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Evolvability of cancer-associated genes under APOBEC3A/B selection.
Song, Joon-Hyun; Dávalos, Liliana M; MacCarthy, Thomas; Damaghi, Mehdi.
Afiliação
  • Song JH; Stony Brook Cancer Center, Stony Brook Medicine, Stony Brook University, Stony Brook, NY, USA.
  • Dávalos LM; Department of Applied Mathematics and Statistics, Stony Brook University, Stony Brook, NY, USA.
  • MacCarthy T; Department of Ecology and Evolution, Stony Brook University, Stony Brook, NY 11794, USA.
  • Damaghi M; Consortium for Inter-Disciplinary Environmental Research, Stony Brook University, Stony Brook, NY 11794, USA.
iScience ; 27(4): 109433, 2024 Apr 19.
Article em En | MEDLINE | ID: mdl-38550998
ABSTRACT
Evolvability is an emergent hallmark of cancer that depends on intra-tumor heterogeneity and genetic variation. Mutations generated by APOBEC3 contribute to genetic variation and tumor evolvability. However, the influence of APOBEC3 on the evolvability of the genome and its differential impact on cancer genes versus non-cancer genes remains unclear. Analyzing over 40,000 human protein-coding transcripts, we identified distinct distribution patterns of APOBEC3A/B TC motifs between cancer and non-cancer genes, suggesting unique associations with cancer. Studying a bat species with numerous APOBEC3 genes, we found distinct motif patterns in orthologs of cancer genes compared to non-cancer genes, as in humans, suggesting APOBEC3 evolution to reduce impacts on the genome rather than the converse. Simulations confirmed that APOBEC3-induced heterogeneity enhances cancer evolution through bimodal patterns of mutations in certain classes of genes. Our results suggest the bimodal distribution of APOBEC-induced mutations can significantly increase cancer heterogeneity.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article