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Review
. 2020 Apr 16:14:354.
doi: 10.3389/fnins.2020.00354. eCollection 2020.

Circulating MicroRNAs as Diagnostic Biomarkers for Motor Neuron Disease

Affiliations
Review

Circulating MicroRNAs as Diagnostic Biomarkers for Motor Neuron Disease

Lin Wang et al. Front Neurosci. .

Abstract

Motor neuron disease (MND) is a kind of neurodegenerative disease that selectively invades spinal cord anterior horn cells, brainstem motor neurons, cortical pyramidal cells and the pyramidal tract. The main clinical features are the symptoms and signs of impaired upper and lower motor neurons, manifested as muscle weakness, atrophy and pyramidal tract signs. Histopathology has shown the disappearance of pyramidal cells in the motor cortex, loss of motor neurons in the anterior horn of the spinal cord and brainstem, and degeneration of the corticospinal tract. Due to the lack of effective treatment methods, the prognosis is generally poor, so it is of great significance to confirm the diagnosis early by various means. However, the current diagnosis of MND mainly relies on the combination of clinical manifestations and neurophysiological examinations, lacking effective means of early diagnosis. Circulating microRNA (CmiRNA) is a kind of stable miRNA molecule in serum, plasma and other body fluids, which has the characteristics of distinct differential expression, sensitive detection and convenient sample collection. As a possible new biomarker of MND, CmiRNA can not only reveal the pathophysiological process of MND, but also monitor disease progression and response to drug therapy. With the development of miRNA detection technology, more and more CmiRNAs as biomarkers with potential diagnostic value have been investigated. In this review, we explored the possibility of circulating samples as different sources of biomarkers for the diagnosis of MND, analyzing the progress of CmiRNA detection techniques, and presenting potential diagnostic MND biomarkers that have been reported.

Keywords: biomarker; blood; cerebral spinal fluid; circulating microRNA; motor neuron disease; neurodegeneration.

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Figures

FIGURE 1
FIGURE 1
Methodological aspects to consider in the study of circulating miRNAs as biomarkers for ALS and other MNDs. The comparison among the common characteristics of miRNA detection platforms are summarized in the figure. qRT-PCR, quantitative Real-Time Polymerase Chain Reaction; NGS, Next Generation Sequencing.

References

    1. Atik A., Stewart T., Zhang J. (2016). Alpha-synuclein as a biomarker for Parkinson’s disease. Brain Pathol. 26 410–418. 10.1111/bpa.12370 - DOI - PMC - PubMed
    1. Bartoletti M., Bosco D. A., Da Cruz S., Lagier-Tourenne C., Liachko N., Markmiller S., et al. (2019). Phenotypic suppression of ALS/FTD-associated neurodegeneration highlights mechanisms of dysfunction. J. Neurosci. 39 8217–8224. 10.1523/JNEUROSCI.1159-19.2019 - DOI - PMC - PubMed
    1. Benigni M., Ricci C., Jones A. R., Giannini F., Al-Chalabi A., Battistini S. (2016). Identification of miRNAs as potential biomarkers in cerebrospinal fluid from amyotrophic lateral sclerosis patients. Neuromol. Med. 18 551–560. - PubMed
    1. Bose M., Bhattacharyya S. N. (2018). Target mRNA-driven biogenesis of cognate MicroRNAs in vitro. Methods Mol. Biol. 1733 27–39. 10.1007/978-1-4939-7601-0_2 - DOI - PubMed
    1. Burgos K., Malenica I., Metpally R., Courtright A., Rakela B., Beach T., et al. (2014). Profiles of extracellular miRNA in cerebrospinal fluid and serum from patients with Alzheimer’s and Parkinson’s diseases correlate with disease status and features of pathology. PLoS One 9:e94839. 10.1371/journal.pone.0094839 - DOI - PMC - PubMed

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