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Review
. 2024 Jul;43(28):2135-2142.
doi: 10.1038/s41388-024-03076-3. Epub 2024 Jun 5.

MicroRNAs: circulating biomarkers for the early detection of imperceptible cancers via biosensor and machine-learning advances

Affiliations
Review

MicroRNAs: circulating biomarkers for the early detection of imperceptible cancers via biosensor and machine-learning advances

Gavin A D Metcalf. Oncogene. 2024 Jul.

Abstract

This review explores the topic of microRNAs (miRNAs) for improved early detection of imperceptible cancers, with potential to advance precision medicine and improve patient outcomes. Historical research exploring miRNA's role in cancer detection collectively revealed initial hurdles in identifying specific miRNA signatures for early-stage and difficult-to-detect cancers. Early studies faced challenges in establishing robust biomarker panels and overcoming the heterogeneity of cancer types. Despite this, recent developments have supported the potential of miRNAs as sensitive and specific biomarkers for early cancer detection as well as having demonstrated remarkable potential as diagnostic tools for imperceptible cancers, such as those with elusive symptoms or challenging diagnostic criteria. This review discusses the advent of high-throughput technologies that have enabled comprehensive detection and profiling of unique miRNA signatures associated with early-stage cancers. Furthermore, advancements in bioinformatics and machine-learning techniques are considered, exploring the integration of multi-omics data which have potential to enhance both the accuracy and reliability of miRNA-based cancer detection assays. Finally, perspectives on the continuing development on technologies as well as discussion around challenges that remain, such as the need for standardised protocols and addressing the complex interplay of miRNAs in cancer biology are conferred.

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Conflict of interest statement

The author declares no competing interests.

Figures

Fig. 1
Fig. 1. MiRNA excretion mechanisms and extracellular survival.
MiRNAs are actively and passively released by cells via various approaches, including multivesicular bodies (MVB) and cellular excretion via exosomes, microvesicle formation achieved via membrane shedding, as well as association with AGO-2 and HDL.

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