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• W2904348526 abstract "Osteoarthritis (OA) is one of the most common degenerative diseases of the joints worldwide, but still the pathogenesis of OA is largely unknown. The purpose of our study is to clarify key candidate genes and relevant signaling pathways in a surgical-induced OA rat model. The microarray raw data of GSE8077 was downloaded from GEO datasets. GeoDiver were employed to screen differentially-expressed genes (DEGs). Enrichment analyses of DEGs were performed using Metascape. Construction of protein–protein interaction (PPI) network and identification of key genes were conducted using STRING, Cytoscape v3.6.0, and Centiscape2.2. Furthermore, miRDB and Cytoscape v3.6.0 were used for visualization of miRNA-mRNA regulatory network. Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analysis for predicted miRNAs was undertaken using DIANA-miRPath v3.0. Several DEGs (188 in comparison between OA and sham-operated group and 160 in comparison between OA and contralateral group) were identified. DEGs mainly enriched in vasculature development, regulation of cell migration, response to growth factor (Gene ontology), and ECM-receptor interaction (KEGG). Two comparison cohorts shared 79 intersection genes, and of these, Ccl2, Col4a1, Col1a1, Aldh1a3, and Itga8 were defined as the hub genes. Predicted miRNAs of seven DEGs from sub-networks mainly enriched in MAPK signaling pathway. The current study shows that some key genes and pathways, such as Ccl2, Col4a1, Col1a1, Aldh1a3, Itga8, ECM-receptor interaction, and MAPK signaling pathway may be associated with OA progression and act as potential biomarkers and therapeutic targets for OA." @default.
• W2904348526 created "2018-12-22" @default.
• W2904348526 creator A5056422933 @default.
• W2904348526 creator A5057348901 @default.
• W2904348526 date "2018-12-01" @default.
• W2904348526 modified "2023-10-18" @default.
• W2904348526 title "Transcriptome analyses identify key genes and potential mechanisms in a rat model of osteoarthritis" @default.
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• W2904348526 doi "https://doi.org/10.1186/s13018-018-1019-3" @default.
• W2904348526 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/6295024" @default.
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• W2904348526 hasPublicationYear "2018" @default.
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