High burden and pervasive positive selection of somatic mutations in normal human skin

Author:

Martincorena Iñigo1,Roshan Amit2,Gerstung Moritz1,Ellis Peter1,Van Loo Peter134,McLaren Stuart1,Wedge David C.1,Fullam Anthony1,Alexandrov Ludmil B.1,Tubio Jose M.1,Stebbings Lucy1,Menzies Andrew1,Widaa Sara1,Stratton Michael R.1,Jones Philip H.2,Campbell Peter J.15

Affiliation:

1. Wellcome Trust Sanger Institute, Hinxton CB10 1SA, Cambridgeshire, UK.

2. MRC Cancer Unit, Hutchison-MRC Research Centre, University of Cambridge, Cambridge, UK.

3. Francis Crick Institute, London, UK.

4. Department of Human Genetics, University of Leuven, Leuven, Belgium.

5. Department of Haematology, University of Cambridge, Cambridge, UK.

Abstract

Normal skin's curiously abnormal genome Within every tumor, a battle is being waged. As individual tumor cells acquire new mutations that promote their survival and growth, they clonally expand at the expense of tumor cells that are “less fit.” Martincorena et al. sequenced 234 biopsies of sun-exposed but physiologically normal skin from four individuals (see the Perspective by Brash). They found a surprisingly high burden of mutations, higher than that of many tumors. Many of the mutations known to drive the growth of cutaneous squamous cell carcinomas were already under strong positive selection. More than a quarter of normal skin cells carried a driver mutation, and every square centimeter of skin contained hundreds of competing mutant clones. Science , this issue p. 880 ; see also p. 867

Funder

EMBO

Wellcome Trust

Medical Research Council

MRC

Cancer Research UK

Wellcome Trust Senior Clinical Research Fellowship

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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