Polymorphisms and haplotypes in TLR9 and MYD88 are associated with the development of Hodgkin's lymphoma: a candidate-gene association study.

Détails

ID Serval
serval:BIB_D5DD8D66EA43
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Titre
Polymorphisms and haplotypes in TLR9 and MYD88 are associated with the development of Hodgkin's lymphoma: a candidate-gene association study.
Périodique
Journal of human genetics
Auteur⸱e⸱s
Mollaki V., Georgiadis T., Tassidou A., Ioannou M., Daniil Z., Koutsokera A., Papathanassiou A.A., Zintzaras E., Vassilopoulos G.
ISSN
1435-232X (Electronic)
ISSN-L
1434-5161
Statut éditorial
Publié
Date de publication
11/2009
Peer-reviewed
Oui
Volume
54
Numéro
11
Pages
655-659
Langue
anglais
Notes
Publication types: Journal Article ; Research Support, Non-U.S. Gov't
Publication Status: ppublish
Résumé
Toll-like receptors (TLRs) and myeloid differentiation primary response protein 88 (MYD88) gene polymorphisms may be involved in the pathogenesis of Hodgkin's lymphoma (HL) through altered immunoregulatory and inflammatory responses. A candidate-gene association study was conducted to investigate the association between TLR9 -1237T>C, TLR9 2848A>G, MYD88 -938C>A and MYD88 1944C>G gene polymorphisms and the risk for HL. The impact of haplotypes was also examined. The study showed that carriership for -1237C and 2848A was associated with an increased risk for HL (odds ratio (OR)=2.53 (1.36-4.71) and OR=6.20 (1.3-28.8)). The MYD88 polymorphisms produced nonsignificant results. The estimated frequencies of the TLR9/1237C-2848A and MYD88/938C-1944G haplotypes were also significantly different between HL and controls (P<0.01). In addition, a significant difference between HL and controls was observed for the TLR9/1237C-TLR9/2848A-MYD88/938C-MYD88/1944C haplotypes (P<0.01). In conclusion, our study showed that TLR polymorphisms, and TLR9 and MYD88 haplotypes are related to the development of HL.
Mots-clé
Adult, Female, Gene Frequency, Genetic Association Studies, Genetic Predisposition to Disease, Genotype, Haplotypes, Hodgkin Disease/genetics, Humans, Linkage Disequilibrium, Male, Middle Aged, Myeloid Differentiation Factor 88/genetics, Odds Ratio, Polymorphism, Single Nucleotide, Toll-Like Receptor 9/genetics, Young Adult
Pubmed
Web of science
Open Access
Oui
Création de la notice
19/07/2019 19:41
Dernière modification de la notice
21/08/2019 6:32
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