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Tumor Invasion Optimization by Mesenchymal-Amoeboid Heterogeneity

Metastasizing tumor cells migrate through the surrounding tissue and extracellular matrix toward the blood vessels, in order to colonize distant organs. They typically move in a dense environment, filled with other cells. In this work we study cooperative effects between neighboring cells of differe...

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Autores principales: Hecht, Inbal, Bar-El, Yasmin, Balmer, Frederic, Natan, Sari, Tsarfaty, Ilan, Schweitzer, Frank, Ben-Jacob, Eshel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4650638/
https://www.ncbi.nlm.nih.gov/pubmed/26013062
http://dx.doi.org/10.1038/srep10622
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author Hecht, Inbal
Bar-El, Yasmin
Balmer, Frederic
Natan, Sari
Tsarfaty, Ilan
Schweitzer, Frank
Ben-Jacob, Eshel
author_facet Hecht, Inbal
Bar-El, Yasmin
Balmer, Frederic
Natan, Sari
Tsarfaty, Ilan
Schweitzer, Frank
Ben-Jacob, Eshel
author_sort Hecht, Inbal
collection PubMed
description Metastasizing tumor cells migrate through the surrounding tissue and extracellular matrix toward the blood vessels, in order to colonize distant organs. They typically move in a dense environment, filled with other cells. In this work we study cooperative effects between neighboring cells of different types, migrating in a maze-like environment with directional cue. Using a computerized model, we measure the percentage of cells that arrive to the defined target, for different mesenchymal/amoeboid ratios. Wall degradation of mesenchymal cells, as well as motility of both types of cells, are coupled to metabolic energy-like resource level. We find that indirect cooperation emerges in mid-level energy, as mesenchymal cells create paths that are used by amoeboids. Therefore, we expect to see a small population of mesenchymals kept in a mostly-amoeboid population. We also study different forms of direct interaction between the cells, and show that energy-dependent interaction strength is optimal for the migration of both mesenchymals and amoeboids. The obtained characteristics of cellular cluster size are in agreement with experimental results. We therefore predict that hybrid states, e.g. epithelial-mesenchymal, should be utilized as a stress-response mechanism.
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spelling pubmed-46506382015-11-24 Tumor Invasion Optimization by Mesenchymal-Amoeboid Heterogeneity Hecht, Inbal Bar-El, Yasmin Balmer, Frederic Natan, Sari Tsarfaty, Ilan Schweitzer, Frank Ben-Jacob, Eshel Sci Rep Article Metastasizing tumor cells migrate through the surrounding tissue and extracellular matrix toward the blood vessels, in order to colonize distant organs. They typically move in a dense environment, filled with other cells. In this work we study cooperative effects between neighboring cells of different types, migrating in a maze-like environment with directional cue. Using a computerized model, we measure the percentage of cells that arrive to the defined target, for different mesenchymal/amoeboid ratios. Wall degradation of mesenchymal cells, as well as motility of both types of cells, are coupled to metabolic energy-like resource level. We find that indirect cooperation emerges in mid-level energy, as mesenchymal cells create paths that are used by amoeboids. Therefore, we expect to see a small population of mesenchymals kept in a mostly-amoeboid population. We also study different forms of direct interaction between the cells, and show that energy-dependent interaction strength is optimal for the migration of both mesenchymals and amoeboids. The obtained characteristics of cellular cluster size are in agreement with experimental results. We therefore predict that hybrid states, e.g. epithelial-mesenchymal, should be utilized as a stress-response mechanism. Nature Publishing Group 2015-05-27 /pmc/articles/PMC4650638/ /pubmed/26013062 http://dx.doi.org/10.1038/srep10622 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Hecht, Inbal
Bar-El, Yasmin
Balmer, Frederic
Natan, Sari
Tsarfaty, Ilan
Schweitzer, Frank
Ben-Jacob, Eshel
Tumor Invasion Optimization by Mesenchymal-Amoeboid Heterogeneity
title Tumor Invasion Optimization by Mesenchymal-Amoeboid Heterogeneity
title_full Tumor Invasion Optimization by Mesenchymal-Amoeboid Heterogeneity
title_fullStr Tumor Invasion Optimization by Mesenchymal-Amoeboid Heterogeneity
title_full_unstemmed Tumor Invasion Optimization by Mesenchymal-Amoeboid Heterogeneity
title_short Tumor Invasion Optimization by Mesenchymal-Amoeboid Heterogeneity
title_sort tumor invasion optimization by mesenchymal-amoeboid heterogeneity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4650638/
https://www.ncbi.nlm.nih.gov/pubmed/26013062
http://dx.doi.org/10.1038/srep10622
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