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系统评估多个 qPCR 平台、NanoString 和 miRNA-Seq 在人体生物液中 miRNA 生物标志物发现中的应用。

Systematic evaluation of multiple qPCR platforms, NanoString and miRNA-Seq for microRNA biomarker discovery in human biofluids.

机构信息

Translational Biomarkers, MSD, Singapore, Singapore.

MiRXES Lab, Singapore, Singapore.

出版信息

Sci Rep. 2021 Feb 24;11(1):4435. doi: 10.1038/s41598-021-83365-z.


DOI:10.1038/s41598-021-83365-z
PMID:33627690
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7904811/
Abstract

Aberrant miRNA expression has been associated with many diseases, and extracellular miRNAs that circulate in the bloodstream are remarkably stable. Recently, there has been growing interest in identifying cell-free circulating miRNAs that can serve as non-invasive biomarkers for early detection of disease or selection of treatment options. However, quantifying miRNA levels in biofluids is technically challenging due to their low abundance. Using reference samples, we performed a cross-platform evaluation in which miRNA profiling was performed on four different qPCR platforms (MiRXES, Qiagen, Applied Biosystems, Exiqon), nCounter technology (NanoString), and miRNA-Seq. Overall, our results suggest that using miRNA-Seq for discovery and targeted qPCR for validation is a rational strategy for miRNA biomarker development in clinical samples that involve limited amounts of biofluids.

摘要

异常的 miRNA 表达与许多疾病有关,并且在血液中循环的细胞外 miRNA 非常稳定。最近,人们越来越感兴趣的是识别可作为疾病早期检测或治疗方案选择的非侵入性生物标志物的无细胞循环 miRNA。然而,由于 miRNA 含量低,定量分析生物流体中的 miRNA 水平在技术上具有挑战性。使用参考样本,我们进行了跨平台评估,其中在四个不同的 qPCR 平台(MiRXES、Qiagen、Applied Biosystems、Exiqon)、nCounter 技术(NanoString)和 miRNA-Seq 上进行了 miRNA 分析。总的来说,我们的结果表明,对于涉及有限量生物流体的临床样本,使用 miRNA-Seq 进行发现和靶向 qPCR 进行验证是 miRNA 生物标志物开发的合理策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/29d2/7904811/e74fccbdab01/41598_2021_83365_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/29d2/7904811/d1063cf106c6/41598_2021_83365_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/29d2/7904811/4f4145aff2c3/41598_2021_83365_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/29d2/7904811/cc1ba8a75604/41598_2021_83365_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/29d2/7904811/e74fccbdab01/41598_2021_83365_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/29d2/7904811/d1063cf106c6/41598_2021_83365_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/29d2/7904811/4f4145aff2c3/41598_2021_83365_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/29d2/7904811/cc1ba8a75604/41598_2021_83365_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/29d2/7904811/e74fccbdab01/41598_2021_83365_Fig4_HTML.jpg

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[5]
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[7]
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[8]
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[9]
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[10]
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本文引用的文献

[1]
Development and validation of a serum microRNA biomarker panel for detecting gastric cancer in a high-risk population.

Gut. 2021-5

[2]
Development of a serum miRNA panel for detection of early stage non-small cell lung cancer.

Proc Natl Acad Sci U S A. 2020-9-17

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Diagnostic potential of circulating cell-free microRNAs for community-acquired pneumonia and pneumonia-related sepsis.

J Cell Mol Med. 2020-10

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Non-Exosomal and Exosomal Circulatory MicroRNAs: Which Are More Valid as Biomarkers?

Front Pharmacol. 2020-1-20

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Clin Chem. 2019-6-24

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BMC Genomics. 2019-6-3

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Plasma Protein and MicroRNA Biomarkers of Insulin Resistance: A Network-Based Integrative -Omics Analysis.

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[10]
Combining Circulating MicroRNA and NT-proBNP to Detect and Categorize Heart Failure Subtypes.

J Am Coll Cardiol. 2019-3-26

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