Literature DB >> 23052692

A two-SNP IL-6 promoter haplotype is associated with increased lung cancer risk.

Jun Chen1, Reng-Yun Liu, Lixin Yang, Jun Zhao, Xueying Zhao, Daru Lu, Nengjun Yi, Baohui Han, Xiao-Feng Chen, Kui Zhang, Jun He, Zhe Lei, Yifeng Zhou, Boris Pasche, Xiangdong Li, Hong-Tao Zhang.   

Abstract

BACKGROUND: Aberrant expression of interleukin-6 (IL-6) may play an important role in lung carcinogenesis. Whether IL-6 promoter haplotypes are associated with lung cancer risk and their functions have not yet been studied. We tested the hypothesis that single-nucleotide polymorphism (SNP) and/or haplotypes of IL-6 promoter are associated with risk of lung cancer.
METHODS: Two functional IL-6 promoter SNPs (-6331T>C and -572C>G) were genotyped in the discovery group including 622 patients and 614 controls, and the results were replicated in an independent validation group including 615 patients and 638 controls. Luciferase reporter gene assays were conducted to examine the function of IL-6 promoter haplotypes.
RESULTS: None of the functional IL-6 promoter SNPs were associated with lung cancer risk in either study. However, a two-SNP CC (-6331C and -572C) IL-6 promoter haplotype was significantly more common among cases than among controls in both groups (P = 0.031 and P = 0.035, respectively), indicating that this haplotype is associated with increased lung cancer risk {adjusted odds ratio [OR], 1.56 [95 % confidence interval (95 % CI), 1.04-2.34] and 1.51 [95 % CI, 1.03-2.22], respectively}. Combined analysis of both studies showed a strong association of this two-SNP haplotype with increased lung cancer risk (adjusted OR, 1.53; 95 % CI, 1.16-2.03; P = 0.003). Comparably, luciferase reporter assays of A549 lung cancer cell lines transfected with the CC haplotype revealed that the two-SNP haplotype had significantly higher IL-6 transcriptional activity compared with cells transfected with the common haplotype.
CONCLUSIONS: This is the first evidence of identifying an IL-6 promoter haplotype (CC) associated with increased risk of lung cancer.

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Year:  2012        PMID: 23052692      PMCID: PMC4535449          DOI: 10.1007/s00432-012-1314-z

Source DB:  PubMed          Journal:  J Cancer Res Clin Oncol        ISSN: 0171-5216            Impact factor:   4.553


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