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微小 RNA 作为良性前列腺增生生物标志物的潜在作用:系统评价和荟萃分析。

The Potential Role of MicroRNAs as Biomarkers in Benign Prostatic Hyperplasia: A Systematic Review and Meta-analysis.

机构信息

Department of Urology, Ospedale Pederzoli, Peschiera del Garda (VR), Italy; Department of Urology, Federico II University, Naples, Italy.

Department of Pathology of Adult and Evolutive Age, University of Messina, Messina, Italy.

出版信息

Eur Urol Focus. 2019 May;5(3):497-507. doi: 10.1016/j.euf.2018.01.008. Epub 2018 Feb 3.

Abstract

CONTEXT

Benign prostate hyperplasia (BPH) is one of the most common urologic diseases. However, the molecular and cellular mechanisms involving the stromal and epithelial components of the prostate that lead to BPH remain unclear.

OBJECTIVE

To review and evaluate the evidence implicating microRNAs (miRNAs) in the pathogenesis of BPH.

EVIDENCE ACQUISITION

A systematic search of the PubMed and Embase databases was performed using the terms "benign prostate hypertrophy and miRNA" or ("benign prostate hypertrophy and microRNAs" or "miRNA" or "miR") on July 31, 2017.

EVIDENCE SYNTHESIS

Sixty-four miRNAs from 37 selected articles were ranked according to p values (p≤0.05). To avoid false positive results, Benjamini-Hochberg correction of p values was performed. Application of the robust rank aggregation method identified miR-221 as significantly associated with BPH (p=0.013). The effect size (ES) was calculated for studies with miR-221 data to generate an estimate of the overall ES and its confidence interval. The ES for miR-221 was measured by the standardized mean difference obtained by dividing the difference in the average gene expression between the PCa and BPH groups by a pooled estimate of standard deviation. The random effects model was used to calculate the pooled ES due to the presence of heterogeneity among studies. Publication bias of the seven included studies was assessed by the Funnel plot and Egger's test and it was detected in the overall analysis of the seven studies (p<0.01). After the trim and fill procedure, Egger's test revealed no evidence of publication bias (p=0.76) CONCLUSIONS: miR-221 has the potential to be used both as a biomarker and novel target in the early diagnosis and therapy of BPH. Technological advances should enable the synthesis of pre-RNA or anti-RNA molecules within carrier vehicles that can be safely delivered into patients. The development of such new pharmacologic therapies should be lastly investigated as possible therapy of one of the most common urologic diseases among elderly men. PATIENT SUMMARY: miR-221 has the potential to be used both as a biomarker and novel target in the early diagnosis and therapy of benign prostate hyperplasia. The development of new pharmacologic therapies enabling the synthesis of anti-miR-221 should be lastly investigated as a possible therapy of one of the most common urologic diseases among elderly men.

摘要

背景

良性前列腺增生(BPH)是最常见的泌尿科疾病之一。然而,导致 BPH 的前列腺基质和上皮成分的分子和细胞机制尚不清楚。

目的

综述和评估 microRNAs(miRNAs)在 BPH 发病机制中的作用。

证据获取

2017 年 7 月 31 日,在 PubMed 和 Embase 数据库中使用“良性前列腺肥大和 miRNA”或(“良性前列腺肥大和 microRNAs”或“miRNA”或“miR”)术语进行系统检索。

证据综合

根据 p 值(p≤0.05),对 37 篇选定文章中的 64 个 miRNA 进行了排名。为避免假阳性结果,对 p 值进行了 Benjamini-Hochberg 校正。应用稳健秩聚合方法发现 miR-221 与 BPH 显著相关(p=0.013)。对于具有 miR-221 数据的研究,计算效应量(ES)以生成总体 ES 及其置信区间的估计值。通过将 PCa 和 BPH 组之间的平均基因表达差异除以标准差的合并估计值,用标准化均数差来衡量 miR-221 的 ES。由于研究之间存在异质性,因此使用随机效应模型计算合并 ES。通过漏斗图和 Egger 检验评估纳入的 7 项研究的发表偏倚,在对 7 项研究的总体分析中发现存在发表偏倚(p<0.01)。在修剪和填充程序后,Egger 检验显示无发表偏倚证据(p=0.76)。结论:miR-221 有可能成为 BPH 早期诊断和治疗的生物标志物和新靶点。技术进步应能使带有载体的前 RNA 或反 RNA 分子合成,可安全递送至患者体内。应最后研究开发此类新型药物治疗方法,作为治疗老年男性最常见的泌尿科疾病之一的可能疗法。患者总结:miR-221 有可能成为 BPH 早期诊断和治疗的生物标志物和新靶点。最后应研究开发能够合成抗 miR-221 的新型药物治疗方法,作为治疗老年男性最常见的泌尿科疾病之一的可能疗法。

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