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Ginkgo biloba extract induce cell apoptosis and G0/G1 cycle arrest in gastric cancer cells

机译:银杏叶提取物诱导胃癌细胞凋亡和G0 / G1周期阻滞

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摘要

Objective: Previous studies have shown that the Ginkgo biloba extract (EGb761) can be used to anti-cancer. However, the mechanism by which EGb761 mediate this effect is still unclear. In the present study, EGb761 inhibited cell proliferation and induced cell apoptosis in gastric cancer cell was explored. Methods: The cell viability was detected by the CCK8 assay. The cell cycle and apoptosis was assessed by flow cytometry. The protein expression of caspase-3, p53 and Bcl-2 were analyzed by western blot. Results: Treatment of human gastric cancer cells with EGb761 induced cell death in a dose-dependent manner by using CCK8 assay. Consistent with the CCK8 assay, the flow cytometry results showed that gastric cancer cells were accumulated in G0/G1 phase when exposed to EGb761. Furthermore, the proportion of apoptosis cells was increased after EGb761 treatment as compared to untreated group. In addition, our results showed that the treatment of AGS cells with EGb761 significantly increased the expression of caspase3 and p53, and decreased the anti-apoptotic Bcl-2 level. Conclusions: Our results demonstrated that EGb761 could inhibit gastric cancer proliferation through adjusting cell cycle and inducing cell apoptosis.
机译:目的:先前的研究表明,银杏叶提取物(EGb761)可用于抗癌。但是,EGb761介导此作用的机制仍不清楚。在本研究中,探索了EGb761在胃癌细胞中抑制细胞增殖并诱导细胞凋亡。方法:采用CCK8法检测细胞活力。通过流式细胞术评估细胞周期和凋亡。通过western blot分析caspase-3,p53和Bcl-2的蛋白表达。结果:通过使用CCK8分析,以剂量依赖性方式用EGb761处理人胃癌细胞诱导的细胞死亡。与CCK8分析一致,流式细胞仪结果表明,暴露于EGb761时,胃癌细胞以G0 / G1期积累。此外,与未处理组相比,EGb761处理后凋亡细胞的比例增加。此外,我们的结果表明,用EGb761处理AGS细胞可显着增加caspase3和p53的表达,并降低抗凋亡Bcl-2的水平。结论:我们的结果表明,EGb761可通过调节细胞周期和诱导细胞凋亡来抑制胃癌的增殖。

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