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PAK4 suppresses PDZ-RhoGEF activity to drive invadopodia maturation in melanoma cells
Cancer cells are thought to use actin rich invadopodia to facilitate matrix degradation. Formation and maturation of invadopodia requires the co-ordained activity of Rho-GTPases, however the molecular mechanisms that underlie the invadopodia lifecycle are not fully elucidated. Previous work has sugg...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5342596/ https://www.ncbi.nlm.nih.gov/pubmed/27765920 http://dx.doi.org/10.18632/oncotarget.12282 |
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author | Nicholas, Nicole S. Pipili, Aikaterini Lesjak, Michaela S. Ameer, Simon M. Geh, Jenny L. C. Healy, Ciaran Ross, Alistair D. MacKenzie Parsons, Maddy Nestle, Frank O. Lacy, Katie E. Wells, Claire M. |
author_facet | Nicholas, Nicole S. Pipili, Aikaterini Lesjak, Michaela S. Ameer, Simon M. Geh, Jenny L. C. Healy, Ciaran Ross, Alistair D. MacKenzie Parsons, Maddy Nestle, Frank O. Lacy, Katie E. Wells, Claire M. |
author_sort | Nicholas, Nicole S. |
collection | PubMed |
description | Cancer cells are thought to use actin rich invadopodia to facilitate matrix degradation. Formation and maturation of invadopodia requires the co-ordained activity of Rho-GTPases, however the molecular mechanisms that underlie the invadopodia lifecycle are not fully elucidated. Previous work has suggested a formation and disassembly role for Rho family effector p-21 activated kinase 1 (PAK1) however, related family member PAK4 has not been explored. Systematic analysis of isoform specific depletion using in vitro and in vivo invasion assays revealed there are differential invadopodia-associated functions. We consolidated a role for PAK1 in the invadopodia formation phase and identified PAK4 as a novel invadopodia protein that is required for successful maturation. Furthermore, we find that PAK4 (but not PAK1) mediates invadopodia maturation likely via inhibition of PDZ-RhoGEF. Our work points to an essential role for both PAKs during melanoma invasion but provides a significant advance in our understanding of differential PAK function. |
format | Online Article Text |
id | pubmed-5342596 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-53425962017-03-24 PAK4 suppresses PDZ-RhoGEF activity to drive invadopodia maturation in melanoma cells Nicholas, Nicole S. Pipili, Aikaterini Lesjak, Michaela S. Ameer, Simon M. Geh, Jenny L. C. Healy, Ciaran Ross, Alistair D. MacKenzie Parsons, Maddy Nestle, Frank O. Lacy, Katie E. Wells, Claire M. Oncotarget Research Paper Cancer cells are thought to use actin rich invadopodia to facilitate matrix degradation. Formation and maturation of invadopodia requires the co-ordained activity of Rho-GTPases, however the molecular mechanisms that underlie the invadopodia lifecycle are not fully elucidated. Previous work has suggested a formation and disassembly role for Rho family effector p-21 activated kinase 1 (PAK1) however, related family member PAK4 has not been explored. Systematic analysis of isoform specific depletion using in vitro and in vivo invasion assays revealed there are differential invadopodia-associated functions. We consolidated a role for PAK1 in the invadopodia formation phase and identified PAK4 as a novel invadopodia protein that is required for successful maturation. Furthermore, we find that PAK4 (but not PAK1) mediates invadopodia maturation likely via inhibition of PDZ-RhoGEF. Our work points to an essential role for both PAKs during melanoma invasion but provides a significant advance in our understanding of differential PAK function. Impact Journals LLC 2016-09-27 /pmc/articles/PMC5342596/ /pubmed/27765920 http://dx.doi.org/10.18632/oncotarget.12282 Text en Copyright: © 2016 Nicholas et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Nicholas, Nicole S. Pipili, Aikaterini Lesjak, Michaela S. Ameer, Simon M. Geh, Jenny L. C. Healy, Ciaran Ross, Alistair D. MacKenzie Parsons, Maddy Nestle, Frank O. Lacy, Katie E. Wells, Claire M. PAK4 suppresses PDZ-RhoGEF activity to drive invadopodia maturation in melanoma cells |
title | PAK4 suppresses PDZ-RhoGEF activity to drive invadopodia maturation in melanoma cells |
title_full | PAK4 suppresses PDZ-RhoGEF activity to drive invadopodia maturation in melanoma cells |
title_fullStr | PAK4 suppresses PDZ-RhoGEF activity to drive invadopodia maturation in melanoma cells |
title_full_unstemmed | PAK4 suppresses PDZ-RhoGEF activity to drive invadopodia maturation in melanoma cells |
title_short | PAK4 suppresses PDZ-RhoGEF activity to drive invadopodia maturation in melanoma cells |
title_sort | pak4 suppresses pdz-rhogef activity to drive invadopodia maturation in melanoma cells |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5342596/ https://www.ncbi.nlm.nih.gov/pubmed/27765920 http://dx.doi.org/10.18632/oncotarget.12282 |
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