Evidence mapPaperPMID 41595739Full record

ReviewBiomedicines2026

The Extracellular Matrix, the Silent 'Architect' of Glioma.

Carmen Rubio, Javier Pérez-Villavicencio, Nadia F Esteban-Román, Ángel Lee, Gervith Reyes-Soto, Moisés Rubio-Osornio

Abstract readReview
In one paragraph

Review in Biomedicines, 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

6 authors.

Carmen RubioDepartment of Neurophysiology, National Institute of Neurology and Neurosurgery, Mexico City 14269, Mexico.ORCID 0000-0002-4775-5043
Javier Pérez-VillavicencioBasic Sciences and Engineering Division, Department of Electrical Engineering, Iztapalapa Campus, Metropolitan Autonomous University, Mexico City 09340, Mexico.ORCID 0000-0002-3184-6522
Nadia F Esteban-RománBiological Sciences and Health Division, Department of Biological Systems, Xochimilco Campus, Metropolitan Autonomous University, Mexico City 04960, Mexico.ORCID 0009-0006-2332-1546
Ángel LeeNational Institute of Public Health, Cuernavaca 62100, Mexico.ORCID 0000-0002-2301-3598
Gervith Reyes-SotoDepartment of Surgery, National Institute of Cancer, Mexico City 14080, Mexico.
Moisés Rubio-OsornioDepartment of Neurochemistry, National Institute of Neurology and Neurosurgery, Av. Insurgentes Sur 3877, Mexico City 14269, Mexico.ORCID 0000-0001-9236-0609

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The brain's extracellular matrix (ECM) serves as a dynamic and instructive regulator of glioma progression. The ECM provides structural support while integrating pharmacological and mechanical signals that influence glioma initiation, progression, and treatment resistance. Deviant ECM remodeling fosters tumor heterogeneity, invasion, and immune evasion by altering stiffness, composition, and cellular matrix signaling. We proposed that ECM remodeling in gliomas not only facilitates tumor growth and heterogeneity but also establishes advantageous biophysical and metabolic conditions that foster treatment resistance and recurrence. Our objective is to analyze current findings regarding the structural, biochemical, and mechanical roles of the brain ECM in glioma growth, emphasizing its contribution to tumor heterogeneity, mechanotransduction, immunological modulation, and its potential as a therapeutic target.

methodA comprehensive literature review was conducted using scientific databases including PubMed, Web of Science, and Scopus. Peer-reviewed literature published between 2000 and 2025 was selected for its relevance to ECM composition, stiffness, remodeling enzymes, extracellular vesicles, and mechanobiological processes in gliomas.

resultsRecent investigations demonstrate that glioma cells actively alter the ECM by secreting collagens, laminins, and metalloproteinases, establishing a feedback loop that facilitates invasion and resistance. DISCUSSION: Mechanical variables, such as ECM stiffness and solid stress, influence glioma growth, metabolism, and immune exclusion. Moreover, extracellular vesicles facilitate significant extracellular matrix remodeling and improve communication between tumors and stromal cells. The disruption of ependymal and subventricular extracellular matrix niches enhances invasion and cerebrospinal fluid-mediated signaling. The remodeling of the ECM influences glioma growth through interconnected biochemical, mechanical, and immunological mechanisms. Examining ECM stiffness, crosslinking enzymes, and vesicle-mediated signaling represents a potential therapeutic approach. Integrative methodologies that combine mechanobiology, imaging, and multiomics analysis could uncover ECM-related vulnerabilities to improve glioma treatment.

Indexed as

ECM reorganizationextracellular matrixglioma advancementmechanotransductiontherapeutic resistancetumor diversity

Identifiers

PMID41595739
PMCPMC12839358

What Socratic holds

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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 Socratic graph.