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Methionine synthase A2756G polymorphism and breast cancer risk: An up-to-date meta-analysis
Authors:Shanliang Zhong  Jinjin Xu  Wenjing Li  Zhiyuan Chen  Tengfei Ma  Jianhua Zhao
Affiliation:1. Center of Clinical Laboratory Science, Jiangsu Cancer Hospital, Nanjing Medical University Affiliated Cancer Hospital, Nanjing 210009, China;2. Department of Clinical Laboratory, Suzhou Municipal Hospital, Suzhou 215002, China;3. Teaching and Research Office of General Surgery, Xuzhou Medical College, Xuzhou 221004, China
Abstract:The methionine synthase (MTR) gene polymorphism A2756G has been linked to the risk of developing breast cancer, but the available results were inconsistent and underpowered. To derive a more precise estimation of the association between A2756G and breast cancer risk, an updated meta-analysis of 16 available studies with 9866 cases and 11,702 controls estimating the association between MTR A2756G and breast cancer risk was conducted. The quality of these studies was generally good except 2 studies with a lowest score 4 according to the Newcastle–Ottawa Scale (NOS). The results suggested that there is no significant association between A2756G and breast cancer risk in overall results. In the stratified analysis by ethnicity, source of controls (population or hospital-based), Hardy–Weinberg equilibrium (HWE) in controls, sample size (≥ 1000 and < 1000 subjects), and menopausal status, the 2756G allele was associated with a decreased risk in Caucasians, PB (population-based) subgroup, and large studies. But the associations disappeared after removing the studies not in HWE. On the contrary, an increased risk was found in small studies. In conclusion, the findings suggest that MTR A2756G polymorphism is not associated with altered susceptibility to breast cancer, while the observed decreased risk in Caucasians, PB subgroup, and large studies and increased risk in small studies may be due to selection bias or other unknown factors.
Keywords:MTR, methionine synthase   HWE, Hardy&ndash  Weinberg equilibrium   PB, population-based   HB, hospital-based   OR, odds ratio   CI, confidence interval   NOS, Newcastle&ndash  Ottawa Scale   MALDI-TOF-MS, matrix-assisted laser desorption/ionization time-of-flight mass spectrometry   PCR-RFLP, polymerase chain reaction-restriction fragment length polymorphism   SNP, single nucleotide polymorphism, LD, linkage disequilibrium
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