Identification of lncRNA–miRNA–mRNA regulatory network associated with primary open angle glaucoma

Abstract Background Primary open angle glaucoma (POAG) is a multifactorial disorder characterized by a progressive permanent degeneration of retinal ganglion cell (RGCs) death. An increasing number of studies have suggested that long noncoding RNAs (lncRNAs) have the ability to regulate gene express...

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Main Authors: Minwen Zhou, Bing Lu, Wei Tan, Mingshui Fu
Format: Article
Language:English
Published: BMC 2020-03-01
Series:BMC Ophthalmology
Subjects:
Online Access:http://link.springer.com/article/10.1186/s12886-020-01365-5
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author Minwen Zhou
Bing Lu
Wei Tan
Mingshui Fu
author_facet Minwen Zhou
Bing Lu
Wei Tan
Mingshui Fu
author_sort Minwen Zhou
collection DOAJ
description Abstract Background Primary open angle glaucoma (POAG) is a multifactorial disorder characterized by a progressive permanent degeneration of retinal ganglion cell (RGCs) death. An increasing number of studies have suggested that long noncoding RNAs (lncRNAs) have the ability to regulate gene expression; however, thus far, the mechanisms and functions of lncRNAs in the development of POAG are still unclear. Methods Using the data from Gene Expression Omnibus (GEO), differentially expressed lncRNAs and differentially expressed mRNAs between POAG patients and controls were identified. Then, the lncRNA–miRNA–mRNA competing endogenous RNA (ceRNA) network was constructed, and the key lncRNAs in POAG were identified. A Gene Ontology (GO) analysis and a Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analysis were performed to assess the enriched biological functions of mRNA in the ceRNA network. Results During this study, a POAG-related ceRNA network with 37 miRNA nodes, 248 lncRNA nodes, 178 mRNA nodes, and 1985 edges was constructed. In addition, four lncRNAs (DNAJC27-AS1, AF121898, OIP5-AS1, and SNX29P2) were established as hub RNAs in this ceRNA network. The functional assay showed that 18 GO terms and 17 pathways were enriched. Conclusion This study provides novel insights into the lncRNA-related ceRNA network in POAG, and the four lncRNAs were identified in the development of POAG.
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spelling doaj.art-82685af724a243338a709d0e862a8d782022-12-22T01:34:33ZengBMCBMC Ophthalmology1471-24152020-03-012011910.1186/s12886-020-01365-5Identification of lncRNA–miRNA–mRNA regulatory network associated with primary open angle glaucomaMinwen Zhou0Bing Lu1Wei Tan2Mingshui Fu3Department of Ophthalmology, Shanghai General Hospital (Shanghai First People’s Hospital), Shanghai Jiao Tong University School of MedicineDepartment of Ophthalmology, Shanghai General Hospital (Shanghai First People’s Hospital), Shanghai Jiao Tong University School of MedicineThe Department of Ophthalmology, The Third Affiliated Hospital of Zunyi Medical UniversityDepartment of Ophthalmology, Shanghai General Hospital (Shanghai First People’s Hospital), Shanghai Jiao Tong University School of MedicineAbstract Background Primary open angle glaucoma (POAG) is a multifactorial disorder characterized by a progressive permanent degeneration of retinal ganglion cell (RGCs) death. An increasing number of studies have suggested that long noncoding RNAs (lncRNAs) have the ability to regulate gene expression; however, thus far, the mechanisms and functions of lncRNAs in the development of POAG are still unclear. Methods Using the data from Gene Expression Omnibus (GEO), differentially expressed lncRNAs and differentially expressed mRNAs between POAG patients and controls were identified. Then, the lncRNA–miRNA–mRNA competing endogenous RNA (ceRNA) network was constructed, and the key lncRNAs in POAG were identified. A Gene Ontology (GO) analysis and a Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analysis were performed to assess the enriched biological functions of mRNA in the ceRNA network. Results During this study, a POAG-related ceRNA network with 37 miRNA nodes, 248 lncRNA nodes, 178 mRNA nodes, and 1985 edges was constructed. In addition, four lncRNAs (DNAJC27-AS1, AF121898, OIP5-AS1, and SNX29P2) were established as hub RNAs in this ceRNA network. The functional assay showed that 18 GO terms and 17 pathways were enriched. Conclusion This study provides novel insights into the lncRNA-related ceRNA network in POAG, and the four lncRNAs were identified in the development of POAG.http://link.springer.com/article/10.1186/s12886-020-01365-5Primary open angle glaucomaLong noncoding RNAlncRNA-miRNA-mRNA regulatory network
spellingShingle Minwen Zhou
Bing Lu
Wei Tan
Mingshui Fu
Identification of lncRNA–miRNA–mRNA regulatory network associated with primary open angle glaucoma
BMC Ophthalmology
Primary open angle glaucoma
Long noncoding RNA
lncRNA-miRNA-mRNA regulatory network
title Identification of lncRNA–miRNA–mRNA regulatory network associated with primary open angle glaucoma
title_full Identification of lncRNA–miRNA–mRNA regulatory network associated with primary open angle glaucoma
title_fullStr Identification of lncRNA–miRNA–mRNA regulatory network associated with primary open angle glaucoma
title_full_unstemmed Identification of lncRNA–miRNA–mRNA regulatory network associated with primary open angle glaucoma
title_short Identification of lncRNA–miRNA–mRNA regulatory network associated with primary open angle glaucoma
title_sort identification of lncrna mirna mrna regulatory network associated with primary open angle glaucoma
topic Primary open angle glaucoma
Long noncoding RNA
lncRNA-miRNA-mRNA regulatory network
url http://link.springer.com/article/10.1186/s12886-020-01365-5
work_keys_str_mv AT minwenzhou identificationoflncrnamirnamrnaregulatorynetworkassociatedwithprimaryopenangleglaucoma
AT binglu identificationoflncrnamirnamrnaregulatorynetworkassociatedwithprimaryopenangleglaucoma
AT weitan identificationoflncrnamirnamrnaregulatorynetworkassociatedwithprimaryopenangleglaucoma
AT mingshuifu identificationoflncrnamirnamrnaregulatorynetworkassociatedwithprimaryopenangleglaucoma