AI Article Synopsis
- - Sickle cell disease (SCD) is caused by genetic defects affecting globin chains, and this study investigated the genes and pathways involved in its development.
- - Researchers analyzed microarray data to identify differentially expressed genes (DEGs) and found 447 DEGs in SCD patients, with 345 up-regulated and 102 down-regulated genes.
- - The study suggests that understanding these hub genes can aid in diagnosing high-risk SCD patients and developing tailored treatment strategies.
Article Abstract
Background: Sickle cell disease (SCD) is one of the hematological disorders characterized by a defect in the structure and function of globin chains. Hereditary factors play an important role in the pathogenesis of SCD. We aimed to investigate the genes and pathways related to the pathogenesis of SCD.
Methods: Microarray dataset was downloaded from the Gene Expression Omnibus (GEO) database. LIMMA package of R-software was used to detect UP and Down regulations between SCD and control subjects. Enrichment analysis and Protein-protein interaction (PPI) networks were performed using GeneCodis4 software and GeneMANIA database, respectively. PrognoScan database was used to evaluate the relationship between the hub genes and patients' survival.
Results: Overall, 447 DEGs were identified in SCD patients compared to control subjects. Out of 447 DEGs, 345 genes were up-regulated and 102 genes were down-regulated. Effective hub genes in SCD pathogenesis include and . In addition, hub genes had a high diagnostic value.
Conclusion: Evaluation of hub genes in SCD can be used as a diagnostic panel to detect high-risk patients. In addition, by identifying the UP and Down stream pathways, treatment strategies in the monitoring and treatment of patients can be designed.
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| http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11488559 | PMC |
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