DNA damage and hormone-related cancer: a repair pathway view

Hum Mol Genet. 2019 Nov 21;28(R2):R180-R186. doi: 10.1093/hmg/ddz206.

Abstract

In this short review, we examine the overlap between genes known to be mutated in the germlines of individuals at risk of breast, ovarian and prostate cancers, and their positions in DNA damage repair pathways. Cancer risk mutations have been consistently reported in certain genes at the top of these pathways, but none have been reported in others. We consider whether some of these gene products are too crucial to life for mutations to be tolerated, whilst others, further down the pathways, are less essential.

Publication types

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

MeSH terms

  • Ataxia Telangiectasia Mutated Proteins / genetics*
  • Ataxia Telangiectasia Mutated Proteins / metabolism
  • BRCA1 Protein / genetics*
  • BRCA2 Protein / genetics*
  • Breast Neoplasms / genetics*
  • DNA Breaks, Double-Stranded
  • DNA End-Joining Repair / genetics
  • DNA Repair / genetics*
  • Female
  • Homologous Recombination / genetics
  • Humans
  • Male
  • Prostatic Neoplasms / genetics*
  • Telomere / genetics
  • Telomere / metabolism

Substances

  • BRCA1 Protein
  • BRCA2 Protein
  • ATM protein, human
  • ATR protein, human
  • Ataxia Telangiectasia Mutated Proteins