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BioMed Central, BMC Biology, 1(12), 2014

DOI: 10.1186/s12915-014-0094-0

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Proteotoxic crisis, the ubiquitin-proteasome system, and cancer therapy

Journal article published in 2014 by Raymond J. Deshaies ORCID
This paper is made freely available by the publisher.
This paper is made freely available by the publisher.

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Abstract

Genomic alterations may make cancer cells more dependent than normal cells on mechanisms of proteostasis, including protein folding and degradation. This proposition is the basis for the clinical use of proteasome inhibitors to treat multiple myeloma and mantle cell lymphoma. However, proteasome inhibitors have not proved effective in treating other cancers, and this has called into question the general applicability of this approach. Here, I consider possible explanations for this apparently limited applicability, and discuss whether inhibiting other broadly acting components of the ubiquitin-proteasome system - including ubiquitin-activating enzyme and the AAA-ATPase p97/VCP - might be more generally effective in cancer therapy.