基础医学与临床 ›› 2013, Vol. 33 ›› Issue (12): 1590-1594.

• 研究论文 • 上一篇    下一篇

EphA2在不同肝癌细胞系中过表达及其与乙肝病毒感染相关

王鹏,朱争艳,李成龙,骆莹,张海鹏,刘辉   

  1. 天津市第三中心医院肝胆疾病研究所,天津市人工细胞重点实验室
  • 收稿日期:2013-06-09 修回日期:2013-07-19 出版日期:2013-12-05 发布日期:2013-11-28
  • 通讯作者: 刘辉 E-mail:liuyangmeimei@163.com
  • 基金资助:
    高新技术产业化专项资金;天津市卫生局科技基金

Over expression of EphA2 in different cell lines of hepatocellular carcinoma and its relationship with HBV infection

  • Received:2013-06-09 Revised:2013-07-19 Online:2013-12-05 Published:2013-11-28
  • Contact: Hui LIU E-mail:liuyangmeimei@163.com

摘要: 目的 观察EphA2在不同肝癌细胞系中的表达及与乙肝病毒(HBV)感染的相关性。方法 体外培养正常人肝细胞系HL7702及HepG2和HepG2.2.15两种肝癌细胞系,用免疫化学染色及蛋白免疫印迹法,检测EphA2蛋白的表达,用流式细胞术检测细胞的增殖指数与凋亡率,分析EphA2表达与肝细胞凋亡、增殖的关系。通过荧光定量聚合酶链反应(PCR)法检测肝癌细胞中HBV DNA的水平,分析EphA2表达与HBV感染的相关性。结果 与正常肝细胞比较,两种肝癌细胞中EphA2蛋白表达均明显增强(P<0.05),且HepG2.2.15细胞中EphA2的表达水平显著高于HepG2细胞中EphA2的表达水平(P<0.01);与正常肝细胞比较,两种肝癌细胞的增殖指数升高、细胞凋亡率降低(P<0.01),且肝细胞的增殖、凋亡与EphA2表达具有明显相关性(P<0.01)。HepG2.2.15细胞中HBV DNA水平显著高于HepG2细胞中HBV DNA水平,且HBV DNA水平与EphA2表达呈显著正相关(r=0.878,P<0.05)。结论 EphA2在肝癌细胞中过表达,可促进肝细胞的恶性生长,抑制肝细胞的凋亡,且EphA2过表达与HBV感染密切相关。

关键词: 肝癌, EphA2, 细胞增殖, 凋亡, 乙型肝炎病毒

Abstract: Objective To investigate the expression of EphA2 in human hepatocellular carcinoma and its relationship with HBV infection. Methods Expressions of EphA2 protein in the cell lines of HL7702, HepG2 and HepG2.2.15 were examined by immunochemistry staining and Western blotting. The proliferation index and apoptotic ratio were determined by FCM, and the relationship between EphA2 expression and cellular apoptosis and proliferation were analyzed. The levels of HBV DNA in hepatocellular carcinoma cells were detected by real-time PCR and its relationship with EphA2 expression were analyzed. Results EphA2 expression increased in hepatocellular carcinoma cells comparing with that in normal hepatic cells (P<0.05) and the expression level of EphA2 in HepG2.2.15 was higher than that in HepG2 (P<0.01). The proliferation index was increased and the apoptotic ratio was decreased in hepatocellular carcinoma cells comparing with that in normal hepatic cells (P<0.01), and the cell apoptosis and proliferation were associated with EphA2 expression (P<0.01). The level of HBV DNA in HepG2.2.15 was higher than that in HepG2 (P<0.01) and the level of HBV DNA in hepatocellular carcinoma cells was positively correlated with EphA2 expression (r=0.878,P<0.05). Conclusion EphA2 protein is over-expressed in hepatocellular carcinoma and the overexpression of EphA2 inhibits the apoptosis and promotes the proliferation of liver cells. EphA2 overexpression is close associated with HBV infection.

Key words: Hepatocellular carcinoma, EphA2, Proliferation, Apoptosis, HBV

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