Whole-genome doubling is a double-edged sword: the heterogeneous role of whole-genome doubling in various cancer types

BMB Rep. 2024 Mar;57(3):125-134. doi: 10.5483/BMBRep.2023-0244.

Abstract

Whole-genome doubling (WGD), characterized by the duplication of an entire set of chromosomes, is commonly observed in various tumors, occurring in approximately 30-40% of patients with different cancer types. The effect of WGD on tumorigenesis varies depending on the context, either promoting or suppressing tumor progression. Recent advances in genomic technologies and large-scale clinical investigations have led to the identification of the complex patterns of genomic alterations underlying WGD and their functional consequences on tumorigenesis progression and prognosis. Our comprehensive review aims to summarize the causes and effects of WGD on tumorigenesis, highlighting its dualistic influence on cancer cells. We then introduce recent findings on WGD-associated molecular signatures and genetic aberrations and a novel subtype related to WGD. Finally, we discuss the clinical implications of WGD in cancer subtype classification and future therapeutic interventions. Overall, a comprehensive understanding of WGD in cancer biology is crucial to unraveling its complex role in tumorigenesis and identifying novel therapeutic strategies. [BMB Reports 2024; 57(3): 125-134].

Publication types

  • Review
  • News

MeSH terms

  • Carcinogenesis / genetics
  • Genome*
  • Genomics
  • Humans
  • Neoplasms* / genetics

Grants and funding

ACKNOWLEDGEMENTS This study was supported by the National Research Foundation of Korea (NRF) grant funded by the Korea government (MSIT) (NRF-2019M3E5D3073568 and NRF-2021R1A4A1029097 to J.Y.A.) and Korea University to J.Y.A. E.H.C. received a scholarship from the Kwanjeong Educational Foundation and the Brain Korea (BK21) FOUR education program.