Department of Urology, Affiliated Hospital of Hebei University, Baoding, 071000, China.
Hebei Key Laboratory of Chronic Kidney Diseases and Bone Metabolism, Baoding, 071000, China.
Pathol Oncol Res. 2020 Apr;26(2):1201-1209. doi: 10.1007/s12253-019-00672-7. Epub 2019 Jun 13.
To assess the associations between O-methylguanine-DNA methyltransferase(MGMT) polymorphisms and prostate cancer risk. We retrieved PubMed, Cochrane Library and Embase electronic database to search for all eligible studies published from Jan 1, 1970 to Sep 31, 2017 to conduct a Meta-analysis. we identified 11 independent studies in 5 eligible reports, including 5143 cases and 8118 controls. The data suggested that rs12917 was associated with higher PCa risk under the contrast of TT vs CC and recessive model in overall population (TT vs CC: OR = 1.599, 95%CI: 1.007-2.539, P = 0.047; TT vs CC + CT: OR = 1.627, 95%CI: 1.026-2.580, P = 0.038). In subgroup analyses stratified by ethnicity, the remarkable association with higher PCa risk was detected under allelic model, dominant model, the contrast of TC vs CC, and the contrast of TC vs CC + TT in Asian population. (T vs C: OR = 1.911, 95%CI: 1.182-3.090, P = 0.008; TC vs CC: OR = 1.948, 95%CI: 1.152-3.295, P = 0.013; TC + TT vs CC: OR = 1.994, 95%CI: 1.190-3.342, P = 0.009; TC vs CC + TT: OR = 1.926, 95%CI: 1.140-3.255, P = 0.014). However, the data suggest the rs2308327 and rs2308321 polymorphisms of the MGMT gene were nor associated with the susceptibility of prostate cancer. Based on the meta-analysis, MGMT rs12917 polymorphism increase the susceptibility to prostate cancer, which can be taken for a diagnosis and screening molecular biomarker for prostate cancer patients.
为了评估 O-甲基鸟嘌呤-DNA 甲基转移酶(MGMT)多态性与前列腺癌风险之间的关联。我们检索了 PubMed、Cochrane Library 和 Embase 电子数据库,以搜索 1970 年 1 月 1 日至 2017 年 9 月 31 日发表的所有符合条件的研究,进行 Meta 分析。我们从 5 份符合条件的报告中确定了 11 项独立研究,共包括 5143 例病例和 8118 例对照。数据表明,在总体人群中,与 CC 相比,TT 与 rs12917 对比与较高的 PCa 风险相关,并且在隐性模型中也是如此(TT 与 CC:OR=1.599,95%CI:1.007-2.539,P=0.047;TT 与 CC+CT:OR=1.627,95%CI:1.026-2.580,P=0.038)。在按种族分层的亚组分析中,在等位基因模型、显性模型、TC 与 CC 的对比以及亚洲人群中 TC 与 CC+TT 的对比中,发现与较高的 PCa 风险有显著关联。(T 与 C:OR=1.911,95%CI:1.182-3.090,P=0.008;TC 与 CC:OR=1.948,95%CI:1.152-3.295,P=0.013;TC+TT 与 CC:OR=1.994,95%CI:1.190-3.342,P=0.009;TC 与 CC+TT:OR=1.926,95%CI:1.140-3.255,P=0.014)。然而,数据表明 MGMT 基因的 rs2308327 和 rs2308321 多态性与前列腺癌的易感性无关。基于荟萃分析,MGMT rs12917 多态性增加了前列腺癌的易感性,可作为前列腺癌患者的诊断和筛查分子生物标志物。