The rs5743836 polymorphism in TLR9 confers a population-based increased risk of non-Hodgkin lymphoma

Detalhes bibliográficos
Autor(a) principal: Carvalho, A
Data de Publicação: 2012
Outros Autores: Cunha, C, Almeida, AJ, Osório, NS, Saraiva, M, Teixeira-Coelho, M, Pedreiro, S, Torrado, E, Domingues, N, Gomes-Alves, AG, Marques, A, Silva MG, Lacerda, JF, Gomes, M, Pinto, AC, Torres, F, Rendeiro, P, Tavares, P, Di Ianni, M, Heutink, P, Bracci, PM, Conde, L, Ludovico, P, Pedrosa, J, Maciel, P, Pitzurra, L, Aversa, F, Marques, H, Paiva, A, Skibola, CF, Romani, L, Castro, AG, Rodrigues, F
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10400.23/565
Resumo: Non-Hodgkin lymphoma (NHL) has been associated with immunological defects, chronic inflammatory and autoimmune conditions. Given the link between immune dysfunction and NHL, genetic variants in toll-like receptors (TLRs) have been regarded as potential predictive factors of susceptibility to NHL. Adequate anti-tumoral responses are known to depend on TLR9 function, such that the use of its synthetic ligand is being targeted as a therapeutic strategy. We investigated the association between the functional rs5743836 polymorphism in the TLR9 promoter and risk for B-cell NHL and its major subtypes in three independent case-control association studies from Portugal (1160 controls, 797 patients), Italy (468 controls, 494 patients) and the US (972 controls, 868 patients). We found that the rs5743836 polymorphism was significantly overtransmitted in both Portuguese (odds ratio (OR), 1.85; P=7.3E-9) and Italian (OR, 1.84; P=6.0E-5) and not in the US cohort of NHL patients. Moreover, the increased transcriptional activity of TLR9 in mononuclear cells from patients harboring rs5743836 further supports a functional effect of this polymorphism on NHL susceptibility in a population-dependent manner.
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spelling The rs5743836 polymorphism in TLR9 confers a population-based increased risk of non-Hodgkin lymphomaLinfoma Não-HodgkinPolimorfismo GenéticoReceptor "Toll-Like" 9Non-Hodgkin lymphoma (NHL) has been associated with immunological defects, chronic inflammatory and autoimmune conditions. Given the link between immune dysfunction and NHL, genetic variants in toll-like receptors (TLRs) have been regarded as potential predictive factors of susceptibility to NHL. Adequate anti-tumoral responses are known to depend on TLR9 function, such that the use of its synthetic ligand is being targeted as a therapeutic strategy. We investigated the association between the functional rs5743836 polymorphism in the TLR9 promoter and risk for B-cell NHL and its major subtypes in three independent case-control association studies from Portugal (1160 controls, 797 patients), Italy (468 controls, 494 patients) and the US (972 controls, 868 patients). We found that the rs5743836 polymorphism was significantly overtransmitted in both Portuguese (odds ratio (OR), 1.85; P=7.3E-9) and Italian (OR, 1.84; P=6.0E-5) and not in the US cohort of NHL patients. Moreover, the increased transcriptional activity of TLR9 in mononuclear cells from patients harboring rs5743836 further supports a functional effect of this polymorphism on NHL susceptibility in a population-dependent manner.Nature Publishing GroupRepositório Científico do Hospital de BragaCarvalho, ACunha, CAlmeida, AJOsório, NSSaraiva, MTeixeira-Coelho, MPedreiro, STorrado, EDomingues, NGomes-Alves, AGMarques, ASilva MGLacerda, JFGomes, MPinto, ACTorres, FRendeiro, PTavares, PDi Ianni, MHeutink, PBracci, PMConde, LLudovico, PPedrosa, JMaciel, PPitzurra, LAversa, FMarques, HPaiva, ASkibola, CFRomani, LCastro, AGRodrigues, F2013-12-13T16:15:46Z2012-01-01T00:00:00Z2012-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10400.23/565engGenes Immun. 2012;13(2):197-201.info:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2022-09-21T09:02:15Zoai:repositorio.hospitaldebraga.pt:10400.23/565Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T15:55:12.961563Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv The rs5743836 polymorphism in TLR9 confers a population-based increased risk of non-Hodgkin lymphoma
title The rs5743836 polymorphism in TLR9 confers a population-based increased risk of non-Hodgkin lymphoma
spellingShingle The rs5743836 polymorphism in TLR9 confers a population-based increased risk of non-Hodgkin lymphoma
Carvalho, A
Linfoma Não-Hodgkin
Polimorfismo Genético
Receptor "Toll-Like" 9
title_short The rs5743836 polymorphism in TLR9 confers a population-based increased risk of non-Hodgkin lymphoma
title_full The rs5743836 polymorphism in TLR9 confers a population-based increased risk of non-Hodgkin lymphoma
title_fullStr The rs5743836 polymorphism in TLR9 confers a population-based increased risk of non-Hodgkin lymphoma
title_full_unstemmed The rs5743836 polymorphism in TLR9 confers a population-based increased risk of non-Hodgkin lymphoma
title_sort The rs5743836 polymorphism in TLR9 confers a population-based increased risk of non-Hodgkin lymphoma
author Carvalho, A
author_facet Carvalho, A
Cunha, C
Almeida, AJ
Osório, NS
Saraiva, M
Teixeira-Coelho, M
Pedreiro, S
Torrado, E
Domingues, N
Gomes-Alves, AG
Marques, A
Silva MG
Lacerda, JF
Gomes, M
Pinto, AC
Torres, F
Rendeiro, P
Tavares, P
Di Ianni, M
Heutink, P
Bracci, PM
Conde, L
Ludovico, P
Pedrosa, J
Maciel, P
Pitzurra, L
Aversa, F
Marques, H
Paiva, A
Skibola, CF
Romani, L
Castro, AG
Rodrigues, F
author_role author
author2 Cunha, C
Almeida, AJ
Osório, NS
Saraiva, M
Teixeira-Coelho, M
Pedreiro, S
Torrado, E
Domingues, N
Gomes-Alves, AG
Marques, A
Silva MG
Lacerda, JF
Gomes, M
Pinto, AC
Torres, F
Rendeiro, P
Tavares, P
Di Ianni, M
Heutink, P
Bracci, PM
Conde, L
Ludovico, P
Pedrosa, J
Maciel, P
Pitzurra, L
Aversa, F
Marques, H
Paiva, A
Skibola, CF
Romani, L
Castro, AG
Rodrigues, F
author2_role author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Repositório Científico do Hospital de Braga
dc.contributor.author.fl_str_mv Carvalho, A
Cunha, C
Almeida, AJ
Osório, NS
Saraiva, M
Teixeira-Coelho, M
Pedreiro, S
Torrado, E
Domingues, N
Gomes-Alves, AG
Marques, A
Silva MG
Lacerda, JF
Gomes, M
Pinto, AC
Torres, F
Rendeiro, P
Tavares, P
Di Ianni, M
Heutink, P
Bracci, PM
Conde, L
Ludovico, P
Pedrosa, J
Maciel, P
Pitzurra, L
Aversa, F
Marques, H
Paiva, A
Skibola, CF
Romani, L
Castro, AG
Rodrigues, F
dc.subject.por.fl_str_mv Linfoma Não-Hodgkin
Polimorfismo Genético
Receptor "Toll-Like" 9
topic Linfoma Não-Hodgkin
Polimorfismo Genético
Receptor "Toll-Like" 9
description Non-Hodgkin lymphoma (NHL) has been associated with immunological defects, chronic inflammatory and autoimmune conditions. Given the link between immune dysfunction and NHL, genetic variants in toll-like receptors (TLRs) have been regarded as potential predictive factors of susceptibility to NHL. Adequate anti-tumoral responses are known to depend on TLR9 function, such that the use of its synthetic ligand is being targeted as a therapeutic strategy. We investigated the association between the functional rs5743836 polymorphism in the TLR9 promoter and risk for B-cell NHL and its major subtypes in three independent case-control association studies from Portugal (1160 controls, 797 patients), Italy (468 controls, 494 patients) and the US (972 controls, 868 patients). We found that the rs5743836 polymorphism was significantly overtransmitted in both Portuguese (odds ratio (OR), 1.85; P=7.3E-9) and Italian (OR, 1.84; P=6.0E-5) and not in the US cohort of NHL patients. Moreover, the increased transcriptional activity of TLR9 in mononuclear cells from patients harboring rs5743836 further supports a functional effect of this polymorphism on NHL susceptibility in a population-dependent manner.
publishDate 2012
dc.date.none.fl_str_mv 2012-01-01T00:00:00Z
2012-01-01T00:00:00Z
2013-12-13T16:15:46Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
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status_str publishedVersion
dc.identifier.uri.fl_str_mv http://hdl.handle.net/10400.23/565
url http://hdl.handle.net/10400.23/565
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Genes Immun. 2012;13(2):197-201.
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dc.publisher.none.fl_str_mv Nature Publishing Group
publisher.none.fl_str_mv Nature Publishing Group
dc.source.none.fl_str_mv reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
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