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作 者:刘峰 何周华[2] LIU Feng;HE Zhou-hua(Department of Pharmacy, Lishui Chinese Medicine Hospital, Lishui 323000, China;Department of Oncology, Lishui Chinese Medicine Hospital, Lishui 323000, China)
机构地区:[1]丽水市中医院药剂科,浙江丽水323000 [2]丽水市中医院肿瘤科,浙江丽水323000
出 处:《中国生化药物杂志》2017年第11期12-13,17,共3页Chinese Journal of Biochemical Pharmaceutics
摘 要:目的探讨没食子酸(gallicacid,GA)对人肝癌SMMC-7721细胞凋亡的影响及其可能的作用机制。方法没食子酸干预SMMC-7721细胞后,MTT法检测其对细胞生长抑制的影响,计算IC50值;DNA琼脂糖凝胶电泳观察SMMC-7721细胞DNA降解情况;流式细胞仪检测细胞凋亡;Westernblot检测相关蛋白表达。结果GA作用SMMC-7721细胞48h的IC50为(31.2±1.8)μg/mL;12.5、25、50μg/mLGA作用SMMC-7721细胞48h后,细胞DNA电泳可见典型的DNA凋亡梯状条带;GA各剂量组SMMC-7721细胞线粒体膜电位降低,峰值明显左移;GA激活了SMMC-7721细胞的caspase-3及9凋亡通路,上调促凋亡蛋白Bax的表达。结论GA可能通过线粒体凋亡途径诱导SMMC-7721细胞的凋亡,抑制肝癌SMMC-7721细胞的增殖。Objective To investigate the effect of gallic acid on the apoptosis of human hepatocellular carcinoma SMMC-7721cells and its possible mechanism.Methods DNA activity was measured by DNA agarose gel electrophoresis.The DNA degradation of SMMC-7721cells was observed by flow cytometry.The apoptosis of SMMC-7721cells was detected by flow cytometry.The expression of IC50was detected by MTT assay.Western blot to detect the expression of related proteins.Results The IC50of SMMC-7721cells treated with GA was(31.2±1.8)μg/mL;12.5,50,50μg/mL GA for48h after SMMC-7721cells,the typical DNA apoptotic bands were observed by DNA electrophoresis.GA inhibited the mitochondrial membrane potential of SMMC-7721cells,and the peak value was significantly shifted to the left.GA activated the caspase-3and9apoptotic pathway of SMMC-7721cells to up-regulate the expression of pro-apoptotic protein Bax.Conclusion GA may induce the apoptosis of SMMC-7721cells by mitochondrial apoptosis and inhibit the proliferation of SMMC-7721cells.
关 键 词:没食子酸 肝癌 SMMC-7721细胞
分 类 号:R197[医药卫生—卫生事业管理]
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