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Updated: Oct 27, 2025

An Orthotopic Bladder Cancer Model for Gene Delivery Studies
Published on: December 1, 2013
Epidermal Growth Factor Based Targeted Toxin for the Treatment of Bladder Cancer
Anie Priscilla Masilamani1,2, Alexandra Fischer1,2, Susanne Schultze-Seemann1,2
1Faculty of Medicine, University of Freiburg, Freiburg, Germany.
Background/Aim:
Reports on over-expression of the epidermal growth factor receptor (EGFR) in bladder cancer and its function in tumorigenesis have suggested to target this antigen.
Materials And Methods:
We generated the targeted toxin EGF-PE40 consisting of the human epidermal growth factor (EGF) as the binding domain and PE40, a truncated version of Pseudomonas Exotoxin A, as the toxin domain. EGF-PE40 was tested on EGFR-expressing bladder cancer cells in view of binding via flow cytometry, and cytotoxicity via WST viability assay. Induction of apoptosis was examined by western blot.
Results:
The targeted toxin specifically triggered cytotoxicity in the bladder cancer cells with 50% inhibitory concentration (IC50) values in the low nanomolar or picomolar range, and was about 1,250- to 1,500-fold more cytotoxic than the EGFR inhibitor erlotinib. Cytotoxicity of EGF-PE40 was based on the induction of apoptosis.
Conclusion:
EGF-PE40 represents a promising candidate for the future treatment of bladder cancer.
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