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Role of proteasomes in disease

A functional ubiquitin proteasome system is essential for all eukaryotic cells and therefore any alteration to its components has potential pathological consequences. Though the exact underlying mechanism is unclear, an age-related decrease in proteasome activity weakens cellular capacity to remove...

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Detalles Bibliográficos
Autor principal: Dahlmann, Burkhardt
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2106367/
https://www.ncbi.nlm.nih.gov/pubmed/18047740
http://dx.doi.org/10.1186/1471-2091-8-S1-S3
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author Dahlmann, Burkhardt
author_facet Dahlmann, Burkhardt
author_sort Dahlmann, Burkhardt
collection PubMed
description A functional ubiquitin proteasome system is essential for all eukaryotic cells and therefore any alteration to its components has potential pathological consequences. Though the exact underlying mechanism is unclear, an age-related decrease in proteasome activity weakens cellular capacity to remove oxidatively modified proteins and favours the development of neurodegenerative and cardiac diseases. Up-regulation of proteasome activity is characteristic of muscle wasting conditions including sepsis, cachexia and uraemia, but may not be rate limiting. Meanwhile, enhanced presence of immunoproteasomes in aging brain and muscle tissue could reflect a persistent inflammatory defence and anti-stress mechanism, whereas in cancer cells, their down-regulation reflects a means by which to escape immune surveillance. Hence, induction of apoptosis by synthetic proteasome inhibitors is a potential treatment strategy for cancer, whereas for other diseases such as neurodegeneration, the use of proteasome-activating or -modulating compounds could be more effective. Publication history: Republished from Current BioData's Targeted Proteins database (TPdb; ).
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spelling pubmed-21063672007-12-05 Role of proteasomes in disease Dahlmann, Burkhardt BMC Biochem Review A functional ubiquitin proteasome system is essential for all eukaryotic cells and therefore any alteration to its components has potential pathological consequences. Though the exact underlying mechanism is unclear, an age-related decrease in proteasome activity weakens cellular capacity to remove oxidatively modified proteins and favours the development of neurodegenerative and cardiac diseases. Up-regulation of proteasome activity is characteristic of muscle wasting conditions including sepsis, cachexia and uraemia, but may not be rate limiting. Meanwhile, enhanced presence of immunoproteasomes in aging brain and muscle tissue could reflect a persistent inflammatory defence and anti-stress mechanism, whereas in cancer cells, their down-regulation reflects a means by which to escape immune surveillance. Hence, induction of apoptosis by synthetic proteasome inhibitors is a potential treatment strategy for cancer, whereas for other diseases such as neurodegeneration, the use of proteasome-activating or -modulating compounds could be more effective. Publication history: Republished from Current BioData's Targeted Proteins database (TPdb; ). BioMed Central 2007-11-22 /pmc/articles/PMC2106367/ /pubmed/18047740 http://dx.doi.org/10.1186/1471-2091-8-S1-S3 Text en Copyright © 2007 Dahlmann; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review
Dahlmann, Burkhardt
Role of proteasomes in disease
title Role of proteasomes in disease
title_full Role of proteasomes in disease
title_fullStr Role of proteasomes in disease
title_full_unstemmed Role of proteasomes in disease
title_short Role of proteasomes in disease
title_sort role of proteasomes in disease
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2106367/
https://www.ncbi.nlm.nih.gov/pubmed/18047740
http://dx.doi.org/10.1186/1471-2091-8-S1-S3
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