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miR-145 在多种肿瘤中的预后价值及调控机制:50 项研究的系统评价和荟萃分析。

The Prognostic Value and Regulatory Mechanisms of microRNA-145 in Various Tumors: A Systematic Review and Meta-analysis of 50 Studies.

机构信息

Department of Liver Surgery, West China Hospital, Sichuan University, Chengdu, Sichuan Province, China.

Center of Infectious Diseases, West China Hospital, Sichuan University, Chengdu, Sichuan Province, China.

出版信息

Cancer Epidemiol Biomarkers Prev. 2019 May;28(5):867-881. doi: 10.1158/1055-9965.EPI-18-0570. Epub 2019 Jan 2.

Abstract

Acting as an important tumor-related miRNA, the clinical significance and underlying mechanisms of miR-145 in various malignant tumors have been investigated by numerous studies. This study aimed to comprehensively estimate the prognostic value and systematically illustrate the regulatory mechanisms of miR-145 based on all eligible literature.Relevant studies were acquired from multiple online databases. Overall survival (OS) and progression-free survival (PFS) were used as primary endpoints. Detailed subgroup analyses were performed to decrease the heterogeneity among studies and recognize the prognostic value of miR-145. All statistical analyses were performed with RevMan software version 5.3 and STATA software version 14.1. A total of 48 articles containing 50 studies were included in the meta-analysis. For OS, the pooled results showed that low miR-145 expression in tumor tissues was significantly associated with worse OS in patients with various tumors [HR = 1.70; 95% confidence interval (CI), 1.46-1.99; < 0.001). Subgroup analysis based on tumor type showed that the downregulation of miR-145 was associated with unfavorable OS in colorectal cancer (HR = 2.17; 95% CI, 1.52-3.08; < 0.001), ovarian cancer (HR = 2.15; 95% CI, 1.29-3.59; = 0.003), gastric cancer (HR = 1.78; 95% CI, 1.35-2.36; < 0.001), glioma (HR = 1.65; 95% CI, 1.30-2.10; < 0.001), and osteosarcoma (HR = 2.28; 95% CI, 1.50-3.47; < 0.001). For PFS, the pooled results also showed that the downregulation of miR-145 was significantly associated with poor PFS in patients with multiple tumors (HR = 1.39; 95% CI, 1.16-1.67; < 0.001), and the subgroup analyses further identified that the low miR-145 expression was associated with worse PFS in patients with lung cancer (HR = 1.97; 95% CI, 1.25-3.09; = 0.003) and those of Asian descent (HR = 1.50; 95% CI, 1.23-1.82; < 0.001). For the regulatory mechanisms, we observed that numerous tumor-related transcripts could be targeted by miR-145-5p or miR-145-3p, as well as the expression and function of miR-145-5p could be regulated by multiple molecules.This meta-analysis indicated that downregulated miR-145 in tumor tissues or peripheral blood predicted unfavorable prognostic outcomes for patients suffering from various malignant tumors. In addition, miR-145 was involved in multiple tumor-related pathways and the functioning of significant biological effects. miR-145 is a well-demonstrated tumor suppressor, and its expression level is significantly correlated with the prognosis of patients with multiple malignant tumors.

摘要

作为一种重要的肿瘤相关 miRNA,miR-145 在各种恶性肿瘤中的临床意义和潜在机制已被大量研究进行了探讨。本研究旨在全面评估 miR-145 的预后价值,并基于所有合格的文献系统地阐明其调控机制。

从多个在线数据库中获取相关研究。总生存期(OS)和无进展生存期(PFS)被用作主要终点。进行了详细的亚组分析,以减少研究之间的异质性,并确定 miR-145 的预后价值。所有统计分析均使用 RevMan 软件版本 5.3 和 STATA 软件版本 14.1 进行。共有 48 篇文章包含 50 项研究被纳入荟萃分析。

对于 OS,汇总结果表明,肿瘤组织中 miR-145 表达水平降低与各种肿瘤患者的 OS 较差显著相关[HR = 1.70;95%置信区间(CI),1.46-1.99;<0.001]。基于肿瘤类型的亚组分析显示,miR-145 的下调与结直肠癌(HR = 2.17;95%CI,1.52-3.08;<0.001)、卵巢癌(HR = 2.15;95%CI,1.29-3.59;=0.003)、胃癌(HR = 1.78;95%CI,1.35-2.36;<0.001)、神经胶质瘤(HR = 1.65;95%CI,1.30-2.10;<0.001)和骨肉瘤(HR = 2.28;95%CI,1.50-3.47;<0.001)患者的不良 OS 相关。

对于 PFS,汇总结果还表明,miR-145 的下调与多种肿瘤患者的不良 PFS 显著相关(HR = 1.39;95%CI,1.16-1.67;<0.001),进一步的亚组分析还确定,miR-145 的低表达与肺癌(HR = 1.97;95%CI,1.25-3.09;=0.003)和亚洲人群(HR = 1.50;95%CI,1.23-1.82;<0.001)患者的较差 PFS 相关。

对于调控机制,我们观察到许多肿瘤相关转录物可以被 miR-145-5p 或 miR-145-3p 靶向,以及 miR-145-5p 的表达和功能可以被多种分子调节。

这项荟萃分析表明,肿瘤组织或外周血中下调的 miR-145 预测患有各种恶性肿瘤的患者预后不良。此外,miR-145 参与多种肿瘤相关途径和重要生物学效应的功能。miR-145 是一种经过充分证实的肿瘤抑制因子,其表达水平与多种恶性肿瘤患者的预后显著相关。

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