Copper(II) Complexes of Halogenated Quinoline Schiff Base Derivatives Enabled Cancer Therapy through Glutathione-Assisted Chemodynamic Therapy and Inhibition of Autophagy Flux.

Twelve new complexes - were designed and synthesized to improve their chemotherapeutic properties. They showed considerable antiproliferative activity against T24 cancer cells but lower cytotoxicity to human normal cells HL-7702 and WI-38. A mechanism study indicated that and were reduced to Fenton-like Cu by glutathione depletion, and the resulting Cu catalyzed the generation of highly toxic hydroxyl radicals from excess HO. Simultaneously, and could decrease the catalase activity to restrain HO transfer to HO for enhanced chemodynamic therapy (CDT). These induced mitochondrial dysfunctions and endoplasmic reticulum stress to induce T24 cell apoptosis. In addition, and inhibited autophagy flux to promote cell apoptosis. and demonstrated strong tumor inhibition ability in the T24 xenograft model. Moreover, showed higher antitumor activity and a better safety profile than the CDT agent . exhibited excellent pharmacokinetic properties. Collectively, and could be developed as potential CDT candidates for cancer treatment.