Association between the NBS1 Glu185Gln polymorphism and lung cancer risk: a systemic review and meta-analysis
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  • 作者:Lixin Wang (1)
    Jinsong Cheng (2)
    Jinyu Gao (3)
    Jipeng Wang (1)
    Xiaoning Liu (4)
    Liwen Xiong (5)
  • 关键词:NBS1 ; Lung cancer ; Polymorphism ; Meta ; analysis
  • 刊名:Molecular Biology Reports
  • 出版年:2013
  • 出版时间:March 2013
  • 年:2013
  • 卷:40
  • 期:3
  • 页码:2711-2715
  • 全文大小:206KB
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  • 作者单位:Lixin Wang (1)
    Jinsong Cheng (2)
    Jinyu Gao (3)
    Jipeng Wang (1)
    Xiaoning Liu (4)
    Liwen Xiong (5)

    1. Department of Respiratory Medicine, Huai’an First People’s Hospital, Nanjing Medical University, 6 Beijing Road West, Huai’an, 223300, Jiangsu, People’s Republic of China
    2. Department of Medical Oncology, Huai’an First People’s Hospital, Nanjing Medical University, 6 Beijing Road West, Huai’an, 223300, Jiangsu, People’s Republic of China
    3. Department of Gynecology and Obstetrics, Huai’an First People’s Hospital, Nanjing Medical University, 6 Beijing Road West, Huai’an, 223300, Jiangsu, People’s Republic of China
    4. Central Laboratory, Huai’an First People’s Hospital, Nanjing Medical University, 6 Beijing Road West, Huai’an, 223300, Jiangsu, People’s Republic of China
    5. Department of Pulmonary Diseases, Shanghai Chest Hospital, Shanghai Jiao Tong University, 241 Huaihai West Road, Shanghai, 200030, People’s Republic of China
  • ISSN:1573-4978
文摘
Nijmegen Breakage Syndrome protein 1 (NBS1) is one of the most important DNA repair proteins playing important roles in maintaining the genomic stability of NDA. Previous studies regarding the association between NBS1 8360G>C (Glu185Gln) polymorphism and lung cancer reported conflicting results. To derive a more precise estimation of this association, a systemic review and meta-analysis was performed. We performed a meta-analysis using eligible case–control studies to summarize the data on the association between the NBS1 Glu185Gln polymorphism and lung cancer risk. Odds ratios (ORs) with corresponding 95?% confidence intervals (95?%CIs) were pooled to assess the association between NBS1 Glu185Gln polymorphism and lung cancer risk. Six case–control studies with a total of 2,348 lung cancer cases and 2,401 controls without canner were included into the meta-analysis. Overall, there was an association between NBS1 Glu185Gln polymorphism and lung cancer risk under the dominant comparison model (fixed-effects OR GluGln/GlnGln vs. GluGlu ?=?1.21, 95?% CI 1.07-.37, P?=?0.002, I 2?=?8.1?%). Subgroup analysis by race suggested a significant association between NBS1 Glu185Gln polymorphism and lung cancer risk in Asians (fixed-effects OR GluGlnGlnGln vs. GluGlu ?=?1.22, 95?% CI 1.06-.41, P?=?0.005) but not in Caucasians (fixed-effects OR GluGlnGlnGln vs. GluGlu ?=?1.17, 95?% CI 0.91-.50, P?=?0.220). This meta-analysis supports that there is an association between NBS1 Glu185Gln polymorphism and lung cancer risk. More studies are needed to further verify this association.
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