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MicroRNA amplification and detection technologies: opportunities and challenges for point of care diagnostics
Technical University of Denmark, Lyngby, Denmark.
Technical University of Denmark, Lyngby, Denmark.
University of Skövde, School of Bioscience. University of Skövde, The Systems Biology Research Centre. (Infection Biology, Infektionsbiologi)ORCID iD: 0000-0003-4221-6013
University of Skövde, School of Bioscience. University of Skövde, The Systems Biology Research Centre. (Infection Biology, Infektionsbiologi)ORCID iD: 0000-0002-8181-4131
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2018 (English)In: Laboratory Investigation, ISSN 0023-6837, E-ISSN 1530-0307, Vol. 99, no 4, p. 452-469Article, review/survey (Refereed) Published
Abstract [en]

The volume of point of care (POC) testing continues to grow steadily due to the increased availability of easy-to-use devices, thus making it possible to deliver less costly care closer to the patient site in a shorter time relative to the central laboratory services. A novel class of molecules called microRNAs have recently gained attention in healthcare management for their potential as biomarkers for human diseases. The increasing interest of miRNAs in clinical practice has led to an unmet need for assays that can rapidly and accurately measure miRNAs at the POC. However, the most widely used methods for analyzing miRNAs, including Northern blot-based platforms, in situ hybridization, reverse transcription qPCR, microarray, and next-generation sequencing, are still far from being used as ideal POC diagnostic tools, due to considerable time, expertize required for sample preparation, and in terms of miniaturizations making them suitable platforms for centralized labs. In this review, we highlight various existing and upcoming technologies for miRNA amplification and detection with a particular emphasis on the POC testing industries. The review summarizes different miRNA targets and signals amplification-based assays, from conventional methods to alternative technologies, such as isothermal amplification, paper-based, oligonucleotide-templated reaction, nanobead-based, electrochemical signaling-based, and microfluidic chip-based strategies. Based on critical analysis of these technologies, the possibilities and feasibilities for further development of POC testing for miRNA diagnostics are addressed and discussed.

Place, publisher, year, edition, pages
Nature Publishing Group, 2018. Vol. 99, no 4, p. 452-469
Keywords [en]
IN-SITU HYBRIDIZATION, ELECTROCHEMICAL BIOSENSORS, CIRCULATING MICRORNAS, MICROFLUIDIC PLATFORM, CANCER DIAGNOSTICS, EXPRESSION, BIOMARKERS, ACID, PROBES, RNA
National Category
Biochemistry and Molecular Biology Medical Biotechnology
Research subject
Infection Biology; INF502 Biomarkers
Identifiers
URN: urn:nbn:se:his:diva-16509DOI: 10.1038/s41374-018-0143-3ISI: 000462161500002PubMedID: 30542067Scopus ID: 2-s2.0-85058447908OAI: oai:DiVA.org:his-16509DiVA, id: diva2:1271897
Projects
SMARTDIAGNOS
Funder
EU, Horizon 2020, 68797
Note

© United States & Canadian Academy of Pathology 2018. The RightsLink Digital Licensing and Rights Management Service (including RightsLink for Open Access) is available (A) to users of copyrighted works found at the websites of participating publishers who are seeking permissions or licenses to use those works, and (B) to authors of articles and other manuscripts who are seeking to pay author publication charges in connection with the submission of their works to publishers.

Available from: 2018-12-18 Created: 2018-12-18 Last updated: 2021-01-07Bibliographically approved

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Pernestig, Anna-KarinTilevik, Diana

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