miR-133b Regulation of Connective Tissue Growth Factor: A Novel Mechanism in Liver Pathology

Am J Pathol. 2016 May;186(5):1092-102. doi: 10.1016/j.ajpath.2015.12.022. Epub 2016 Mar 3.

Abstract

miRNAs are involved in liver regeneration, and their expression is dysregulated in hepatocellular carcinoma (HCC). Connective tissue growth factor (CTGF), a direct target of miR-133b, is crucial in the ductular reaction (DR)/oval cell (OC) response for generating new hepatocyte lineages during liver injury in the context of hepatotoxin-inhibited hepatocyte proliferation. Herein, we investigate whether miR-133b regulation of CTGF influences HCC cell proliferation and migration, and DR/OC response. We analyzed miR-133b expression and found it to be down-regulated in HCC patient samples and induced in the rat DR/OC activation model of 2-acetylaminofluorene with partial hepatectomy. Furthermore, overexpression of miR-133b via adenoviral system in vitro led to decreased CTGF expression and reduced proliferation and Transwell migration of both HepG2 HCC cells and WBF-344 rat OCs. In vivo, overexpression of miR-133b in DR/OC activation models of 2-acetylaminofluorene with partial hepatectomy in rats, and 3,5-diethoxycarbonyl-1,4-dihydrocollidine in mice, led to down-regulation of CTGF expression and OC proliferation. Collectively, these results show that miR-133b regulation of CTGF is a novel mechanism critical for the proliferation and migration of HCC cells and OC response.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, N.I.H., Extramural

MeSH terms

  • 2-Acetylaminofluorene / pharmacology
  • Adenoviridae / genetics
  • Aged
  • Animals
  • Carcinogens / pharmacology
  • Carcinoma, Hepatocellular / physiopathology
  • Cell Movement / physiology
  • Cell Proliferation / physiology
  • Connective Tissue Growth Factor / metabolism*
  • Disease Models, Animal
  • Down-Regulation / physiology
  • Female
  • Genetic Vectors
  • HEK293 Cells
  • Hep G2 Cells
  • Humans
  • Liver Neoplasms / physiopathology
  • Male
  • Mice
  • MicroRNAs / metabolism
  • MicroRNAs / physiology*
  • Middle Aged
  • Rats
  • Transfection

Substances

  • Carcinogens
  • MIRN133 microRNA, human
  • MicroRNAs
  • Connective Tissue Growth Factor
  • 2-Acetylaminofluorene