Please use this identifier to cite or link to this item: http://hdl.handle.net/10553/47001
DC FieldValueLanguage
dc.contributor.authorValerón, Pilar F.en_US
dc.contributor.authorChirino, Ricardoen_US
dc.contributor.authorVega Benítez, Víctor Manuelen_US
dc.contributor.authorFalcón, Orlandoen_US
dc.contributor.authorRivero, Juan F.en_US
dc.contributor.authorTorres Curbelo, Santiagoen_US
dc.contributor.authorLeón Arencibia, Laureanoen_US
dc.contributor.authorFernández, Leandroen_US
dc.contributor.authorPestano, Jen_US
dc.contributor.authorDíaz-Chico, Bonifacioen_US
dc.contributor.authorDiazChico, JCen_US
dc.contributor.otherPestano Brito, Jose Juan-
dc.contributor.otherDiaz-Chico, Juan-
dc.contributor.otherFernandez-Perez, Leandro-
dc.date.accessioned2018-11-23T10:03:39Z-
dc.date.available2018-11-23T10:03:39Z-
dc.date.issued1997en_US
dc.identifier.issn0020-7136en_US
dc.identifier.urihttp://hdl.handle.net/10553/47001-
dc.description.abstractThe total cellular p185(HER-2/neu) protein (p185) content was measured by ELISA in 346 invasive primary breast cancers, and the results were compared with those of estrogen (ER) and progesterone (PR) receptors, pS2 and Cathepsin D (Cat D) content. At a cut-off level of 260 fmol/mg protein, 53 of the 346 tumors (15%) were p185 positive. A significant positive correlation was observed between p185 levels and those of Cat D, and a weaker, though significant, positive correlation with ER, and pS2 levels, but not with those of PR. However, when only the 293 p185-negative tumors were considered, the correlation between p185 and ER improved substantially, and statistical significance was reached for PR. p185-positive tumors exhibited lower ER and PR content and higher Cat D content than p185-negative tumors. The pS2 content, in contrast, did not undergo significant variation, Tumors considered to be p185-positive were significantly more frequently positive for Cat D at the cut-off of 45 pmol/mg protein, and were more frequently negative for ER and/or PR, but only significant at the cut-off of 15 fmol/mg or higher for both steroid receptors. Finally, p185 status was not associated with menopausal status, tumor size, axillary-lymph-node invasiveness or distant metastases. These results suggest that 260 fmol/mg protein as the cut-off for p185 allows the identification of a tumoral sub-population with a more aggresive phenotype.en_US
dc.languageengen_US
dc.relation.ispartofInternational Journal of Canceren_US
dc.sourceInternational Journal Of Cancer[ISSN 0020-7136],v. 74 (2), p. 175-179en_US
dc.subject32 Ciencias médicasen_US
dc.subject320101 Oncologíaen_US
dc.subject.otherCathepsin-D Expressionen_US
dc.subject.otherHer-2/Neu Amplificationen_US
dc.subject.otherEstrogen-Receptoren_US
dc.subject.otherOncogeneen_US
dc.subject.otherAssayen_US
dc.subject.otherCellsen_US
dc.subject.otherP185en_US
dc.titleQuantitative analysis of p185(HER-2/neu) protein in breast cancer and its association with other prognostic factorsen_US
dc.typeinfo:eu-repo/semantics/Articleen_US
dc.typeArticleen_US
dc.identifier.doi10.1002/(SICI)1097-0215(19970422)74:2<175::AID-IJC6>3.0.CO;2-Wen_US
dc.identifier.scopus0030945762-
dc.identifier.isiA1997WX43400006-
dcterms.isPartOfInternational Journal Of Cancer-
dcterms.sourceInternational Journal Of Cancer[ISSN 0020-7136],v. 74 (2), p. 175-179-
dc.contributor.authorscopusid6603469417-
dc.contributor.authorscopusid6701324062-
dc.contributor.authorscopusid7003826494-
dc.contributor.authorscopusid6603752888-
dc.contributor.authorscopusid7006478821-
dc.contributor.authorscopusid57192268038-
dc.contributor.authorscopusid19234933700-
dc.contributor.authorscopusid7202848203-
dc.contributor.authorscopusid56149756400-
dc.contributor.authorscopusid7003603506-
dc.contributor.authorscopusid6508301282-
dc.description.lastpage179en_US
dc.description.firstpage175en_US
dc.relation.volume74en_US
dc.investigacionCiencias de la Saluden_US
dc.type2Artículoen_US
dc.identifier.wosWOS:A1997WX43400006-
dc.contributor.daisngid1146740-
dc.contributor.daisngid6115168-
dc.contributor.daisngid880609-
dc.contributor.daisngid994925-
dc.contributor.daisngid1217537-
dc.contributor.daisngid29398789-
dc.contributor.daisngid1397582-
dc.contributor.daisngid30389612-
dc.contributor.daisngid5422159-
dc.contributor.daisngid411603-
dc.contributor.daisngid795544-
dc.contributor.daisngid865329-
dc.contributor.daisngid1724161-
dc.contributor.daisngid749099-
dc.identifier.investigatorRIDA-9640-2017-
dc.identifier.investigatorRIDH-1527-2015-
dc.identifier.investigatorRIDH-1493-2015-
dc.description.numberofpages5en_US
dc.utils.revisionen_US
dc.contributor.wosstandardWOS:Valeron, PF-
dc.contributor.wosstandardWOS:Chirino, R-
dc.contributor.wosstandardWOS:Vega, V-
dc.contributor.wosstandardWOS:Falcon, O-
dc.contributor.wosstandardWOS:Rivero, JF-
dc.contributor.wosstandardWOS:Torres, S-
dc.contributor.wosstandardWOS:Leon, L-
dc.contributor.wosstandardWOS:Fernandez, L-
dc.contributor.wosstandardWOS:Pestano, J-
dc.contributor.wosstandardWOS:DiazChico, B-
dc.contributor.wosstandardWOS:DiazChico, JC-
dc.date.coverdateAbril 1997en_US
dc.identifier.ulpgcen_US
dc.contributor.buulpgcBU-MEDen_US
dc.description.jcr3,362-
dc.description.jcrqQ1-
dc.description.scieSCIE-
item.grantfulltextnone-
item.fulltextSin texto completo-
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.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.deptDepartamento de Ciencias Médicas y Quirúrgicas-
crisitem.author.deptDepartamento de Bioquímica y Biología Molecular, Fisiología, Genética e Inmunología-
crisitem.author.deptDepartamento de Morfología-
crisitem.author.deptGIR IUIBS: Farmacología Molecular y Traslacional-
crisitem.author.deptIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.deptDepartamento de Ciencias Clínicas-
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.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.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.orcid0000-0001-5865-7003-
crisitem.author.orcid0000-0002-5681-8931-
crisitem.author.orcid0000-0002-0596-3880-
crisitem.author.orcid0000-0001-7802-465X-
crisitem.author.orcid0000-0001-6454-4785-
crisitem.author.orcid0000-0002-0944-990X-
crisitem.author.orcid0000-0002-0944-990X-
crisitem.author.parentorgIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.parentorgIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.parentorgIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.parentorgIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.parentorgIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.parentorgIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.fullNameFernández Valerón, Josefa Pilar-
crisitem.author.fullNameChirino Godoy, Ricardo-
crisitem.author.fullNameVega Benítez, Víctor Manuel-
crisitem.author.fullNameTorres Curbelo, Santiago-
crisitem.author.fullNameLeón Arencibia, Laureano-
crisitem.author.fullNameFernández Pérez, Leandro Francisco-
crisitem.author.fullNamePestano Brito, José Juan-
crisitem.author.fullNameDíaz Chico, Juan Carlos-
crisitem.author.fullNameDíaz Chico, Juan Carlos-
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