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JCR 2016
جستجوی مقالات
یکشنبه 23 آذر 1404
Iranian Biomedical Journal
، جلد ۲۸، شماره ۴، صفحات ۱۷۹-۱۹۱
عنوان فارسی
چکیده فارسی مقاله
کلیدواژههای فارسی مقاله
عنوان انگلیسی
Deciphering Molecular Mechanisms of Cutaneous Leishmaniasis, Pathogenesis and Drug Repurposing through Systems Biology
چکیده انگلیسی مقاله
Background:
Cutaneous leishmaniasis (CL) is a major health problem caused by an intracellular pathogen of the genus
Leishmania
. CL results in morphologically distinct skin injuries, ranging from nodules to plaques and ulcers, which persist as a recuperating incessant injury depending on the type of contaminating parasite. There is still no effective treatment to reduce the skin lesions in patients infected with CL. The aim of this study was to develop strategies to treat skin lesions in CL patients.
Methods:
We retrieved the transcriptomic data of skin lesions from patients with CL and normal skin from the
g
ene Expression Omnibus (GEO) database. The
protein-protein interaction network
(PPIN) was constructed using the STRING database and Cytoscape v3.10.1 software. Critical genes were identified by topological network analysis and cluster detection. Finally, gene ontology and repurposing drugs for critical genes were determined.
Results:
CD8A, IFNG, IL-6, PTPRC, CCR7, TLR2, GSTA5, CYBB, IL-12RB2,
ITGB2, FCGR3A, CTLA4, and IFNG
were identified as the critical genes in PPIN
and subnetworks.
Enrichment analysis revealed that T-cell receptor signaling, toll-like receptor signaling, cytokine-cytokine receptor interaction, graft-versus-host disease, leishmaniasis, chemokine signaling, primary immunodeficiency, and Th17 cell differentiation were the major pathways associated with critical genes.
The drug repurposing results identified cyclosporine, rituximab, infliximab, blinatumomab, and methylprednisolone as candidates for treatment of CL.
Conclusion:
After validating our model with available experimental data, we found that critical molecules and drug candidates play a crucial role in the treatment of skin lesions caused by Leishmania in prospective studies.
کلیدواژههای انگلیسی مقاله
Cutaneous leishmaniasis, Gene ontology, Repurpose drug, Systems biology
نویسندگان مقاله
| Fatemeh Saberi
Student Research Committee, Department of Medical Biotechnology, School of Advanced Technologies in Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran
| Zeinab Dehghan
Department of Comparative Biomedical Sciences, School of Advanced Medical Sciences and Technologies, Shiraz University of Medical Sciences, Shiraz, Iran
| Zahra Taheri
Department of Biology and Biotechnology, Pavia University, Pavia, Italy
| Tayyebeh Pilehchi
Student Research Committee, Department of Medical Biotechnology, School of Advanced Technologies in Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran
| Hakimeh Zali
Department of Tissue Engineering and Applied Cell Sciences, School of Advanced Technologies in Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran
نشانی اینترنتی
http://ibj.pasteur.ac.ir/browse.php?a_code=A-10-5777-1&slc_lang=en&sid=1
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زبان مقاله منتشر شده
en
موضوعات مقاله منتشر شده
Molecular Genetics & Genomics
نوع مقاله منتشر شده
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