Wnt5A and TGFβ1 Converges through YAP1 Activity and Integrin Alpha v Up-Regulation Promoting Epithelial to Mesenchymal Transition in Ovarian Cancer Cells and Mesothelial Cell Activation

Cells. 2022 Jan 11;11(2):237. doi: 10.3390/cells11020237.

Abstract

In this paper, we investigate whether Wnt5A is associated with the TGF-β1/Smad2/3 and Hippo-YAP1/TAZ-TEAD pathways, implicated in epithelial to mesenchymal transition (EMT) in epithelial ovarian cancer. We used 3D and 2D cultures of human epithelial ovarian cancer cell lines SKOV-3, OVCAR-3, CAOV-4, and different subtypes of human serous ovarian cancer compared to normal ovary specimens. Wnt5A showed a positive correlation with TAZ and TGFβ1 in high- and low-grade serous ovarian cancer specimens compared to borderline serous and normal ovaries. Silencing Wnt5A by siRNAs significantly decreased Smad2/3 activation and YAP1 expression and nuclear shuttling in ovarian cancer (OvCa) cells. Furthermore, Wnt5A was required for TGFβ1-induced cell migration and invasion. In addition, inhibition of YAP1 transcriptional activity by Verteporfin (VP) altered OvCa cell migration and invasion through decreased Wnt5A expression and inhibition of Smad2/3 activation, which was reverted in the presence of exogenous Wnt5A. We found that the activation of TGFβ1 and YAP1 nuclear shuttling was promoted by Wnt5A-induced integrin alpha v. Lastly, Wnt5A was implicated in activating human primary omental mesothelial cells and subsequent invasion of ovarian cancer cells. Together, we propose that Wnt5A could be a critical mediator of EMT-associated pathways.

Keywords: TGFβ1/Smad signaling; Wnt5A; epithelial to mesenchymal transition; hippo-YAP1/TAZ signaling; integrin alpha v; mesothelial cell activation; ovarian cancer.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Line, Tumor
  • Cell Movement / genetics
  • Cell Nucleus / metabolism
  • Epithelial-Mesenchymal Transition / genetics*
  • Epithelium / pathology*
  • Feedback, Physiological
  • Female
  • Gene Expression Regulation, Neoplastic
  • Hippo Signaling Pathway / genetics
  • Humans
  • Integrin alphaV / metabolism*
  • Models, Biological
  • Neoplasm Invasiveness
  • Ovarian Neoplasms / genetics*
  • Ovarian Neoplasms / pathology
  • Phosphorylation
  • Smad2 Protein / metabolism
  • Smad3 Protein / metabolism
  • Transcription, Genetic
  • Transforming Growth Factor beta1 / metabolism*
  • Up-Regulation* / genetics
  • Wnt-5a Protein / metabolism*
  • YAP-Signaling Proteins / metabolism*

Substances

  • Integrin alphaV
  • Smad2 Protein
  • Smad3 Protein
  • Transforming Growth Factor beta1
  • Wnt-5a Protein
  • YAP-Signaling Proteins
  • YAP1 protein, human