Evidence map›Paper›PMID 42160268›Full record

ArticlePloS one2026

Modeling cell migratory persistence through temporal correlations and angular noise.

Ignacio Montenegro-Rojas, Martín Andaur-Lobos, Karol Soler-Orozco, Diego Castelli-Lacunza, Cristina Bertocchi, Anastasios Matzavinos, Andrea Ravasio

Abstract read
In one paragraph

Article in PloS one, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

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

7 authors.

Ignacio Montenegro-RojasInstitute for Biological and Medical Engineering, Schools of Engineering, Medicine and Biological Sciences, Pontificia Universidad Católica de Chile, Santiago, Chile.ORCID https://orcid.org/0009-0009-0828-5358
Martín Andaur-LobosInstitute for Biological and Medical Engineering, Schools of Engineering, Medicine and Biological Sciences, Pontificia Universidad Católica de Chile, Santiago, Chile.
Karol Soler-OrozcoInstitute for Biological and Medical Engineering, Schools of Engineering, Medicine and Biological Sciences, Pontificia Universidad Católica de Chile, Santiago, Chile.
Diego Castelli-LacunzaInstitute for Mathematical and Computational Engineering, School of Engineering, Pontificia Universidad Católica de Chile, Santiago, Chile.
Cristina BertocchiFaculty of Biological Sciences, Pontificia Universidad Católica de Chile, Santiago, Chile.
Anastasios MatzavinosInstitute for Mathematical and Computational Engineering, School of Engineering, Pontificia Universidad Católica de Chile, Santiago, Chile.
Andrea RavasioInstitute for Biological and Medical Engineering, Schools of Engineering, Medicine and Biological Sciences, Pontificia Universidad Católica de Chile, Santiago, Chile.ORCID https://orcid.org/0000-0001-7835-5133

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The persistence of cell migration is a fundamental property of motile behavior, enabling cells to maintain directionality while adapting to fluctuations and external cues. This feature underlies essential processes such as development, immune responses, and cancer invasion. Classical mathematical models have offered key insights into directed migration, yet they often neglect temporal correlations arising from cellular mechanisms that stabilize polarity and protrusion dynamics. Here, we introduce an agent-based model based on stochastic differential equations that integrates fractional Brownian motion to explicitly incorporate translational autocorrelation in cell trajectories. We simulate migration as a function of angular reorientation and the strength of correlated noise. In this framework, temporal correlation stabilizes trajectory features inherited from initial conditions, whereas angular reorientation introduces variability that enables transitions between erratic and directed motion. Our simulations show that, unlike models driven by white noise, positive correlation markedly enhances persistence even under strong angular reorientation. Moreover, the combination of [Formula: see text] and [Formula: see text] gives rise to emergent behaviors, particularly in the presence of taxis, where persistence and responsiveness are jointly tuned. These results identify correlated noise as a proxy for intrinsic cellular memory and provide a versatile computational framework to interpret the diversity and complexity of migratory behaviors.

Indexed as

Cell MovementModels, BiologicalComputer SimulationStochastic Processes

Identifiers

PMID42160268
PMCPMC13189357

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.