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作 者:李宁[1] 李建[1] 吴克瑾[1] 费哲为[1] 欧敬民[1] 叶敏[1]
机构地区:[1]上海交通大学附属新华医院普外科,上海200092
出 处:《现代肿瘤医学》2008年第6期921-924,共4页Journal of Modern Oncology
基 金:上海市科委基金资助项目(编号:05ZR14064)
摘 要:目的:观察沙培林在体外对人胃癌SGC7901细胞的作用。方法:以不同浓度的沙培林(0、0.001KE/ml、0.01KE/ml、0.1KE/ml和0.5KE/ml)处理6h、12h、24h和48h后,噻唑蓝(MTT)比色法观察SGC7901细胞的生长情况;0.5 KE/ml沙培林作用于胃癌SGC7901细胞48h后,流式细胞仪检测细胞周期的变化;免疫组化染色观察药物处理前后的p53、p27、PCNA蛋白的表达。结果:沙培林对SGC7901胃癌细胞具有抑制增殖效应,并在一定范围呈现时间和浓度依赖性;沙培林(0.5KE/ml)作用48h后,周期检测发现SGC7901细胞G0/G1期细胞下降,S期增加(P<0.01);免疫组化结果显示:沙培林干预可使SGC7901细胞p53蛋白表达下调,p27蛋白表达上调(P<0.01),PCNA蛋白表达组间无统计学差异(P>0.01)。结论:沙培林可改变SGC7901细胞周期分布,抑制细胞增殖;可使细胞p53表达减少,p27表达增加。Objective :To study the effects of Sapyhn on human gastric cancer cell SGC7901 in vitro. Methods: SGC7901 cells were treated with 0,0. 001,0.01,0.1 and 0.5 KE/ml Sapylin for6,12,24,48 hours respectively. The cell growth condition was observed by MTT assey ;The cell cycle was analyzed by flow cytometry ;Immunocytochemical staining was used to analyze the expression of p53, p27 and PCNA protein in SGC7901 cell between control group and treated group. Results: Sapyin inhibited the proliferation of SGC7901 cells by. dose-dependent and time -dependent manner. SGC7901 cells were treated with 0.5 KE/ml Sapylin for 48 hours ,cells in G0/G1 - phase were decreased in cell cycle, but increased in S -phase (P 〈 0.01 ). Results of immunocytochemical staining showed that Sapylin can down- regulated the expression of p53 protein ,up-regulated the p27 protein (P 〈 0.01 ). The expression of PCNA showed no significant difference between control group and treated group( P 〉 0.01 ). Conclusion : Sapylin can change the cell cycle, inhibit the proliferation of human gastric cancer SGC7901cell. It can also increase the expression of p53 protein,but decrease the p27 protein.
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