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机构地区:[1]南华大学医学院肿瘤研究所,湖南衡阳421001 [2]南华大学医学院病理学教研室,湖南衡阳421001 [3]湖南浏阳市人民医院妇科,湖南浏阳410300 [4]湖南浏阳市人民医院烧伤科,湖南浏阳410300
出 处:《现代生物医学进展》2011年第15期2840-2843,共4页Progress in Modern Biomedicine
摘 要:目的:初步探讨EGCG对卵巢癌HO-8910细胞增殖的抑制作用及其机制。方法:通过绘制细胞生长曲线、平皿克隆和软琼脂集落形成实验观察EGCG对HO-8910细胞增殖的抑制作用;Western-blotting检测AKT1、Mdm-2与p53蛋白的表达。结果:(1)细胞生长曲线、平皿克隆和软琼脂集落形成实验结果显示,EGCG可有效抑制HO-8910细胞的增殖(n=3,P<0.05)。(2)Westernblotting检测结果显示,EGCG处理后AKT1与Mdm-2蛋白表达均降低,而p53蛋白表达升高(P<0.05)。结论:EGCG通过抑制HO-8910细胞中AKT1与Mdm-2蛋白表达,促使p53蛋白表达而发挥其对细胞增殖的抑制作用。Objective: To investigate mechanism of Epigallocatechin-3-gallate (EGCG) inhibited the proliferation of ovarian cancer HO-8910 cells. Methods: EGCG inhibited HO-8910 cellular proliferation was observed by the drawing cellular growth curve, plate colony formation and soft agar colony formation. The expressions of AKT1, Mdm-2 and p53 proteins were detected by Western-blotting. Results: 1. The results of cellular growth curve, plate colony formation and soft agar colony formation showed that EGCG active depressed the proliferation of HO-8910 cells with treatment time extended (n=3, P 〈 0.05). 2. The western-blotting results exhibited that the expressions of AKT1 and Mdm-2 proteins in HO-8910 cells obviously decreased, but the expression of p53 protein increased after EGCG dealing with it (P 〈 0.05). Conclusion: EGCG depressed the expressions of AKT1, Mdm-2 proteins in HO-8910 cells and increased the expression of p53 protein to inhibit the cellular proliferation.
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