Polymorphisms of COMT and XPD and risk of esophageal squamous cell carcinoma in a population of Yili Prefecture, in Xinjiang, China

被引:10
|
作者
Huang, Cong-Gai [1 ]
Iv, Guo-dong [1 ]
Liu, Tao [1 ]
Liu, Qing [1 ]
Feng, Jun-guo [1 ]
Lu, Xiao-mei [1 ]
机构
[1] Xinjiang Med Univ, Affiliated Hosp 1, Med Res Ctr, Urumqi 830054, Xinjiang Uygur, Peoples R China
关键词
Esophageal squamous cell carcinoma; COMT gene; XPD gene; polymorphisms; CATECHOL-O-METHYLTRANSFERASE; NUCLEOTIDE EXCISION-REPAIR; DNA-REPAIR; CANCER-RISK; GENES; FREQUENCIES; VARIANTS; GENOTYPE;
D O I
10.3109/1354750X.2010.522732
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Objective: To investigate polymorphisms of COMT (Rs4680) and XPD (Rs13181) and risk of esophageal squamous cell carcinoma (ESCC) in a population from Yili Prefecture, Xinjiang, China. Methods: A hospital-based case-control study was designed. Genotypes were determined by polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP). Odds ratios (OR) and 95% confidence intervals (CI) were analysed using unconditional logistic regression. Results: An increased risk of ESCC was discovered with COMT in relation to the frequency of the presence of the A allele (Rs4680; OR 1.30, 95% CI 1.00-1.68). An individual with combined COMT 158 (Val/Met or Met/Met) and XPD 751 (Lys/Gln or Gln/Gln) genotype had an increased ESCC risk. Conclusions: Polymorphic variation in COMT Val158Met and XPD Lys751Gln may be important for ESCC susceptibility.
引用
收藏
页码:37 / 41
页数:5
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