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Updated: May 29, 2025

Generation of CAR T Cells for Adoptive Therapy in the Context of Glioblastoma Standard of Care
Published on: February 16, 2015
Advances on the therapeutic potential of cell receptor activation in glioblastoma
Gerson G Contreras-Chávez1, Luis A Zapi-Colin1, José A Estrada1
1Neurochemistry Laboratory, Faculty of Medicine, Universidad Autónoma del Estado de México, Toluca, México.
Abstract:
Glioblastoma multiforme is the most common and aggressive malignant brain tumor. Current therapies have been unable to improve life expectancy in patients. This cancer is frequently accompanied by overexpression of receptors, such as EGFR, VEGFR and TLRs, involved in the regulation of inflammation, cell proliferation, differentiation, and survival. The present review summarizes current knowledge from preclinical and clinical studies investigating the role of pattern recognition and tyrosine kinase receptors in glioblastoma development and evolution, and their possible use to improve treatment outcomes and patient survival.
Insights
Glioblastoma multiforme, an aggressive brain cancer, shows receptor overexpression linked to poor outcomes. Targeting these receptors may improve glioblastoma treatment and patient survival.
Area of Science:
- Neuro-oncology
- Molecular Biology
- Immunology
Background:
- Glioblastoma multiforme is the most aggressive primary brain tumor, with limited therapeutic options and poor patient survival rates.
- Overexpression of receptors like EGFR, VEGFR, and TLRs is common in glioblastoma and influences tumor progression.
- These receptors play critical roles in inflammation, cell growth, and survival pathways essential for glioblastoma development.
Purpose of the Study:
- To review current preclinical and clinical research on pattern recognition and tyrosine kinase receptors in glioblastoma.
- To investigate the role of these receptors in glioblastoma development and progression.
- To explore the potential of targeting these receptors for improved glioblastoma treatment outcomes and survival.
Main Methods:
- Systematic review of preclinical studies.
- Analysis of clinical trial data.
- Literature search for pattern recognition receptors (PRRs) and tyrosine kinase receptors (TKRs) in glioblastoma.
Main Results:
- Receptor tyrosine kinases (RTKs) like EGFR and VEGFR are implicated in glioblastoma proliferation and angiogenesis.
- Pattern recognition receptors (PRRs) like Toll-like receptors (TLRs) modulate the tumor microenvironment and immune response.
- Dysregulation of these receptors contributes significantly to glioblastoma pathogenesis.
Conclusions:
- Targeting EGFR, VEGFR, and TLRs presents a promising therapeutic strategy for glioblastoma.
- Further research into the complex interplay of these receptors is crucial for developing effective treatments.
- Modulating receptor signaling pathways holds potential for enhancing patient survival in glioblastoma.
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