银杏叶提取物可诱导胃癌细胞凋亡和 G0/G1 周期停滞。

IF 0.2 Q4 MEDICINE, RESEARCH & EXPERIMENTAL International journal of clinical and experimental medicine Pub Date : 2015-11-15 eCollection Date: 2015-01-01
Yu Bai, Feng Zhao, Yan Li, Lei Wang, Xiang-Jie Fang, Chen-Yu Wang
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引用次数: 0

摘要

研究目的以往的研究表明,银杏叶提取物(EGb761)可用于抗癌。然而,EGb761 的作用机制尚不清楚。本研究探讨了 EGb761 在胃癌细胞中抑制细胞增殖和诱导细胞凋亡的作用:方法:采用 CCK8 检测法检测细胞活力。流式细胞术评估细胞周期和细胞凋亡。结果:CCK8 可诱导胃癌细胞凋亡:结果:采用 CCK8 检测法,EGb761 以剂量依赖性方式诱导人胃癌细胞死亡。与 CCK8 试验结果一致,流式细胞术结果显示,暴露于 EGb761 的胃癌细胞在 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,我们的研究结果表明,用EGb761处理AGS细胞可显著增加caspase3和p53的表达,并降低抗凋亡的Bcl-2水平:我们的研究结果表明,EGb761可通过调整细胞周期和诱导细胞凋亡来抑制胃癌细胞的增殖。
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Ginkgo biloba extract induce cell apoptosis and G0/G1 cycle arrest in gastric cancer cells.

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.

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