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Collective cell migration and metastases induced by an epithelial-to-mesenchymal transition in Drosophila intestinal tumors

Metastasis underlies the majority of cancer-related deaths yet remains poorly understood due, in part, to the lack of models in vivo. Here we show that expression of the EMT master inducer Snail in primary adult Drosophila intestinal tumors leads to the dissemination of tumor cells and formation of...

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Autores principales: Campbell, Kyra, Rossi, Fabrizio, Adams, Jamie, Pitsidianaki, Ioanna, Barriga, Francisco M., Garcia-Gerique, Laura, Batlle, Eduard, Casanova, Jordi, Casali, Andreu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6534551/
https://www.ncbi.nlm.nih.gov/pubmed/31127094
http://dx.doi.org/10.1038/s41467-019-10269-y
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author Campbell, Kyra
Rossi, Fabrizio
Adams, Jamie
Pitsidianaki, Ioanna
Barriga, Francisco M.
Garcia-Gerique, Laura
Batlle, Eduard
Casanova, Jordi
Casali, Andreu
author_facet Campbell, Kyra
Rossi, Fabrizio
Adams, Jamie
Pitsidianaki, Ioanna
Barriga, Francisco M.
Garcia-Gerique, Laura
Batlle, Eduard
Casanova, Jordi
Casali, Andreu
author_sort Campbell, Kyra
collection PubMed
description Metastasis underlies the majority of cancer-related deaths yet remains poorly understood due, in part, to the lack of models in vivo. Here we show that expression of the EMT master inducer Snail in primary adult Drosophila intestinal tumors leads to the dissemination of tumor cells and formation of macrometastases. Snail drives an EMT in tumor cells, which, although retaining some epithelial markers, subsequently break through the basal lamina of the midgut, undergo a collective migration and seed polyclonal metastases. While metastases re-epithelialize over time, we found that early metastases are remarkably mesenchymal, discarding the requirement for a mesenchymal-to-epithelial transition for early stages of metastatic growth. Our results demonstrate the formation of metastases in adult flies, and identify a key role for partial-EMTs in driving it. This model opens the door to investigate the basic mechanisms underlying metastasis, in a powerful in vivo system suited for rapid genetic and drug screens.
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spelling pubmed-65345512019-05-28 Collective cell migration and metastases induced by an epithelial-to-mesenchymal transition in Drosophila intestinal tumors Campbell, Kyra Rossi, Fabrizio Adams, Jamie Pitsidianaki, Ioanna Barriga, Francisco M. Garcia-Gerique, Laura Batlle, Eduard Casanova, Jordi Casali, Andreu Nat Commun Article Metastasis underlies the majority of cancer-related deaths yet remains poorly understood due, in part, to the lack of models in vivo. Here we show that expression of the EMT master inducer Snail in primary adult Drosophila intestinal tumors leads to the dissemination of tumor cells and formation of macrometastases. Snail drives an EMT in tumor cells, which, although retaining some epithelial markers, subsequently break through the basal lamina of the midgut, undergo a collective migration and seed polyclonal metastases. While metastases re-epithelialize over time, we found that early metastases are remarkably mesenchymal, discarding the requirement for a mesenchymal-to-epithelial transition for early stages of metastatic growth. Our results demonstrate the formation of metastases in adult flies, and identify a key role for partial-EMTs in driving it. This model opens the door to investigate the basic mechanisms underlying metastasis, in a powerful in vivo system suited for rapid genetic and drug screens. Nature Publishing Group UK 2019-05-24 /pmc/articles/PMC6534551/ /pubmed/31127094 http://dx.doi.org/10.1038/s41467-019-10269-y Text en © The Author(s) 2019 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
Campbell, Kyra
Rossi, Fabrizio
Adams, Jamie
Pitsidianaki, Ioanna
Barriga, Francisco M.
Garcia-Gerique, Laura
Batlle, Eduard
Casanova, Jordi
Casali, Andreu
Collective cell migration and metastases induced by an epithelial-to-mesenchymal transition in Drosophila intestinal tumors
title Collective cell migration and metastases induced by an epithelial-to-mesenchymal transition in Drosophila intestinal tumors
title_full Collective cell migration and metastases induced by an epithelial-to-mesenchymal transition in Drosophila intestinal tumors
title_fullStr Collective cell migration and metastases induced by an epithelial-to-mesenchymal transition in Drosophila intestinal tumors
title_full_unstemmed Collective cell migration and metastases induced by an epithelial-to-mesenchymal transition in Drosophila intestinal tumors
title_short Collective cell migration and metastases induced by an epithelial-to-mesenchymal transition in Drosophila intestinal tumors
title_sort collective cell migration and metastases induced by an epithelial-to-mesenchymal transition in drosophila intestinal tumors
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6534551/
https://www.ncbi.nlm.nih.gov/pubmed/31127094
http://dx.doi.org/10.1038/s41467-019-10269-y
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