Downregulation of HER2 by RIG1 involves the PI3K/Akt pathway in ovarian cancer cells

Carcinogenesis. 2008 Feb;29(2):299-306. doi: 10.1093/carcin/bgm263. Epub 2008 Jan 3.

Abstract

Interferon-gamma (IFN-gamma) is known to downregulate HER2 oncoprotein (p185(HER2) or briefly p185) in prostate cancer cells. We demonstrate that the IFN-gamma-induced retinoid-inducible gene 1 (RIG1) acts as a transrepressor of p185. Furthermore, we exhibit that RIG1 downregulates the activated (phosphorylated) form of p185 and phosphoinositide-3 kinase (PI3K)/serine/threonine-specific protein kinase (Akt) and the mammalian target of rapamycin (mTOR), downstream substrates of HER2. We also elucidate that heregulin (HRG) specifically restores the activation of p185 and Akt after their activities are reduced by RIG1. Additionally, expression of vascular endothelial growth factor (VEGF) increases through the HER2- and Akt/mTOR-signaling pathways, indicating that VEGF is downregulated by RIG1 within the cell. These findings suggest that RIG1 plays a role in IFN-gamma-mediated therapy by downregulating p185 and its downstream PI3K/Akt/mTOR/VEGF-signaling pathway. These results may provide a new therapeutic mechanism for the clinical use of IFN-gamma and RIG1.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Line, Tumor
  • Down-Regulation
  • Enzyme Activation
  • Female
  • Gene Expression Regulation, Neoplastic*
  • Humans
  • Interferon-gamma / metabolism
  • Models, Biological
  • Neuregulin-1 / metabolism
  • Ovarian Neoplasms / metabolism*
  • Phosphatidylinositol 3-Kinases / metabolism*
  • Receptor, ErbB-2 / biosynthesis*
  • Receptor, ErbB-2 / metabolism
  • Receptors, Retinoic Acid / biosynthesis*
  • Signal Transduction

Substances

  • Neuregulin-1
  • PLAAT4 protein, human
  • Receptors, Retinoic Acid
  • Interferon-gamma
  • Phosphatidylinositol 3-Kinases
  • ERBB2 protein, human
  • Receptor, ErbB-2