Show simple item record

dc.contributor.authorWoodcock, DJ
dc.contributor.authorSahli, A
dc.contributor.authorTeslo, R
dc.contributor.authorBhandari, V
dc.contributor.authorGruber, AJ
dc.contributor.authorZiubroniewicz, A
dc.contributor.authorGundem, G
dc.contributor.authorXu, Y
dc.contributor.authorButler, A
dc.contributor.authorAnokian, E
dc.contributor.authorPope, BJ
dc.contributor.authorJung, C-H
dc.contributor.authorTarabichi, M
dc.contributor.authorDentro, SC
dc.contributor.authorFarmery, JHR
dc.contributor.authorCRUK ICGC Prostate Group,
dc.contributor.authorVan Loo, P
dc.contributor.authorWarren, AY
dc.contributor.authorGnanapragasam, V
dc.contributor.authorHamdy, FC
dc.contributor.authorBova, GS
dc.contributor.authorFoster, CS
dc.contributor.authorNeal, DE
dc.contributor.authorLu, Y-J
dc.contributor.authorKote-Jarai, Z
dc.contributor.authorFraser, M
dc.contributor.authorBristow, RG
dc.contributor.authorBoutros, PC
dc.contributor.authorCostello, AJ
dc.contributor.authorCorcoran, NM
dc.contributor.authorHovens, CM
dc.contributor.authorMassie, CE
dc.contributor.authorLynch, AG
dc.contributor.authorBrewer, DS
dc.contributor.authorEeles, RA
dc.contributor.authorCooper, CS
dc.contributor.authorWedge, DC
dc.coverage.spatialUnited States
dc.date.accessioned2024-04-08T09:38:54Z
dc.date.available2024-04-08T09:38:54Z
dc.date.issued2024-03-13
dc.identifier100511
dc.identifierS2666-979X(24)00038-7
dc.identifier.citationCell Genomics, 2024, pp. 100511 -
dc.identifier.issn2666-979X
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/6193
dc.identifier.eissn2666-979X
dc.identifier.eissn2666-979X
dc.identifier.doi10.1016/j.xgen.2024.100511
dc.identifier.doi10.1016/j.xgen.2024.100511
dc.description.abstractThe development of cancer is an evolutionary process involving the sequential acquisition of genetic alterations that disrupt normal biological processes, enabling tumor cells to rapidly proliferate and eventually invade and metastasize to other tissues. We investigated the genomic evolution of prostate cancer through the application of three separate classification methods, each designed to investigate a different aspect of tumor evolution. Integrating the results revealed the existence of two distinct types of prostate cancer that arise from divergent evolutionary trajectories, designated as the Canonical and Alternative evolutionary disease types. We therefore propose the evotype model for prostate cancer evolution wherein Alternative-evotype tumors diverge from those of the Canonical-evotype through the stochastic accumulation of genetic alterations associated with disruptions to androgen receptor DNA binding. Our model unifies many previous molecular observations, providing a powerful new framework to investigate prostate cancer disease progression.
dc.formatPrint-Electronic
dc.format.extent100511 -
dc.languageeng
dc.language.isoeng
dc.publisherELSEVIER
dc.relation.ispartofCell Genomics
dc.rights.urihttps://creativecommons.org/licenses/by-nc/4.0
dc.subjectAR binding
dc.subjectcancer evolution
dc.subjectevotype model
dc.subjectevotypes
dc.subjectordering
dc.subjectprostate cancer
dc.titleGenomic evolution shapes prostate cancer disease type.
dc.typeJournal Article
dcterms.dateAccepted2024-02-08
dc.date.updated2024-03-14T11:38:22Z
rioxxterms.versionVoR
rioxxterms.versionofrecord10.1016/j.xgen.2024.100511
rioxxterms.licenseref.startdate2024-02-28
rioxxterms.typeJournal Article/Review
pubs.author-urlhttps://www.ncbi.nlm.nih.gov/pubmed/38428419
pubs.organisational-groupICR
pubs.organisational-groupICR/Primary Group
pubs.organisational-groupICR/Primary Group/ICR Divisions
pubs.organisational-groupICR/Primary Group/ICR Divisions/Genetics and Epidemiology
pubs.organisational-groupICR/Primary Group/ICR Divisions/Genetics and Epidemiology/Oncogenetics
pubs.organisational-groupICR/Primary Group/ICR Divisions/Radiotherapy and Imaging
pubs.organisational-groupICR/Primary Group/ICR Divisions/Radiotherapy and Imaging/Oncogenetics
pubs.publication-statusPublished online
pubs.publisher-urlhttp://dx.doi.org/10.1016/j.xgen.2024.100511
icr.researchteamOncogenetics
dc.contributor.icrauthorKote-Jarai, Zsofia
dc.contributor.icrauthorEeles, Rosalind
icr.provenanceDeposited by Miss Fay Allen (impersonating Prof Ros Eeles) on 2024-03-14. Deposit type is initial. No. of files: 1. Files: evotypes_full_ms_editorial_comments.pdf


Files in this item

Thumbnail

This item appears in the following collection(s)

Show simple item record

https://creativecommons.org/licenses/by-nc/4.0
Except where otherwise noted, this item's license is described as https://creativecommons.org/licenses/by-nc/4.0