Evidence map›Paper›PMID 39246099›Full record

ArticleAdvanced healthcare materials2024

Tunable Hybrid Hydrogels of Alginate and Cell-Derived dECM to Study the Impact of Matrix Alterations on Epithelial-to-Mesenchymal Transition.

P Barros da Silva, Xiaoyu Zhao, Sílvia J Bidarra, Diana S Nascimento, Vernon LaLone, Bianca N Lourenço, Joana Paredes, Molly M Stevens, C C Barrias

Abstract read
In one paragraph

Article in Advanced healthcare materials, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. Biomimetic Scaffold-Based 3D Models for Decoding Cancer Biology and Advancing Therapy.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Review
  2. Article
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  10. Frontiers in bioengineering and biotechnology · 2026
    Article
  11. Dynamic Hydrogels in Breast Tumor Models.Gels (Basel, Switzerland) · 2025
    Review
  12. Article
  13. 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

9 authors.

P Barros da Silvai3S - Instituto de Investigação e Inovação em Saúde, Universidade do Porto, Rua Alfredo Allen 208, Porto, 4200-135, Portugal.ORCID 0000-0003-0306-5259
Xiaoyu ZhaoDepartment of Bioengineering, Imperial College London, Exhibition Rd, London, SW7 2AZ, UK.
Sílvia J Bidarrai3S - Instituto de Investigação e Inovação em Saúde, Universidade do Porto, Rua Alfredo Allen 208, Porto, 4200-135, Portugal.
Diana S Nascimentoi3S - Instituto de Investigação e Inovação em Saúde, Universidade do Porto, Rua Alfredo Allen 208, Porto, 4200-135, Portugal.
Vernon LaLoneDepartment of Bioengineering, Imperial College London, Exhibition Rd, London, SW7 2AZ, UK.
Bianca N Lourençoi3S - Instituto de Investigação e Inovação em Saúde, Universidade do Porto, Rua Alfredo Allen 208, Porto, 4200-135, Portugal.
Joana Paredesi3S - Instituto de Investigação e Inovação em Saúde, Universidade do Porto, Rua Alfredo Allen 208, Porto, 4200-135, Portugal.
Molly M StevensDepartment of Bioengineering, Imperial College London, Exhibition Rd, London, SW7 2AZ, UK.
C C Barriasi3S - Instituto de Investigação e Inovação em Saúde, Universidade do Porto, Rua Alfredo Allen 208, Porto, 4200-135, Portugal.

Funding

Fundação para a Ciência e a Tecnologia DL 57/2016/CP1360/CT0006Fundação para a Ciência e Tecnologia COVID/BD/152422/2022Fundação para a Ciência e Tecnologia IF/00296/2015Fundação para a Ciência e Tecnologia PTDC/BTM-ORG/5154/2020Fundação para a Ciência e Tecnologia SFRH/BD/131757/2017H2020 Marie Skłodowska-Curie Actions 890854Medical Research Council MR/R015651/1Research Council of Norway 262613Royal Academy of Engineering CiET2021\94
6 · The paper itself

Abstract

Epithelial-to-mesenchymal transition (EMT) is crucial for tumor progression, being linked to alterations in the extracellular matrix (ECM). Understanding the ECM's role in EMT can uncover new therapeutic targets, yet replicating these interactions in vitro remains challenging. It is shown that hybrid hydrogels of alginate (ALG) and cell-derived decellularized ECM (dECM), with independently tunable composition and stiffness, are useful 3D-models to explore the impact of the breast tumor matrix on EMT. Soft RGD-ALG hydrogels (200 Pa), used as neutral bulk material, supported mammary epithelial cells morphogenesis without spontaneous EMT, allowing to define the gene, protein, and biochemical profiles of cells at different TGFβ1-induced EMT states. To mimic the breast tumor composition, dECM from TGFβ1-activated fibroblasts (adECM) are generated, which shows upregulation of tumor-associated proteins compared to ndECM from normal fibroblasts. Using hybrid adECM-ALG hydrogels, it is shown that the presence of adECM induces partial EMT in normal epithelial cells, and amplifes TGF-β1 effects compared to ALG and ndECM-ALG. Increasing the hydrogel stiffness to tumor-like levels (2.5 kPa) have a synergistic effect, promoting a more evident EMT. These findings shed light on the complex interplay between matrix composition and stiffness in EMT, underscoring the utility of dECM-ALG hydrogels as a valuable in vitro platform for cancer research.

Indexed as

AlginatesEpithelial-Mesenchymal TransitionExtracellular MatrixHydrogelsTransforming Growth Factor beta1Breast NeoplasmsEpithelial CellsFemaleFibroblastsHumansAlginatesHydrogelsTransforming Growth Factor beta1cell‐derived decellularized ECMdefined hydrogeltumor microenvironmenttunable hydrogel

Identifiers

PMID39246099
PMCPMC11582509

What OpenQuestion holds

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LicenceCC BY
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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.