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Prognostic value of low microRNA-34a expression in human gastrointestinal cancer: a systematic review and meta-analysis

机译:低MicroRNA-34A表达在人胃肠癌中的预后价值:系统评价与荟萃分析

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Mounting evidence shows that microRNA-34a (miR-34a) is involved in cancer prognosis. Therefore, we summarize the predictive role of miR-34a for survival in patients with gastrointestinal cancers (GICs). All eligible studies were found by searching PubMed, Web of Science and EMBASE, and survival results were extracted. Then, the hazard ratio (HR) with the corresponding 95% confidence interval (CI) was calculated to evaluate the prognostic role of miR-34a in GICs. The association between miR-34a expression and clinicopathological characteristics was estimated by odds ratios (ORs) and 95% CIs. A total of 20 studies were included in this meta-analysis. For overall survival (OS), lower miR-34a expression could probably predict poorer outcome in GICs, with a pooled HR of 1.86 (95% CI: 1.52–2.28, P??0.01). For disease-free survival (DFS), progression-free survival (PFS), and recurrence-free survival (RFS), lower miR-34a expression was related to worse DFS/PFS/RFS with a pooled HR of 1.86 (95% CI: 1.31–2.63, P 0.01). A significant relation of differentiation/TNM stage/lymphatic metastasis and the expression level of miR-34a was identified. This meta-analysis revealed that lower miR-34a expression is significantly connected with worse OS and DFS/PFS/RFS in GIC patients. In addition, the miR-34a expression level is relatively lower in patients with lymph node metastasis than in patients without lymph node metastasis, and decreased miR-34a expression levels are linked to poor tumour differentiation and late TNM stage. MiR-34a may become a new factor for the prognosis prediction and progression of GICs.
机译:安装证据表明,MicroRNA-34A(miR-34a)参与癌症预后。因此,我们总结了miR-34a对胃肠道癌患者存活的预测性作用(GICS)。通过搜索PubMed,科学网和Embase,提取所有合格的研究,提取生存结果。然后,计算具有相应的95%置信区间(CI)的危害比(HR)以评估miR-34a在GICS中的预后作用。 miR-34a表达与临床病理特征之间的关联估计了大量比率(或)和95%的顺应性。该荟萃分析中共有20项研究。对于总体存活(OS),较低的miR-34a表达可能可能预测GICS的较差结果,汇集的HR为1.86(95%CI:1.52-28,P≤≤0.01)。对于无疾病存活(DFS),无进展生存期(PFS)和无复发存活(RFS),较低的miR-34a表达与汇总的HR的较差的DFS / PFS / RF有关,其中1.86(95%CI :1.31-2.63,p& 0.01)。鉴定了分化/ TNM阶段/淋巴结转移和miR-34a的表达水平的显着关系。该荟萃分析显示,较低的miR-34a表达与GIC患者中的更差的OS和DFS / PFS / RF显着连接。此外,淋巴结转移患者的miR-34a表达水平比没有淋巴结转移的患者相对较低,并且降低miR-34a表达水平与肿瘤分化差和晚期阶段。 MiR-34A可能成为GICS预后预测和进展的新因素。

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