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Identifying the hub genes and immune infiltration related to pyroptosis in rheumatoid arthritis
1Department of Orthopedics, Minzu Hospital of Guangxi Zhuang Autonomous Region, Nanning, China.
Abstract:
Rheumatoid arthritis (RA) is one of the most common autoimmune joint disorders globally, but its pathophysiological mechanisms have not been thoroughly investigated. Pyroptosis significantly correlates with programmed cell death. However, targeting pyroptosis has not been considered as a therapeutic strategy in RA due to a lack of systematic studies on validated biomarkers. The present study aimed to identify hub pyroptosis biomarkers and immune infiltration in RA. The gene expression profiles of synovial tissues were obtained from the Gene Expression Omnibus (GEO) database to identify differentially expressed pyroptosis genes (DEPGs). Meanwhile, the CIBERSORT algorithm was used to explore the association between immune infiltration and RA. Consequently, two hub DEPGs (EGFR and JUN) were identified as critical genes in RA. Through gene ontology and pathway enrichment analysis. EGFR and JUN were found to be primarily involved in the ErbB signaling pathway, PD-1 checkpoint pathway, GnRH signaling pathway, etc. Furthermore, for immune infiltration analysis, the pyroptosis genes EGFR and JUN were closely connected with four and one immune cell types, respectively. Overall, this study presents a novel method to identify hub DEPGs and their correlation with immune infiltration, which may provide novel perspectives into the diagnosis and treatment of patients with RA.
Insights
This study identifies key pyroptosis biomarkers, EGFR and JUN, in rheumatoid arthritis (RA). These findings offer new insights into RA
Area of Science:
- Immunology
- Genetics
- Molecular Biology
Background:
- Rheumatoid arthritis (RA) is a prevalent autoimmune joint disorder with incompletely understood mechanisms.
- Pyroptosis, a form of programmed cell death, is linked to RA pathogenesis.
- Validated biomarkers for targeting pyroptosis in RA therapy are lacking.
Purpose of the Study:
- To identify crucial pyroptosis biomarkers in rheumatoid arthritis (RA).
- To investigate the relationship between pyroptosis and immune cell infiltration in RA.
- To explore potential therapeutic targets for RA based on pyroptosis pathways.
Main Methods:
- Utilized Gene Expression Omnibus (GEO) database for synovial tissue gene expression profiles.
- Identified differentially expressed pyroptosis genes (DEPGs) in RA.
- Employed the CIBERSORT algorithm to analyze immune infiltration patterns.
- Performed Gene Ontology and pathway enrichment analyses for identified hub genes.
Main Results:
- Identified EGFR and JUN as two hub differentially expressed pyroptosis genes (DEPGs) in RA.
- EGFR and JUN are implicated in signaling pathways including ErbB, PD-1 checkpoint, and GnRH.
- Found significant correlations between pyroptosis genes (EGFR, JUN) and specific immune cell types.
Conclusions:
- This study introduces a novel approach to pinpointing hub DEPGs in RA.
- Identified EGFR and JUN as critical genes linking pyroptosis and immune infiltration in RA.
- Findings may offer new diagnostic and therapeutic strategies for rheumatoid arthritis patients.
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