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Circulating microRNAs as promising diagnostic biomarkers for pancreatic cancer: a systematic review

机译:循环microRNAs作为胰腺癌有希望的诊断生物标志物:系统综述

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摘要

Pancreatic cancer (PC) is one of the most common forms of malignant tumors and causes of tumor-related death worldwide. The current prognosis of PC still remains poor due to the lack of effective early detection method. Recently, there is strong support that circulating miRNAs can be used as biomarkers for early detection of various cancers, including PC. The purpose of this review is to provide an overview of previous published studies on circulating miRNAs in plasma/serum for early detection of PC and summarize their diagnostic value. PubMed, Embase and Web of Science were systematically searched for eligible studies on circulating miRNAs for PC detection. Overall, 29 studies published between 2009 and 2018 evaluating 51 individual miRNAs (no P -value exceeding 0.05) and 13 miRNAs panels were included. Generally, the diagnostic performance of circulating miRNAs for PC detection was strong, with both the sensitivity and specificity of 36% individual miRNAs and 40% miRNAs panels exceeding 80%. Moreover, two promising miRNA panels were discovered and verified externally with all AUC values exceeding 0.95. Therefore, circulating miRNAs may hold potential to be used as noninvasive diagnostic biomarkers for PC, but large-scale studies are still needed to validate the promising miRNAs and optimize the miRNA panels. Since, the tremendous heterogeneity of studies in this field hampers translating miRNA markers into clinical practice, miRNA analytical procedures are also needed to be standardized in the future.
机译:胰腺癌(PC)是恶性肿瘤的最常见形式之一,并且是全世界范围内与肿瘤相关的死亡的原因。由于缺乏有效的早期检测方法,目前PC的预后仍然很差。最近,强烈支持将循环的miRNA用作早期检测各种癌症(包括PC)的生物标志物。这篇综述的目的是概述先前发表的关于血浆/血清中循环miRNA的研究,以早期检测PC并总结其诊断价值。系统搜索了PubMed,Embase和Web of Science,以寻找有关可检测PC的循环miRNA的合格研究。总体而言,包括2009年至2018年发表的29项研究,评估了51种单个miRNA(P值均不超过0.05)和13个miRNA组。通常,循环miRNA对PC检测的诊断性能强,36%的单个miRNA和40%的miRNA面板的灵敏度和特异性都超过80%。此外,还发现了两个有希望的miRNA面板,并在外部进行了验证,所有AUC值均超过0.95。因此,循环中的miRNA可能具有用作PC的非侵入性诊断生物标志物的潜力,但仍需要进行大规模研究来验证有前途的miRNA和优化miRNA面板。由于该领域研究的巨大异质性阻碍了将miRNA标记物转化为临床实践,因此将来还需要对miRNA分析程序进行标准化。

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