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Article Dans Une Revue Cell Death and Differentiation Année : 2021

Beyond DNA repair and chromosome instability—Fanconi anaemia as a cellular senescence-associated syndrome

Anne Helbling-Leclerc
Cécile Garcin
  • Fonction : Auteur
Filippo Rosselli

Résumé

Abstract Fanconi anaemia (FA) is the most frequent inherited bone marrow failure syndrome, due to mutations in genes encoding proteins involved in replication fork protection, DNA interstrand crosslink repair and replication rescue through inducing double-strand break repair and homologous recombination. Clinically, FA is characterised by aplastic anaemia, congenital defects and cancer predisposition. In in vitro studies, FA cells presented hallmarks defining senescent cells, including p53-p21 axis activation, altered telomere length, mitochondrial dysfunction, chromatin alterations, and a pro-inflammatory status. Senescence is a programme leading to proliferation arrest that is involved in different physiological contexts, such as embryogenesis, tissue remodelling and repair and guarantees tumour suppression activity. However, senescence can become a driving force for developmental abnormalities, aging and cancer. Herein, we summarise the current knowledge in the field to highlight the mutual relationships between FA and senescence that lead us to consider FA not only as a DNA repair and chromosome fragility syndrome but also as a “senescence syndrome”.
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Dates et versions

hal-03376720 , version 1 (20-10-2021)

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Anne Helbling-Leclerc, Cécile Garcin, Filippo Rosselli. Beyond DNA repair and chromosome instability—Fanconi anaemia as a cellular senescence-associated syndrome. Cell Death and Differentiation, 2021, 28 (4), pp.1159-1173. ⟨10.1038/s41418-021-00764-5⟩. ⟨hal-03376720⟩
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