miR-203 inhibits arecoline-induced epithelial-mesenchymal transition by regulating secreted frizzled-related protein 4 and transmembrane-4 L six family member 1 in oral submucous fibrosis

Oncol Rep. 2015 Jun;33(6):2753-60. doi: 10.3892/or.2015.3909. Epub 2015 Apr 9.

Abstract

Oral submucous fibrosis (OSF) is a potentially malignant disease predominantly found in Asian people. The areca nut has been implicated in this disease. Arecoline, one of the areca alkaloids, induces epithelial-mesenchymal transition (EMT)-related factors in primary human buccal mucosal fibroblasts. Yet, the mechanisms of the underlying arecoline-induced EMT in OSF remain unknown. In the present study, we aimed to investigate the role of microRNAs (miRNAs) in arecoline-induced EMT in HaCaT cells. We found that miR-203 was significantly downregulated in OSF tissues compared to that in normal buccal mucosa tissues, and that miR-203 negatively regulated secreted frizzled-related protein 4 (SFRP4) and positively regulated transmembrane-4 L six family member 1 (TM4SF1). We observed that upregulation of miR-203 significantly decreased the cell proliferation of HaCaT cells, and significantly upregulated the expression of cytokeratin 19 (CK19) and E-cadherin proteins, whereas it significantly downregulated the expression of N-cadherin and vimentin compared to these levels in the vehicle control cells. Thus, we provide evidence to illustrate that miR-203 plays a role in the pathogenesis of OSF, which may be a target for OSF management.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antigens, Surface / biosynthesis*
  • Antigens, Surface / genetics
  • Arecoline / adverse effects
  • Cell Line
  • Cell Proliferation / drug effects
  • Epithelial-Mesenchymal Transition / drug effects
  • Fibroblasts / drug effects
  • Humans
  • MicroRNAs / biosynthesis
  • MicroRNAs / genetics*
  • Mouth Mucosa / drug effects
  • Mouth Mucosa / pathology
  • Neoplasm Proteins / biosynthesis*
  • Neoplasm Proteins / genetics
  • Oral Submucous Fibrosis / genetics*
  • Oral Submucous Fibrosis / pathology
  • Proto-Oncogene Proteins / biosynthesis*
  • Proto-Oncogene Proteins / genetics

Substances

  • Antigens, Surface
  • MIRN203 microRNA, human
  • MicroRNAs
  • Neoplasm Proteins
  • Proto-Oncogene Proteins
  • SFRP4 protein, human
  • TM4SF1 protein, human
  • Arecoline