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作 者:潘敏[1] 刘纯伦[1] 方晓杰[1] 石建华[1]
机构地区:[1]重庆医科大学附属第一医院消化内科,重庆400016
出 处:《中国药理学通报》2009年第4期523-527,共5页Chinese Pharmacological Bulletin
基 金:重庆市卫生局资助课题(No05-2-155)
摘 要:目的观察环氧合酶-2/5-脂氧合酶双重抑制剂dar-bufelone对胃癌SGC-7901细胞生长的影响。方法MTT法测定darbufelone对胃癌SGC-7901细胞增殖的影响;TUNEL法检测细胞凋亡;RT-PCR法分析SGC-7901细胞中5-LOX和COX-2 mRNA的表达;免疫细胞化学法检测胃癌SGC-7901细胞中5-LOX和COX-2蛋白质的表达。结果dar-bufelone以时间剂量依赖的方式抑制SGC-7901细胞增殖;1.5×10-5、1.0×10-5和5×10-6mol.L-1darbufelone作用72 h后,细胞凋亡率分别为(30.3±2.1)%、(23.0±2.0)%和(15.0±1.5)%,均高于对照组(0.6±0.1)%(P<0.01);1.5×10-5、1.0×10-5和5×10-6mol.L-1darbufelone处理胃癌SGC-7901细胞72 h后,5-LOX和COX-2 mRNA及其蛋白质表达均减少(P<0.05)。结论环氧合酶-2/5-脂氧合酶双重抑制剂darbufelone对人胃癌SGC-7901细胞株有抑制增殖、诱导凋亡的作用。Aim To investigate the effects of dual COX-2/5-LOX inhibitor darbufelone on the inhibition of gastric adenocarcinoma in vitro. Methods MTT assay was used to detect the inhibition of gastric adenocarcinoma cell line SGC-7901 by darbufelone in different concentrations and at different times. TUNEL staining was used to evaluate the apoptosis of SGC-7901 cells. The changes of 5-LOX and COX-2 mRNA expression were studied by reverse transcription polymerase chain reaction. 5-LOX and COX-2 protein expressions were analyzed by immunocytochemistry in SGC- 7901 cells. Results darbufelone could decrease the proliferation significantly in a dose-dependent and time-dependent manner in SGC-7901 cells. After treating SGC-7901 with darbufelone at concentration of 1.5 × 10^-5,1.0 ×10^-5, 5 ×10^-6mol · L^-1 for72 hs, apoptosis index (% ) of SGC-7901 was (30. 3 ± 2.1)%, (23.0±2.0)%,(15.0 ± 1.5)%, respectively, which was significantly higher than (0.6 ±0. 1 )% that in control group(P 〈0.01 ). 1.5× 10^-5, 1.0 × 10^ -5, 5 × 10^ -6 mol · L^-1 darbufelone effectively inhibited the protein and mRNA expression of COX-2 and 5-LOX ( P 〈 0.05 ). Conclusions darbufelone can inhibit the proliferation and induce apoptosis of SGC-7901 cells.
关 键 词:SGC-7901细胞 环氧合酶-2 5-脂氧合酶 增殖 凋亡
分 类 号:R329.24[医药卫生—人体解剖和组织胚胎学] R329.25[医药卫生—基础医学]
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