Role of the transcriptional coactivators YAP/TAZ in liver cancer

Curr Opin Cell Biol. 2019 Dec:61:64-71. doi: 10.1016/j.ceb.2019.07.006. Epub 2019 Aug 3.

Abstract

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.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Acyltransferases
  • Adaptor Proteins, Signal Transducing / metabolism
  • Carcinogenesis
  • Carcinoma, Hepatocellular / pathology*
  • Cell Cycle Proteins / metabolism*
  • Hippo Signaling Pathway
  • Humans
  • Liver Neoplasms / pathology*
  • Organ Size
  • Phosphoproteins
  • Protein Serine-Threonine Kinases / metabolism*
  • Signal Transduction
  • Transcription Factors / metabolism*

Substances

  • Adaptor Proteins, Signal Transducing
  • Cell Cycle Proteins
  • Phosphoproteins
  • Transcription Factors
  • YY1AP1 protein, human
  • Acyltransferases
  • TAFAZZIN protein, human
  • Protein Serine-Threonine Kinases