实用肿瘤学杂志 ›› 2011, Vol. 25 ›› Issue (5): 406-410.doi: 10.3969/j.issn.1002-3070.2011.05.002

• 论著 • 上一篇    下一篇

利用RNA干扰技术分析Pokemon对Lovo增殖过程的影响

白玉贤, 刘磊, 隋红, 魏孝礼, 苑珩珩   

  1. 哈尔滨医科大学附属第三医院肿瘤内科(哈尔滨 150081)
  • 收稿日期:2011-06-03 出版日期:2011-10-28 发布日期:2014-12-02
  • 通讯作者: 白玉贤,E-mail:Bai_yuxian@126.com
  • 作者简介:白玉贤,女,(1962-),主任医师,从事消化道肿瘤的化疗及靶向治疗
  • 基金资助:
    黑龙江省教育厅科学技术研究项目(11521179)

Analysis of biological role of pokemon in cultured Lovo cells by RNA interference

BAI Yuxian1,LIU Lei,SUI Hong,WEI Xiaoli,YUAN Hengheng   

  1. 1.Medical Department,The Tumor Hospital Affiliated Harbin Medical University,Harbin 150081;
    2.Laboratory of Medical Genetics,Harbin Medical University,Harbin 150081
  • Received:2011-06-03 Online:2011-10-28 Published:2014-12-02

摘要: 目的 探索干扰Pokemon基因对大肠癌细胞系Lovo增殖和细胞周期的影响。方法 采用miRNA技术干扰Pokemon基因不同位点,运用q-PCR检测干扰后Lovo细胞中Pokemon mRNA的表达,MTT和流式细胞仪分析转染后细胞增殖和细胞周期的变化。结果 成功构建含miRNA片段的重组质粒,依次命名为mR22-1、2、3、4。转染Lovo细胞后,Pokemon基因的mRNA表达水平明显下调,以mR22-1最强,干扰效率为50%±2.7%,对照组之间有统计学意义(P<0.01)。MTT显示mR22-1可明显抑制细胞增殖,24 h、48 h和72 h的抑制率分别为23%±2.1%、47%±3.0%和69%±2.5%,呈时间依赖性;流式细胞仪测定转染后Lovo细胞周期阻滞在G1期。结论 采用RNAi技术可以特异性阻断Pokemon基因的表达;Pokemon基因有促进大肠癌细胞株Lovo增殖的作用。

Abstract: Objective To construct recombinant plasmids containing microRNA targeting the Pokemon gene and investigate the effects of miRNA-mediated downregulation of the Pokemon gene on the proliferation and cell-cycle progression of colorectal cancer cells,Lovo.Methods Four miRNAs were designed according to the coding sequence of the Pokemon gene and used to construct recombinant plasmids.The recombinant plasmids were transfected into Lovo cells using Lipofectamine 2000.The expression of Pokemon mRNA was detected by Quantitative polymerase chain reaction(qPCR)assays.Cellular proliferation was measured by methyl thiazolyl tetrazolium(MTT)assay.Cell-cycle progression was analyzed by flow cytometry.Results Four recombinant plasmids were successfully constructed,named mR22-1,mR22-2,mR22-3 and mR22-4.The expression of Pokemon mRNA was obviously downregulated in Lovo cells transfected with the recombinant plasmids.The best silencing effect was achieved in cells transfected with the mR22-1 plasmid.The expression levels of Pokemon mRNA were downregulated by 50%±2.7%.MTT assay indicated that mR22-1 transfection could inhibit cellular proliferation.Flow cytometry assay indicated that mR22-1 transfection lead to Lovo cell cycle arrest in G1-phase.Conclusion The recombinant plasmids containing miRNA targeting the Pokemon gene specifically downregulate Pokemon expression.Pokemon gene can promote proliferation in Lovo cells.Results suggest that the microRNA interference developed in this study represents a novel anti-tumor strategy that may be applicable to most research involving cancer therapy and,thus,has promising potential as a colorectal cancer treatment.

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