22 results on '"Meiyan Qi"'
Search Results
2. Shizukaol D, a Dimeric Sesquiterpene Isolated from Chloranthus serratus, Represses the Growth of Human Liver Cancer Cells by Modulating Wnt Signalling Pathway.
- Author
-
Lisha Tang, Hengrui Zhu, Xianmei Yang, Fang Xie, Jingtao Peng, Deke Jiang, Jun Xie, Meiyan Qi, and Long Yu
- Subjects
Medicine ,Science - Abstract
Natural products have become sources of developing new drugs for the treatment of cancer. To seek candidate compounds that inhibit the growth of liver cancer, components of Chloranthus serratus were tested. Here, we report that shizukaol D, a dimeric sesquiterpene from Chloranthus serratus, exerted a growth inhibition effect on liver cancer cells in a dose- and time-dependent manner. We demonstrated that shizukaol D induced cells to undergo apoptosis. More importantly, shizukaol D attenuated Wnt signalling and reduced the expression of endogenous Wnt target genes, which resulted in decreased expression of β-catenin. Collectively, this study demonstrated that shizukaol D inhibited the growth of liver cancer cells by modulating Wnt pathway.
- Published
- 2016
- Full Text
- View/download PDF
3. Polarity Protein AF6 Controls Hepatic Glucose Homeostasis and Insulin Sensitivity by Modulating IRS1/AKT Insulin Pathway in an SHP2-Dependent Manner
- Author
-
Yanjun Wu, Lixing Zhan, Yi Xu, Weiwei Ji, Cheng Dai, Xinyu Wang, Shu Zhuo, and Meiyan Qi
- Subjects
Male ,0301 basic medicine ,medicine.medical_specialty ,Endocrinology, Diabetes and Metabolism ,Kinesins ,Protein Tyrosine Phosphatase, Non-Receptor Type 11 ,030209 endocrinology & metabolism ,Myosins ,Carbohydrate metabolism ,Diet, High-Fat ,Cell Line ,Diabetes Mellitus, Experimental ,Mice ,03 medical and health sciences ,chemistry.chemical_compound ,0302 clinical medicine ,Insulin resistance ,Internal medicine ,Internal Medicine ,medicine ,Animals ,Homeostasis ,Insulin ,Protein kinase B ,Mice, Knockout ,Glucose tolerance test ,medicine.diagnostic_test ,biology ,Glycogen ,Chemistry ,Glucose Tolerance Test ,medicine.disease ,IRS1 ,Insulin receptor ,Glucose ,030104 developmental biology ,Endocrinology ,Liver ,Knockout mouse ,Hepatocytes ,Insulin Receptor Substrate Proteins ,biology.protein ,Insulin Resistance ,Proto-Oncogene Proteins c-akt ,Signal Transduction - Abstract
Insulin resistance is a major contributing factor in the development of metabolic disease. Although numerous functions of the polarity protein AF6 (afadin and MLLT4) have been identified, a direct effect on insulin sensitivity has not been previously described. We show that AF6 is elevated in the liver tissues of dietary and genetic mouse models of diabetes. We generated liver-specific AF6 knockout mice and show that these animals exhibit enhanced insulin sensitivity and liver glycogen storage, whereas overexpression of AF6 in wild-type mice by adenovirus-expressing AF6 led to the opposite phenotype. Similar observations were obtained from in vitro studies. In addition, we discovered that AF6 directly regulates IRS1/AKT kinase-mediated insulin signaling through its interaction with Src homology 2 domain-containing phosphatase 2 (SHP2) and its regulation of SHP2’s tyrosine phosphatase activity. Finally, we show that knockdown of hepatic AF6 ameliorates hyperglycemia and insulin resistance in high-fat diet–fed or db/db diabetic mice. These results demonstrate a novel function for hepatic AF6 in the regulation of insulin sensitivity, providing important insights about the metabolic role of AF6.
- Published
- 2019
4. Lin28B-high breast cancer cells promote immune suppression in the lung pre-metastatic niche via exosomes and support cancer progression
- Author
-
Meiyan Qi, Yun Xia, Yanjun Wu, Zhuo Zhang, Xinyu Wang, Liying Lu, Cheng Dai, Yanan Song, Keying Xu, Weiwei Ji, and Lixing Zhan
- Subjects
CD4-Positive T-Lymphocytes ,Lung Neoplasms ,Neutrophils ,General Physics and Astronomy ,Breast Neoplasms ,CD8-Positive T-Lymphocytes ,Exosomes ,General Biochemistry, Genetics and Molecular Biology ,Mice ,Cell Line, Tumor ,Immune Tolerance ,Animals ,Humans ,Lung ,Mice, Inbred BALB C ,Multidisciplinary ,Macrophages ,RNA-Binding Proteins ,General Chemistry ,Fibroblasts ,Prognosis ,Gene Expression Regulation, Neoplastic ,Mice, Inbred C57BL ,MicroRNAs ,HEK293 Cells ,Neutrophil Infiltration ,Female - Abstract
The formation of pre-metastatic niche is a key step in the metastatic burden. The pluripotent factor Lin28B is frequently expressed in breast tumors and is particularly upregulated in the triple negative breast cancer subtype. Here, we demonstrate that Lin28B promotes lung metastasis of breast cancer by building an immune-suppressive pre-metastatic niche. Lin28B enables neutrophil recruitment and N2 conversion. The N2 neutrophils are then essential for immune suppression in pre-metastatic lung by PD-L2 up-regulation and a dysregulated cytokine milieu. We also identify that breast cancer-released exosomes with low let-7s are a prerequisite for Lin28B-induced immune suppression. Moreover, Lin28B-induced breast cancer stem cells are the main sources of low-let-7s exosomes. Clinical data further verify that high Lin28B and low let-7s in tumors are both indicators for poor prognosis and lung metastasis in breast cancer patients. Together, these data reveal a mechanism by which Lin28B directs the formation of an immune-suppressive pre-metastatic niche.
- Published
- 2021
5. Experience of verbal violence among Chinese nursing students in clinical practice: a qualitative study
- Author
-
Meiyan Qian, Pingting Zhu, Qiwei Wu, Wen Wang, Guanghui Shi, Yinwen Ding, Hui Zhang, Xinyue Gu, Ting Xu, and QianQian Zhang
- Subjects
Chinese ,Nursing students ,Qualitative research ,Verbal violence ,Workplace violence ,Special aspects of education ,LC8-6691 ,Medicine - Abstract
Abstract Background Workplace violence is prevalent in the nursing profession, and as a relatively junior link of the professional hierarchy, nursing students are not immune to it. Among these, verbal violence may have more serious consequences for the victims than physical violence, but the literature on verbal violence among nursing students in Chinese clinical settings is limited. Aims To explore the verbal violence experience among Chinese nursing students in clinical practice, and the strategies used by nursing students to cope with violence. Design A descriptive qualitative study. Methods From January 2022 to June 2022, semi-structured interviews were conducted with 21 nursing students in clinical practice by purposive snowball sampling. Nvivo12 software and inductive content analysis were used for data analysis. This paper followed the COREQ (Consolidated criteria for Reporting Qualitative Research) guidance. Results Through data analysis, three themes were defined:(1) Multiform verbal violence; (2) Hurting and impacting and (3) Struggling or Coping. The findings indicated that nursing students were subjected to multiple forms of verbal violence in clinical practice, not only from patients and caregivers, but also from peers such as clinical tutors and doctors, which not only harmed students’ personal health and well-being, but may also contribute to the nursing industry’s future loss of human resources. Seeking emotional support from others and forcing themselves to grow up were the most commonly used coping strategies. Conclusion Nursing educators and nursing managers need to pay attention to verbal violence in the clinical environment, and actively develop the ability of nursing students to deal with uncivilized behavior. Establishing relevant courses and training such as communication, resilience, and violence prevention, establishing a stricter clinical mentor appointment system, and teaching assessment system may be strategies to help nursing students better perform clinical practice.
- Published
- 2023
- Full Text
- View/download PDF
6. Trajectory analysis of the work and life experience of healthcare workers during the COVID-19 pandemic: a longitudinal qualitative study
- Author
-
Pingting Zhu, Meiyan Qian, Amanda Lee, Mark Hayter, Wen Wang, Guanghui Shi, Qiwei Wu, Qiaoying Ji, Xinyue Gu, Hui Zhang, and Yinwen Ding
- Subjects
COVID-19 ,Experience ,Healthcare workers ,Longitudinal study ,Nurses ,Qualitative research ,Nursing ,RT1-120 - Abstract
Abstract Background The COVID-19 pandemic has posed a global health threat and has had a profoundly negative impact on the work and lives of healthcare workers. However, few people know how their experiences have evolved over time. Aims To describe healthcare workers’ experiences during clinical responses to COVID-19 and how they changed over time. Design A longitudinal qualitative study. Methods We undertook a series of four semi-structured qualitative interviews of 14 healthcare workers called as 1st responders to the COVID-19 pandemic. Participants were recruited through purposive snowball sampling. Interviews were undertaken between May 2020 and May 2022 and trajectory approach was used to reveal individual experiences over time. This paper follows the COREQ (Consolidated criteria for Reporting Qualitative Research) guidance. Results Data analysis yielded the following four themes: (1) Changes in emotions; (2) Changes in organization and management of care; (3) Changes in knowledge and capabilities; and (4) Changes in outlook on life and career. Conclusion Healthcare workers have become stronger in the pandemic and have demonstrated a high degree of professional loyalty and responsibility. However, there is a need to focus on the issue of jealousy and create a harmonious and safe work environment to reduce harm to healthcare workers. Additionally, human resource management strategies must support well-being of healthcare workers and maximize the efficiency of human resource utilization to enable them to respond to current and future needs and emergencies.
- Published
- 2023
- Full Text
- View/download PDF
7. Loss of Scribble Promotes Snail Translation through Translocation of HuR and Enhances Cancer Drug Resistance
- Author
-
Meiyan Qi, Weiwei Ji, Yi Xu, Yi Zhou, Renxu Chang, Lixing Zhan, Na Wang, and Jingyu Guo
- Subjects
0301 basic medicine ,Tumor suppressor gene ,Mice, Nude ,cisplatin ,Apoptosis ,Snail ,Biology ,Models, Biological ,p38 Mitogen-Activated Protein Kinases ,Biochemistry ,ELAV-Like Protein 1 ,Scribble ,03 medical and health sciences ,Cell Line, Tumor ,Neoplasms ,biology.animal ,Cell polarity ,Protein biosynthesis ,Animals ,Humans ,RNA, Messenger ,Molecular Biology ,Transcription factor ,cancer biology ,Gene knockdown ,drug resistance ,Tumor Suppressor Proteins ,Membrane Proteins ,Cell Biology ,Transport protein ,Cell biology ,Enzyme Activation ,Gene Expression Regulation, Neoplastic ,Protein Transport ,cell polarity ,030104 developmental biology ,Drug Resistance, Neoplasm ,Gene Knockdown Techniques ,Polyribosomes ,Protein Biosynthesis ,Cancer cell ,cancer therapy ,HuR ,Snail Family Transcription Factors ,Transcription Factors - Abstract
Drug resistance of cancer cells to various therapeutic agents and molecular targets is a major problem facing current cancer research. The tumor suppressor gene Scribble encodes a polarity protein that is conserved between Drosophila and mammals; loss of the locus disrupts cell polarity, inhibits apoptosis, and mediates cancer process. However, the role of Scribble in drug resistance remains unknown. We show here that knockdown of Scribble enhances drug resistance by permitting accumulation of Snail, which functions as a transcription factor during the epithelial-mesenchymal transition. Then, loss of Scribble activates the mRNA-binding protein human antigen R (HuR) by facilitating translocation of HuR from the nucleus to the cytoplasm. Furthermore, we demonstrate HuR can recognize AU-rich elements of the Snail-encoding mRNA, thereby regulating Snail translation. Moreover, loss of Scribble-induced HuR translocation mediates the accumulation of Snail via activation of the p38 MAPK pathway. Thus, this work clarifies the role of polarity protein Scribble, which is directly implicated in the regulation of developmental transcription factor Snail, and suggesting a mechanism for Scribble mediating cancer drug resistance.
- Published
- 2016
8. Long non-coding RNA CUDR promotes malignant phenotypes in pancreatic ductal adenocarcinoma via activating AKT and ERK signaling pathways
- Author
-
Wei Li, Rui Wu, Jun Chen, Xing Liang, Lixing Zhan, Xiangui Hu, Chenghao Shao, Danlei Chen, Meiyan Qi, Anan Liu, and Liang Tang
- Subjects
Adult ,Male ,0301 basic medicine ,Cancer Research ,Epithelial-Mesenchymal Transition ,endocrine system diseases ,MAP Kinase Signaling System ,Cell ,Biology ,Mice ,03 medical and health sciences ,0302 clinical medicine ,Downregulation and upregulation ,Cell Movement ,Cell Line, Tumor ,medicine ,Animals ,Humans ,Epithelial–mesenchymal transition ,Protein kinase B ,Aged ,Cell Proliferation ,Oligonucleotide Array Sequence Analysis ,Oncogene ,Gene Expression Profiling ,Cancer ,Middle Aged ,Cell cycle ,medicine.disease ,digestive system diseases ,Long non-coding RNA ,Up-Regulation ,Gene Expression Regulation, Neoplastic ,Pancreatic Neoplasms ,030104 developmental biology ,medicine.anatomical_structure ,Oncology ,030220 oncology & carcinogenesis ,Cancer research ,Female ,RNA, Long Noncoding ,Proto-Oncogene Proteins c-akt ,Neoplasm Transplantation ,Carcinoma, Pancreatic Ductal - Abstract
Pancreatic ductal adenocarcinoma (PDAC) is one of the most lethal malignancies, with a marked potential for invasion and metastasis. Emerging evidence has suggested that dysregulation of long non-coding RNAs (lncRNAs) is associated with the development of multiple types of cancer. However, the function of lncRNAs in PDAC is poorly known. In the present study, a microarray assay was used to screen for differently expressed lncRNAs in PDAC and it was identified that cancer upregulated drug resistance (CUDR) was upregulated in PDAC. CUDR increased PDAC cell proliferation, migration and invasion, inhibited apoptosis, and promoted drug resistance; it also regulated the PDAC cell epithelial-mesenchymal transition. The CUDR-induced PDAC malignant phenotypes is via the protein kinase B and extracellular-signal-regulated kinase signaling pathways. Downregulation of CUDR may be a novel therapeutic strategy to prevent PDAC development and drug resistance in the future.
- Published
- 2018
9. Psychological distress and academic self-efficacy of nursing undergraduates under the normalization of COVID-19: multiple mediating roles of social support and mindfulness
- Author
-
Ting Xu, Pingting Zhu, Qiaoying Ji, Wen Wang, Meiyan Qian, and Guanghui Shi
- Subjects
COVID-19 epidemic ,Academic self-efficacy ,Psychological distress ,Social support ,Mindfulness ,Special aspects of education ,LC8-6691 ,Medicine - Abstract
Abstract Background Nursing undergraduates’ academic self-efficacy is a significant factor in determining their learning motivation, cognition, and emotions. It has a significant impact on improving academic performance and achieving learning goals. Methods To explore the mechanism of psychological distress affecting the academic self-efficacy of nursing undergraduates, the generalized anxiety disorder scale-7, patient health questionnaire-9, academic self-efficacy scale, perceived social support scale and mindful attention awareness scale were conducted. Results Model fitness indexes of the structural equation model is good (CMIN/DF = 1.404, RMSEA = 0.042, GFI = 0.977, IFI = 0.977, TLI = 0.954, CFI = 0.975, NFI = 0.923). Structural equation model analysis showed that social support and mindfulness were the mediating variables of psychological distress on academic self-efficacy. Mediating variables accounted for 44% of the total effect value (− 0.3) with a value of − 0.132. Three paths were verified: psychological distress indirectly affected academic self-efficacy through social support (− 0.064); psychological distress indirectly affected academic self-efficacy through mindfulness (− 0.053); psychological distress indirectly affected academic self-efficacy through social support and mindfulness (− 0.015). Conclusions Social support and mindfulness play significant mediating roles in the effect of psychological distress on academic self-efficacy, and the chain mediating role of social support and mindfulness is also significant. Educators may mitigate the impact of psychological distress on academic self-efficacy by enhancing students’ social support and mindfulness.
- Published
- 2023
- Full Text
- View/download PDF
10. Severe Loneliness and Isolation in Nursing Students during COVID-19 Lockdown: A Phenomenological Study
- Author
-
Pingting Zhu, Wen Wang, Meiyan Qian, Guanghui Shi, Qianqian Zhang, Ting Xu, Huiwen Xu, Hui Zhang, Xinyue Gu, Yinwen Ding, Amanda Lee, and Mark Hayter
- Subjects
COVID-19 ,nursing students ,mental health ,lockdown ,loneliness ,phenomenological study ,Medicine - Abstract
In 2022, COVID-19 continued to spread across the globe, and to stop the spread of the virus and protect people’s health, universities across China continued to remain in a lockdown state. Loneliness is an important topic among college students, and the coronavirus pandemic has exacerbated loneliness. This prolonged school lockdown was unprecedented and it caused severe social isolation and emotional loneliness for students. Few people know how nursing students experience loneliness and find a way through their experience. This qualitative phenomenological study was conducted to reveal the lived experiences of nursing students who indicated COVID-19 lockdown-related loneliness in a previous quantitative survey. We performed 20 semi-structured interviews with nursing students aged 19–23 yrs during their lockdown (April 2022 to June 2022). Our research applied Colaizzi’s seven-step data analysis processes to reveal shared patterns in terms of how nursing students experienced lockdown and found the following four themes: emotional challenges associated with loneliness; causes of loneliness; positive and negative motivation to learn; and accepting solitude and reconstructing real life.
- Published
- 2023
- Full Text
- View/download PDF
11. Shizukaol D, a Dimeric Sesquiterpene Isolated from Chloranthus serratus, Represses the Growth of Human Liver Cancer Cells by Modulating Wnt Signalling Pathway
- Author
-
Jingtao Peng, Hengrui Zhu, Deke Jiang, Jun Xie, Xianmei Yang, Fang Xie, Meiyan Qi, Lisha Tang, and Long Yu
- Subjects
0301 basic medicine ,Cytotoxicity ,Cancer Treatment ,lcsh:Medicine ,Apoptosis ,Toxicology ,Pathology and Laboratory Medicine ,chemistry.chemical_compound ,Cell Signaling ,Medicine and Health Sciences ,lcsh:Science ,Wnt Signaling Pathway ,WNT Signaling Cascade ,Multidisciplinary ,Cell Death ,Liver Diseases ,Liver Neoplasms ,Wnt signaling pathway ,Transfection ,Signaling Cascades ,Cell biology ,Oncology ,Liver ,Biochemistry ,Cell Processes ,Growth inhibition ,Liver cancer ,Research Article ,Signal Transduction ,Cell signaling ,Signal Inhibition ,Gastroenterology and Hepatology ,Biology ,Research and Analysis Methods ,Carcinomas ,Magnoliopsida ,03 medical and health sciences ,Cell Line, Tumor ,Gastrointestinal Tumors ,medicine ,Humans ,Molecular Biology Techniques ,Molecular Biology ,Cell Proliferation ,Cell growth ,lcsh:R ,Cancers and Neoplasms ,Biology and Life Sciences ,Cancer ,Hepatocellular Carcinoma ,Cell Biology ,medicine.disease ,Antineoplastic Agents, Phytogenic ,Triterpenes ,030104 developmental biology ,chemistry ,Cell culture ,lcsh:Q - Abstract
Natural products have become sources of developing new drugs for the treatment of cancer. To seek candidate compounds that inhibit the growth of liver cancer, components of Chloranthus serratus were tested. Here, we report that shizukaol D, a dimeric sesquiterpene from Chloranthus serratus, exerted a growth inhibition effect on liver cancer cells in a dose- and time-dependent manner. We demonstrated that shizukaol D induced cells to undergo apoptosis. More importantly, shizukaol D attenuated Wnt signalling and reduced the expression of endogenous Wnt target genes, which resulted in decreased expression of β-catenin. Collectively, this study demonstrated that shizukaol D inhibited the growth of liver cancer cells by modulating Wnt pathway.
- Published
- 2016
12. Molecular cloning and expression analysis of a new gene for short-chain dehydrogenase/reductase 9
- Author
-
Long Yu, Dawei Li, Chaoqun Huang, Shen Liu, Meiyan Qi, Weihua Ren, Haoxing Zhang, and Xin Li
- Subjects
Signal peptide ,Oxidoreductases Acting on CH-CH Group Donors ,7-Dehydrocholesterol reductase ,17-Hydroxysteroid Dehydrogenases ,Molecular Sequence Data ,Biology ,Molecular cloning ,General Biochemistry, Genetics and Molecular Biology ,Mice ,Animals ,Humans ,Amino Acid Sequence ,Cloning, Molecular ,Peptide sequence ,Gene ,Short-chain dehydrogenase ,Expression vector ,Base Sequence ,cDNA library ,Chromosome Mapping ,Molecular biology ,Recombinant Proteins ,Rats ,Liver ,Chromosomes, Human, Pair 4 ,Oxidoreductases ,Sequence Alignment - Abstract
We report here the cloning and characterization of a novel human short-chain dehydrogenases/reductase gene SCDR9, isolated from a human liver cDNA library, and mapped to 4q22.1 by browsing the UCSC genomic database. SCDR9 containing an ORF with a length of 900 bp, encoding a protein with a signal peptide sequence and an adh_short domain. GFP localization shows SCDR9 protein concentrated in some site of the cytoplasm, but not in the ER. Expression pattern in eighteen tissues revealed that SCDR9 is expressed highly in liver. Soluble recombinant protein was successfully purified from Escherichia coli using pET28A(+) expression vector. Our data provides important information for further study of the function of the SCDR9 gene and its products.
- Published
- 2007
13. Polarity Protein AF6 Controls Hepatic Glucose Homeostasis and Insulin Sensitivity by Modulating IRS1/AKT Insulin Pathway in an SHP2-Dependent Manner.
- Author
-
Cheng Dai, Xinyu Wang, Yanjun Wu, Yi Xu, Shu Zhuo, Meiyan Qi, Weiwei Ji, Lixing Zhan, Dai, Cheng, Wang, Xinyu, Wu, Yanjun, Xu, Yi, Zhuo, Shu, Qi, Meiyan, Ji, Weiwei, and Zhan, Lixing
- Subjects
INSULIN resistance ,INSULIN regulation ,PROTEIN-tyrosine phosphatase ,INSULIN ,METABOLIC disorders ,GLUCOSE - Abstract
Insulin resistance is a major contributing factor in the development of metabolic disease. Although numerous functions of the polarity protein AF6 (afadin and MLLT4) have been identified, a direct effect on insulin sensitivity has not been previously described. We show that AF6 is elevated in the liver tissues of dietary and genetic mouse models of diabetes. We generated liver-specific AF6 knockout mice and show that these animals exhibit enhanced insulin sensitivity and liver glycogen storage, whereas overexpression of AF6 in wild-type mice by adenovirus-expressing AF6 led to the opposite phenotype. Similar observations were obtained from in vitro studies. In addition, we discovered that AF6 directly regulates IRS1/AKT kinase-mediated insulin signaling through its interaction with Src homology 2 domain-containing phosphatase 2 (SHP2) and its regulation of SHP2's tyrosine phosphatase activity. Finally, we show that knockdown of hepatic AF6 ameliorates hyperglycemia and insulin resistance in high-fat diet-fed or db/db diabetic mice. These results demonstrate a novel function for hepatic AF6 in the regulation of insulin sensitivity, providing important insights about the metabolic role of AF6. [ABSTRACT FROM AUTHOR]
- Published
- 2019
- Full Text
- View/download PDF
14. [Untitled]
- Author
-
Guangjin Zhou, Meiyan Qi, Fengjue Shu, Ying Zhang, Shuguang Guo, Chaoqun Wu, Zekun Guo, Long Yu, Yongjun Dang, and Shouyuan Zhao
- Subjects
Immunoprecipitation ,Clinical Biochemistry ,Aurora B kinase ,macromolecular substances ,Cell Biology ,General Medicine ,Plasma protein binding ,Cell cycle ,Biology ,Molecular biology ,Cell biology ,enzymes and coenzymes (carbohydrates) ,Proteasome ,embryonic structures ,Proteasome inhibitor ,medicine ,Aurora Kinase B ,biological phenomena, cell phenomena, and immunity ,Molecular Biology ,Mitosis ,medicine.drug - Abstract
Human Aurora/Ipl1-related kinase 2 (Aurora-B) is a key regulator of mitosis. Here human proteasome α-subunit C8 (HC8) was identified to interact with the Aurora-B by yeast two-hybrid screen. This finding was confirmed by GST pull-down assays and immunoprecipitation experiments. The Aurora-B protein level increased in HeLa cells cultured with proteasome inhibitor ALLN. Our data suggest that Aurora-B might undergo degradation by binding to HC8 in a proteasome-dependent manner during mitosis.
- Published
- 2003
15. The phosphoproteome in regenerating protoplasts from Physcomitrella patens protonemata shows changes paralleling postembryonic development in higher plants
- Author
-
Yong Hu, Meiyan Qi, Fang Bao, Zhongzhong Ji, Jingyun Li, Ramamurthy Mahalingam, Yikun He, and Xiaoqin Wang
- Subjects
Proteome ,Physiology ,Organogenesis ,Plant Science ,protoplast regeneration ,Physcomitrella patens ,Polymerase Chain Reaction ,Bryopsida ,TiO2 enrichment ,Tandem Mass Spectrometry ,Botany ,Regeneration ,LC-MS/MS ,Protonema ,Plant Proteins ,biology ,Cell growth ,Cell morphogenesis ,Protoplasts ,fungi ,phosphoproteome ,food and beverages ,postembryonic development ,biochemical phenomena, metabolism, and nutrition ,Protoplast ,equipment and supplies ,biology.organism_classification ,Phosphoproteins ,Cell biology ,bacteria ,Chromatography, Liquid ,Research Paper - Abstract
Summary During protoplast regeneration, proteins related to cell morphogenesis, organogenesis and development adjustment were phosphorylated in Physcomitrella patens. These proteins play important roles in regulating postembryonic development in higher plants., The moss Physcomitrella patens is an ideal model plant to study plant developmental processes. To better understand the mechanism of protoplast regeneration, a phosphoproteome analysis was performed. Protoplasts were prepared from protonemata. By 4 d of protoplast regeneration, the first cell divisions had ensued. Through a highly selective titanium dioxide (TiO2)-based phosphopeptide enrichment method and mass spectrometric technology, more than 300 phosphoproteins were identified as protoplast regeneration responsive. Of these, 108 phosphoproteins were present on day 4 but not in fresh protoplasts or those cultured for 2 d. These proteins are catalogued here. They were involved in cell-wall metabolism, transcription, signal transduction, cell growth/division, and cell structure. These protein functions are related to cell morphogenesis, organogenesis, and development adjustment. This study presents a comprehensive analysis of phosphoproteome involved in protoplast regeneration and indicates that the mechanism of plant protoplast regeneration is similar to that of postembryonic development.
- Published
- 2014
16. Let7a inhibits the growth of endometrial carcinoma cells by targeting Aurora-B
- Author
-
Yan Liu, Guoying Lao, Chengbin Ma, Yingzi Liu, Ping Liu, Meiyan Qi, and Yu Liu
- Subjects
Cell Survival ,Genetic enhancement ,Biophysics ,Aurora B kinase ,Protein Serine-Threonine Kinases ,medicine.disease_cause ,Bioinformatics ,Biochemistry ,Gene Expression Regulation, Enzymologic ,HeLa ,Endometrium ,Structural Biology ,Aurora Kinases ,Carcinoma Cell ,microRNA ,Genetics ,Carcinoma ,medicine ,Aurora Kinase B ,Humans ,Molecular Biology ,Cell Proliferation ,Oligonucleotide Array Sequence Analysis ,Targeting Aurora-B ,biology ,Endometrial cancer ,Gene Expression Profiling ,MicroRNA ,Let-7a ,Cell Biology ,medicine.disease ,biology.organism_classification ,Endometrial carcinoma cell ,Endometrial Neoplasms ,Gene Expression Regulation, Neoplastic ,MicroRNAs ,Cancer research ,Female ,Carcinogenesis ,HeLa Cells - Abstract
MicroRNAs negatively regulate target gene expression at the post-transcriptional level during carcinogenesis. Recent advances revealed that the expression levels of several miRNAs are up- or down-regulated in endometrial carcinoma (EC). Here we identify dysregulated miRNAs in EC and we elucidate the essential role of let-7a. The expression of 86 miRNAs in EC was found to be different from adjacent normal endometrial tissues. Moreover, miR-let-7 members are down-regulated in EC and let-7 miRNAs are highly associated with endometrial cancer. A functional investigation revealed that let-7a suppressed proliferation of HeLa cells by targeting Aurora-B. Let-7a also antagonizes Aurora-B functions in promoting carcinoma cell proliferation by down-regulating Aurora-B protein level. Let-7a could be applied for gene therapy against endometrial carcinogenesis.
- Published
- 2013
17. Septin1, a new interaction partner for human serine/threonine kinase aurora-B
- Author
-
Shen Liu, Xiaomei Yan, Bo Wan, Meiyan Qi, Shouyuan Zhao, Huijue Jia, Hexige Saiyin, Lisha Tang, Qingyu Lang, Long Yu, Wenbo Yu, and Mingjuan Shen
- Subjects
Serine/threonine-specific protein kinase ,Biophysics ,Aurora B kinase ,macromolecular substances ,Cell Biology ,Polo-like kinase ,Biology ,Protein Serine-Threonine Kinases ,Septin ,Biochemistry ,Phosphoric Monoester Hydrolases ,Cell biology ,Midbody ,Phosphoserine ,Aurora Kinases ,Two-Hybrid System Techniques ,Aurora Kinase B ,Humans ,Cleavage furrow ,Phosphorylation ,Molecular Biology ,Mitosis ,Cytokinesis ,HeLa Cells - Abstract
Several families of kinases work together to ensure the rate and precision of mitosis. Aurora-B is an important serine/threonine kinase required for chromosome segregation and cytokinesis. Identification of Aurora-B substrates will help to enhance our understanding of the molecular mechanism of mitosis. Through a yeast two-hybrid screen, we found a novel partner of Aurora-B, Septin1, belonging to a conserved family of GTPase proteins that localize to the cleavage furrow and are involved in cytokinesis. We confirmed this interaction using Co-immunoprecipitation experiments in mammalian cells and GST-pull-down analysis in vitro. Moreover, Aurora-B can phosphorylate Septin1 in vitro. We identified that Ser248, Ser307, and Ser315 are the main phosphorylation sites in Septin1. These two proteins partially co-localize to the midbody during cytokinesis. So, it is possible that Septin1's role in the regulation of cytokinesis is related to its phosphorylation by Aurora-B. Unlike previous reports that Septins function in cytokinesis and localize to the cleavage furrow, we found that Septin1 localizes to the spindle pole throughout mitosis, indicating that Septin1 may function in chromosome segregation as well.
- Published
- 2005
18. Human aurora-B binds to a proteasome alpha-subunit HC8 and undergoes degradation in a proteasome-dependent manner
- Author
-
Fengjue, Shu, Shuguang, Guo, Yongjun, Dang, Meiyan, Qi, Guangjin, Zhou, Zekun, Guo, Ying, Zhang, Chaoqun, Wu, Shouyuan, Zhao, and Long, Yu
- Subjects
Proteasome Endopeptidase Complex ,DNA, Complementary ,Cell Cycle ,Immunoblotting ,Mitosis ,Protein Serine-Threonine Kinases ,Precipitin Tests ,Cysteine Endopeptidases ,Aurora Kinases ,Multienzyme Complexes ,Protein Biosynthesis ,Two-Hybrid System Techniques ,Aurora Kinase B ,Humans ,Electrophoresis, Polyacrylamide Gel ,Glutathione Transferase ,HeLa Cells ,Plasmids ,Protein Binding - Abstract
Human Aurora/Ipl1-related kinase 2 (Aurora-B) is a key regulator of mitosis. Here human proteasome alpha-subunit C8 (HC8) was identified to interact with the Aurora-B by yeast two-hybrid screen. This finding was confirmed by GST pull-down assays and immunoprecipitation experiments. The Aurora-B protein level increased in HeLa cells cultured with proteasome inhibitor ALLN. Our data suggest that Aurora-B might undergo degradation by binding to HC8 in a proteasome-dependent manner during mitosis.
- Published
- 2003
19. Nirvana: A Qualitative Study of Posttraumatic Growth in Adolescents and Young Adults with Inflammatory Bowel Disease
- Author
-
Qiwei Wu, Pingting Zhu, Xinyi Liu, Qiaoying Ji, and Meiyan Qian
- Subjects
adolescents and young adults ,inflammatory bowel disease ,posttraumatic growth ,a qualitative study ,Pediatrics ,RJ1-570 - Abstract
(1) Background: Psychosomatic discomfort is prevalent among adolescents and young adults (AYAs) with inflammatory bowel disease (IBD). Post-traumatic growth (PTG) has been a protective factor in earlier research. However, little is known regarding PTG among AYAs with IBD. This study investigates the generation of PTG in adolescents and young adults with inflammatory bowel disease (IBD) and finds positive coping skills employed in clinical nursing practice. (2) Methods: In 2021, 32 individuals were interviewed utilizing a semi-structured interview guide. This study used qualitative content analysis. (3) Results: The interviews revealed five themes: spiritual change, internalized supportiveness, cognitive re-shaping, externalized behaviors, and future-oriented thinking. (4) Conclusions: The research revealed the presence of PTG in AYAs with IBD. To give tailored care to patients, medical professionals must monitor the state of their PTG development in a planned and focused manner.
- Published
- 2022
- Full Text
- View/download PDF
20. Enhancement of High-Order Harmonic Generation due to the Large Gradient of the Electric Field Amplitude
- Author
-
Meiyan Qin, Yi Zeng, Xin Zeng, and Qing Liao
- Subjects
circularly polarized laser pulse ,strong field physics ,high-order harmonic generation ,pulse duration dependence of the harmonic yield ,Technology ,Engineering (General). Civil engineering (General) ,TA1-2040 ,Biology (General) ,QH301-705.5 ,Physics ,QC1-999 ,Chemistry ,QD1-999 - Abstract
The influence of the waveform of circularly polarized laser field on high-order harmonic (HH) generation from atoms is investigated by solving the time-dependent Schrödinger equation (TDSE) and by classical trajectory analysis, without assuming an initial transverse velocity. Both the HH simulation and the classical trajectory calculation demonstrate that the positive temporal gradient of the electric field amplitude is a key factor that makes the electron return to the parent ion possible. Moreover, the larger the temporal gradient of the field amplitude is, the more the electron trajectories will revisit the parent ion. Correspondingly, the enhancement of HH is observed. This is confirmed by the pulse-duration dependence of the harmonic yield driven by a circularly polarized laser field.
- Published
- 2019
- Full Text
- View/download PDF
21. Pogostone alleviates angiotensin II-induced cardiomyocyte hypertrophy in H9c2 cells through MAPK and Nrf2 pathway.
- Author
-
Ying Yang, Yuan Xie, Xinna Zhao, Meiyan Qi, and Xuebo Liu
- Subjects
- *
NUCLEAR factor E2 related factor , *ATRIAL natriuretic peptides , *ANGIOTENSIN receptors , *BRAIN natriuretic factor , *ANGIOTENSINS - Abstract
Purpose: To investigate the effect of pogostone on cardiac hypertrophy. Methods: An in vitro model of myocardial hypertrophy was first established by stimulating H9c2 (rat cardiomyocytes) with angiotensin II (Ang II), and the cells treated with or without pogostone. Atrial natriuretic peptide (ANP) and brain natriuretic peptide (BNP) were measured by western blot. Immunofluorescence staining was performed for a-actinin while cell surface area was quantified. Dichlorodihydrofluorescein diacetate (DCFH-DA) fluorescent probe and malondialdehyde (MDA) assay kit were used to determine reactive oxygen species (ROS) and MDA levels respectively. Apoptosis was evaluated by flow cytometry while Nrf2, p38, ERK, and JNK protein expression levels were determined by western-blot assay. Results: Compared with the control group, ANP and BNP protein expression levels, cell surface area, ROS, MDA, and apoptosis were all elevated in H9c2 cells after stimulation with Ang II (p < 0.001). Varying doses of pogostone decreased protein expressions of ANP and BNP, reduced cell surface area, decreased ROS and MDA levels, and inhibited apoptosis. Pogostone also up-regulated and inhibited the phosphorylation levels of p38 and ERK, and JNK levels in H9c2 cells. Conclusion: Pogostone reduces protein expression of ANP and BNP and up-regulated Nrf2 protein expression in H9c2 cells stimulated with angiotensin II. [ABSTRACT FROM AUTHOR]
- Published
- 2023
- Full Text
- View/download PDF
22. Loss of Scribble Promotes Snail Translation through Translocation of HuR and Enhances Cancer Drug Resistance.
- Author
-
Yi Zhou, Renxu Chang, Weiwei Ji, Na Wang, Meiyan Qi, Yi Xu, Jingyu Guo, and Lixing Zhan
- Subjects
- *
SNAILS , *DRUG resistance in cancer cells , *TUMOR suppressor genes , *DROSOPHILA physiology , *ANTIGENS , *CYTOPLASM , *TRANSCRIPTION factors , *PHYSIOLOGY - Abstract
Drug resistance of cancer cells to various therapeutic agents and molecular targets is a major problem facing current cancer research. The tumor suppressor gene Scribble encodes a polarity protein that is conserved between Drosophila and mammals; loss of the locus disrupts cell polarity, inhibits apoptosis, and mediates cancer process. However, the role of Scribble in drug resistance remains unknown. We show here that knockdown of Scribble enhances drug resistance by permitting accumulation of Snail, which functions as a transcription factor during the epithelial-mesenchymal transition. Then, loss of Scribble activates the mRNA-binding protein human antigen R (HuR) by facilitating translocation of HuR from the nucleus to the cytoplasm. Furthermore, we demonstrate HuR can recognize AU-rich elements of the Snail-encoding mRNA, thereby regulating Snail translation. Moreover, loss of Scribble-induced HuR translocation mediates the accumulation of Snail via activation of the p38 MAPK pathway. Thus, this work clarifies the role of polarity protein Scribble, which is directly implicated in the regulation of developmental transcription factor Snail, and suggesting a mechanism for Scribble mediating cancer drug resistance. [ABSTRACT FROM AUTHOR]
- Published
- 2016
- Full Text
- View/download PDF
Catalog
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.