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Patterns of somatic mutation in human cancer genomes
Authors:Greenman Christopher  Stephens Philip  Smith Raffaella  Dalgliesh Gillian L  Hunter Christopher  Bignell Graham  Davies Helen  Teague Jon  Butler Adam  Stevens Claire  Edkins Sarah  O'Meara Sarah  Vastrik Imre  Schmidt Esther E  Avis Tim  Barthorpe Syd  Bhamra Gurpreet  Buck Gemma  Choudhury Bhudipa  Clements Jody  Cole Jennifer  Dicks Ed  Forbes Simon  Gray Kris  Halliday Kelly  Harrison Rachel  Hills Katy  Hinton Jon  Jenkinson Andy  Jones David  Menzies Andy  Mironenko Tatiana  Perry Janet  Raine Keiran  Richardson Dave  Shepherd Rebecca  Small Alexandra  Tofts Calli  Varian Jennifer  Webb Tony  West Sofie  Widaa Sara  Yates Andy
Institution:Cancer Genome Project, Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge CB10 1SA, UK.
Abstract:Cancers arise owing to mutations in a subset of genes that confer growth advantage. The availability of the human genome sequence led us to propose that systematic resequencing of cancer genomes for mutations would lead to the discovery of many additional cancer genes. Here we report more than 1,000 somatic mutations found in 274 megabases (Mb) of DNA corresponding to the coding exons of 518 protein kinase genes in 210 diverse human cancers. There was substantial variation in the number and pattern of mutations in individual cancers reflecting different exposures, DNA repair defects and cellular origins. Most somatic mutations are likely to be 'passengers' that do not contribute to oncogenesis. However, there was evidence for 'driver' mutations contributing to the development of the cancers studied in approximately 120 genes. Systematic sequencing of cancer genomes therefore reveals the evolutionary diversity of cancers and implicates a larger repertoire of cancer genes than previously anticipated.
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