Polymorphisms of the CYP1A1 and CYP2E1 genes in head and neck squamous cell carcinoma risk

Polymorphisms in genes that encode P450 cytochrome enzymes may increase carcinogen activation or decrease their inactivation and consequently, promote the development of cancer. The aims of this study were to identify the Msp I- CYP1A1 , Pst I- CYP2E1 and Dra I- CYP2E1 polymorphisms in patients with...

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Published in:Molecular biology reports Vol. 39; no. 2; pp. 1055 - 1063
Main Authors: Cury, Nathália Moreno, Russo, Anelise, Galbiatti, Ana Lívia Silva, Ruiz, Mariângela Torreglosa, Raposo, Luiz Sérgio, Maniglia, José Victor, Pavarino, Érika Cristina, Goloni-Bertollo, Eny Maria
Format: Journal Article
Language:English
Published: Dordrecht Springer Netherlands 01-02-2012
Springer Nature B.V
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Summary:Polymorphisms in genes that encode P450 cytochrome enzymes may increase carcinogen activation or decrease their inactivation and consequently, promote the development of cancer. The aims of this study were to identify the Msp I- CYP1A1 , Pst I- CYP2E1 and Dra I- CYP2E1 polymorphisms in patients with head and neck cancer and to compare with individuals without cancer; to evaluate the association of these polymorphisms with risk factors and clinical histopathological parameters. In the study group, 313 patients were evaluated for CYP1A1 , 217 for CYP2E1 ( Pst I) and 211 for CYP2E1 ( Dra I) and in the control group 417, 334 and 374 individuals, respectively . Molecular analysis was performed by PCR–RFLP technique, and chi-square and multiple logistic regression tests were used for statistical analysis. The result of analysis regarding individuals evaluated for CYP1A1 ( Msp I) showed that age (OR: 8.15; 95% CI 5.57–11.92) and smoking (OR: 5.37; 95% CI 3.52–8.21) were predictors for the disease; for the CYP2E1 ( Pst I and Dra I), there were associations with age ( Pst I-OR: 9.10; 95% CI 5.86–14.14/ Dra I-OR: 8.07; 95% CI 5.12–12.72), smoking ( Pst I-OR: 4.10; 95% CI 2.44–6.89/ Dra I-OR: 5.73; 95% CI 3.34–9.82), alcohol ( Pst I-OR: 1.93; 95% CI 1.18–3.16/ Dra I-OR: 1.69; 95% CI 1.02–2.81), respectively, with disease development. CYP2E1 ( Pst I) was less frequent in patient group (OR: 0.48; 95% CI 0.23–0.98). Regarding clinical histopathological parameters, CYP1A1 polymorphism was less frequent in the larynx primary anatomic site (OR = 0.45; 95% CI = 0.28–0.73; P  = 0.014). In conclusion, we confirm that age, smoking and alcohol consumption are risk factors for this disease and the polymorphisms investigated have no association with the development of head and neck cancer.
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ISSN:0301-4851
1573-4978
DOI:10.1007/s11033-011-0831-1