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Studies on the Role of circRNAs in Osteoarthritis
Insights
Circular RNAs (circRNAs) are increasingly studied for their role in osteoarthritis (OA) mechanisms. CircRNA VWF shows promise as a diagnostic biomarker for OA.
Area of Science:
- Molecular Biology
- Genetics
- Biochemistry
Background:
- Osteoarthritis (OA) is a degenerative joint disease with complex molecular underpinnings.
- Circular RNAs (circRNAs) have emerged as key regulators in various biological processes, including disease pathogenesis.
- Understanding the role of circRNAs in OA is crucial for developing novel diagnostic and therapeutic strategies.
Purpose of the Study:
- To elucidate the regulatory mechanisms of circRNAs in osteoarthritis (OA).
- To identify potential clinical applications of circRNAs in OA diagnosis and treatment.
Main Methods:
- Systematic review of recent literature (5 years) on circRNAs and OA.
- Differential expression analysis of circRNAs in OA.
- Bioinformatic analyses including Protein-Protein Interaction (PPI), Gene Ontology (GO), and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analysis.
- Identification of key circRNAs and associated signaling pathways.
Main Results:
- 33 studies were included, identifying 27 upregulated and 8 downregulated circRNAs in OA.
- 31 circRNAs were analyzed via PPI, GO, and KEGG, revealing significant interactions and functions.
- Vascular Endothelial Growth Factor (VWF) exhibited prominent node and edge size in PPI and major functions in GO and KEGG analyses.
- Enrichment analysis identified PI3K/AKT, human papillomavirus infection (HPI), and focal adhesion (FA) pathways as significantly associated with circRNAs in OA.
Conclusions:
- Recent research on circRNAs in OA primarily focuses on their regulatory mechanisms, particularly circ-miRNA sponge activity.
- Extracellular Matrix (ECM) and PI3K/AKT/mTOR signaling pathways are frequently implicated in circRNA functions related to OA.
- CircRNA VWF demonstrates significant potential as a biomarker for OA detection due to its functions and interactions.
Objective:
Provide a reference to elucidate the mechanism of circRNAs regulating osteoarthritis (OA) and the clinical treatment.
Methods:
Herein, articles about circRNAs (hsa-circ) and osteoarthritis in the recent 5 years have been reviewed and the differential expression and regulatory effect of circRNAs in OA deduced. Based on these conclusions and Protein-Protein Interaction (PPI), Gene Ontology (GO), and Kyoto Encyclopedia of Genes and Genomes (KEGG) analyses of the acquired circRNAs, the potential functions and interactions of circRNAs in OA and the involved signaling pathways are discussed.
Results:
A total of 33 studies meeting the inclusion criteria were included in this study, and 27 circRNAs were upregulated and 8 circRNAs were downregulated in OA. A total of 31 circRNAs were finally included in the PPI, GO, and KEGG analyses. From PPI, 12 map nodes and 7 map edges were interrelated. VWF had the biggest node and edge size. From GO, VWF showed a majority of the functions. From KEGG, circRNAs are enriched in PI3K/AKT, human papillomavirus infection (HPI), and focal adhesion (FA) pathways, and VWF was involved in major pathways.
Conclusion:
We found that most articles about circRNAs regulating OA in the recent 5 years focused on the mechanism, especially the absorption effect of circ-miRNA as sponges in the recent 2 years, while most of the articles about their functions addressed ECM and PI3K, AKT, and mTOR signaling pathways. Future studies might focus on the functions of circRNAs, and circRNA VWF, with preferable functions, interactions, and involvement, can be used as a biological indicator to detect OA in clinical practice.
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