Angewandte Chemie International Edition · 2018 · 102 citations · 19 references
Life SciencesOncologyPharmacologyCancer PharmacologyChemotherapyMitochondrial BiologyAnticancer Prodrug DesignMitochondrial BiochemistryMitochondrial FunctionMitochondrial MembranesReactive Oxygen SpeciesTumor-activated ProdrugsAnticancer ActivityAnticancer ChemotherapyMitochondria-targeted Redox ProdrugsMitochondrial TargetsOxidative Stress In CancerReactive Oxygen Species GenerationReactive Oxygen Species-activated ProdrugsRedox-activated Anticancer Prodrugs
Mitochondrial membrane potential is more negative in cancer cells than in normal cells, allowing cancer targeting by delocalized lipophilic cations (DLCs). However, as the difference is rather small, these drugs affect also normal cells. Now a concept of pro-DLCs is proposed based on an N-alkylaminoferrocene structure. These prodrugs are activated by the reaction with reactive oxygen species (ROS) forming ferrocenium-based DLCs. Since ROS are overproduced in cancer, the high-efficiency cancer-cell-specific targeting of mitochondria could be achieved as demonstrated by fluorescence microscopy in combination with two fluorogenic pro-DLCs in vitro and in vivo. We prepared a conjugate of another pro-DLC with a clinically approved drug carboplatin and confirmed that its accumulation in mitochondria was higher than that of the free drug. This was reflected in the substantially higher anticancer effect of the conjugate.
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Otto Warbürg · Science · 1956 · 13.3K citations
Steven O’Day, Alexander M.M. Eggermont, Vanna Chiarion‐Sileni et al. · Journal of Clinical Oncology · 2013 · 386 citations · Full text
Medicine, Oncology, Pharmacology +17
Zejia Yang, Lisa M. Schumaker, Merrill J. Egorin et al. · Clinical Cancer Research · 2006 · 266 citations
A novel mitochondriotoxic small molecule that selectively inhibits tumor cell growth
Valeria R. Fantin, Marcelo J. Berardi, Luca Scorrano et al. · Cancer Cell · 2002 · 230 citations · Full text
Medicine, Oncology, Pharmacology +14