首页> 外文期刊>Evidence-based complementary and alternative medicine: eCAM >A C_(21)-Steroidal Glycoside Isolated from the Roots of Cynanchum auriculatum Induces Cell Cycle Arrest and Apoptosis in Human Gastric Cancer SGC-7901 Cells
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A C_(21)-Steroidal Glycoside Isolated from the Roots of Cynanchum auriculatum Induces Cell Cycle Arrest and Apoptosis in Human Gastric Cancer SGC-7901 Cells

机译:C_(21)-甾体糖苷从虎耳草根中分离诱导人胃癌SGC-7901细胞的细胞周期阻滞和凋亡。

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摘要

Caudatin3-O-beta-D-cymaropyranosyl-(l —> 4)-j3-D-oleandropyranosyl-(l —> 4)-betaD-cymaropyranosyl-(l —> 4)-betaD-cymaro-pyranoside (CGII) is one of the C_(21)-steroidal glycosides isolated from the roots of Cynanchum auriculatum ROYLE ex WIGHT. This study aimed to determine the cell growth, cell proliferation,apoptotic cell death of human gastric cancer cells after CGII treatment. MTT assay was used to determine cell growth; fluorescence-activated cell sorting analysis was used to evaluate cell cycle distribution and apoptotic cell death. Immunoblotting was applied for measuring the expression of proteins involved in the cell cycle progression. The activities of caspase-3, -8,-9 were detected by colorimetric caspase activity assays. CGII inhibited cell growth of human gastric cancer SGC-7901 cells in a concentration- and time-dependent manner. Treatment of SGC-7901 cells with CGII resulted in Gl phase cell cycle arrest, accompanied with decreased expression of cyclin Dl and cyclin-dependent kinases 4 and 6. CGII induced cell apoptosis and activated caspase-3, caspase-8,caspase-9. In contrast, pan-caspase inhibitor z-VAD-fmk partially abolished the CGII-induced growth inhibition of SGC-7901 cells. In conclusion, CGII inhibits cell growth of human gastric cancer cells by inducing Gl phase cell cycle arrest and caspase-dependent apoptosis cascades.
机译:Caudatin3-O-β-D-环吡喃糖基-(1-4)-j3-D-油基吡喃糖基-(1-4)-βD-环吡喃糖基-(1-4)-βD-环吡喃吡喃糖苷(CGII)为从Cynanchum auriculatum ROYLE ex WIGHT的根中分离出的一种C_(21)-甾体糖苷。本研究旨在确定CGII处理后人胃癌细胞的生长,细胞增殖,凋亡细胞死亡。用MTT法测定细胞生长。荧光激活细胞分选分析用于评估细胞周期分布和凋亡细胞死亡。免疫印迹法用于测量参与细胞周期进程的蛋白质的表达。通过比色半胱天冬酶活性测定法检测半胱天冬酶3,-8,-9的活性。 CGII以浓度和时间依赖性方式抑制人胃癌SGC-7901细胞的生长。用CGII处理SGC-7901细胞导致G1期细胞周期停滞,伴随着细胞周期蛋白D1和细胞周期蛋白依赖性激酶4和6的表达降低。CGII诱导细胞凋亡并激活了caspase-3,caspase-8,caspase-9。相反,泛半胱天冬酶抑制剂z-VAD-fmk部分取消了CGII诱导的SGC-7901细胞的生长抑制。总之,CGII通过诱导G1期细胞周期停滞和胱天蛋白酶依赖性凋亡级联反应而抑制人胃癌细胞的细胞生长。

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