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Published on: December 6, 2016
Identifying Obstructive Sleep Apnea Syndrome-Associated Genes and Pathways through Weighted Gene Coexpression Network
1Department of Respiratory, Minhang Hospital, Fudan University, 170 Xinsong Road, Minhang District, Shanghai, China 201199.
Background:
Obstructive sleep apnea syndrome (OSAS) is the most common type of sleep apnea disorder. The disease seriously affects the patient's respiratory system. At present, the prognosis of the disease is poor and there is a lack of effective treatments. Therefore, it is urgent to explore its pathogenesis and treatment methods.
Method:
We downloaded a set of expression profile data from GSE75097 related to OSAS based on the Gene Expression Omnibus (GEO) database and selected the representative differentially expressed genes (DEGs) from the sample of the GSE75097 dataset. WGCNA was used to find genes related to OSAS and obtain coexpression modules. The Gene Ontology (GO) function and the Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway were used to analyze genes from key modules. Finally, Cytoscape software was used to construct a protein-protein interaction (PPI) network and analyze the hub genes.
Result:
We obtained a total of 7565 DEGs. Through WGCNA, we got four coexpression modules and the modules most related to OSAS were green-yellow, magenta, purple, and turquoise, and we screened out eight hub genes (DDX46, RNF115, COPA, FBXO4, PA2G4, NHP2L1, CDC20, and PCNA). GO and KEGG analyses indicated that the key modules were mainly enriched in tRNA modification, nucleobase metabolic process, DNA ligation, regulation of cellular component movement, basal transcription factors, Huntington disease, and vitamin digestion and absorption.
Conclusion:
These pathways and hub genes can facilitate understanding the molecular mechanism of OSAS and provide a meaningful reference for finding biological targets of OSAS treatment.
Insights
Obstructive sleep apnea syndrome (OSAS) research identified key genes and pathways. This study offers insights into OSAS molecular mechanisms and potential therapeutic targets for this common sleep disorder.
Area of Science:
- Genomics
- Molecular Biology
- Sleep Medicine
Background:
- Obstructive sleep apnea syndrome (OSAS) is a prevalent sleep disorder with significant respiratory impact.
- Current treatment options for OSAS are limited, and its prognosis is often poor.
- Understanding OSAS pathogenesis is crucial for developing effective therapies.
Purpose of the Study:
- To identify key molecular mechanisms and potential therapeutic targets for Obstructive sleep apnea syndrome (OSAS).
- To analyze differentially expressed genes (DEGs) and coexpression modules associated with OSAS.
- To investigate hub genes and enriched pathways in OSAS pathogenesis.
Main Methods:
- Downloaded and analyzed gene expression data (GSE75097) from the Gene Expression Omnibus (GEO) database.
- Utilized Weighted Gene Coexpression Network Analysis (WGCNA) to identify OSAS-related gene modules.
- Performed Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analyses.
- Constructed a protein-protein interaction (PPI) network to identify hub genes using Cytoscape.
Main Results:
- Identified 7565 differentially expressed genes (DEGs) in OSAS.
- Discovered four key coexpression modules (green-yellow, magenta, purple, turquoise) associated with OSAS via WGCNA.
- Screened eight hub genes (DDX46, RNF115, COPA, FBXO4, PA2G4, NHP2L1, CDC20, PCNA).
- Found enrichment in tRNA modification, nucleobase metabolism, DNA ligation, and basal transcription factors.
Conclusions:
- The identified hub genes and pathways provide a foundation for understanding OSAS molecular mechanisms.
- This research offers a valuable reference for discovering novel biological targets for OSAS treatment.
- Further investigation into these molecular players could lead to improved therapeutic strategies for OSAS.
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