A 5-gene classifier from the carcinoma-associated fibroblast transcriptomic profile and clinical outcome in colorectal cancer

dc.contributor.authorBerdiel Acer, Mireia
dc.contributor.authorBerenguer, Antoni
dc.contributor.authorSanz Pamplona, Rebeca
dc.contributor.authorCuadras, Daniel
dc.contributor.authorSanjuan, Xavier
dc.contributor.authorPaules, María José
dc.contributor.authorSantos, Cristina
dc.contributor.authorSalazar Soler, Ramón
dc.contributor.authorMoreno Aguado, Víctor
dc.contributor.authorCapellá, G. (Gabriel)
dc.contributor.authorVillanueva Garatachea, Alberto
dc.contributor.authorMolleví, David G.
dc.date.accessioned2021-06-30T16:05:56Z
dc.date.available2021-06-30T16:05:56Z
dc.date.issued2014-08-15
dc.date.updated2021-06-30T16:05:57Z
dc.description.abstractBased on 108 differentially expressed genes between carcinoma-associated fibroblasts (CAFs) and paired normal colonic fibroblasts we recently reported, a 5-gene classifier for relapse prediction in Stage II/III colorectal cancer (CRC ) was developed. Its predictive value was validated in datasets GSE17538, GSE33113 and GSE14095. An additional validation was performed in a metacohort (n=317) and 142 CRC patients by means of RT-PCR. The 5-gene classifier was significantly associated with increased relapse risk and death from CRC across all validation series of Stage II/III patients used. Multivariate Cox regression analyses confirmed the independent prognostic value of the stromal classifier (HR=2.67; P=0.002). Post-test probabilities provided evidence of the suitability of the 5-gene classifier in clinical practice, identifying a subgroup of Stage-II patients who were at high risk of relapse. Moreover, the a priory worst prognosis mesenchymal subtype of tumours can be stratified according to the physiological status of their carcinoma-associated fibroblasts. In conclusion the CAFs-derived 5-gene classifier provides more accurate information about outcome than conventional clinicopathological criteria and it could be useful to take clinical decisions, especially in Stage II. Additionally, the classifier put into relevance the CAF's intratumoral heterogeneity and might contribute to find relevant targets for depleting adequate CAFS subtypes.
dc.format.extent16 p.
dc.format.mimetypeapplication/pdf
dc.identifier.idgrec648503
dc.identifier.issn1949-2553
dc.identifier.pmid25115384
dc.identifier.urihttps://hdl.handle.net/2445/178753
dc.language.isoeng
dc.publisherImpact Journals
dc.relation.isformatofReproducció del document publicat a: https://doi.org/10.18632/oncotarget.2237
dc.relation.ispartofOncotarget, 2014, vol. 5, num. 15, p. 6437-6452
dc.relation.urihttps://doi.org/10.18632/oncotarget.2237
dc.rightscc-by (c) Berdiel Acer, Mireia et al., 2014
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.sourceArticles publicats en revistes (Ciències Clíniques)
dc.subject.classificationCàncer colorectal
dc.subject.classificationFibroblasts
dc.subject.classificationGenètica
dc.subject.classificationMetabolisme
dc.subject.otherColorectal cancer
dc.subject.otherFibroblasts
dc.subject.otherGenetics
dc.subject.otherMetabolism
dc.titleA 5-gene classifier from the carcinoma-associated fibroblast transcriptomic profile and clinical outcome in colorectal cancer
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion

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