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机构地区:[1]惠州市第三人民医院心胸外科,广东惠州516000
出 处:《现代肿瘤医学》2017年第21期3402-3406,共5页Journal of Modern Oncology
基 金:惠州市科学计划项目(编号:20130802)
摘 要:目的:探讨白藜芦醇(Resveratrol,Res)对肺癌H460细胞增殖与凋亡的影响并探讨其可能的机制。方法:分别用浓度为0、25、100、200μmol/L的Res作用于H460细胞48 h后,采用CCK-8法检测Res对H460细胞增殖的影响;流式细胞术检测细胞凋亡率;JC-1试剂盒检测细胞内线粒体膜电位水平;ATP试剂盒检测细胞内ATP水平;Western blot法检测细胞内Bcl-2、Bax和Cytochrome c蛋白表达情况。结果:与对照组比较,CCK-8及流式结果显示Res可抑制H460细胞的增殖,并使其凋亡率升高(P<0.01);JC-1及ATP检测结果显示Res可降低H460细胞内线粒体膜电位及ATP水平(P<0.01),且在该浓度范围内呈剂量相关性;Western blot检测发现随着Res浓度的增加,Bcl-2蛋白的表达水平下降,而Bax和Cytochrome c蛋白的表达水平升高。结论:实验浓度的Res可抑制H460细胞的增殖并诱导其凋亡,这一作用的机制可能与Res激活了线粒体凋亡通路进而诱发H460细胞凋亡有关。Objectlve:To observe the effect of Resveratrol on proliferation and apoptosis of lung cancer H460 cells and explore the possible mechanisms. Methods:H460 cells were treated with Res (0,25,100,200 μmol/L) for 48 hours. The cell proliferation was measured by eel1 counting Kit - 8, the apoptosis assays were performed by flow cytom- etry, the mitoehondrial membrane potential level was detected by JC - 1. The ATP levels in H460 cells were measured using an ATP assay kit, and the expression level of Bax, Bcl - 2 and Cytochrome c protein in H460 cells were analysed by Western blot. Results: Compared with the control group, treated with Res inhibiteyd the proliferation of H460 cells, and enhanced the apoptosis rate through the CCK - 8 and flow cytometry ( P 〈 0.01 ), and the JC - 1 and ATP detec- tion showed that Res decreased the mitochondrial membrane potential and ATP levels in H460 cells in a dose - de- pendent manner( P 〈 0.01 ). Meanwhile, the expression level of Bcl - 2 was downregulated, however the Bax and Cyto- chrome were upregulated with the increase of the Res concentration. Conclusion: Res inhibited the proliferation and induced the apoptosis of H460 cells, and which was involved in mitoehondfial signaling pathway of apoptosis, poten- tially.
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