BRCA1 and PALB2 in a Messy Breakup

Cancer Res. 2020 Oct 1;80(19):4044-4045. doi: 10.1158/0008-5472.CAN-20-2731.

Abstract

Mutations in the BRCA1 gene cause an extremely high lifetime risk of breast and ovarian cancer, but the exact mechanism by which the BRCA1 protein acts to prevent cancer onset remains unclear. In this edition of Cancer Research, Park and colleagues describe a new mouse model featuring a single amino acid substitution in the coiled-coil motif of BRCA1. This change prevents BRCA1 from interacting with PALB2 (partner and localizer of BRCA2), causing rapid cancer onset and a loss of blood cells similar to Fanconi anemia.See related article by Park et al., p. 4172.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Comment

MeSH terms

  • Animals
  • BRCA1 Protein* / genetics
  • BRCA2 Protein / genetics
  • Fanconi Anemia Complementation Group N Protein / genetics
  • Fanconi Anemia* / genetics
  • Female
  • Genes, BRCA1
  • Genes, BRCA2
  • Humans
  • Mice
  • Tumor Suppressor Proteins / genetics

Substances

  • BRCA1 Protein
  • BRCA1 protein, human
  • BRCA2 Protein
  • Fanconi Anemia Complementation Group N Protein
  • PALB2 protein, human
  • Tumor Suppressor Proteins