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dc.contributor.authorRodríguez, Nuriaes_ES
dc.contributor.authorPeláez, A.es_ES
dc.contributor.authorBarderas, Rodrigoes_ES
dc.contributor.authorDomínguez, Gemmaes_ES
dc.date.accessioned2019-08-13T06:56:36Z-
dc.date.available2019-08-13T06:56:36Z-
dc.date.issued2018-
dc.identifier.citationClinical and Translational Oncology 20(7): 827-836 (2018)es_ES
dc.identifier.issn1699-048X-
dc.identifier.urihttp://hdl.handle.net/10261/188101-
dc.description.abstractTP73 is a member of the TP53 family whose expression has been observed altered in most human cancers and associated with the prognosis. TP73 translates into a complex number of isoforms with both oncogenic and tumour-suppressor functions and presents a complex cross-talk with other members of the family (TP53 and TP63). In this revision, we focus on the evidence that may support TP73 variants as prognostic markers in cancer. Nowadays, most publications in this topic highlight the association between overexpression of the oncogenic variants and failure to respond to chemotherapy and/or shorter survival. In addition, we comment on the putative possibilities that the detection through a liquid biopsy of TP73 variants may provide, and finally, the significance of determining the value of the combined alteration of the TP53 family members in the clinical setting.es_ES
dc.description.sponsorshipWe acknowledge ISCIII, FIS, FEDER and Cátedra de Patrocinio UAM-Roche for funding our current research through the PI15/00246 Grant and the Grant from the MINECO (SAF2014-53209-R) and CIBERONC.es_ES
dc.language.isoenges_ES
dc.publisherSpringer Naturees_ES
dc.relationinfo:eu-repo/grantAgreement/MINECO/Plan Estatal de Investigación Científica y Técnica y de Innovación 2013-2016/SAF2014-53209-Res_ES
dc.rightsclosedAccesses_ES
dc.subjectClinical translationes_ES
dc.subjectCanceres_ES
dc.subjectHuman patientses_ES
dc.subjectPrognosises_ES
dc.subjectTP73 isoformses_ES
dc.titleClinical implications of the deregulated TP73 isoforms expression in canceres_ES
dc.typeartículoes_ES
dc.identifier.doi10.1007/s12094-017-1802-3-
dc.description.peerreviewedPeer reviewedes_ES
dc.relation.publisherversionhttps://doi.org/10.1007/s12094-017-1802-3es_ES
dc.identifier.e-issn1699-3055-
dc.contributor.funderInstituto de Salud Carlos IIIes_ES
dc.contributor.funderMinisterio de Economía y Competitividad (España)es_ES
dc.contributor.funderFederación Española de Enfermedades Rarases_ES
dc.contributor.funderUniversidad Autónoma de Madrides_ES
dc.relation.csices_ES
oprm.item.hasRevisionno ko 0 false*
dc.identifier.funderhttp://dx.doi.org/10.13039/501100004587es_ES
dc.identifier.funderhttp://dx.doi.org/10.13039/501100002924es_ES
dc.identifier.funderhttp://dx.doi.org/10.13039/501100003329es_ES
dc.identifier.funderhttp://dx.doi.org/10.13039/501100004593es_ES
dc.contributor.orcidDomínguez, Gemma [0000-0002-2802-6806]es_ES
dc.identifier.pmid29230693-
dc.type.coarhttp://purl.org/coar/resource_type/c_6501es_ES
item.grantfulltextnone-
item.cerifentitytypePublications-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.languageiso639-1en-
item.fulltextNo Fulltext-
item.openairetypeartículo-
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