Evidence map›Paper›PMID 41022685›Full record

ArticleNature communications2025

Biomimetic organo-hydrogels reveal the adipose tissue local mechanical anisotropy regulates ovarian cancer invasion.

Jordi Gonzalez-Molina, Parisa Nabili, Daniele Marciano, Sara Abdelnabi, Okan Gultekin, Mohammed Fatih Rasul, Yikun Zhang, Clémence Nadal, Alexandra Chrysanthou, Twana Alkasalias and 4 more

Abstract read
In one paragraph

Article in Nature communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Review
  3. 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

14 authors.

Jordi Gonzalez-MolinaDepartment of Microbiology, Tumor and Cell Biology, Karolinska Institutet, Solnavägen 9, Solna, Sweden. jordigonzalezmolina@gmail.com.ORCID http://orcid.org/0000-0003-4306-1498
Parisa NabiliDepartment of Microbiology, Tumor and Cell Biology, Karolinska Institutet, Solnavägen 9, Solna, Sweden.
Daniele MarcianoSchool of Engineering and Materials Science, Queen Mary University of London, Mile End Road, London, United Kingdom.ORCID http://orcid.org/0000-0002-2996-6146
Sara AbdelnabiDepartment of Microbiology, Tumor and Cell Biology, Karolinska Institutet, Solnavägen 9, Solna, Sweden.
Okan GultekinDepartment of Microbiology, Tumor and Cell Biology, Karolinska Institutet, Solnavägen 9, Solna, Sweden.ORCID http://orcid.org/0000-0003-0248-2384
Mohammed Fatih RasulDepartment of Women's and Children's Health, Division of Obstetrics and Gynecology, Karolinska Institutet, Solnavägen, Solna, Sweden.
Yikun ZhangSchool of Engineering and Materials Science, Queen Mary University of London, Mile End Road, London, United Kingdom.
Clémence NadalSchool of Engineering and Materials Science, Queen Mary University of London, Mile End Road, London, United Kingdom.
Alexandra ChrysanthouSchool of Engineering and Materials Science, Queen Mary University of London, Mile End Road, London, United Kingdom.
Twana AlkasaliasDepartment of Women's and Children's Health, Division of Obstetrics and Gynecology, Karolinska Institutet, Solnavägen, Solna, Sweden.ORCID http://orcid.org/0000-0003-4567-2364
Sahar SalehiDepartment of Women's and Children's Health, Division of Obstetrics and Gynecology, Karolinska Institutet, Solnavägen, Solna, Sweden.
Frances BalkwillBarts Cancer Institute, Queen Mary University of London, Charterhouse Square, EC1M6BQ, London, UK.ORCID http://orcid.org/0000-0002-5587-9759
Kaisa LehtiDepartment of Microbiology, Tumor and Cell Biology, Karolinska Institutet, Solnavägen 9, Solna, Sweden.ORCID http://orcid.org/0000-0001-9110-8719
Julien E GautrotSchool of Engineering and Materials Science, Queen Mary University of London, Mile End Road, London, United Kingdom. j.gautrot@qmul.ac.uk.ORCID http://orcid.org/0000-0002-1614-2578

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

High-grade serous ovarian cancer, the most common and aggressive ovarian cancer subtype, frequently metastasises to visceral adipose tissues. In these tissues, the extracellular matrix through which ovarian cancer cells migrate is constrained by the presence and preponderance of adipocytes. How cells migrate in this unique environment is not known, yet critical to understanding metastatic progression. To study these processes, we developed biomimetic organo-hydrogels that recreate structural, mechanical, and biochemical properties of human adipose tissues. We show that ovarian cancer cells present invasive tropism towards organo-hydrogels, replicating the behaviour observed in native adipose tissues. This migration is facilitated by the mechanical anisotropy and microstructure of organo-hydrogels and adipose tissues, allowing the formation of migratory tracks. These results highlight the contribution of adipocytes to tissue biophysical features as a key regulatory factor of ovarian cancer cell migration and demonstrate that organo-hydrogels are particularly relevant tools to develop in vitro models of complex tissue architectures with high cellularity.

Indexed as

Adipose TissueBiomimetic MaterialsHydrogelsOvarian NeoplasmsAdipocytesAnisotropyBiomimeticsCell Line, TumorCell MovementExtracellular MatrixFemaleHumansNeoplasm InvasivenessHydrogels

Identifiers

PMID41022685
PMCPMC12480658

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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.