Genistein and curcumin block TGF-beta 1-induced u-PA expression and migratory and invasive phenotype in mouse epidermal keratinocytes

Nutr Cancer. 2000;37(1):49-54. doi: 10.1207/S15327914NC3701_6.

Abstract

Transforming growth factor-beta 1 (TGF-beta 1) stimulates migration/invasion of mouse transformed keratinocytes and increases urokinase (u-PA) expression/secretion. In this report, we analyzed the biological behavior of two naturally occurring inhibitors of protein tyrosine kinases, genistein and curcumin, that could abrogate the enhancement of u-PA levels induced by TGF-beta 1 in transformed keratinocytes. Our results showed that genistein and curcumin blocked this response in a dose-dependent manner and also inhibited the TGF-beta 1-induced synthesis of fibronectin, an early responsive gene to the growth factor. Both compounds also reduced TGF-beta 1-stimulated cell migration and invasiveness. These results suggest that a tyrosine kinase-signaling pathway should be involved in TGF-beta 1-mediated increased malignancy of transformed keratinocytes and that genistein and curcumin could play an important role in inhibiting tumor progression.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Blotting, Western
  • Cell Movement / drug effects
  • Cells, Cultured
  • Curcumin / pharmacology*
  • Epidermal Cells
  • Epidermis / drug effects
  • Fluorescent Antibody Technique
  • Genistein / antagonists & inhibitors
  • Genistein / pharmacology*
  • Keratinocytes / cytology
  • Keratinocytes / drug effects*
  • Keratinocytes / metabolism
  • Mice
  • Protein-Tyrosine Kinases / metabolism
  • Transforming Growth Factor beta / pharmacology*
  • Urokinase-Type Plasminogen Activator / drug effects*
  • Urokinase-Type Plasminogen Activator / metabolism

Substances

  • Transforming Growth Factor beta
  • Genistein
  • Protein-Tyrosine Kinases
  • Urokinase-Type Plasminogen Activator
  • Curcumin