Identification of Potential Key Genes Involved in the Carotid Atherosclerosis
Youshi Meng1,2, Chunli Zhang1,2, Lucong Liang1,2
1Department of Neurology, The Fifth Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi, 530022, People's Republic of China.
Purpose:
Carotid atherosclerosis is a kind of systemic atherosclerosis in the carotid arteries. However, the efficiency of treatment is insufficient. Therefore, it is urgent to find therapeutic targets and deepen the understanding of carotid atherosclerosis.
Materials And Methods:
In this study, we analyzed differentially expressed genes (DEGs) between atheroma plaque and macroscopically intact tissue (control samples). Furthermore, we performed Gene Ontology (GO) and Kyoto Encyclopedia of Gene and Genomes (KEGG) enrichment analysis based on the DEGs. Four methods were used to identify the hub genes in the protein-protein interaction networks of the DEGs. Furthermore, we also performed network module analysis to reveal carotid atherosclerosis-related gene modules and biological functions.
Results:
The enrichment results showed that the biological functions were related to inflammation, immunity, chemokine and cell adhesion molecule, such as PIK-Akt signaling pathway, Rap1 signaling pathway, MAPK signaling pathway, NOD-like receptor signaling pathway and B cell receptor signaling pathway. In addition, we screened the hub genes. A total of 16 up-regulated genes (C3AR1, CCR1, CCR2, CD33, CD53, CXCL10, CXCL8, CXCR4, CYBB, FCER1G, FPR2, ITGAL, ITGAM, ITGAX, ITGB2, and LILRB2) were identified as hub genes. A total of 5 gene modules were obtained. We found that biological functions obtained for each cluster were mostly related to immunity, chemokines and cell adhesion molecules.
Conclusion:
The present study identified key DEGs in atheroma plaque compared with control samples. The key genes involved in the development of carotid atherosclerosis may provide valuable therapeutic targets for carotid atherosclerosis.
Insights
Researchers identified key genes involved in carotid atherosclerosis by analyzing gene expression differences. These findings offer potential new therapeutic targets for this systemic vascular disease.
Area of Science:
- Cardiovascular Biology
- Molecular Biology
- Genomics
Background:
- Carotid atherosclerosis is a systemic vascular disease affecting carotid arteries.
- Current treatments for carotid atherosclerosis have limited efficacy.
- Understanding the molecular mechanisms underlying carotid atherosclerosis is crucial for developing new therapies.
Purpose of the Study:
- To identify key differentially expressed genes (DEGs) in carotid atheroma plaque compared to control tissues.
- To elucidate the biological functions and pathways associated with these DEGs.
- To discover potential therapeutic targets for carotid atherosclerosis.
Main Methods:
- Differential gene expression analysis between atheroma plaque and control samples.
- Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment analyses of DEGs.
- Identification of hub genes using four network analysis methods.
- Network module analysis to identify disease-related gene clusters.
Main Results:
- Enrichment analysis revealed significant involvement of inflammation, immunity, chemokines, and cell adhesion molecules.
- Key signaling pathways identified include PI3K-Akt, Rap1, MAPK, NOD-like receptor, and B cell receptor signaling.
- Sixteen upregulated hub genes were identified, including C3AR1, CCR1, CCR2, CD33, CD53, CXCL10, CXCL8, CXCR4, CYBB, FCER1G, FPR2, ITGAL, ITGAM, ITGAX, ITGB2, and LILRB2.
- Five gene modules related to immunity, chemokines, and cell adhesion were identified.
Conclusions:
- This study identified critical DEGs in carotid atheroma plaque.
- The identified key genes and pathways are implicated in the development of carotid atherosclerosis.
- These findings provide potential novel therapeutic targets for managing carotid atherosclerosis.
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