Show simple item record

dc.contributor.authorGarcía Tuñón Llanio, Ignacio 
dc.contributor.authorRicote Belinchón, Mónica 
dc.contributor.authorRuiz A., Antonio
dc.contributor.authorFraile Laiz, Benito 
dc.contributor.authorPaniagua Gómez-Álvarez, Ricardo 
dc.contributor.authorRoyuela García, María del Mar 
dc.date.accessioned2010-03-12T12:42:08Z
dc.date.available2010-03-12T12:42:08Z
dc.date.issued2007
dc.identifier.bibliographicCitationBMC Cancer, 2007, v. 7, p. 158en
dc.identifier.issn1471-2407
dc.identifier.urihttp://hdl.handle.net/10017/5918
dc.description.abstractInterferons are a group of proteins that trigger multiple responses including prevention of viral replication, inhibition of cell growth, and modulation of cell differentiation. In different mammary carcinoma cell lines IFNγ induces growth arrest at mid-G1. At the present there are no in vivo studies in human breast. The aim of this study was to investigate the expression patterns of IFNγ and its two receptors (IFNγ-Rα and IFNγ-Rβ) by Western blot and immunohistochem., in order to elucidate its role in the different types of human breast cancer (in situ and infiltrative). Methods: Immunohistochem. and semiquant. study of IFNγ, its receptors types (IFNγ-Rα and IFNγ-Rβ), cell proliferation (proliferating cell nuclear antigen, also named PCNA), and apoptosis (Tunel method) was carried between the three breast groups (fibrocystic lesions, in situ tumors and infiltrating tumors). Results: In the three groups of patients, IFNγ and IFNγ-Rα immunoreactions appeared in the cytoplasm while IFNγ-Rβ also was found in the nucleus. The optical d. of IFNγ was higher in in situ carcinoma than in benign and infiltrating tumors. When we obsd. IFNγ-Rα, the optical d. was lower in infiltrating carcinoma than in benign and in situ tumors (the higher d.). To IFNγ-Rβ, the optical d. was similar in the three group samples. In tumor samples PCNA and TUNEL index was significantly higher; than in benign diseases. PCNA index increased with the malignance. No significant differences were found between cancer types to TUNEL. IFNγ could be a potential therapeutic tool in breast cancer. However, tumor cells are able to escape from the control of this cytokine in the early tumor stages; this is probably due to a decreased expression of IFNγ, or also to an alteration of either its receptors or some transduction elements. Conclusions: We conclude that the decrease in the % pos. samples that expressed IFNγ and IFNγ-Rα together with the nuclear localization of IFNγ-Rβ, could be a tumoral cell response, although perhaps insufficient to inhibit the uncontrolled cell proliferation. Perhaps, IFNγ might be unable to activate p21 to stop the cell cycle, suggesting a possible participation in breast cancer development.en
dc.format.mimetypeapplication/pdfen
dc.language.isoengen
dc.publisherBioMed Centralen
dc.rightsAtribución-NoComercial-SinDerivadas 3.0 Españaes_ES
dc.rights© García-Tuñón et al; licensee BioMed Central Ltd., 2007en
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/es/
dc.subjectBreast canceren
dc.subjectInterferonsen
dc.subjectIFNγ receptorsen
dc.titleInfluence of IFN-gamma and its receptors in human breast canceren
dc.typeinfo:eu-repo/semantics/articleen
dc.subject.ecienciaBiologíaes_ES
dc.subject.ecienciaBiologyen
dc.subject.ecienciaGenéticaes_ES
dc.subject.ecienciaGeneticsen
dc.subject.ecienciaCienciaes_ES
dc.subject.ecienciaScienceen
dc.contributor.affiliationUniversidad de Alcalá. Departamento de Biología Celular y Genética
dc.relation.publisherversionhttp://dx.doi.org/10.1186/1471-2407-7-158
dc.type.versioninfo:eu-repo/semantics/publishedVersionen
dc.identifier.doi10.1186/1471-2407-7-158
dc.rights.accessRightsinfo:eu-repo/semantics/openAccessen


Files in this item

Thumbnail

This item appears in the following Collection(s)

Atribución-NoComercial-SinDerivadas 3.0 España
Este ítem está sujeto a una licencia Creative Commons.