9 results on '"Liu, Yan"'
Search Results
2. Synthesis, characterization, and in vitro antitumor properties of gold(III) compounds with the traditional Chinese medicine (TCM) active ingredient liriodenine.
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Chen, Zhen-Feng, Liu, Yan-Cheng, Peng, Yan, Hong, Xue, Wang, Hong-Hong, Zhang, Min-Min, and Liang, Hong
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ANTINEOPLASTIC agents , *GOLD compounds , *CHINESE medicine , *BIOACTIVE compounds , *DNA topoisomerase I , *CELL-mediated cytotoxicity , *DNA-ligand interactions , *CANCER cells , *X-ray crystallography ,THERAPEUTIC use of alkaloids - Abstract
Liriodenine, an oxoaporphine alkaloid with anticancer activity isolated from Zanthoxylum nitidum (rutaceous anticancer traditional Chinese medicine), was selected as a bioactive ligand to react with HAuCl and NaAuCl to afford [LH][AuCl] ( 1) and [AuClL] ( 2), respectively (where L is liriodenine). The structures of 1 and 2 were characterized by IR spectroscopy, electrospray ionization mass spectrometry, H-NMR spectroscopy, and elemental analysis. The single-crystal X-ray diffraction analysis of 1 revealed that it is an ionic compound consisting of protonated liriodenine cation [LH] and [AuCl] anion. The spectroscopic analysis showed that 2 is a coordination compound, in which one liriodenine coordinates to gold via its 7-N donor. In aqueous solution, 1 is relatively stable, but 2 undergoes rapid hydrolysis. The in vitro cytotoxicity towards five human tumor cell lines shows that 1 and 2 manifest roughly similar biological behavior and appreciable antiproliferative properties, with IC values falling in the 2-16 μM range. The flow-cytometric analysis of 1 and 2 suggests that both compounds induced an S-phase arrest. Compounds 1 and 2 significantly poison topoisomerase I in vitro at low concentration (25 μM or less). DNA binding studies indicate that both 1 and 2 interact with DNA mainly via intercalation between the neighboring base pairs of the DNA double helix. Electrostatic interactions of 1 and 2 with the polyanionic DNA phosphate backbone may reinforce the intercalation because both 1 and 2 are composed of planar cationic species. Graphical abstract: Two liriodenine (L) gold(III) compounds [LH][AuCl] ( 1) and [AuClL] ( 2) were synthesized. The in vitro cytotoxicity towards five human tumor cell lines was tested and shows that 1 and 2 manifest appreciable antiproliferative properties, with IC values falling in the 2-16 μM range. Both 1 and 2 interact with DNA mainly via an intercalation mode, but electrostatic binding may exist. They both inhibit topoisomerase I activity at low concentration (25 μM or less). [Figure not available: see fulltext.] [ABSTRACT FROM AUTHOR]
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- 2012
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3. Moderate static magnetic fields enhance antitumor CD8+ T cell function by promoting mitochondrial respiration.
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Zhu, Xiaoyan, Liu, Yan, Cao, Xianxia, Liu, Haifeng, Sun, Ao, Shen, Hao, Zhao, Jingyao, Li, Ronghong, Wu, Ligang, Fang, Zhicai, Wang, Hui, and Zhai, Qiwei
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ANTINEOPLASTIC agents , *T cells , *ANIMAL behavior , *MAGNETIC fields , *MITOCHONDRIAL physiology - Abstract
With the discovery of magnetoreceptor mechanisms in animals, it materialized the novel applications of controlling cell and animal behaviors using magnetic fields. T cells have shown to be sensitive to magnetic fields. Here, we reported that exposure to moderate SMFs (static magnetic fields) led to increased granule and cytokine secretion as well as ATP production and mitochondrial respiration from CD8+ T cells. These effects were inhibited by knocking down the Uqcrb and Ndufs6 genes of mitochondrial respiratory chain, whose transcriptions were regulated by candidate magnetoreceptor genes Isca1 and Cry1/Cry2. SMF exposure also promoted CD8+ T cell granule and cytokine secretion and repressed tumor growth in vivo. SMFs enhanced CD8+ T cell cytotoxicity, and the adoptive transfer into tumor-bearing mice resulted in enhanced antitumor effects. Collectively, our study suggests that moderate SMFs enhance CD8+ T cell cytotoxicity by promoting mitochondrial respiration and promoted the antitumor function of CD8+ T cells. [ABSTRACT FROM AUTHOR]
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- 2020
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4. QSAR analysis of substituted benzylamino- and heterocyclylmethylamino-carbodithioate derivatives of 4-(3H)-quinazolinone using CoMFA and SCORE2.0.
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Liu Feng, Liu Shiying, Liu Yan, Han Daxiong, Jiang Yuyang, Cao Shengli, and Zhao Yufen
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ANTINEOPLASTIC agents , *DNA synthesis , *QSAR models , *BIOCHEMISTRY , *ENZYMES - Abstract
Thymidylate synthase (TS) is a critical enzyme for DNA biosynthesis and many nonclassical lipophilic antifolates targeting this enzyme are quite eflicient and encouraging as antitumor drugs. In this paper, the binding model of 14 antifolates of substituted benzylamino- and heterocyclylmethylamino-carbodithioate derivatives of 4-(3H)-quinazolinone with TS is examined using molecular simulation methods—FlexiDock and SCORE2.0. The resulting conformation and orientation of these antifolates are directly applied to CoMFA study. The robust QSAR model, its three-dimensional contour map, and binding score of these antifolates derived from SCORE2.0 provide guidelines for structural optimization of current antifolates. The experiment indicates that deletion of cancer chemopreventive structure of dithiocarbamate is unfavorable for interaction between TS and antifolates. [ABSTRACT FROM AUTHOR]
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- 2007
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5. Glycine metabolomic changes induced by anticancer agents in A549 cells.
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Guo, Kaiqiang, Cao, Yin, Li, Zan, Zhou, Xiaoxiao, Ding, Rong, Chen, Kejing, Liu, Yan, Qiu, Yingkun, Wu, Zhen, and Fang, Meijuan
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BETAINE , *GLYCINE , *ANTINEOPLASTIC agents , *GLYCINE receptors , *CANCER cell proliferation , *PRINCIPAL components analysis , *METHIONINE metabolism , *CELL metabolism - Abstract
Glycine plays a key role in rapidly proliferating cancer cells such as A549 cells. Targeting glycine metabolism is considered as a potential means for cancer treatment. However, the drug-induced alterations in glycine metabolism have not yet been investigated. Herein, a total of 34 glycine metabolites were examined in A549 cells with or without anticancer drug treatment. This work showed all tested anticancer agents could alter glycine metabolism in A549 cells including inhibition of pyruvate metabolism and down-regulation of betaine aldehyde and 5′-phosphoribosylglycinamide. Principal component analysis and orthogonal partial least-squares discrimination analysis exhibited the difference between control and each drug-treated group. In general, cisplatin, camptothecin, and SAHA could induce the significant down-regulation of more metabolites, compared with afatinib, gefitinib, and targretin. Both glycine, serine and threonine metabolism, and purine metabolism were significantly disturbed by the treatment with afatinib, gefitinib, and targretin. However, the treatment using cisplatin, camptothecin, and SAHA was considered to be highly responsible for the perturbation of glycine, serine and threonine metabolism, and cysteine and methionine metabolism. Finally, multivariate analysis for control and all drug-treated groups revealed 11 altered metabolites with a significant difference. It implies anti-cancer agents with different mechanisms of action might induce different comprehensive changes of glycine metabolomics. The current study provides fundamental insights into the acquisition of the role of anti-cancer agents in glycine metabolism while suppressing cancer cell proliferation, and may aid the development of cancer treatment targeting glycine metabolism. [ABSTRACT FROM AUTHOR]
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- 2020
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6. WBP2 modulates G1/S transition in ER+ breast cancer cells and is a direct target of miR-206.
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Ren, Yong-qiang, Wang, Hui-jun, Zhang, Yong-qing, and Liu, Yan-bing
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BREAST cancer prognosis , *TARGETED drug delivery , *MICRORNA , *CARRIER proteins , *TAMOXIFEN , *BREAST cancer treatment , *GENETIC overexpression , *ANTINEOPLASTIC agents , *BINDING sites , *BREAST tumors , *CELL lines , *CELL physiology , *DRUG resistance in cancer cells , *GENETIC techniques , *PROGNOSIS , *PROTEINS , *RNA , *CELL cycle proteins , *PHARMACODYNAMICS - Abstract
Purpose: The mechanisms underlying the oncogenic properties of WW domain binding protein 2 (WBP2) in breast cancer have not been fully understood. In this study, we explored the role of WBP2 in cell cycle regulation in ER+ breast cancer cells and how it is regulated in the cancer cells.Methods: The association between WBP2 expression and prognosis in ER+ breast cancer was assessed by data mining in Breast Cancer Gene-Expression Miner v4.0. Cell cycle was assessed by PI staining and flow cytometry. EdU staining was applied to visualize cells in S phase. The binding between miR-206 and WBP2 were verified by dual luciferase assay. CCK-8 assay and flow cytometric analysis were applied to assess the functional role of WBP2 and miR-206 in the cancer cells.Results: High WBP2 expression correlates with higher risk of any events (AE) and metastatic relapse (MR) and also indicates shorter AE-free survival and MR-free survival in ER+ breast cancer patients. In both MCF-7 and BT474 cells, WBP can influence the expression of G1/S-related cell cycle proteins, including p21, CDK4, and cyclin D1. In addition, WBP2 overexpression resulted in facilitated G1/S transition, while WBP2 knockdown impaired the transition. The 3'UTR of WBP2 has a conserved miR-206 binding site. Functionally, miR-206 knockdown decreased tamoxifen sensitivity in tamoxifen-sensitive (TamS) MCF-7 cells, while miR-206 overexpression and WBP2 knockdown enhanced the sensitivity in tamoxifen-resistant (TamR) MCF-7 cells.Conclusion: Based on these findings, we infer that the miR-206/WBP2 axis can modulate tamoxifen sensitivity via regulating G1/S progression in ER+ breast cancer. [ABSTRACT FROM AUTHOR]- Published
- 2017
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7. Pterocarpans from the Stems and Leaves of Ochrosia elliptica.
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Chen, A-Hong, Liu, Qing-Long, Ma, Yan-Lei, Jiang, Zhi-Hua, Tang, Jin-Ying, Liu, Yan-Ping, Chen, Guang-Ying, Xu, Wei, and Fu, Yan-Hui
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PTEROCARPANS , *PLANT stems , *LEAVES , *APOCYNACEAE , *ANTINEOPLASTIC agents - Published
- 2018
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8. Enhanced antitumor efficacy of a novel oncolytic adenovirus combined with temozolomide in the treatment of melanoma in vivo.
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Jiang, Guan, Sun, Chao, Li, Rong-Hua, Wei, Zhi-Ping, Zheng, Jun-Nian, and Liu, Yan-Qun
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ANTINEOPLASTIC agents , *DRUG efficacy , *ADENOVIRUS diseases , *MELANOMA treatment , *TEMOZOLOMIDE , *COMBINATION drug therapy , *THERAPEUTICS - Abstract
Purpose: The aim of this study was to investigate the effect of Ki67-ZD55-IL-24 with temozolomide (TMZ) against melanoma in mice. Methods: Seventy-eight mice with subcutaneous injection of A375 cells (2 × 10) into the right flank were randomized to receive phosphate buffered saline (PBS), Ki67-ZD55, Ki67-ZD55-IL-24, TMZ, TMZ + Ki67-ZD55, and TMZ + Ki67-ZD55-IL-24. Six mice were killed in each group 10 days after intervention for detecting IL-24 mRNA and protein expression. The remaining mice were monitored to draw the body weight change curve and tumor growth curve, and killed 30 days after intervention. Tumors were excised and weighted. The morphology of tumor tissues was determined by hematoxylin and eosin (HE) staining, and the apoptosis index and rate of apoptotic cells were determined by TUNEL assay and AnnexinV-FITC/PI double staining, respectively. Results: The Ki67-ZD55-IL-24-treated group generated much more reactive oxygen species than the untreated group. There was no significant difference in IL-24 expression between Ki67-ZD55-IL-24 and TMZ + Ki67-ZD55-IL-24 groups. Immunohistochemical analysis and Western blot revealed that both the Ki67-ZD55 and Ki67-ZD55-IL-24 could significantly reduce the expression of MGMT. Toxicity assessments demonstrated that mice in the three groups that received TMZ exhibited significant body weight loss following treatment. HE staining showed that TMZ + Ki67-ZD55-IL-24 group had much fewer karyokinesis in the tumors, compared with other groups. The apoptosis index of tumor tissues and the rate of apoptotic cells were significantly higher in TMZ + Ki67-ZD55-IL-24 group than in other groups (all P < 0.05). Conclusions: These findings indicate this novel strategy holds promising potentials for treatment of malignant melanoma. [ABSTRACT FROM AUTHOR]
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- 2015
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9. Inhibition of autophagy enhances anticancer effects of bevacizumab in hepatocarcinoma.
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Guo, Xian-ling, Li, Ding, Sun, Kai, Wang, Jin, Liu, Yan, Song, Jian-rui, Zhao, Qiu-dong, Zhang, Shan-shan, Deng, Wei-jie, Zhao, Xue, Wu, Meng-chao, and Wei, Li-xin
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LIVER cancer , *BEVACIZUMAB , *AUTOPHAGY , *ANTINEOPLASTIC agents , *REACTIVE oxygen species - Abstract
Angiogenesis inhibitors have long been considered desirable anticancer agents. However, it was found that many tumors could develop resistance to antiangiogenesis inhibitors. Antiangiogenic therapy results in metabolic stress. Autophagy is an important survival mechanism in cancer cells under metabolic stress; however, it remains unknown if autophagy contributes to antiangiogenesis resistance. In this study, we reported that bevacizumab treatment reduced the development of new blood vessels and inhibited cell growth in xenografts of hepatocellular carcinoma (HCC) tumors. Bevacizumab treatment also upregulated expression of the autophagy-related genes (Beclin1 and LC3) and increased autophagosome formation. Our in vitro studies demonstrated that autophagy inhibition significantly increased apoptosis of HCC cells during nutrient starvation or hypoxia. In addition, the combined treatment of an autophagy inhibitor and bevacizumab markedly inhibited the tumor growth of HCC xenografts, led to enhanced apoptosis, and impaired the proliferation of tumor cells compared with treatment with either drug alone. Furthermore, autophagy inhibition led to enhanced reactive oxygen species (ROS) generation in HCC cells exposed to nutrient starvation or hypoxia in vitro and increased DNA oxidative damage in vivo. Antioxidants reduced nutrient starvation or the hypoxia-induced cell death of HCC cells after autophagy inhibition. Our results suggest that autophagy modulates ROS generation and contributes to cell survival under metabolic stress. Therefore, autophagy inhibition may be a novel way of increasing the efficicacy of antiangiogenic agents in the treatment of HCC. [ABSTRACT FROM AUTHOR]
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- 2013
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