Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/162994
Title: Pan-cancer analysis of whole genomes
Author: ICGC/TCGA Pan-Cancer Analysis of Whole Genomes Consortium
Rabionet Janssen, Raquel
Gelpi Buchaca, Josep Lluís
Aymerich, Marta
López Guillermo, Armando
Campo Güerri, Elias
Estivill, Xavier, 1955-
Escaramis Babiano, Georgia
Martín-Subero, José Ignacio
Keywords: Càncer
Genètica
Cancer
Genetics
Issue Date: 5-Feb-2020
Publisher: Nature Publishing Group
Abstract: Cancer is driven by genetic change, and the advent of massively parallel sequencing has enabled systematic documentation of this variation at the whole-genome scale1,2,3. Here we report the integrative analysis of 2,658 whole-cancer genomes and their matching normal tissues across 38 tumour types from the Pan-Cancer Analysis of Whole Genomes (PCAWG) Consortium of the International Cancer Genome Consortium (ICGC) and The Cancer Genome Atlas (TCGA). We describe the generation of the PCAWG resource, facilitated by international data sharing using compute clouds. On average, cancer genomes contained 4-5 driver mutations when combining coding and non-coding genomic elements; however, in around 5% of cases no drivers were identified, suggesting that cancer driver discovery is not yet complete. Chromothripsis, in which many clustered structural variants arise in a single catastrophic event, is frequently an early event in tumour evolution; in acral melanoma, for example, these events precede most somatic point mutations and affect several cancer-associated genes simultaneously. Cancers with abnormal telomere maintenance often originate from tissues with low replicative activity and show several mechanisms of preventing telomere attrition to critical levels. Common and rare germline variants affect patterns of somatic mutation, including point mutations, structural variants and somatic retrotransposition. A collection of papers from the PCAWG Consortium describes non-coding mutations that drive cancer beyond those in the TERT promoter4; identifies new signatures of mutational processes that cause base substitutions, small insertions and deletions and structural variation5,6; analyses timings and patterns of tumour evolution7; describes the diverse transcriptional consequences of somatic mutation on splicing, expression levels, fusion genes and promoter activity8,9; and evaluates a range of more-specialized features of cancer genomes8,10,11,12,13,14,15,16,17,18.
Note: Versió postprint del document publicat a: https://doi.org/10.1038/s41586-020-1969-6
It is part of: Nature, 2020, vol. 578, num. 7793, p. 82-93
URI: http://hdl.handle.net/2445/162994
Related resource: https://doi.org/10.1038/s41586-020-1969-6
ISSN: 0028-0836
Appears in Collections:Articles publicats en revistes (Bioquímica i Biomedicina Molecular)
Articles publicats en revistes (Genètica, Microbiologia i Estadística)

Files in This Item:
File Description SizeFormat 
695946.pdf23.13 MBAdobe PDFView/Open


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.