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Association between microsomal epoxide hydrolase 1 T113C polymorphism and susceptibility to lung cancer
Authors:Siwen Wang  Jie Zhu  Ruxin Zhang  Siyang Wang  Zongheng Gu
Affiliation:1. Department of Emergency, the Fourth Affiliated Hospital of China Medical University, No. 102 Nan Qi Road, Heping District, Shenyang City, 110005, Liaoning Province, People’s Republic of China
2. Department of Infectious Diseases, the First Affiliated Hospital, China Medical University, Shenyang, 110001, China
Abstract:Previous case–control studies assessing the association between microsomal epoxide hydrolase 1 (EPHX1) T113C and susceptibility to lung cancer reported conflicting results. Thus, a systemic review and meta-analysis of published studies were performed to assess the possible association. PubMed and Embase databases were searched for all eligible studies. The strength of the association between EPHX1 T113C polymorphism and lung cancer risk was estimated by the pooled odds ratios (ORs) with its 95 % confidence interval. Twenty-four individual case–control studies involving a total of 4,970 lung cancer cases and 8,917 controls were finally included into the meta-analysis. When all 24 studies were included into the meta-analysis, the pooled results suggested that there was no association between EPHX1 T113C polymorphism and lung cancer risk under all four comparison models, and all P values for the pooled ORs were more than 0.05. In the subgroup analysis of Caucasians, the pooled results suggested that EPHX1 T113C polymorphism was associated with decreased risk of lung cancer under all four comparison models, and all P values for the pooled ORs were less than 0.05. However, in the subgroup analysis of Asians, the pooled results suggested that EPHX1 T113C polymorphism was associated with increased risk of lung cancer under three comparison models, and all P values for the pooled ORs were less than 0.05. There was no risk of publication bias. This current meta-analysis suggests that EPHX1 T113C polymorphism is associated with lung cancer risk, and there is an obvious race-specific effect in the association.
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