Published in Gene Therapy Weekly, September 28th, 1998
Most enzyme/prodrug systems are based on herpes simplex virus type 1 thymidine kinase and the antiviral drug ganciclovir or cytosine deaminase and the prodrug 5-fluorocytosine. These suicide gene therapy combinations work as antimetabolites, whose toxicity is dependent upon ongoing DNA replication. As such, growth-arrested cells are not significantly altered by these therapies and their application to some cancers is limited.
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Source: Gene Therapy Weekly (1998-09-28)
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