Detalhes do Documento

The rs5743836 polymorphism in TLR9 confers a population-based increased risk of...

Autor(es): Carvalho, A cv logo 1 ; Cunha, C cv logo 2 ; Almeida, AJ cv logo 3 ; Osório, NS cv logo 4 ; Saraiva, M cv logo 5 ; Teixeira-Coelho, M cv logo 6 ; Pedreiro, S cv logo 7 ; Torrado, E cv logo 8 ; Domingues, N cv logo 9 ; Gomes-Alves, AG cv logo 10 ; Marques, A cv logo 11 ; Silva MG cv logo 12 ; Lacerda, JF cv logo 13 ; Gomes, M cv logo 14 ; Pinto, AC cv logo 15 ; Torres, F cv logo 16 ; Rendeiro, P cv logo 17 ; Tavares, P cv logo 18 ; Di Ianni, M cv logo 19 ; Heutink, P cv logo 20 ; Bracci, PM cv logo 21 ; Conde, L cv logo 22 ; Ludovico, P cv logo 23 ; Pedrosa, J cv logo 24 ; Maciel, P cv logo 25 ; Pitzurra, L cv logo 26 ; Aversa, F cv logo 27 ; Marques, H cv logo 28 ; Paiva, A cv logo 29 ; Skibola, CF cv logo 30 ; Romani, L cv logo 31 ; Castro, AG cv logo 32 ; Rodrigues, F cv logo 33

Data: 2012

Identificador Persistente: http://hdl.handle.net/10400.23/565

Origem: Repositório Científico do Hospital de Braga

Assunto(s): Linfoma Não-Hodgkin; Polimorfismo Genético; Receptor "Toll-Like" 9


Descrição
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.
Tipo de Documento Artigo
Idioma Inglês
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