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Author Tengfei, Wang
Author Marei, Hany E.
Available date 2016-07-20T10:22:41Z
Publication Date 2016-02-01
Publication Name Biomedicine and Pharmacotherapyen_US
Identifier http://dx.doi.org/10.1016/j.biopha.2015.12.011en_US
ISSN 0753-3322
URI http://hdl.handle.net/10576/4682
Abstract PURPOSE: The prevalence of phenotypes of Arylamine N-acetyltransferase-2(NAT2) gene (i.e. fast, intermediate and slow acetylators) among ethnic groups, as well as the association studies regarding NAT2 polymorphisms and risk of breast cancer produced inconsistent results. This meta-analysis aimed to clarify whether the selected NAT2 phenotypes have an effect on the susceptibility to breast cancer. METHODS: After aggregating the frequencies of fast, intermediate and slow phenotypes of NAT2 in breast cancer subjects, the odds ratio and relevant 95% confidence intervals were examined using combined data from all published 36 articles. RESULTS: Overall, our results did not produce statistical significance for the proposed association, suggesting that there is no association between the selected phenotypes of NAT2 polymorphisms and breast cancer. In subgroup analyses, it was revealed that, as compared with the fast phenotype, intermediate acetylator is protective of the vulnerable White population to breast cancer. In addition, an obvious ethnic/geographic difference was found in the prevalence of fast, intermediate and slow acetylators among world-wide populations. CONCLUSIONS: Although ethnic and geographic differences in NAT2 polymorphisms were present, this was not associated with the risk of breast cancer in general. Intermediate acetylator is protective for particular ethnic groups, a finding which should be carefully viewed and confirmed in the future studies.en_US
Sponsor BRC, QUen_US
Language enen_US
Publisher Elsevier Massonen_US
Subject NAT2en_US
Subject Polymorphismen_US
Subject Frequencyen_US
Subject Breast canceren_US
Subject Ethnicen_US
Subject Geographic differenceen_US
Title Landscape of NAT2 polymorphisms among breast cancer.en_US
Type Articleen_US
Pagination 191-196
Volume Number 77


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