基础医学与临床 ›› 2014, Vol. 34 ›› Issue (9): 1199-1203.

• 研究论文 • 上一篇    下一篇

顺铂通过促进microRNA-214表达抑制肝癌细胞增殖

刘子文1,杜永星2,由磊3,舒红1,赵玉沛4   

  1. 1. 中国医学科学院北京协和医院
    2. 北京协和医院
    3. 中国医学科学院北京协和医院整形美容外科
    4. 北京协和医院外科
  • 收稿日期:2014-07-02 修回日期:2014-07-09 出版日期:2014-09-05 发布日期:2014-09-02
  • 通讯作者: 赵玉沛 E-mail:zhao8028@263.net
  • 基金资助:
    AKR1B10蛋白翻译后修饰在肝癌细胞脂代谢紊乱和化疗敏感性中的作用机制研究

Cisplatin suppresses human hepatocellular carcinoma cell growth via regulating microRNA-214-mediatedΒ-CATENIN axis

  • Received:2014-07-02 Revised:2014-07-09 Online:2014-09-05 Published:2014-09-02

摘要: 目的 研究顺铂对microRNA-214(miR-214)在肝癌细胞中表达的影响及其抑制肝癌细胞增殖的分子机制。方法 用Real-Time PCR方法分析miR-214在肝细胞癌组织及细胞系中的表达;利用CCK-8细胞增殖分析法确定顺铂在肝癌细胞系HepG2及Hep3b中的半数致死浓度(IC50),并用Real-Time PCR和 Western blot 方法检测经不同浓度顺铂处理的肝癌细胞HepG2及Hep3b中miR-214及其靶基因Β-CATENIN的表达变化;设计拯救实验研究顺铂、miR-214与肝癌细胞增殖的关系。结果miR-214在肝细胞癌组织及细胞系中表达下调(P<0.01);顺铂处理的肝癌细胞系HepG2、Hep3b内源性miR-214表达水平明显上调(P<0.01),而其靶基因Β-CATENIN的表达水平明显下调(P<0.05)。结论 顺铂通过调控miR-214介导的Β-CATENIN表达发挥抑制肝癌细胞增殖的作用。

关键词: miR-214, 肝细胞癌, 化疗

Abstract: Objective To investigate the impact of cisplatin on microRNA-214 (miR-214) expression in human hepatocellular carcinoma (HCC) cell lines and to elucidate the molecular mechanism of cisplatin for HCC chemotherapy. Methods Real-time PCR analysis was conducted to determine the expression levels of miR-214 in HCC tissue specimens and HCC cell lines. The IC 50 value of cisplatin was determined both in HepG2 and Hep3b cell lines. The expression of miR-214 was evaluated in HepG2 and Hep3b cells with cisplatin treatment by using real-time PCR and we also performed western blot analysis to detect the protein levels ofΒ-CATENIN in HCC cells with the same treatment as described above. A rescue assay was conducted by using cisplatin treatment in combination with miR-214 inhibitor (Anti-214) to further investigate the correlation among cisplatin, miR-214, and cell growth. Results miR-214 expression depicted a significant downregulation in HCC tissues and cell lines (P<0.01). Cisplatin treatment led to an augment of miR-214 expression in HepG2 and Hep3b cells (P<0.01) and resulted in a decrease ofΒ-CATENIN protein levels, which was verified as a direct target of miR-214 in HCC cells (P<0.05). Conclusion Cisplatin represents its suppressive effect on HCC growth at least partly via miR-214-mediatedΒ-CATENIN axis.

Key words: miR-214, HCC, chemotherapy

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