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出 处:《中国医药导报》2009年第3期21-22,共2页China Medical Herald
基 金:辽宁省教育厅科研基金项目(No.20060070)
摘 要:目的:探讨人参皂苷化学修饰物PM1体外诱导肝癌HepG2细胞凋亡作用。方法:采用四甲基偶氮唑蓝(MTT)还原法检测不同浓度的人参皂苷化学修饰物PM1对肝癌HepG2细胞增殖的作用;流式细胞仪分析肿瘤细胞凋亡周期及细胞凋亡率。结果:PM1抑制肝癌HepG2细胞生长,呈浓度依赖关系。用50和100mg/LPM1处理细胞24h后,PM1诱导了细胞凋亡和调节细胞周期,凋亡率与对照组比较明显升高(P<0.01)。结论:PM1抑制肝癌HepG2细胞生长,其机制可能是通过诱导凋亡来发挥作用的。Objective: To study the effect of PM1 on inducing apoptosis of HepG2 ceils in vitro. Methods: The HepG2 ceils were treated with different doses of PM1. Cell proliferation was measured by MTT assay. Cell cycle and apoptosis rate were analyzed by flow cytometry. Results: PM1 inhibited proliferation of HepG2 ceils in concentration-dependent manner. FCM assay showed that PM1 regulated cell cycle and induced apoptosis of HepG2 cells after treated with 50 and 100 mg/L PM1 for 24 h. The apoptosis rates were increased (P〈0.01). Conclusion: PM1 probably inhibits the proliferation of HepG2 cells by inducing apoptosis.
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