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Published on: January 19, 2019
An alternative to the magic bullet paradigm for specific cancer therapy
1VA Medical Center, Bedford, MA 01730.
Abstract:
To improve on current cancer therapies, which attack cells on the basis of their proliferative tendencies, much effort has been devoted to a search for properties of tumor cells that are tumor-specific rather than proliferation specific. Evidence from molecular genetic studies suggests, however, that most tumors may lack such properties. An alternative approach to therapy is described that is based on a property known to characterize the majority of human tumors; viz., a monoclonal origin. The strategy requires the prophylactic induction in tissues of mosaicism for genes dictating sensitivity or resistance to chemotherapeutic agents, and exploits the observation that any clone of cells arising in a mosaic tissue must inevitably differ from some other cells in the mosaic. Recent advances in genetic technology imply that the strategy is likely to be testable soon in animals, and that it may significantly improve the results of cancer therapy when a technology safe and efficient enough for its human implementation becomes available.
Insights
This study proposes a novel cancer therapy approach targeting the monoclonal origin of tumors. By creating tissue mosaicism for drug sensitivity, it aims to improve cancer treatment outcomes.
Area of Science:
- Oncology
- Molecular Genetics
- Cancer Therapy
Background:
- Current cancer therapies target cell proliferation, lacking tumor specificity.
- Most tumors may not possess unique tumor-specific properties.
- Tumors are characterized by their monoclonal origin.
Purpose of the Study:
- To explore an alternative cancer therapy strategy.
- To leverage the monoclonal origin of tumors for therapeutic benefit.
Main Methods:
- Prophylactic induction of tissue mosaicism for drug sensitivity/resistance genes.
- Exploiting cellular differences within mosaic tissues.
Main Results:
- The proposed strategy is theoretically sound and exploits inherent tumor properties.
- Advances in genetic technology suggest feasibility in animal models soon.
Conclusions:
- This approach offers a potential improvement over current cancer therapies.
- Human implementation requires safe and efficient technology development.
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