Identificador persistente para citar o vincular este elemento: http://hdl.handle.net/10553/42586
Campo DC Valoridioma
dc.contributor.authorBohn, Urielen_US
dc.contributor.authorAguiar, Joséen_US
dc.contributor.authorBilbao Sieyro, Cristinaen_US
dc.contributor.authorMurias, Adolfoen_US
dc.contributor.authorVega, Victoren_US
dc.contributor.authorChirino Godoy, Ricardoen_US
dc.contributor.authorDíaz-Chico, Nicolasen_US
dc.contributor.authorDíaz Chico, Juan Carlosen_US
dc.contributor.otherBILBAO SIEYRO, CRISTINA-
dc.contributor.otherDiaz-Chico, Juan-
dc.date.accessioned2018-11-21T10:14:38Z-
dc.date.available2018-11-21T10:14:38Z-
dc.date.issued2002en_US
dc.identifier.issn0020-7136en_US
dc.identifier.urihttp://hdl.handle.net/10553/42586-
dc.description.abstractOur study attempts to determine the prognostic value of the quantitative measurement of the oncoprotein p185Her‐2/neu in a group of patients with breast cancer and positive node involvement. In a series of 217 patients with breast cancer and positive nodes in whom the oncoprotein p185 was quantitatively determined by ELISA, we analyzed the clinico‐pathological variables including age, menopausal status, tumor size, number of affected nodes, type and histology grade and the molecular variables such as the oestrogen and progesterone receptors (ER and PR, respectively), pS2 and Cathepsin D (CD). Using 260 fmol/mg protein as a cut‐off point, 18% of the tumors presented as overexpressing p185. The p185 showed no relationship with any of the clinico‐pathological variables studied except that its concentration was elevated in ductal and lobular histology types and in the moderate and poorly differentiated histology grades. With a median follow‐up of 50 months (range 1–90), the univariate analysis of disease‐free survival (DFS) and overall survival (OS) showed that the histology grade, tumor size, the number of infiltrated nodes, the p185 and the ER were the variables associated with the clinical course of the disease in the patients. In the multivariate analysis, however, only the tumor size, number of affected ganglia, the p185 and the ER remained associated with the clinical progression of the disease. The patients with p185 overexpression had a risk, not only of relapse but also death from the disease, of more than twice that of the patients who had normal p185 concentrations. When the p185 was divided into 3 categories based on ±1 × SD above or below the mean, the patients with high and low p185 showed, in the univariate analysis, a similar relationship with DFS but not with OS. In the multivariate analysis, both with the DFS as with the OS, only a high p185 concentration retained its association with the clinical course of the disease in the patients. Our results suggest that by quantitatively determining (using ELISA) the p185 oncoprotein, groups of cancer patients of high risk could be better identified for more effective clinical management.en_US
dc.languageengen_US
dc.publisher0020-7136-
dc.relation.ispartofInternational Journal of Canceren_US
dc.sourceInternational Journal Of Cancer [ISSN 0020-7136],v. 101 (6), p. 539-544en_US
dc.subject320101 Oncologíaen_US
dc.subject.otherBreast canceren_US
dc.subject.otherp185 oncoproteinen_US
dc.subject.otherELISAen_US
dc.subject.otherHer-2 Neu Oncogeneen_US
dc.subject.otherC-Erbb-2 Expressionen_US
dc.subject.otherProtein Overexpressionen_US
dc.subject.otherMultivariate-Analysisen_US
dc.subject.otherRecurrent Diseaseen_US
dc.subject.otherIncreased Risken_US
dc.subject.otherLymph-Nodesen_US
dc.subject.otherCathepsin-Den_US
dc.titlePrognostic value of the quantitative measurement of the oncoprotein p185(Her-2/neu) in a group of patients with breast cancer and positive node involvementen_US
dc.typeinfo:eu-repo/semantics/articleen_US
dc.typeArticleen_US
dc.identifier.doi10.1002/ijc.10612en_US
dc.identifier.scopus2-s2.0-0037145315-
dc.identifier.isi000178250900006-
dcterms.isPartOfInternational Journal Of Cancer-
dcterms.sourceInternational Journal Of Cancer[ISSN 0020-7136],v. 101 (6), p. 539-544-
dc.contributor.authorscopusid6602628770-
dc.contributor.authorscopusid57198008231-
dc.contributor.authorscopusid12759635600-
dc.contributor.authorscopusid19836805600-
dc.contributor.authorscopusid7003826494-
dc.contributor.authorscopusid6701324062-
dc.contributor.authorscopusid25723175700-
dc.contributor.authorscopusid6701492347-
dc.description.lastpage544en_US
dc.identifier.issue6-
dc.description.firstpage539en_US
dc.relation.volume101en_US
dc.investigacionCiencias de la Saluden_US
dc.type2Artículoen_US
dc.identifier.wosWOS:000178250900006-
dc.contributor.daisngid1265214-
dc.contributor.daisngid23629369-
dc.contributor.daisngid2205075-
dc.contributor.daisngid963987-
dc.contributor.daisngid994925-
dc.contributor.daisngid880609-
dc.contributor.daisngid6115168-
dc.contributor.daisngid4287772-
dc.contributor.daisngid1724161-
dc.contributor.daisngid749099-
dc.identifier.investigatorRIDR-6779-2018-
dc.identifier.investigatorRIDH-1527-2015-
dc.utils.revisionen_US
dc.contributor.wosstandardWOS:Bohn, U-
dc.contributor.wosstandardWOS:Aguiar, J-
dc.contributor.wosstandardWOS:Bilbao, C-
dc.contributor.wosstandardWOS:Murias, A-
dc.contributor.wosstandardWOS:Vega, V-
dc.contributor.wosstandardWOS:Chirino, R-
dc.contributor.wosstandardWOS:Diaz-Chico, N-
dc.contributor.wosstandardWOS:Diaz-Chico, JC-
dc.date.coverdateOctubre 2002en_US
dc.identifier.ulpgces
dc.description.jcr4,056
dc.description.jcrqQ1
dc.description.scieSCIE
item.fulltextCon texto completo-
item.grantfulltextopen-
crisitem.author.deptDepartamento de Morfología-
crisitem.author.deptGIR IUIBS: Diabetes y endocrinología aplicada-
crisitem.author.deptIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.deptDepartamento de Bioquímica y Biología Molecular, Fisiología, Genética e Inmunología-
crisitem.author.deptGIR IUIBS: Bioquímica-
crisitem.author.deptIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.deptDepartamento de Bioquímica y Biología Molecular, Fisiología, Genética e Inmunología-
crisitem.author.orcid0000-0002-4796-1445-
crisitem.author.orcid0000-0002-5681-8931-
crisitem.author.orcid0000-0002-0944-990X-
crisitem.author.parentorgIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.parentorgIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.fullNameBilbao Sieyro, Cristina-
crisitem.author.fullNameChirino Godoy, Ricardo-
crisitem.author.fullNameDíaz Chico, Juan Carlos-
Colección:Artículos
miniatura
PDF
Adobe PDF (99,15 kB)
Vista resumida

Citas SCOPUSTM   

7
actualizado el 13-oct-2024

Citas de WEB OF SCIENCETM
Citations

7
actualizado el 13-oct-2024

Visitas

112
actualizado el 03-ago-2024

Descargas

145
actualizado el 03-ago-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.