Polymorphisms of the TLR2 and TLR4 genes are associated with risk of gastric cancer in a Brazilian population
Autor(a) principal: | |
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Data de Publicação: | 2012 |
Outros Autores: | |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNESP |
Texto Completo: | http://dx.doi.org/10.3748/wjg.v18.i11.1235 http://hdl.handle.net/11449/21622 |
Resumo: | AIM: 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. |
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oai:repositorio.unesp.br:11449/21622 |
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Repositório Institucional da UNESP |
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2946 |
spelling |
Polymorphisms of the TLR2 and TLR4 genes are associated with risk of gastric cancer in a Brazilian populationPolymorphismToll-like receptor 2Toll-like receptor 4Gastric cancerGastritisAIM: 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.Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)UNESP São Paulo State Univ, Dept Biol, BR-15054000 São Paulo, SP, BrazilUNESP São Paulo State Univ, Dept Biol, BR-15054000 São Paulo, SP, BrazilFAPESP: 10/00507-0CNPq: 471908/2010-0Baishideng Publ Grp Co LtdUniversidade Estadual Paulista (Unesp)de Oliveira, Juliana Garcia [UNESP]Silva, Ana Elizabete [UNESP]2014-05-20T14:01:11Z2014-05-20T14:01:11Z2012-03-21info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article1235-1242http://dx.doi.org/10.3748/wjg.v18.i11.1235World Journal of Gastroenterology. Beijing: Baishideng Publ Grp Co Ltd, v. 18, n. 11, p. 1235-1242, 2012.1007-9327http://hdl.handle.net/11449/2162210.3748/wjg.v18.i11.1235WOS:000302190400012Web of Sciencereponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengWorld Journal of Gastroenterology3.3001,409info:eu-repo/semantics/openAccess2021-10-23T03:21:57Zoai:repositorio.unesp.br:11449/21622Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T21:06:45.901771Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
dc.title.none.fl_str_mv |
Polymorphisms of the TLR2 and TLR4 genes are associated with risk of gastric cancer in a Brazilian population |
title |
Polymorphisms of the TLR2 and TLR4 genes are associated with risk of gastric cancer in a Brazilian population |
spellingShingle |
Polymorphisms of the TLR2 and TLR4 genes are associated with risk of gastric cancer in a Brazilian population de Oliveira, Juliana Garcia [UNESP] Polymorphism Toll-like receptor 2 Toll-like receptor 4 Gastric cancer Gastritis |
title_short |
Polymorphisms of the TLR2 and TLR4 genes are associated with risk of gastric cancer in a Brazilian population |
title_full |
Polymorphisms of the TLR2 and TLR4 genes are associated with risk of gastric cancer in a Brazilian population |
title_fullStr |
Polymorphisms of the TLR2 and TLR4 genes are associated with risk of gastric cancer in a Brazilian population |
title_full_unstemmed |
Polymorphisms of the TLR2 and TLR4 genes are associated with risk of gastric cancer in a Brazilian population |
title_sort |
Polymorphisms of the TLR2 and TLR4 genes are associated with risk of gastric cancer in a Brazilian population |
author |
de Oliveira, Juliana Garcia [UNESP] |
author_facet |
de Oliveira, Juliana Garcia [UNESP] Silva, Ana Elizabete [UNESP] |
author_role |
author |
author2 |
Silva, Ana Elizabete [UNESP] |
author2_role |
author |
dc.contributor.none.fl_str_mv |
Universidade Estadual Paulista (Unesp) |
dc.contributor.author.fl_str_mv |
de Oliveira, Juliana Garcia [UNESP] Silva, Ana Elizabete [UNESP] |
dc.subject.por.fl_str_mv |
Polymorphism Toll-like receptor 2 Toll-like receptor 4 Gastric cancer Gastritis |
topic |
Polymorphism Toll-like receptor 2 Toll-like receptor 4 Gastric cancer Gastritis |
description |
AIM: 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. |
publishDate |
2012 |
dc.date.none.fl_str_mv |
2012-03-21 2014-05-20T14:01:11Z 2014-05-20T14:01:11Z |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://dx.doi.org/10.3748/wjg.v18.i11.1235 World Journal of Gastroenterology. Beijing: Baishideng Publ Grp Co Ltd, v. 18, n. 11, p. 1235-1242, 2012. 1007-9327 http://hdl.handle.net/11449/21622 10.3748/wjg.v18.i11.1235 WOS:000302190400012 |
url |
http://dx.doi.org/10.3748/wjg.v18.i11.1235 http://hdl.handle.net/11449/21622 |
identifier_str_mv |
World Journal of Gastroenterology. Beijing: Baishideng Publ Grp Co Ltd, v. 18, n. 11, p. 1235-1242, 2012. 1007-9327 10.3748/wjg.v18.i11.1235 WOS:000302190400012 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
World Journal of Gastroenterology 3.300 1,409 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
1235-1242 |
dc.publisher.none.fl_str_mv |
Baishideng Publ Grp Co Ltd |
publisher.none.fl_str_mv |
Baishideng Publ Grp Co Ltd |
dc.source.none.fl_str_mv |
Web of Science reponame:Repositório Institucional da UNESP instname:Universidade Estadual Paulista (UNESP) instacron:UNESP |
instname_str |
Universidade Estadual Paulista (UNESP) |
instacron_str |
UNESP |
institution |
UNESP |
reponame_str |
Repositório Institucional da UNESP |
collection |
Repositório Institucional da UNESP |
repository.name.fl_str_mv |
Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP) |
repository.mail.fl_str_mv |
|
_version_ |
1808129286035472384 |