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Updated: Jun 10, 2026

Initial Evaluation of Antibody-conjugates Modified with Viral-derived Peptides for Increasing Cellular Accumulation and Improving Tumor Targeting
Published on: March 8, 2018
Encapsulated cells to focus the metabolic activation of anticancer drugs
Brian Salmons1, Eva M Brandtner, Kay Hettrich
1Austrianova Singapore Pte Ltd, 20 Biopolis Way, #05-518 Centros, Singapore 138668. salmons@sgaustria.com
Abstract:
One of the first strategies for cancer gene therapy was the use of suicide gene/prodrug combinations, originally delivered to tumor cells using viral vectors. A major limitation of this approach was the inefficiency of suicide gene delivery. An alternative strategy, in which the suicide genes are physically juxtaposed to the tumor, involves the implantation of encapsulated, genetically modified cells. Cell encapsulation technologies were originally developed for the treatment of acquired and genetic diseases, such as diabetes. In the application of this technology for the treatment of tumors, cells that are genetically modified to overexpress suicide genes are encapsulated and implanted near solid tumors; this process is then followed by systemic prodrug administration. This review discusses the various cells types, suicide genes and prodrugs that have been used in preclinical and clinical trials, as well as the data that have been obtained from these studies. Future improvements for the production of second-generation approaches are also discussed.
Insights
Encapsulated, genetically modified cells offer a promising cancer gene therapy approach. This method overcomes limitations of viral vector delivery by implanting cells near tumors for effective suicide gene/prodrug treatment.
Area of Science:
- Oncology
- Gene Therapy
- Biotechnology
Background:
- Suicide gene/prodrug cancer therapy initially used viral vectors.
- Viral delivery faced limitations due to inefficient gene transfer to tumor cells.
Purpose of the Study:
- To review encapsulated cell technology for cancer gene therapy.
- To discuss cell types, suicide genes, and prodrugs used in trials.
- To explore future advancements in this therapeutic strategy.
Main Methods:
- Encapsulation of genetically modified cells overexpressing suicide genes.
- Implantation of encapsulated cells adjacent to solid tumors.
- Systemic administration of prodrugs to activate the suicide gene therapy.
Main Results:
- Review of preclinical and clinical trial data for various cell types, genes, and prodrugs.
- Demonstrated potential of encapsulated cells to overcome delivery inefficiencies.
- Identified key components and outcomes of this therapeutic approach.
Conclusions:
- Encapsulated suicide gene-modified cells represent an effective alternative for cancer gene therapy.
- This strategy enhances localized prodrug activation and minimizes systemic toxicity.
- Further development of second-generation approaches is crucial for improved efficacy.
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