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GRIM-19基因对前列腺癌DU145细胞的促凋亡作用
引用本文:刘艳波,葛贺,盖晓东,李冰,赵雪俭,芦丽莉.GRIM-19基因对前列腺癌DU145细胞的促凋亡作用[J].吉林林学院学报,2012(1):58-61.
作者姓名:刘艳波  葛贺  盖晓东  李冰  赵雪俭  芦丽莉
作者单位:[1]北华大学基础医学院,吉林吉林132013 [2]吉林大学前列腺疾病防治研究中心,吉林长春130001
基金项目:吉林省教育厅科学技术研究项目(2011146);吉林市科技局科研项目(201133139;01032235).
摘    要:目的探讨GRIM-19基因对前列腺癌DU145细胞的促凋亡作用,并分析相关机制.方法将构建成功的pGRIM-19重组质粒转染DU145细胞株,应用MTT法检测其对细胞增殖能力的影响,通过流式细胞术检测细胞周期及凋亡率,应用半定量RT-PCR检测GRIM-19及caspase-3 mRNA转录水平.结果流式细胞术结果显示:与对照组比较,pGRIM-19重组质粒明显抑制DU145细胞增殖,并使细胞周期发生改变,多数细胞抑制在G0/G1期,细胞凋亡率增加明显;通过RT—PCR电泳结果证实:pGRIM-19重组质粒明显促进GRIM-19的表达,同时激活caspase-3.结论重组质粒pGRIM-19可明显抑制DU145细胞增殖,并促进其凋亡,其凋亡的发生机制与激活caspase-3有关.

关 键 词:GRIM-19  前列腺癌  质粒  凋亡

Pro-apoptosis Effect of GRIM-19 Gene on Prostatic Cancer DU145 Cells
Authors:LIU Yan-bo  GE He  GAI Xiao-dong  LI Bing  ZHAO Xue-jian  LU Li-li
Institution:1. Basic Medical College, Beihua University Jilin 132013, China; 2. Prevention and Cure Center of Prostate Disease, Jilin University, Changchun 130021, China)
Abstract:Objective To explore the pro-apoptosis effect of GRIM-19 gene on prostatic cancer DU145 cells and analyze the related mechanisms. Method The constructed recombinant plasmid pGRIM-19 was transfected into prostatic carcinoma DU145 cells. The growth inhibitory rate was determined by MTT, cell cycle distribution and apoptosis rate were determined with flow cytometry and GRIM-19 and caspase-3 mRNA expression levels were measured by using RT-PCR assay. Results Compared with control group,pGRIM-19 could inhibit DU145 cells proliferation obviously. The cell cycle changed, most cells remained in G0/G1 phase with obvious apoptotic rate by flow cytometry; pGRIM-19 could promote GRIM-19 expression and activate caspase-3 through RT-PCR detection. Conclusion The recombinant plasmid pGRIM-19 could significantly inhibit DU145 cells proliferation and promote their apoptosis. The mechanism was related to high caspase-3 level.
Keywords:GRIM-19  prostatic cancer  plasmids  apoptosis
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