Identificador persistente para citar o vincular este elemento: http://hdl.handle.net/10553/43060
Campo DC Valoridioma
dc.contributor.authorValenciano, Almudenaen_US
dc.contributor.authorHenríquez-Hernández, Luis Albertoen_US
dc.contributor.authorMoreno, Mercedesen_US
dc.contributor.authorLloret, Martaen_US
dc.contributor.authorLara, Pedro Carlosen_US
dc.date.accessioned2018-11-21T12:18:18Z-
dc.date.available2018-11-21T12:18:18Z-
dc.date.issued2012en_US
dc.identifier.issn1936-5233en_US
dc.identifier.otherWoS-
dc.identifier.urihttp://hdl.handle.net/10553/43060-
dc.description.abstractInsulin-like growth factor 1 receptor (IGF-1R) is a transmembrane receptor tyrosine kinase involved in the development and progression of cancer whose activation strongly promotes cell growth and survival. IGF-1R exerts its main actions through the activation of the mitogen-activated protein kinase and phosphoinositide 3-kinase pathways. In addition to their traditional roles, IGF-1R activation has been associated with increased radioresistance both in vitro and in vivo, although the molecular mechanisms behind this process are still unclear. Recently, IGF-1R has been associated to new partners as major vault proteins, BCL-2, BAX, or Ku70/80, related to radiochemotherapy resistance, regulation of apoptosis, and nonhomologous end-joining DNA repair. Here, we review these novel associations of IGF-1R trying to explain the resistance to radiotherapy mediated by IGF-1R. Finally, we revised the role of new therapies leading to block the receptor to enhance the efficacy of radiation. © 2012 Neoplasia Press, Inc. All rights reserved.en_US
dc.languageengen_US
dc.relationFIS 1035/98en_US
dc.relation0855/01en_US
dc.relation.ispartofTranslational Oncologyen_US
dc.sourceTranslational Oncology [ISSN 1936-5233],v. 5(1), p. 1-9en_US
dc.subject320101 Oncologíaen_US
dc.subject3208 Farmacodinámicaen_US
dc.subject.otherGrowth-Factor-Ien_US
dc.subject.otherSquamous-Cell Carcinomaen_US
dc.subject.otherStrand-Break Repairen_US
dc.subject.otherLung-Cancer Cellsen_US
dc.subject.otherAnnexin-Iien_US
dc.subject.otherPrognostic-Significanceen_US
dc.subject.otherInsulin-Receptoren_US
dc.subject.otherDna-Damageen_US
dc.subject.otherKinaseen_US
dc.subject.otherExpressionen_US
dc.titleRole of IGF-1 receptor in radiation responseen_US
dc.typeinfo:eu-repo/semantics/reviewen_US
dc.typereviewen_US
dc.identifier.doi10.1593/tlo.11265en_US
dc.identifier.scopus84856006155-
dc.identifier.isi000304817600001-
dc.contributor.authorscopusid54904204300-
dc.contributor.authorscopusid15829708200-
dc.contributor.authorscopusid56328294100-
dc.contributor.authorscopusid7003855087-
dc.contributor.authorscopusid7004374085-
dc.description.lastpage9en_US
dc.identifier.issue1-
dc.description.firstpage1en_US
dc.relation.volume5en_US
dc.investigacionCiencias de la Saluden_US
dc.type2Reseñaen_US
dc.contributor.daisngid4100074-
dc.contributor.daisngid465624-
dc.contributor.daisngid3955607-
dc.contributor.daisngid802813-
dc.contributor.daisngid591076-
dc.description.numberofpages9en_US
dc.utils.revisionen_US
dc.contributor.wosstandardWOS:Valenciano, A-
dc.contributor.wosstandardWOS:Henriquez-Hernandez, LA-
dc.contributor.wosstandardWOS:Moreno, M-
dc.contributor.wosstandardWOS:Lloret, M-
dc.contributor.wosstandardWOS:Lara, PC-
dc.date.coverdateEnero 2012en_US
dc.identifier.ulpgcen_US
dc.identifier.ulpgcen_US
dc.identifier.ulpgcen_US
dc.identifier.ulpgcen_US
dc.contributor.buulpgcBU-MEDen_US
dc.description.sjr1,423
dc.description.sjrqQ1
dc.description.scieSCIE
item.grantfulltextopen-
item.fulltextCon texto completo-
crisitem.author.deptGIR IUIBS: Medio Ambiente y Salud-
crisitem.author.deptIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.deptDepartamento de Ciencias Clínicas-
crisitem.author.deptDepartamento de Ciencias Clínicas-
crisitem.author.orcid0000-0003-3237-0316-
crisitem.author.parentorgIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.fullNameHenríquez Hernández, Luis Alberto-
crisitem.author.fullNameLloret Sáez-Bravo, Marta-
Colección:Reseña
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