芪术抗癌方对肝癌HepG2细胞增殖和凋亡的影响
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深圳市基础学科布局项目(JCYJ20170817094901026);深圳市科技计划项目(JCYJ201803023000674)


Effects of Qizhu Kangai Formula on Proliferation and Apoptosis of HepG2 Heptoma Cells of Liver Cancer
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    摘要:

    目的:探讨芪术抗癌方对肝癌HepG2细胞增殖与凋亡的调控作用。方法:体外培养HepG2细胞,加入不同浓度芪术抗癌方(0,250,500,1 000 mg/L)处理48 h。采用细胞计数试剂盒8(CCK-8)检测细胞活力,采用免疫印记法检测凋亡相关蛋白c-Caspase-3和c-Caspase-9表达变化。结果:CCK-8结果显示芪术抗癌方可呈浓度依赖性抑制HepG2细胞增殖,与对照组比较,差异有统计学意义(P<0.05),1 000 mg/L组抑制效果最好,芪术抗癌方刺激HepG2细胞后,凋亡相关蛋白c-Caspase3及c-Caspase9表达增加,呈浓度依赖性,在1 000 mg/L组达到最高且差异有统计学意义(c-Caspase3增加1.83倍,P<0.05;c-Caspase9增加1.06倍,P<0.05)。结论:芪术抗癌方可抑制肝癌HepG2细胞增殖并诱导细胞凋亡。

    Abstract:

    To study the effects of Qizhu Kangai Formula on the proliferation and apoptosis of HepG2 heptoma cells of liver cancer.Methods:The HepG2 cells were cultured in vitro and treated with different concentration of Qizhu Kangai Formula (0,250,500,1 000 mg/L ) for 48 h.The living cells were detected by cell counting kit 8 ( CCK8 ) and the protein expression of c-caspase3 and c-caspase9 were observed by Western-blot.Results:CCK8 showed that Qizhu Kangai Formula could inhibit HepG2 cells proliferation in concentration-dependent manner and had significant differences with the control group (P<0.05).Among them,the 1000 mg/L group had the best inhibition effects.Further studies found that the expression of the apoptotic proteins c-caspase3 and c-caspase9 increased after the stimulating HepG2 cells by Qizhu Kangai Formula and was concentration-dependent and was highest in the 1000 mg/L group with statistical significance ( c-caspase3 increased 1.83 times,P<0.05; c-caspase9 increases by 1.06 times,P<0.05 ).Conclusion:Qizhu Kangai Formula could inhibit the proliferation and induce apoptosis of HepG2 heptoma cells.

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冯文杏,周小舟,韩志毅,孙新锋,马文峰,张卫.芪术抗癌方对肝癌HepG2细胞增殖和凋亡的影响[J].世界中医药,2020,(11).

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  • 收稿日期:2019-03-25
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  • 在线发布日期: 2020-06-25
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