干扰素γ诱导肝癌HepG2细胞表达B7分子的实验研究  

Study of Interferon-γ on B7 Expression in HepG2 Cell Line of Human Liver Neoplasm

作　　者：张顺明 袁小敏 

机构地区：[1]江苏省南京市六合区人民医院,211500

出　　处：《中国医药指南》2009年第19期27-29,共3页Guide of China Medicine

摘　　要：目的研究干扰素γ(IFN-γ)对人肝癌细胞B7分子表达的影响。方法选用人肝癌HepG2细胞进行体外培养,经过不同浓度的IFN-γ干预后,采用MTT法检测细胞增殖作用,RT-PCR检测B7-1和B7-2mRNA的表达。结果不同浓度的IFN-γ对HepG2细胞体外生长有明显抑制作用;干预后HepG2细胞的B7基因表达明显增加。结论IFN-γ能直接抑制HepG2细胞增殖,显著上调HepG2细胞B7基因的表达,具有一定的抗肿瘤效应。Objective To study the effects of IFN-γ on expression of B7 molecules in human liver neoplasm cell line. Methods Human liver neoplasm HepG2 cells were cultured in vitro in the medium with IFN-γ respectively, cell proliferation effect was measured by MTT assay; expression of B7-1 and B7-2 mRNA was determined by RT-PCR. Results MTT shows that IFN-γ could reduce the HepG2 cell proliferation, expression of B7-1 and B7-2 significantly increased in the IFN-γ group. Conclusion IFN-3, can inhibit cell proliferation. IFN-γ markedly enhance the expression of B7-1 and B7-2 in HepG2 line and olavs a role in anti-cancer effect.

关 键 词：干扰素Γ HEPG2细胞系 B7分子 

分 类 号：R735.7[医药卫生—肿瘤]