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Updated: Oct 5, 2025

A 3D Spheroid Model for Glioblastoma
Published on: April 9, 2020
Establishing an In Vitro 3D Spheroid Model to Study Medulloblastoma Drug Response and Tumor Dissemination
1Children's Brain Tumor Research Centre, School of Medicine, Biodiscovery Institute, University of Nottingham, Nottingham, UK.
Abstract:
Medulloblastoma is the most common malignant pediatric brain tumor. Current treatment involves surgery, chemotherapy, and craniospinal radiotherapy, and these are associated with a significant reduction in quality of life. Metastatic dissemination at diagnosis is found in up to 30% of medulloblastoma cases and, alongside therapy resistance, is a significant feature in determining poor outcome. Development of new therapeutic approaches requires models where drug resistance and migration can be readily quantified and that are representative of patient disease. 3D medulloblastoma (3D-MB) spheroids are a simple yet effective means of bridging the gap between 2D culture and in vivo methods, providing users with highly reproducible in vitro models that more accurately recapitulate tumor morphology, drug response, and migration from a tumor mass. Unlike other cancer types, medulloblastoma spheroids fail to grow in their different standard cell culture media; instead, each cell line requires the same stem cell-enriching conditions. This requirement, however, has the advantage that it allows direct comparison of growth and response between cell lines in the absence of any potential media bias. In addition, spheroids can be used to model the initial stages of metastatic dissemination, something that cannot be achieved in 2D culture, providing insight into key changes occurring in migratory cells. Here, we provide protocols that detail the initial generation and maintenance of 3D-MB spheroids from sonic-hedgehog, Group 3, and Group 4 medulloblastoma subgroups, as well as describing functional assays to study drug response and cell migration across hyaluronan matrices, which represent the extracellular matrix backbone of the brain parenchyma. Through application of these simple yet highly representative models, it will be possible to test novel therapeutics targeting metastasis and drug resistance, as well as to develop insights into the mechanistic processes driving relapse in this malignant pediatric brain tumor. © 2022 The Authors. Current Protocols published by Wiley Periodicals LLC. Basic Protocol 1: Generation and maintenance of 3D medulloblastoma (3D-MB) spheroids Support Protocol 1: Measuring spheroid size for coefficient-of-variation analysis Basic Protocol 2: Assessing drug response in 3D-MB spheroids Support Protocol 2: 384-well 3D-MB spheroid generation Basic Protocol 3: Immunohistochemical staining of 3D-MB spheroids Basic Protocol 4: Modeling metastatic dissemination using 3D-MB migration models Support Protocol 3: RNA extraction from 3D-MB spheroids.
Insights
This study introduces 3D medulloblastoma (3D-MB) spheroids as a novel model for pediatric brain tumor research. These models accurately mimic drug resistance and metastasis, aiding the development of new therapies for medulloblastoma.
Area of Science:
- Oncology
- Biomedical Engineering
- Pediatric Medicine
Background:
- Medulloblastoma is the most common malignant pediatric brain tumor.
- Current treatments cause significant quality of life reductions.
- Metastasis and therapy resistance are key factors in poor medulloblastoma outcomes.
Purpose of the Study:
- To develop advanced in vitro models for studying medulloblastoma drug resistance and metastasis.
- To provide reproducible models that better represent patient disease compared to 2D cultures.
- To facilitate the testing of novel therapeutic strategies targeting medulloblastoma relapse.
Main Methods:
- Generation and maintenance of 3D medulloblastoma (3D-MB) spheroids from different medulloblastoma subgroups.
- Development of functional assays for drug response assessment in 3D-MB spheroids.
- Modeling of metastatic dissemination using 3D-MB migration assays across hyaluronan matrices.
Main Results:
- 3D-MB spheroids accurately recapitulate tumor morphology, drug response, and migration.
- These models allow for direct comparison of cell line responses without media bias.
- The models effectively simulate early-stage metastatic dissemination, offering insights into migratory cell changes.
Conclusions:
- 3D-MB spheroids offer a highly reproducible and representative in vitro model for medulloblastoma research.
- These models are crucial for testing novel therapeutics targeting metastasis and drug resistance.
- The application of these models can provide mechanistic insights into medulloblastoma relapse.

