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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/37555
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dc.contributor.authorDuarte, Marcia Cristina-
dc.contributor.authorColombo, Jucimara-
dc.contributor.authorBaptista Rossit, Andrea Regina-
dc.contributor.authorCaetano, Alaor-
dc.contributor.authorBorim, Aldenis Albaneze-
dc.contributor.authorWornrath, Durval-
dc.contributor.authorSilva, Ana Elizabete-
dc.date.accessioned2014-05-20T15:27:36Z-
dc.date.accessioned2016-10-25T18:02:28Z-
dc.date.available2014-05-20T15:27:36Z-
dc.date.available2016-10-25T18:02:28Z-
dc.date.issued2005-11-14-
dc.identifierhttp://www.wjgnet.com/1007-9327/full/v11/i42/6593.htm-
dc.identifier.citationWorld Journal of Gastroenterology. Beijing: Baishideng Publ Grp Co Ltd, v. 11, n. 42, p. 6593-6600, 2005.-
dc.identifier.issn1007-9327-
dc.identifier.urihttp://hdl.handle.net/11449/37555-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/37555-
dc.description.abstractAIM: To evaluate the association between polymorphisms XRCC1 Arg194Trp and Arg399Gln and XRCC3 Thr241Met and the risk for chronic gastritis and gastric cancer, in a Southeastern Brazilian population.METHODS: Genotyping by PCR-RFLP was carried out on 202 patients with chronic gastritis (CG) and 160 patients with gastric cancer (GC), matched to 202 (C1) and 150 (C2) controls, respectively.RESULTS: No differences were observed among the studied groups with regard to the genotype distribution of XRCC1 codons 194 and 399 and of XRCC3 codon 241. However, the combined analyses of the three variant alleles (194Trp, 399Gln and 241Met) showed an increased risk for chronic gastritis when compared to the GC group. Moreover, an interaction between the polymorphic alleles and demographic and environmental factors was observed in the CG and GC groups. XRCC1 194Trp was associated with smoking in the CG group, while the variant alleles XRCC1 399Gln and XRCC3 241Met were related with gender, smoking, drinking and H pylori infection in the CG and GC groups.CONCLUSION: Our results showed no evidence of a rela-tionship between the polymorphisms XRCC1 Arg194Trp and Arg399Gln and XRCC3 Thr241Met and the risk of chronic gastritis and gastric cancer in the Brazilian population, but the combined effect of these variants may interact to increase the risk for chronic gastritis, considered a premalignant lesion. Our data also indicate a gene-environment interaction in the susceptibility to chronic gastritis and gastric cancer. (C) 2005 the WJG Press and Elsevier B.V. All rights reserved.en
dc.description.sponsorshipCoordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)-
dc.format.extent6593-6600-
dc.language.isoeng-
dc.publisherBaishideng Publ Grp Co Ltd-
dc.sourceWeb of Science-
dc.subjectGastric cancerpt
dc.subjectGastritispt
dc.subjectXRCC1pt
dc.subjectXRCC3pt
dc.subjectPolymorphismpt
dc.subjectEnvironmental exposurept
dc.titlePolymorphisms of DNA repair genes XRCC1 and XRCC3, interaction with environmental exposure and risk of chronic gastritis and gastric canceren
dc.typeoutro-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.contributor.institutionUniversidade de São Paulo (USP)-
dc.contributor.institutionPio XII Fdn-
dc.description.affiliationUNESP São Paulo State Univ, Dept Biol, Campus Sao Jose Rio Pret, SP, Brazil-
dc.description.affiliationFAMERP Sao Jose do Rio Preto Sch Med, Microorganism Invest Ctr, Sao Jose do Rio Preto, SP, Brazil-
dc.description.affiliationHosp Base, FAMERP Sao Jose do Rio Preto Sch Med, Sao Jose do Rio Preto, SP, Brazil-
dc.description.affiliationPio XII Fdn, Barretos, SP, Brazil-
dc.description.affiliationUnespUNESP São Paulo State Univ, Dept Biol, Campus Sao Jose Rio Pret, SP, Brazil-
dc.identifier.wosWOS:000208224700005-
dc.rights.accessRightsAcesso aberto-
dc.relation.ispartofWorld Journal of Gastroenterology-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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