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Signatures of mutational processes in human cancer.

Authors :
Alexandrov LB
Nik-Zainal S
Wedge DC
Aparicio SA
Behjati S
Biankin AV
Bignell GR
Bolli N
Borg A
Børresen-Dale AL
Boyault S
Burkhardt B
Butler AP
Caldas C
Davies HR
Desmedt C
Eils R
Eyfjörd JE
Foekens JA
Greaves M
Hosoda F
Hutter B
Ilicic T
Imbeaud S
Imielinski M
Jäger N
Jones DT
Jones D
Knappskog S
Kool M
Lakhani SR
López-Otín C
Martin S
Munshi NC
Nakamura H
Northcott PA
Pajic M
Papaemmanuil E
Paradiso A
Pearson JV
Puente XS
Raine K
Ramakrishna M
Richardson AL
Richter J
Rosenstiel P
Schlesner M
Schumacher TN
Span PN
Teague JW
Totoki Y
Tutt AN
Valdés-Mas R
van Buuren MM
van 't Veer L
Vincent-Salomon A
Waddell N
Yates LR
Zucman-Rossi J
Futreal PA
McDermott U
Lichter P
Meyerson M
Grimmond SM
Siebert R
Campo E
Shibata T
Pfister SM
Campbell PJ
Stratton MR
Source :
Nature [Nature] 2013 Aug 22; Vol. 500 (7463), pp. 415-21. Date of Electronic Publication: 2013 Aug 14.
Publication Year :
2013

Abstract

All cancers are caused by somatic mutations; however, understanding of the biological processes generating these mutations is limited. The catalogue of somatic mutations from a cancer genome bears the signatures of the mutational processes that have been operative. Here we analysed 4,938,362 mutations from 7,042 cancers and extracted more than 20 distinct mutational signatures. Some are present in many cancer types, notably a signature attributed to the APOBEC family of cytidine deaminases, whereas others are confined to a single cancer class. Certain signatures are associated with age of the patient at cancer diagnosis, known mutagenic exposures or defects in DNA maintenance, but many are of cryptic origin. In addition to these genome-wide mutational signatures, hypermutation localized to small genomic regions, 'kataegis', is found in many cancer types. The results reveal the diversity of mutational processes underlying the development of cancer, with potential implications for understanding of cancer aetiology, prevention and therapy.

Details

Language :
English
ISSN :
1476-4687
Volume :
500
Issue :
7463
Database :
MEDLINE
Journal :
Nature
Publication Type :
Academic Journal
Accession number :
23945592
Full Text :
https://doi.org/10.1038/nature12477