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作 者:邹飞雁[1] 刘晓[1] 刘婉君[1] 王秋兰[2] 晏光荣[3] 白顺[1]
机构地区:[1]暨南大学生殖免疫研究所,广州510632 [2]暨南大学化学系,广州510632 [3]暨南大学生命与健康工程研究院,广州510632
出 处:《生物技术通报》2011年第5期200-204,共5页Biotechnology Bulletin
基 金:国家自然科学基金资助项目(30471954);中国博士后科学基金资助项目(2003034467);中央高校基本科研业务费专项资金(21600201)
摘 要:应用原子力显微镜(Atomic Force Microscope,AFM)技术、Real-time PCR及Western blotting方法,分别检测金雀异黄素(genistein)对SGC-7901胃癌细胞超微结构、Aurora-A基因mRNA和蛋白表达的影响。AFM扫描显示,经20μg/mLgenistein处理SGC-7901胃癌细胞48 h,细胞的超微结构呈现凋亡形态特征改变;Aurora-A表达分析,5μg/mL组、10μg/mL组和20μg/mL组与对照组比较,其mRNA表达量分别下降(31.6±0.02)%、(38.8±0.04)%和(59.9±0.02)%,其中5μg/mL组与10μg/mL组间比较无显著性差异(P>0.05),其余组间比较均有显著性差异(P<0.05);其蛋白表达量分别下降(26.8±0.04)%、(33.0±0.10)%和(48.5±0.09)%,组间比较均有显著性差异(P<0.05)。由此推断金雀异黄素诱导SGC-7901胃癌细胞凋亡的分子机制可能涉及极光激酶A mRNA及蛋白表达下调。The nano-microstructure of SGC-7901 gastric carcinoma cells was determined by Atomic Force Microscope;the expression of Aurora-A mRNA and protein were evaluated by Real-time PCR and Western blotting respectively.The nano-microstructure of SGC-7901 gastric carcinoma cells altered apparently,showed apoptosis during the treatment of 20 μg/mL genistein after 48 h.Compared with group of control,Aurora-A mRNAs were down-regulated after genistein treatment,which were(31.6±0.02)%,(38.8±0.04)%,(59.9±0.02)%,between the group of 5 μg/mL and the group of control,there was no significant difference(P0.05),while among other groups,there were significant differences(P0.05);Aurora-A proteins were also down-regulated,which were(26.8±0.04)%,(33.0±0.10)%,(48.5±0.09)%,there were significant differences among all the group(P0.05).The present study indicated that the mechanism of SGC-7901 gastric carcinoma cells apoptosis induced by genistein may be due to the down-regulation of expression of Aurora-A mRNA and protein.
关 键 词:金雀异黄素 SGC-7901胃癌细胞 原子力显微镜 凋亡 极光激酶A
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