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The regulation of snail: on the ubiquitin edge

Metastasis accounts for a majority of cancer death. One key feature during metastasis is epithelial-mesenchymal transition (EMT), which is regulated by transcription factors such as Snail and Twist. In non-malignant cells, Snail has a short half-life and is degraded via ubiquitination, but its stabi...

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Detalles Bibliográficos
Autores principales: Yu, Qian, Zhou, Binhua P., Wu, Yadi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5685547/
https://www.ncbi.nlm.nih.gov/pubmed/29147673
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author Yu, Qian
Zhou, Binhua P.
Wu, Yadi
author_facet Yu, Qian
Zhou, Binhua P.
Wu, Yadi
author_sort Yu, Qian
collection PubMed
description Metastasis accounts for a majority of cancer death. One key feature during metastasis is epithelial-mesenchymal transition (EMT), which is regulated by transcription factors such as Snail and Twist. In non-malignant cells, Snail has a short half-life and is degraded via ubiquitination, but its stability is increased in cancer cell. However, the mechanism by which Snail escapes ubiquitination and degradation remains unknown. Recently, we found that Dub3 is a deubiquinase of Snail. Most importantly, we determined that Dub3 responded to extracellular signals such as IL-6, and that the resultant signaling prevented Snail degradation, and promoted cancer growth, invasion, and migration. In this highlight, we present a concise picture of how the transcription factor Snail is regulated by ubiquitination in cancer cells, the role of Dub3 in this process, and its potential use as a treatment target.
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spelling pubmed-56855472017-11-14 The regulation of snail: on the ubiquitin edge Yu, Qian Zhou, Binhua P. Wu, Yadi Cancer Cell Microenviron Article Metastasis accounts for a majority of cancer death. One key feature during metastasis is epithelial-mesenchymal transition (EMT), which is regulated by transcription factors such as Snail and Twist. In non-malignant cells, Snail has a short half-life and is degraded via ubiquitination, but its stability is increased in cancer cell. However, the mechanism by which Snail escapes ubiquitination and degradation remains unknown. Recently, we found that Dub3 is a deubiquinase of Snail. Most importantly, we determined that Dub3 responded to extracellular signals such as IL-6, and that the resultant signaling prevented Snail degradation, and promoted cancer growth, invasion, and migration. In this highlight, we present a concise picture of how the transcription factor Snail is regulated by ubiquitination in cancer cells, the role of Dub3 in this process, and its potential use as a treatment target. 2017-07-03 2017 /pmc/articles/PMC5685547/ /pubmed/29147673 Text en http://creativecommons.org/licenses/by/4.0/ Licensed under a Creative Commons Attribution 4.0 International License which allows users including authors of articles to copy and redistribute the material in any medium or format, in addition to remix, transform, and build upon the material for any purpose, even commercially, as long as the author and original source are properly cited or credited.
spellingShingle Article
Yu, Qian
Zhou, Binhua P.
Wu, Yadi
The regulation of snail: on the ubiquitin edge
title The regulation of snail: on the ubiquitin edge
title_full The regulation of snail: on the ubiquitin edge
title_fullStr The regulation of snail: on the ubiquitin edge
title_full_unstemmed The regulation of snail: on the ubiquitin edge
title_short The regulation of snail: on the ubiquitin edge
title_sort regulation of snail: on the ubiquitin edge
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5685547/
https://www.ncbi.nlm.nih.gov/pubmed/29147673
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