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首页> 外文期刊>BioMed research international >The Molecular Mechanisms of Tanshinone IIA on the Apoptosis and Arrest of Human Esophageal Carcinoma Cells
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The Molecular Mechanisms of Tanshinone IIA on the Apoptosis and Arrest of Human Esophageal Carcinoma Cells

机译:丹参酮IIA对人食管癌细胞凋亡和阻滞的分子机制

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Objective.To explore the possible mechanisms of Tanshinone IIA (TanIIA) on esophageal carcinoma cell lines.Methods.Two human esophageal carcinoma cell lines (EC-1 cells and ECa-109 cells) were treated with different concentrations of TanIIA. Cell proliferation was measured by CCK-8, colony-forming efficiency was calculated, cell cycle and apoptosis were measured, and changes in cell cycle- and apoptosis-related gene expression were measured by Western blotting.Results.The CCK-8 and colony formation assay indicated that TanIIA inhibited the cell proliferation of human esophageal cancer cells (IC50 below 1 μg/mL) at 48 h. Hoechst 33258 and flow cytometry showed that TanIIA induced apoptosis in both esophageal cancer cell lines. Flow cytometry showed that TanIIA arrested cell cycle in S phase and G2/M phase. Western blotting analysis showed that Akt1 and its phosphorylation were inhibited, the Bax/Bcl-2 ratio increased, and both caspase-9 and caspase-3 were activated after treatment with 1.3 μg/mL TanIIA at 48 h. Meanwhile, p53 and p21 protein levels increased, whereas cyclin B1, CDC2, and CDC2 phosphorylation were inhibited.Conclusion.TanIIA inhibits the growth of esophageal cancer cells and induces apoptosis in a time-dependent and concentration-dependent manner, possibly by affecting cell cycle- and apoptosis-related signaling pathways.
机译:目的:探讨丹参酮IIA(TanIIA)对食管癌细胞系的作用机制。方法:用不同浓度的TanIIA处理两种人食管癌细胞系(EC-1细胞和ECa-109细胞)。 CCK-8检测细胞增殖,计算菌落形成效率,测定细胞周期和凋亡,Western blotting检测细胞周期及凋亡相关基因表达的变化。结果,CCK-8和菌落形成实验表明,TanIIA在48 h抑制人食道癌细胞的增殖(IC50低于1μg/ mL)。 Hoechst 33258和流式细胞仪显示,TanIIA诱导了两种食道癌细胞系的凋亡。流式细胞仪检测表明,TanIIA阻滞了S期和G2 / M期的细胞周期。 Western blotting分析显示,在1.3μg/ mL的TanIIA处理后48h,Akt1及其磷酸化受到抑制,Bax / Bcl-2比增加,caspase-9和caspase-3均被激活。同时,p53和p21蛋白水平升高,而细胞周期蛋白B1,CDC2和CDC2磷酸化受到抑制。结论:TanIIA抑制食管癌细胞的生长,并以时间依赖性和浓度依赖性的方式诱导细胞凋亡,可能是通过影响细胞周期-和凋亡相关的信号通路。

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