Estrogen-related receptor alpha induces the expression of vascular endothelial growth factor in breast cancer cells.

Journal Article (Journal Article)

Estrogen-related receptor alpha (ERRalpha) is an orphan member of the nuclear receptor family of transcription factors. In addition to its function as a metabolic regulator, ERRalpha has been implicated in the growth and progression of several malignancies. In the setting of breast cancer, not only is ERRalpha a putative negative prognostic factor, but we have recently found that knock-down of its expression retards tumor growth in a xenograft model of this disease. The specific aspects of ERRalpha function that are responsible for its actions in breast cancer, however, remain unclear. Using the coactivator PGC-1alpha as a protein ligand to regulate ERRalpha activity, we analyzed the effects of this receptor on gene expression in the ERalpha-positive MCF-7 cell line. This analysis led to the identification of a large number of potential ERRalpha target genes, many of which were subsequently validated in other breast cancer cell lines. Importantly, we demonstrate in this study that activation of ERRalpha in several different breast cancer cell lines leads to a significant increase in VEGF mRNA expression, an activity that translates into an increase in VEGF protein secretion. The induction of VEGF results from the interaction of ERRalpha with specific ERR-responsive elements within the VEGF promoter. These findings suggest that ERRalpha-dependent induction of VEGF may contribute to the overall negative phenotype observed in tumors in which ERRalpha is expressed and provide validation for its use as a therapeutic target in cancer.

Full Text

Duke Authors

Cited Authors

  • Stein, RA; Gaillard, S; McDonnell, DP

Published Date

  • March 2009

Published In

Volume / Issue

  • 114 / 1-2

Start / End Page

  • 106 - 112

PubMed ID

  • 19429439

Pubmed Central ID

  • PMC2680788

Electronic International Standard Serial Number (EISSN)

  • 1879-1220

Digital Object Identifier (DOI)

  • 10.1016/j.jsbmb.2009.02.010


  • eng

Conference Location

  • England