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dc.contributor.authorZhang, GuangJun
dc.contributor.authorHoersch, Sebastian
dc.contributor.authorAmsterdam, Adam
dc.contributor.authorWhittaker, Charles A.
dc.contributor.authorBeert, Eline
dc.contributor.authorCatchen, Julian M.
dc.contributor.authorPostlethwait, John H.
dc.contributor.authorLegius, Eric
dc.contributor.authorFarrington, Sarah M.
dc.contributor.authorHopkins, Nancy H.
dc.contributor.authorLees, Jacqueline
dc.date.accessioned2013-09-30T17:15:17Z
dc.date.available2013-09-30T17:15:17Z
dc.date.issued2013-08
dc.date.submitted2013-03
dc.identifier.issn1553-7404
dc.identifier.issn1553-7390
dc.identifier.urihttp://hdl.handle.net/1721.1/81246
dc.description.abstractThe identification of cancer drivers is a major goal of current cancer research. Finding driver genes within large chromosomal events is especially challenging because such alterations encompass many genes. Previously, we demonstrated that zebrafish malignant peripheral nerve sheath tumors (MPNSTs) are highly aneuploid, much like human tumors. In this study, we examined 147 zebrafish MPNSTs by massively parallel sequencing and identified both large and focal copy number alterations (CNAs). Given the low degree of conserved synteny between fish and mammals, we reasoned that comparative analyses of CNAs from fish versus human MPNSTs would enable elimination of a large proportion of passenger mutations, especially on large CNAs. We established a list of orthologous genes between human and zebrafish, which includes approximately two-thirds of human protein-coding genes. For the subset of these genes found in human MPNST CNAs, only one quarter of their orthologues were co-gained or co-lost in zebrafish, dramatically narrowing the list of candidate cancer drivers for both focal and large CNAs. We conclude that zebrafish-human comparative analysis represents a powerful, and broadly applicable, tool to enrich for evolutionarily conserved cancer drivers.en_US
dc.description.sponsorshipKathy and Curt Marble Cancer Research Funden_US
dc.description.sponsorshipArthur C. Merrillen_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grant CA106416)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grant ROI RR020833)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grant 1F32GM095213-01)en_US
dc.language.isoen_US
dc.publisherPublic Library of Scienceen_US
dc.relation.isversionofhttp://dx.doi.org/10.1371/journal.pgen.1003734en_US
dc.rightsCreative Commons Attributionen_US
dc.rights.urihttp://creativecommons.org/licenses/by/2.5/en_US
dc.sourcePLoSen_US
dc.titleComparative Oncogenomic Analysis of Copy Number Alterations in Human and Zebrafish Tumors Enables Cancer Driver Discoveryen_US
dc.typeArticleen_US
dc.identifier.citationZhang, GuangJun, Sebastian Hoersch, Adam Amsterdam, Charles A. Whittaker, Eline Beert, Julian M. Catchen, Sarah Farrington, et al. “Comparative Oncogenomic Analysis of Copy Number Alterations in Human and Zebrafish Tumors Enables Cancer Driver Discovery.” Edited by Marshall S. Horwitz. PLoS Genetics 9, no. 8 (August 29, 2013): e1003734.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biologyen_US
dc.contributor.departmentKoch Institute for Integrative Cancer Research at MITen_US
dc.contributor.mitauthorAmsterdam, Adamen_US
dc.contributor.mitauthorWhittaker, Charles A.en_US
dc.contributor.mitauthorFarrington, Sarah M.en_US
dc.contributor.mitauthorHopkins, Nancy H.en_US
dc.contributor.mitauthorLees, Jacquelineen_US
dc.contributor.mitauthorZhang, GuangJunen_US
dc.contributor.mitauthorHoersch, Sebastianen_US
dc.relation.journalPLoS Geneticsen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsZhang, GuangJun; Hoersch, Sebastian; Amsterdam, Adam; Whittaker, Charles A.; Beert, Eline; Catchen, Julian M.; Farrington, Sarah; Postlethwait, John H.; Legius, Eric; Hopkins, Nancy; Lees, Jacqueline A.en_US
dc.identifier.orcidhttps://orcid.org/0000-0001-9451-2194
dc.identifier.orcidhttps://orcid.org/0000-0001-9804-536X
mit.licensePUBLISHER_CCen_US
mit.metadata.statusComplete


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