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机构地区:[1]大连医科大学,辽宁大连116044 [2]大连第六人民医院
出 处:《胃肠病学和肝病学杂志》2010年第9期859-863,共5页Chinese Journal of Gastroenterology and Hepatology
基 金:2008年大连市卫生局科研基金项目(20080423)
摘 要:目的探讨IFN-γ对肝癌细胞肿瘤抗原甲胎蛋白和MAGE-1表达的影响与机制。方法用重组人干扰素处理人肝癌细胞系SMMC-7721,用四氮唑比色法检测人肝癌细胞增殖活性,用间接免疫荧光检测MAGE-1表达,ELISA法检测甲胎蛋白表达,用BSP法测MAGE-1基因启动子甲基化状态,用免疫沉淀测JNK活性。结果在IFN-γ作用下,SMMC-7721细胞甲胎蛋白表达量下降,MAGE-1表达下降,MAGE-1基因启动子甲基化程度增加而JNK活性降低。结论 IFN-γ可增强MAGE-1基因启动子甲基化程度,下调MAGE-1表达,降低JNK活性,抑制细胞增殖。Objective To investigate the effects and mechanisms of Interferon-γ(IFN-γ) on the expression of hepatocellular carcinoma-associated antigens AFP and MAGE-1. Methods Human hepatocellular carcinoma cell line SMMC-7721 cells were treated with recombinant IFN-γ.MTT colorimetry was used to reveal the proliferative activity.ELISA method was applied to detect the AFP expression.Indirect immunofluorescence was used to detect MAGE-1 expression.Bisulfite-sequencing PCR(BSP) was used to assay the methylation status of MAGE-1 gene promoter of SMMC-7721.Immunoprecipitation was used to assay the activity of the c-Jun N-terminal kinases. Results The results of indirect immunofluorescence showed that the expression of MAGE-1 and AFP in IFN-γ-treated SMMC-7721 were weaker than those in untreated cells.The methylation status of MAGE-1 gene promoter in IFN-γ-treated SMMC-7721 was higher than that in untreated cells.The activity of JNK decreased in IFN-γ-treated cells. Conclusion IFN-γ may enhance methylation status of MAGE-1 gene promoter,down-regulate the expression of MAGE-1 and decrease JNK activity.
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