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作 者:张青松[1] 曹立赢[1] 王明君[1] 温英武[1] 费乐学[1] 高建超[1] 郑景珍[1] 李浩[1] 戴世龙[1]
出 处:《安徽医药》2017年第4期646-649,共4页Anhui Medical and Pharmaceutical Journal
基 金:唐山市科技支撑项目(14130260)
摘 要:目的研究5-甲基硫代腺苷(MTA)对结肠癌Hct116细胞增殖的影响及其相关机制。方法采用MTT比色法及软琼脂克隆形成试验分析MTA对结肠癌Hct116细胞增殖的影响,采用Realtime PCR的方法分析RNA聚合酶Ⅲ依赖基因(tRNAs、5S rRNA)及TFⅢB亚单位TBP、Bdp1和Brf1基因mRNA水平的变化,并采用Western Blot的方法分析了TFⅢB亚单位Bdp1蛋白水平的变化。结果 MTA对结肠癌Hct116细胞具有明显的增殖抑制作用,在这一过程中,RNA聚合酶Ⅲ依赖基因(tRNAs、5S rRNA)的mRNA水平明显下调;同时TFⅢB亚单位Bdp1在mRNA水平和蛋白水平也出现了明显下调。结论 MTA对结肠癌Hct116细胞具有明显增殖抑制作用;RNA聚合酶Ⅲ依赖基因转录的下调、TFⅢB亚单位Bdp1蛋白的下调可能在这一抗肿瘤过程中起到重要作用。Objective To study the role and mechanism of methylthioadenosine in cell proliferation of colon cancer Hctl 16 cells. Meth-ods MTT assay and anchorage-independent growth were used to detect the effects of methylthioadenosine on proliferation in Hctl 16 cells;the level of RNA Pol Ⅲ-dependent (tRNAs,5SrRNA) and the subunits of TFⅢB (TBP,Bdp1 and Bif l) transcription were de-tected with the method of Realtime PCR;the level of subunit of TFⅢB (Bdp1) protein was detected with the method of Western Blot. Results Methylthioadenosine could significantly inhibitthe proliferation of Hctl 16 cells; RNA Pol Ⅲ-dependent (tRNAs,5S rRNA) transcription was downregulated significantly ; mRNA and protein of the Bdp1 were also downregulated significantly in this course. Con-clusions Methylthioadenosine could inhibit significantly the proliferation ofHctll6 cells and downregulate RNA Pol Ⅲ-dependent (tRNAs,5S rRNA) transcription and protein of the subunit of the TFⅢB Bdp1,which might play a major role in the treatment of cancer.
关 键 词:5-甲基硫代腺苷结肠癌细胞增殖 RNA 聚合酶Ⅲ
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