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

被引:10
作者
Cui, Shangbin [1 ,2 ]
Zhou, Zhiyu [1 ,3 ]
Liu, Xizhe [1 ]
Richards, Robert Geoff [1 ,2 ]
Alini, Mauro [2 ]
Peng, Songlin [4 ]
Liu, Shaoyu [1 ,3 ,4 ]
Zou, Xuenong [1 ]
Li, Zhen [2 ]
Grad, Sibylle [2 ]
机构
[1] Sun Yat Sen Univ, Affiliated Hosp 1, Guangdong Prov Key Lab Orthoped & Traumatol, Guangzhou 510000, Peoples R China
[2] AO Res Inst Davos, CH-7270 Davos, Switzerland
[3] Sun Yat Sen Univ, Affiliated Hosp 7, Shenzhen 518107, Peoples R China
[4] Shenzhen Peoples Hosp, Dept Spine Surg, Shenzhen 518020, Peoples R China
基金
中国国家自然科学基金;
关键词
circulating microRNA; intervertebral disc; degeneration; disc herniation; biomarker; CIRCULATING MICRORNAS; MICROARRAY ANALYSIS; EXPRESSION; CELLS; PROTEIN; INFLAMMATION; DISEASE; KINASE; GENES;
D O I
10.3390/diagnostics10121063
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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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页数:22
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