Apoptosis gene polymorphisms, age, smoking and the risk of non-small cell lung cancer

被引:47
|
作者
Ter-Minassian, Monica [1 ]
Zhai, Rihong [1 ]
Asomaning, Kofi [1 ]
Su, Li [1 ]
Zhou, Wei [1 ]
Liu, Geoffrey [4 ,7 ]
Heist, Rebecca Suk [1 ,4 ]
Lynch, Thomas J. [3 ]
Wain, John C. [2 ]
Lin, Xihong [5 ]
DeVivo, Immaculata [6 ]
Christiani, David C. [1 ,3 ,6 ]
机构
[1] Harvard Univ, Sch Publ Hlth, Dept Environm Hlth, Boston, MA 02115 USA
[2] Harvard Univ, Massachusetts Gen Hosp, Sch Med, Thorac Surg Unit,Dept Med, Boston, MA 02114 USA
[3] Harvard Univ, Massachusetts Gen Hosp, Sch Med, Pulm & Crit Care Unit, Boston, MA 02114 USA
[4] Harvard Univ, Massachusetts Gen Hosp, Sch Med, Massachusetts Gen Hosp Canc Ctr, Boston, MA 02114 USA
[5] Harvard Univ, Sch Publ Hlth, Dept Biostat, Boston, MA 02115 USA
[6] Harvard Univ, Sch Publ Hlth, Dept Epidemiol, Boston, MA 02115 USA
[7] Princess Margaret Hosp, Ontario Canc Inst, Appl Mol Oncol & Dept Med Oncol, Toronto, ON M5G 2M9, Canada
基金
美国国家卫生研究院;
关键词
D O I
10.1093/carcin/bgn205
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Apoptosis is important for targeting cancer cells for destruction. Various single-nucleotide polymorphisms (SNPs) in apoptotic genes have been associated with increased risks in lung cancer, particularly FAS -1377 G > A (rs2234767), FASLG -844 C > T (rs763110), IL1B +3954 C > T Phe105Phe (rs1143634) and BAT3 Ser625Pro (rs1052486). We studied the association of these SNPs with non-small cell lung cancer (NSCLC) in a large case-control study (N = 4263: 2644 cases and 1619 controls). No associations with NSCLC were observed in the main effects analysis for all four SNPs, adjusting for age, gender, smoking status, pack-years and years since smoking cessation. In subjects under age 60, for FASLG -844 C > T polymorphism, CT compared with the CC genotype, was significantly associated with increased risk of NSCLC, adjusted odds ratio (aOR) = 1.58 (1.22, 2.05), P = 0.0006 and TT aOR = 1.45 (1.01, 2.04), P = 0.04. In contrast, for those over age 60, the CT aOR = 0.91 (0.73, 1.13), P = 0.37 and TT aOR = 0.86 (0.64, 1.16), P = 0.32. The P-value for the age-genotype interaction was 0.004. For the IL1B +3954 C > T polymorphism, compared with the CC genotype, TT showed significant associations in former smokers and in men but tests of interaction were not significant (P-smoking = 0.24, P-gender = 0.17). No interactions were observed for FAS -1377 G > A and BAT3 Ser625Pro polymorphisms. Our findings indicate that age and smoking may modify the association of the FASLG -844 and IL1B + 3954 SNPs with the risk of NSCLC.
引用
收藏
页码:2147 / 2152
页数:6
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