Upregulated YAP promotes oncogenic CTNNB1 expression contributing to molecular pathology of hepatoblastoma

Pediatr Blood Cancer. 2022 Sep;69(9):e29705. doi: 10.1002/pbc.29705. Epub 2022 Apr 11.

Abstract

Background: Hepatoblastoma (HB) is one of the most common cancers in children. Recent studies have shown that the occurrence of nuclear accumulation of β-catenin reaches 90%-100% because of the anomalous activation of the Wnt pathway in HB patients. Furthermore, emerging studies have shown that concomitant activated forms of YAP and β-catenin trigger the formation and progression of HB. YAP might play a vital role in β-catenin-mediated HB development. However, the molecular mechanisms by which YAP/TEAD4 transcription factor regulates CTNNB1 underlying HB pathogenesis are still unclear.

Procedure: YAP and CTNNB1 expression and correlation were analyzed by a combination of network enrichment analysis and gene set enrichment analysis of the public microarray datasets (GSE131329 and GSE81928). The protein levels of YAP and β-catenin were further validated by Western blotting in paired patients' samples. The direct interplay between YAP/TEAD4 and the promoter region of CTNNB1 was proven by the combination of dual-luciferase report assay and chromatin immunoprecipitation assay.

Results: YAP-conserved signature and WNT signaling pathway were significantly enriched in HB patients, with upregulated expression of YAP and β-catenin compared to non-HB patients. Further functional assays demonstrated that YAP/TEAD4 transcription factor complex could bind to the CTNNB1 promoter region directly to promote β-catenin expression and cell proliferation. Targeting the YAP/TEAD4 complex with a specific small-molecule compound markedly suppressed HepaG2 cell proliferation.

Conclusions: As the upstream transcription factor of CTNNB1, YAP/TEAD4 is a promising target for the treatment of HB patients with high levels of YAP and β-catenin.

Keywords: YAP/TEAD4; hepatoblastoma; liver; proliferation; β-catenin.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Carcinogenesis / genetics
  • Cell Line, Tumor
  • Cell Proliferation / genetics
  • Child
  • DNA-Binding Proteins / genetics
  • DNA-Binding Proteins / metabolism
  • Hepatoblastoma* / pathology
  • Humans
  • Liver Neoplasms* / pathology
  • Muscle Proteins
  • Pathology, Molecular
  • TEA Domain Transcription Factors
  • Transcription Factors / genetics
  • Transcription Factors / metabolism
  • YAP-Signaling Proteins* / genetics
  • beta Catenin* / genetics
  • beta Catenin* / metabolism

Substances

  • CTNNB1 protein, human
  • DNA-Binding Proteins
  • Muscle Proteins
  • TEA Domain Transcription Factors
  • TEAD4 protein, human
  • Transcription Factors
  • YAP-Signaling Proteins
  • YAP1 protein, human
  • beta Catenin