- Volume 14 Issue 11
DOI QR Code
CYP1A1 Genetic Polymorphisms and Risk for Esophageal Cancer: a Case-control Study in Central China
- Yun, Yu-Xia (Department of Epidemiology and Biostatistics, College of Public Health) ;
- Wang, Yan-Ping (Department of Epidemiology and Biostatistics, College of Public Health) ;
- Wang, Peng (Department of Epidemiology and Biostatistics, College of Public Health) ;
- Cui, Li-Hong (Digestive System Department, PLA Navy General Hospital) ;
- Wang, Kai-Juan (Department of Epidemiology and Biostatistics, College of Public Health) ;
- Zhang, Jian-Ying (Department of Epidemiology and Biostatistics, College of Public Health) ;
- Dai, Li-Ping (Department of Epidemiology and Biostatistics, College of Public Health)
- Published : 2013.11.30
The purpose of this study was to evaluate the associations of CYP1A1 genetic polymorphisms with the risk of developing esophageal cancer (EC). A case-control study was carried out in a Chinese population in which 157 hospital based EC cases and 157 population based healthy controls with 1:1 match by age and sex were included. PCR based restriction fragment length polymorphisms (PCR-RFLP) were used to detect genotypes in case and control groups. For the CYP1A1 Ile/Val polymorphism, comparing with wild genotype Ile/Ile, both the heterozygote genotype Ile/Val and the combined variant genotype Ile/Val+Val/Val increased the risk of esophageal cancer (OR: 2.05, 95%CI: 1.19-3.54, OR: 1.86, 95%CI: 1.11-3.12). No significant association was found between the CYP1A1 MspI polymorphism and EC. According to analysis of combined genotypes, the TC/AG combined genotype which contained both variant alleles of these two polymorphisms increased the risk of developing EC (OR: 2.12, 95%CI: 1.16-3.85). Our results suggested that genetic polymorphisms of CYP1A1 may increase the susceptibility to EC.
Polymorphisms;CYP1A1;esophageal cancer;susceptibility;Central China
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