Source:http://linkedlifedata.com/resource/pubmed/id/16702361
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
5
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pubmed:dateCreated |
2006-5-16
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pubmed:abstractText |
Nasopharyngeal carcinoma (NPC) is a common malignancy in southern China and Southeast Asia. Genetic susceptibility is a major factor in determining the individual risk of NPC in these areas. To test the association between NPC and variants in Toll-like receptor 10 (TLR10), we conducted a hospital-based case-control study in a Cantonese-speaking population in Guangdong province. Seven single nucleotide polymorphisms in TLR10, selected with a tagging algorithm, were genotyped. When assessing each unique haplotype compared with the most common haplotype, "GAGTGAA," with the expectation-maximization algorithm in Haplo.stats, the risk of developing NPC was significantly elevated among men who carried the haplotype "GCGTGGC" (P = 0.005). After adjusting for age, gender, and VCA-IgA antibody titers, this association was more significant (P = 0.0007). To further assess the overall differences of haplotype frequency profiles between cases and healthy controls, the global score test, considering all haplotypes and adjusting for age, gender, and VCA-IgA antibody titers, gave a haplo score of 27.52 with P = 0.002. The haplotype specific odds ratio was 2.66 (confidence interval, 1.34-3.82) for GCGTGGC. We concluded that in this Cantonese population-based study, haplotype GCGTGGC with frequency of 11.4% in TLR10 was found to be associated with NPC and this association was statistically significant after adjusting for age, gender, and VCA-IgA antibody titers. It is possible that this is not a causal haplotype for NPC; rather, it is in strong linkage disequilibrium with a causal single nucleotide polymorphism in close proximity.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
May
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pubmed:issn |
1055-9965
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
15
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
862-6
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pubmed:dateRevised |
2008-11-21
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pubmed:meshHeading |
pubmed-meshheading:16702361-Adult,
pubmed-meshheading:16702361-Algorithms,
pubmed-meshheading:16702361-Case-Control Studies,
pubmed-meshheading:16702361-Chi-Square Distribution,
pubmed-meshheading:16702361-China,
pubmed-meshheading:16702361-Genetic Predisposition to Disease,
pubmed-meshheading:16702361-Genetic Variation,
pubmed-meshheading:16702361-Genotype,
pubmed-meshheading:16702361-Haplotypes,
pubmed-meshheading:16702361-Humans,
pubmed-meshheading:16702361-Logistic Models,
pubmed-meshheading:16702361-Male,
pubmed-meshheading:16702361-Middle Aged,
pubmed-meshheading:16702361-Nasopharyngeal Neoplasms,
pubmed-meshheading:16702361-Polymorphism, Single Nucleotide,
pubmed-meshheading:16702361-Toll-Like Receptor 10
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pubmed:year |
2006
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pubmed:articleTitle |
Sequence variants in toll-like receptor 10 are associated with nasopharyngeal carcinoma risk.
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pubmed:affiliation |
Sun Yat-sen University, Cancer Center, 651 Dong-Feng Road East, 510060 Guangzhou, China.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't,
Research Support, N.I.H., Extramural
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