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Roles of Rap1 signaling in tumor cell migration and invasion

Ras-associated protein-1 (Rap1), a small GTPase in the Ras-related protein family, is an important regulator of basic cellular functions (e.g., formation and control of cell adhesions and junctions), cellular migration, and polarization. Through its interaction with other proteins, Rap1 plays many r...

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Autores principales: Zhang, Yi-Lei, Wang, Ruo-Chen, Cheng, Ken, Ring, Brian Z., Su, Li
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Chinese Anti-Cancer Association 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5365179/
https://www.ncbi.nlm.nih.gov/pubmed/28443208
http://dx.doi.org/10.20892/j.issn.2095-3941.2016.0086
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author Zhang, Yi-Lei
Wang, Ruo-Chen
Cheng, Ken
Ring, Brian Z.
Su, Li
author_facet Zhang, Yi-Lei
Wang, Ruo-Chen
Cheng, Ken
Ring, Brian Z.
Su, Li
author_sort Zhang, Yi-Lei
collection PubMed
description Ras-associated protein-1 (Rap1), a small GTPase in the Ras-related protein family, is an important regulator of basic cellular functions (e.g., formation and control of cell adhesions and junctions), cellular migration, and polarization. Through its interaction with other proteins, Rap1 plays many roles during cell invasion and metastasis in different cancers. The basic function of Rap1 is straightforward; it acts as a switch during cellular signaling transduction and regulated by its binding to either guanosine triphosphate (GTP) or guanosine diphosphate (GDP). However, its remarkably diverse function is rendered by its interplay with a large number of distinct Rap guanine nucleotide exchange factors and Rap GTPase activating proteins. This review summarizes the mechanisms by which Rap1 signaling can regulate cell invasion and metastasis, focusing on its roles in integrin and cadherin regulation, Rho GTPase control, and matrix metalloproteinase expression.
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spelling pubmed-53651792017-04-25 Roles of Rap1 signaling in tumor cell migration and invasion Zhang, Yi-Lei Wang, Ruo-Chen Cheng, Ken Ring, Brian Z. Su, Li Cancer Biol Med Review Ras-associated protein-1 (Rap1), a small GTPase in the Ras-related protein family, is an important regulator of basic cellular functions (e.g., formation and control of cell adhesions and junctions), cellular migration, and polarization. Through its interaction with other proteins, Rap1 plays many roles during cell invasion and metastasis in different cancers. The basic function of Rap1 is straightforward; it acts as a switch during cellular signaling transduction and regulated by its binding to either guanosine triphosphate (GTP) or guanosine diphosphate (GDP). However, its remarkably diverse function is rendered by its interplay with a large number of distinct Rap guanine nucleotide exchange factors and Rap GTPase activating proteins. This review summarizes the mechanisms by which Rap1 signaling can regulate cell invasion and metastasis, focusing on its roles in integrin and cadherin regulation, Rho GTPase control, and matrix metalloproteinase expression. Chinese Anti-Cancer Association 2017-02 /pmc/articles/PMC5365179/ /pubmed/28443208 http://dx.doi.org/10.20892/j.issn.2095-3941.2016.0086 Text en Copyright 2017 Cancer Biology & Medicine http://creativecommons.org/licenses/by-nc-sa/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-Share Alike 4.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/4.0/
spellingShingle Review
Zhang, Yi-Lei
Wang, Ruo-Chen
Cheng, Ken
Ring, Brian Z.
Su, Li
Roles of Rap1 signaling in tumor cell migration and invasion
title Roles of Rap1 signaling in tumor cell migration and invasion
title_full Roles of Rap1 signaling in tumor cell migration and invasion
title_fullStr Roles of Rap1 signaling in tumor cell migration and invasion
title_full_unstemmed Roles of Rap1 signaling in tumor cell migration and invasion
title_short Roles of Rap1 signaling in tumor cell migration and invasion
title_sort roles of rap1 signaling in tumor cell migration and invasion
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5365179/
https://www.ncbi.nlm.nih.gov/pubmed/28443208
http://dx.doi.org/10.20892/j.issn.2095-3941.2016.0086
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