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DUBs, New Members in the Hypoxia Signaling clUb

Cellular protein homeostasis is tightly regulated by ubiquitination. Responsible for target protein ubiquitination is a class of enzymes, the so-called ubiquitin E3 ligases. They are opposed to a second class of enzymes, called deubiquitinating enzymes (DUBs), which can remove polyubiquitin chains f...

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Detalles Bibliográficos
Autores principales: Schober, Amelie S., Berra, Edurne
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4783435/
https://www.ncbi.nlm.nih.gov/pubmed/27014628
http://dx.doi.org/10.3389/fonc.2016.00053
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author Schober, Amelie S.
Berra, Edurne
author_facet Schober, Amelie S.
Berra, Edurne
author_sort Schober, Amelie S.
collection PubMed
description Cellular protein homeostasis is tightly regulated by ubiquitination. Responsible for target protein ubiquitination is a class of enzymes, the so-called ubiquitin E3 ligases. They are opposed to a second class of enzymes, called deubiquitinating enzymes (DUBs), which can remove polyubiquitin chains from their specific target proteins. The coaction of the two sets of enzymes allows the cell to adapt its overall protein content and the abundance of particular proteins to a variety of cellular and environmental stresses, including hypoxia. In recent years, DUBs have been highlighted to play major roles in many diseases, including cancer, both as tumor suppressors and oncogenes. Therefore, DUBs are emerging as promising targets for cancer-cell specific treatment. Here, we will review the current understanding of DUBs implicated in the control of hypoxia-inducible factor, the regulation of DUBs by hypoxia, and the use of DUB-specific drugs to target tumor hypoxia-signaling.
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spelling pubmed-47834352016-03-24 DUBs, New Members in the Hypoxia Signaling clUb Schober, Amelie S. Berra, Edurne Front Oncol Oncology Cellular protein homeostasis is tightly regulated by ubiquitination. Responsible for target protein ubiquitination is a class of enzymes, the so-called ubiquitin E3 ligases. They are opposed to a second class of enzymes, called deubiquitinating enzymes (DUBs), which can remove polyubiquitin chains from their specific target proteins. The coaction of the two sets of enzymes allows the cell to adapt its overall protein content and the abundance of particular proteins to a variety of cellular and environmental stresses, including hypoxia. In recent years, DUBs have been highlighted to play major roles in many diseases, including cancer, both as tumor suppressors and oncogenes. Therefore, DUBs are emerging as promising targets for cancer-cell specific treatment. Here, we will review the current understanding of DUBs implicated in the control of hypoxia-inducible factor, the regulation of DUBs by hypoxia, and the use of DUB-specific drugs to target tumor hypoxia-signaling. Frontiers Media S.A. 2016-03-09 /pmc/articles/PMC4783435/ /pubmed/27014628 http://dx.doi.org/10.3389/fonc.2016.00053 Text en Copyright © 2016 Schober and Berra. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Oncology
Schober, Amelie S.
Berra, Edurne
DUBs, New Members in the Hypoxia Signaling clUb
title DUBs, New Members in the Hypoxia Signaling clUb
title_full DUBs, New Members in the Hypoxia Signaling clUb
title_fullStr DUBs, New Members in the Hypoxia Signaling clUb
title_full_unstemmed DUBs, New Members in the Hypoxia Signaling clUb
title_short DUBs, New Members in the Hypoxia Signaling clUb
title_sort dubs, new members in the hypoxia signaling club
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4783435/
https://www.ncbi.nlm.nih.gov/pubmed/27014628
http://dx.doi.org/10.3389/fonc.2016.00053
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