Epigenetic regulation of miR-212 expression in lung cancer

PLoS One. 2011;6(11):e27722. doi: 10.1371/journal.pone.0027722. Epub 2011 Nov 15.

Abstract

Many studies have shown that microRNA expression in cancer may be regulated by epigenetic events. Recently, we found that in lung cancer miR-212 was strongly down-regulated. However, mechanisms involved in the regulation of miR-212 expression are unknown. Therefore, we addressed this point by investigating the molecular mechanisms of miR-212 silencing in lung cancer. We identified histone modifications rather than DNA hypermethylation as epigenetic events that regulate miR-212 levels in NSCLC. Moreover, we found that miR-212 silencing in vivo is closely associated with the severity of the disease.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetylation / drug effects
  • Aged
  • Aged, 80 and over
  • Apoptosis / drug effects
  • Apoptosis / genetics
  • Carcinoma, Non-Small-Cell Lung / genetics*
  • Carcinoma, Non-Small-Cell Lung / pathology
  • Cell Line, Tumor
  • CpG Islands / drug effects
  • CpG Islands / genetics
  • DNA Methylation / drug effects
  • DNA Methylation / genetics
  • DNA-Binding Proteins / antagonists & inhibitors
  • Enhancer of Zeste Homolog 2 Protein
  • Epigenesis, Genetic* / drug effects
  • Female
  • Gene Expression Regulation, Neoplastic / drug effects
  • Gene Expression Regulation, Neoplastic / genetics*
  • Gene Silencing
  • Histocompatibility Antigens
  • Histone Deacetylase Inhibitors / pharmacology
  • Histone Deacetylases / metabolism
  • Histone-Lysine N-Methyltransferase / antagonists & inhibitors
  • Histones / metabolism
  • Humans
  • Lung Neoplasms / genetics*
  • Lung Neoplasms / pathology
  • Male
  • MicroRNAs / genetics*
  • Middle Aged
  • Neoplasm Staging
  • Polycomb Repressive Complex 2
  • Promoter Regions, Genetic / drug effects
  • Promoter Regions, Genetic / genetics
  • Transcription Factors / antagonists & inhibitors
  • Transcription Initiation Site / drug effects

Substances

  • DNA-Binding Proteins
  • Histocompatibility Antigens
  • Histone Deacetylase Inhibitors
  • Histones
  • MIRN212 microRNA, human
  • MicroRNAs
  • Transcription Factors
  • EHMT2 protein, human
  • EZH2 protein, human
  • Enhancer of Zeste Homolog 2 Protein
  • Histone-Lysine N-Methyltransferase
  • Polycomb Repressive Complex 2
  • Histone Deacetylases