中华实验外科杂志
中華實驗外科雜誌
중화실험외과잡지
CHINESE JOURNAL OF EXPERIMENTAL SURGERY
2015年
6期
1355-1357
,共3页
王惟佳%徐姗%王珊珊%胡雪梅%王淳良%梅金红
王惟佳%徐姍%王珊珊%鬍雪梅%王淳良%梅金紅
왕유가%서산%왕산산%호설매%왕순량%매금홍
脑膜瘤%人类表皮生长因子受体-2%RNA干扰%增殖
腦膜瘤%人類錶皮生長因子受體-2%RNA榦擾%增殖
뇌막류%인류표피생장인자수체-2%RNA간우%증식
Meningioma%Human epidermalgrowth factor receptor-2%Small interfering RNA%Proliferation
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.
目的 觀察人類錶皮生長因子受體-2(Her-2)/neu基因對腦膜瘤細胞增殖能力的影響.方法 收集腦膜瘤Her-2暘性患者術後新鮮標本5例,原代培養細胞,用脂質體法榦擾細胞Her-2基因後,分彆採用反轉錄-聚閤酶鏈反應(RT-PCR)、Western blot法檢測Her-2 mRNA和蛋白的錶達;噻唑藍(MTT)法、流式細胞術檢測細胞增殖活性及週期的變化.結果 轉染後72 h,榦擾組與陰性對照組比較,Her-2 mRNA和蛋白錶達水平分彆下降56.3%和52.7%,差異有統計學意義(P<0.05);榦擾組轉染後72 h的抑製作用最彊,細胞增殖抑製率為50.08%,細胞週期中G0/G1期細胞比例上升18.11%,S期比例下降39.34%,差異有統計學意義(P<0.05).結論 Her-2/neu小分子榦擾RNA可抑製腦膜瘤細胞的增殖活性.
목적 관찰인류표피생장인자수체-2(Her-2)/neu기인대뇌막류세포증식능력적영향.방법 수집뇌막류Her-2양성환자술후신선표본5례,원대배양세포,용지질체법간우세포Her-2기인후,분별채용반전록-취합매련반응(RT-PCR)、Western blot법검측Her-2 mRNA화단백적표체;새서람(MTT)법、류식세포술검측세포증식활성급주기적변화.결과 전염후72 h,간우조여음성대조조비교,Her-2 mRNA화단백표체수평분별하강56.3%화52.7%,차이유통계학의의(P<0.05);간우조전염후72 h적억제작용최강,세포증식억제솔위50.08%,세포주기중G0/G1기세포비례상승18.11%,S기비례하강39.34%,차이유통계학의의(P<0.05).결론 Her-2/neu소분자간우RNA가억제뇌막류세포적증식활성.
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.