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Arf proteins in cancer cell migration

Members of the ADP-ribosylation factor (Arf) family of small GTP-binding (G) proteins regulate several aspects of membrane trafficking, such as vesicle budding, tethering and cytoskeleton organization. Arf family members, including Arf-like (Arl) proteins have been implicated in several essential ce...

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Detalles Bibliográficos
Autores principales: Casalou, Cristina, Faustino, Alexandra, Barral, Duarte C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5129889/
https://www.ncbi.nlm.nih.gov/pubmed/27589148
http://dx.doi.org/10.1080/21541248.2016.1228792
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author Casalou, Cristina
Faustino, Alexandra
Barral, Duarte C.
author_facet Casalou, Cristina
Faustino, Alexandra
Barral, Duarte C.
author_sort Casalou, Cristina
collection PubMed
description Members of the ADP-ribosylation factor (Arf) family of small GTP-binding (G) proteins regulate several aspects of membrane trafficking, such as vesicle budding, tethering and cytoskeleton organization. Arf family members, including Arf-like (Arl) proteins have been implicated in several essential cellular functions, like cell spreading and migration. These functions are used by cancer cells to disseminate and invade the tissues surrounding the primary tumor, leading to the formation of metastases. Indeed, Arf and Arl proteins, as well as their guanine nucleotide exchange factors (GEFs) and GTPase-activating proteins (GAPs) have been found to be abnormally expressed in different cancer cell types and human cancers. Here, we review the current evidence supporting the involvement of Arf family proteins and their GEFs and GAPs in cancer progression, focusing on 3 different mechanisms: cell-cell adhesion, integrin internalization and recycling, and actin cytoskeleton remodeling.
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spelling pubmed-51298892016-12-19 Arf proteins in cancer cell migration Casalou, Cristina Faustino, Alexandra Barral, Duarte C. Small GTPases Commentary Members of the ADP-ribosylation factor (Arf) family of small GTP-binding (G) proteins regulate several aspects of membrane trafficking, such as vesicle budding, tethering and cytoskeleton organization. Arf family members, including Arf-like (Arl) proteins have been implicated in several essential cellular functions, like cell spreading and migration. These functions are used by cancer cells to disseminate and invade the tissues surrounding the primary tumor, leading to the formation of metastases. Indeed, Arf and Arl proteins, as well as their guanine nucleotide exchange factors (GEFs) and GTPase-activating proteins (GAPs) have been found to be abnormally expressed in different cancer cell types and human cancers. Here, we review the current evidence supporting the involvement of Arf family proteins and their GEFs and GAPs in cancer progression, focusing on 3 different mechanisms: cell-cell adhesion, integrin internalization and recycling, and actin cytoskeleton remodeling. Taylor & Francis 2016-09-02 /pmc/articles/PMC5129889/ /pubmed/27589148 http://dx.doi.org/10.1080/21541248.2016.1228792 Text en © 2016 The Author(s). Published with license by Taylor & Francis http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. The moral rights of the named author(s) have been asserted.
spellingShingle Commentary
Casalou, Cristina
Faustino, Alexandra
Barral, Duarte C.
Arf proteins in cancer cell migration
title Arf proteins in cancer cell migration
title_full Arf proteins in cancer cell migration
title_fullStr Arf proteins in cancer cell migration
title_full_unstemmed Arf proteins in cancer cell migration
title_short Arf proteins in cancer cell migration
title_sort arf proteins in cancer cell migration
topic Commentary
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5129889/
https://www.ncbi.nlm.nih.gov/pubmed/27589148
http://dx.doi.org/10.1080/21541248.2016.1228792
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