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首页> 外文期刊>Medicine. >Promoter hypermethylation of MGMT gene may contribute to the pathogenesis of gastric cancer: A PRISMA-compliant meta-analysis
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Promoter hypermethylation of MGMT gene may contribute to the pathogenesis of gastric cancer: A PRISMA-compliant meta-analysis

机译:MGMT基因的启动子高甲基化可能与胃癌的发病机制有关:符合PRISMA的荟萃分析

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摘要

Beckground: The association of MGMT (O6-methyguanine deoxyribonucleic acid methyltransferase) promoter hypermethylation with gastric cancer (GC) risk has been studied extensively, but the results remained unclear. Here, we performed a meta-analysis to evaluate whether promoter hypermethylation of the MGMT gene contributed to gastric pathogenesis. Methods: Relevant studies were identified by retrieving the PubMed, Web of Science, Embase, and China National Knowledge Infrastructure (CNKI) databases. The Newcastle–Ottawa Scale was applied to assess methodological quality of the included studies. Pooled odds ratios (ORs) and 95% confidence intervals (95% CIs) were calculated to evaluate the association of MGMT promoter hypermethylation with gastric pathogenesis. Moreover, STATA 12.0 software was used to summarize the extracted data in this meta-analysis. Results: Seventeen studies, comprising 1736 cases and 1291 controls, were included in this meta-analysis. The frequency of MGMT promoter hypermethylation in the GC group (32.97%) was significantly higher than those in the control group (18.00%) (OR = 2.83, CI = 1.93–4.15, P < .05). When stratified by cancer subtype, the results indicated that the frequency of MGMT promoter hypermethylation was significantly higher in gastric adenocarcinoma than in control group (OR = 3.47, CI = 1.06–11.35, P < .05). In addition, MGMT promoter hypermethylation significantly promoted distant metastasis and lymph node (LN) metastasis of gastric tumor (for distant metastasis, OR = 4.22, CI = 2.42–7.37, P < .05; for LN metastasis, OR = 1.56, CI = 1.14–2.13, P < .05). A significant association between MGMT promoter hypermethylation and TNM-stage was also found in the present meta-analysis (OR = 2.70, CI = 1.79–4.08, P < .05). Conclusion: The results of this meta-analysis suggested that MGMT gene-promoter hypermethylation was significantly associated with an increased risk of GC, especially in Asians. Furthermore, MGMT gene-promoter hypermethylation might be correlated with the distant metastasis and LN metastasis of GC.
机译:Beckground:MGMT(O 6 -甲鸟嘌呤脱氧核糖核酸甲基转移酶)启动子过甲基化与胃癌(GC)风险的关联已经进行了广泛的研究,但结果仍不清楚。在这里,我们进行了荟萃分析,以评估MGMT基因的启动子过度甲基化是否有助于胃部发病。方法:通过检索PubMed,Web of Science,Embase和中国国家知识基础设施(CNKI)数据库来鉴定相关研究。纽卡斯尔-渥太华量表用于评估纳入研究的方法学质量。计算合并的优势比(OR)和95%置信区间(95%CI),以评估MGMT启动子高甲基化与胃病发病机制的关系。此外,在该荟萃分析中,使用了STATA 12.0软件对提取的数据进行汇总。结果:这项荟萃分析包括17项研究,包括1736例病例和1291例对照。 GC组中MGMT启动子甲基化的频率(32.97%)显着高于对照组(18.00%)(OR = 2.83,CI = 1.93–4.15,P <.05)。当按癌症亚型进行分层时,结果表明胃腺癌中MGMT启动子高甲基化的频率显着高于对照组(OR = 3.47,CI = 1.06-11.35,P <.05)。此外,MGMT启动子甲基化显着促进了胃癌的远处转移和淋巴结转移(远处转移,OR = 4.22,CI = 2.42-7.37,P <.05; LN转移,OR = 1.56,CI = 1.14–2.13,P <.05)。在本荟萃分析中还发现MGMT启动子甲基化过度与TNM分期之间存在显着关联(OR = 2.70,CI = 1.79-4.08,P <.05)。结论:这项荟萃分析的结果表明,MGMT基因启动子高甲基化与GC风险增加显着相关,尤其是在亚洲人中。此外,MGMT基因启动子的高甲基化可能与GC的远处转移和LN转移有关。

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