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DNA methylation in the CTCF-binding site I and the expression pattern of the H19 gene: Does positive expression predict poor prognosis in early stage head and neck carcinomas?

dc.contributor.authorEsteves, LICV
dc.contributor.authorJavaroni, A. C.
dc.contributor.authorNishimoto, I. N.
dc.contributor.authorMagrin, J.
dc.contributor.authorSquire, J. A.
dc.contributor.authorKowalski, L. P.
dc.contributor.authorRainho, C. A.
dc.contributor.authorRogatto, Silvia Regina [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionUniversidade de São Paulo (USP)
dc.contributor.institutionAC Camargo Hosp
dc.contributor.institutionUniv Toronto
dc.contributor.institutionOntario Canc Inst
dc.date.accessioned2014-05-20T13:38:45Z
dc.date.available2014-05-20T13:38:45Z
dc.date.issued2005-10-01
dc.description.abstractLoss of allele-specific expression by the imprinted genes IGF2 and H19 has been correlated with a differentially methylated region (DMR) upstream to the H19 gene. The H19-DMR contains seven potential CCCTC-binding factor (CTCF) binding sites. CTCF is a chromatin insulator and a multifunctional transcription factor whose binding to the H19-DMR is suppressed by DNA methylation. Our study included a group of 41 head and neck squamous cell carcinoma (HNSCC) samples. The imprinting status of the H19 gene was analyzed in 11 out of 35 positive cases for H19 gene expression, and only 1 of them showed loss of imprinting. We detected a significant correlation (P=0.041, Fisher's exact test) between H19 expression and tumor recurrence. Among H19 positive cases, six were T2, in which five developed recurrence and/or metastasis. Inversely, in the group of tumors that showed no H19 gene expression, 5 out of 24 were T2 and only I presented regional recurrence. These data support the hypothesis that H19 expression could be used as a prognostic marker to indicate recurrence in early stage tumors. We also examined the methylation of the CTCF binding site 1 in a subgroup of these samples. The H19 gene silencing and loss of imprinting were not correlated with the methylation pattern of the CTCF binding site 1. However, the significant correlation between H19 expression and tumor recurrence suggest that this transcript could be a marker for the progression of HNSCC. (c) 2005 Wiley-Liss, Inc.en
dc.description.affiliationSão Paulo State Univ, UNESP, Fac Med, Dept Urol,NeoGene Lab, BR-18618000 Botucatu, SP, Brazil
dc.description.affiliationSão Paulo State Univ, UNESP, Inst Biosci, Dept Genet, BR-18618000 Botucatu, SP, Brazil
dc.description.affiliationAmaral Carvalho Hosp, Dept Head & Neck Surg, Jau, SP, Brazil
dc.description.affiliationAC Camargo Hosp, Dept Head & Neck Surg & Otorhinolaryngol, São Paulo, Brazil
dc.description.affiliationUniv Toronto, Princess Margaret Hosp, Dept Lab Med & Pathobiol, Toronto, ON, Canada
dc.description.affiliationOntario Canc Inst, Toronto, ON M4X 1K9, Canada
dc.description.affiliationUnespSão Paulo State Univ, UNESP, Fac Med, Dept Urol,NeoGene Lab, BR-18618000 Botucatu, SP, Brazil
dc.description.affiliationUnespSão Paulo State Univ, UNESP, Inst Biosci, Dept Genet, BR-18618000 Botucatu, SP, Brazil
dc.format.extent102-110
dc.identifierhttp://dx.doi.org/10.1002/mc.20126
dc.identifier.citationMolecular Carcinogenesis. Hoboken: Wiley-liss, v. 44, n. 2, p. 102-110, 2005.
dc.identifier.doi10.1002/mc.20126
dc.identifier.issn0899-1987
dc.identifier.lattes8814823545159504
dc.identifier.lattes2259986546265579
dc.identifier.orcid0000-0002-0285-1162
dc.identifier.urihttp://hdl.handle.net/11449/13431
dc.identifier.wosWOS:000232075800004
dc.language.isoeng
dc.publisherWiley-Blackwell
dc.relation.ispartofMolecular Carcinogenesis
dc.relation.ispartofjcr3.851
dc.relation.ispartofsjr1,277
dc.rights.accessRightsAcesso restrito
dc.sourceWeb of Science
dc.subjectimprinted genept
dc.subjectdifferentially methylated regionpt
dc.subjecttumor suppressor genept
dc.subjecttumor progressionpt
dc.titleDNA methylation in the CTCF-binding site I and the expression pattern of the H19 gene: Does positive expression predict poor prognosis in early stage head and neck carcinomas?en
dc.typeArtigo
dcterms.licensehttp://olabout.wiley.com/WileyCDA/Section/id-406071.html
dcterms.rightsHolderWiley-Blackwell
dspace.entity.typePublication
unesp.author.lattes2259986546265579
unesp.author.lattes8814823545159504[7]
unesp.author.orcid0000-0001-5865-9308[6]
unesp.author.orcid0000-0002-9863-468X[5]
unesp.author.orcid0000-0002-0481-156X[6]
unesp.author.orcid0000-0002-0285-1162[7]
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Biociências, Botucatupt
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Medicina, Botucatupt
unesp.departmentUrologia - FMBpt
unesp.departmentGenética - IBBpt

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