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Updated: Feb 10, 2026

Laboratory-Engineered Glioblastoma Organoid Culture and Drug Screening
Published on: January 10, 2025
Hydrogel Microdroplet Based Glioblastoma Drug Screening Platform
Brittany A Payan1, Annika Carrillo Diaz De Leon1, Tejasvi Anand2
1Department of Bioengineering, University of Illinois at Urbana-Champaign, Urbana, Illinois, USA.
Abstract:
Glioblastoma is the most common primary malignant brain tumor with a 5-year survival rate < 5%. The standard of care involves surgical resection followed by treatment with the alkylating agent temozolomide (TMZ). GBM cells that evade surgery eventually become resistant to TMZ and lead to recurrence of tumors in patients. With only four drugs currently FDA-approved for GBM treatment, there is a need for a clinically relevant model capable of accelerating the identification of new therapies. Microgels are microscale (~10-1000 μm) hydrogel particles that can be used to encapsulate cells in a tailorable 3D matrix. Microdroplets offer short diffusion lengths relative to conventional hydrogel constructs (> 1 mm) to limit spatial distributions of hypoxia and potentially screen therapeutics in a controlled and physiologically relevant environment. Here, we establish a method to encapsulate GBM cells in gelatin and polyethylene glycol (PEG) microgels. We show that microgel composition can affect cell morphology and further, that collections of GBM-laden hydrogels can be used to quantify the effect of single versus metronomic doses of TMZ. GBM metabolic activity is maintained in microgel culture and GBM cells display drug response kinetics similar to previously established literature using macro-scale hydrogel constructs. Finally, we show microgels can be integrated with a liquid handler to enable high-throughput screening using cell-laden microgels.
Insights
Researchers developed a novel microgel method to culture glioblastoma (GBM) cells, enabling faster drug screening. This 3D model mimics tumor environments, accelerating the search for new glioblastoma treatments.
Area of Science:
- Biomedical Engineering
- Oncology
- Drug Discovery
Background:
- Glioblastoma (GBM) is an aggressive brain tumor with poor prognosis.
- Current treatments like surgery and temozolomide (TMZ) face challenges due to drug resistance and recurrence.
- There is a critical need for advanced models to accelerate the development of new GBM therapies.
Purpose of the Study:
- To establish a microgel-based culture system for glioblastoma (GBM) cells.
- To evaluate the utility of microgels for drug screening and therapeutic response assessment.
- To enable high-throughput screening of potential GBM treatments.
Main Methods:
- Encapsulation of GBM cells within gelatin and polyethylene glycol (PEG) microgels.
- Assessment of microgel composition effects on cell morphology and metabolic activity.
- Quantification of TMZ drug response in microgel cultures.
- Integration of microgels with liquid handling systems for high-throughput screening.
Main Results:
- Microgel composition influences GBM cell morphology.
- GBM cells maintain metabolic activity and exhibit predictable drug response kinetics in microgels.
- The microgel system effectively quantifies responses to single and metronomic TMZ dosing.
- Microgels are compatible with liquid handlers for automated, high-throughput drug screening.
Conclusions:
- Microgels provide a tailorable 3D environment for culturing GBM cells.
- This microgel platform facilitates physiologically relevant drug screening and accelerates therapeutic discovery for glioblastoma.
- The developed method supports high-throughput screening, addressing the urgent need for new GBM treatments.
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10:28Flow Cytometry-based Drug Screening System for the Identification of Small Molecules That Promote Cellular Differentiation of Glioblastoma Stem Cells
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