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Deciphering the Molecular Basis of Systemic Manifestations in Cutaneous Leishmaniasis Using Integrated Bioinformatics
Zeinab Dehghan1, Zeinab Zarei-Behjani2, Masoud Rezaei3
1Autoimmune Diseases Research Center, Shiraz University of Medical Sciences, Shiraz, Iran. dehghan8590@gmail.com.
Acta Parasitologica
|June 1, 2026
Summary
Bioinformatics identified key genes like ICAM1 and CD274 in cutaneous leishmaniasis systemic disease. This research reveals molecular pathways and potential therapeutic targets for this neglected parasitic infection.
Area of Science:
- Parasitology
- Bioinformatics
- Molecular Biology
Background:
- Cutaneous leishmaniasis (CL) is a neglected parasitic disease causing skin lesions and potential systemic effects.
- Understanding the molecular basis of CL systemic manifestations is crucial for effective treatment.
Purpose of the Study:
- To identify key molecular markers and mechanisms in cutaneous leishmaniasis systemic disease using bioinformatics.
- To analyze gene expression data from CL patients to uncover pathways driving systemic involvement.
Main Methods:
- Utilized bioinformatics to analyze gene expression datasets from the GEO database.
- Constructed protein-protein interaction and gene regulatory networks using STRING, HIPPIE, and miRTarBase.
- Identified key genes through network centrality analysis and performed functional enrichment using DAVID.
Main Results:
- Identified 221 differentially expressed genes (192 up-regulated, 29 down-regulated).
- Network analysis pinpointed critical genes including ICAM1, CD274, BIRC3, EZH2, and CTLA4.
- Key genes are implicated in apoptosis, autophagy, immune regulation, and TNF signaling pathways.
Conclusions:
- This study provides molecular insights into cutaneous leishmaniasis systemic effects.
- Identified potential biomarkers and therapeutic targets for targeted treatment development.
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