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Updated: Jul 16, 2026

Defining Gene Functions in Tumorigenesis by Ex vivo Ablation of Floxed Alleles in Malignant Peripheral Nerve Sheath Tumor Cells
Published on: August 25, 2021
Gene therapy of cancer
1Faculty of Sciences and Mathematics, Department of Biology and Ecology, Nis, Serbia and Montenegro.
Abstract:
The original concept of gene therapy was the introduction of a healthy copy of gene into an ill human cell in order to correct gene defects in monogenic hereditary diseases. Since then the idea of gene therapy was expanded to cure or slow down the progression of numerous inherited and acquired diseases. Presently, there are 918 ongoing gene therapy clinical trials worldwide. The major indication in these trials is cancer (608 trials or 66% of the total number). Gene therapy of cancer can be defined as transfer of nucleic acids into tumor or normal cells aiming at eradicating or reducing the tumor mass by direct killing of cells, immunomodulation or correction of genetic errors and reversion of the malignant status. Initially started with lots of optimism and enthusiasm, cancer genet therapy has shown limited success in the treatment of patients. This lesson highlights current limitations and almost endless possibilities of cancer gene therapy. The major difficulty in advancing gene therapy technology for the lab bench to clinical practice is the problem with gene delivery vehicles (so-called vectors) needed to ferry genetic material into a cell. Despite few reports of therapeutic responses in some patients, there is still no proof of clinical efficacy of most cancer gene therapy approaches, primarily due to very low transduction and expression efficacy in vivo of available vectors. An "ideal" gene therapy vector should: be administered through a noninvasive route; target not only the primary tumor mass but disseminated tumor cells and micrometastases at distant and unreachable sites as well; carry a therapeutic gene with tumor-restricted and time-regulated and sustained expression. Current strategies for combating cancer with gene therapy can be subdivided into 4 basic concepts: 1) replacement of missing tumor suppressor gene and/or blocking of oncogenes or proinflammatory genes; 2) suicide gene strategies; 3) induction of immune-mediated destruction; and 4) inhibition of tumor angiogenesis. Clinical advance will probably come first from cooperation with standard cancer treatment such as chemotherapy, radiotherapy and immunotherapy.
Insights
Gene therapy aims to correct genetic defects, but cancer gene therapy faces challenges, primarily with effective gene delivery vectors. Future success relies on improved vectors and combination treatments.
Area of Science:
- Oncology
- Molecular Biology
- Biotechnology
Background:
- Gene therapy initially targeted monogenic diseases but has expanded to acquired conditions.
- Cancer represents the largest area for gene therapy clinical trials (66%).
- Cancer gene therapy seeks tumor eradication via direct killing, immunomodulation, or genetic correction.
Purpose of the Study:
- To review current limitations and future possibilities in cancer gene therapy.
- To highlight challenges in translating gene therapy from laboratory to clinical practice.
- To discuss the essential characteristics of an ideal gene therapy vector.
Main Methods:
- Overview of current gene therapy strategies for cancer.
- Analysis of gene delivery vehicle (vector) limitations.
- Discussion of potential therapeutic approaches including gene replacement, suicide gene therapy, immunotherapy, and anti-angiogenesis.
Main Results:
- Cancer gene therapy has shown limited clinical success to date.
- Low in vivo transduction and expression efficacy of current vectors are major hurdles.
- No definitive clinical efficacy has been proven for most cancer gene therapy approaches.
Conclusions:
- Advancements in gene therapy for cancer are hindered by vector delivery issues.
- An ideal vector requires noninvasive administration, broad tumor targeting, and controlled gene expression.
- Future clinical progress likely involves integrating gene therapy with standard treatments like chemotherapy, radiotherapy, and immunotherapy.
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