Isfahan University of Medical Sciences

Science Communicator Platform

Stay connected! Follow us on X network (Twitter):
Share this content! On (X network) By
Identification and Prediction of Common Molecular Culprits Between Psoriasis and Melanoma Via Bioinformatical Analysis Publisher



Mousavi SR1 ; Khosravian F2, 3, 4 ; Mondeali M5 ; Safi A1 ; Feizbakhshan S2, 3 ; Salmanizadeh S2, 3 ; Foroutan FS2, 3, 6 ; Ghaedi K7 ; Salehi M1, 2, 3
Authors
Show Affiliations
Authors Affiliations
  1. 1. Department of Medical Genetics, Faculty of Medicine, Tabriz University of Medical Sciences, Tabriz, Iran
  2. 2. Cellular, Molecular and Genetics Research Center, Isfahan University of Medical Sciences, Isfahan, Iran
  3. 3. Medical Genetics Research Center of Genome, Isfahan University of Medical Sciences, Isfahan, Iran
  4. 4. Department of Genetics and Molecular Biology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran
  5. 5. Department of Medical Genetics, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran
  6. 6. Legal Medicine Research Center, Legal Medicine Organization, Tehran, Iran
  7. 7. Department of Cell and Molecular Biology and Microbiology, Faculty of Biological Science and Technology, University of Isfahan, Isfahan, Iran

Source: Gene Reports Published:2021


Abstract

Background: Psoriasis is an autoimmune, chronic inflammatory dermatosis characterized by excessive hyperproliferation of keratinocytes, manifested by skin lesions. Melanoma is a type of skin cancer that develops from melanocytes. Growing epidemiology evidence has indicated psoriasis could be associated with melanoma. This study aims to explore the common molecular mechanisms that connect psoriasis with melanoma. Methods: Differentially expressed genes (DEGs) were obtained from melanoma and psoriasis GEO datasets. Next, using the GEO2R tool, common DEGs between melanoma and psoriasis samples were picked out. Finally, using in silico analysis, the hub genes and their significant molecular mechanisms were identified. Results: 244 DEGs (p < 0.05, │LogFC│ ≥ 1) were shared between psoriasis and melanoma. Of these, 116 were down-regulated, and 62 were up-regulated. In the protein-protein interaction (PPI) network, 19 DEGs were obtained as central nodes with criteria of interaction numbers and considered as hubs. Besides, the most crucial axis (module) among DEGs was predicted. Finally, Toll-like receptors and chemokine signaling pathways were identified as potential mechanisms underlying psoriasis and melanoma. Conclusion: This in-silico study may shed light on the molecular culprits that predispose psoriasis patients to melanoma. © 2021 Elsevier Inc.
Other Related Docs
12. Olfactory Receptors Contribute to Progression of Kidney Fibrosis, npj Systems Biology and Applications (2022)
14. Mir-193B Deregulation Is Associated With Parkinson's Disease, Journal of Cellular and Molecular Medicine (2021)