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ShRNA沉默基因DNA甲基转移酶3b的表达对膀胱癌T24细胞增殖的影响
引用本文:张士龙,曾甫清,董继华,朱朝辉,廖贵益,彭世波.ShRNA沉默基因DNA甲基转移酶3b的表达对膀胱癌T24细胞增殖的影响[J].中国医师杂志,2008,10(9):1156-1159.
作者姓名:张士龙  曾甫清  董继华  朱朝辉  廖贵益  彭世波
作者单位:1. 华中科技大学同济医学院附属协和医院泌尿外科,湖北,武汉,430022
2. 华中科技大学同济医学院附属协和医院中心实验室,湖北,武汉,430022
基金项目:湖北省科技公关计划项目 
摘    要:目的体外研究重组质粒pshRNA-DNMT3b对膀胱癌T24细胞中DNMT3bmRNA和蛋白的沉默效应以及细胞增殖抑制的影响,初步探讨DNMT3b在膀胱肿瘤发生过程中的作用。方法实验分为空白对照组、HK组及pshRNA-DNMT3b组(24、48、72h);常规培养T24细胞,用脂质体lipofectamine2000将重组质粒pshRNA-DNMT3b转染进入T24细胞,后进行RT.PCR、WesternBlot、MTY检测,观察pshRNA-DNMT3b对T24细胞中DNMT3bmRNA、蛋白质水平变化以及细胞增殖的影响。结果重组质粒pshRNA-DNMT3b成功的转染进入T24细胞;RT-PCR电泳结果用Gel-proanalyzer图像分析系统进行灰度分析,空白对照组、HK组、pshRNA-DNMT3b组(24、48、72h)条带的IOD相对比值(DNMT3/β-actin)分别是(99.56±1.24)%、(99.12±1.35)%、(75.77±1.42)%、(44.69±1.05)%和(20.52±0.89)%;Westernblot图像分析结果各组的相对比值分别是(99.43±1.28)%、(98.90±1.31)%、(67.83±1.02)%、(43.43±1.05)%和(21.92±0.89)%;在MTF检测中空白对照组和HK组之间差异无统计学意义(P〉0.05),pshRNA-DNMT3b组仅在72h后和前2组之间差异有统计学意义(P〈0.01),但抑制率仅增加0.45%左右。结论重组质粒pshRNA-DNMT3b能有效的降低膀胱癌1、24细胞中基因DNMT3bmRNA的转录及蛋白的表达,但在抑制细胞增殖上作用甚微。

关 键 词:DNA(胞嘧啶-5-)-甲基转移酶  RNA干扰  膀胱肿瘤

Effect of silencing gene DNA methyltransferase 3b expression by shRNA on proliferation of bladder cancer T24 cells
ZHANG Shi-long,ZENG Fu-qing,DONG Ji-hua,ZHU Chao-hui,LIAO Gui-yi,PENG Shi-bo.Effect of silencing gene DNA methyltransferase 3b expression by shRNA on proliferation of bladder cancer T24 cells[J].Journal of Chinese Physician,2008,10(9):1156-1159.
Authors:ZHANG Shi-long  ZENG Fu-qing  DONG Ji-hua  ZHU Chao-hui  LIAO Gui-yi  PENG Shi-bo
Institution:ZHANG Shi-long, ZENG Fu-qing, DONG Ji-hua, ZHU Chao-hui, LIAO Gui-yi, PENG Shi-bo. (Department of Urology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430022, China)
Abstract:Objective To investigate the effect of recombinant plasmid pshRNA-DNMT3b on expression of DNMT3b mRNA and protein and on the proliferation of bladder cancer T24 cells,and research the function of DNMT3b in the process of bladder tumor formation.Methods There were three groups in this study,which are blank controller,HK and pshRNA-DNMT3b(24h,48h,72h),respectively.T24 cells were cultured routinely and transfected by the recombinant plasmids with lipfectamine 2000.The cells were detected by methods of RT-PCR,western blot and MTT.The varying level of DNMT3b mRNA and expression protein,and the conditions of cellular survival rate were observed.Results The recombinant plasmids were successfully transfected into T24 cell lines.The grey valHe of RT-PCR elctrophoretogram was analyzed by the software of Gel-pro analyzer,the rate of blank controller,HK and pshRNA-DNMT3b(24h,48h,72h),was (99.56±1.24)%,(99.12±1.35)%,(75.77±1.42)%,(44.69±1.05)%and(20.52±0.89)%,respectively.The analytical resuit of western blot image was(99.43±1.28)%,(98.90±1.31)%,(67.83±1.02)%,(43.43±1.05)%and(21.92±0.89)%.There was no statistically difference in survival between blank control and HK(P>0.05).The group of pshRNA-DNMT3b and other two groups had statistical difference only at the 72th hour and the cell inhibitory growth rate only increase 0.45%.Conclusions The recombinant ptasmid pshRNA-DNMT3b can inhibit the expression of mRNA and protein of DNMT3b effectively.However,it has slight function on inhibiting cell proliferation.
Keywords:DNA(cytosine-5-)-methyhransferase  RNA interference  Bladder neoplasms
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