Transglutaminase 2 as a therapeutic target for neurological conditions.
Alzheimer’s disease
CNS injury
Huntington’s disease
Parkinson’s disease
TG2 inhibitors
Transglutaminase 2
multiple sclerosis
neurodegenerative diseases
Journal
Expert opinion on therapeutic targets
ISSN: 1744-7631
Titre abrégé: Expert Opin Ther Targets
Pays: England
ID NLM: 101127833
Informations de publication
Date de publication:
09 2021
09 2021
Historique:
pubmed:
6
10
2021
medline:
3
3
2022
entrez:
5
10
2021
Statut:
ppublish
Résumé
Transglutaminase 2 (TG2) has been implicated in numerous neurological conditions, including neurodegenerative diseases, multiple sclerosis, and CNS injury. Early studies on the role of TG2 in neurodegenerative conditions focused on its ability to 'crosslink' proteins into insoluble aggregates. However, more recent studies have suggested that this is unlikely to be the primary mechanism by which TG2 contributes to the pathogenic processes. Although the specific mechanisms by which TG2 is involved in neurological conditions have not been clearly defined, TG2 regulates numerous cellular processes through which it could contribute to a specific disease. Given the fact that TG2 is a stress-induced gene and elevated in disease or injury conditions, TG2 inhibitors may be useful neurotherapeutics. Overview of TG2 and different TG2 inhibitors. A brief review of TG2 in neurodegenerative diseases, multiple sclerosis and CNS injury and inhibitors that have been tested in different models. Database search: https://pubmed.ncbi.nlm.nih.gov prior to 1 July 2021. Currently, it appears unlikely that inhibiting TG2 in the context of neurodegenerative diseases would be therapeutically advantageous. However, for multiple sclerosis and CNS injuries, TG2 inhibitors may have the potential to be therapeutically useful and thus there is rationale for their further development.
Identifiants
pubmed: 34607527
doi: 10.1080/14728222.2021.1989410
doi:
Substances chimiques
Protein Glutamine gamma Glutamyltransferase 2
EC 2.3.2.13
Transglutaminases
EC 2.3.2.13
GTP-Binding Proteins
EC 3.6.1.-
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
721-731Subventions
Organisme : NINDS NIH HHS
ID : R21 NS119673
Pays : United States
Organisme : CIHR
ID : PJT-162180
Pays : Canada