DNA-dependent protein kinase: Epigenetic alterations and the role in genomic stability of cancer

Mutat Res Rev Mutat Res. 2019 Apr-Jun:780:92-105. doi: 10.1016/j.mrrev.2018.06.001. Epub 2018 Jun 19.

Abstract

DNA-dependent protein kinase (DNA-PK), a member of phosphatidylinositol-kinase family, is a key protein in mammalian DNA double-strand break (DSB) repair that helps to maintain genomic integrity. DNA-PK also plays a central role in immune cell development and protects telomerase during cellular aging. Epigenetic deregulation due to endogenous and exogenous factors may affect the normal function of DNA-PK, which in turn could impair DNA repair and contribute to genomic instability. Recent studies implicate a role for epigenetics in the regulation of DNA-PK expression in normal and cancer cells, which may impact cancer progression and metastasis as well as provide opportunities for treatment and use of DNA-PK as a novel cancer biomarker. In addition, several small molecules and biological agents have been recently identified that can inhibit DNA-PK function or expression, and thus hold promise for cancer treatments. This review discusses the impact of epigenetic alterations and the expression of DNA-PK in relation to the DNA repair mechanisms with a focus on its differential levels in normal and cancer cells.

Keywords: Cancer; DNA damage; DNA repair; DNA-PK; Epigenetic alternations; Genomic stability.

Publication types

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

MeSH terms

  • Animals
  • DNA Breaks, Double-Stranded
  • DNA Damage / genetics
  • DNA Repair / genetics
  • DNA-Activated Protein Kinase / genetics*
  • Epigenesis, Genetic / genetics*
  • Genomic Instability / genetics*
  • Humans
  • Neoplasms / genetics*

Substances

  • DNA-Activated Protein Kinase