Wang Yue, Fang Runping, Cui Ming, Zhang Weiying, Bai Xiao, Wang Huawei, Liu Bowen, Zhang Xiaodong, Ye Lihong
State Key Laboratory of Medicinal Chemical Biology, Department of Biochemistry, College of Life Sciences, Nankai University, Tianjin, People's Republic of China.
State Key Laboratory of Medicinal Chemical Biology, Department of Cancer Research, College of Life Sciences, Nankai University, Tianjin, People's Republic of China.
Cancer Lett. 2017 Jan 28;385:234-242. doi: 10.1016/j.canlet.2016.10.018. Epub 2016 Oct 17.
The oncoprotein Yes-associated protein (YAP) in Hippo pathway plays crucial roles in the development of cancer. However, the mechanism of YAP regulation in cancer remains poorly understood. Here, we supposed that the oncoprotein hepatitis B X-interacting protein (HBXIP) might be involved in the modulation of YAP in liver cancer. Interestingly, our data showed that the expression levels of HBXIP were positively associated with those of YAP in clinical hepatocellular carcinoma (HCC) samples by immunohistochemistry (IHC) staining and real-time PCR assays. HBXIP was able to up-regulate YAP in hepatoma cells at the levels of promoter, mRNA and protein. Mechanistically, we identified that HBXIP up-regulated YAP through co-activating the transcription factor c-Myb in hepatoma cells. Functionally, silencing YAP abolished the proliferation of hepatoma cells mediated by HBXIP in vitro. Moreover, knockdown of YAP strongly blocked the HBXIP-enhanced tumor growth in mice. Thus, we conclude that HBXIP up-regulates YAP expression via activating transcription factor c-Myb to facilitate the growth of hepatoma cells. Our finding provides new insights into the mechanism of YAP regulation. Therapeutically, the oncoprotein HBXIP and YAP might serve as targets in liver cancer.
河马通路中的癌蛋白Yes相关蛋白(YAP)在癌症发展中起关键作用。然而,YAP在癌症中的调控机制仍知之甚少。在此,我们推测癌蛋白乙型肝炎X相互作用蛋白(HBXIP)可能参与肝癌中YAP的调控。有趣的是,我们的数据通过免疫组织化学(IHC)染色和实时PCR分析表明,在临床肝细胞癌(HCC)样本中,HBXIP的表达水平与YAP的表达水平呈正相关。HBXIP能够在启动子、mRNA和蛋白质水平上调肝癌细胞中的YAP。机制上,我们发现在肝癌细胞中HBXIP通过共激活转录因子c-Myb上调YAP。功能上,沉默YAP消除了体外HBXIP介导的肝癌细胞增殖。此外,敲低YAP强烈阻断了HBXIP增强的小鼠肿瘤生长。因此,我们得出结论,HBXIP通过激活转录因子c-Myb上调YAP表达,以促进肝癌细胞生长。我们的发现为YAP调控机制提供了新的见解。在治疗方面,癌蛋白HBXIP和YAP可能成为肝癌的治疗靶点。