Signatures of mutational processes in human cancer

阿波贝克 体细胞突变 生物 遗传学 基因组 癌症 体细胞 计算生物学 突变 种系突变 基因 抗体 B细胞
作者
Ludmil B. Alexandrov,Serena Nik-Zainal,David C. Wedge,Samuel Aparicio,Sam Behjati,Andrew V. Biankin,Graham R. Bignell,Niccolò Bolli,Åke Borg,Anne‐Lise Børresen‐Dale,Sandrine Boyault,Birgit Burkhardt,Adam Butler,Carlos Caldas,Helen Davies,Christine Desmedt,Roland Eils,Jórunn E. Eyfjörd,John A. Foekens,Mel Greaves,Fumie Hosoda,Barbara Hutter,Tomislav Ilicic,Sandrine Imbeaud,Marcin Imieliński,Natalie Jäger,David Jones,David R. Jones,Stian Knappskog,Marcel Kool,Sunil R. Lakhani,Carlos López-Otı́n,Sancha Martin,Nikhil C. Munshi,Hiromi Nakamura,Paul A. Northcott,Marina Pajic,Elli Papaemmanuil,Angelo Paradiso,John V. Pearson,Xosé S. Puente,Keiran Raine,Manasa Ramakrishna,Andrea L. Richardson,Julia Richter,Philip Rosenstiel,Matthias Schlesner,Ton N. Schumacher,Paul N. Span,Jon W. Teague,Yasushi Totoki,Andrew Tutt,Rafael Valdés-Mas,Marit M. van Buuren,Laura van ‘t Veer,Anne Vincent‐Salomon,Nicola Waddell,Lucy R. Yates,Jessica Zucman‐Rossi,P. Andrew Futreal,Ultan McDermott,Peter Lichter,Matthew Meyerson,Sean M. Grimmond,Reiner Siebert,Elı́as Campo,Tatsuhiro Shibata,Stefan M. Pfister,Peter J. Campbell,Michael R. Stratton
出处
期刊:Nature [Springer Nature]
卷期号:500 (7463): 415-421 被引量:7832
标识
DOI:10.1038/nature12477
摘要

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.
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