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dc.contributor.authorCRUK-ICGC Prostate Group
dc.contributor.authorWoodcock, Dan J
dc.contributor.authorSahli, Atef
dc.contributor.authorTeslo, Ruxandra
dc.contributor.authorBhandari, Vinayak
dc.contributor.authorGruber, Andreas J
dc.contributor.authorZiubroniewicz, Aleksandra
dc.contributor.authorGundem, Gunes
dc.contributor.authorXu, Yaobo
dc.contributor.authorButler, Adam
dc.contributor.authorAnokian, Ezequiel
dc.contributor.authorPope, Bernard J
dc.contributor.authorJung, Chol-Hee
dc.contributor.authorTarabichi, Maxime
dc.contributor.authorDentro, Stefan C
dc.contributor.authorFarmery, J Henry R
dc.contributor.authorVan Loo, Peter
dc.contributor.authorWarren, Anne Y
dc.contributor.authorGnanapragasam, Vincent
dc.contributor.authorHamdy, Freddie C
dc.contributor.authorBova, G Steven
dc.contributor.authorFoster, Christopher S
dc.contributor.authorNeal, David E
dc.contributor.authorLu, Yong-Jie
dc.contributor.authorKote-Jarai, Zsofia
dc.contributor.authorBristow, Robert G
dc.contributor.authorBoutros, Paul C
dc.contributor.authorCostello, Anthony J
dc.contributor.authorCorcoran, Niall M
dc.contributor.authorHovens, Christopher M
dc.contributor.authorMassie, Charlie E
dc.contributor.authorLynch, Andy G
dc.contributor.authorBrewer, Daniel S
dc.contributor.authorEeles, Rosalind A
dc.contributor.authorCooper, Colin S
dc.contributor.authorWedge, David C
dc.date.accessioned2024-03-14T15:30:09Z
dc.date.available2024-03-14T15:30:09Z
dc.date.issued2024-03-13
dc.identifier300069797
dc.identifier2608d7f1-f04d-4ef9-b6c5-89108c7f4bbd
dc.identifier38428419
dc.identifier85186331848
dc.identifier.citationCRUK-ICGC Prostate Group , Woodcock , D J , Sahli , A , Teslo , R , Bhandari , V , Gruber , A J , Ziubroniewicz , A , Gundem , G , Xu , Y , Butler , A , Anokian , E , Pope , B J , Jung , C-H , Tarabichi , M , Dentro , S C , Farmery , J H R , Van Loo , P , Warren , A Y , Gnanapragasam , V , Hamdy , F C , Bova , G S , Foster , C S , Neal , D E , Lu , Y-J , Kote-Jarai , Z , Bristow , R G , Boutros , P C , Costello , A J , Corcoran , N M , Hovens , C M , Massie , C E , Lynch , A G , Brewer , D S , Eeles , R A , Cooper , C S & Wedge , D C 2024 , ' Genomic evolution shapes prostate cancer disease type ' , Cell Genomics , vol. 4 , no. 13 , 100511 . https://doi.org/10.1016/j.xgen.2024.100511en
dc.identifier.issn2666-979X
dc.identifier.otherORCID: /0000-0002-7876-7338/work/155069488
dc.identifier.urihttps://hdl.handle.net/10023/29492
dc.descriptionH.R.F. was supported by a Cancer Research UK Programme Grant to Simon Tavaré (C14303/A17197), as, partially, was A.G.L. A.G.L. acknowledges the support of the University of St Andrews. A.G.L. and J.H.R.F. also acknowledge the support of the Cambridge Cancer Research Fund.en
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 Aalternative 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.format.extent31
dc.format.extent6500271
dc.language.isoeng
dc.relation.ispartofCell Genomicsen
dc.subjectProstate canceren
dc.subjectCancer evolutionen
dc.subjectEvotype modelen
dc.subjectEvotypesen
dc.subjectAR bindingen
dc.subjectOrderingen
dc.subjectI-PWen
dc.subjectSDG 3 - Good Health and Well-beingen
dc.titleGenomic evolution shapes prostate cancer disease typeen
dc.typeJournal articleen
dc.contributor.institutionUniversity of St Andrews. School of Mathematics and Statisticsen
dc.contributor.institutionUniversity of St Andrews. School of Medicineen
dc.identifier.doihttps://doi.org/10.1016/j.xgen.2024.100511
dc.description.statusPeer revieweden


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