Hide metadata

dc.date.accessioned2020-05-16T19:24:53Z
dc.date.available2020-05-16T19:24:53Z
dc.date.created2020-01-08T09:26:11Z
dc.date.issued2019
dc.identifier.citationWong, Kim van der Weyden, Louise Schott, Courtney R. Foote, Alastair Constantino-Casas, Fernando Smith, Sionagh Dobson, Jane M. Murchison, Elizabeth P. Wu, Hong Yeh, Iwei Fullen, Douglas R. Joseph, Nancy Bastian, Boris C. Patel, Rajiv M. Martincorena, Inigo Robles-Espinoza, Carla Daniela Iyer, Vivek Kuijjer, Marieke Lydia Arends, Mark J. Brenn, Thomas Harms, Paul W. Wood, Geoffrey A. Adams, David J. . Cross-species genomic landscape comparison of human mucosal melanoma with canine oral and equine melanoma. Nature Communications. 2019
dc.identifier.urihttp://hdl.handle.net/10852/75820
dc.description.abstractMucosal melanoma is a rare and poorly characterized subtype of human melanoma. Here we perform a cross-species analysis by sequencing tumor-germline pairs from 46 primary human muscosal, 65 primary canine oral and 28 primary equine melanoma cases from mucosal sites. Analysis of these data reveals recurrently mutated driver genes shared between species such as NRAS, FAT4, PTPRJ, TP53 and PTEN, and pathogenic germline alleles of BRCA1, BRCA2 and TP53. We identify a UV mutation signature in a small number of samples, including human cases from the lip and nasal mucosa. A cross-species comparative analysis of recurrent copy number alterations identifies several candidate drivers including MDM2, B2M, KNSTRN and BUB1B. Comparison of somatic mutations in recurrences and metastases to those in the primary tumor suggests pervasive intra-tumor heterogeneity. Collectively, these studies suggest a convergence of some genetic changes in mucosal melanomas between species but also distinctly different paths to tumorigenesis.
dc.languageEN
dc.rightsAttribution 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.titleCross-species genomic landscape comparison of human mucosal melanoma with canine oral and equine melanoma
dc.typeJournal article
dc.creator.authorWong, Kim
dc.creator.authorvan der Weyden, Louise
dc.creator.authorSchott, Courtney R.
dc.creator.authorFoote, Alastair
dc.creator.authorConstantino-Casas, Fernando
dc.creator.authorSmith, Sionagh
dc.creator.authorDobson, Jane M.
dc.creator.authorMurchison, Elizabeth P.
dc.creator.authorWu, Hong
dc.creator.authorYeh, Iwei
dc.creator.authorFullen, Douglas R.
dc.creator.authorJoseph, Nancy
dc.creator.authorBastian, Boris C.
dc.creator.authorPatel, Rajiv M.
dc.creator.authorMartincorena, Inigo
dc.creator.authorRobles-Espinoza, Carla Daniela
dc.creator.authorIyer, Vivek
dc.creator.authorKuijjer, Marieke Lydia
dc.creator.authorArends, Mark J.
dc.creator.authorBrenn, Thomas
dc.creator.authorHarms, Paul W.
dc.creator.authorWood, Geoffrey A.
dc.creator.authorAdams, David J.
cristin.unitcode185,57,55,0
cristin.unitnameMarieke Kuijjer Group - Computational Biology and Systems Medicine
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode2
dc.identifier.cristin1768214
dc.identifier.bibliographiccitationinfo:ofi/fmt:kev:mtx:ctx&ctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Nature Communications&rft.volume=&rft.spage=&rft.date=2019
dc.identifier.jtitleNature Communications
dc.identifier.volume10
dc.identifier.issue1
dc.identifier.doihttps://doi.org/10.1038/s41467-018-08081-1
dc.identifier.urnURN:NBN:no-78839
dc.type.documentTidsskriftartikkel
dc.type.peerreviewedPeer reviewed
dc.source.issn2041-1723
dc.identifier.fulltextFulltext https://www.duo.uio.no/bitstream/handle/10852/75820/1/2019-01-21_wong_nat_comm.pdf
dc.type.versionPublishedVersion
cristin.articleid353
dc.relation.projectNFR/187615


Files in this item

Appears in the following Collection

Hide metadata

Attribution 4.0 International
This item's license is: Attribution 4.0 International