Evidence map›Paper›PMID 40963997›Full record

ArticleJournal of extracellular biology2025

Tumoural Hypoxic Extracellular Vesicles Foster a Protective Microenvironment in Triple-Negative Breast Cancer.

Bianca Cruz Pachane, Pedro Henrique Teixeira Bottaro, Aline Maria Machado, Cynthia Aparecida de Castro, Gabriela Guerra, Larissa Thabata Gozzer, Marina Mantellatto Grigoli, Arthur Deponte Zutião, Angelina Maria Fuzer, Marcia Regina Cominetti and 2 more

Abstract read
In one paragraph

Article in Journal of extracellular biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. 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

12 authors.

Bianca Cruz PachaneBiochemistry and Molecular Biology Laboratory, Department of Physiological Sciences Universidade Federal de São Carlos - UFSCar São Carlos São Paulo Brazil.ORCID https://orcid.org/0000-0002-7302-4498
Pedro Henrique Teixeira BottaroBiochemistry and Molecular Biology Laboratory, Department of Physiological Sciences Universidade Federal de São Carlos - UFSCar São Carlos São Paulo Brazil.ORCID https://orcid.org/0000-0002-6456-6244
Aline Maria MachadoBiochemistry and Molecular Biology Laboratory, Department of Physiological Sciences Universidade Federal de São Carlos - UFSCar São Carlos São Paulo Brazil.ORCID https://orcid.org/0000-0001-8047-8482
Cynthia Aparecida de CastroPathology and Biocompatibility Laboratory, Department of Morphology and Pathology Universidade Federal de São Carlos - UFSCar São Carlos São Paulo Brazil.ORCID https://orcid.org/0000-0002-2675-8069
Gabriela GuerraBiochemistry and Molecular Biology Laboratory, Department of Physiological Sciences Universidade Federal de São Carlos - UFSCar São Carlos São Paulo Brazil.ORCID https://orcid.org/0009-0008-9975-1125
Larissa Thabata GozzerBiochemistry and Molecular Biology Laboratory, Department of Physiological Sciences Universidade Federal de São Carlos - UFSCar São Carlos São Paulo Brazil.
Marina Mantellatto GrigoliDepartment of Gerontology Universidade Federal de São Carlos - UFSCar São Carlos São Paulo Brazil.ORCID https://orcid.org/0000-0002-8212-9574
Arthur Deponte ZutiãoDepartment of Gerontology Universidade Federal de São Carlos - UFSCar São Carlos São Paulo Brazil.ORCID https://orcid.org/0009-0005-8844-8866
Angelina Maria FuzerDepartment of Gerontology Universidade Federal de São Carlos - UFSCar São Carlos São Paulo Brazil.ORCID https://orcid.org/0000-0003-0673-8287
Marcia Regina CominettiDepartment of Gerontology Universidade Federal de São Carlos - UFSCar São Carlos São Paulo Brazil.ORCID https://orcid.org/0000-0001-6385-7392
Wanessa Fernanda AlteiMolecular Oncology Research Center Barretos Cancer Hospital Barretos São Paulo Brazil.ORCID https://orcid.org/0000-0002-6636-7951
Heloisa Sobreiro Selistre-de-AraujoBiochemistry and Molecular Biology Laboratory, Department of Physiological Sciences Universidade Federal de São Carlos - UFSCar São Carlos São Paulo Brazil.ORCID https://orcid.org/0000-0002-2372-7814

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The highly metastatic triple-negative breast cancer (TNBC) relies on the tumour microenvironment (TME) to maintain phenotypic heterogeneity and progression. Extracellular vesicles from hypoxic TNBC (EVh) have been previously shown to facilitate tumoural invasion; however, their function in the TME remains unclear. We used a novel method to investigate the TME in vitro called multicellular circulating co-culture, to characterise how EVh interferes with tumoural and endothelial cells, fibroblasts, monocytes and macrophages. EVh promoted monocyte differentiation to M2-like macrophages and inhibited macrophage-derived phagocytosis in endothelial and tumoural cells. The protection of endothelial, tumoural and stromal cellular integrity by EVh increased pro-tumoural and pro-angiogenic signalling, collagen matrix synthesis and showed a potential differentiation to cancer-associated fibroblasts. Our findings highlight the critical role of EVh in protecting tumour cells, indicating its cooperation towards a protective TME, which was demonstrated by the multicellular circulating co-culture and conventional co-culture protocols. These findings lead to an adequate system with potential for investigating other tumour-related processes, including circulating tumour cells and metastasis.

Indexed as

extracellular vesicleshypoxiaphagocytosistumour microenvironment

Identifiers

PMID40963997
PMCPMC12438445

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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.