Cheng Xiao-Ke, Yu Guo-Zheng, Li Xiao-Dong, Ren Xue-Qun
Center for Evidence-Based Medicine, Huaihe Hospital of Henan University, Kaifeng 475000, Henan Province, China.
Department of General Surgery, Huangshi Central Hospital, Affiliated Hospital of Hubei Polytechnic University, Huangshi 435000, Hubei Province, China.
Oncotarget. 2017 Jan 3;8(1):1132-1140. doi: 10.18632/oncotarget.13586.
Raf kinase inhibitor protein (RKIP) has been shown to be a suppressor of the mitogen-activated protein kinase pathway and is reported to be involved in human malignancy. However, the molecular mechanism of hepatitis B virus (HBV) in regulating RKIP expression is not yet clarified. In this study, we compared RKIP expression in 107 pairs of matched liver cancer and adjacent non-cancerous liver tissues. Among seven HBV-encoded proteins, we found HBV X (HBX) protein could significantly inhibit the expression level of RKIP, indicating that HBV could suppress RKIP expression through regulating HBX. To further elucidate the mechanism, analyses on transcriptional regulation and promoter methylation inhibition were conducted in Huh7 cells. Our results showed that HBX can interact with AP1 protein to inhibit the RKIP transcription. Moreover, we observed that the promoter methylation level of RKIP could be enhanced by HBV. In conclusion, our study revealed that RKIP could act as a molecular marker for HBV-infected liver cancer, but had no tumor-suppressing effect.
raf激酶抑制蛋白(RKIP)已被证明是丝裂原活化蛋白激酶途径的抑制剂,据报道与人类恶性肿瘤有关。然而,乙型肝炎病毒(HBV)调节RKIP表达的分子机制尚未阐明。在本研究中,我们比较了107对匹配的肝癌组织和癌旁非癌肝组织中RKIP的表达。在七种HBV编码蛋白中,我们发现HBV X(HBX)蛋白可显著抑制RKIP的表达水平,表明HBV可通过调节HBX抑制RKIP表达。为进一步阐明其机制,我们在Huh7细胞中进行了转录调控和启动子甲基化抑制分析。我们的结果表明,HBX可与AP1蛋白相互作用以抑制RKIP转录。此外,我们观察到HBV可提高RKIP的启动子甲基化水平。总之,我们的研究表明,RKIP可作为HBV感染肝癌的分子标志物,但无抑癌作用。