Vascular endothelial growth factor up-regulation via p21-activated kinase-1 signaling regulates heregulin-beta1-mediated angiogenesis

J Biol Chem. 2000 Dec 15;275(50):39451-7. doi: 10.1074/jbc.M006150200.

Abstract

Heregulin-beta1 promotes the activation of p21-activated kinase 1 (Pak1) and the motility and invasiveness of breast cancer cells. In this study, we identified vascular endothelial growth factor (VEGF) as a gene product induced by heregulin-beta1. The stimulation by heregulin-beta1 of breast cancer epithelial cells induced the expression of the VEGF mRNA and protein and its promoter activity. Heregulin-beta1 also stimulated angiogenesis in a VEGF-dependent manner. Herceptin, an anti-HER2 antibody inhibited heregulin-beta1-mediated stimulation of both VEGF expression in epithelial cells and angiogenesis in endothelial cells. Because the activation of Pak1 and VEGF expression are positively regulated by heregulin-beta1, we hypothesized that Pak1 regulates VEGF expression, and hence explored the role of Pak1 in angiogenesis. We provide new evidence to implicate Pak1 signaling in VEGF expression. Overexpression of a kinase-dead K299R Pak1 leads to suppression of VEGF promoter activity, as well as VEGF mRNA expression and secretion of VEGF protein. Conversely, kinase-active T423E Pak1 promotes the expression and secretion of VEGF. Furthermore, expression of the heregulin-beta1 transgene, HRG, in harderian tumors in mice enhances the activation of Pak1 as well as expression of VEGF and angiogenic marker CD34 antigen. These results suggest that heregulin-beta1 regulates angiogenesis via up-regulation of VEGF expression and that Pak1 plays an important role in controlling VEGF expression and, consequently, VEGF secretion and function.

Publication types

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

MeSH terms

  • 3T3 Cells
  • Animals
  • Antigens, CD34 / metabolism
  • Blotting, Northern
  • Breast Neoplasms / metabolism
  • Cell Movement
  • Collagen / metabolism
  • Drug Combinations
  • Endothelial Growth Factors / genetics*
  • Endothelial Growth Factors / metabolism*
  • Genes, Dominant
  • Genes, Reporter
  • Humans
  • Laminin / metabolism
  • Lymphokines / genetics*
  • Lymphokines / metabolism*
  • Mice
  • Mice, Transgenic
  • Mutagenesis
  • Neovascularization, Physiologic*
  • Neuregulin-1 / metabolism*
  • Phosphotransferases / metabolism
  • Precipitin Tests
  • Promoter Regions, Genetic
  • Protein Serine-Threonine Kinases / metabolism*
  • Proteoglycans / metabolism
  • RNA, Messenger / metabolism
  • Signal Transduction*
  • Transgenes
  • Tumor Cells, Cultured
  • Up-Regulation*
  • Vascular Endothelial Growth Factor A
  • Vascular Endothelial Growth Factors
  • p21-Activated Kinases

Substances

  • Antigens, CD34
  • Drug Combinations
  • Endothelial Growth Factors
  • Laminin
  • Lymphokines
  • Neuregulin-1
  • Proteoglycans
  • RNA, Messenger
  • Vascular Endothelial Growth Factor A
  • Vascular Endothelial Growth Factors
  • matrigel
  • heregulin beta1
  • Collagen
  • Phosphotransferases
  • PAK1 protein, human
  • Pak1 protein, mouse
  • Protein Serine-Threonine Kinases
  • p21-Activated Kinases