Evidence map›Paper›PMID 37011021›Full record

ArticleThe journal of physical chemistry. B2023

Multiscale Modeling of Spheroid Tumors: Effect of Nutrient Availability on Tumor Evolution.

Jakob Rosenbauer, Marco Berghoff, James A Glazier, Alexander Schug

Abstract read
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Article in The journal of physical chemistry. B, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Jakob RosenbauerJülich Supercomputing Center, Forschungszentrum Jülich, Jülich, Nordrhein-Westfalen 52425, Germany.
Marco BerghoffSteinbuch Center for Computing, Karlsruhe Institute of Technology, Karlsruhe, Baden-Württemberg 76021, Germany.
James A GlazierBiocomplexity Institute, Indiana University, Bloomington, Indiana 47408, United States.
Alexander SchugJülich Supercomputing Center, Forschungszentrum Jülich, Jülich, Nordrhein-Westfalen 52425, Germany.ORCID 0000-0002-0534-502X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

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.

Indexed as

NeoplasmsCell MovementComputer SimulationHumansNutrientsTumor MicroenvironmentNutrients

Identifiers

PMID37011021
PMCPMC10150357

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.