基础医学与临床 ›› 2015, Vol. 35 ›› Issue (3): 383-386.

• 研究论文 • 上一篇    下一篇

Runx3对人肝癌HepG2细胞增殖、凋亡及侵袭的影响

刘俊斌,吴卫红,靳君华   

  1. 内蒙古医科大学附属医院
  • 收稿日期:2014-10-13 修回日期:2014-12-03 出版日期:2015-03-05 发布日期:2015-03-03
  • 通讯作者: 刘俊斌 E-mail:qihoney@gmail.com

Effect of Runx3 on the proliferation, apoptosis and invasion of HepG2 cells

  • Received:2014-10-13 Revised:2014-12-03 Online:2015-03-05 Published:2015-03-03

摘要: 目的 探讨siRNA干扰Runx3对人肝癌HepG2细胞增殖、凋亡和侵袭能力的影响。方法 以人肝癌HepG2细胞为研究对象,构建Runx3-siRNA,转染入细胞。将细胞分为对照组、脂质体组、NC-siRNA组和Runx3-siRNA组。用RT-PCR法检测Runx3 mRNA表达,用Western blotting检测Runx3蛋白表达。用MTT法、流式细胞法和Transwell小室法观察Runx3对HepG2细胞增殖、凋亡和侵袭的影响。结果Runx3-siRNA可抑制HepG2细胞的增殖(P<0.05);Runx3-siRNA可促进HepG2细胞凋亡(P<0.05);Runx3-siRNA可抑制HepG2细胞的侵袭(P<0.05)。结论Runx3基因在肝癌的发生发展中发挥一定的促进作用,有可能成为肝癌治疗的新靶点。

关键词: Runt相关转录因子3, HepG2细胞, 增殖, 凋亡, 侵袭

Abstract: Objective To explore the effect of siRNA targeting Runx3 on proliferation, apoptosis, and invasive ability of HepG2 cells. Methods The Runx3-siRNA was transfected into HepG2 cells. HepG2 cells were divided into four groups: control group, liposomes group, NC-siRNA group and Runx3-siRNA group. The expression levels of Runx3 mRNA and Runx3 protein were examined by RT-PCR and Western blotting. MTT assay, flow cytometry and Transwell chamber were used to determine the effect of Runx3 on HepG2 cells proliferation, apoptosis and migration. Results MTT assay showed that the proliferation of HepG2 cells was obviously inhibited by Runx3-siRNA. The result of flow cytometry demonstrated that the apoptosis of HepG2 cells was promoted by Runx3-siRNA. The invasion of HepG2 cells was also significantly inhibited by Runx3-siRNA according to Transwell chamber assay. Conclusions Silence Runx3 could effectively inhibit cell proliferation and migration, and promote apoptosis in HepG2 cells. Our study shows that Runx3 gene plays an important role on the occurrence and development in hepatocellular carcinoma. Runx3 could be a new target for the treatment of hepatocellular carcinoma.