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Dysregulation of Rho GTPases in Human Cancers
Rho GTPases play central roles in numerous cellular processes, including cell motility, cell polarity, and cell cycle progression, by regulating actin cytoskeletal dynamics and cell adhesion. Dysregulation of Rho GTPase signaling is observed in a broad range of human cancers, and is associated with...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7281333/ https://www.ncbi.nlm.nih.gov/pubmed/32392742 http://dx.doi.org/10.3390/cancers12051179 |
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author | Jung, Haiyoung Yoon, Suk Ran Lim, Jeewon Cho, Hee Jun Lee, Hee Gu |
author_facet | Jung, Haiyoung Yoon, Suk Ran Lim, Jeewon Cho, Hee Jun Lee, Hee Gu |
author_sort | Jung, Haiyoung |
collection | PubMed |
description | Rho GTPases play central roles in numerous cellular processes, including cell motility, cell polarity, and cell cycle progression, by regulating actin cytoskeletal dynamics and cell adhesion. Dysregulation of Rho GTPase signaling is observed in a broad range of human cancers, and is associated with cancer development and malignant phenotypes, including metastasis and chemoresistance. Rho GTPase activity is precisely controlled by guanine nucleotide exchange factors, GTPase-activating proteins, and guanine nucleotide dissociation inhibitors. Recent evidence demonstrates that it is also regulated by post-translational modifications, such as phosphorylation, ubiquitination, and sumoylation. Here, we review the current knowledge on the role of Rho GTPases, and the precise mechanisms controlling their activity in the regulation of cancer progression. In addition, we discuss targeting strategies for the development of new drugs to improve cancer therapy. |
format | Online Article Text |
id | pubmed-7281333 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-72813332020-06-19 Dysregulation of Rho GTPases in Human Cancers Jung, Haiyoung Yoon, Suk Ran Lim, Jeewon Cho, Hee Jun Lee, Hee Gu Cancers (Basel) Review Rho GTPases play central roles in numerous cellular processes, including cell motility, cell polarity, and cell cycle progression, by regulating actin cytoskeletal dynamics and cell adhesion. Dysregulation of Rho GTPase signaling is observed in a broad range of human cancers, and is associated with cancer development and malignant phenotypes, including metastasis and chemoresistance. Rho GTPase activity is precisely controlled by guanine nucleotide exchange factors, GTPase-activating proteins, and guanine nucleotide dissociation inhibitors. Recent evidence demonstrates that it is also regulated by post-translational modifications, such as phosphorylation, ubiquitination, and sumoylation. Here, we review the current knowledge on the role of Rho GTPases, and the precise mechanisms controlling their activity in the regulation of cancer progression. In addition, we discuss targeting strategies for the development of new drugs to improve cancer therapy. MDPI 2020-05-07 /pmc/articles/PMC7281333/ /pubmed/32392742 http://dx.doi.org/10.3390/cancers12051179 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Jung, Haiyoung Yoon, Suk Ran Lim, Jeewon Cho, Hee Jun Lee, Hee Gu Dysregulation of Rho GTPases in Human Cancers |
title | Dysregulation of Rho GTPases in Human Cancers |
title_full | Dysregulation of Rho GTPases in Human Cancers |
title_fullStr | Dysregulation of Rho GTPases in Human Cancers |
title_full_unstemmed | Dysregulation of Rho GTPases in Human Cancers |
title_short | Dysregulation of Rho GTPases in Human Cancers |
title_sort | dysregulation of rho gtpases in human cancers |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7281333/ https://www.ncbi.nlm.nih.gov/pubmed/32392742 http://dx.doi.org/10.3390/cancers12051179 |
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