| Literature DB >> 20061363 |
Takashi Kohno1, Hideo Kunitoh, Yoko Shimada, Kouya Shiraishi, Yuko Ishii, Koichi Goto, Yuichiro Ohe, Yutaka Nishiwaki, Aya Kuchiba, Seiichiro Yamamoto, Hiroshi Hirose, Akira Oka, Noriko Yanagitani, Ryusei Saito, Hidetoshi Inoko, Jun Yokota.
Abstract
Adenocarcinoma (ADC) is the commonest histological type of lung cancer, and its weak association with smoking indicates the necessity to identify high-risk individuals for targeted screening and/or prevention. By a genome-wide association study (GWAS), we identified an association of polymorphisms in the 6p21.31 locus containing four human leukocyte antigen (HLA) class II genes with lung ADC risk. DQA1*03 of the HLA-DQA1 gene was defined as a risk allele with odds ratio (OR) of 1.36 [95% confidence interval (CI) = 1.21-1.54, P = 5.3 x 10(-7)] by analysis of 1656 ADC cases and 1173 controls. DQA1*03 and the minor allele for a polymorphism, rs2736100, in TERT, another lung cancer susceptibility locus identified in recent GWASs on Europeans and Americans, were indicated to independently contribute to ADC risk with per allele OR of 1.43 (95% CI = 1.31-1.56, P = 7.8 x 10(-16)). Individuals homozygous both for the DQA1*03 and minor TERT alleles were defined as high-risk individuals with an OR of 4.76 (95% CI = 2.53-9.47, P = 4.2 x 10(-7)). The present results indicated that individuals susceptible to lung ADC can be defined by combined genotypes of HLA-DQA1 and TERT.Entities:
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Year: 2010 PMID: 20061363 DOI: 10.1093/carcin/bgq003
Source DB: PubMed Journal: Carcinogenesis ISSN: 0143-3334 Impact factor: 4.944