Bioengineering (Focus Group – BE)
Gene-directed enzyme prodrug therapy (GDEPT) has been developed as a targeted cancer treatment aimed at minimizing toxicity to healthy cells [1]. This approach involves three key components: a non-toxic prodrug, a gene encoding an enzyme that converts the prodrug into an active chemotherapy drug, and a gene carrier to target cancer cells. In this study, the prodrug doxifluridine was converted into the chemotherapy drug 5-FU via thymidine phosphorylase (TP), using human mesenchymal stem cells (hMSCs) as delivery vehicles due to their tumor-tropic nature and low immunogenicity [2, 3].
Ching-An Peng, PhD
Prof.
University of Idaho, United States