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作 者:沈汉斌 吴耀辉[2] 龙浩成 郑启昌[2] 龚建平[3]
机构地区:[1]武汉市第五医院普外Ⅰ科,430050 [2]华中科技大学同济医学院附属协和医院外科 [3]华中科技大学同济医学院附属同济医院外科
出 处:《中华实验外科杂志》2009年第12期1600-1602,共3页Chinese Journal of Experimental Surgery
摘 要:目的观察重组质粒pEGFP—Survivin对胆囊癌细胞(GBC—SD)化疗敏感性的影响。方法以噻唑蓝(MTr)比色法检测GBC-SD、GBC-SD/EGFP和GBC—SD/Survivin3种细胞的增殖活性;用逆转录-聚合酶链反应(RT—PCR)和Westernblot测各组细胞中SurvivinmRNA和蛋白质水平的表达;以合适浓度的顺铂(DDP,3.0mg/L)作用相同的时间后,用MTY法检测3种细胞存活率,流式细胞仪测细胞凋亡,并用MTT法筛选IC50值,TUNEL法观察细胞核改变;另外检测DDP作用后各组细胞的Caspase.3蛋白酶活性的变化。结果GBC—SD和GBC—SD/EGFP细胞的增殖活性大致相同,而GBC—SD/Survivin细胞的增殖活性明显下降;RT—PCR和Westemblot均发现GBC—SD/Survivin细胞中的Survivin表达水平较其余两种细胞明显下降(分别下降了74.7%和71.5%);在给予了DDP作用后,GBC—SD/Survivin细胞存活率和IC50[(2.03±0.24)mg/L]明显较低,细胞凋亡率较高(84.3%),而3种细胞用TUNEL法染色后均可见棕色凋亡细胞核。给予了DDP作用后,各组细胞Caspase-3活性均呈现先升高后下降的趋势,但GBC—SD/Survivin细胞中Caspase-3的活性明显高于另外两种细胞。结论pEGFP—Survivin表达的SurvivinshRNA能明显降低GBC—SD细胞中Survivin的表达.提高对化疗药物的敏感性。Objective To investigate the effect of Survivin shRNA on chemotherapy resistance of GBC-SD cells. Methods They were divided into three group which are GBC-SD, GBC-SD/EGFP and GBC-SD/survivin. MTT assay was used to detect cells viability in three groups, and mRNA and protein of survivin were tested by RT-PCR and Western blot. Then cells were treated with proper construction DDP (3.0 mg/L) for the same time,cell survival rate and IC50 was detected with MTT respectively,cells apoptosis was detected through FACS, and the alteration of nucleus was observed by TUNEL. In addition, caspase-3 activity was detected by using colorimetric method. Results Cell viability was reduced remarkably in GBC-SD/survivin and survivin expression was decreased obviously (74.7% ,71.5% ). After treated with DDP,cell survival rate and IC50 was decreased obviously [ (2.03 ±0.24) mg/L] in GBC-SD/ survivin, apoptosis rate (84.3%) were elevated remarkably compared with other group. There were brownly nucleuses in three groups. Caspase-3 activity all ascend first and then descent,but it exceeded in GBC- SD/survivin than that in other two groups. Conclusion The survivin shRNA could down-regulate the expression of survivin in GBC-SD cells remarkably and improve the sensibility to chemotherapy. The alteration of caspase-3 activity followed with survivin contrarily.
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