TY - JOUR T1 - Epidermal Growth Factor Based Targeted Toxin for the Treatment of Bladder Cancer JF - Anticancer Research JO - Anticancer Res SP - 3741 LP - 3746 DO - 10.21873/anticanres.15165 VL - 41 IS - 8 AU - ANIE PRISCILLA MASILAMANI AU - ALEXANDRA FISCHER AU - SUSANNE SCHULTZE-SEEMANN AU - IRINA KUCKUCK AU - ISIS WOLF AU - FRANZ FRIEDRICH DRESSLER AU - CHRISTIAN GRATZKE AU - PHILIPP WOLF Y1 - 2021/08/01 UR - http://ar.iiarjournals.org/content/41/8/3741.abstract N2 - 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. ER -