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The Proteasome Activator PA200/PSME4: An Emerging New Player in Health and Disease

Proteasomes comprise a family of proteasomal complexes essential for maintaining protein homeostasis. Accordingly, proteasomes represent promising therapeutic targets in multiple human diseases. Several proteasome inhibitors are approved for treating hematological cancers. However, their side effect...

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Detalles Bibliográficos
Autores principales: Yazgili, Ayse Seda, Ebstein, Frédéric, Meiners, Silke
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9406137/
https://www.ncbi.nlm.nih.gov/pubmed/36009043
http://dx.doi.org/10.3390/biom12081150
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author Yazgili, Ayse Seda
Ebstein, Frédéric
Meiners, Silke
author_facet Yazgili, Ayse Seda
Ebstein, Frédéric
Meiners, Silke
author_sort Yazgili, Ayse Seda
collection PubMed
description Proteasomes comprise a family of proteasomal complexes essential for maintaining protein homeostasis. Accordingly, proteasomes represent promising therapeutic targets in multiple human diseases. Several proteasome inhibitors are approved for treating hematological cancers. However, their side effects impede their efficacy and broader therapeutic applications. Therefore, understanding the biology of the different proteasome complexes present in the cell is crucial for developing tailor-made inhibitors against specific proteasome complexes. Here, we will discuss the structure, biology, and function of the alternative Proteasome Activator 200 (PA200), also known as PSME4, and summarize the current evidence for its dysregulation in different human diseases. We hereby aim to stimulate research on this enigmatic proteasome regulator that has the potential to serve as a therapeutic target in cancer.
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spelling pubmed-94061372022-08-26 The Proteasome Activator PA200/PSME4: An Emerging New Player in Health and Disease Yazgili, Ayse Seda Ebstein, Frédéric Meiners, Silke Biomolecules Review Proteasomes comprise a family of proteasomal complexes essential for maintaining protein homeostasis. Accordingly, proteasomes represent promising therapeutic targets in multiple human diseases. Several proteasome inhibitors are approved for treating hematological cancers. However, their side effects impede their efficacy and broader therapeutic applications. Therefore, understanding the biology of the different proteasome complexes present in the cell is crucial for developing tailor-made inhibitors against specific proteasome complexes. Here, we will discuss the structure, biology, and function of the alternative Proteasome Activator 200 (PA200), also known as PSME4, and summarize the current evidence for its dysregulation in different human diseases. We hereby aim to stimulate research on this enigmatic proteasome regulator that has the potential to serve as a therapeutic target in cancer. MDPI 2022-08-20 /pmc/articles/PMC9406137/ /pubmed/36009043 http://dx.doi.org/10.3390/biom12081150 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Yazgili, Ayse Seda
Ebstein, Frédéric
Meiners, Silke
The Proteasome Activator PA200/PSME4: An Emerging New Player in Health and Disease
title The Proteasome Activator PA200/PSME4: An Emerging New Player in Health and Disease
title_full The Proteasome Activator PA200/PSME4: An Emerging New Player in Health and Disease
title_fullStr The Proteasome Activator PA200/PSME4: An Emerging New Player in Health and Disease
title_full_unstemmed The Proteasome Activator PA200/PSME4: An Emerging New Player in Health and Disease
title_short The Proteasome Activator PA200/PSME4: An Emerging New Player in Health and Disease
title_sort proteasome activator pa200/psme4: an emerging new player in health and disease
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9406137/
https://www.ncbi.nlm.nih.gov/pubmed/36009043
http://dx.doi.org/10.3390/biom12081150
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