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GSK3α: An Important Paralog in Neurodegenerative Disorders and Cancer
The biological activity of the enzyme glycogen synthase kinase-3 (GSK3) is fulfilled by two paralogs named GSK3α and GSK3β, which possess both redundancy and specific functions. The upregulated activity of these proteins is linked to the development of disorders such as neurodegenerative disorders (...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7765659/ https://www.ncbi.nlm.nih.gov/pubmed/33339170 http://dx.doi.org/10.3390/biom10121683 |
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author | Silva-García, Octavio Cortés-Vieyra, Ricarda Mendoza-Ambrosio, Francisco N. Ramírez-Galicia, Guillermo Baizabal-Aguirre, Víctor M. |
author_facet | Silva-García, Octavio Cortés-Vieyra, Ricarda Mendoza-Ambrosio, Francisco N. Ramírez-Galicia, Guillermo Baizabal-Aguirre, Víctor M. |
author_sort | Silva-García, Octavio |
collection | PubMed |
description | The biological activity of the enzyme glycogen synthase kinase-3 (GSK3) is fulfilled by two paralogs named GSK3α and GSK3β, which possess both redundancy and specific functions. The upregulated activity of these proteins is linked to the development of disorders such as neurodegenerative disorders (ND) and cancer. Although various chemical inhibitors of these enzymes restore the brain functions in models of ND such as Alzheimer’s disease (AD), and reduce the proliferation and survival of cancer cells, the particular contribution of each paralog to these effects remains unclear as these molecules downregulate the activity of both paralogs with a similar efficacy. Moreover, given that GSK3 paralogs phosphorylate more than 100 substrates, the simultaneous inhibition of both enzymes has detrimental effects during long-term inhibition. Although the GSK3β kinase function has usually been taken as the global GSK3 activity, in the last few years, a growing interest in the study of GSK3α has emerged because several studies have recognized it as the main GSK3 paralog involved in a variety of diseases. This review summarizes the current biological evidence on the role of GSK3α in AD and various types of cancer. We also provide a discussion on some strategies that may lead to the design of the paralog-specific inhibition of GSK3α. |
format | Online Article Text |
id | pubmed-7765659 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-77656592020-12-27 GSK3α: An Important Paralog in Neurodegenerative Disorders and Cancer Silva-García, Octavio Cortés-Vieyra, Ricarda Mendoza-Ambrosio, Francisco N. Ramírez-Galicia, Guillermo Baizabal-Aguirre, Víctor M. Biomolecules Review The biological activity of the enzyme glycogen synthase kinase-3 (GSK3) is fulfilled by two paralogs named GSK3α and GSK3β, which possess both redundancy and specific functions. The upregulated activity of these proteins is linked to the development of disorders such as neurodegenerative disorders (ND) and cancer. Although various chemical inhibitors of these enzymes restore the brain functions in models of ND such as Alzheimer’s disease (AD), and reduce the proliferation and survival of cancer cells, the particular contribution of each paralog to these effects remains unclear as these molecules downregulate the activity of both paralogs with a similar efficacy. Moreover, given that GSK3 paralogs phosphorylate more than 100 substrates, the simultaneous inhibition of both enzymes has detrimental effects during long-term inhibition. Although the GSK3β kinase function has usually been taken as the global GSK3 activity, in the last few years, a growing interest in the study of GSK3α has emerged because several studies have recognized it as the main GSK3 paralog involved in a variety of diseases. This review summarizes the current biological evidence on the role of GSK3α in AD and various types of cancer. We also provide a discussion on some strategies that may lead to the design of the paralog-specific inhibition of GSK3α. MDPI 2020-12-16 /pmc/articles/PMC7765659/ /pubmed/33339170 http://dx.doi.org/10.3390/biom10121683 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Silva-García, Octavio Cortés-Vieyra, Ricarda Mendoza-Ambrosio, Francisco N. Ramírez-Galicia, Guillermo Baizabal-Aguirre, Víctor M. GSK3α: An Important Paralog in Neurodegenerative Disorders and Cancer |
title | GSK3α: An Important Paralog in Neurodegenerative Disorders and Cancer |
title_full | GSK3α: An Important Paralog in Neurodegenerative Disorders and Cancer |
title_fullStr | GSK3α: An Important Paralog in Neurodegenerative Disorders and Cancer |
title_full_unstemmed | GSK3α: An Important Paralog in Neurodegenerative Disorders and Cancer |
title_short | GSK3α: An Important Paralog in Neurodegenerative Disorders and Cancer |
title_sort | gsk3α: an important paralog in neurodegenerative disorders and cancer |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7765659/ https://www.ncbi.nlm.nih.gov/pubmed/33339170 http://dx.doi.org/10.3390/biom10121683 |
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