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http://dx.doi.org/10.7314/APJCP.2015.16.16.6953

Influence of the CYP1A1 T3801C Polymorphism on Tobacco and Alcohol-Associated Head and Neck Cancer Susceptibility in Northeast India  

Singh, Seram Anil (Molecular Medicine Laboratory, Department of Biotechnology, Assam University)
Choudhury, Javed Hussain (Molecular Medicine Laboratory, Department of Biotechnology, Assam University)
Kapfo, Wetetsho (Molecular Medicine Laboratory, Department of Biotechnology, Assam University)
Kundu, Sharbadeb (Molecular Medicine Laboratory, Department of Biotechnology, Assam University)
Dhar, Bishal (Molecular Medicine Laboratory, Department of Biotechnology, Assam University)
Laskar, Shaheen (Molecular Medicine Laboratory, Department of Biotechnology, Assam University)
Das, Raima (Molecular Medicine Laboratory, Department of Biotechnology, Assam University)
Kumar, Manish (Molecular Medicine Laboratory, Department of Biotechnology, Assam University)
Ghosh, Sankar Kumar (Molecular Medicine Laboratory, Department of Biotechnology, Assam University)
Publication Information
Asian Pacific Journal of Cancer Prevention / v.16, no.16, 2015 , pp. 6953-6961 More about this Journal
Abstract
Background: Tobacco and alcohol contain or may generate carcinogenic compounds related to cancers. CYP1A1 enzymes act upon these carcinogens before elimination from the body. The aim of this study was to investigate whether CYP1A1 T3801C polymorphism modulates the relationship between tobacco and alcohol-associated head and neck cancer (HNC) susceptibility among the northeast Indian population. Materials and Methods: One hundred and seventy histologically confirmed HNC cases and 230 controls were included within the study. The CYP1A1 T3801C polymorphism was determined using PCR-RFLP, and the results were confirmed by DNA sequencing. Logistic regression (LR) and multifactor dimensionality reduction (MDR) approaches were applied for statistical analysis. Results: The CYP1A1 CC genotype was significantly associated with HNC risk (P=0.045). A significantly increased risk of HNC (OR=6.09; P<0.0001) was observed in individuals with combined habits of smoking, alcohol drinking and tobacco-betel quid chewing. Further, gene-environment interactions revealed enhanced risks of HNC among smokers, alcohol drinkers and tobacco-betel quid chewers carrying CYP1A1 TC or CC genotypes. The highest risk of HNC was observed among smokers (OR=7.55; P=0.009) and chewers (OR=10.8; P<0.0001) carrying the CYP1A1 CC genotype. In MDR analysis, the best model for HNC risk was the three-factor model combination of smoking, tobacco-betel quid chewing and the CYP1A1 variant genotype (CVC=99/100; TBA=0.605; P<0.0001); whereas interaction entropy graphs showed synergistic interaction between tobacco habits and CYP1A1. Conclusions: Our results confirm that the CYP1A1 T3801C polymorphism modifies the risk of HNC and further demonstrated importance of gene-environment interaction.
Keywords
Head and neck cancer; CYP1A1 T3801C polymorphism; tobacco; alcohol; northeast India;
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Times Cited By KSCI : 8  (Citation Analysis)
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