Epigenetic silencing of 14-3-3sigma in cancer

Semin Cancer Biol. 2006 Jun;16(3):214-24. doi: 10.1016/j.semcancer.2006.03.008. Epub 2006 Apr 1.

Abstract

The 14-3-3sigma gene is a direct target of the p53 tumor suppressor and its product inhibits cell cycle progression. Recently, a proteomic analysis revealed that 14-3-3sigma regulates additional cellular processes relevant to carcinogenesis, as migration and MAP-kinase signalling. The expression of 14-3-3sigma is down-regulated by CpG methylation in several types of human cancer, among them prostate, lung, breast and several types of skin cancer. The epigenetic inactivation of 14-3-3sigma occurs at an early stage of tumor development and may allow evasion from senescence and promote genomic instability. In the future the detection of CpG methylation of 14-3-3sigma may be used for diagnostic and prognostic purposes.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • 14-3-3 Proteins
  • Animals
  • Biomarkers, Tumor / metabolism*
  • DNA Methylation
  • Disease Models, Animal
  • Epigenesis, Genetic
  • Exonucleases / metabolism*
  • Exoribonucleases
  • Female
  • Gene Silencing*
  • Histone Deacetylases / metabolism
  • Humans
  • Male
  • Neoplasm Proteins / metabolism*
  • Neoplasms / genetics*
  • Neoplasms / metabolism
  • Prostatic Neoplasms / genetics
  • Prostatic Neoplasms / metabolism
  • Protein Binding
  • Signal Transduction / physiology*
  • Tumor Suppressor Protein p53 / metabolism*

Substances

  • 14-3-3 Proteins
  • Biomarkers, Tumor
  • Neoplasm Proteins
  • Tumor Suppressor Protein p53
  • Exonucleases
  • Exoribonucleases
  • SFN protein, human
  • Histone Deacetylases