Genetic polymorphisms involved in the inflammatory response and lung cancer risk: A case-control study in Japan

被引:29
作者
Kiyohara, Chikako [1 ]
Horiuchi, Takahiko [2 ]
Takayama, Koichi [3 ]
Nakanishi, Yoichi [3 ]
机构
[1] Kyushu Univ, Grad Sch Med Sci, Dept Prevent Med, Higashi Ku, Fukuoka 8128582, Japan
[2] Kyushu Univ, Beppu Hosp, Dept Internal Med, Beppu, Oita 8740838, Japan
[3] Kyushu Univ, Grad Sch Med Sci, Chest Dis Res Inst, Higashi Ku, Fukuoka 8128582, Japan
关键词
Epidemiology; Genetic polymorphism; Inflammatory cytokine; Lung cancer; Smoking; C-REACTIVE PROTEIN; NECROSIS-FACTOR-ALPHA; ACUTE-PHASE RESPONSE; BREAST-CANCER; CYTOKINE RECEPTORS; CIRCULATING LEVELS; SERUM-LEVELS; TNF-ALPHA; INTERLEUKIN-6; MYELOPEROXIDASE;
D O I
10.1016/j.cyto.2013.09.015
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Evidence is accumulating that chronic inflammation may have an important mechanism for the development and progression of lung cancer. Therefore, genetic polymorphisms in genes that involved in the inflammatory response may be associated with lung cancer risk. We evaluated the role of tumor necrosis factor alpha (TNFA) rs1799724, interleukin 1 beta (IL1B) rs16944, IL6 rs1800796, myeloperoxidase (MPO) rs2333227 and C-reactive protein (CRP) rs2794520 in a case-control study comprised of 462 lung cancer cases and 379 controls in a Japanese population. Unconditional logistic regression was used to assess the adjusted odds ratios (OR) and 95% confidence intervals (95% CI). CRP rs2794520 (OR = 1.64, 95% CI = 1.19-2.26) and IL6 rs1800796 (OR=1.41,95% CI=1.02-1.96) were associated with lung cancer risk. In addition, we assessed interactions between the polymorphisms and smoking. The polymorphisms did not significantly modify the association between smoking and lung cancer. As TNFA triggers a cytokine cascade, the modifying effect of the TNFA rs1799724 genotypes on the association of any of the remaining polymorphisms with lung cancer risk was also examined. There was a significant interaction between TNFA rs1799724 and MPO rs2333227 (P-interaction = 0.058). Future studies involving larger control and case populations will undoubtedly lead to a more thorough understanding of the role of the polymorphisms involved in the inflammation pathway in lung cancer. (C) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:88 / 94
页数:7
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