奥沙利铂
药品
化学
荧光
癌症
癌症研究
药理学
癌细胞
医学
结直肠癌
内科学
量子力学
物理
作者
Monika Caban,Philipp Fronik,Alessio Terenzi,Anja Federa,Julia H. Bormio Nunes,Rastislav Pitek,Dominik Kirchhofer,Hemma Schueffl,Walter Berger,Bernhard K. Keppler,Christian R. Kowol,Petra Heffeter
摘要
Platinum chemotherapy is part of every second anticancer treatment regimen. However, its application is limited by severe side effects and drug resistance. The combination of platinum-based chemotherapeutics with EGFR inhibitors has shown remarkable synergism in clinical treatment. To enhance the tolerability of this combination, we designed a novel multi-action oxaliplatin-based platinum(iv) complex with an EGFR-inhibiting moiety (KP2749). KP2749 releases two independent cytotoxic agents upon reduction: oxaliplatin and the EGFR inhibitor KP2187, which was selected for its strong intrinsic fluorescence that became quenched upon complexation to metal ions. In particular, KP2749 demonstrated high stability and specific KP2187 release, with quenched fluorescent properties in its intact form, facilitating the investigation of its intracellular reduction. Notably, by exploiting its fluorescence, we demonstrated that intact KP2749 itself exhibited EGFR-inhibitory properties. Furthermore, subsequent experiments indicated that our complex was able to overcome resistance to oxaliplatin and EGFR inhibitors
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