Please use this identifier to cite or link to this item: http://hdl.handle.net/10553/44143
DC FieldValueLanguage
dc.contributor.authorSánchez-Céspedes, R.en_US
dc.contributor.authorSuárez-Bonnet, A.en_US
dc.contributor.authorMillán, Y.en_US
dc.contributor.authorGuil-Luna, S.en_US
dc.contributor.authorReymundo, C.en_US
dc.contributor.authorHerráez, P.en_US
dc.contributor.authorEspinosa De Los Monteros Y Zayas, Antonioen_US
dc.contributor.authorMartin de las Mulas, J.en_US
dc.date.accessioned2018-11-21T20:33:26Z-
dc.date.available2018-11-21T20:33:26Z-
dc.date.issued2013en_US
dc.identifier.issn1090-0233en_US
dc.identifier.urihttp://hdl.handle.net/10553/44143-
dc.description.abstractCD10 is an important cell marker in the diagnosis of acute lymphoblastic leukaemia and of breast myoepithelial (ME) cells in humans. The objective of this study was to assess the value of CD10 as a marker of canine ME cells using immunohistochemistry on routinely processed normal, dysplastic and neoplastic mammary tissue. Five different CD10 positive cell types were identified on the basis of cell morphology, pattern of immunoreactivity, and on the co-expression of additional cell lineage-specific markers.Type 1 cells were typical fusiform cells with a ME cell phenotype (calponin- and cytokeratin [CK] 14-positive, CK8/18-negative). Type 2 cells were typical or atypical polyhedral cells with a luminal epithelial (LE) cell phenotype (calponin- and CK14-negative, CK8/18-positive). Type 3 cells had a type 1 phenotype with variable morphology, and type 4 were atypical neoplastic cells with a mixed ME/LE phenotype. Type 5 cells were typical fusiform cells with a stromal phenotype.Type 1 cells were considered normal ME cells and were found in all sample types; type 2 cells were considered normal or neoplastic LE cells and were also found in all sample types; types 3 and 4 cells were restricted to tumour samples and to malignant tumours, respectively, and type 5 cells were found in all sample types, although predominantly in neoplastic tissue. The findings indicate that the CD10 antigen is a sensitive (although not specific) marker of canine ME cells in normal, dysplastic and neoplastic mammary tissue. Differences in the distribution and staining intensity of CD10-positive cells suggest a number of potential roles for this protein in the pathogenesis of canine mammary neoplasia. (C) 2012 Elsevier Ltd. All rights reserved.en_US
dc.languageengen_US
dc.publisher1090-0233
dc.relation.ispartofVeterinary Journalen_US
dc.sourceVeterinary Journal[ISSN 1090-0233],v. 195, p. 192-199en_US
dc.subject.otherLymphoblastic-Leukemia Antigenen_US
dc.subject.otherSmooth Muscle Actinen_US
dc.subject.otherImmunohistochemical Detectionen_US
dc.subject.otherMonoclonal-Antibodiesen_US
dc.subject.otherMembrane-Antigensen_US
dc.subject.otherBreast-Canceren_US
dc.subject.otherCommonen_US
dc.subject.otherExpressionen_US
dc.subject.otherCarcinomaen_US
dc.subject.otherBenignen_US
dc.titleUse of CD10 as a marker of canine mammary myoepithelial cellsen_US
dc.typeinfo:eu-repo/semantics/Articleen_US
dc.typeArticleen_US
dc.identifier.doi10.1016/j.tvjl.2012.06.003en_US
dc.identifier.scopus84873165470-
dc.identifier.isi000315066100012-
dc.contributor.authorscopusid35068575800-
dc.contributor.authorscopusid25636181300-
dc.contributor.authorscopusid6603640503-
dc.contributor.authorscopusid26632922000-
dc.contributor.authorscopusid6602625041-
dc.contributor.authorscopusid57194503614-
dc.contributor.authorscopusid36928058400-
dc.contributor.authorscopusid7003394672-
dc.contributor.authorscopusid57211742924-
dc.description.lastpage199en_US
dc.description.firstpage192en_US
dc.relation.volume195en_US
dc.investigacionCiencias de la Saluden_US
dc.type2Artículoen_US
dc.contributor.daisngid19758239-
dc.contributor.daisngid1256449-
dc.contributor.daisngid619515-
dc.contributor.daisngid1353334-
dc.contributor.daisngid1431295-
dc.contributor.daisngid30335206-
dc.contributor.daisngid700159-
dc.contributor.daisngid407245-
dc.utils.revisionen_US
dc.contributor.wosstandardWOS:Sanchez-Cespedes, R-
dc.contributor.wosstandardWOS:Suarez-Bonnet, A-
dc.contributor.wosstandardWOS:Millan, Y-
dc.contributor.wosstandardWOS:Guil-Luna, S-
dc.contributor.wosstandardWOS:Reymundo, C-
dc.contributor.wosstandardWOS:Herraez, P-
dc.contributor.wosstandardWOS:de los Monteros, AE-
dc.contributor.wosstandardWOS:de las Mulas, JM-
dc.date.coverdateFebrero 2013en_US
dc.identifier.ulpgcen_US
dc.contributor.buulpgcBU-MEDen_US
dc.description.sjr1,034
dc.description.jcr2,165
dc.description.sjrqQ1
dc.description.jcrqQ1
dc.description.scieSCIE
item.grantfulltextnone-
item.fulltextSin texto completo-
crisitem.author.deptGIR IUSA-ONEHEALTH 3: Histología y Patología Veterinaria y Forense (Terrestre y Marina)-
crisitem.author.deptIU de Sanidad Animal y Seguridad Alimentaria-
crisitem.author.deptGIR IUSA-ONEHEALTH 3: Histología y Patología Veterinaria y Forense (Terrestre y Marina)-
crisitem.author.deptIU de Sanidad Animal y Seguridad Alimentaria-
crisitem.author.deptDepartamento de Morfología-
crisitem.author.deptGIR IUSA-ONEHEALTH 3: Histología y Patología Veterinaria y Forense (Terrestre y Marina)-
crisitem.author.deptIU de Sanidad Animal y Seguridad Alimentaria-
crisitem.author.deptDepartamento de Morfología-
crisitem.author.orcid0000-0001-9316-2882-
crisitem.author.orcid0000-0002-7736-3139-
crisitem.author.parentorgIU de Sanidad Animal y Seguridad Alimentaria-
crisitem.author.parentorgIU de Sanidad Animal y Seguridad Alimentaria-
crisitem.author.parentorgIU de Sanidad Animal y Seguridad Alimentaria-
crisitem.author.fullNameSuarez Bonnet,Alejandro-
crisitem.author.fullNameHerráez Thomas, Pedro Manuel-
crisitem.author.fullNameEspinosa De Los Monteros Y Zayas, Antonio-
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