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Experimental Studies on Cyclooxygenase-2 Inhibitor Induced Cervical Cancer Hela Cell Apoptosis and Its Molecular Mechanism 被引量:1
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作者 Ling YIN Li-bei WEI Qiu-hong QU Xiao-peng GUO 《Journal of Reproduction and Contraception》 CAS 2007年第4期271-277,共7页
Objective To investigate the Hela cells growth inhibition and apoptosis possible molecular mechanisms. Methods Hela cells were treated with various concentrations (100μmol/L,200μmol/L, 300 μmol/L, 400 μmol/L) of... Objective To investigate the Hela cells growth inhibition and apoptosis possible molecular mechanisms. Methods Hela cells were treated with various concentrations (100μmol/L,200μmol/L, 300 μmol/L, 400 μmol/L) of NS-398 (selective for COX-2 inhibition). Cell growth was measured by MTT (Thiazolyl blue). Apoptosis was detected by double staining flow cytometry (FCM). Levels of PGE: were measured by radioimmunoassay. The expressions of COX-2 protein were also examined by Western blot analysis. Results After treated with different concentrations of NS-398, the growth of Hela cells was suppressed significantly in a dose-and time-dependent manner (P〈0.01). The NS-398 can induce apoptosis with the apoptosis rates at 8.53%-43.46% by FCM in a dose-dependent manner. The release of PGE2 was reduced in Hela cells with the values of 69.26 ± 2.13, 47.46 ± 2.18, 28.15 ± 1.64 and 17.01 ± 1.12, respectively, there was significant difference compared with control group (83.78 ± 1.11) (P〈0.01). The NS-398 could inhibit the activity and expression of COX-2 in a dose- dependent manner and down-regulated the expression of COX-2 protein greatly. Conclusion NS-398 could inhibit the proliferation and increase apoptosis in human Hela cells. These effects may be depended on the inhibition of the expression of COX-2 and PGE2 by NS-398. 展开更多
关键词 cyclooxygenase-2 ns-398 Hela cell apoptosis
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NS-398对结直肠癌细胞HT-29放射增敏机制的初探
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作者 王振波 胡立宽 +1 位作者 竺鑫丽 宋轶鹏 《中国肿瘤临床》 CAS CSCD 北大核心 2006年第19期1112-1116,共5页
目的:探讨COX-2抑制剂NS-398对结直肠癌细胞系HT-29的放射增敏作用及其相关机制。方法:COX-2高表达细胞系HT-29经25μmol/LNS-398处理24h后,给以不同剂量(0、2、4、6、8Gy)X-ray照射,应用克隆形成实验测NS-398对HT-29细胞的放射增敏作用... 目的:探讨COX-2抑制剂NS-398对结直肠癌细胞系HT-29的放射增敏作用及其相关机制。方法:COX-2高表达细胞系HT-29经25μmol/LNS-398处理24h后,给以不同剂量(0、2、4、6、8Gy)X-ray照射,应用克隆形成实验测NS-398对HT-29细胞的放射增敏作用,流式细胞仪(FCM)分析NS-398对HT-29细胞凋亡及细胞周期的影响,RT-PCR和FCM观察NS-398处理后Bax、Bcl-2在mRNA及蛋白水平的表达变化。结果:25μmol/LNS-398对HT-29有明显增敏作用,细胞存活分数(SF)为0.1时,放射增敏比SER为1.76;NS-398诱导HT-29凋亡、增强HT-29对放射诱导凋亡的敏感性,同时抑制细胞增殖;BaxmRNA及蛋白表达呈NS-398剂量依赖性增高,而Bcl-2的表达无明显变化。结论:NS-398对HT-29有放射增敏作用,其机制与诱导凋亡、直接抑制细胞增殖有关。 展开更多
关键词 环氧合酶抑制剂 放射增敏 凋亡 ns-398
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