Drugs targeting adenosine signaling pathways: A current view.


Journal

Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie
ISSN: 1950-6007
Titre abrégé: Biomed Pharmacother
Pays: France
ID NLM: 8213295

Informations de publication

Date de publication:
Sep 2023
Historique:
received: 18 05 2023
revised: 06 07 2023
accepted: 18 07 2023
medline: 17 8 2023
pubmed: 29 7 2023
entrez: 28 7 2023
Statut: ppublish

Résumé

Adenosine is an endogenous nucleoside that regulates many physiological and pathological processes. It is derived from either the intracellular or extracellular dephosphorylation of adenosine triphosphate and interacts with cell-surface G-protein-coupled receptors. Adenosine plays a substantial role in protecting against cell damage in areas of increased tissue metabolism and preventing organ dysfunction in pathological states. Targeting adenosine metabolism and receptor signaling may be an effective therapeutic approach for human diseases, including cardiovascular and central nervous system disorders, rheumatoid arthritis, asthma, renal diseases, and cancer. Several lines of evidence have shown that many drugs exert their beneficial effects by modulating adenosine signaling pathways but this knowledge urgently needs to be summarized, and most importantly, actualized. The present review collects pharmaceuticals and pharmacological or diagnostic tools that target adenosine signaling in their primary or secondary mode of action. We overviewed FDA-approved drugs as well as those currently being studied in clinical trials. Among them are already used in clinic A2A adenosine receptor modulators like istradefylline or regadenoson, but also plenty of anti-platelet, anti-inflammatory, or immunosuppressive, and anti-cancer drugs. On the other hand, we investigated dozens of specific adenosine pathway regulators that are tested in clinical trials to treat human infectious and noninfectious diseases. In conclusion, targeting purinergic signaling represents a great therapeutic challenge. The actual knowledge of the involvement of adenosinergic signaling as part of the mechanism of action of old drugs has open a path not only for drug-repurposing but also for new therapeutic strategies.

Identifiants

pubmed: 37506580
pii: S0753-3322(23)00975-7
doi: 10.1016/j.biopha.2023.115184
pii:
doi:

Substances chimiques

Adenosine K72T3FS567
Adenosine Triphosphate 8L70Q75FXE
Receptors, Purinergic P1 0

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

115184

Informations de copyright

Copyright © 2023 The Authors. Published by Elsevier Masson SAS.. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest There is no conflict of interest associated with the publication entitled: “Drugs targeting adenosine signaling pathways: A current view” by Kutryb-Zajac, Kawecka, Nasadiuk, Braczko, Stawarska, Caiazzo, Koszalka, and Cicala that has been submitted to the Biomedicine & Pharmacotherapy.

Auteurs

Barbara Kutryb-Zając (B)

Department of Biochemistry, Medical University of Gdańsk, 80-211 Gdańsk, Poland. Electronic address: b.kutryb-zajac@gumed.edu.pl.

Ada Kawecka (A)

Department of Biochemistry, Medical University of Gdańsk, 80-211 Gdańsk, Poland.

Khrystyna Nasadiuk (K)

Department of Biochemistry, Medical University of Gdańsk, 80-211 Gdańsk, Poland.

Alicja Braczko (A)

Department of Biochemistry, Medical University of Gdańsk, 80-211 Gdańsk, Poland.

Klaudia Stawarska (K)

Department of Biochemistry, Medical University of Gdańsk, 80-211 Gdańsk, Poland.

Elisabetta Caiazzo (E)

Department of Pharmacy, School of Medicine, University of Naple Federico II, 80131 Naples, Italy.

Patrycja Koszałka (P)

Laboratory of Cell Biology and Immunology, Institute of Medical Biotechnology and Experimental Oncology, Intercollegiate Faculty of Biotechnology University of Gdańsk and Medical University of Gdańsk, Medical University of Gdańsk, 80-211 Gdańsk, Poland.

Carla Cicala (C)

Department of Pharmacy, School of Medicine, University of Naple Federico II, 80131 Naples, Italy.

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Classifications MeSH