Recent insights into the molecular basis of Fanconi anemia: genes, modifiers, and drivers

Int J Hematol. 2017 Sep;106(3):335-344. doi: 10.1007/s12185-017-2283-4. Epub 2017 Jun 19.

Abstract

Fanconi anemia (FA), the most common form of inherited bone marrow failure, predisposes to leukemia and solid tumors. FA is caused by the genetic disruption of a cellular pathway that repairs DNA interstrand crosslinks. The impaired function of this pathway, and the genetic instability that results, is considered the main pathogenic mechanism behind this disease. The identification of breast cancer susceptibility genes (for example, BRCA1/FANCS and BRCA2/FANCD1) as being major players in the FA pathway has led to a surge in molecular studies, resulting in the concept of the FA-BRCA pathway. In this review, we discuss recent advances in the molecular pathogenesis of FA from three viewpoints: (a) new FA genes, (b) modifier pathways that influence the cellular and clinical phenotypes of FA and (c) non-canonical functions of FA genes that may drive disease progression independently of deficient DNA repair. Potential therapeutic approaches for FA that are relevant to each will also be proposed.

Keywords: Aldehydes; Autophagy; Bone marrow failure; DNA interstrand crosslink repair; TGFβ.

Publication types

  • Review

MeSH terms

  • Aldehydes
  • Autophagy / genetics
  • BRCA1 Protein / genetics*
  • BRCA2 Protein / genetics*
  • Breast Neoplasms / genetics
  • DNA Repair / genetics*
  • Disease Progression
  • Fanconi Anemia / genetics*
  • Female
  • Genetic Predisposition to Disease / genetics
  • Humans
  • Male
  • Molecular Targeted Therapy
  • Transforming Growth Factor beta

Substances

  • Aldehydes
  • BRCA1 Protein
  • BRCA1 protein, human
  • BRCA2 Protein
  • BRCA2 protein, human
  • Transforming Growth Factor beta