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Intravital characterization of tumor cell migration in pancreatic cancer
Curing pancreatic cancer is difficult as metastases often determine the poor clinical outcome. To gain more insight into the metastatic behavior of pancreatic cancer cells, we characterized migratory cells in primary pancreatic tumors using intravital microscopy. We visualized the migratory behavior...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5226006/ https://www.ncbi.nlm.nih.gov/pubmed/28243522 http://dx.doi.org/10.1080/21659087.2016.1261773 |
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author | Beerling, Evelyne Oosterom, Ilse Voest, Emile Lolkema, Martijn van Rheenen, Jacco |
author_facet | Beerling, Evelyne Oosterom, Ilse Voest, Emile Lolkema, Martijn van Rheenen, Jacco |
author_sort | Beerling, Evelyne |
collection | PubMed |
description | Curing pancreatic cancer is difficult as metastases often determine the poor clinical outcome. To gain more insight into the metastatic behavior of pancreatic cancer cells, we characterized migratory cells in primary pancreatic tumors using intravital microscopy. We visualized the migratory behavior of primary tumor cells of a genetically engineered pancreatic cancer mouse model and found that pancreatic tumor cells migrate with a mesenchymal morphology as single individual cells or collectively as a stream of non-cohesive single motile cells. These findings may improve our ability to conceive treatments that block metastatic behavior. |
format | Online Article Text |
id | pubmed-5226006 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-52260062017-02-27 Intravital characterization of tumor cell migration in pancreatic cancer Beerling, Evelyne Oosterom, Ilse Voest, Emile Lolkema, Martijn van Rheenen, Jacco Intravital Short Report Curing pancreatic cancer is difficult as metastases often determine the poor clinical outcome. To gain more insight into the metastatic behavior of pancreatic cancer cells, we characterized migratory cells in primary pancreatic tumors using intravital microscopy. We visualized the migratory behavior of primary tumor cells of a genetically engineered pancreatic cancer mouse model and found that pancreatic tumor cells migrate with a mesenchymal morphology as single individual cells or collectively as a stream of non-cohesive single motile cells. These findings may improve our ability to conceive treatments that block metastatic behavior. Taylor & Francis 2016-11-18 /pmc/articles/PMC5226006/ /pubmed/28243522 http://dx.doi.org/10.1080/21659087.2016.1261773 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 | Short Report Beerling, Evelyne Oosterom, Ilse Voest, Emile Lolkema, Martijn van Rheenen, Jacco Intravital characterization of tumor cell migration in pancreatic cancer |
title | Intravital characterization of tumor cell migration in pancreatic cancer |
title_full | Intravital characterization of tumor cell migration in pancreatic cancer |
title_fullStr | Intravital characterization of tumor cell migration in pancreatic cancer |
title_full_unstemmed | Intravital characterization of tumor cell migration in pancreatic cancer |
title_short | Intravital characterization of tumor cell migration in pancreatic cancer |
title_sort | intravital characterization of tumor cell migration in pancreatic cancer |
topic | Short Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5226006/ https://www.ncbi.nlm.nih.gov/pubmed/28243522 http://dx.doi.org/10.1080/21659087.2016.1261773 |
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