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作 者:王惟佳 徐姗[1] 王珊珊[1] 胡雪梅[1] 王淳良[2] 梅金红[1]
机构地区:[1]南昌大学第一附属医院病理科,330006 [2]南昌大学第一附属医院神经外科,330006
出 处:《中华实验外科杂志》2015年第6期1355-1357,共3页Chinese Journal of Experimental Surgery
基 金:国家自然科学基金资助项目(81260372);江西省教育厅科学技术研究重点项目(GJJ 11013);江西省科技厅重大攻关计划资助项目(20114004)
摘 要:目的 观察人类表皮生长因子受体-2(Her-2)/neu基因对脑膜瘤细胞增殖能力的影响.方法 收集脑膜瘤Her-2阳性患者术后新鲜标本5例,原代培养细胞,用脂质体法干扰细胞Her-2基因后,分别采用反转录-聚合酶链反应(RT-PCR)、Western blot法检测Her-2 mRNA和蛋白的表达;噻唑蓝(MTT)法、流式细胞术检测细胞增殖活性及周期的变化.结果 转染后72 h,干扰组与阴性对照组比较,Her-2 mRNA和蛋白表达水平分别下降56.3%和52.7%,差异有统计学意义(P<0.05);干扰组转染后72 h的抑制作用最强,细胞增殖抑制率为50.08%,细胞周期中G0/G1期细胞比例上升18.11%,S期比例下降39.34%,差异有统计学意义(P<0.05).结论 Her-2/neu小分子干扰RNA可抑制脑膜瘤细胞的增殖活性.Objective To investigate the effects of human epidermal growth factor receptor-2 (Her-2)/neu gene on cell proliferative activity in human meningiomas.Methods The surgicall resected fresh samples from 5 cases of human meningiomas with Her-2 overexpression were selected,and cells were primarily cultured.The expression of Her-2 mRNA and protein was detected by reverse transcriptase-polymerase chain reaction (RT-PCR) and Western blotting respectively.Methyl thiazol tetrazolium (MTT) assay was employed to examined the cell viability.The cell cycle distribution was measured by flow cytometry.Results At 72nd h after transfection,as compared with the silencing group and the negative control group,the Her-2 mRNA and protein expression was reduced by 56.3% and 52.7% respectively (P < 0.05).At 72nd h after transfection,the proliferation inhibition rate was 50.08%.The proportion of cells in G0/G1 phase was increased by 18.11%,and that in S phase decreased by 39.34% (P <0.05).Conclusion Her-2 small interfering RNA (siRNA)-mediated gene may inhibit the proliferative ablity of human meningiomas.
关 键 词:脑膜瘤 人类表皮生长因子受体-2 RNA干扰 增殖
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