Corilagin Represses Epithelial to Mesenchymal Transition Process Through Modulating Wnt/β-Catenin Signaling Cascade

Biomolecules. 2020 Oct 5;10(10):1406. doi: 10.3390/biom10101406.

Abstract

Corilagin (CLG), a major component of several medicinal plants, can exhibit diverse pharmacological properties including those of anti-cancer, anti-inflammatory, and hepatoprotective qualities. However, there are no prior studies on its potential impact on the epithelial-to-mesenchymal transition (EMT) process. EMT can lead to dissemination of tumor cells into other organs and promote cancer progression. Hence, we aimed to investigate the effect of CLG on EMT and its mechanism(s) of action in tumor cells. We noted that CLG reduced the expression of various epithelial markers and up-regulated the expression of Occludin and E-cadherin in both basal and TGFβ-stimulated tumor cells. CLG treatment also abrogated cellular invasion and migration in colon and prostate carcinoma cells. In addition, CLG effectively attenuated the Wnt/β-catenin signaling cascade in TGFβ-stimulated cells. Overall, our study suggests that CLG may function as and effective modulator of EMT and metastasis in neoplastic cells.

Keywords: Wnt/β-catenin; corilagin; epithelial-to-mesenchymal transition; invasion; migration.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cadherins / metabolism
  • Cell Movement / drug effects*
  • Colonic Neoplasms / drug therapy
  • Colonic Neoplasms / metabolism*
  • Colonic Neoplasms / pathology
  • Epithelial-Mesenchymal Transition / drug effects*
  • Glucosides / pharmacology*
  • Humans
  • Hydrolyzable Tannins / pharmacology*
  • MCF-7 Cells
  • Male
  • Neoplasm Invasiveness
  • Neoplasm Proteins / metabolism
  • Occludin / metabolism
  • Prostatic Neoplasms / drug therapy
  • Prostatic Neoplasms / metabolism*
  • Prostatic Neoplasms / pathology
  • Transforming Growth Factor beta / metabolism
  • Wnt Signaling Pathway / drug effects*

Substances

  • Cadherins
  • Cdh1 protein, mouse
  • Glucosides
  • Hydrolyzable Tannins
  • Neoplasm Proteins
  • OCLN protein, human
  • Occludin
  • Transforming Growth Factor beta
  • corilagin