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Updated: Aug 23, 2026

Monitoring Functionality and Morphology of Vasculature Recruited by Factors Secreted by Fast-growing Tumor-generating Cells
Published on: November 23, 2014
Antiangiogenic gene therapy of cancer: recent developments
Anita Tandle1, Dan G Blazer, Steven K Libutti
1Surgery Branch, Center for Cancer Research, National Cancer Institute, Bethesda, MD 20892 USA. libuttis@mail.nih.gov
Abstract:
With the role of angiogenesis in tumor growth and progression firmly established, considerable effort has been directed to antiangiogenic therapy as a new modality to treat human cancers. Antiangiogenic agents have recently received much widespread attention but strategies for their optimal use are still being developed. Gene therapy represents an attractive alternative to recombinant protein administration for several reasons. This review evaluates the potential advantages of gene transfer for antiangiogenic cancer therapy and describes preclinical gene transfer work with endogenous angiogenesis inhibitors demonstrating the feasibility of effectively suppressing and even eradicating tumors in animal models. Additionally, we describe the advantages and disadvantages of currently available gene transfer vectors and update novel developments in this field. In conclusion, gene therapy holds great promise in advancing antiangiogenesis as an effective cancer therapy and will undoubtedly be evaluated in human clinical trials in the near future.
Insights
Gene therapy offers a promising approach for antiangiogenic cancer treatment by utilizing gene transfer to deliver endogenous angiogenesis inhibitors. Preclinical studies show this method can suppress and eradicate tumors, paving the way for clinical trials.
Area of Science:
- Oncology
- Molecular Biology
- Biotechnology
Background:
- Angiogenesis is crucial for tumor growth and progression.
- Antiangiogenic therapy is a developing cancer treatment modality.
- Gene therapy presents an alternative to recombinant protein administration.
Purpose of the Study:
- To evaluate gene transfer advantages for antiangiogenic cancer therapy.
- To review preclinical gene transfer studies using endogenous angiogenesis inhibitors.
- To discuss gene transfer vectors and novel developments.
Main Methods:
- Review of preclinical gene transfer studies.
- Evaluation of gene transfer vectors for antiangiogenic therapy.
- Analysis of endogenous angiogenesis inhibitors via gene transfer.
Main Results:
- Preclinical studies demonstrate tumor suppression and eradication in animal models.
- Gene transfer of endogenous angiogenesis inhibitors is feasible.
- Various gene transfer vectors have distinct advantages and disadvantages.
Conclusions:
- Gene therapy holds significant promise for advancing antiangiogenesis in cancer treatment.
- Further development and clinical trials are anticipated for gene therapy in oncology.
- Gene transfer offers a viable strategy for effective cancer suppression.
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