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The Molecular Mechanisms of Tanshinone IIA on the Apoptosis and Arrest of Human Esophageal Carcinoma Cells

机译:丹石IIA对人食管癌细胞凋亡和捕获的分子机制

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摘要

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:客观的。探讨丹参酮IIA(Taniia)对食管癌细胞系的可能机制。方法。用不同浓度的坦苗治疗两种人食管癌细胞系(EC-1细胞和ECA-109细胞)。通过CCK-8测量细胞增殖,计算菌落形成效率,测量细胞周期和细胞凋亡,并通过Western印迹测定细胞周期和凋亡相关基因表达的变化。结果。 CCK-8和菌落形成测定表明,坦苗在48小时下抑制人食管细胞(IC50低于1μg/ mL)的细胞增殖。 Hoechst 33258和流式细胞仪表明,Taniia诱导两种食管癌细胞系中的细胞凋亡。流式细胞术显示Taniia在S期和G2 / m相中停止了细胞周期。蛋白质印迹分析表明,抑制AkT1及其磷酸化,Bax / Bcl-2比增加,并在48小时下用1.3μg/ ml坦苗处理后激活Caspase-9和Caspase-3。同时,P53和P21蛋白水平增加,而细胞周期蛋白B1,CDC2和CDC2磷酸化被抑制。结论。坦苗抑制食管癌细胞的生长,并以时间依赖性和浓度依赖性方式诱导细胞凋亡,可能通过影响细胞周期和凋亡相关的信号通路。

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