COX-2 polymorphisms-765G→C and-1195A→G and hepatocellular carcinoma risk

被引:15
作者
Gharib, Arnl F. [1 ]
Karam, Rehab A. [1 ,2 ]
Abd El Rahman, Tamer M. [3 ,4 ]
Elsawy, Wael H. [5 ]
机构
[1] Zagazig Univ, Fac Med, Dept Biochem, Zagazig, Egypt
[2] Taif Univ, Fac Med, Dept Biochem, Al Taif, Saudi Arabia
[3] Taif Univ, Fac Med, Dept Surg, Al Taif, Saudi Arabia
[4] Benha Teaching Hosp, Dept Surg, Banha, Egypt
[5] Zagazig Univ, Fac Med, Dept Oncol, Zagazig, Egypt
关键词
Cyclooxygenase-2; gene; Single nucleotide polymorphisms; Hepatocellular carcinoma; SQUAMOUS-CELL CARCINOMA; CYCLOOXYGENASE-2; EXPRESSION; FUNCTIONAL POLYMORPHISMS; CHINESE POPULATION; GENETIC-VARIANTS; CANCER; DISEASE; ASSOCIATION; INFECTION; INDIA;
D O I
10.1016/j.gene.2014.04.014
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Cyclooxygenase-2 (COX-2) is overexpressed in hepatocellular carcinoma (HCC) and considered to play a role in hepatic carcinogenesis. Our aim was to examine the associations between polymorphisms in COX-2 - 765G -> C and - 1195A -> G and risk of HCC. We conducted a case-control study including 120 patients with HCC and 130 age- and gender-matched controls. Genotypes of the COX-2 polymorphisms - 765G -> C and - 1195A -> G were determined by polymerase chain reaction-based restriction fragment length polymorphism. No significant difference was observed in the genotype distribution of the - 765G -> C polymorphism between patients and controls. The - 1195AA genotype was associated with an increased risk of developing HCC (OR, 2.5; 95%CI, 1.18-537). The A allele was present significantly more often in HCC patients (OR 1.5; 95%CI, 1.05-2.14). In conclusion, our results demonstrated that the - 1195AA genotype and A allele have an important role in HCC risk in Egyptian patients. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:234 / 236
页数:3
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