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作 者:姚友春[1,2] 王晓翊[1] 姚爱香[2] 王泽华[1]
机构地区:[1]华中科技大学同济医学院附属协和医院妇科,武汉430022 [2]荆门市第一人民医院妇科
出 处:《现代妇产科进展》2009年第1期26-30,共5页Progress in Obstetrics and Gynecology
摘 要:目的:研究选择性环氧合酶-2(COX-2)抑制剂NS-398对宫颈癌HeLa,SiHa细胞系的增殖、凋亡作用及其对凋亡抑制基因survivin表达的影响。方法:体外培养宫颈癌HeLa,SiHa细胞系,用四甲基偶氮唑蓝(MTT)比色法分析不同浓度的NS-398分别作用于HeLa,SiHa细胞系24h、48h后对细胞增殖的作用;流式细胞仪(FCM)检测对细胞凋亡的作用;RT-PCR分析对凋亡抑制基因survivin表达的影响。结果:MTT检测显示,NS-398可抑制宫颈癌HeLa,SiHa细胞系增殖,并有浓度时间依赖性,与对照组相比差异有统计学意义(P<0.05)。FCM检测提示,NS-398可诱导HeLa,SiHa细胞系凋亡,有浓度依赖性,与对照组相比差异有统计学意义(P<0.05)。RT-PCR分析表明,NS-398可抑制HeLa,SiHa细胞系凋亡抑制基因survivinmRNA表达,与对照组的差异有统计学意义(P<0.05)。结论:NS-398可抑制宫颈癌HeLa,SiHa细胞增殖,诱导凋亡,其机制与抑制凋亡抑制基因survivin mRNA表达有关,为宫颈癌治疗提供了新的靶点和理论依据。Objective: To investigate the effects of the selective inhibitor of cyclooxygenase-2(COX-2) NS-398 on the proliferation and the pro-apoptosis in human cervical carcinoma cell lines HeLa and SiHa in vitro, and to explore its influence on the expression of survivin mRNA. Methods:Cervical cancer cells HeLa and SiHa were cultured in vitro respectively under the irritation of NS-398 with different concent rations (25,50, 100μmol/L) for 24h and 48h. The inhibition rates were detected by methyl thiazolyl tetrazolium (MTF). Flow cytometry (FCM) was prepared to determine its pro-apoptosis activity at 48h after the administration of NS-398 with different concentrations (25,50,100txmol/L). The expressions of survivin mRNA were detected by reverse transcription-polymerase chain reaction(RT-PCR) at 48h after admin istrated with NS-398 of different concentrations (25,50,100μmol/L). Results: The results of MTF showed that NS-398 significantly inhibited the proliferation of cervical cancer cells in a dose and time dependent manner. NS-398 at 100μmol/L obviously inhibited the proliferation of HeLa and SiHa cells, and there was significant difference between the experimental groups and the control groups (P 〈 0. 05 ). By FCM, NS-398 could induce apoptosis, especially at 100μmol/L. The difference was significant between the experimental groups and the control groups ( P 〈 0.05 ). Using RT-PCR, the alteration of survivin mRNA decreased after administration of NS-398 for 48h. The difference was significant between the experimental groups and the control groups. ( P 〈 0.05 ). Conclusion: The selective inhibitor of COX-2 NS-398 can inhibit proliferation and induce the development of apoptosis of cervical cancer cells HeLa and SiHa via downregulating the expression of survivin mRNA.
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