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dc.contributor.authorDressler, Len_US
dc.contributor.authorBortolomeazzi, Men_US
dc.contributor.authorKeddar, MRen_US
dc.contributor.authorMisetic, Hen_US
dc.contributor.authorSartini, Gen_US
dc.contributor.authorAcha-Sagredo, Aen_US
dc.contributor.authorMontorsi, Len_US
dc.contributor.authorWijewardhane, Nen_US
dc.contributor.authorRepana, Den_US
dc.contributor.authorNulsen, Jen_US
dc.contributor.authorGoldman, Jen_US
dc.contributor.authorPollitt, Men_US
dc.contributor.authorDavis, Pen_US
dc.contributor.authorStrange, Aen_US
dc.contributor.authorAmbrose, Ken_US
dc.contributor.authorCiccarelli, FDen_US
dc.date.accessioned2024-01-08T09:37:39Z
dc.date.available2022-01-10en_US
dc.date.issued2022-01-26en_US
dc.identifier.urihttps://qmro.qmul.ac.uk/xmlui/handle/123456789/93494
dc.description.abstractBACKGROUND: Genetic alterations of somatic cells can drive non-malignant clone formation and promote cancer initiation. However, the link between these processes remains unclear and hampers our understanding of tissue homeostasis and cancer development. RESULTS: Here, we collect a literature-based repertoire of 3355 well-known or predicted drivers of cancer and non-cancer somatic evolution in 122 cancer types and 12 non-cancer tissues. Mapping the alterations of these genes in 7953 pan-cancer samples reveals that, despite the large size, the known compendium of drivers is still incomplete and biased towards frequently occurring coding mutations. High overlap exists between drivers of cancer and non-cancer somatic evolution, although significant differences emerge in their recurrence. We confirm and expand the unique properties of drivers and identify a core of evolutionarily conserved and essential genes whose germline variation is strongly counter-selected. Somatic alteration in even one of these genes is sufficient to drive clonal expansion but not malignant transformation. CONCLUSIONS: Our study offers a comprehensive overview of our current understanding of the genetic events initiating clone expansion and cancer revealing significant gaps and biases that still need to be addressed. The compendium of cancer and non-cancer somatic drivers, their literature support, and properties are accessible in the Network of Cancer Genes and Healthy Drivers resource at http://www.network-cancer-genes.org/ .en_US
dc.format.extent35 - ?en_US
dc.languageengen_US
dc.relation.ispartofGenome Biolen_US
dc.rightsAttribution 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/us/*
dc.subjectCancer initiationen_US
dc.subjectDriver genesen_US
dc.subjectSomatic evolutionen_US
dc.subjectSystems-level propertiesen_US
dc.subjectClonal Evolutionen_US
dc.subjectHumansen_US
dc.subjectMutationen_US
dc.subjectNeoplasmsen_US
dc.subjectOncogenesen_US
dc.titleComparative assessment of genes driving cancer and somatic evolution in non-cancer tissues: an update of the Network of Cancer Genes (NCG) resource.en_US
dc.typeArticle
dc.identifier.doi10.1186/s13059-022-02607-zen_US
pubs.author-urlhttps://www.ncbi.nlm.nih.gov/pubmed/35078504en_US
pubs.issue1en_US
pubs.notesNot knownen_US
pubs.publication-statusPublished onlineen_US
pubs.volume23en_US
dcterms.dateAccepted2022-01-10en_US
rioxxterms.funderDefault funderen_US
rioxxterms.identifier.projectDefault projecten_US


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Attribution 3.0 United States
Except where otherwise noted, this item's license is described as Attribution 3.0 United States