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Identification and Verification of Key MiRNAs Associated with Intervertebral Disc Degeneration

BACKGROUND: Intervertebral Disc Degeneration (IDD) is a heterogeneous spinal disease whose underlying molecular mechanism is unclear. OBJECTIVES: This study aimed to identify, profile, and analyze microRNAs (miRNAs) related to IDD. METHODS: Microarray Gene Expression IDD data (GSE63492) were downloa...

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Detalles Bibliográficos
Autores principales: Liu, Jianwei, Li, Rong, Lyv, Peizhen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bentham Science Publishers 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10242762/
https://www.ncbi.nlm.nih.gov/pubmed/36111773
http://dx.doi.org/10.2174/1386207325666220915113438
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author Liu, Jianwei
Li, Rong
Lyv, Peizhen
author_facet Liu, Jianwei
Li, Rong
Lyv, Peizhen
author_sort Liu, Jianwei
collection PubMed
description BACKGROUND: Intervertebral Disc Degeneration (IDD) is a heterogeneous spinal disease whose underlying molecular mechanism is unclear. OBJECTIVES: This study aimed to identify, profile, and analyze microRNAs (miRNAs) related to IDD. METHODS: Microarray Gene Expression IDD data (GSE63492) were downloaded from Gene Expression Omnibus datasets. We employed Weighted Gene Co-Expression Network Analysis (WGCNA) to construct a miRNA co-expression network, and the miRNAs related to the IDD stage were detected. The number of differentially expressed miRNAs between normal and degenerated nucleus pulposus tissues was calculated. Twenty-three clinical specimens were used to validate the expression of miRNAs using qRT-PCR. RESULTS: WGCNA identified 48 miRNAs significantly related to the IDD stage, and 94 miRNAs that were significantly different between normal and degenerated nucleus pulposus tissues. We selected 32 overlapping miRNAs and identified 347 corresponding target genes. The integrative analysis revealed the biological function and pathways of these targeted genes. Analysis of clinical specimens validated that hsa-miR-4534 was upregulated in IDD, whereas hsa-miR-1827 and hsa-miR-185-5p were downregulated in IDD. CONCLUSION: This study has identified a subset of miRNAs that are related to IDD pathogenesis and hub miRNAs that are keys to the IDD co-expression network, which may potentially be utilized as indicators for treatment.
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spelling pubmed-102427622023-06-07 Identification and Verification of Key MiRNAs Associated with Intervertebral Disc Degeneration Liu, Jianwei Li, Rong Lyv, Peizhen Comb Chem High Throughput Screen Chemistry, Combinatorial Chemistry and High Throughput Screening, BIOCHEMICAL RESEARCH METHODS, Chemistry, APPLIED CHEMISTRY, Pharmacology BACKGROUND: Intervertebral Disc Degeneration (IDD) is a heterogeneous spinal disease whose underlying molecular mechanism is unclear. OBJECTIVES: This study aimed to identify, profile, and analyze microRNAs (miRNAs) related to IDD. METHODS: Microarray Gene Expression IDD data (GSE63492) were downloaded from Gene Expression Omnibus datasets. We employed Weighted Gene Co-Expression Network Analysis (WGCNA) to construct a miRNA co-expression network, and the miRNAs related to the IDD stage were detected. The number of differentially expressed miRNAs between normal and degenerated nucleus pulposus tissues was calculated. Twenty-three clinical specimens were used to validate the expression of miRNAs using qRT-PCR. RESULTS: WGCNA identified 48 miRNAs significantly related to the IDD stage, and 94 miRNAs that were significantly different between normal and degenerated nucleus pulposus tissues. We selected 32 overlapping miRNAs and identified 347 corresponding target genes. The integrative analysis revealed the biological function and pathways of these targeted genes. Analysis of clinical specimens validated that hsa-miR-4534 was upregulated in IDD, whereas hsa-miR-1827 and hsa-miR-185-5p were downregulated in IDD. CONCLUSION: This study has identified a subset of miRNAs that are related to IDD pathogenesis and hub miRNAs that are keys to the IDD co-expression network, which may potentially be utilized as indicators for treatment. Bentham Science Publishers 2023-04-27 2023-04-27 /pmc/articles/PMC10242762/ /pubmed/36111773 http://dx.doi.org/10.2174/1386207325666220915113438 Text en © 2023 Bentham Science Publishers https://creativecommons.org/licenses/by/4.0/This is an Open Access article published under CC BY 4.0 https://creativecommons.org/licenses/by/4.0/legalcode
spellingShingle Chemistry, Combinatorial Chemistry and High Throughput Screening, BIOCHEMICAL RESEARCH METHODS, Chemistry, APPLIED CHEMISTRY, Pharmacology
Liu, Jianwei
Li, Rong
Lyv, Peizhen
Identification and Verification of Key MiRNAs Associated with Intervertebral Disc Degeneration
title Identification and Verification of Key MiRNAs Associated with Intervertebral Disc Degeneration
title_full Identification and Verification of Key MiRNAs Associated with Intervertebral Disc Degeneration
title_fullStr Identification and Verification of Key MiRNAs Associated with Intervertebral Disc Degeneration
title_full_unstemmed Identification and Verification of Key MiRNAs Associated with Intervertebral Disc Degeneration
title_short Identification and Verification of Key MiRNAs Associated with Intervertebral Disc Degeneration
title_sort identification and verification of key mirnas associated with intervertebral disc degeneration
topic Chemistry, Combinatorial Chemistry and High Throughput Screening, BIOCHEMICAL RESEARCH METHODS, Chemistry, APPLIED CHEMISTRY, Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10242762/
https://www.ncbi.nlm.nih.gov/pubmed/36111773
http://dx.doi.org/10.2174/1386207325666220915113438
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AT lirong identificationandverificationofkeymirnasassociatedwithintervertebraldiscdegeneration
AT lyvpeizhen identificationandverificationofkeymirnasassociatedwithintervertebraldiscdegeneration