miR-137 suppresses cell growth in ovarian cancer by targeting AEG-1

Biochem Biophys Res Commun. 2013 Nov 15;441(2):357-63. doi: 10.1016/j.bbrc.2013.10.052. Epub 2013 Oct 19.

Abstract

Astrocyte elevated gene-1 (AEG-1) is an oncogene overexpressed in multiple types of human cancers including ovarian cancer (OC). However, the underlying mechanism of AEG-1 up-regulation in OC is not well understood. In this study, we showed that miR-137 downregulated AEG-1 expression through interaction with its 3' untranslated region (3'UTR) and that miR-137 expression was inversely correlated with AEG-1 levels in OC specimens. Similar to the downregulation of AEG-1, overexpression of miR-137 in OC cell lines decreased in vitro cell growth, clonogenicity, and also induced G1 arrest. Importantly, miR-137 overexpression suppressed in vivo tumor growth in nude mice models. Furthermore, we found that restoring the AEG-1 (without the 3'UTR) significantly rescued miR-137-induced cell growth inhibition and cell-cycle arrest. Taken together, these findings indicate that miR-137 functions as a tumor suppressor by inhibition of AEG-1. These molecules might be targets for prevention or treatment of OC.

Keywords: AEG-1; Cell growth; Ovarian cancer; miR-137.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 3' Untranslated Regions / genetics
  • Animals
  • Carcinogenesis / genetics*
  • Cell Adhesion Molecules / antagonists & inhibitors
  • Cell Adhesion Molecules / genetics*
  • Cell Line, Tumor
  • Cell Proliferation
  • Down-Regulation
  • Female
  • G1 Phase Cell Cycle Checkpoints / genetics
  • Gene Expression Regulation, Neoplastic*
  • Genes, Tumor Suppressor / physiology*
  • Humans
  • Membrane Proteins
  • Mice
  • Mice, Nude
  • MicroRNAs / genetics
  • MicroRNAs / physiology*
  • Ovarian Neoplasms / genetics*
  • Ovarian Neoplasms / pathology*
  • RNA-Binding Proteins

Substances

  • 3' Untranslated Regions
  • Cell Adhesion Molecules
  • MIRN137 microRNA, human
  • MTDH protein, human
  • Membrane Proteins
  • MicroRNAs
  • RNA-Binding Proteins