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Relationship among oxidative DNA damage, gastric mucosal density and the relevance of cagA, vacA and iceA genotypes of Helicobacter pylori

dc.contributor.authorLadeira, Marcelo S. P. [UNESP]
dc.contributor.authorBueno, Roberta C. A. [UNESP]
dc.contributor.authorDos Santos, Bruna Fornazari [UNESP]
dc.contributor.authorPinto, Carla L. S. [UNESP]
dc.contributor.authorPrado, Renato P. [UNESP]
dc.contributor.authorSilveira, Marcela G. [UNESP]
dc.contributor.authorRodrigues, Maria Aparecida Marchesan [UNESP]
dc.contributor.authorBartchewsky, Waldemar
dc.contributor.authorPedrazzoli, Jose
dc.contributor.authorRibeiro, Marcelo Lima
dc.contributor.authorSalvadori, Daisy Maria Favero [UNESP]
dc.contributor.institutionUniv Sao Francisco
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2014-05-20T13:33:17Z
dc.date.available2014-05-20T13:33:17Z
dc.date.issued2008-01-01
dc.description.abstractThe aim of this study was to evaluate the relationship among oxidative DNA damage, density of Helicobacter pylori and the relevance of cagA, vacA and iceA genotypes of H. pylori. Gastric epithelial cells were isolated from 24 uninfected patients, 42 H. pylori infected patients with gastritis, and 61 patients with gastric cancer. Oxidative DNA damage was analyzed by the Comet assay, the density of H. pylori was measured by real-time polymerase chain reaction (PCR), and allelic variants of cagA, vacA and iceA were identified using the PCR. Infected patients by Helicobacter pylori cagA(+), vacAs1 m1 and iceA1 genotype showed higher levels of oxidative DNA damage than infected patients with H. pylori cagA(-), vacAs2 m2 and iceA2 genotypes and uninfected patients. Density of H. pylori did not influence oxidative DNA damage. Our results indicate that H. pylori genotype is more relevant than density for oxidative DNA damage.en
dc.description.affiliationUniv Sao Francisco, Unid Integrad Farmacol & Gastroenterol, Braganca Paulista, SP, Brazil
dc.description.affiliationUNESP, Dept Clin Med, Lab Biol Mol Clin Med, Botucatu, SP, Brazil
dc.description.affiliationUNESP, Dept Patol, Lab Toxigenom & Epidemiol Mol, Botucatu, SP, Brazil
dc.description.affiliationUNESP, Fac Med, Dept Patol, Botucatu, SP, Brazil
dc.description.affiliationUnespUNESP, Dept Clin Med, Lab Biol Mol Clin Med, Botucatu, SP, Brazil
dc.description.affiliationUnespUNESP, Dept Patol, Lab Toxigenom & Epidemiol Mol, Botucatu, SP, Brazil
dc.description.affiliationUnespUNESP, Fac Med, Dept Patol, Botucatu, SP, Brazil
dc.format.extent248-255
dc.identifierhttp://dx.doi.org/10.1007/s10620-007-9850-0
dc.identifier.citationDigestive Diseases and Sciences. Dordrecht: Springer, v. 53, n. 1, p. 248-255, 2008.
dc.identifier.doi10.1007/s10620-007-9850-0
dc.identifier.issn0163-2116
dc.identifier.lattes5051118752980903
dc.identifier.urihttp://hdl.handle.net/11449/11381
dc.identifier.wosWOS:000251650300037
dc.language.isoeng
dc.publisherSpringer
dc.relation.ispartofDigestive Diseases and Sciences
dc.relation.ispartofjcr2.819
dc.relation.ispartofsjr1,330
dc.rights.accessRightsAcesso restrito
dc.sourceWeb of Science
dc.subjectoxidative DNA damageen
dc.subjectHelicobacter pylorien
dc.subjectreal-time PCRen
dc.subjectComet assayen
dc.subjectgastric canceren
dc.subjectinflammationen
dc.titleRelationship among oxidative DNA damage, gastric mucosal density and the relevance of cagA, vacA and iceA genotypes of Helicobacter pylorien
dc.typeArtigo
dcterms.licensehttp://www.springer.com/open+access/authors+rights?SGWID=0-176704-12-683201-0
dcterms.rightsHolderSpringer
dspace.entity.typePublication
unesp.author.lattes5051118752980903
unesp.author.orcid0000-0003-4529-7832[10]
unesp.author.orcid0000-0001-9323-3134[11]
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Medicina, Botucatupt
unesp.departmentClínica Médica - FMBpt
unesp.departmentPatologia - FMBpt

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