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A comprehensive catalogue of somatic mutations from a human cancer genome

Author

Listed:
  • Erin D. Pleasance

    (Wellcome Trust Sanger Institute)

  • R. Keira Cheetham

    (Illumina Cambridge Ltd, Chesterford Research Park, Little Chesterford, Essex CB10 1XL, UK)

  • Philip J. Stephens

    (Wellcome Trust Sanger Institute)

  • David J. McBride

    (Wellcome Trust Sanger Institute)

  • Sean J. Humphray

    (Illumina Cambridge Ltd, Chesterford Research Park, Little Chesterford, Essex CB10 1XL, UK)

  • Chris D. Greenman

    (Wellcome Trust Sanger Institute)

  • Ignacio Varela

    (Wellcome Trust Sanger Institute)

  • Meng-Lay Lin

    (Wellcome Trust Sanger Institute)

  • Gonzalo R. Ordóñez

    (Wellcome Trust Sanger Institute)

  • Graham R. Bignell

    (Wellcome Trust Sanger Institute)

  • Kai Ye

    (Medical Statistics and Bioinformatics, Leiden University Medical Center, Einthovenweg 20, 2333 ZC Leiden, the Netherlands)

  • Julie Alipaz

    (Illumina Inc., Corporate Headquarters, 9865 Towne Centre Drive, San Diego, California 92121, USA)

  • Markus J. Bauer

    (Illumina Cambridge Ltd, Chesterford Research Park, Little Chesterford, Essex CB10 1XL, UK)

  • David Beare

    (Wellcome Trust Sanger Institute)

  • Adam Butler

    (Wellcome Trust Sanger Institute)

  • Richard J. Carter

    (Illumina Cambridge Ltd, Chesterford Research Park, Little Chesterford, Essex CB10 1XL, UK)

  • Lina Chen

    (Wellcome Trust Sanger Institute)

  • Anthony J. Cox

    (Illumina Cambridge Ltd, Chesterford Research Park, Little Chesterford, Essex CB10 1XL, UK)

  • Sarah Edkins

    (Wellcome Trust Sanger Institute)

  • Paula I. Kokko-Gonzales

    (Illumina Cambridge Ltd, Chesterford Research Park, Little Chesterford, Essex CB10 1XL, UK)

  • Niall A. Gormley

    (Illumina Cambridge Ltd, Chesterford Research Park, Little Chesterford, Essex CB10 1XL, UK)

  • Russell J. Grocock

    (Illumina Cambridge Ltd, Chesterford Research Park, Little Chesterford, Essex CB10 1XL, UK)

  • Christian D. Haudenschild

    (Illumina Hayward, 25861 Industrial Bvld, Hayward, California 94545, USA)

  • Matthew M. Hims

    (Illumina Cambridge Ltd, Chesterford Research Park, Little Chesterford, Essex CB10 1XL, UK)

  • Terena James

    (Illumina Cambridge Ltd, Chesterford Research Park, Little Chesterford, Essex CB10 1XL, UK)

  • Mingming Jia

    (Wellcome Trust Sanger Institute)

  • Zoya Kingsbury

    (Illumina Cambridge Ltd, Chesterford Research Park, Little Chesterford, Essex CB10 1XL, UK)

  • Catherine Leroy

    (Wellcome Trust Sanger Institute)

  • John Marshall

    (Wellcome Trust Sanger Institute)

  • Andrew Menzies

    (Wellcome Trust Sanger Institute)

  • Laura J. Mudie

    (Wellcome Trust Sanger Institute)

  • Zemin Ning

    (Wellcome Trust Sanger Institute)

  • Tom Royce

    (Illumina Inc., Corporate Headquarters, 9865 Towne Centre Drive, San Diego, California 92121, USA)

  • Ole B. Schulz-Trieglaff

    (Illumina Cambridge Ltd, Chesterford Research Park, Little Chesterford, Essex CB10 1XL, UK)

  • Anastassia Spiridou

    (Illumina Cambridge Ltd, Chesterford Research Park, Little Chesterford, Essex CB10 1XL, UK)

  • Lucy A. Stebbings

    (Wellcome Trust Sanger Institute)

  • Lukasz Szajkowski

    (Illumina Cambridge Ltd, Chesterford Research Park, Little Chesterford, Essex CB10 1XL, UK)

  • Jon Teague

    (Wellcome Trust Sanger Institute)

  • David Williamson

    (Illumina Hayward, 25861 Industrial Bvld, Hayward, California 94545, USA)

  • Lynda Chin

    (Dana-Farber Cancer Institute, 44 Binney Street, Boston, Massachusetts 02115, USA)

  • Mark T. Ross

    (Illumina Cambridge Ltd, Chesterford Research Park, Little Chesterford, Essex CB10 1XL, UK)

  • Peter J. Campbell

    (Wellcome Trust Sanger Institute)

  • David R. Bentley

    (Illumina Cambridge Ltd, Chesterford Research Park, Little Chesterford, Essex CB10 1XL, UK)

  • P. Andrew Futreal

    (Wellcome Trust Sanger Institute)

  • Michael R. Stratton

    (Wellcome Trust Sanger Institute
    Institute of Cancer Research, Sutton, Surrey SM2 5NG, UK)

Abstract

All cancers carry somatic mutations. A subset of these somatic alterations, termed driver mutations, confer selective growth advantage and are implicated in cancer development, whereas the remainder are passengers. Here we have sequenced the genomes of a malignant melanoma and a lymphoblastoid cell line from the same person, providing the first comprehensive catalogue of somatic mutations from an individual cancer. The catalogue provides remarkable insights into the forces that have shaped this cancer genome. The dominant mutational signature reflects DNA damage due to ultraviolet light exposure, a known risk factor for malignant melanoma, whereas the uneven distribution of mutations across the genome, with a lower prevalence in gene footprints, indicates that DNA repair has been preferentially deployed towards transcribed regions. The results illustrate the power of a cancer genome sequence to reveal traces of the DNA damage, repair, mutation and selection processes that were operative years before the cancer became symptomatic.

Suggested Citation

  • Erin D. Pleasance & R. Keira Cheetham & Philip J. Stephens & David J. McBride & Sean J. Humphray & Chris D. Greenman & Ignacio Varela & Meng-Lay Lin & Gonzalo R. Ordóñez & Graham R. Bignell & Kai Ye &, 2010. "A comprehensive catalogue of somatic mutations from a human cancer genome," Nature, Nature, vol. 463(7278), pages 191-196, January.
  • Handle: RePEc:nat:nature:v:463:y:2010:i:7278:d:10.1038_nature08658
    DOI: 10.1038/nature08658
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    Citations

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    Cited by:

    1. Yuchao Xia & Zijie Jin & Chengsheng Zhang & Linkun Ouyang & Yuhao Dong & Juan Li & Lvze Guo & Biyang Jing & Yang Shi & Susheng Miao & Ruibin Xi, 2023. "TAGET: a toolkit for analyzing full-length transcripts from long-read sequencing," Nature Communications, Nature, vol. 14(1), pages 1-12, December.
    2. Kathiresan Selvam & Smitha Sivapragasam & Gregory M. K. Poon & John J. Wyrick, 2023. "Detecting recurrent passenger mutations in melanoma by targeted UV damage sequencing," Nature Communications, Nature, vol. 14(1), pages 1-13, December.

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