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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/13483
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dc.contributor.authorPereira, Michele C.-
dc.contributor.authorOliveira, Denise T.-
dc.contributor.authorOlivieri, Eloisa H. R.-
dc.contributor.authorRogatto, Silvia Regina-
dc.contributor.authorCarvalho, Andre L.-
dc.contributor.authorLandman, Gilles-
dc.contributor.authorKowalski, Luiz P.-
dc.date.accessioned2014-05-20T13:38:52Z-
dc.date.accessioned2016-10-25T16:54:54Z-
dc.date.available2014-05-20T13:38:52Z-
dc.date.available2016-10-25T16:54:54Z-
dc.date.issued2010-01-01-
dc.identifierhttp://dx.doi.org/10.1111/j.1600-0714.2009.00795.x-
dc.identifier.citationJournal of Oral Pathology & Medicine. Malden: Wiley-blackwell Publishing, Inc, v. 39, n. 1, p. 56-62, 2010.-
dc.identifier.issn0904-2512-
dc.identifier.urihttp://hdl.handle.net/11449/13483-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/13483-
dc.description.abstractObjective: The aim of this study was to investigate the prevalence of the Eosinophil cationic protein (ECP)-gene polymorphism 434(G > C) in oral squamous cell carcinoma (OSCC) patients and its association with tumor-associated tissue eosinophilia (TATE), demographic, clinical, and microscopic variables. Methods: The ECP genotypes of 165 healthy individuals and 157 OSCC patients were detected by PCR-RFLP analysis after cleavage of the amplified DNA sequence with enzyme PstI. TATE was obtained by morphometric analysis. Chi-square test or Fisher's exact test was used to analyze the association of ECP-gene polymorphism 434(G > C) with TATE, demographic, clinical, and microscopic variables in OSCC patients. Disease-free survival and overall survival were calculated by the Kaplan-Meier product-limit actuarial method and the comparison of the survival curves were performed using log rank test. Results: Most of healthy individuals (53.33%) and OSCC patients (57.97%) were heterozygous for the ECP 434(G > C) polymorphism. Based on numerical differences, our results showed that OSCC patients with intense TATE and at least one C allele had a higher frequency of bilateral neck dissection, local recurrence, vascular embolization, involved resection margins, and postoperative radiotherapy. No statistically significant differences on survival rates were found in OSCC patients presenting different ECP 434(G > C) genotypes. Conclusions: These results suggest a tendency towards a poor clinical outcome in OSCC patients with intense TATE and 434GC/CC genotypes, probably due to an ECP genetic variant with altered cytotoxic activity.en
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)-
dc.description.sponsorshipCoordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)-
dc.format.extent56-62-
dc.language.isoeng-
dc.publisherWiley-Blackwell Publishing, Inc-
dc.sourceWeb of Science-
dc.subjecteosinophil cationic proteinen
dc.subjecteosinophilsen
dc.subjectgene polymorphismen
dc.subjectprognosisen
dc.subjectsquamous cell carcinomaen
dc.titleThe 434(G > C) polymorphism in the eosinophil cationic protein gene and its association with tissue eosinophilia in oral squamous cell carcinomasen
dc.typeoutro-
dc.contributor.institutionUniversidade de São Paulo (USP)-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.contributor.institutionCanc Hosp AC Camargo-
dc.contributor.institutionCanc Hosp Barretos-
dc.description.affiliationUniv São Paulo, Dept Stomatol, Area Pathol, Bauru Sch Dent, BR-17012901 São Paulo, Brazil-
dc.description.affiliationSão Paulo State Univ, Dept Genet, Inst Biosci, São Paulo, Brazil-
dc.description.affiliationSão Paulo State Univ, Dept Urol, Fac Med, São Paulo, Brazil-
dc.description.affiliationCanc Hosp AC Camargo, Dept Pathol, São Paulo, Brazil-
dc.description.affiliationCanc Hosp Barretos, Dept Head & Neck Surg, Fundação Pio 12, São Paulo, Brazil-
dc.description.affiliationCanc Hosp AC Camargo, Dept Head & Neck Surg & Otorhinolaryngol, São Paulo, Brazil-
dc.description.affiliationUnespSão Paulo State Univ, Dept Genet, Inst Biosci, São Paulo, Brazil-
dc.description.affiliationUnespSão Paulo State Univ, Dept Urol, Fac Med, São Paulo, Brazil-
dc.description.sponsorshipIdFAPESP: 06/03830-0-
dc.identifier.doi10.1111/j.1600-0714.2009.00795.x-
dc.identifier.wosWOS:000273313200009-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofJournal of Oral Pathology & Medicine-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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