Targeting Protein Aggregation in ALS.
amyotrophic lateral sclerosis
clinical trials
drug discovery
inflammation
neurodegeneration
protein aggregation
protein homeostasis
therapeutics
Journal
Biomolecules
ISSN: 2218-273X
Titre abrégé: Biomolecules
Pays: Switzerland
ID NLM: 101596414
Informations de publication
Date de publication:
18 Oct 2024
18 Oct 2024
Historique:
received:
23
08
2024
revised:
03
10
2024
accepted:
14
10
2024
medline:
26
10
2024
pubmed:
26
10
2024
entrez:
26
10
2024
Statut:
epublish
Résumé
Proteinopathies involve the abnormal accumulation of specific proteins. Maintaining the balance of the proteome is a finely regulated process managed by a complex network of cellular machinery responsible for protein synthesis, folding, and degradation. However, stress and ageing can disrupt this balance, leading to widespread protein aggregation. Currently, several therapies targeting protein aggregation are in clinical trials for ALS. These approaches mainly focus on two strategies: addressing proteins that are prone to aggregation due to mutations and targeting the cellular mechanisms that maintain protein homeostasis to prevent aggregation. This review will cover these emerging drugs. Advances in ALS research not only offer hope for better outcomes for ALS patients but also provide valuable insights and methodologies that can benefit the broader field of neurodegenerative disease drug discovery.
Identifiants
pubmed: 39456257
pii: biom14101324
doi: 10.3390/biom14101324
pii:
doi:
Substances chimiques
Protein Aggregates
0
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM