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机构地区:[1]上海交通大学第六人民医院妇产科,上海200233
出 处:《上海交通大学学报(医学版)》2006年第12期1343-1346,共4页Journal of Shanghai Jiao tong University:Medical Science
基 金:上海市科委基金(04JC14064);上海市卫生局基金(2005ZD006)资助项目
摘 要:目的探讨环氧化酶-2(COX-2)选择性抑制剂塞来昔布对人子宫内膜腺癌细胞系HEC-1B增殖及凋亡的影响及其作用机制。方法噻唑蓝(MTT)法检测不同浓度塞来昔布作用HEC-1B细胞后细胞增殖的变化;不同浓度塞来昔布作用HEC-1B细胞24h后,流式细胞仪检测细胞周期和凋亡;RT—PCR检测细胞中COX-2 mRNA的表达。结果MTT结果显示.塞来昔布对HEC-1B细胞的增殖抑制作用呈现时间依赖性和浓度依赖性;不同浓度塞来昔布作用HEC-1B细胞24h后,流式细胞仪结果显示G0/G1期细胞增加,S期和G2/M细胞减少,细胞凋亡率增加,各药物组与对照组相比差异均有统计学意义(P〈0.05);RT—PCR结果显示,在50~200μmol/L塞来昔布组,随着药物浓度的增加COX-2 mRNA的表达逐渐减弱(P〈0.05)。结论塞来昔布能抑制HEC-1B细胞的增殖,并能改变细胞周期和诱导凋亡,其机制可能与下调细胞中COX-2 mRNA的表达有关。Objective To study the effects of cyclooxygenase-2 ( COX-2 ) selective inhibitor celecoxib on proliferation and apoptosis of human endometrial adenocarcinoma HEC-1B cell line. Methods Methabenzthiazuron (MTT) assay was used to examine the effects of different concentrations of celecoxib on proliferation of HEC-1B cells. When HEC-1B cells were treated with different concentrations of celecoxib for 24 h, cell cycle and apoptosis were detected by flow cytometry. The expression of COX-2 mRNA was analyzed by RT-PCR. Results MTT results indicated that celecoxib could inhibit HEC-1 B cell proliferation in a time- and dose-dependent manner. When HEC-1B cells were treated with different concentrations of celecoxib for 24 h, flow cytometry results showed that the cell percent of G0/G1 phase increased, S and G2/M phase decreased, and cell apoptosis rate also increased, which was significantly different from that of the control group ( P 〈 0.05 ). The results of RT-PCR indicated that the expression of COX-2 mRNA gradually decreased with the increasing dose of celecoxib ( 50 - 200 μmol/L) ( P 〈 0.05 ). Conclusion Celecoxib can inhibit the proliferation of HEC-1B cells, alter cell cycle and induce cell apoptosis. The mechanism might be associated with the down-regulation of COX-2 mRNA expression in HEC-1B cells.
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