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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/74546
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dc.contributor.authorMartinho, Olga-
dc.contributor.authorSimões, Kleber-
dc.contributor.authorLongatto-Filho, Adhemar-
dc.contributor.authorJacob, Carlos Eduardo-
dc.contributor.authorZilberstein, Bruno-
dc.contributor.authorBresciani, Cláudio-
dc.contributor.authorGama-Rodrigues, Joaquim-
dc.contributor.authorCecconello, Ivan-
dc.contributor.authorAlves, Venâncio-
dc.contributor.authorReis, Rui Manuel-
dc.date.accessioned2014-05-27T11:28:21Z-
dc.date.accessioned2016-10-25T18:43:31Z-
dc.date.available2014-05-27T11:28:21Z-
dc.date.available2016-10-25T18:43:31Z-
dc.date.issued2013-02-01-
dc.identifierhttp://dx.doi.org/10.3892/or.2012.2179-
dc.identifier.citationOncology Reports, v. 29, n. 2, p. 690-696, 2013.-
dc.identifier.issn1021-335X-
dc.identifier.issn1791-2431-
dc.identifier.urihttp://hdl.handle.net/11449/74546-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/74546-
dc.description.abstractGastric cancer is a leading cause of cancer-related mortality, and the presence of lymph node metastasis an important prognostic factor. Downregulation of RKIP has been associated with tumor progression and metastasis in several types of neoplasms, being currently categorized as a metastasis suppressor gene. Our aim was to determine the expression levels of RKIP in gastric tissues and to evaluate its impact in the clinical outcome of gastric carcinoma patients. RKIP expression levels were studied by immunohistochemistry in a series of gastric tissues. Overall, we analysed 222 non-neoplastic gastric tissues, 152 primary tumors and 42 lymph node metastasis samples. We observed that RKIP was highly expressed in ∼83% of non-neoplastic tissues (including normal tissue and metaplasia), was lost in ∼56% of primary tumors and in ∼90% of lymph node metastasis samples. Loss of RKIP expression was significantly associated with several markers of poor clinical outcome, including the presence of lymph node metastasis. Furthermore, the absence of RKIP protein constitutes an independent prognostic marker for these patients. In conclusion, RKIP expression is significantly lost during gastric carcinoma progression being almost absent in lymph node metastasis samples. Of note, we showed that the absence of RKIP expression is associated with poor outcome features of gastric cancer patients, this being also an independent prognostic marker.en
dc.format.extent690-696-
dc.language.isoeng-
dc.sourceScopus-
dc.subjectGastric carcinomas-
dc.subjectPrognosis-
dc.subjectRKIP-
dc.subjectbiological marker-
dc.subjectphosphatidylethanolamine binding protein-
dc.subjectadult-
dc.subjectaged-
dc.subjectcancer grading-
dc.subjectcancer incidence-
dc.subjectcancer patient-
dc.subjectcancer prognosis-
dc.subjectcancer staging-
dc.subjectcontrolled study-
dc.subjectfemale-
dc.subjecthuman-
dc.subjecthuman tissue-
dc.subjectimmunohistochemistry-
dc.subjectlymph node metastasis-
dc.subjectmajor clinical study-
dc.subjectmale-
dc.subjectmetaplasia-
dc.subjectprimary tumor-
dc.subjectpriority journal-
dc.subjectprotein expression-
dc.subjectstomach cancer-
dc.subjectstomach carcinoma-
dc.subjecttissue microarray-
dc.subjecttumor volume-
dc.subjectAdult-
dc.subjectAged-
dc.subjectAged, 80 and over-
dc.subjectCarcinoma-
dc.subjectChi-Square Distribution-
dc.subjectFemale-
dc.subjectHumans-
dc.subjectKaplan-Meier Estimate-
dc.subjectLymphatic Metastasis-
dc.subjectMale-
dc.subjectMiddle Aged-
dc.subjectMultivariate Analysis-
dc.subjectPhosphatidylethanolamine Binding Protein-
dc.subjectProportional Hazards Models-
dc.subjectStomach Neoplasms-
dc.subjectTumor Markers, Biological-
dc.titleAbsence of RKIP expression is an independent prognostic biomarker for gastric cancer patientsen
dc.typeoutro-
dc.contributor.institutionUniversity of Minho-
dc.contributor.institutionICVS/3B's - PT Government Associate Laboratory-
dc.contributor.institutionUniversidade de São Paulo (USP)-
dc.contributor.institutionBarretos Cancer Hospital-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.description.affiliationLife and Health Sciences Research Institute (ICVS) Health Sciences School University of Minho, Braga-
dc.description.affiliationICVS/3B's - PT Government Associate Laboratory, Braga/Guimarães-
dc.description.affiliationDepartment of Pathology University of São Paulo School of Medicine, São Paulo-
dc.description.affiliationMolecular Oncology Research Center Barretos Cancer Hospital, Rua Antenor Duarte Villela, 1331, CEP 14784400 Barretos, S. Paulo-
dc.description.affiliationLaboratory of Medical Investigation (LIM) 14 Faculty of Medicine São Paulo State University, São Paulo-
dc.description.affiliationDepartment of Gastroenterology Faculty of Medicine University of São Paulo, São Paulo-
dc.description.affiliationUnespLaboratory of Medical Investigation (LIM) 14 Faculty of Medicine São Paulo State University, São Paulo-
dc.identifier.doi10.3892/or.2012.2179-
dc.identifier.wosWOS:000313605100039-
dc.rights.accessRightsAcesso restrito-
dc.identifier.file2-s2.0-84872803648.pdf-
dc.relation.ispartofOncology Reports-
dc.identifier.scopus2-s2.0-84872803648-
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