Polymorphisms associated with the risk of lung cancer in a healthy Mexican Mestizo population: Application of the additive model for cancer

• Published in: Genetics and molecular biology 2011-01, Vol.34 (4), p.546-552
• Main Authors: Pérez-Morales, Rebeca, Méndez-Ramírez, Ignacio, Castro-Hernández, Clementina, Martínez-Ramírez, Ollin C, Gonsebatt, María Eugenia, Rubio, Julieta
• Format: Article
• Language: English
• Subjects: additive model; BIOCHEMISTRY & MOLECULAR BIOLOGY; genetic polymorphism; GENETICS & HEREDITY; Human and Medical Genetics; lung cancer; Mexicans; molecular epidemiology
• ISSN: 1415-4757; 1678-4685; 1678-4685
• DOI: 10.1590/S1415-47572011005000053

Lung cancer is the leading cause of cancer mortality in Mexico and worldwide. In the past decade, there has been an increase in the number of lung cancer cases in young people, which suggests an important role for genetic background in the etiology of this disease. In this study, we genetically characterized 16 polymorphisms in 12 low penetrance genes (AhR, CYP1A1, CYP2E1, EPHX1, GSTM1, GSTT1, GSTPI, XRCC1, ERCC2, MGMT, CCND1 and TP53) in 382 healthy Mexican Mestizos as the first step in elucidating the genetic structure of this population and identifying high risk individuals. All of the genotypes analyzed were in Hardy-Weinberg equilibrium, but different degrees of linkage were observed for polymorphisms in the CYP1A1 and EPHX1 genes. The genetic variability of this population was distributed in six clusters that were defined based on their genetic characteristics. The use of a polygenic model to assess the additive effect of low penetrance risk alleles identified combinations of risk genotypes that could be useful in predicting a predisposition to lung cancer. Estimation of the level of genetic susceptibility showed that the individual calculated risk value (iCRV) ranged from 1 to 16, with a higher iCRV indicating a greater genetic susceptibility to lung cancer.