Therapeutic inhibition of ferroptosis in neurodegenerative disease.

ALS Alzheimer's Parkinson's drug discovery ferroptosis inhibitor iron lipid peroxidation neurodegeneration therapeutics treatment

Journal

Trends in pharmacological sciences
ISSN: 1873-3735
Titre abrégé: Trends Pharmacol Sci
Pays: England
ID NLM: 7906158

Informations de publication

Date de publication:
10 2023
Historique:
received: 07 07 2023
revised: 28 07 2023
accepted: 28 07 2023
medline: 18 9 2023
pubmed: 2 9 2023
entrez: 1 9 2023
Statut: ppublish

Résumé

Iron accumulation has been associated with the etiology and progression of multiple neurodegenerative diseases (NDDs). The exact role of iron in these diseases is not fully understood, but an iron-dependent form of regulated cell death called ferroptosis could be key. Although there is substantial preclinical and clinical evidence that ferroptosis plays a role in NDD, there are still questions regarding how to target ferroptosis therapeutically, including which proteins to target, identification of clinically relevant biomarkers, and which patients might benefit most. Clinical trials of iron- and ferroptosis-targeted therapies are beginning to provide some answers, but there is growing interest in developing new ferroptosis inhibitors. We describe newly identified ferroptosis targets, opportunities, and challenges in NDD, as well as key considerations for progressing new therapeutics to the clinic.

Identifiants

pubmed: 37657967
pii: S0165-6147(23)00169-4
doi: 10.1016/j.tips.2023.07.007
pii:
doi:

Substances chimiques

Iron E1UOL152H7

Types de publication

Journal Article Review Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

674-688

Informations de copyright

Copyright © 2023 Elsevier Ltd. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of interests S.K.R. and T.R.H. were employees of Sanofi at the time this review was conducted and declare no other competing interests. The remaining authors have no interests to declare.

Auteurs

Sean K Ryan (SK)

Sanofi, Rare and Neurologic Diseases, Cambridge, MA, USA.

Cathryn L Ugalde (CL)

The ALBORADA Drug Discovery Institute, University of Cambridge, Island Research Building, Cambridge Biomedical Campus, Hills Road, Cambridge CB2 0AH, UK.

Anne-Sophie Rolland (AS)

Department of Medical Pharmacology, Expert Center of Parkinson's Disease, ALS, and Neurogenetics, University of Lille, LilNCog, Lille Neuroscience and Cognition, INSERM UMR S1172, CHU de Lille, LICEND, COEN, Center, NS-PARK Network, France.

John Skidmore (J)

The ALBORADA Drug Discovery Institute, University of Cambridge, Island Research Building, Cambridge Biomedical Campus, Hills Road, Cambridge CB2 0AH, UK.

David Devos (D)

Department of Medical Pharmacology, Expert Center of Parkinson's Disease, ALS, and Neurogenetics, University of Lille, LilNCog, Lille Neuroscience and Cognition, INSERM UMR S1172, CHU de Lille, LICEND, COEN, Center, NS-PARK Network, France.

Timothy R Hammond (TR)

Sanofi, Rare and Neurologic Diseases, Cambridge, MA, USA. Electronic address: Timothy.Hammond@sanofi.com.

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Classifications MeSH