Evidence map›Paper›PMID 41091123›Full record

ArticleeLife2025

BEHAV3D Tumor Profiler to map heterogeneous cancer cell behavior in the tumor microenvironment.

Emilio Rios-Jimenez, Anoek Zomer, Raphael Collot, Mario Barrera Román, Sandra F Archidona, Hendrikus Ariese, Ravian van Ineveld, Michiel Kleinnijenhuis, Nils Bessler, Hannah Johnson and 3 more

Abstract read
In one paragraph

Article in eLife, 2025. 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

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

1 citing paper in PubMed.

  1. Article
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

13 authors.

Emilio Rios-Jimenez *Institute for Biomedical Research Sols-Morreale (IIBM), Spanish National Research Council- Universidad Autónoma de Madrid, Madrid, Spain.ORCID https://orcid.org/0009-0002-4032-8716
Anoek Zomer *Princess Máxima Center for Pediatric Oncology, Utrecht, Netherlands.
Raphael CollotPrincess Máxima Center for Pediatric Oncology, Utrecht, Netherlands.
Mario Barrera RománPrincess Máxima Center for Pediatric Oncology, Utrecht, Netherlands.ORCID https://orcid.org/0000-0002-5919-2962
Sandra F ArchidonaInstitute for Biomedical Research Sols-Morreale (IIBM), Spanish National Research Council- Universidad Autónoma de Madrid, Madrid, Spain.
Hendrikus AriesePrincess Máxima Center for Pediatric Oncology, Utrecht, Netherlands.
Ravian van IneveldPrincess Máxima Center for Pediatric Oncology, Utrecht, Netherlands.
Michiel KleinnijenhuisPrincess Máxima Center for Pediatric Oncology, Utrecht, Netherlands.
Nils BesslerPrincess Máxima Center for Pediatric Oncology, Utrecht, Netherlands.
Hannah JohnsonPrincess Máxima Center for Pediatric Oncology, Utrecht, Netherlands.
Caleb A DawsonACRF Cancer Biology and Stem Cells Division, The Walter and Eliza Hall Institute of Medical Research, Parkville, Australia.
Anne RiosPrincess Máxima Center for Pediatric Oncology, Utrecht, Netherlands.
Maria AlievaInstitute for Biomedical Research Sols-Morreale (IIBM), Spanish National Research Council- Universidad Autónoma de Madrid, Madrid, Spain.ORCID https://orcid.org/0000-0002-1425-9908

Funding

Comunidad de Madrid 2022-T1/BMD-24021European Research Council 804412Leonardo Grant for Scientific Research and Cultural Creation, BBVA Foundation LEO23-2-10305-BBM-BAS-144Veni fellowship by the Netherlands Organization for Scientific Research 09150161910076V FERO ASEICA Research Award BFERO2024.04
6 · The paper itself

Abstract

Intravital microscopy (IVM) enables live imaging of animals at single-cell level, offering essential insights into cancer progression. This technique allows for the observation of single-cell behaviors within their natural 3D tissue environments, shedding light on how genetic and microenvironmental changes influence the complex dynamics of tumors. IVM generates highly complex datasets that often exceed the analytical capacity of traditional uni-parametric approaches, which can neglect single-cell heterogeneous in vivo behavior and limit insights into microenvironmental influences on cellular behavior. To overcome these limitations, we present BEHAV3D Tumor Profiler (BEHAV3D-TP), a computational framework that enables unbiased single-cell classification based on a range of morphological, environmental, and dynamic single-cell features. BEHAV3D-TP integrates with widely used 2D and 3D image processing pipelines, enabling researchers without advanced computational expertise to profile cancer and healthy cell dynamics in IVM data from mouse models. Here, we apply BEHAV3D-TP to study diffuse midline glioma (DMG), a highly aggressive pediatric brain tumor characterized by invasive progression. By extending BEHAV3D-TP to incorporate tumor microenvironment (TME) data from IVM or fixed correlative imaging, we demonstrate that distinct migratory behaviors of DMG cells are associated with specific TME components, including tumor-associated macrophages and vasculature. BEHAV3D-TP enhances the accessibility of computational tools for analyzing the complex behaviors of cancer cells and their interactions with the TME in IVM data.

Indexed as

Brain NeoplasmsGliomaIntravital MicroscopySingle-Cell AnalysisTumor MicroenvironmentAnimalsHumansImaging, Three-DimensionalMicecancer biologycell migrationcomputational biologyconfocal microscopyimage analysismousesystems biology

Identifiers

PMID41091123
PMCPMC12527384

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.