You are in the accessibility menu

Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/21622
Full metadata record
DC FieldValueLanguage
dc.contributor.authorde Oliveira, Juliana Garcia-
dc.contributor.authorSilva, Ana Elizabete-
dc.date.accessioned2014-05-20T14:01:11Z-
dc.date.accessioned2016-10-25T17:08:29Z-
dc.date.available2014-05-20T14:01:11Z-
dc.date.available2016-10-25T17:08:29Z-
dc.date.issued2012-03-21-
dc.identifierhttp://dx.doi.org/10.3748/wjg.v18.i11.1235-
dc.identifier.citationWorld Journal of Gastroenterology. Beijing: Baishideng Publ Grp Co Ltd, v. 18, n. 11, p. 1235-1242, 2012.-
dc.identifier.issn1007-9327-
dc.identifier.urihttp://hdl.handle.net/11449/21622-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/21622-
dc.description.abstractAIM: To investigate toll-like receptor 2 (TLR2) -196 to -174 del, and TLR4 (+896A/G rs4986790 and +1196C/T rs4986791) polymorphisms at risk of chronic gastritis and gastric cancer in a Brazilian population and association of gastric lesions with risk factors such as smoking, alcohol intake and Helicobacter pylori infection.METHODS: In this case-control study, polymorphism at TLR2 496 to -174 del was investigated by using the polymerase chain reaction (PCR) method, while the PCR-restriction fragment length polymorphism technique was carried out to identify the TLR4 (rs4986790 and rs4986791) genotypes in 607 Brazilian individuals (208 with chronic gastritis-CG, 174 with gastric cancer-GC and 225 controls -C).RESULTS: The single nucleotide polymorphisms TLR4+1196C/T was not associated with risk of chronic gastritis or gastric cancer and the homozygous genotypes TLR4+896GG and TLR4+1196TT were absent in the studied population. However, the frequency of TLR2 -196 to -174 ins/del + del/del and TLR4+896AG genotypes was significantly higher (P < 0.01 and P = 0.01, respectively) in the cancer group (33.4% and 11.5%, respectively) than in the control group (16.9% and 4.5%, respectively). It was also observed that the G-C haplotype of the TLR4+896A/G+1196C/T (P = 0.02) and the combination of variant alleles of the TLR2/TLR4+896G (P = 0.02) are associated with susceptibility to gastric cancer. In addition, the multiple logistic regression showed that male gender [odds ratio (OR) = 2.70; 95% CI: 1.66-4.41; P < 0.01], alcohol intake (OR = 2.93; 95% CI: 1.76-4.87; P < 0.01), TLR2 -196 to -174 del (OR = 2.64; 95% CI: 1.56-4.44; P < 0.01) and TLR4+896G (OR = 3.19; 95% CI: 1.34-7.61; P < 0.01) polymorphisms were associated with a higher susceptibility to developing this neoplasm.CONCLUSION: Our data indicate that TLR2 -196 to -174 del and TLR4+896G may increase the risk of gastric cancer in a Brazilian population. (C) 2012 Baishideng. All rights reserved.en
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)-
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)-
dc.format.extent1235-1242-
dc.language.isoeng-
dc.publisherBaishideng Publ Grp Co Ltd-
dc.sourceWeb of Science-
dc.subjectPolymorphismen
dc.subjectToll-like receptor 2en
dc.subjectToll-like receptor 4en
dc.subjectGastric canceren
dc.subjectGastritisen
dc.titlePolymorphisms of the TLR2 and TLR4 genes are associated with risk of gastric cancer in a Brazilian populationen
dc.typeoutro-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.description.affiliationUNESP São Paulo State Univ, Dept Biol, BR-15054000 São Paulo, SP, Brazil-
dc.description.affiliationUnespUNESP São Paulo State Univ, Dept Biol, BR-15054000 São Paulo, SP, Brazil-
dc.description.sponsorshipIdFAPESP: 10/00507-0-
dc.description.sponsorshipIdCNPq: 471908/2010-0-
dc.identifier.doi10.3748/wjg.v18.i11.1235-
dc.identifier.wosWOS:000302190400012-
dc.rights.accessRightsAcesso aberto-
dc.relation.ispartofWorld Journal of Gastroenterology-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

There are no files associated with this item.
 

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.