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作 者:王庆亮[1] 郭敏毅[2] 李洋[3] 叶小鸣[1]
机构地区:[1]中山大学附属第三医院岭南医院普通外科,510530 [2]中山大学附属第三医院药剂科,510630 [3]中山大学附属第三医院肝脏外科,510630
出 处:《新医学》2012年第3期174-178,共5页Journal of New Medicine
基 金:广东省科技计划项目(2011B031300016);广东省科委社会发展计划资助项目(2006B36002002)
摘 要:目的:观察热疗对哺乳动物雷帕霉素靶蛋白(mTOR)靶向基因治疗在人肝癌细胞SMMC-7721中体外杀伤作用的影响。方法:观察不同温度热疗处理后SMMC-7721的形态学变化,并采用CCK-8试剂检测细胞增殖确定合适热疗温度,以该温度与转染pEGFP-C1-mTOR反义质粒相结合,设置联合组、转染组及对照组,CCK-8试剂检测处理后各组细胞增殖变化;流式细胞仪分析凋亡;逆转录PCR(RT-PCR)和蛋白免疫印记法检测mTOR基因表达。结果:热疗后细胞皱缩、变圆,胞浆空泡化,坏死细胞比例增加。CCK-8检测示温度越高,热疗对细胞增殖抑制作用越明显,42℃热疗后抑制率达(29.7±1.7)%。联合处理后细胞增殖能力降低,流式细胞仪分析示细胞凋亡比例增加,差异有统计学意义(P<0.05)。转染后mTOR基因表达在mR-NA水平和蛋白水平均受到抑制,而联合处理后表达水平进一步下降。结论:热疗可以增强mTOR靶向基因治疗对SMMC-7721细胞的体外杀伤作用。Objective : To investigate the enhanced killing effect of hyperthermia of mammalian target of rapa- mycin (mTOR) -targeted gene therapy on human hepatocellular carcinoma cell line SMMC-7721 in vitro. Methods: The morphological change of SMMC-7721 was observed after hyperthermia at different temperatures, thus the optimal temperature was determined with assistance of CCK-8 assay. Optimal hyperthermia was executed after trans fection of antisense plasmid pEGFP-CI-mTOR. Cell proliferation and apoptosis were evaluated by using CCK-8 as say and flow cytometry, respectively. The expression of mTOR mRNA and protein were analyzed by RT-PCR and Western blot. Results: After hyperthermia, cell shrinkage, rounded and blebbing, and also the proportion of necrotic cell were increased. According to CCK-8 assay, the inhibition effect was in consistent with the elevation of temperature, and reached 29.7± 1.7% at 42℃. After combined treatment, cell proliferation was significantly re- duced and with increased apoptosis (P 〈 0.05 ). The expression of mTOR mRNA and protein were reduced after transfection, and more prominent combined treatment group. Conclusion: Hyperthermia enhances the killing effect of mTOR-targeted gene therapy on human hepatocellular carcinoma cell line SMMC-7721 in vitro.
关 键 词:热疗 靶向基因治疗 哺乳动物雷帕霉素靶蛋白 质粒 肝癌
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