Department of Chemistry & Biochemistry, Utah State University, 0300 Old Main Hill, Logan, UT 84322-0300, United States.
Department of Animal, Dairy and Veterinary Sciences, Utah State University, 4815 Old Main Hill, Logan, UT 84322-4815, United States.
ChemMedChem. 2024 Jun 3;19(11):e202300682. doi: 10.1002/cmdc.202300682. Epub 2024 Mar 13.
Carbon monoxide (CO) delivery molecules are of significant current interest as potential therapeutics, including for anticancer applications. A recent approach toward generating new types of materials-based anticancer agents involves combining the Fenton reactivity of a redox active metal ion with CO delivery. However, small molecule examples of these types of entities have not been systematically studied to evaluate the combined effect on cellular toxicity. Herein we describe a Cu(II) flavonolato complex which produces anticancer effects through a combination of copper-mediated reactive oxygen species (ROS) generation and light-induced flavonol CO release. Confocal microscopy studies provide evidence of enhanced flavonol uptake in the copper flavonolato system relative to the free flavonol, which leads to an increased amount of CO delivery within cells. Importantly, this work demonstrates that a metal flavonolato species can be used to produce enhanced toxicity effects resulting from both metal ion-induced Fenton reactivity and increased cellular uptake of a flavonol CO donor.
一氧化碳(CO)传递分子是目前非常关注的潜在治疗药物,包括用于抗癌应用。最近一种生成新型基于材料的抗癌剂的方法涉及将氧化还原活性金属离子的芬顿反应与 CO 传递相结合。然而,这些类型的实体的小分子示例尚未被系统地研究以评估对细胞毒性的联合影响。在此,我们描述了一种 Cu(II) 黄酮醇配合物,它通过铜介导的活性氧 (ROS) 生成和光诱导黄酮醇 CO 释放的组合产生抗癌作用。共焦显微镜研究提供了证据,表明相对于游离黄酮醇,铜黄酮醇配合物系统中黄酮醇的摄取增强,从而导致细胞内 CO 传递量增加。重要的是,这项工作表明,金属黄酮醇配合物可用于产生增强的毒性作用,这是由金属离子诱导的芬顿反应和黄酮醇 CO 供体的细胞摄取增加共同导致的。