The browser you are using is not supported by this website. All versions of Internet Explorer are no longer supported, either by us or Microsoft (read more here: https://www.microsoft.com/en-us/microsoft-365/windows/end-of-ie-support).

Please use a modern browser to fully experience our website, such as the newest versions of Edge, Chrome, Firefox or Safari etc.

Åke Borg

Åke Borg

Principal investigator

Åke Borg

Mutational Processes Molding the Genomes of 21 Breast Cancers

Author

  • Serena Nik-Zainal
  • Ludmil B. Alexandrov
  • David C. Wedge
  • Peter Van Loo
  • Christopher D. Greenman
  • Keiran Raine
  • David Jones
  • Jonathan Hinton
  • John Marshall
  • Lucy A. Stebbings
  • Andrew Menzies
  • Sancha Martin
  • Kenric Leung
  • Lina Chen
  • Catherine Leroy
  • Manasa Ramakrishna
  • Richard Rance
  • King Wai Lau
  • Laura J. Mudie
  • Ignacio Varela
  • David J. McBride
  • Graham R. Bignell
  • Susanna L. Cooke
  • Adam Shlien
  • John Gamble
  • Ian Whitmore
  • Mark Maddison
  • Patrick S. Tarpey
  • Helen R. Davies
  • Elli Papaemmanuil
  • Philip J. Stephens
  • Stuart McLaren
  • Adam P. Butler
  • Jon W. Teague
  • Göran B Jönsson
  • Judy E. Garber
  • Daniel Silver
  • Penelope Miron
  • Aquila Fatima
  • Sandrine Boyault
  • Anita Langerod
  • Andrew Tutt
  • John W. M. Martens
  • Samuel A. J. R. Aparicio
  • Åke Borg
  • Anne Vincent Salomon
  • Gilles Thomas
  • Anne-Lise Borresen-Dale
  • Andrea L. Richardson
  • Michael S. Neuberger
  • P. Andrew Futreal
  • Peter J. Campbell
  • Michael R. Stratton

Summary, in English

All cancers carry somatic mutations. The patterns of mutation in cancer genomes reflect the DNA damage and repair processes to which cancer cells and their precursors have been exposed. To explore these mechanisms further, we generated catalogs of somatic mutation from 21 breast cancers and applied mathematical methods to extract mutational signatures of the underlying processes. Multiple distinct single- and double-nucleotide substitution signatures were discernible. Cancers with BRCA1 or BRCA2 mutations exhibited a characteristic combination of substitution mutation signatures and a distinctive profile of deletions. Complex relationships between somatic mutation prevalence and transcription were detected. A remarkable phenomenon of localized hypermutation, termed "kataegis,'' was observed. Regions of kataegis differed between cancers but usually colocalized with somatic rearrangements. Base substitutions in these regions were almost exclusively of cytosine at TpC dinucleotides. The mechanisms underlying most of these mutational signatures are unknown. However, a role for the APOBEC family of cytidine deaminases is proposed.

Department/s

  • Breastcancer-genetics
  • BioCARE: Biomarkers in Cancer Medicine improving Health Care, Education and Innovation

Publishing year

2012

Language

English

Pages

979-993

Publication/Series

Cell

Volume

149

Issue

5

Document type

Journal article

Publisher

Cell Press

Topic

  • Cancer and Oncology

Status

Published

ISBN/ISSN/Other

  • ISSN: 1097-4172