MTA1-activated Epi-microRNA-22 regulates E-cadherin and prostate cancer invasiveness

FEBS Lett. 2017 Mar;591(6):924-933. doi: 10.1002/1873-3468.12603. Epub 2017 Mar 12.

Abstract

We have previously shown that metastasis-associated protein 1 (MTA1), a chromatin remodeler, plays an important role in prostate cancer invasiveness, likely through regulation of epithelial-to-mesenchymal transition. Here, we identified miR-22 as an epigenetic-microRNA (Epi-miR) directly induced by MTA1 and predicted to target E-cadherin. Loss-of-function and overexpression studies of MTA1 reinforced its regulatory role in miR-22 expression. MiR-22 directly targets the 3'-untranslated region of E-cadherin, and ectopic overexpression of miR-22 diminishes E-cadherin expression. Overexpression of miR-22 in prostate cancer cells promotes cell invasiveness and migration. Meta-analysis of patient tumor samples indicates a positive correlation between MTA1 and miR-22, supporting their inhibitory effect on E-cadherin expression. Our findings implicate the MTA1/Epi-miR-22/E-cadherin axis as a new epigenetic signaling pathway that promotes tumor invasion in prostate cancer.

Keywords: E-cadherin; MTA1; miR-22; prostate cancer.

MeSH terms

  • 3' Untranslated Regions / genetics
  • Animals
  • Antigens, CD
  • Base Sequence
  • Cadherins / genetics*
  • Cadherins / metabolism
  • Cell Line, Tumor
  • Cell Movement / genetics
  • Epigenesis, Genetic
  • Gene Expression Profiling / methods
  • Gene Expression Regulation, Neoplastic
  • Histone Deacetylases / genetics*
  • Histone Deacetylases / metabolism
  • Humans
  • Immunoblotting
  • Male
  • Mice, Knockout
  • Mice, Transgenic
  • MicroRNAs / genetics*
  • Microscopy, Fluorescence
  • Neoplasm Invasiveness
  • Prostatic Neoplasms / genetics*
  • Prostatic Neoplasms / metabolism
  • Prostatic Neoplasms / pathology
  • RNA Interference
  • Repressor Proteins / genetics*
  • Repressor Proteins / metabolism
  • Reverse Transcriptase Polymerase Chain Reaction
  • Sequence Homology, Nucleic Acid
  • Trans-Activators

Substances

  • 3' Untranslated Regions
  • Antigens, CD
  • CDH1 protein, human
  • Cadherins
  • MIRN22 microRNA, human
  • MicroRNAs
  • MTA1 protein, human
  • Repressor Proteins
  • Trans-Activators
  • Histone Deacetylases