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DLC-1:a Rho GTPase-activating protein and tumour suppressor

The deleted in liver cancer 1 (DLC-1) gene encodes a GTPase activating protein that acts as a negative regulator of the Rho family of small GTPases. Rho proteins transduce signals that influence cell morphology and physiology, and their aberrant up-regulation is a key factor in the neoplastic proces...

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Autores principales: Durkin, Marian E, Yuan, Bao-Zhu, Zhou, Xiaoling, Zimonjic, Drazen B, Lowy, Douglas R, Thorgeirsson, Snorri S, Popescu, Nicholas C
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4401278/
https://www.ncbi.nlm.nih.gov/pubmed/17979893
http://dx.doi.org/10.1111/j.1582-4934.2007.00098.x
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author Durkin, Marian E
Yuan, Bao-Zhu
Zhou, Xiaoling
Zimonjic, Drazen B
Lowy, Douglas R
Thorgeirsson, Snorri S
Popescu, Nicholas C
author_facet Durkin, Marian E
Yuan, Bao-Zhu
Zhou, Xiaoling
Zimonjic, Drazen B
Lowy, Douglas R
Thorgeirsson, Snorri S
Popescu, Nicholas C
author_sort Durkin, Marian E
collection PubMed
description The deleted in liver cancer 1 (DLC-1) gene encodes a GTPase activating protein that acts as a negative regulator of the Rho family of small GTPases. Rho proteins transduce signals that influence cell morphology and physiology, and their aberrant up-regulation is a key factor in the neoplastic process, including metastasis. Since its discovery, compelling evidence has accumulated that demonstrates a role for DLC-1 as a bona fide tumour suppressor gene in different types of human cancer. Loss of DLC-1 expression mediated by genetic and epigenetic mechanisms has been associated with the development of many human cancers, and restoration of DLC-1 expression inhibited the growth of tumour cells in vivo and in vitro. Two closely related genes, DLC-2 and DLC-3, may also be tumour suppressors. This review presents the current status of progress in understanding the biological functions of DLC-1 and its relatives and their roles in neoplasia.
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spelling pubmed-44012782015-04-27 DLC-1:a Rho GTPase-activating protein and tumour suppressor Durkin, Marian E Yuan, Bao-Zhu Zhou, Xiaoling Zimonjic, Drazen B Lowy, Douglas R Thorgeirsson, Snorri S Popescu, Nicholas C J Cell Mol Med Special Review Article The deleted in liver cancer 1 (DLC-1) gene encodes a GTPase activating protein that acts as a negative regulator of the Rho family of small GTPases. Rho proteins transduce signals that influence cell morphology and physiology, and their aberrant up-regulation is a key factor in the neoplastic process, including metastasis. Since its discovery, compelling evidence has accumulated that demonstrates a role for DLC-1 as a bona fide tumour suppressor gene in different types of human cancer. Loss of DLC-1 expression mediated by genetic and epigenetic mechanisms has been associated with the development of many human cancers, and restoration of DLC-1 expression inhibited the growth of tumour cells in vivo and in vitro. Two closely related genes, DLC-2 and DLC-3, may also be tumour suppressors. This review presents the current status of progress in understanding the biological functions of DLC-1 and its relatives and their roles in neoplasia. Blackwell Publishing Ltd 2007-09 2007-08-13 /pmc/articles/PMC4401278/ /pubmed/17979893 http://dx.doi.org/10.1111/j.1582-4934.2007.00098.x Text en
spellingShingle Special Review Article
Durkin, Marian E
Yuan, Bao-Zhu
Zhou, Xiaoling
Zimonjic, Drazen B
Lowy, Douglas R
Thorgeirsson, Snorri S
Popescu, Nicholas C
DLC-1:a Rho GTPase-activating protein and tumour suppressor
title DLC-1:a Rho GTPase-activating protein and tumour suppressor
title_full DLC-1:a Rho GTPase-activating protein and tumour suppressor
title_fullStr DLC-1:a Rho GTPase-activating protein and tumour suppressor
title_full_unstemmed DLC-1:a Rho GTPase-activating protein and tumour suppressor
title_short DLC-1:a Rho GTPase-activating protein and tumour suppressor
title_sort dlc-1:a rho gtpase-activating protein and tumour suppressor
topic Special Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4401278/
https://www.ncbi.nlm.nih.gov/pubmed/17979893
http://dx.doi.org/10.1111/j.1582-4934.2007.00098.x
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