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Signatures of mutational processes in human cancer

Authors :
Alexandrov, Ludmil B
Nik-Zainal, Serena
Wedge, David C
Aparicio, Samuel AJR
Behjati, Sam
Biankin, Andrew V
Bignell, Graham R
Bolli, Niccolò
Borg, Ake
Børresen-Dale, Anne-Lise
Boyault, Sandrine
Burkhardt, Birgit
Butler, Adam P
Caldas, Carlos
Davies, Helen R
Desmedt, Christine
Eils, Roland
Eyfjörd, Jórunn Erla
Foekens, John A
Greaves, Mel
Hosoda, Fumie
Hutter, Barbara
Ilicic, Tomislav
Imbeaud, Sandrine
Imielinski, Marcin
Jäger, Natalie
Jones, David TW
Jones, David
Knappskog, Stian
Kool, Marcel
Lakhani, Sunil R
López-Otín, Carlos
Martin, Sancha
Munshi, Nikhil C
Nakamura, Hiromi
Northcott, Paul A
Pajic, Marina
Papaemmanuil, Elli
Paradiso, Angelo
Pearson, John V
Puente, Xose S
Raine, Keiran
Ramakrishna, Manasa
Richardson, Andrea L
Richter, Julia
Rosenstiel, Philip
Schlesner, Matthias
Schumacher, Ton N
Span, Paul N
Teague, Jon W
Totoki, Yasushi
Tutt, Andrew NJ
Valdés-Mas, Rafael
van Buuren, Marit M
van 't Veer, Laura
Vincent-Salomon, Anne
Waddell, Nicola
Yates, Lucy R
Australian Pancreatic Cancer Genome Initiative
ICGC Breast Cancer Consortium
ICGC MMML-Seq Consortium
ICGC PedBrain
Zucman-Rossi, Jessica
Futreal, P Andrew
McDermott, Ultan
Lichter, Peter
Meyerson, Matthew
Grimmond, Sean M
Siebert, Reiner
Campo, Elías
Shibata, Tatsuhiro
Pfister, Stefan M
Campbell, Peter J
Stratton, Michael R
Nik-Zainal Abidin, Serena [0000-0001-5054-1727]
Caldas, Carlos [0000-0003-3547-1489]
Apollo - University of Cambridge Repository
Publication Year :
2013
Publisher :
Springer Science and Business Media LLC, 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

Database :
OpenAIRE
Accession number :
edsair.od.......109..6e577c103a18e0cba7d99001cfcb581a