Lee Kyoung-Mu, Shen Min, Chapman Robert S, Yeager Meredith, Welch Robert, He Xingzhou, Zheng Tongzhang, Hosgood H Dean, Yang Dongyun, Berndt Sonja I, Chanock Stephen, Lan Qing
Division of Cancer Epidemiology and Genetics, National Cancer Institute, Bethesda, MD 20892-7240, USA.
Carcinogenesis. 2007 Jul;28(7):1437-41. doi: 10.1093/carcin/bgm030. Epub 2007 Mar 14.
We conducted a population-based case-control study in Xuan Wei, China, where lung cancer rates are among the highest in China due to exposure to indoor coal combustion products, to evaluate the association between polymorphisms in immunoregulatory genes and lung cancer risk. A total of 122 incident primary lung cancer cases and 122 individually matched controls were enrolled in Xuan Wei, China. Fifty single-nucleotide polymorphisms (SNPs) in 23 immunoregulatory genes involved in inflammation were genotyped and analyzed by logistic regression to assess the risk of lung cancer. A global test of association for 42 SNPs, which excluded eight SNPs that were in very tight linkage disequilibrium with other SNPs, was statistically significant (P = 0.01), suggesting that overall genetic variation in this pathway contributes to lung cancer risk. In addition, the IL1B -1060TT (i.e. -511TT) genotype was associated with increased lung cancer risk compared with the CC genotype [odds ratio (OR) = 2.27, 95% confidence interval (CI) = 1.05-4.91]. The IL8RA Ex2+860 GC or CC (OR = 0.27, 95% CI = 0.11-0.67), ICAM1 Ex2+100 AT or TT (OR = 0.39, 95% CI = 0.18-0.88) and IL12A Ex7+277 GA or AA (OR = 0.43, 95% CI = 0.22-0.84) genotypes were associated with decreased lung cancer risk. The protective effect of the IL8RA variant was stronger among subjects with high cumulative smoky coal use (> or = 130 tons) (OR = 0.11, 95% CI = 0.03-0.44; P(interaction) = 0.03). In conclusion, genetic variation in immunoregulatory genes may play an important role in the development of lung cancer in this population.
我们在中国宣威开展了一项基于人群的病例对照研究,该地由于接触室内燃煤产物,肺癌发病率位居中国前列,旨在评估免疫调节基因多态性与肺癌风险之间的关联。在中国宣威,共纳入了122例原发性肺癌新发病例以及122例个体匹配对照。对参与炎症反应的23个免疫调节基因中的50个单核苷酸多态性(SNP)进行基因分型,并通过逻辑回归分析来评估肺癌风险。对42个SNP进行的整体关联性检验具有统计学意义(P = 0.01),该检验排除了与其他SNP处于紧密连锁不平衡状态的8个SNP,这表明该通路中的整体基因变异会导致肺癌风险。此外,与CC基因型相比,IL1B -1060TT(即-511TT)基因型与肺癌风险增加相关[比值比(OR)= 2.27,95%置信区间(CI)= 1.05 - 4.91]。IL8RA Ex2+860 GC或CC(OR = 0.27,95% CI = 0.11 - 0.67)、ICAM1 Ex2+100 AT或TT(OR = 0.39,95% CI = 0.18 - 0.88)以及IL12A Ex7+277 GA或AA(OR = 0.43,95% CI = 0.22 - 0.84)基因型与肺癌风险降低相关。IL8RA变异体在累积使用高量烟煤(≥130吨)的受试者中具有更强的保护作用(OR = 0.11,95% CI = 0.03 - 0.44;P(交互作用)= 0.03)。总之,免疫调节基因的遗传变异可能在该人群肺癌的发生发展中起重要作用。