Molecular-subtype-specific biomarkers improve prediction of prognosis in colorectal cancer

dc.contributor.authorBertram Bramsen, Jesper
dc.contributor.authorHeilskov Rasmussen, Mads
dc.contributor.authorOngen, Halit
dc.contributor.authorBlock Mattesen, Trine
dc.contributor.authorWorm Ørntoft, Mai-Britt
dc.contributor.authorSalling Árnadóttir, Sigrid
dc.contributor.authorSandoval, Juan
dc.contributor.authorLaguna, Teresa
dc.contributor.authorVang, Søren
dc.contributor.authorØster, Bodil
dc.contributor.authorLamy, Philippe
dc.contributor.authorRørbæk Madsen, Mogens
dc.contributor.authorLaurberg, Søren
dc.contributor.authorEsteller, Manel
dc.contributor.authorTheophilos Dermitzakis, Emmanouil
dc.contributor.authorFalck Ørntoft, Torben
dc.contributor.authorLindbjerg Andersen, Claus
dc.date.accessioned2018-05-07T12:42:23Z
dc.date.available2018-05-07T12:42:23Z
dc.date.issued2017-05-09
dc.date.updated2018-05-07T12:42:23Z
dc.description.abstractColorectal cancer (CRC) is characterized by major inter-tumor diversity that complicates the prediction of disease and treatment outcomes. Recent efforts help resolve this by sub-classification of CRC into natural molecular subtypes; however, this strategy is not yet able to provide clinicians with improved tools for decision making. We here present an extended framework for CRC stratification that specifically aims to improve patient prognostication. Using transcriptional profiles from 1,100 CRCs, including >300 previously unpublished samples, we identify cancer cell and tumor archetypes and suggest the tumor microenvironment as a major prognostic determinant that can be influenced by the microbiome. Notably, our subtyping strategy allowed identification of archetype-specific prognostic biomarkers that provided information beyond and independent of UICC-TNM staging, MSI status, and consensus molecular subtyping. The results illustrate that our extended subtyping framework, combining subtyping and subtype-specific biomarkers, could contribute to improved patient prognostication and may form a strong basis for future studies
dc.format.extent13 p.
dc.format.mimetypeapplication/pdf
dc.identifier.idgrec673494
dc.identifier.issn2211-1247
dc.identifier.pmid28494874
dc.identifier.urihttps://hdl.handle.net/2445/122137
dc.language.isoeng
dc.publisherElsevier
dc.relation.isformatofReproducció del document publicat a: https://doi.org/10.1016/j.celrep.2017.04.045
dc.relation.ispartofCell Reports, 2017, vol. 19, num. 6, p. 1268-1280
dc.relation.projectIDinfo:eu-repo/grantAgreement/EC/FP7/258236/EU//SYSCOL
dc.relation.urihttps://doi.org/10.1016/j.celrep.2017.04.045
dc.rightscc-by (c) Bertram Bramsen, Jesper et al., 2017
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es
dc.sourceArticles publicats en revistes (Ciències Fisiològiques)
dc.subject.classificationMarcadors bioquímics
dc.subject.classificationPronòstic mèdic
dc.subject.classificationCàncer colorectal
dc.subject.classificationCèl·lules canceroses
dc.subject.otherBiochemical markers
dc.subject.otherPrognosis
dc.subject.otherColorectal cancer
dc.subject.otherCancer cells
dc.titleMolecular-subtype-specific biomarkers improve prediction of prognosis in colorectal cancer
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion

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