Τετάρτη 16 Μαΐου 2018

Predictive value of excision repair cross-complementing group 2 gene Lys751Gln and Asp312Asn polymorphisms in melanoma risk

Epidemiological studies have assessed the association between excision repair cross-complementing group 2 (ERCC2) Lys751Gln and Asp312Asn polymorphisms and melanoma risk with conflicting results. Relevant articles were searched from PubMed, Embase, and Web of Science with a time limit of 3 September 2016. Pooled odds ratio (OR) with 95% confidence interval (CI) was used to assess the strength of the association. We performed this meta-analysis with 12 studies including 6157 cases and 8873 controls for Lys751Gln and nine studies including 5037 cases and 7542 controls for Asp312Asn polymorphism. Overall, no significant associations were found under all the models for Lys751Gln polymorphism, and significant associations were found for Asp312Asn polymorphism for AA versus GG (OR=1.12, 95% CI=1.00–1.26) and for the recessive model (OR=1.11, 95% CI=1.00–1.24). In the stratification analyses by source of control: for Lys751Gln polymorphism, significant associations were found for CC versus AA (OR=1.19, 95% CI=1.04–1.36) and the recessive model (OR=1.15, 95% CI=1.02–1.30); for Asp312Asn polymorphism, significant associations were found for AA versus GG (OR=1.31, 95% CI=1.11–1.53) and the recessive model (OR=1.29, 95% CI=1.11–1.50). This meta-analysis suggested that both the Lys751Gln and Asp312Asn polymorphisms were risk factors for melanoma risk in population-based subgroup. * Xue Zhou and Yong Zeng contributed equally to the writing of this article. Correspondence to Limei Xia, MSc, Department of Gynaecology, The Fourth People's Hospital of Shanghai, Shanghai 200081, China Tel: +86 215 666 3031; e-mail: limeixiadoc@163.com or Correspondence to Chuan Liu, MD, Department of Oncology, Shanghai General Hospital, 100 Haining Road, Shanghai 200080, China Tel: +86 216 324 0090; e-mail: chuanliu2005@163.com Received October 26, 2016 Accepted April 21, 2018 Copyright © 2018 Wolters Kluwer Health, Inc. All rights reserved.

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