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Deubiquitinating enzymes as oncotargets

Carcinogenesis is a complex process tightly regulated at multiple levels by post-translational modifications. Epigenetics plays a major role in cancer development, all stable changes to the gene expression process that are not a result of a direct change in the DNA code are described as epigenetics....

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Autores principales: McClurg, Urszula L., Robson, Craig N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4496387/
https://www.ncbi.nlm.nih.gov/pubmed/25962961
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author McClurg, Urszula L.
Robson, Craig N.
author_facet McClurg, Urszula L.
Robson, Craig N.
author_sort McClurg, Urszula L.
collection PubMed
description Carcinogenesis is a complex process tightly regulated at multiple levels by post-translational modifications. Epigenetics plays a major role in cancer development, all stable changes to the gene expression process that are not a result of a direct change in the DNA code are described as epigenetics. Epigenetic processes are regulated by post-translational modifications including ubiquitination which can directly affect either histones or transcription factors or may target their co-factors and interacting partners exerting an indirect effect. Deubiquitination of these target proteins is equally important and alterations in this pathway can also lead to cancer development, progression and metastasis. Only the correct, unaltered balance between ubiquitination and deubiquitination ensures healthy cellular homeostasis. In this review we focus on the role of deubiquitinating (DUB) enzymes in various aspects of epigenetics including the regulation of transcription factors, histone modifications, DNA damage repair pathways and cell cycle regulation. We discuss the impact of those processes on tumourigenesis and potential therapeutic applications of DUBs for cancer treatment.
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spelling pubmed-44963872015-07-15 Deubiquitinating enzymes as oncotargets McClurg, Urszula L. Robson, Craig N. Oncotarget Review Carcinogenesis is a complex process tightly regulated at multiple levels by post-translational modifications. Epigenetics plays a major role in cancer development, all stable changes to the gene expression process that are not a result of a direct change in the DNA code are described as epigenetics. Epigenetic processes are regulated by post-translational modifications including ubiquitination which can directly affect either histones or transcription factors or may target their co-factors and interacting partners exerting an indirect effect. Deubiquitination of these target proteins is equally important and alterations in this pathway can also lead to cancer development, progression and metastasis. Only the correct, unaltered balance between ubiquitination and deubiquitination ensures healthy cellular homeostasis. In this review we focus on the role of deubiquitinating (DUB) enzymes in various aspects of epigenetics including the regulation of transcription factors, histone modifications, DNA damage repair pathways and cell cycle regulation. We discuss the impact of those processes on tumourigenesis and potential therapeutic applications of DUBs for cancer treatment. Impact Journals LLC 2015-04-23 /pmc/articles/PMC4496387/ /pubmed/25962961 Text en Copyright: © 2015 McClurg and Robson http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Review
McClurg, Urszula L.
Robson, Craig N.
Deubiquitinating enzymes as oncotargets
title Deubiquitinating enzymes as oncotargets
title_full Deubiquitinating enzymes as oncotargets
title_fullStr Deubiquitinating enzymes as oncotargets
title_full_unstemmed Deubiquitinating enzymes as oncotargets
title_short Deubiquitinating enzymes as oncotargets
title_sort deubiquitinating enzymes as oncotargets
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4496387/
https://www.ncbi.nlm.nih.gov/pubmed/25962961
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