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Multiscale Modeling of Spheroid Tumors: Effect of Nutrient Availability on Tumor Evolution
[Image: see text] Recent years have revealed a large number of complex mechanisms and interactions that drive the development of malignant tumors. Tumor evolution is a framework that explains tumor development as a process driven by survival of the fittest, with tumor cells of different properties c...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10150357/ https://www.ncbi.nlm.nih.gov/pubmed/37011021 http://dx.doi.org/10.1021/acs.jpcb.2c08114 |
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author | Rosenbauer, Jakob Berghoff, Marco Glazier, James A. Schug, Alexander |
author_facet | Rosenbauer, Jakob Berghoff, Marco Glazier, James A. Schug, Alexander |
author_sort | Rosenbauer, Jakob |
collection | PubMed |
description | [Image: see text] Recent years have revealed a large number of complex mechanisms and interactions that drive the development of malignant tumors. Tumor evolution is a framework that explains tumor development as a process driven by survival of the fittest, with tumor cells of different properties competing for limited available resources. To predict the evolutionary trajectory of a tumor, knowledge of how cellular properties influence the fitness of a subpopulation in the context of the microenvironment is required and is often inaccessible. Computational multiscale-modeling of tissues enables the observation of the full trajectory of each cell within the tumor environment. Here, we model a 3D spheroid tumor with subcellular resolution. The fitness of individual cells and the evolutionary behavior of the tumor are quantified and linked to cellular and environmental parameters. The fitness of cells is solely influenced by their position in the tumor, which in turn is influenced by the two variable parameters of our model: cell–cell adhesion and cell motility. We observe the influence of nutrient independence and static and dynamically changing nutrient availability on the evolutionary trajectories of heterogeneous tumors in a high-resolution computational model. Regardless of nutrient availability, we find a fitness advantage of low-adhesion cells, which are favorable for tumor invasion. We find that the introduction of nutrient-dependent cell division and death accelerates the evolutionary speed. The evolutionary speed can be increased by fluctuations in nutrients. We identify a distinct frequency domain in which the evolutionary speed increases significantly over a tumor with constant nutrient supply. The findings suggest that an unstable supply of nutrients can accelerate tumor evolution and, thus, the transition to malignancy. |
format | Online Article Text |
id | pubmed-10150357 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-101503572023-05-02 Multiscale Modeling of Spheroid Tumors: Effect of Nutrient Availability on Tumor Evolution Rosenbauer, Jakob Berghoff, Marco Glazier, James A. Schug, Alexander J Phys Chem B [Image: see text] Recent years have revealed a large number of complex mechanisms and interactions that drive the development of malignant tumors. Tumor evolution is a framework that explains tumor development as a process driven by survival of the fittest, with tumor cells of different properties competing for limited available resources. To predict the evolutionary trajectory of a tumor, knowledge of how cellular properties influence the fitness of a subpopulation in the context of the microenvironment is required and is often inaccessible. Computational multiscale-modeling of tissues enables the observation of the full trajectory of each cell within the tumor environment. Here, we model a 3D spheroid tumor with subcellular resolution. The fitness of individual cells and the evolutionary behavior of the tumor are quantified and linked to cellular and environmental parameters. The fitness of cells is solely influenced by their position in the tumor, which in turn is influenced by the two variable parameters of our model: cell–cell adhesion and cell motility. We observe the influence of nutrient independence and static and dynamically changing nutrient availability on the evolutionary trajectories of heterogeneous tumors in a high-resolution computational model. Regardless of nutrient availability, we find a fitness advantage of low-adhesion cells, which are favorable for tumor invasion. We find that the introduction of nutrient-dependent cell division and death accelerates the evolutionary speed. The evolutionary speed can be increased by fluctuations in nutrients. We identify a distinct frequency domain in which the evolutionary speed increases significantly over a tumor with constant nutrient supply. The findings suggest that an unstable supply of nutrients can accelerate tumor evolution and, thus, the transition to malignancy. American Chemical Society 2023-04-03 /pmc/articles/PMC10150357/ /pubmed/37011021 http://dx.doi.org/10.1021/acs.jpcb.2c08114 Text en © 2023 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Rosenbauer, Jakob Berghoff, Marco Glazier, James A. Schug, Alexander Multiscale Modeling of Spheroid Tumors: Effect of Nutrient Availability on Tumor Evolution |
title | Multiscale Modeling of Spheroid Tumors: Effect of
Nutrient Availability on Tumor Evolution |
title_full | Multiscale Modeling of Spheroid Tumors: Effect of
Nutrient Availability on Tumor Evolution |
title_fullStr | Multiscale Modeling of Spheroid Tumors: Effect of
Nutrient Availability on Tumor Evolution |
title_full_unstemmed | Multiscale Modeling of Spheroid Tumors: Effect of
Nutrient Availability on Tumor Evolution |
title_short | Multiscale Modeling of Spheroid Tumors: Effect of
Nutrient Availability on Tumor Evolution |
title_sort | multiscale modeling of spheroid tumors: effect of
nutrient availability on tumor evolution |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10150357/ https://www.ncbi.nlm.nih.gov/pubmed/37011021 http://dx.doi.org/10.1021/acs.jpcb.2c08114 |
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