Literature DB >> 24535266

The rs7003908 (T>G) polymorphism in the XRCC7 gene and the risk of cancers.

Min Xiao1, Yongchun Shen, Lei Chen, Zenglin Liao, Fuqiang Wen.   

Abstract

The association between the rs7003908 (T>G) polymorphism in the XRCC7 gene and the risk of cancers had been widely studied; however, the results were inconsistent. The objective of the current study was to investigate the association between the rs7003908 polymorphism in the XRCC7 gene and the risk of cancers by meta-analysis. We searched PubMed, EMbase, CNKI and Wanfang databases; the last search was performed on January 10th, 2014. Statistical analysis was performed using the Revman4.2 and STATA10.0 softwares. A total of 3,684 cancer cases and 5,232 controls from 11 case-control studies were included for data analysis. In the dominant model analysis, the results suggested a lack of association between the polymorphism and the risk of cancers: OR 1.01, 95% CI 0.83-1.16, P = 0.70. In the subgroup analysis by ethnicity, no significant association was found either for Asians or Caucasians. In the subgroup analysis by cancer types, significant association was found for prostate cancer, but not for bladder cancer, breast cancer and glioma. In summary, the current meta-analysis confirmed that the rs7003908 polymorphism in the XRCC7 gene might be a risk factor for prostate cancer. In the future, more studies are needed to validate these results.

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Year:  2014        PMID: 24535266     DOI: 10.1007/s11033-014-3220-8

Source DB:  PubMed          Journal:  Mol Biol Rep        ISSN: 0301-4851            Impact factor:   2.316


  21 in total

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Journal:  Int J Cancer       Date:  2008-01-01       Impact factor: 7.396

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Journal:  Nature       Date:  2013-12-04       Impact factor: 49.962

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Journal:  Exp Ther Med       Date:  2012-11-23       Impact factor: 2.447

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  1 in total

1.  DNA double-strand break repair gene XRCC7 genotypes were associated with hepatocellular carcinoma risk in Taiwanese males and alcohol drinkers.

Authors:  Yi-Hsien Hsieh; Wen-Shin Chang; Chia-Wen Tsai; Jen-Pi Tsai; Chin-Mu Hsu; Long-Bin Jeng; Da-Tian Bau
Journal:  Tumour Biol       Date:  2015-05-06
  1 in total

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