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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/74901
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dc.contributor.authorAfonso, Julieta-
dc.contributor.authorLongatto-Filho, Adhemar-
dc.contributor.authorMartinho, Olga-
dc.contributor.authorLobo, Francisco-
dc.contributor.authorAmaro, Teresina-
dc.contributor.authorReis, Rui M.-
dc.contributor.authorSantos, Lúcio L.-
dc.date.accessioned2014-05-27T11:28:44Z-
dc.date.accessioned2016-10-25T18:45:57Z-
dc.date.available2014-05-27T11:28:44Z-
dc.date.available2016-10-25T18:45:57Z-
dc.date.issued2013-04-01-
dc.identifierhttp://dx.doi.org/10.1007/s00428-013-1388-2-
dc.identifier.citationVirchows Archiv, v. 462, n. 4, p. 445-453, 2013.-
dc.identifier.issn0945-6317-
dc.identifier.issn1432-2307-
dc.identifier.urihttp://hdl.handle.net/11449/74901-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/74901-
dc.description.abstractUrothelial bladder cancer (UBC) is a heterogeneous type of disease. It is urgent to screen biomarkers of tumour aggressiveness in order to clarify the clinical behaviour and to personalize therapy in UBC patients. Raf kinase inhibitory protein (RKIP) is a metastasis suppressor, and its downregulation is associated with metastatic events in an increasing number of solid tumours. We evaluated the clinical and prognostic significance of RKIP expression in patients with high risk of progression UBC. Using immunohistochemistry, we determined RKIP expression levels in a series of 81 patients with high-grade pT1/pTis or muscle-invasive UBC. Staining of CD31 and D2-40 was used to assess blood and lymphatic vessels, in order to distinguish between blood and lymphatic vessel invasion (LVI). We found that 90 % of pT1/pTis tumours, 94 % of non-muscle invasive papillary tumours and 76 % of the cases without LVI occurrence expressed RKIP in >10 % of cells. In this group, we observed a subgroup of tumours (42 %) in which the tumour centre was significantly more intensely stained than the invasion front. This heterogeneous pattern was observed in 63 % of the cases with LVI. Low RKIP expression was associated with poorer 5-year disease-free and overall survival rates, and remained as an independent prognostic factor for disease-free survival. Loss of RKIP expression may be an important prognostic factor for patients with high risk of progression bladder cancer. © 2013 Springer-Verlag Berlin Heidelberg.en
dc.format.extent445-453-
dc.language.isoeng-
dc.sourceScopus-
dc.subjectBiomarkers-
dc.subjectBladder cancer-
dc.subjectLymphovascular invasion-
dc.subjectPrognosis-
dc.subjectRKIP-
dc.subjectCD31 antigen-
dc.subjectmonoclonal antibody D2-40-
dc.subjectphosphatidylethanolamine binding protein-
dc.subjectadult-
dc.subjectaged-
dc.subjectbladder cancer-
dc.subjectblood-
dc.subjectcancer growth-
dc.subjectcancer invasion-
dc.subjectcancer patient-
dc.subjectcancer prognosis-
dc.subjectcancer survival-
dc.subjectcancer tissue-
dc.subjectcontrolled study-
dc.subjectdisease free survival-
dc.subjectfemale-
dc.subjecthigh risk patient-
dc.subjecthuman-
dc.subjecthuman tissue-
dc.subjectimmunohistochemistry-
dc.subjectlymph vessel-
dc.subjectmale-
dc.subjectoverall survival-
dc.subjectpriority journal-
dc.subjectprotein expression-
dc.subjecturothelial bladder cancer-
dc.subjectAdult-
dc.subjectAged-
dc.subjectAged, 80 and over-
dc.subjectFemale-
dc.subjectHumans-
dc.subjectImmunohistochemistry-
dc.subjectMale-
dc.subjectMiddle Aged-
dc.subjectPhosphatidylethanolamine Binding Protein-
dc.subjectUrinary Bladder Neoplasms-
dc.titleLow RKIP expression associates with poor prognosis in bladder cancer patientsen
dc.typeoutro-
dc.contributor.institutionUniversity of Minho-
dc.contributor.institutionICVS/3B's-PT Government Associate Laboratory-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.contributor.institutionPortuguese Institute of Oncology-IPO-
dc.contributor.institutionBarretos Cancer Hospital-
dc.contributor.institutionUniversity Fernando Pessoa-UFP-
dc.description.affiliationLife and Health Sciences Research Institute-ICVS University of Minho, Braga-
dc.description.affiliationICVS/3B's-PT Government Associate Laboratory, Braga-
dc.description.affiliationLaboratory of Medical Investigation (LIM 14) Faculty of Medicine São Paulo State University, São Paulo-
dc.description.affiliationDepartment of Urology Portuguese Institute of Oncology-IPO, Porto-
dc.description.affiliationExperimental Pathology and Therapeutics Research Center Portuguese Institute of Oncology-IPO, Porto-
dc.description.affiliationMolecular Oncology Research Center Barretos Cancer Hospital, São Paulo-
dc.description.affiliationUniversity Fernando Pessoa-UFP, Porto-
dc.description.affiliationUnespLaboratory of Medical Investigation (LIM 14) Faculty of Medicine São Paulo State University, São Paulo-
dc.identifier.doi10.1007/s00428-013-1388-2-
dc.identifier.wosWOS:000317856400009-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofVirchows Archiv-
dc.identifier.scopus2-s2.0-84876502122-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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