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Association between RUNX3 promoter methylation and gastric cancer: a meta-analysis

机译:RUNX3启动子甲基化与胃癌之间的关联:META分析

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Background Runt-related transcription factor 3 (RUNX3) is a member of the runt-domain family of transcription factors and has been reported to be a candidate tumor suppressor in gastric cancer. However, the association between RUNX3 promoter methylation and gastric cancer remains unclear. Methods We systematically reviewed studies of RUNX3 promoter methylation and gastric cancer published in English or Chinese from January 2000 to January 2011, and quantified the association between RUNX3 promoter methylation and gastric cancer using meta-analysis methods. Results A total of 1740 samples in 974 participants from seventeen studies were included in the meta-analysis. A significant association was observed between RUNX3 promoter methylation and gastric cancer, with an aggregated odds ratio (OR) of 5.63 (95%CI 3.15, 10.07). There was obvious heterogeneity among studies. Subgroup analyses (including by tissue origin, country and age), meta-regression were performed to determine the source of the heterogeneity. Meta-regression showed that the trend in ORs was inversely correlated with age. No publication bias was detected. The ORs for RUNX3 methylation in well-differentiated vs undifferentiated gastric cancers, and in intestinal-type vs diffuse-type carcinomas were 0.59 (95%CI: 0.30, 1.16) and 2.62 (95%CI: 1.33, 5.14), respectively. There were no significant differences in RUNX3 methylation in cancer tissues in relation to age, gender, TNM stage, invasion of tumors into blood vessel or lymphatic ducts, or tumor stage. Conclusions This meta-analysis identified a strong association between methylation of the RUNX3 promoter and gastric cancer, confirming the role of RUNX3 as a tumor suppressor gene.
机译:背景技术Runt相关的转录因子3(Runx3)是Runt-Domain系列转录因子的成员,并且已据报道是胃癌中的候选肿瘤抑制因子。然而,RUNX3启动子甲基化与胃癌之间的关联仍不清楚。方法从2000年1月到2011年1月到2011年1月,系统地审查了对英语或中文发表的Runx3启动子甲基化和胃癌的研究,并使用Meta分析方法量化了Runx3启动子甲基化和胃癌之间的关联。结果在荟萃分析中,共有1740名从774名参与者中的样本中包含1740个样本。在Runx3启动子甲基化和胃癌之间观察到显着的关联,其聚集的差距(或)为5.63(95%CI 3.15,10.07)。研究中有明显的异质性。亚组分析(包括组织来源,国家和年龄),进行了荟萃回归以确定异质性的来源。元回归表明,趋势与年龄相反。没有检测到出版物偏见。在良好分化的与未分化的胃癌和肠型VS漫射型癌中的runx3甲基化的ORS分别为0.59(95%CI:0.30,1.16)和2.62(95%CI:1.33,5.14)。在血管或淋巴管或淋巴管或肿瘤阶段,癌组织中癌组织中runx3甲基化无显着差异。结论该META分析确定了RUNX3启动子和胃癌的甲基化与胃癌之间的强烈关联,确认RUNX3作为肿瘤抑制基因的作用。

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