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Novel functions for Rab GTPases in multiple aspects of tumour progression
Rab GTPases are master regulators of intracellular trafficking and, in recent years, their role in the control of different aspects of tumour progression has emerged. In the present review, we show that Rab GTPases are disregulated in many cancers and have central roles in tumour cell migration, inv...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Portland Press Ltd.
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3554041/ https://www.ncbi.nlm.nih.gov/pubmed/23176488 http://dx.doi.org/10.1042/BST20120199 |
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author | Recchi, Chiara Seabra, Miguel C. |
author_facet | Recchi, Chiara Seabra, Miguel C. |
author_sort | Recchi, Chiara |
collection | PubMed |
description | Rab GTPases are master regulators of intracellular trafficking and, in recent years, their role in the control of different aspects of tumour progression has emerged. In the present review, we show that Rab GTPases are disregulated in many cancers and have central roles in tumour cell migration, invasion, proliferation, communication with stromal cells and the development of drug resistance. As a consequence, Rab proteins may be novel potential candidates for the development of anticancer drugs and, in this context, the preliminary results obtained with an inhibitor of Rab function are also discussed. |
format | Online Article Text |
id | pubmed-3554041 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Portland Press Ltd. |
record_format | MEDLINE/PubMed |
spelling | pubmed-35540412013-01-31 Novel functions for Rab GTPases in multiple aspects of tumour progression Recchi, Chiara Seabra, Miguel C. Biochem Soc Trans Biochemical Society Focused Meetings Rab GTPases are master regulators of intracellular trafficking and, in recent years, their role in the control of different aspects of tumour progression has emerged. In the present review, we show that Rab GTPases are disregulated in many cancers and have central roles in tumour cell migration, invasion, proliferation, communication with stromal cells and the development of drug resistance. As a consequence, Rab proteins may be novel potential candidates for the development of anticancer drugs and, in this context, the preliminary results obtained with an inhibitor of Rab function are also discussed. Portland Press Ltd. 2012-11-21 2012-12-01 /pmc/articles/PMC3554041/ /pubmed/23176488 http://dx.doi.org/10.1042/BST20120199 Text en © 2012 The Author(s) The author(s) has paid for this article to be freely available under the terms of the Creative Commons Attribution Non-Commercial Licence (http://creativecommons.org/licenses/by-nc/2.5/) which permits unrestricted non-commercial use, distribution and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/licenses/by-nc/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Biochemical Society Focused Meetings Recchi, Chiara Seabra, Miguel C. Novel functions for Rab GTPases in multiple aspects of tumour progression |
title | Novel functions for Rab GTPases in multiple aspects of tumour progression |
title_full | Novel functions for Rab GTPases in multiple aspects of tumour progression |
title_fullStr | Novel functions for Rab GTPases in multiple aspects of tumour progression |
title_full_unstemmed | Novel functions for Rab GTPases in multiple aspects of tumour progression |
title_short | Novel functions for Rab GTPases in multiple aspects of tumour progression |
title_sort | novel functions for rab gtpases in multiple aspects of tumour progression |
topic | Biochemical Society Focused Meetings |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3554041/ https://www.ncbi.nlm.nih.gov/pubmed/23176488 http://dx.doi.org/10.1042/BST20120199 |
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