State Key Laboratory of Cellular Stress Biology, Innovation Center for Cell Signaling Network, School of Life Sciences, Xiamen University, Xiamen, Fujian 361102, China.
State Key Laboratory of Cellular Stress Biology, Innovation Center for Cell Signaling Network, School of Life Sciences, Xiamen University, Xiamen, Fujian 361102, China.
Curr Opin Cell Biol. 2019 Dec;61:64-71. doi: 10.1016/j.ceb.2019.07.006. Epub 2019 Aug 3.
Liver cancer, hepatocellular carcinoma (HCC) in particular, is one of the deadliest cancers worldwide. Although the etiologies for liver oncogenesis are relatively well defined, the exact mechanisms leading to cancer development remain elusive. The Hippo signaling pathway, an evolutionarily conserved signaling module, plays critical roles in organ size control and tumorigenesis. The aberrant activation of the transcriptional coactivator YAP or TAZ, downstream effectors of the Hippo signaling pathway, has been implicated in several human cancers including HCC. YAP/TAZ therefore have emerged as an attractive target for cancer therapeutics. In this review, we summarize the recent findings regarding the role of YAP/TAZ in HCC development, and discuss the multifarious mechanisms regulating their activities and their potential contribution to human liver tumorigenesis.
肝癌,特别是肝细胞癌 (HCC),是全球最致命的癌症之一。尽管肝癌发生的病因相对明确,但导致癌症发展的确切机制仍难以捉摸。Hippo 信号通路是一种进化上保守的信号模块,在器官大小控制和肿瘤发生中发挥着关键作用。Hippo 信号通路的下游效应因子转录共激活因子 YAP 或 TAZ 的异常激活与包括 HCC 在内的多种人类癌症有关。因此,YAP/TAZ 已成为癌症治疗的一个有吸引力的靶点。在这篇综述中,我们总结了最近关于 YAP/TAZ 在 HCC 发展中的作用的研究结果,并讨论了调节它们活性的多种机制及其对人类肝肿瘤发生的潜在贡献。