Genetic therapy in gliomas: historical analysis and future perspectives
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Stereotactic Adoptive Transfer of Cytotoxic Immune Cells in Murine Models of Orthotopic Human Glioblastoma Multiforme Xenografts
Published on: September 1, 2018
Tobias Alécio Mattei1, Ricardo Ramina, Flavio Key Miura
1Department of Neurosurgery, São Paulo Medical School, Rua Capote Valente 725, ap. 302, CEP 05409-002 São Paulo, Brazil. tobiasmattei@hotmail.com
Abstract:
High-grade gliomas are relatively frequent in adults, and consist of the most malignant kind of primary brain tumor. Being resistant to standard treatment modalities such as surgery, radiation, and chemotherapy, it is fatal within 1 to 2 years of onset of symptoms. Although several gene therapy systems proved to be efficient in controlling or eradicating these tumors in animal models, the clinical studies performed so far were not equally successful. Most clinical studies showed that methodologies that increase tumor infection/transduction and, consequently confer more permanent activity against the tumor, will lead to enhanced therapeutic results. Due to the promising practical clinical benefits that can be expected for the near future, an exposition to the practicing neurosurgeon about the basic issues in genetic therapy of gliomas seems convenient. Among the main topics, we shall discuss anti-tumoral mechanisms of various genes that can be transfected, the advantages and drawbacks of the different vectors utilized, the possibilities of tumor targeting by modifications in the native tropism of virus vectors, as well as the different physical methods for vector delivery to the tumors. Along with the exposition we will also review of the history of the genetic therapy for gliomas, with special focus on the main problems found during the advancement of scientific discoveries in this area. A general analysis is also made of the present state of this promising therapeutic modality, with reference to the problems that still must be solved and the new paradigms for future research in this area.
Insights
Gene therapy shows promise for treating aggressive brain tumors (high-grade gliomas) that resist conventional treatments. Enhancing tumor targeting and gene delivery is key to improving clinical outcomes.
Area of Science:
- Neuro-oncology
- Molecular biology
- Gene therapy
Background:
- High-grade gliomas are aggressive brain tumors with poor prognoses, often resistant to standard treatments like surgery, radiation, and chemotherapy.
- Current clinical gene therapy trials for gliomas have shown limited success, highlighting the need for improved methodologies.
Observation:
- Animal models demonstrate gene therapy's potential for tumor control and eradication.
- Clinical success is linked to methods that enhance tumor cell infection and transduction, leading to sustained anti-tumor activity.
Findings:
- Various anti-tumoral genes and gene delivery vectors (viral vectors) offer different advantages and drawbacks.
- Strategies for improving therapeutic efficacy include modifying viral vector tropism for tumor targeting and employing physical methods for vector delivery.
Implications:
- Understanding gene therapy's basic principles, vector technologies, and delivery methods is crucial for neurosurgeons.
- Addressing current challenges and exploring new research paradigms are essential for advancing glioma gene therapy.
- Future research should focus on optimizing tumor targeting and gene delivery for enhanced clinical benefits in high-grade glioma treatment.
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