High levels of oestrogen receptor-alpha in tumorigenesis: inhibition of cell growth and angiogenic factors

Cell Prolif. 2001 Aug;34(4):223-31. doi: 10.1046/j.0960-7722.2001.00207.x.

Abstract

We previously found that the stable overexpression of oestrogen receptor-alpha in the human endothelial cell line ECV304* inhibits its growth in vitro, and that this inhibition is possibly mediated through a down-regulation of the vasoactive agents endothelin-1 and vascular endothelial growth factor. Here we show an in vivo growth-inhibitory effect of oestrogen receptor-alpha overexpression in tumours initiated in nude mice from the same clone of ECV304. In addition, we show that this growth inhibition is accompanied by an alphavbeta3-mediated inhibition of cell migration in vitro, and a down-regulation of the integrin alphavbeta3, vascular endothelial growth factor and vascularization in vivo. The levels of vascular endothelial growth factor and integrin alphavbeta3, through their effect on cell growth and migration, contribute to the process of angiogenesis and to the pathogenesis of atherosclerosis and cancer. The results shown here demonstrate that a higher level of oestrogen receptor-alpha in the cell, through its effect on certain angiogenic factors, may play a role in the control of angiogenesis.

MeSH terms

  • Animals
  • Antibodies / pharmacology
  • Cell Division / drug effects
  • Cell Division / genetics
  • Cell Line, Transformed
  • Cell Movement / drug effects
  • Clone Cells
  • Down-Regulation / drug effects
  • Down-Regulation / genetics
  • Endothelial Growth Factors / metabolism
  • Endothelial Growth Factors / pharmacology
  • Estradiol / pharmacology
  • Estrogen Receptor alpha
  • Female
  • Gene Expression / genetics
  • Humans
  • Imidazoles / pharmacology
  • Lymphokines / metabolism
  • Lymphokines / pharmacology
  • Mice
  • Mice, Nude
  • Neoplasm Transplantation
  • Neoplasms, Vascular Tissue / genetics
  • Neoplasms, Vascular Tissue / metabolism*
  • Neoplasms, Vascular Tissue / pathology
  • Neovascularization, Pathologic / metabolism
  • Neovascularization, Pathologic / physiopathology
  • Receptors, Estrogen / genetics
  • Receptors, Estrogen / metabolism*
  • Receptors, Vitronectin / antagonists & inhibitors
  • Receptors, Vitronectin / metabolism
  • Transfection
  • Vascular Endothelial Growth Factor A
  • Vascular Endothelial Growth Factors

Substances

  • 3-(3-(3-(4,5-dihydroimidazol-2-ylamino)propyloxylisoxazol-5-yl)carbonylamino)-2-(phenylsulfonylamino)propionic acid
  • Antibodies
  • Endothelial Growth Factors
  • Estrogen Receptor alpha
  • Imidazoles
  • Lymphokines
  • Receptors, Estrogen
  • Receptors, Vitronectin
  • Vascular Endothelial Growth Factor A
  • Vascular Endothelial Growth Factors
  • Estradiol