» Articles » PMID: 37828541

Janus Kinase Inhibitors Are Potential Therapeutics for Amyotrophic Lateral Sclerosis

Overview
Publisher Biomed Central
Date 2023 Oct 12
PMID 37828541
Authors
Affiliations
Soon will be listed here.
Abstract

Amyotrophic lateral sclerosis (ALS) is a poorly treated multifactorial neurodegenerative disease associated with multiple cell types and subcellular organelles. As with other multifactorial diseases, it is likely that drugs will need to target multiple disease processes and cell types to be effective. We review here the role of Janus kinase (JAK)/Signal transducer and activator of transcription (STAT) signalling in ALS, confirm the association of this signalling with fundamental ALS disease processes using the BenevolentAI Knowledge Graph, and demonstrate that inhibitors of this pathway could reduce the ALS pathophysiology in neurons, glia, muscle fibres, and blood cells. Specifically, we suggest that inhibition of the JAK enzymes by approved inhibitors known as Jakinibs could reduce STAT3 activation and modify the progress of this disease. Analysis of the Jakinibs highlights baricitinib as a suitable candidate due to its ability to penetrate the central nervous system and exert beneficial effects on the immune system. Therefore, we recommend that this drug be tested in appropriately designed clinical trials for ALS.

Citing Articles

The Crucial Role of the Blood-Brain Barrier in Neurodegenerative Diseases: Mechanisms of Disruption and Therapeutic Implications.

Kim S, Jung U, Kim S J Clin Med. 2025; 14(2).

PMID: 39860392 PMC: 11765772. DOI: 10.3390/jcm14020386.


Biochemical dissection of STAT3 signaling in amyotrophic lateral sclerosis.

Apolloni S, DAmbrosi N Neural Regen Res. 2024; 20(11):3229-3230.

PMID: 39589500 PMC: 11881706. DOI: 10.4103/NRR.NRR-D-24-00862.


Novel insights into the ROCK-JAK-STAT signaling pathway in upper respiratory tract infections and neurodegenerative diseases.

Li J, Mao N, Wang Y, Deng S, Chen K Mol Ther. 2024; 33(1):32-50.

PMID: 39511889 PMC: 11764622. DOI: 10.1016/j.ymthe.2024.11.011.


Multi-Omics Approach Reveals Genes and Pathways Affected in Miller-Dieker Syndrome.

Mahendran G, Breger K, McCown P, Hulewicz J, Bhandari T, Addepalli B Mol Neurobiol. 2024; 62(4):5073-5094.

PMID: 39508990 PMC: 11880102. DOI: 10.1007/s12035-024-04532-7.


The Scientific and Therapeutic Rationale for Off-Label Treatments in Amyotrophic Lateral Sclerosis.

Bedlack R, Li X, Evangelista B, Panzetta M, Kwan J, Gittings L Ann Neurol. 2024; .

PMID: 39503319 PMC: 11683184. DOI: 10.1002/ana.27126.


References
1.
Gordon D, Jang G, Bouhaddou M, Xu J, Obernier K, White K . A SARS-CoV-2 protein interaction map reveals targets for drug repurposing. Nature. 2020; 583(7816):459-468. PMC: 7431030. DOI: 10.1038/s41586-020-2286-9. View

2.
Rodriguez S, Sahin A, Schrank B, Al-Lawati H, Costantino I, Benz E . Genome-encoded cytoplasmic double-stranded RNAs, found in ALS-FTD brain, propagate neuronal loss. Sci Transl Med. 2021; 13(601). PMC: 8779652. DOI: 10.1126/scitranslmed.aaz4699. View

3.
Zhao W, Beers D, Hooten K, Sieglaff D, Zhang A, Kalyana-Sundaram S . Characterization of Gene Expression Phenotype in Amyotrophic Lateral Sclerosis Monocytes. JAMA Neurol. 2017; 74(6):677-685. PMC: 5822209. DOI: 10.1001/jamaneurol.2017.0357. View

4.
Bright F, Chan G, van Hummel A, Ittner L, Ke Y . TDP-43 and Inflammation: Implications for Amyotrophic Lateral Sclerosis and Frontotemporal Dementia. Int J Mol Sci. 2021; 22(15). PMC: 8346169. DOI: 10.3390/ijms22157781. View

5.
Boillee S . Local and remote interactions between macrophages and microglia in neurological conditions. Curr Opin Immunol. 2021; 74:118-124. DOI: 10.1016/j.coi.2021.11.006. View