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DOI 10.1007/s13277-013-1380-0

Медицинская библиотека · Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2014

A pooled analysis of the ERCC2 Asp312Asn polymorphism and esophageal cancer susceptibility.

Wen Fang, Zhao Zhiyong, Liu Chuan, Yin Qinghua, Weng Jie, Wang Yajie, Ma Yuchen

СтатьяМетаанализПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

Published data regarding the association between the excision repair cross-complimentary group 2 (ERCC2) Asp312Asn polymorphisms and esophageal cancer susceptibility remained controversial. This meta-analysis of literatures was performed to assess the strength of association between the ERCC2 and esophageal cancer susceptibility using random effects model. We systematically searched PubMed, Embase and Web of Science with a time limit of September 15, 2013. Summary odds ratios (ORs) with 95 % confidence intervals (CIs) were used to assess the strength of association between the ERCC2 Asp312Asn polymorphism and esophageal cancer susceptibility using random effects model. A total of seven case-control studies including 1,831 cases and 2,728 controls were included for analysis. Overall, a significant association was found between ERCC2 Asp312Asn polymorphism and esophageal cancer susceptibility for GA vs. GG (OR = 1.20, 95 % CI = 1.03-1.40) and for the dominant model GA/AA vs. GG (OR = 1.18, 95 % CI = 1.03-1.35). However, the ERCC2 Asp312Asn polymorphism was a protective factor for AA vs. GA/GG (OR = 0.63, 95 % CI = 1.15-2.65) in esophageal squamous cell carcinoma. Our meta-analysis suggested that the ERCC2 Asp312Asn polymorphism might be associated with increased risk of esophageal adenocarcinoma and a protective factor for esophageal squamous cell carcinoma.

Для цитирования: Wen Fang, Zhao Zhiyong, Liu Chuan, Yin Qinghua, Weng Jie, Wang Yajie, Ma Yuchen. A pooled analysis of the ERCC2 Asp312Asn polymorphism and esophageal cancer susceptibility.. Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine. 2014. DOI: 10.1007/s13277-013-1380-0.

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