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DYRK1A: the double-edged kinase as a protagonist in cell growth and tumorigenesis

dc.contributor.authorFernández-Martínez, P
dc.contributor.authorZahonero, Cristina
dc.contributor.authorSánchez-Gómez, Pilar
dc.contributor.funderMinisterio de Economía y Competitividad (España)
dc.contributor.funderInstituto de Salud Carlos III
dc.contributor.funderRed Temática de Investigación Cooperativa en Cáncer (RTICC) (España)
dc.date.accessioned2019-07-12T07:53:54Z
dc.date.available2019-07-12T07:53:54Z
dc.date.issued2015
dc.description.abstractDYRK1A (dual-specificity tyrosine-regulated kinase 1A) is a kinase with multiple implications for embryonic development, especially in the nervous system where it regulates the balance between proliferation and differentiation of neural progenitors. The DYRK1A gene is located in the Down syndrome critical region and may play a significant role in the developmental brain defects, early neurodegeneration, and cancer susceptibility of individuals with this syndrome. DYRK1A is also expressed in adults, where it might participate in the regulation of cell cycle, survival, and tumorigenesis, thus representing a potential therapeutic target for certain types of cancer. However, the final readout of DYRK1A overexpression or inhibition depends strongly on the cellular context, as it has both tumor suppressor and oncogenic activities. Here, we will discuss the functions and substrates of DYRK1A associated with the control of cell growth and tumorigenesis with a focus on the potential use of DYRK1A inhibitors in cancer therapy.es_ES
dc.description.peerreviewedes_ES
dc.description.sponsorshipThis study was supported by grants from Ministerio de Economía y Competitividad, Fondo de Investigación Sanitaria, PI12/00775 and from Ministerio de Economía y Competitividad, Red Temática de Investigación Cooperativa en Cancer (RD12/0036/0027) to PSG.es_ES
dc.format.number1es_ES
dc.format.pagee970048es_ES
dc.format.volume2es_ES
dc.identifier.citationMolecular & Cellular Oncology, 2:1, e970048es_ES
dc.identifier.doi10.4161/23723548.2014.970048es_ES
dc.identifier.issn2372-3556es_ES
dc.identifier.journalMolecular & Cellular Oncologyes_ES
dc.identifier.pubmedID27308401es_ES
dc.identifier.urihttp://hdl.handle.net/20.500.12105/7898
dc.language.isoenges_ES
dc.publisherTaylor & Francis
dc.relation.projectIDinfo:eu-repo/grantAgreement/ES/PI12/00775es_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/ES/RD12/0036/0027es_ES
dc.relation.publisherversionhttps://doi.org/10.4161/23723548.2014.970048es_ES
dc.repisalud.centroISCIII::Unidad Funcional de Investigación de Enfermedades Crónicas (UFIEC)es_ES
dc.repisalud.institucionISCIIIes_ES
dc.rights.accessRightsopen accesses_ES
dc.rights.licenseAtribución-NoComercial 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc/4.0/*
dc.subjectDYRK1Aes_ES
dc.subjectCanceres_ES
dc.subjectCell differentiationes_ES
dc.subjectCell proliferationes_ES
dc.subjectNeural progenitorses_ES
dc.titleDYRK1A: the double-edged kinase as a protagonist in cell growth and tumorigenesises_ES
dc.typeresearch articlees_ES
dc.type.hasVersionVoRes_ES
dspace.entity.typePublication
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