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机构地区:[1]中国人民解放军第四军医大学西京医院妇产科,陕西西安710032
出 处:《世界肿瘤杂志》2008年第2期94-97,共4页Tumour Journal of the World
基 金:国家自然科学基金(30772305)
摘 要:目的观察腺病毒介导的针对Her2/neu基因RNAi表达载体对Her2/neu的抑制及抑制后对卵巢癌SKOV-3细胞的生长的影响。方法通过构建的针对Her2neu的siRNA重组腺病毒(滴度为1.6×10^8PFU/mL)感染卵巢癌细胞SKOV-3后,采用Western—blot法观察Her2/neu基因的沉默效果,流式细胞仪分析细胞周期变化,cell Proliferation法检查细胞体外增殖能力。结果构建的重组腺病毒Adeno—Her2siRNA感染卵巢癌细胞SKOV-3后Her2/neu的蛋白表达降低;S期细胞较对照组未感染细胞比例增加;肿瘤细胞胞增殖速度缓慢(P〈0.05)。结论成功构建的重组腺病毒Adeno-Her2siRNA感染后可有效降低Her2/neu蛋白水平表达,阻滞细胞感染于S期,造成感染细胞生长速度减慢,有望为卵巢癌的基因治疗提供一种选择手段。Objective To observe the Her2siRNA mediated adenovirus down-regulate Her2/neu gene and study the RNAi effect on the cell cycle and tumor growth of ovarian cancer SKOV-3 cells. Methods The ovarian cancer SKOV-3 cells was infected by the recombinant adenovirus vector Adeno-Her2siRNA(the titer was 1.6×10^8 PFU/mL), the protein was detected by Western blot. FCM analysis and cell proliferation method were applied to measure cell cycle and cell growth respectively. Results The results from infection of SKOV-3 cells with siRNA-expressing adenovirus demonstrated that adenovirus-mediated RNAi could downregulate Her2/neu expression efficiently through Western blot. It can increase the number of cells in S phase, and inhibit the tumor cell growth (P〈0.05). Conclusions The adenovirus-mediated Her2siRNA could effectively silence Her2/neu gene, increase the number of cells in S phase, and then slow down the growth of tumor cells. This may be a useful therapeutic strategy for ovarian cancer over-expressing Her2/neu.
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