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Dynamic functions of RhoA in tumor cell migration and invasion

RhoA is one of the more extensively studied members of the Rho family of small GTPase where it is most readily recognized for its contributions to actin-myosin contractility and stress fiber formation. Accordingly, RhoA function during cell migration has been relegated to the rear of the cell where...

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Autores principales: O'Connor, Kathleen, Chen, Min
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Landes Bioscience 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3976970/
https://www.ncbi.nlm.nih.gov/pubmed/24025634
http://dx.doi.org/10.4161/sgtp.25131
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author O'Connor, Kathleen
Chen, Min
author_facet O'Connor, Kathleen
Chen, Min
author_sort O'Connor, Kathleen
collection PubMed
description RhoA is one of the more extensively studied members of the Rho family of small GTPase where it is most readily recognized for its contributions to actin-myosin contractility and stress fiber formation. Accordingly, RhoA function during cell migration has been relegated to the rear of the cell where it mediates retraction of the trailing edge. However, RhoA can also mediate membrane ruffling, lamellae formation and membrane blebbing, thus suggesting an active role in membrane protrusions at the leading edge. With the advent of fluorescence resonance energy transfer (FRET)-based Rho activity reporters, RhoA has been shown to be active at the leading edge of migrating cells where it precedes Rac and Cdc42 activation. These observations demonstrate a remarkable versatility to RhoA signaling, but how RhoA function can switch between contraction and protrusion has remained an enigma. This review highlights recent advances regarding how the cooperation of Rho effector Rhotekin and S100A4 suppresses stress fiber generation to permit RhoA-mediated lamellae formation.
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spelling pubmed-39769702014-04-07 Dynamic functions of RhoA in tumor cell migration and invasion O'Connor, Kathleen Chen, Min Small GTPases Mini Review RhoA is one of the more extensively studied members of the Rho family of small GTPase where it is most readily recognized for its contributions to actin-myosin contractility and stress fiber formation. Accordingly, RhoA function during cell migration has been relegated to the rear of the cell where it mediates retraction of the trailing edge. However, RhoA can also mediate membrane ruffling, lamellae formation and membrane blebbing, thus suggesting an active role in membrane protrusions at the leading edge. With the advent of fluorescence resonance energy transfer (FRET)-based Rho activity reporters, RhoA has been shown to be active at the leading edge of migrating cells where it precedes Rac and Cdc42 activation. These observations demonstrate a remarkable versatility to RhoA signaling, but how RhoA function can switch between contraction and protrusion has remained an enigma. This review highlights recent advances regarding how the cooperation of Rho effector Rhotekin and S100A4 suppresses stress fiber generation to permit RhoA-mediated lamellae formation. Landes Bioscience 2013-07-01 2013-06-10 /pmc/articles/PMC3976970/ /pubmed/24025634 http://dx.doi.org/10.4161/sgtp.25131 Text en Copyright © 2013 Landes Bioscience http://creativecommons.org/licenses/by-nc/3.0/ This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited.
spellingShingle Mini Review
O'Connor, Kathleen
Chen, Min
Dynamic functions of RhoA in tumor cell migration and invasion
title Dynamic functions of RhoA in tumor cell migration and invasion
title_full Dynamic functions of RhoA in tumor cell migration and invasion
title_fullStr Dynamic functions of RhoA in tumor cell migration and invasion
title_full_unstemmed Dynamic functions of RhoA in tumor cell migration and invasion
title_short Dynamic functions of RhoA in tumor cell migration and invasion
title_sort dynamic functions of rhoa in tumor cell migration and invasion
topic Mini Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3976970/
https://www.ncbi.nlm.nih.gov/pubmed/24025634
http://dx.doi.org/10.4161/sgtp.25131
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