Abstract

Glioblastoma (GBM), the most common and aggressive primary brain tumor in adults, remains one of the least treatable cancers. Current standard of care—combining surgical resection, radiation, and alkylating chemotherapy—results in a median survival of only 15 months. Despite decades of investment and research into the development of new therapies, most candidate anti-glioma compounds fail to translate into effective treatments in clinical trials. One key issue underlying this failure of therapies that work in pre-clinical models to generate meaningful improvement in human patients is the profound mismatch between drug discovery systems—cell cultures and mouse models—and the actual tumors they are supposed to imitate. Indeed, current strategies that evaluate the effects of novel treatments on GBM cells in vitro fail to account for a wide range of factors known to influence tumor growth. These include secreted factors, the brain’s unique extracellular matrix, circulatory structures, the presence of non-tumor brain cells, and nutrient sources available for tumor metabolism. While mouse models provide a more realistic testing ground for potential therapies, they still fail to account for the full complexity of tumor-microenvironment interactions, as well as the role of the immune system. Based on the limitations of current models, researchers have begun to develop and implement novel culture systems that better recapitulate the complex reality of brain tumors growing in situ. A rise in the use of patient derived cells, creative combinations of added growth factors and supplements, may provide a more effective proving ground for the development of novel therapies. This review will summarize and analyze these exciting developments in 3D culturing systems. Special attention will be paid to how they enhance the design and identification of compounds that increase the efficacy of radiotherapy, a bedrock of GBM treatment.

Highlights

  • In glioblastoma (GBM), we have seen the disastrous result of insufficiently realistic drug screening and testing systems

  • The failure of current radiotherapy paradigms to provide long-term tumor control in GBM has been linked to all these factors [8]

  • Colorectal cancer cell lines cultured in similar laminin-rich extracellular matrix (ECM) 3D conditions exhibited changes in cellular morphology, phenotype and gene expression and were resistant to treatment with epidermal growth factor receptor (EGFR) inhibitors compared to cells cultured in 2D conditions [13,17]

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Summary

Introduction

In glioblastoma (GBM), we have seen the disastrous result of insufficiently realistic drug screening and testing systems. From cilengitide to target therapies, drugs developed using contemporary pre-clinical systems have roundly failed to predict clinical efficacy. The failure of current radiotherapy paradigms to provide long-term tumor control in GBM has been linked to all these factors [8]. In addition to these tumor factors, GBM remains intractable because of its ability to interact with its environment, including healthy astrocytes and blood vessels. The challenge of pre-clinical drug development is to create culture systems and animal models that faithfully recapitulate these complex behaviors and systems, thereby enabling researchers to identify compounds that effectively translate success targeting cancer cells in vitro models to meaningful improvement for patients. This review will analyze the limitations of current GBM drug development models and summarize and discuss novel culture systems under development

Limits of Current Pre-Clinical Systems
Current Practices for Pre-Clinical GBM Modeling
Tumor Intrinsic Factors
Inter and Intratumoral Genetic Heterogeneity
Cellular Plasticity
Microenvironmental Factors
Brain Extracellular Matrix
Regional Differences in the Tumor Microenvironment
Nutrient Availability and Metabolism
Non-Tumor Cells
Dynamic Surroundings
Novel Strategies for GBM Cell Culture
Suspension-Based Culture Models
Summary
Hydrogels
Matrigel-Coating for 2D Growth
Matrigel Plugs for 3D Growth
Microfluidic Systems
Brain Slices
Mini-Brains
Tumor Organoids
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