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The Protease Activated Receptor2 Promotes Rab5a Mediated Generation of Pro-metastatic Microvesicles
Metastasis, the hallmark of cancer propagation is attributed by the modification of phenotypic/functional behavior of cells to break attachment and migrate to distant body parts. Cancer cell-secreted microvesicles (MVs) contribute immensely in disease propagation. These nano-vesicles, generated from...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5943449/ https://www.ncbi.nlm.nih.gov/pubmed/29743547 http://dx.doi.org/10.1038/s41598-018-25725-w |
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author | Das, Kaushik Prasad, Ramesh Roy, Sreetama Mukherjee, Ashis Sen, Prosenjit |
author_facet | Das, Kaushik Prasad, Ramesh Roy, Sreetama Mukherjee, Ashis Sen, Prosenjit |
author_sort | Das, Kaushik |
collection | PubMed |
description | Metastasis, the hallmark of cancer propagation is attributed by the modification of phenotypic/functional behavior of cells to break attachment and migrate to distant body parts. Cancer cell-secreted microvesicles (MVs) contribute immensely in disease propagation. These nano-vesicles, generated from plasma membrane outward budding are taken up by nearby healthy cells thereby inducing phenotypic alterations in those recipient cells. Protease activated receptor 2 (PAR2), activated by trypsin, also contributes to cancer progression by increasing metastasis, angiogenesis etc. Here, we report that PAR2 activation promotes pro-metastatic MVs generation from human breast cancer cell line, MDA-MB-231. Rab5a, located at the plasma membrane plays vital roles in MVs biogenesis. We show that PAR2 stimulation promotes AKT phosphorylation which activates Rab5a by converting inactive Rab5a-GDP to active Rab5a-GTP. Active Rab5a polymerizes actin which critically regulates MVs shedding. Not only MVs generation, has this Rab5a activation also promoted cell migration and invasion. We reveal that Rab5a is over-expressed in human breast tumor specimen and contributes MVs generation in those patients. The involvement of p38 MAPK in MVs-induced cell metastasis has also been highlighted in the present study. Blockade of Rab5a activation can be a potential therapeutic approach to restrict MVs shedding and associated breast cancer metastasis. |
format | Online Article Text |
id | pubmed-5943449 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-59434492018-05-14 The Protease Activated Receptor2 Promotes Rab5a Mediated Generation of Pro-metastatic Microvesicles Das, Kaushik Prasad, Ramesh Roy, Sreetama Mukherjee, Ashis Sen, Prosenjit Sci Rep Article Metastasis, the hallmark of cancer propagation is attributed by the modification of phenotypic/functional behavior of cells to break attachment and migrate to distant body parts. Cancer cell-secreted microvesicles (MVs) contribute immensely in disease propagation. These nano-vesicles, generated from plasma membrane outward budding are taken up by nearby healthy cells thereby inducing phenotypic alterations in those recipient cells. Protease activated receptor 2 (PAR2), activated by trypsin, also contributes to cancer progression by increasing metastasis, angiogenesis etc. Here, we report that PAR2 activation promotes pro-metastatic MVs generation from human breast cancer cell line, MDA-MB-231. Rab5a, located at the plasma membrane plays vital roles in MVs biogenesis. We show that PAR2 stimulation promotes AKT phosphorylation which activates Rab5a by converting inactive Rab5a-GDP to active Rab5a-GTP. Active Rab5a polymerizes actin which critically regulates MVs shedding. Not only MVs generation, has this Rab5a activation also promoted cell migration and invasion. We reveal that Rab5a is over-expressed in human breast tumor specimen and contributes MVs generation in those patients. The involvement of p38 MAPK in MVs-induced cell metastasis has also been highlighted in the present study. Blockade of Rab5a activation can be a potential therapeutic approach to restrict MVs shedding and associated breast cancer metastasis. Nature Publishing Group UK 2018-05-09 /pmc/articles/PMC5943449/ /pubmed/29743547 http://dx.doi.org/10.1038/s41598-018-25725-w Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Das, Kaushik Prasad, Ramesh Roy, Sreetama Mukherjee, Ashis Sen, Prosenjit The Protease Activated Receptor2 Promotes Rab5a Mediated Generation of Pro-metastatic Microvesicles |
title | The Protease Activated Receptor2 Promotes Rab5a Mediated Generation of Pro-metastatic Microvesicles |
title_full | The Protease Activated Receptor2 Promotes Rab5a Mediated Generation of Pro-metastatic Microvesicles |
title_fullStr | The Protease Activated Receptor2 Promotes Rab5a Mediated Generation of Pro-metastatic Microvesicles |
title_full_unstemmed | The Protease Activated Receptor2 Promotes Rab5a Mediated Generation of Pro-metastatic Microvesicles |
title_short | The Protease Activated Receptor2 Promotes Rab5a Mediated Generation of Pro-metastatic Microvesicles |
title_sort | protease activated receptor2 promotes rab5a mediated generation of pro-metastatic microvesicles |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5943449/ https://www.ncbi.nlm.nih.gov/pubmed/29743547 http://dx.doi.org/10.1038/s41598-018-25725-w |
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