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Network analysis of potential risk genes for psoriasis
Huilin Wang1, Wenjun Chen1, Jin He1
1Department of Dermatology, General Hospital of Xinjiang Military Command, No. 359 Youhao North Road, Saybak District, Urumqi, 830001, Xinjiang, China.
This study identifies key genes and molecular pathways involved in psoriasis, a chronic inflammatory skin condition. CXCL9, SPRR1B, TGM6, and S100A9 show potential as diagnostic and therapeutic targets for psoriasis.
Area of Science:
- Dermatology
- Immunology
- Genetics
Background:
- Psoriasis is a complex chronic inflammatory skin disease.
- Understanding its genetic and molecular underpinnings is crucial for effective management.
Purpose of the Study:
- To identify potential risk genes and molecular mechanisms associated with psoriasis.
- To explore gene expression and methylation patterns in psoriatic skin.
Main Methods:
- Analysis of gene expression datasets (GSE54456, GSE114286, GSE121212) to identify differentially expressed genes (DEGs).
- Enrichment analysis and protein-protein interaction (PPI) network construction to identify hub genes.
- Logistic regression and nomogram analysis to evaluate gene risk for psoriasis.
- Analysis of methylation data (GSE115797) to identify methylation markers.
Main Results:
- 118 common DEGs were identified, primarily linked to keratinocyte differentiation and the IL-17 signaling pathway.
- CXCL9 and SPRR1B were identified as potential risk factors for psoriasis based on high expression and hub gene analysis.
- TGM6 and S100A9 were associated with increased psoriasis risk, supported by nomogram analysis and methylation markers.
Conclusions:
- Immune and inflammatory responses are active in the keratinocytes of psoriatic skin.
- CXCL9, SPRR1B, TGM6, and S100A9 represent potential diagnostic and therapeutic targets for psoriasis.
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