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作 者:吴倩[1] 袁凯[2] 钱成[3] 王勇 童继春[2] 袁卫东[2]
机构地区:[1]南京医科大学附属常州第二人民医院血液肿瘤科,江苏常州213003 [2]南京医科大学附属常州第二人民医院胸心外科,江苏常州213003 [3]复旦大学附属中山医院胸外科,上海200032
出 处:《中国临床医学》2013年第6期772-775,共4页Chinese Journal of Clinical Medicine
基 金:江苏省常州市卫生局青年基金项目(编号:QN201003)
摘 要:目的:探讨小干扰RNA(small interfering RNA,siRNA)沉默缺氧诱导因子2α(hypoxia inducible factor-2 alpha,HIF-2α)基因表达后,人肺腺癌A549细胞株对顺铂耐药性的变化。方法:构建靶向HIF-2α基因的siRNA真核表达载体并转染A549细胞,采用Real-time PCR检测HIF-2αmRNA的表达,采用Western blotting检测HIF-2α及多药耐药基因1(multidrug resistance-1,Mdr-1)蛋白的表达,采用MTT法检测顺铂处理后细胞的存活率。结果:在HIF-2αsiRNA转染A549细胞后24、48 h后,HIF-2α在mRNA和蛋白水平的表达与空白对照组相比均显著下调(均P<0.01),Mdr-1蛋白的表达水平也明显降低(均P<0.05)。与空白对照组相比,HIF-2αsiRNA组细胞对顺铂的敏感性明显增加,各时间点的IC50值均显著降低,差异有统计学意义(均P<0.01)。结论:靶向HIF-2α的siRNA表达载体能够有效抑制HIF-2α基因的表达,从而逆转A549细胞对顺铂的化疗耐药性。Objective:To investigate the effect of silencing hypoxia inducible factor-2 alpha (HIF-2α) gene expression by small interfering RNA (siRNA) on chemotherapy resistance of A549 cells to cisplatin.Methods:The siRNA eukaryotic expression vectors targeting HIF-2α gene were constructed and transfected into A549 cells.The expression of HIF-2α mRNA was detected by real-time PCR.The expression of HIF-2α and multidrug resistance-1 (Mdr-1) proteins were detected by Western blotting.MTT assay was used to explore the survival rate of A549 cells under the treatment of cisplatin.Results:After transfection of HIF-2α siRNA into A549 cells for 24 and 48 h,the expression levels of HIF-2α mRNA and protein were both down-regulated significantly compared with those in the blank group (all P<0.01).Meanwhile,the protein expression level of Mdr-1 also decreased significantly (all P<0.05).The sensitivity of A549 cells to cisplatin was significantly increased in HIF-2α siRNA transfection group compared with that in the blank group.The IC50 value at each time point was significantly decreased,and the difference was statistically significant (all P<0.01).Conclusions:The siRNA expression vector targeting HIF 2α constructed in this study can effectively inhibit the expression of HIF-2α gene,and thus reversing the chemotherapy resistance of A549 cells to cisplatin.
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