Tehran University of Medical Sciences

Science Communicator Platform

Stay connected! Follow us on X network (Twitter):
Share this content! On (X network) By
Identification of Celecoxib-Targeted Proteins Using Label-Free Thermal Proteome Profiling on Rat Hippocampus Publisher Pubmed



Gholizadeh E1 ; Karbalaei R2 ; Khaleghian A1 ; Salimi M3 ; Gilany K4 ; Soliymani R5 ; Tanoli Z6 ; Rezadoost H7 ; Baumann M5 ; Jafari M6 ; Tang J6
Authors
Show Affiliations
Authors Affiliations
  1. 1. Department of Biochemistry, Faculty of Medicine, Semnan University of Medical Sciences, Semnan, Iran
  2. 2. Department of Psychology, College of Science and Technology, Temple University, Philadelphia, PA, United States
  3. 3. Physiology and Pharmacology Department, Pasteur Institute of Iran, Tehran, Iran
  4. 4. Reproductive Immunology Research Center, Avicenna Research Institute, and Integrative Oncology Department, Breast Cancer Research Center, Motamed Cancer Institute, Acecr, Tehran, Iran
  5. 5. Meilahti Clinical Proteomics Core Facility, University of Helsinki, Medicum, Biochemistry/Developmental Biology and HiLIFE, Helsinki, Finland
  6. 6. Research Program in Systems Oncology, Faculty of Medicine, University of Helsinki, Helsinki, Finland
  7. 7. Medicinal Plants and Drugs Research Institute, Shahid Beheshti University, Tehran, Iran

Source: Molecular Pharmacology Published:2021


Abstract

Celecoxib, or Celebrex, a nonsteroidal anti-inflammatory drug, is one of the most common medicines for treating inflammatory diseases. Recently, it has been shown that celecoxib is associated with implications in complex diseases, such as Alzheimer disease and cancer as well as with cardiovascular risk assessment and toxicity, suggesting that celecoxib may affect multiple unknown targets. In this project, we detected targets of celecoxib within the nervous system using a label-free thermal proteome profiling method. First, proteins of the rat hippocampus were treated with multiple drug concentrations and temperatures. Next, we separated the soluble proteins from the denatured and sedimented total protein load by ultracentrifugation. Subsequently, the soluble proteins were analyzed by nano-liquid chromatography tandem mass spectrometry to determine the identity of the celecoxib-targeted proteins based on structural changes by thermal stability variation of targeted proteins toward higher solubility in the higher temperatures. In the analysis of the soluble protein extract at 67°C, 44 proteins were uniquely detected in drug-treated samples out of all 478 identified proteins at this temperature. Ras-associated binding protein 4a, 1 out of these 44 proteins, has previously been reported as one of the celecoxib off targets in the rat central nervous system. Furthermore, we provide more molecular details through biomedical enrichment analysis to explore the potential role of all detected proteins in the biologic systems. We show that the determined proteins play a role in the signaling pathways related to neurodegenerative disease-and cancer pathways. Finally, we fill out molecular supporting evidence for using celecoxib toward the drug-repurposing approach by exploring drug targets. © 2021 American Society for Pharmacology and Experimental Therapy. All rights reserved.