Evidence map›Paper›PMID 40719870›Full record

ArticleJournal of mathematical biology2025

Reducing phenotype-structured partial differential equations models of cancer evolution to systems of ordinary differential equations: a generalised moment dynamics approach.

Chiara Villa, Philip K Maini, Alexander P Browning, Adrianne L Jenner, Sara Hamis, Tyler Cassidy

Abstract read
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Article in Journal of mathematical biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Adaptive dynamics of diverging fitness optima.Journal of mathematical biology · 2025
    Article
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4 · The record

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PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Chiara VillaUniversité Paris-Saclay, Inria, Centre Inria de Saclay, Palaiseau, 91120, France. chiara.villa@inria.fr.ORCID http://orcid.org/0000-0003-3127-0532
Philip K MainiMathematical Institute, University of Oxford, Oxford, UK.ORCID http://orcid.org/0000-0002-0146-9164
Alexander P BrowningMathematical Institute, University of Oxford, Oxford, UK.ORCID http://orcid.org/0000-0002-8753-1538
Adrianne L JennerSchool of Mathematical Sciences, Queensland University of Technology, Brisbane, Australia.ORCID http://orcid.org/0000-0001-9103-7092
Sara HamisDepartment of Information Technology, Uppsala University, Uppsala, Sweden.ORCID http://orcid.org/0000-0002-1105-8078
Tyler CassidySchool of Mathematics, University of Leeds, Leeds, UK. t.cassidy1@leeds.ac.uk.ORCID http://orcid.org/0000-0003-0757-0017

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Intratumour phenotypic heterogeneity is understood to play a critical role in disease progression and treatment failure. Accordingly, there has been increasing interest in the development of mathematical models capable of capturing its role in cancer cell adaptation. This can be systematically achieved by means of models comprising phenotype-structured nonlocal partial differential equations, tracking the evolution of the phenotypic density distribution of the cell population, which may be compared to gene and protein expression distributions obtained experimentally. Nevertheless, given the high analytical and computational cost of solving these models, much is to be gained from reducing them to systems of ordinary differential equations for the moments of the distribution. We propose a generalised method of model-reduction, relying on the use of a moment generating function, Taylor series expansion and truncation closure, to reduce a nonlocal reaction-advection-diffusion equation, with general phenotypic drift and proliferation rate functions, to a system of moment equations up to arbitrary order. Our method extends previous results in the literature, which we address via three examples, by removing any a priori assumption on the shape of the distribution, and provides a flexible framework for mathematical modellers to account for the role of phenotypic heterogeneity in cancer adaptive dynamics, in a simpler mathematical framework.

Indexed as

Models, BiologicalNeoplasmsCell ProliferationComputer SimulationDisease ProgressionHumansMathematical ConceptsPhenotype

Identifiers

PMID40719870
PMCPMC12304065

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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.