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microRNA-9 might be a novel protective factor for osteoarthritis patients

BACKGROUND: The study aimed to identify the targeting genes and miRNAs using the microarray expression profile dataset for Osteoarthritis (OA) patients. Differentially expressed genes (DEGs) between OA and control samples were identified using Bayes method of limma package. Subsequently, a protein-p...

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Autores principales: Jiang, Lei, Sun, Xu, Kong, Hongyang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7178977/
https://www.ncbi.nlm.nih.gov/pubmed/32321579
http://dx.doi.org/10.1186/s41065-020-00128-y
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author Jiang, Lei
Sun, Xu
Kong, Hongyang
author_facet Jiang, Lei
Sun, Xu
Kong, Hongyang
author_sort Jiang, Lei
collection PubMed
description BACKGROUND: The study aimed to identify the targeting genes and miRNAs using the microarray expression profile dataset for Osteoarthritis (OA) patients. Differentially expressed genes (DEGs) between OA and control samples were identified using Bayes method of limma package. Subsequently, a protein-protein interaction (PPI) network was constructed. miRNAs and transcription factor (TFs) based on DEGs in PPI network were identified using Webgestalt and ENCODE, respectively. Finally, MCODE, Gene Ontology (GO) function, and Kyoto Encyclopedia of Genes and Genomes (KEGG) were performed. The expressions of several DEGs and predicted miRNAs in OA rats were detected by RT-PCR. RESULTS: A total of 594 DEGs were identified. In PPI network, there were 313 upregulated DEGs and 22 downregulated DEGs. Besides, the regulatory relationships included 467 upregulated interactions and 85 downregulated interactions (miR-124A → QKI and MAP 1B) between miRNA and DEGs in PPI network. The module from downregulated DEGs-TFs-miRNA networks was mainly enriched to low-density lipoprotein particle clearance, response to linoleic acid, and small molecule metabolic process BP terms. Moreover, QKI, MAP 1B mRNA and miR-9 expressions were significantly reduced in OA rats. CONCLUSION: miR-9 might be a protective factor for OA patients via inhibiting proliferation and differentiation of cartilage progenitor cells. miR-124A might play an important role in progression of OA through targeting QKI and MAP 1B.
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spelling pubmed-71789772020-04-26 microRNA-9 might be a novel protective factor for osteoarthritis patients Jiang, Lei Sun, Xu Kong, Hongyang Hereditas Research BACKGROUND: The study aimed to identify the targeting genes and miRNAs using the microarray expression profile dataset for Osteoarthritis (OA) patients. Differentially expressed genes (DEGs) between OA and control samples were identified using Bayes method of limma package. Subsequently, a protein-protein interaction (PPI) network was constructed. miRNAs and transcription factor (TFs) based on DEGs in PPI network were identified using Webgestalt and ENCODE, respectively. Finally, MCODE, Gene Ontology (GO) function, and Kyoto Encyclopedia of Genes and Genomes (KEGG) were performed. The expressions of several DEGs and predicted miRNAs in OA rats were detected by RT-PCR. RESULTS: A total of 594 DEGs were identified. In PPI network, there were 313 upregulated DEGs and 22 downregulated DEGs. Besides, the regulatory relationships included 467 upregulated interactions and 85 downregulated interactions (miR-124A → QKI and MAP 1B) between miRNA and DEGs in PPI network. The module from downregulated DEGs-TFs-miRNA networks was mainly enriched to low-density lipoprotein particle clearance, response to linoleic acid, and small molecule metabolic process BP terms. Moreover, QKI, MAP 1B mRNA and miR-9 expressions were significantly reduced in OA rats. CONCLUSION: miR-9 might be a protective factor for OA patients via inhibiting proliferation and differentiation of cartilage progenitor cells. miR-124A might play an important role in progression of OA through targeting QKI and MAP 1B. BioMed Central 2020-04-22 /pmc/articles/PMC7178977/ /pubmed/32321579 http://dx.doi.org/10.1186/s41065-020-00128-y Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Jiang, Lei
Sun, Xu
Kong, Hongyang
microRNA-9 might be a novel protective factor for osteoarthritis patients
title microRNA-9 might be a novel protective factor for osteoarthritis patients
title_full microRNA-9 might be a novel protective factor for osteoarthritis patients
title_fullStr microRNA-9 might be a novel protective factor for osteoarthritis patients
title_full_unstemmed microRNA-9 might be a novel protective factor for osteoarthritis patients
title_short microRNA-9 might be a novel protective factor for osteoarthritis patients
title_sort microrna-9 might be a novel protective factor for osteoarthritis patients
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7178977/
https://www.ncbi.nlm.nih.gov/pubmed/32321579
http://dx.doi.org/10.1186/s41065-020-00128-y
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