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Bioinformatics analysis of neutrophil-associated hub genes and ceRNA network construction in septic cardiomyopathy
Qingfei Cao1, Jing Li2, Meixue Chen2
1Department of Urology, The First Affiliated Hospital of Jinzhou Medical University, Jinzhou, China.
Insights
Septic cardiomyopathy (SCM) involves heart dysfunction during sepsis. This study identifies MRC1 as a key neutrophil-related gene involved in SCM, offering potential biomarkers for early diagnosis and treatment.
Area of Science:
- Cardiology
- Immunology
- Molecular Biology
Background:
- Septic cardiomyopathy (SCM) is a serious sepsis complication causing cardiac depression.
- Neutrophils play a role in sepsis-induced organ damage, but their specific function in SCM is unclear.
- Identifying Neutrophil-Related Genes (NRGs) is crucial for understanding SCM and finding diagnostic/treatment biomarkers.
Purpose of the Study:
- To investigate the role of Neutrophil-Related Genes (NRGs) in the pathogenesis of septic cardiomyopathy (SCM).
- To identify potential diagnostic and therapeutic biomarkers for SCM based on NRGs.
- To elucidate the molecular mechanisms involving neutrophils in SCM.
Main Methods:
- Differential gene expression analysis of datasets GSE79962 and GSE44363 to identify shared DEGs.
- Utilized Cytoscape software and the cytoHubba plugin to pinpoint hub DEGs.
- Integrated hub DEGs with NRGs from WGCNA to identify the Neutrophil-Related Hub Gene (NRHG) MRC1.
- Validated MRC1 expression in SCM using internal and external datasets.
- Constructed and validated a neutrophil-related competing endogenous RNA (ceRNA) network (AC145207.5/miR-23a-3p/MRC1).
Main Results:
- Identified shared differentially expressed genes (DEGs) between sepsis and control groups.
- Pinpointed MRC1 as a key Neutrophil-Related Hub Gene (NRHG) implicated in SCM.
- Confirmed abnormal expression of MRC1 in SCM patients through validation studies.
- Established a functional neutrophil-related ceRNA network involving AC145207.5, miR-23a-3p, and MRC1.
Conclusions:
- MRC1 is identified as a potential NRHG contributing to SCM pathogenesis.
- The study provides insights into neutrophil-mediated mechanisms underlying SCM.
- MRC1 emerges as a promising molecular target for the early diagnosis and therapeutic intervention of SCM.
Abstract:
Septic cardiomyopathy (SCM) is a critical sepsis complication characterized by reversible cardiac depression during early septic shock. Neutrophils, integral to innate immunity, can mediate organ damage when abnormal, but their specific role in sepsis-induced myocardial damage remains elusive. Our study focuses on elucidating the role of Neutrophil-Related Genes (NRGs) in SCM, finding early diagnosis and treatment biomarkers. We identified shared differentially expressed genes (DEGs) from datasets GSE79962 and GSE44363 and pinpointed hub DEGs using the cytoHubba plugin in Cytoscape software. The Neutrophil-Related Hub Gene (NRHG) MRC1 was identified via intersecting hub DEGs with NRGs from WGCNA. We validated MRC1's abnormal expression in SCM using our data and external datasets. Furthermore, a neutrophil-related ceRNA network (AC145207.5/ miR-23a-3p/MRC1) was constructed and validated. Our findings reveal MRC1 as a potential NRHG in SCM pathogenesis, offering insights into neutrophil-mediated mechanisms in SCM and providing a novel molecular target for early diagnosis and intervention in SCM.
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