Protein kinase C and cancer: what we know and what we do not

cic.isFulltexttruees
cic.isPeerReviewedtruees
cic.lugarDesarrolloCentro de Investigaciones Inmunológicas Básicas y Aplicadas es
cic.versioninfo:eu-repo/semantics/submittedVersiones
dc.date.accessioned2017-09-27T12:05:12Z
dc.date.available2017-09-27T12:05:12Z
dc.identifier.urihttps://digital.cic.gba.gob.ar/handle/11746/6197
dc.titleProtein kinase C and cancer: what we know and what we do noten
dc.typeArtículoes
dcterms.abstractSince their discovery in the late 1970’s, protein kinase C (PKC) isozymes represent one of the most extensively studied signaling kinases. PKCs signal through multiple pathways and control the expression of genes relevant for cell cycle progression, tumorigenesis and metastatic dissemination. Despite the vast amount of information concerning the mechanisms that control PKC activation and function in cellular models, the relevance of individual PKC isozymes in the progression of human cancer is still a matter of controversy. Although the expression of PKC isozymes is altered in multiple cancer types, the causal relationship between such changes and the initiation and progression of the disease remains poorly defined. Animal models developed in the last years helped to better understand the involvement of individual PKCs in various cancer types and in the context of specific oncogenic alterations. Unraveling the enormous complexity in the mechanisms by which PKC isozymes impact on tumorigenesis and metastasis is key for reassessing their potential as pharmacological targets for cancer treatment.en
dcterms.creator.authorGarg, Rachanaes
dcterms.creator.authorBenedetti, Lorena G.es
dcterms.creator.authorAbera, Mahlet B.es
dcterms.creator.authorWang, HongBines
dcterms.creator.authorAbba, Martín Carloses
dcterms.creator.authorKazanietz, Marcelo G.es
dcterms.extent34 p.es
dcterms.identifier.otherDOI:10.1038/onc.2013.524es
dcterms.isPartOf.issuevol. 33, no. 45es
dcterms.isPartOf.seriesOncogenees
dcterms.issued2014-11
dcterms.languageIngléses
dcterms.licenseAttribution-NonCommercial 4.0 International (BY-NC 4.0)es
dcterms.subjectProtein kinase C (PKC)en
dcterms.subjectmitogenesisen
dcterms.subjectapoptosisen
dcterms.subjectsurvivalen
dcterms.subjecttumorigenesisen
dcterms.subjectmetastasisen
dcterms.subjectanimal modelses
dcterms.subject.materiaCiencias Médicases

Archivos

Bloque original
Mostrando 1 - 1 de 1
Cargando...
Miniatura
Nombre:
nihms688403.pdf-PDFA.pdf
Tamaño:
1.22 MB
Formato:
Adobe Portable Document Format
Descripción:
Documento completo