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Article type: Research Article
Authors: Xia, Zongjianga | Duan, Fujiaob | Jing, Changc | Guo, Zhihuab | Nie, Changfud | Song, Chunhuae; *
Affiliations: [a] Department of Surgery Medicine, Division of Thoracic Surgery, The First Affiliated Hospital, Zhengzhou University, Zhengzhou, Henan, China | [b] Department of Hospital Infection Management, Affiliated Cancer Hospital of Zhengzhou University, Zhengzhou, Henan, China | [c] Department of Medical, Affiliated Cancer Hospital of Zhengzhou University, Henan Cancer Hospital, Zhengzhou, Henan, China | [d] Hepatobiliary and Pancreatic Surgery, Affiliated Cancer Hospital of Zhengzhou University, Henan Cancer Hospital, Zhengzhou, Henan, China | [e] Department of Epidemiology, College of Public Health, Zhengzhou University, Zhengzhou, Henan, China
Correspondence: [*] Corresponding author: Chunhua Song, Department of Epidemiology, College of Public Health, Zhengzhou University, Zhengzhou, Henan, China. E-mail:sch16@zzu.edu.cn
Abstract: BACKGROUND: DNA methyltransferase 3B (DNMT3B) has been discovered to play an important role in tumorigenesis. However, the association between DNMT3B-579G>T and the cancer risk has not been demonstrated. OBJECTIVE: The aim of this study is to provide a precise quantification for the association between DNMT3B-579G>T and the cancer susceptibility. METHODS: We performed a systematic literature review and assessed the methodological quality of included case-control designed studies based on Newcastle-Ottawa Scale (NOS). Pooled odds ratios (ORs) and corresponding 95% confidence intervals (95%CIs) were calculated to assess the strengths of the association. RESULTS: We identified 18 studies for pooled analyses. Overall, the results demonstrated that the DNMT3B-579G>T polymorphism was significantly associated with a subtly decreased cancer risk (GT vs TT: OR = 0.78, 95%CI: 0.70-0.87, P< 0.01; GT + GG vs TT: OR = 0.81, 95%CI: 0.68-0.97, P= 0.02), especially in the Asian population and in colorectal cancer subgroup. In addition, when stratified for source of controls, the results of population-based subgroup showed the GT genotype might have a significantly decreased cancer risk, but not hospital-based subgroups. CONCLUSIONS: DNMT3B-579G>T polymorphism might contribute to the susceptibility of cancers especially in the Asian population and for colorectal cancer.
Keywords: DNMT3B, polymorphism, cancer, quantitative assessment
DOI: 10.3233/CBM-150512
Journal: Cancer Biomarkers, vol. 15, no. 5, pp. 707-716, 2015
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