Abstract
Lung cancer (LCa) is the leading cause of death by cancer in men. Genetic and environmental factors play a synergistic role in its etiology. We explore in 111 lung cancer cases and 133 unrelated noncancer controls the gene-environment interaction (G × E) between p53cd72 polymorphism variants and smoking and the effect on LCa risk in two kinds of case-control designs. We assessed the interaction odds ratio (IOR) using an adjusted unconditional logistic model. We found a significant and positive interaction association between Pro* allele carriers and smoking habits in both case-control and case-only designs: IOR = 3.90 (95% confidence interval [CI] = 1.10–13.81) and 3.05 (95% CI = 1.63–5.72), respectively. These exploratory results suggest a synergistic effect of the smoking habit and the susceptibility of the Pro allele on lung cancer risk compared with each risk factor alone.
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Acknowledgments
The National Fund of Scientific Development and Technology (FONDECYT) (Grant No. 2990019) supported this work. Dr. Dante Cáceres thanks Dr. Nevin Schrimshaw and the Ellison Medical Foundation-International Nutrition Foundation.
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Cáceres, D.D., Quiñones, L.A., Schroeder, J.C. et al. Association Between p53 codon 72 Genetic Polymorphism and Tobacco Use and Lung Cancer Risk. Lung 187, 110–115 (2009). https://doi.org/10.1007/s00408-008-9133-3
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DOI: https://doi.org/10.1007/s00408-008-9133-3