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Updated: Jun 3, 2025

A 3D Spheroid Model for Glioblastoma
Published on: April 9, 2020
Cell-Based Glioma Models for Anticancer Drug Screening: From Conventional Adherent Cell Cultures to Tumor-Specific
Daria Lanskikh1, Olga Kuziakova1, Ivan Baklanov1
1School of Medicine and Life Sciences, Far Eastern Federal University, 690922 Vladivostok, Russia.
Abstract:
Gliomas are a group of primary brain tumors characterized by their aggressive nature and resistance to treatment. Infiltration of surrounding normal tissues limits surgical approaches, wide inter- and intratumor heterogeneity hinders the development of universal therapeutics, and the presence of the blood-brain barrier reduces the efficiency of their delivery. As a result, patients diagnosed with gliomas often face a poor prognosis and low survival rates. The spectrum of anti-glioma drugs used in clinical practice is quite narrow. Alkylating agents are often used as first-line therapy, but their effectiveness varies depending on the molecular subtypes of gliomas. This highlights the need for new, more effective therapeutic approaches. Standard drug-screening methods involve the use of two-dimensional cell cultures. However, these models cannot fully replicate the conditions present in real tumors, making it difficult to extrapolate the results to humans. We describe the advantages and disadvantages of existing glioma cell-based models designed to improve the situation and build future prospects to make drug discovery comprehensive and more effective for each patient according to personalized therapy paradigms.
Insights
Glioma treatment faces challenges due to tumor infiltration and drug resistance. This study reviews current glioma cell models, highlighting the need for better drug discovery methods for personalized therapy.
Area of Science:
- Neuro-oncology
- Cancer Biology
- Drug Discovery
Background:
- Gliomas are aggressive primary brain tumors with poor prognoses.
- Treatment is limited by tumor infiltration, heterogeneity, and the blood-brain barrier.
- Current therapies, like alkylating agents, have variable efficacy based on glioma subtypes.
Purpose of the Study:
- To review existing glioma cell-based models for drug screening.
- To identify limitations of current models in replicating tumor microenvironments.
- To propose future directions for comprehensive and personalized glioma drug discovery.
Main Methods:
- Analysis of existing literature on glioma cell-based models.
- Comparison of 2D cell cultures with more advanced in vitro models.
- Evaluation of model suitability for predicting therapeutic response.
Main Results:
- Standard 2D cell cultures inadequately mimic in vivo glioma conditions.
- Existing models present both advantages and disadvantages for drug screening.
- Improved models are crucial for advancing therapeutic development.
Conclusions:
- There is a critical need for improved glioma cell models.
- Advanced models can enhance the effectiveness of drug discovery pipelines.
- Personalized therapy paradigms require better preclinical models for gliomas.
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