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Clinical effect of DAPK promoter methylation in gastric cancer: A systematic meta-analysis

机译:DAPK启动子甲基化在胃癌中的临床疗效:系统性荟萃分析

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摘要

Background:The loss of death-associated protein kinase (DAPK) gene expression through promoter methylation is involved in many tumors. However, the relationship between DAPK promoter methylation and clinicopathological features of gastric cancer (GC) remains to be done. Therefore, we performed a meta-analysis to assess the role of DAPK promoter methylation in GC.Methods:Literature databases were searched to retrieve eligible studies. The pooled odds ratios (ORs) with its 95% confidence intervals (CIs) were calculated using the Stata 12.0 software.Results:Final 22 available studies with 1606 GC patients and 1508 nonmalignant controls were analyzed. A significant correlation was found between DAPK promoter methylation and GC (OR = 3.23, 95% CI = 1.70-6.14, P<0.001), but we did not find any significant association in Caucasian population, and in blood samples in subgroup analyses. DAPK promoter methylation was associated with tumor stage and lymph node status (OR = 0.69, 95% CI = 0.49-0.96, P = 0.03; OR = 1.50, 95% CI = 1.12-2.01, P = 0.007; respectively). However, we did not find that DAPK promoter methylation was associated with gender status and tumor histology.Conclusion:Our findings suggested that DAPK promoter methylation may play a key role in the carcinogenesis and progression of GC. In addition, methylated DAPK was a susceptible gene for Asian population. However, more studies with larger subjects should be done to further evaluate the effect of DAPK promoter methylation in GC patients, especially in blood and Caucasian population subgroup.
机译:背景:通过启动子甲基化的死亡相关蛋白激酶(DAPK)基因表达的丧失涉及许多肿瘤。然而,DAPK启动子甲基化与胃癌(GC)的临床病理特征之间的关系仍有待完成。因此,我们进行了荟萃分析,以评估DAPK启动子甲基化在GC.Methods中的作用:搜查文献数据库来检索合格的研究。使用STATA 12.0软件计算汇总的差距(或者)具有95%置信区间(CIS)。结果:最终22种可用的1606名GC患者和1508名非无产量控制的研究。在DAPK启动子甲基化和GC之间发现了显着的相关性(或= 3.23,95%CI = 1.70-6.14,P <0.001),但我们没有发现在白种人人群中有任何重大关联,并且在亚组分析中的血液样本中。 DAPK启动子甲基化与肿瘤阶段和淋巴结状态有关(或= 0.69,95%CI = 0.49-0.96,P = 0.03;或= 1.50,95%CI = 1.12-2.01,P = 0.007;然而,我们发现DAPK启动子甲基化与性别状态和肿瘤组织学有关。结论:我们的研究结果表明DAPK启动子甲基化可能在癌症发生和GC的进展中发挥关键作用。此外,甲基化的DAPK是亚洲人口的敏感基因。然而,应采取更多对受试者进行更多的研究,以进一步评估GC患者的DAPK启动子甲基化的作用,特别是在血液和高加索人群亚组中。

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  • 来源
    《Medicine.》 |2016年第43期|共8页
  • 作者单位

    Beijing Hosp Dept Gen Surg Natl Ctr Gerontol Beijing Peoples R China;

    Beijing Hosp Dept Gen Surg Natl Ctr Gerontol Beijing Peoples R China;

    Beijing Hosp Dept Gen Surg Natl Ctr Gerontol Beijing Peoples R China;

    Beijing Hosp Dept Gen Surg Natl Ctr Gerontol Beijing Peoples R China;

    Beijing Hosp Dept Gen Surg Natl Ctr Gerontol Beijing Peoples R China;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 医药、卫生;
  • 关键词

    clinicopathological features; DAPK; GC; promoter methylation;

    机译:临床病理特征;DAPK;GC;启动子甲基化;

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