Evidence map›Paper›PMID 41536151›Full record

ArticleMacromolecular bioscience2026

High-Throughput 3D Glioblastoma Model in Glycosaminoglycan Hydrogels for Personalized Therapeutic Screening.

Rajvinder Kaur Trautmann, Nicholas Dennison, Kathleen McCortney, Solveig Klier, Mehmet Ilyas Cosacak, Carsten Werner, Goktug Akyoldas, Craig M Horbinski, Uwe Freudenberg, Caghan Kizil

Abstract read
In one paragraph

Article in Macromolecular bioscience, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. 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

10 authors.

Rajvinder Kaur TrautmannNeuron-D GmbH, Dresden, Germany.ORCID 0000-0002-9417-3716
Nicholas DennisonNeuron-D GmbH, Dresden, Germany.
Kathleen McCortneyNervous System Tumor Bank, Department of Neurological Surgery, Feinberg School of Medicine, Northwestern University, Chicago, Illinois, USA.
Solveig KlierNeuron-D GmbH, Dresden, Germany.
Mehmet Ilyas CosacakGerman Center for Neurodegenerative Diseases (DZNE), Dresden, Germany.
Carsten WernerLeibniz Institute of Polymer Research Dresden (IPF), Dresden, Germany.
Goktug AkyoldasKoc University Hospital, İstanbul, Türkiye.
Craig M HorbinskiNervous System Tumor Bank, Department of Neurological Surgery, Feinberg School of Medicine, Northwestern University, Chicago, Illinois, USA.
Uwe FreudenbergLeibniz Institute of Polymer Research Dresden (IPF), Dresden, Germany.
Caghan KizilDepartment of Neurology, Vagelos College of Physicians and Surgeons, Columbia University Irving Medical Center, New York, New York, USA.

Funding

STINGing GBM: A First-in- Man Clinical Trial in Surgical Resectable Recurrent GBMP50CA221747 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI Hui Zhang · 2018 to 2026
$21.4M
European Union Regional Development Fund (EFRE) and Sachsische Aufbaubank (SAB) 100545782NCI NIH HHS P50 CA221747
6 · The paper itself

Abstract

Glioblastoma (GBM) is a devastating brain tumor with limited treatment success, partly because in vitro models poorly mimic in vivo complexity. This study introduces a high-throughput 3D culture platform utilizing modular starPEG-glycosaminoglycan (GAG) hydrogels that enable independent control of extracellular matrix (ECM) cues: stiffness, cytokine affinity, matrix metalloproteinase-responsive remodeling, and cell adhesiveness via integrin-binding RGD peptides. This platform supports encapsulation of patient-derived GBM cells, recreates physiologically relevant tumor microenvironments in 384-well plates, and enables automated drug testing on primary cells. Transcriptomic analyses show that 3D cultures recapitulate primary and recurrent GBM programs- including hypoxia-, immune-, and ECM-regulatory pathways driving growth, invasion, and resistance, without externally imposed hypoxia. The platform's versatility extends to drug screening, where single and combinatorial treatments produce reproducible cytoskeletal and transcriptomic responses. Notably, the system revealed dose-dependent reductions in invasive filaments and spheroid architecture with 5-fluorouracil/uridine and carmustine, demonstrating its potential for optimizing combinatorial therapies. This 3D model surpasses 2D cultures, capturing tumor-specific molecular programs and offering a robust tool for translational research. Despite lacking vascular or immune components, its tunability, scalability, and clinical relevance make it a strong basis for advanced co-cultures. By delivering reliable, individualized therapeutic data within a short timeframe, this model holds transformative potential for personalized GBM treatment.

Indexed as

Brain NeoplasmsCell Culture Techniques, Three DimensionalGlioblastomaGlycosaminoglycansHigh-Throughput Screening AssaysHydrogelsPrecision MedicineCell Line, TumorExtracellular MatrixHumansTumor MicroenvironmentGlycosaminoglycansHydrogelsbioengineered tumor microenvironmentGlioblastomahigh‐throughput screeningpatient‐derived cellspersonalized medicinestarPEG‐heparin hydrogel

Identifiers

PMID41536151
PMCPMC12805317

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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.