Caspase activation during Huaier-induced apoptosis was confirmed by pan-caspase inhibitor, Z-VAD-fmk. As expected, the inhibitor decreased Huaier-induced apoptosis in both cell lines. Based on our findings, Huaier can induce cell apoptosis in both ER-positive and ER-negative breast cancer cell lines and is an effective complementary agent for breast cancer treatment., (© 2010 Japanese Cancer Association.)
- Published
- 2010
- Full Text
- View/download PDF
38. A model of ischemia and reperfusion increases JNK activity, inhibits the association of BAD and 14-3-3, and induces apoptosis of rabbit spinal neurocytes.
- Author
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Fan J, Xu G, Nagel DJ, Hua Z, Zhang N, and Yin G
- Subjects
- Animals, Ischemia metabolism, MAP Kinase Kinase 4 antagonists & inhibitors, Mitochondria metabolism, Rabbits, Random Allocation, Signal Transduction, Spinal Cord metabolism, 14-3-3 Proteins metabolism, Apoptosis, Ischemia pathology, MAP Kinase Kinase 4 metabolism, Neurons pathology, Reperfusion Injury pathology, Spinal Cord blood supply, Spinal Cord pathology, bcl-Associated Death Protein metabolism
- Abstract
It is now well established that the protein BAD (a pro-apoptotic Bcl-2 family protein) plays a pivotal role in determining cell death and survival. The c-Jun N-terminal kinase (JNK) pathway has been hypothesized to be involved in regulation of BAD. To clarify the role of BAD within the JNK pathway, a randomized, controlled study was designed using a rabbit model of ischemic spinal cord injury [5,8]. Forty-five white adult New England rabbits were randomly assigned to one of the three groups: sham-operation group (n=5), vehicle group (n=20), and JNK inhibitor group (n=20). We examined alterations in spinal tissue morphology, local concentration and cellular locations of key regulatory proteins, and protein-protein interactions. Changes in spinal cord morphology were observed with hematoxylin and eosin (H&E) staining and electron microscopy. In the vehicle group, the amount of JNK phosphorylation, cytochrome c release, and the interaction between BAD and Bcl-XL or Bcl-2 were increased compared with the JNK inhibitor group. Similarly, the phosphorylation of BAD (Ser136) and the interaction between BAD and 14-3-3 were decreased in the vehicle group. Immunohistochemical studies showed that cytoplasmic location of 14-3-3 and p-BAD (Ser136) were decreased in the vehicle group compared with the JNK inhibitor group. In addition, mitochondrial morphology was better preserved and the percentage of apoptosis was lower when JNK was inhibited. These results indicate that the JNK pathway has a critical role in the survival of neurocytes by regulating the interaction between BAD and 14-3-3., (Published by Elsevier Ireland Ltd.)
- Published
- 2010
- Full Text
- View/download PDF
39. NSC606985 induces apoptosis, exerts synergistic effects with cisplatin, and inhibits hypoxia-stabilized HIF-1alpha protein in human ovarian cancer cells.
- Author
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Zhang N, Zhang H, Xia L, Zheng Y, Yu Y, Zhu Y, Chen G, and Di W
- Subjects
- Camptothecin pharmacology, Caspase 3 metabolism, Cell Line, Tumor, Drug Synergism, Female, Humans, Ovarian Neoplasms pathology, Protein Kinase C-delta metabolism, Antineoplastic Agents pharmacology, Apoptosis drug effects, Camptothecin analogs & derivatives, Cisplatin pharmacology, Hypoxia-Inducible Factor 1, alpha Subunit antagonists & inhibitors, Ovarian Neoplasms drug therapy
- Abstract
The camptothecins, which target the intranuclear enzyme topoisomerase I, have advanced to the forefront of several areas of developmental chemotherapy of cancers. In the present study, we investigated the potential anti-human ovarian cancer effects of NSC606985, a novel and rarely studied camptothecin analog, and its combination with cisplatin (CDDP). Human ovarian cancer cell line COC1 cells were treated with different nanomolar of NSC606985 with or without CDDP, and cell growth and apoptosis were evaluated, respectively, by MTT assay and annexin-V assay on flow cytometry. Chou-Talalay analysis was used to evaluate combined effect of NSC606985 and CDDP. Western blot was used to detect protein kinase Cdelta (PKCdelta), caspase-3 and hypoxia-inducible factor-1alpha (HIF-1alpha) proteins. Our results showed that NSC606985 at nanomolar concentration induced apoptosis with the activation of PKCdelta in COC1 cells. Especially, NSC606985 presented the significant combined effects on COC1 cells in terms of growth inhibition and apoptosis induction. In addition, NSC606985 significantly antagonized the accumulation of HIF-1alpha stabilized by hypoxia or hypoxia-mimetic agent. These results suggest that NSC606985 and its combination with CDDP present the therapeutic potential on ovarian cancer, and deserve further preclinical and clinical studies.
- Published
- 2009
- Full Text
- View/download PDF
40. Melittin, a major component of bee venom, sensitizes human hepatocellular carcinoma cells to tumor necrosis factor-related apoptosis-inducing ligand (TRAIL)-induced apoptosis by activating CaMKII-TAK1-JNK/p38 and inhibiting IkappaBalpha kinase-NFkappaB.
- Author
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Wang C, Chen T, Zhang N, Yang M, Li B, Lü X, Cao X, and Ling C
- Subjects
- Animals, Bees, Carcinoma, Hepatocellular drug therapy, Drug Resistance, Neoplasm drug effects, Enzyme Activation drug effects, HeLa Cells, Humans, I-kappa B Kinase metabolism, Jurkat Cells, NF-kappa B metabolism, Apoptosis drug effects, Calcium-Calmodulin-Dependent Protein Kinase Type 2 metabolism, Carcinoma, Hepatocellular enzymology, Insect Proteins pharmacology, MAP Kinase Kinase 4 metabolism, MAP Kinase Kinase Kinases metabolism, Melitten pharmacology, Neoplasm Proteins metabolism, TNF-Related Apoptosis-Inducing Ligand pharmacology, p38 Mitogen-Activated Protein Kinases metabolism
- Abstract
Promoting apoptosis is a strategy for cancer drug discovery. Tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) induces apoptosis in a wide range of malignant cells. However, several cancers, including human hepatocellular carcinoma (HCC), exhibit a major resistance to TRAIL-induced cell death. Melittin, a water-soluble 26-amino acid peptide derived from bee venom of Apis mellifera, can exert toxic or inhibitory effects on many types of tumor cells. Here we report that melittin can induce apoptosis of HCC cells by activating Ca2+/calmodulin-dependent protein kinase, transforming growth factor-beta-activated kinase 1 (TAK1), and JNK/p38 MAPK. We show that melittin-induced apoptosis can be inhibited by calcium chelator, by inhibitors for Ca2+/calmodulin-dependent protein kinase, JNK and p38, and by dominant negative TAK1. In the presence of melittin, TRAIL-induced apoptosis is significantly increased in TRAIL-resistant HCC cells, which may be attributed to melittin-induced TAK1-JNK/p38 activation and melittin-mediated inhibition of IkappaBalpha kinase-NFkappaB. Our data suggest that melittin can synergize with TRAIL in the induction of HCC cell apoptosis by activating the TAK1-JNK/p38 pathway but inhibiting the IkappaBalpha kinase-NFkappaB pathway. Therefore, the combination of melittin with TRAIL may be a promising therapeutic approach in the treatment of TRAIL-resistant human cancer.
- Published
- 2009
- Full Text
- View/download PDF
41. Ischemic preconditioning suppresses apoptosis of rabbit spinal neurocytes by inhibiting ASK1-14-3-3 dissociation.
- Author
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Yang C, Ren Y, Liu F, Cai W, Zhang N, Nagel DJ, and Yin G
- Subjects
- Animals, Apoptosis Regulatory Proteins metabolism, Brain Ischemia metabolism, Brain Ischemia pathology, Brain Ischemia physiopathology, Disease Models, Animal, JNK Mitogen-Activated Protein Kinases metabolism, Microscopy, Electron, Transmission, Nerve Degeneration metabolism, Nerve Degeneration pathology, Nerve Degeneration physiopathology, Neurons pathology, Phosphorylation, Rabbits, Reperfusion Injury metabolism, Reperfusion Injury pathology, Reperfusion Injury physiopathology, Signal Transduction physiology, Spinal Cord pathology, p38 Mitogen-Activated Protein Kinases metabolism, 14-3-3 Proteins metabolism, Apoptosis physiology, Ischemic Preconditioning, MAP Kinase Kinase Kinase 5 metabolism, Neurons metabolism, Spinal Cord metabolism
- Abstract
The mechanism by which a brief episode of sublethal ischemia followed by reperfusion (ischemic preconditioning, IPC) prevents the lethal effects of subsequent periods of prolonged ischemia, are poorly understood. A completely randomized, controlled study was designed to study the effect of IPC using a rabbit model of ischemic spinal cord injury. Twenty-four white adult New England rabbits were randomly assigned to one of 3 groups (n=8 per group); the groups were assigned as follows: Group I: sham-operation group, Group II: ischemic reperfusion (I/R) group, and Group III: ischemic preconditioning group. Spinal cord ischemia was induced by introducing an infra renal aortic cross-clamp for 30min. Following injury, rabbits were subjected to 30min, 2h, or 8h of reperfusion in Group II. In Group III, subjects underwent three cycles, 5min each, of ischemia followed by 5min of reperfusion, before receiving 30min of ischemia. We previously reported that the association between ASK1 (apoptosis signal-regulating kinase 1) and 14-3-3 played an important role in regulating ischemia/reperfusion spinal cord injuries. To evaluate the effect of ischemic preconditioning in injured spinal cords, we examined alterations in spinal tissue morphology, activation of key members of the ASK1-mediated signaling pathway, and the association between ASK1 and 14-3-3. Changes in spinal cord morphology were observed with hematoxylin and eosin (H&E) staining and electron microscopy. The phosphorylation levels of ASK1, JNK, and p38 were assessed by immunoblot analysis. The association between ASK1 and 14-3-3 was analyzed by co-immunoprecipitation experiments. We observed that swelling of the neurocyte bodies and hemorrhage of the spinal cord were dramatically decreased in Group III compared to Group II. In addition, the degree of apoptosis among neurocytes was reduced in Group III compared to Group II. Finally, the phosphorylation of ASK1, JNK, p38 and the dissociation of ASK1 from 14-3-3 were dramatically decreased in Group III compared with Group II. These results indicate that ischemic preconditioning may have a protective affect against ASK1/14-3-3 dissociation-induced spinal cord injuries.
- Published
- 2008
- Full Text
- View/download PDF
42. Depletion of mitochondrial DNA by ethidium bromide treatment inhibits the proliferation and tumorigenesis of T47D human breast cancer cells.
- Author
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Yu M, Shi Y, Wei X, Yang Y, Zhou Y, Hao X, Zhang N, and Niu R
- Subjects
- Animals, Breast Neoplasms pathology, Cell Line, Tumor, DNA, Mitochondrial metabolism, DNA, Mitochondrial ultrastructure, Female, Humans, Mice, Microscopy, Electron, Transmission, Mitochondrial Membranes metabolism, Mitochondrial Membranes ultrastructure, Neoplasm Transplantation, Neoplasms, Experimental metabolism, Neoplasms, Experimental pathology, Apoptosis drug effects, Cell Proliferation drug effects, DNA, Mitochondrial drug effects, Ethidium pharmacology, Membrane Potential, Mitochondrial drug effects, Mitochondrial Membranes drug effects
- Abstract
In order to investigate the role of mitochondrial DNA (mtDNA) in human breast cancer cell proliferation and apoptosis, a mtDNA-deficient cell line, T47D rho(0), was generated following a long-term exposure to ethidium bromide (EtBr). T47D rho(0) cells showed a marked decrease in mitochondrial membrane potential (DeltaPsi(m)). However, the apoptosis rate of T47D rho(0) cells was the same as that of their parental cells, suggesting that the change in DeltaPsi(m) was insufficient to induce cell death. Electromicroscopy revealed a profound alteration of mitochondrial morphology, which was consistent with the loss of mtDNA and the decrease in DeltaPsi(m). Disruption of mtDNA resulted in a slower proliferation rate in tissue culture and a reduction in anchorage-independent growth. An in vivo assay revealed a severe impairment of tumorigenicity in T47D rho(0) cells, indicating the biological relevance of in vitro studies. Taken together, our results suggest that the integrity of mtDNA plays a critical role in human breast cancer cell proliferation and tumorigenesis.
- Published
- 2007
- Full Text
- View/download PDF
43. [Regulatory function of nuclear factor kappa B on lymphocyte proliferation and apoptosis in bronchial asthmatic rats and effect of triptolide on the regulation].
- Author
-
Zhang N, Xu YJ, and Zhang ZX
- Subjects
- Animals, Anti-Inflammatory Agents, Non-Steroidal pharmacology, Asthma pathology, Cell Division drug effects, Dexamethasone pharmacology, Epoxy Compounds, Lung metabolism, Male, Random Allocation, Rats, Rats, Wistar, Transcription Factor RelA, Apoptosis drug effects, Asthma metabolism, Diterpenes pharmacology, Lymphocytes pathology, NF-kappa B metabolism, Phenanthrenes pharmacology
- Abstract
Objective: To investigate whether nuclear factor kappa B (NF-kappa B) participates in the regulatory function of lymphocyte proliferation and apoptosis in bronchial asthma and whether the regulatory effect of triptolide on lymphocyte proliferation and apoptosis is conducted through NF-kappa B., Methods: Intervention with dexamethasone, triptolide and PDTC, a NF-kappa B inhibitor, were used to treat astmatic rats respectively. Pathological examination, airway response were determined, the NF-kappa B P65 expression in lung tissue and splenic lymphocytes by immunofluorescent assay were adopted, proliferative cell nuclear antigen (PCNA) in splenic lymphocytes was measured by immunohistochemistry, apoptosis of splenic lymphocytes were monitored by flow cytometry and NF-kappa B activity was investigated by electrophoresis mobility shift assay (EMSA)., Results: The nuclear expression and DNA binding activity of lung tissue and splenic lymphocytes in asthmatic rats were all significantly higher than those in the control (all P < 0.05), so was the proliferation rate of splenic lymphocytes (P < 0.05), while the apoptosis rate was much lower than that of normal control (P < 0.05). Administration of PDTC could reduce the up-regulated expression and activity of NF-kappa B, the proliferation of splenic lymphocytes lowered, while the apoptosis increased. NF-kappa B activity showed an obviously positive correlation with proliferation of splenic lymphocytes (r = 0.89, P < 0.05) and a significantly negative correlation with apoptosis rate (r = -0.54, P < 0.05). After asthmatic rats had been treated with triptolide in vivo, the NF-kappa B nuclear expression and activity in airway and splenic lymphocytes, as well as the proliferation rate of splenic lymphocytes all lowered significantly (all P < 0.05), the apoptosis rate increased significantly (P < 0.05), at the same time, the inflammatory cell infiltration and high reactivity of airway were significantly alleviated (both P < 0.05). There were obviously positive correlation between the amount of airway eosinophils and reactivity with activity of NF-kappa B (r = 0.79 and r = 0.68, P < 0.05), which indicated that the effect of triptolide was not significantly different from that of dexamethasone (P > 0.05)., Conclusion: (1) NF-kappa B participates the formation of airway inflammation and hyper-reactivity in asthmatic rats by positive regulation on proliferation and negative regulation on apoptosis of lymphocytes. (2) Triptolide reduces airway inflammation by way of inhibiting NF-kappa B, and further inhibiting the proliferation of lymphocytes, so that to give full play of the role of anti-asthmatic airway inflammatory agents. Whether the molecular mechanism of triptolide in inhibiting NF-kappa B simulates that of glucocorticoid needs further studying.
- Published
- 2004
44. [Experimental study of apoptosis and proliferation of gastric mucosal cells in chronic atrophic gastritis].
- Author
-
Zhang LX, Zhang L, Xu JR, Jia CH, Zhang NX, and Cao GZ
- Subjects
- Animals, Cell Division, DNA analysis, Gastric Mucosa metabolism, Gastritis, Atrophic metabolism, Male, Proliferating Cell Nuclear Antigen biosynthesis, Proto-Oncogene Proteins c-bcl-2 biosynthesis, Rats, Rats, Sprague-Dawley, fas Receptor biosynthesis, Apoptosis, Gastric Mucosa pathology, Gastritis, Atrophic pathology
- Abstract
Objective: To study the relationship between long-term high-salt hot diet and chronic atrophic gastritis (CAG). The expression of apoptosis cells, proliferation cells, bcl-2 and Fas proteins were detected in the gastric mucosa of CAG rates induced by high-salt hot water., Methods: TUNEL technique and immunohistochemical method were used in the experiment. Flow cytometry method was used to detect the DNA content of apoptosis cells., Results: (1) The detection of apoptosis with TUNEL showed that the apoptosis cells in CAG rates induced by high-salt hot water were high. These cells could be seen in all layers of gastric mucosa, apoptosis index of model rates was higher than that of normal rates (P < 0.05). (2) The result of detecting apoptosis gene and proliferating cell nuclear antigen (PCNA) by immunohistochemical method showed that the expression of bcl-2, Fas and PCNA in the CAG rates induced by high-salt hot water was much higher than that of normal gastric mucosa (P < 0.05). The expression rates of bcl-2, Fas proteins were higher with time going on. After being given high-salt hot water intragastrically for 4, 8, 12 weeks, the bcl-2 protein expression rates were 12.5%, 16.7%, 76.5%, the Fas protein expression rates were 18.7%, 22.2% and 64.7%. (3) Flow cytometry technique showed that there was a second G(0)/G(1) peek, which was apoptosis cells peak, but was not seen in the normal gastric mucosa., Conclusions: Abnormality of proliferation and apoptosis in gastric mucosa could be induced by high-salt hot water. bcl-2, Fas gene played an important role in this course.
- Published
- 2003
45. Mechanisms of ammonotelism, epithelium damage, cellular apoptosis, and proliferation in gill of Litopenaeus vannamei under NH4Cl exposure
- Author
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Li, Yaobing, Zhang, Xin, Tong, Ruixue, Xu, Qiuhong, Zhang, Ning, Liao, Qilong, and Pan, Luqing
- Published
- 2024
- Full Text
- View/download PDF
46. Huogu injection protects against SONFH by promoting osteogenic differentiation of BMSCs and preventing osteoblast apoptosis
- Author
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Zhang, Xin, Li, Ziyu, Xu, Xilin, Liu, Zhao, Hao, Yuanyuan, Yang, Fubiao, Li, Xiaodong, Zhang, Ning, Hou, Yunlong, and Zhang, Xiaofeng
- Published
- 2024
- Full Text
- View/download PDF
47. Radix Scrophulariae Extracts Exert Effect on Hyperthyroidism via MST1/Hippo Signaling Pathway
- Author
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Zhang, Ning, Ye, Tao, Lu, Xu, Li, Zi-hui, and Li, Ling
- Published
- 2023
- Full Text
- View/download PDF
48. Potential pathway and mechanisms underlining the immunotoxicity of benzo[a]pyrene to Chlamys farreri
- Author
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Lei, Fengjun, Zhang, Ning, Miao, Jingjing, Tong, Ruixue, Li, Yaobing, and Pan, Luqing
- Published
- 2023
- Full Text
- View/download PDF
49. Bcl-2 and Noxa are potential prognostic indicators for patients with gastroenteropancreatic neuroendocrine neoplasms
- Author
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Guo, Yu, Zhang, Lin, Zhang, Ning, Chen, Luohai, Luo, Qiuyun, Liu, Man, Yang, Dajun, and Chen, Jie
- Published
- 2022
- Full Text
- View/download PDF
50. The Role of Ferroptosis in Amyotrophic Lateral Sclerosis Treatment.
- Author
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Wang, Le Yi, Zhang, Lei, Bai, Xin Yue, Qiang, Rong Rong, Zhang, Ning, Hu, Qian Qian, Cheng, Jun Zhi, Yang, Yan Ling, and Xiang, Yang
- Subjects
AMYOTROPHIC lateral sclerosis ,APOPTOSIS ,DRUG accessibility ,NEURODEGENERATION ,REACTIVE oxygen species - Abstract
Amyotrophic lateral sclerosis (ALS) is a rare neurodegenerative disease with a challenging treatment landscape, due to its complex pathogenesis and limited availability of clinical drugs. Ferroptosis, an iron-dependent form of programmed cell death (PCD), stands distinct from apoptosis, necrosis, autophagy, and other cell death mechanisms. Recent studies have increasingly highlighted the role of iron deposition, reactive oxygen species (ROS) accumulation, oxidative stress, as well as systemic Xc- and glutamate accumulation in the antioxidant system in the pathogenesis of amyotrophic lateral sclerosis. Therefore, targeting ferroptosis emerges as a promising strategy for amyotrophic lateral sclerosis treatment. This review introduces the regulatory mechanism of ferroptosis, the relationship between amyotrophic lateral sclerosis and ferroptosis, and the drugs used in the clinic, then discusses the current status of amyotrophic lateral sclerosis treatment, hoping to provide new directions and targets for its treatment. [ABSTRACT FROM AUTHOR]
- Published
- 2024
- Full Text
- View/download PDF
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