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The 434(G > C) polymorphism in the eosinophil cationic protein gene and its association with tissue eosinophilia in oral squamous cell carcinomas

dc.contributor.authorPereira, Michele C.
dc.contributor.authorOliveira, Denise T.
dc.contributor.authorOlivieri, Eloisa H. R. [UNESP]
dc.contributor.authorRogatto, Silvia Regina [UNESP]
dc.contributor.authorCarvalho, Andre L.
dc.contributor.authorLandman, Gilles
dc.contributor.authorKowalski, Luiz P.
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.date.accessioned2014-05-20T13:38:52Z
dc.date.available2014-05-20T13:38:52Z
dc.date.issued2010-01-01
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.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.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
dc.description.sponsorshipCoordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)
dc.description.sponsorshipIdFAPESP: 06/03830-0
dc.format.extent56-62
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.doi10.1111/j.1600-0714.2009.00795.x
dc.identifier.issn0904-2512
dc.identifier.lattes5240998569868081
dc.identifier.lattes2259986546265579
dc.identifier.urihttp://hdl.handle.net/11449/13483
dc.identifier.wosWOS:000273313200009
dc.language.isoeng
dc.publisherWiley-Blackwell Publishing, Inc
dc.relation.ispartofJournal of Oral Pathology & Medicine
dc.relation.ispartofjcr2.237
dc.relation.ispartofsjr0,791
dc.rights.accessRightsAcesso restrito
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.typeArtigo
dcterms.licensehttp://olabout.wiley.com/WileyCDA/Section/id-406071.html
dcterms.rightsHolderWiley-blackwell Publishing, Inc
dspace.entity.typePublication
unesp.author.lattes5240998569868081
unesp.author.lattes2259986546265579
unesp.author.orcid0000-0002-4628-7129[2]
unesp.author.orcid0000-0001-7027-5550[3]
unesp.author.orcid0000-0001-7214-6402[5]
unesp.author.orcid0000-0001-5865-9308[7]
unesp.author.orcid0000-0002-0481-156X[7]
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Medicina, Botucatupt
unesp.departmentUrologia - FMBpt

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