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作 者:胡世颉[1] 李兵[1] 邹西峰[1] 胡学安[1] 张磊[1] 王冰[1] 曹宝萍[1] 罗鹏[1] 吕超[1] 费舟[1]
机构地区:[1]第四军医大学西京医院神经外科,陕西西安710032
出 处:《现代生物医学进展》2014年第24期4634-4636,4615,共4页Progress in Modern Biomedicine
基 金:国家自然科学基金青年科学基金项目(81101710)
摘 要:目的:通过动物实验探讨传输靶向COX-2siRNA联合化疗药物对大鼠胃癌细胞生长的抑制作用。方法:24只健康SD大鼠平分为三组,治疗组用COX-2-siRNA转染的胃癌SGC7901细胞接种,同时进行环磷酰胺、丝裂霉素C化疗治疗;阴性对照组,用阴性对照siRNA转染的胃癌SGC7901细胞接种,同时进行环磷酰胺、丝裂霉素C化疗治疗;对照组(n=8),用未经转染的胃癌SGC7901细胞接种,不进行化疗治疗;三组转染后都接种了裸鼠。结果:治疗组、阴性对照组及对照组胃癌细胞凋亡率分别为(22.28±0.12)%、(1.23±0.17)%和(1.03±0.14)%,治疗组与阴性对照组和对照组比较差异都有统计学意义(t=18.152,17.555,P<0.05)。治疗组的抑瘤率为76.7%,阴性对照组和对照组分别为12.8%和6.89%,治疗组的抑瘤率明显高于其他两组(x2=15.211,13.899,P<0.05)。Western blotting检测结果显示治疗组的COX-2蛋白表达含量得到了明显抑制。结论:传输靶向COX-2siRNA和化疗药物的配合应用可有效抑制COX-2蛋白的表达,从而抑制胃癌细胞的生长,从而起到更好的治疗效果。Objective: To investigate the effects of COX2 siRNA combined with chemotherapeutics on the inhibition of gastric carcinoma cells of rats. Methods: 24 healthy SD rats were selected equally divided into three groups, which including the treatment group (n=8) that were given the SGC7901 cells with COX-2-siRNA transfection and treated by the cyclophosphamide and mitomycin C in chemotherapy; the negative control group (n=8) that were given the negative control siRNA transfected cells with gastric cancer SGC7901, and treated by the cyclophosphamide and the mitomycin C in chemotherapy; the control group (n=8) that were given the untransfected SGC7901 without the chemotherapy; Then the mice in the three groups were vaccinated. Results: The rate of the cells' apoptosis in the three groups was (22.28± 0,12)%, (1.23± 0.17)% and (1.03± 0.14)% , respectively with statistically significant differences (t=18.152, 17.555, P〈0.05). The rate of antitumor in the three groups was 76.7 %, 12.8% and 6.89%, respectively. The inhibition rate in the treatment group was significantly higher than those of the other two groups (X^2=15.211,13.899, P〈0.05). Western blotting analysis showed that COX-2 protein expression levels in the treatment group was significantly inhibited. Conclusion: Transmission targeting COX-2 siRNA combined with the chemotherapy drugs can effectively inhibit the expression of COX-2 protein, thereby inhibite the growth of gastric cancer cells, which played better therapeutic effect.
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