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Identification and Characterization of Serum microRNAs as Biomarkers for Human Disc Degeneration: An RNA Sequencing Analysis

Circulating microRNAs (miRNAs) have been associated with various degenerative diseases, including intervertebral disc (IVD) degeneration. Lumbar disc herniation (LDH) often occurs in young patients, although the underlying mechanisms are poorly understood. The aim of this work was to generate RNA de...

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Autores principales: Cui, Shangbin, Zhou, Zhiyu, Liu, Xizhe, Richards, Robert Geoff, Alini, Mauro, Peng, Songlin, Liu, Shaoyu, Zou, Xuenong, Li, Zhen, Grad, Sibylle
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7762572/
https://www.ncbi.nlm.nih.gov/pubmed/33302347
http://dx.doi.org/10.3390/diagnostics10121063
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author Cui, Shangbin
Zhou, Zhiyu
Liu, Xizhe
Richards, Robert Geoff
Alini, Mauro
Peng, Songlin
Liu, Shaoyu
Zou, Xuenong
Li, Zhen
Grad, Sibylle
author_facet Cui, Shangbin
Zhou, Zhiyu
Liu, Xizhe
Richards, Robert Geoff
Alini, Mauro
Peng, Songlin
Liu, Shaoyu
Zou, Xuenong
Li, Zhen
Grad, Sibylle
author_sort Cui, Shangbin
collection PubMed
description Circulating microRNAs (miRNAs) have been associated with various degenerative diseases, including intervertebral disc (IVD) degeneration. Lumbar disc herniation (LDH) often occurs in young patients, although the underlying mechanisms are poorly understood. The aim of this work was to generate RNA deep sequencing data of peripheral blood samples from patients suffering from LDH, identify circulating miRNAs, and analyze them using bioinformatics applications. Serum was collected from 10 patients with LDH (Disc Degeneration Group); 10 patients without LDH served as the Control Group. RNA sequencing analysis identified 73 differential circulating miRNAs (p < 0.05) between the Disc Degeneration Group and Control Group. Gene ontology enrichment analysis (p < 0.05) showed that these differentially expressed miRNAs were associated with extracellular matrix, damage reactions, inflammatory reactions, and regulation of apoptosis. Kyoto Encyclopedia of Genes and Genomes analysis showed that the differentially expressed genes were involved in diverse signaling pathways. The profile of miR-766-3p, miR-6749-3p, and miR-4632-5p serum miRNAs was significantly enriched (p < 0.05) in multiple pathways associated with IVD degeneration. miR-766-3p, miR-6749-3p, and miR-4632-5p signature from serum may serve as a noninvasive diagnostic biomarker for LHD manifestation of IVD degeneration. Furthermore, several dysregulated miRNAs may be involved in the pathogenesis of IVD degeneration. Further study is needed to confirm the functional role of the identified miRNAs.
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spelling pubmed-77625722020-12-26 Identification and Characterization of Serum microRNAs as Biomarkers for Human Disc Degeneration: An RNA Sequencing Analysis Cui, Shangbin Zhou, Zhiyu Liu, Xizhe Richards, Robert Geoff Alini, Mauro Peng, Songlin Liu, Shaoyu Zou, Xuenong Li, Zhen Grad, Sibylle Diagnostics (Basel) Article Circulating microRNAs (miRNAs) have been associated with various degenerative diseases, including intervertebral disc (IVD) degeneration. Lumbar disc herniation (LDH) often occurs in young patients, although the underlying mechanisms are poorly understood. The aim of this work was to generate RNA deep sequencing data of peripheral blood samples from patients suffering from LDH, identify circulating miRNAs, and analyze them using bioinformatics applications. Serum was collected from 10 patients with LDH (Disc Degeneration Group); 10 patients without LDH served as the Control Group. RNA sequencing analysis identified 73 differential circulating miRNAs (p < 0.05) between the Disc Degeneration Group and Control Group. Gene ontology enrichment analysis (p < 0.05) showed that these differentially expressed miRNAs were associated with extracellular matrix, damage reactions, inflammatory reactions, and regulation of apoptosis. Kyoto Encyclopedia of Genes and Genomes analysis showed that the differentially expressed genes were involved in diverse signaling pathways. The profile of miR-766-3p, miR-6749-3p, and miR-4632-5p serum miRNAs was significantly enriched (p < 0.05) in multiple pathways associated with IVD degeneration. miR-766-3p, miR-6749-3p, and miR-4632-5p signature from serum may serve as a noninvasive diagnostic biomarker for LHD manifestation of IVD degeneration. Furthermore, several dysregulated miRNAs may be involved in the pathogenesis of IVD degeneration. Further study is needed to confirm the functional role of the identified miRNAs. MDPI 2020-12-08 /pmc/articles/PMC7762572/ /pubmed/33302347 http://dx.doi.org/10.3390/diagnostics10121063 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Cui, Shangbin
Zhou, Zhiyu
Liu, Xizhe
Richards, Robert Geoff
Alini, Mauro
Peng, Songlin
Liu, Shaoyu
Zou, Xuenong
Li, Zhen
Grad, Sibylle
Identification and Characterization of Serum microRNAs as Biomarkers for Human Disc Degeneration: An RNA Sequencing Analysis
title Identification and Characterization of Serum microRNAs as Biomarkers for Human Disc Degeneration: An RNA Sequencing Analysis
title_full Identification and Characterization of Serum microRNAs as Biomarkers for Human Disc Degeneration: An RNA Sequencing Analysis
title_fullStr Identification and Characterization of Serum microRNAs as Biomarkers for Human Disc Degeneration: An RNA Sequencing Analysis
title_full_unstemmed Identification and Characterization of Serum microRNAs as Biomarkers for Human Disc Degeneration: An RNA Sequencing Analysis
title_short Identification and Characterization of Serum microRNAs as Biomarkers for Human Disc Degeneration: An RNA Sequencing Analysis
title_sort identification and characterization of serum micrornas as biomarkers for human disc degeneration: an rna sequencing analysis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7762572/
https://www.ncbi.nlm.nih.gov/pubmed/33302347
http://dx.doi.org/10.3390/diagnostics10121063
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