Literature DB >> 33632781

Identification of Celecoxib-Targeted Proteins Using Label-Free Thermal Proteome Profiling on Rat Hippocampus.

Elham Gholizadeh1, Reza Karbalaei1, Ali Khaleghian1, Mona Salimi1, Kambiz Gilany1, Rabah Soliymani1, Ziaurrehman Tanoli1, Hassan Rezadoost1, Marc Baumann1, Mohieddin Jafari2, Jing Tang2.   

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. SIGNIFICANCE STATEMENT: This study determined 44 off-target proteins of celecoxib, a nonsteroidal anti-inflammatory and one of the most common medicines for treating inflammatory diseases. It shows that these proteins play a role in the signaling pathways related to neurodegenerative disease and cancer pathways. Finally, the study provides molecular supporting evidence for using celecoxib toward the drug-repurposing approach by exploring drug targets.
Copyright © 2021 The Author(s).

Entities:  

Year:  2021        PMID: 33632781     DOI: 10.1124/molpharm.120.000210

Source DB:  PubMed          Journal:  Mol Pharmacol        ISSN: 0026-895X            Impact factor:   4.436


  2 in total

1.  Isotope-labeled amyloid-β does not transmit to the brain in a prion-like manner after peripheral administration.

Authors:  Mirjam Brackhan; Giulio Calza; Kristiina Lundgren; Pablo Bascuñana; Thomas Brüning; Rabah Soliymani; Rakesh Kumar; Axel Abelein; Marc Baumann; Maciej Lalowski; Jens Pahnke
Journal:  EMBO Rep       Date:  2022-05-27       Impact factor: 9.071

2.  Bipartite network models to design combination therapies in acute myeloid leukaemia.

Authors:  Mohieddin Jafari; Mehdi Mirzaie; Jie Bao; Farnaz Barneh; Shuyu Zheng; Johanna Eriksson; Caroline A Heckman; Jing Tang
Journal:  Nat Commun       Date:  2022-04-19       Impact factor: 17.694

  2 in total

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