Evidence map›Paper›PMID 33212726›Full record

ArticlePhysical review. E2020

Comparative study between discrete and continuum models for the evolution of competing phenotype-structured cell populations in dynamical environments.

Aleksandra Ardaševa, Alexander R A Anderson, Robert A Gatenby, Helen M Byrne, Philip K Maini, Tommaso Lorenzi

Abstract readComparative Study
In one paragraph

Article in Physical review. E, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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

What it found

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Aleksandra ArdaševaWolfson Centre for Mathematical Biology, University of Oxford, Oxford OX2 6GG, United Kingdom.
Alexander R A AndersonDepartment of Integrated Mathematical Oncology, H. Lee Moffitt Cancer Center, Tampa, Florida 33612, USA.
Robert A GatenbyDepartment of Integrated Mathematical Oncology, H. Lee Moffitt Cancer Center, Tampa, Florida 33612, USA.
Helen M ByrneWolfson Centre for Mathematical Biology, University of Oxford, Oxford OX2 6GG, United Kingdom.
Philip K MainiWolfson Centre for Mathematical Biology, University of Oxford, Oxford OX2 6GG, United Kingdom.
Tommaso LorenziDepartment of Mathematical Sciences "G. L. Lagrange", Dipartimento di Eccellenza 2018-2022, Politecnico di Torino, Italy.

Funding

"Research Supplement to Promote Diversity in Health-Related Research", as part of Moffitt PS-OC, "Cancer as a Complex adaptive System"U54CA193489 · NCI · H. LEE MOFFITT CANCER CTR & RES INST · PI ANDERSON, ALEXANDER ROBERTSON ALLAN, GATENBY, ROBERT A · 2015 to 2020
$12.5M
Eco-Evolutionary dynamics of NSCLC to immunotherapy: Response and ResistanceU01CA232382 · NCI · H. LEE MOFFITT CANCER CTR & RES INST · PI ANDERSON, ALEXANDER ROBERTSON ALLAN, ANTONIA, SCOTT J. · 2018 to 2022
$3.3M
NCI NIH HHS U01 CA232382NCI NIH HHS U54 CA193489
6 · The paper itself

Abstract

Deterministic continuum models formulated as nonlocal partial differential equations for the evolutionary dynamics of populations structured by phenotypic traits have been used recently to address open questions concerning the adaptation of asexual species to periodically fluctuating environmental conditions. These models are usually defined on the basis of population-scale phenomenological assumptions and cannot capture adaptive phenomena that are driven by stochastic variability in the evolutionary paths of single individuals. In light of these considerations, in this paper we develop a stochastic individual-based model for the coevolution of two competing phenotype-structured cell populations that are exposed to time-varying nutrient levels and undergo spontaneous, heritable phenotypic changes with different probabilities. Here, the evolution of every cell is described by a set of rules that result in a discrete-time branching random walk on the space of phenotypic states, and nutrient levels are governed by a difference equation in which a sink term models nutrient consumption by the cells. We formally show that the deterministic continuum counterpart of this model comprises a system of nonlocal partial differential equations for the cell population density functions coupled with an ordinary differential equation for the nutrient concentration. We compare the individual-based model and its continuum analog, focusing on scenarios whereby the predictions of the two models differ. The results obtained clarify the conditions under which significant differences between the two models can emerge due to bottleneck effects that bring about both lower regularity of the density functions of the two populations and more pronounced demographic stochasticity. In particular, bottleneck effects emerge in the presence of lower probabilities of phenotypic variation and are more apparent when the two populations are characterized by lower fitness initial mean phenotypes and smaller initial levels of phenotypic heterogeneity. The emergence of these effects, and thus the agreement between the two modeling approaches, is also dependent on the initial proportions of the two populations. As an illustrative example, we demonstrate the implications of these results in the context of the mathematical modeling of the early stage of metastatic colonization of distant organs.

Indexed as

Evolution, MolecularModels, GeneticPhenotypeAdaptation, PhysiologicalEnvironmentStochastic Processes

Identifiers

PMID33212726
PMCPMC10900972

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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.