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Janus kinase inhibitors are potential therapeutics for amyotrophic lateral sclerosis

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 effectiv...

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Autores principales: Richardson, Peter J., Smith, Daniel P., de Giorgio, Alex, Snetkov, Xenia, Almond-Thynne, Joshua, Cronin, Sara, Mead, Richard J., McDermott, Christopher J., Shaw, Pamela J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10568794/
https://www.ncbi.nlm.nih.gov/pubmed/37828541
http://dx.doi.org/10.1186/s40035-023-00380-y
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author Richardson, Peter J.
Smith, Daniel P.
de Giorgio, Alex
Snetkov, Xenia
Almond-Thynne, Joshua
Cronin, Sara
Mead, Richard J.
McDermott, Christopher J.
Shaw, Pamela J.
author_facet Richardson, Peter J.
Smith, Daniel P.
de Giorgio, Alex
Snetkov, Xenia
Almond-Thynne, Joshua
Cronin, Sara
Mead, Richard J.
McDermott, Christopher J.
Shaw, Pamela J.
author_sort Richardson, Peter J.
collection PubMed
description 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.
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spelling pubmed-105687942023-10-13 Janus kinase inhibitors are potential therapeutics for amyotrophic lateral sclerosis Richardson, Peter J. Smith, Daniel P. de Giorgio, Alex Snetkov, Xenia Almond-Thynne, Joshua Cronin, Sara Mead, Richard J. McDermott, Christopher J. Shaw, Pamela J. Transl Neurodegener Review 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. BioMed Central 2023-10-12 /pmc/articles/PMC10568794/ /pubmed/37828541 http://dx.doi.org/10.1186/s40035-023-00380-y Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Review
Richardson, Peter J.
Smith, Daniel P.
de Giorgio, Alex
Snetkov, Xenia
Almond-Thynne, Joshua
Cronin, Sara
Mead, Richard J.
McDermott, Christopher J.
Shaw, Pamela J.
Janus kinase inhibitors are potential therapeutics for amyotrophic lateral sclerosis
title Janus kinase inhibitors are potential therapeutics for amyotrophic lateral sclerosis
title_full Janus kinase inhibitors are potential therapeutics for amyotrophic lateral sclerosis
title_fullStr Janus kinase inhibitors are potential therapeutics for amyotrophic lateral sclerosis
title_full_unstemmed Janus kinase inhibitors are potential therapeutics for amyotrophic lateral sclerosis
title_short Janus kinase inhibitors are potential therapeutics for amyotrophic lateral sclerosis
title_sort janus kinase inhibitors are potential therapeutics for amyotrophic lateral sclerosis
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10568794/
https://www.ncbi.nlm.nih.gov/pubmed/37828541
http://dx.doi.org/10.1186/s40035-023-00380-y
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