Identificador persistente para citar o vincular este elemento: http://hdl.handle.net/10553/49494
Campo DC Valoridioma
dc.contributor.authorAznar Benitah, Salvadoren_US
dc.contributor.authorFernández-Valerón, Pilaren_US
dc.contributor.authorEspina, Carolinaen_US
dc.contributor.authorLacal, Juan Carlosen_US
dc.date.accessioned2018-11-24T08:02:48Z-
dc.date.available2018-11-24T08:02:48Z-
dc.date.issued2004en_US
dc.identifier.issn0304-3835en_US
dc.identifier.urihttp://hdl.handle.net/10553/49494-
dc.description.abstractLow molecular weight Rho GTPases are proteins that, in response to diverse stimuli, control key cellular processes such as cell proliferation, apoptosis, lipid metabolism, cytoarchitecture, adhesion, migration, cell polarity, and transcriptional regulation. The high incidence of overexpression of some members of the Rho family of GTPases in human tumors suggests that these proteins are important in the carcinogenic process, and therefore potential candidates for a therapeutic intervention. In recent years, the characterization of downstream effectors to Rho GTPases has increased our understanding of the general cellular effects that permit aberrant proliferation and motility of tumor cells. In addition, several transcription factors have been identified to play important roles at various levels of Rho-induced tumorigenesis. Accordingly, drugs that specifically alter Rho signaling display antineoplastic properties both at the level of tumor growth and tumor metastasis. In this review, a brief summary of the progress made in understanding the biological functions elicited by Rho GTPases that contribute to tumor biology will be made. In addition, a description of new drugs available targeted to specific elements of Rho signaling with antineoplastic or antimetastatic activity is included.en_US
dc.languageengen_US
dc.relation.ispartofCancer Lettersen_US
dc.sourceCancer Letters[ISSN 0304-3835],v. 206(2), p. 181-191 (Abril 2004)en_US
dc.subject32 Ciencias médicasen_US
dc.subject320713 Oncologíaen_US
dc.subject.otherRho GTPasesen_US
dc.subject.otherHuman carcinogenesisen_US
dc.subject.otherRho effectorsen_US
dc.subject.otherWiskott–Aldrich syndrome protein familyen_US
dc.subject.otherIQGAPen_US
dc.subject.otherROCKen_US
dc.subject.otherp21-Activated kinaseen_US
dc.subject.otherTranscriptional regulationen_US
dc.subject.otherApoptosisen_US
dc.subject.otherAnticancer drugsen_US
dc.titleRho GTPases: Potential candidates for anticancer therapyen_US
dc.typeinfo:eu-repo/semantics/reviewen_US
dc.typeReviewen_US
dc.identifier.doi10.1016/j.canlet.2003.08.035en_US
dc.identifier.scopus1542328238-
dc.contributor.authorscopusid8702853600-
dc.contributor.authorscopusid6603469417-
dc.contributor.authorscopusid57155313100-
dc.contributor.authorscopusid7004811766-
dc.description.lastpage191en_US
dc.description.firstpage181en_US
dc.relation.volume206en_US
dc.investigacionCiencias de la Saluden_US
dc.type2Reseñaen_US
dc.description.numberofpages11en_US
dc.utils.revisionen_US
dc.date.coverdateAbril 2004en_US
dc.identifier.ulpgcen_US
dc.identifier.ulpgcen_US
dc.identifier.ulpgcen_US
dc.identifier.ulpgcen_US
dc.contributor.buulpgcBU-MEDen_US
dc.description.jcr2,938-
dc.description.jcrqQ2-
dc.description.scieSCIE-
item.fulltextSin texto completo-
item.grantfulltextnone-
crisitem.author.deptGIR IUIBS: Medio Ambiente y Salud-
crisitem.author.deptIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.deptDepartamento de Bioquímica y Biología Molecular, Fisiología, Genética e Inmunología-
crisitem.author.orcid0000-0001-5865-7003-
crisitem.author.parentorgIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.fullNameFernández Valerón, Josefa Pilar-
Colección:Reseña
Vista resumida

Citas SCOPUSTM   

107
actualizado el 21-abr-2024

Visitas

29
actualizado el 02-mar-2024

Google ScholarTM

Verifica

Altmetric


Comparte



Exporta metadatos



Los elementos en ULPGC accedaCRIS están protegidos por derechos de autor con todos los derechos reservados, a menos que se indique lo contrario.