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作 者:牛海静[1] 王邦茂[1] 方维丽[1] 曹晓沧[1] 丁娟娟[1]
机构地区:[1]天津医科大学总医院消化内科,天津300052
出 处:《天津医科大学学报》2008年第2期157-159,163,共4页Journal of Tianjin Medical University
基 金:天津市科学技术委员会资助项目(05KYZ79)
摘 要:目的:观察胰岛素样生长因子-Ⅰ受体(IGF-ⅠR)基因特异的siRNA对胃癌细胞体外增殖及凋亡的影响。方法:设计并体外合成2条靶向IGF-ⅠR的siRNAs,脂质体法瞬时转染MGC803细胞,Western Blot法检测IGF-ⅠR蛋白表达,MTT法检测细胞活力,细胞计数并描记生长曲线,流式细胞仪(FCM)检测凋亡。结果:转染后48h,Western Blot检测显示干扰组(siRNA2-L组、siRNA2-H组、siRNA1组)IGF-ⅠR蛋白抑制率分别为64.41%±4.11%、74.14%±6.15%、89.8%±4.10%;siRNA1组转染后第2~5天细胞活力逐渐减少(分别达49.9%±1.2%、45.9%±4.4%、39.1%±5.1%、29%±4.0%);同期生长曲线显示细胞数分别为对照组的65.58%±4.89%、55.59%±0.82%、44.18%±3.17%、21.15%±1.1%;但FCM检测各组细胞凋亡没有显著差异。结论:特异的siRNAs可显著抑制胃癌细胞中的IGF-ⅠR基因的表达,主要是通过抑制增生而不是增加凋亡导致的。Objective: To observe the expression of IGF- ⅠR on human gastric cancer MGC803 cells inhibited by special siRNAs and investigate the following effects of the cell proliferation and apoptosis. Methods: Two different siRNAs targeted to IGF- ⅠR were designed ,synthesized and transfected into MGC803 cells, the changes of IGF- ⅠR protein level were detected by Western Blot at 48 h after transfection, then the cell proliferation were examined by MTT, the growth curve was obtained and the apoptosis was detected by Flow Cytometry (FCM). Results: The 48th hour after transfection, the inhibition ratio of IGF- ⅠR protein of interfering groups (siRNA2-low dose group, siRNA2-high dose group, siRNA1 group) were 64.41%±4.11%,74.14%±6.15%,89.8%±4.10%; On the 2-5 day after transfection, the cell proliferation gradually decreased by 49.9%±1.2%, 45.9%±4.4%, 39.1%±5.1%, 29%±4.0% in siRNA1 group; the cell number decreased by 65.58%±4.89%, 55.59%±0.82%, 44.18%±3.17%, 21.15%±1.1% at the same time; but the early-stage cell apoptosis didn't show differences among the groups. Conclusion: Special siRNAs can remarkably inhibit the expression of IGF-ⅠR in gastric cancer cells, the cell survival decreased mainly through the inhibition of the cell proliferation, but not the increasing of the cell apoptosis.
关 键 词:小干扰RNA 胰岛素样生长因子-Ⅰ受体 胃癌细胞
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