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Viral vector: potential therapeutic for glioblastoma multiforme
Ceera Manikandan1, Akshita Kaushik1, Dwaipayan Sen2
1Cellular and Molecular Therapeutics Laboratory, Centre for Biomaterials, Cellular and Molecular Theranostics, Vellore Institute of Technology (VIT) University, Vellore, Tamil Nadu, 632014, India.
Abstract:
Glioblastoma multiforme is a highly malignant primary brain tumour found in adults and is highlighted as the most devastating among all the other grades of glioma. Well-established standard treatment methods, such as chemotherapy, radiation and surgery, have resulted in modest improvement in the survival of patients. Hence, the arduous search for novel treatments backed by advancements in molecular biology still persists. Glioblastoma has many distinctive characteristics, which makes it a potential candidate for gene therapy. Gene therapy involves the delivery of genetic material of therapeutic use into tumour cells, which produces a specific antitumour response. Moreover, viruses stimulate a vigorous cytotoxic effect, they are easily modifiable and the inherent property of horizontal transfer of genetic material makes them valuable tools for genetic engineering. In this review, we have enlisted the various viral vectors employed in gene therapy for glioblastoma.
Insights
Gene therapy offers a promising new avenue for treating glioblastoma, a deadly brain cancer. This review explores various viral vectors being investigated for their potential to deliver therapeutic genetic material directly to tumor cells.
Area of Science:
- Neuro-oncology
- Molecular biology
- Gene therapy
Background:
- Glioblastoma multiforme is a highly malignant primary brain tumor in adults, representing the most aggressive form of glioma.
- Current treatments (chemotherapy, radiation, surgery) offer limited survival benefits, necessitating novel therapeutic strategies.
- Advancements in molecular biology highlight glioblastoma's unique characteristics, making it a candidate for gene therapy.
Purpose of the Study:
- To review the application of gene therapy for glioblastoma treatment.
- To explore the potential of viral vectors in delivering therapeutic genetic material to glioblastoma cells.
Main Methods:
- Literature review of existing research on gene therapy for glioblastoma.
- Analysis of viral vectors utilized for genetic material delivery in preclinical and clinical studies.
- Discussion of the mechanisms by which viruses can induce an anti-tumor response.
Main Results:
- Viruses possess inherent cytotoxic effects and are easily modifiable for therapeutic purposes.
- The horizontal transfer of genetic material by viruses makes them valuable tools for genetic engineering in cancer treatment.
- Various viral vectors have been identified and employed in experimental glioblastoma gene therapy.
Conclusions:
- Gene therapy, particularly using viral vectors, presents a promising frontier for overcoming the limitations of conventional glioblastoma treatments.
- Further research into optimizing viral vector design and delivery is crucial for clinical translation.
- Viral vectors offer a targeted approach to combat glioblastoma by inducing specific anti-tumor responses.
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