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垂盆草醇提物抑制HepG2细胞STAT-3信号通路诱导细胞凋亡的研究
引用本文:曾军英,李胜华,伍贤进,刘丹,万雄.垂盆草醇提物抑制HepG2细胞STAT-3信号通路诱导细胞凋亡的研究[J].中国中药杂志,2014,39(17):3349-3352.
作者姓名:曾军英  李胜华  伍贤进  刘丹  万雄
作者单位:民族药用植物资源研究与利用湖南省重点实验室 怀化学院 生命科学系, 湖南 怀化 418008;民族药用植物资源研究与利用湖南省重点实验室 怀化学院 生命科学系, 湖南 怀化 418008;民族药用植物资源研究与利用湖南省重点实验室 怀化学院 生命科学系, 湖南 怀化 418008;民族药用植物资源研究与利用湖南省重点实验室 怀化学院 生命科学系, 湖南 怀化 418008;民族药用植物资源研究与利用湖南省重点实验室 怀化学院 生命科学系, 湖南 怀化 418008
基金项目:湖南省教育厅平台项目(11K052,09K105);湖南省高等学校产业化培育项目(13cy026);湖南省科技计划项目(2013FJ6090);民族药用植物资源研究与利用湖南省重点实验室开放基金项目(HHUW2010-65);湖南省植物学“十二五”重点建设学科(湘教发[2011]42号)
摘    要:目的:研究垂盆草醇提物对STAT-3信号通路的影响,及其诱导细胞凋亡的分子机制。方法:MTT法检测垂盆草醇提物对HepG2细胞增殖的影响;流式细胞术分析结合FITC-Annexin V/PI双标记检测对肝癌细胞凋亡的影响,免疫印迹试验检测细胞凋亡Caspase-3,Caspase-9,PARP,P-STAT-3(Tyr705),STAT-3,Bcl-2,Mcl-1相关蛋白表达水平。结果:垂盆草醇提物可明显抑制HepG2细胞的增殖,诱导HepG2细胞凋亡,且抑制作用呈剂量依赖效应。垂盆草醇提物作用后,抑制STAT-3信号转导通路,下调Mcl-1和Bcl-2的表达,引起凋亡相关蛋白Caspase-3,Caspase-9的降解/活化及PARP的降解,并呈剂量依赖效应。结论:垂盆草醇提物通过抑制STAT-3信号转导通路和Mcl-1和Bcl-2的表达,进而抑制HepG2细胞的增殖,诱导其凋亡。

关 键 词:垂盆草  细胞增殖  细胞凋亡  STAT-3  Mcl-1  Bcl-2  信号转导  HepG2细胞株
收稿时间:2013/12/4 0:00:00

Study on impact of ethanol extracts from Sedum sarmentosum in inhibiting STAT-3 signaling and inducing apoptosis of human hepatocellular carcinoma cell line HepG2
ZENG Jun-ying,LI Sheng-hu,WU Xian-jin,LIU Dan and WAN Xiong.Study on impact of ethanol extracts from Sedum sarmentosum in inhibiting STAT-3 signaling and inducing apoptosis of human hepatocellular carcinoma cell line HepG2[J].China Journal of Chinese Materia Medica,2014,39(17):3349-3352.
Authors:ZENG Jun-ying  LI Sheng-hu  WU Xian-jin  LIU Dan and WAN Xiong
Institution:Key Laboratory of Hunan Province for Study and Utilization of Ethnic Medicinal Plant Resources, Department of Life Sciences, Huaihua University, Huaihua 418008, China;Key Laboratory of Hunan Province for Study and Utilization of Ethnic Medicinal Plant Resources, Department of Life Sciences, Huaihua University, Huaihua 418008, China;Key Laboratory of Hunan Province for Study and Utilization of Ethnic Medicinal Plant Resources, Department of Life Sciences, Huaihua University, Huaihua 418008, China;Key Laboratory of Hunan Province for Study and Utilization of Ethnic Medicinal Plant Resources, Department of Life Sciences, Huaihua University, Huaihua 418008, China;Key Laboratory of Hunan Province for Study and Utilization of Ethnic Medicinal Plant Resources, Department of Life Sciences, Huaihua University, Huaihua 418008, China
Abstract:Objective: To investigate the impact of ethanol extracts from Sedum sarmentosum (ESB) on STAT-3 signaling and its probable molecular mechanism in inducing apoptosis. Method: MTT assay was used to detect the impact of ESB on HepG2 cell proliferation. FITC-Annexin V-FITC/PI double-labeling were used to investigate the impact on hepatoma carcinoma cell apoptosis. Western blot analysis was used to test the expression levels of cell apoptosis-related proteins Caspase-3, Caspase-9, PARP, P-STAT-3(Tyr705), STAT-3, Bcl-2, Mcl-1. Result: ESB could notably inhibit proliferation of HepG2 cells, and induce HepG2 cell apoptosis, with the dose-dependent inhibitory effect. In addition, ESB could inhibit STAT-3 signaling, down-regulate Mcl-1 and Bcl-2 expressions, and induce degradation/activation of apoptosis-related proteins Caspase-3 and Caspase-9 and PARP degradation in a dose-dependent manner. Conclusion: ESB inhibits HepG2 cell proliferation and induces apoptosis by inhibiting STAT-3 signaling and Mcl-1 and Bcl-2 expressions.
Keywords:Sedum sarmentosum  cell proliferation  cell apoptosis  STAT-3  Mcl-1  Bcl-2  signal transduction  HepG2 cell line
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