Department of Chemical Biology, The MOE Laboratory of Spectrochemical Analysis & Instrumentation, and the Key Laboratory for Chemical Biology of Fujian Province, College of Chemistry and Chemical Engineering, Xiamen University, Xiamen, 361005, China.
Angew Chem Int Ed Engl. 2021 Jan 18;60(3):1403-1410. doi: 10.1002/anie.202012237. Epub 2020 Nov 13.
Despite widespread applications for cancer treatment, chemotherapy is restricted by several limitations, including low targeting specificity, acquired drug resistance, and concomitant adverse side effects. It remains challenging to overcome these drawbacks. Herein, we report a new bioenergetic approach for treating cancer efficiently. As a proof-of-concept, we construct activatable mitochondria-targeting organoarsenic prodrugs from organoarsenic compounds and traditional chemotherapeutics. These prodrugs could accomplish selective delivery and controlled release of both therapeutic agents to mitochondria, which synergistically promote mitochondrial ROS production and induce mitochondrial DNA damage, finally leading to mitochondria-mediated apoptosis of cancer cells. Our in vitro and in vivo experiments reveal the excellent anticancer efficacy of these prodrugs, underscoring the encouraging outlook of this strategy for effective cancer therapy.
尽管在癌症治疗中有广泛的应用,但化疗受到多种限制,包括靶向特异性低、获得性药物耐药性和伴随的不良反应。克服这些缺点仍然具有挑战性。在这里,我们报告了一种新的生物能量方法来有效治疗癌症。作为概念验证,我们从有机砷化合物和传统化疗药物构建了可激活的靶向线粒体的有机砷前药。这些前药可以选择性地将治疗剂递送到线粒体并进行控制释放,协同促进线粒体 ROS 的产生和诱导线粒体 DNA 损伤,最终导致线粒体介导的癌细胞凋亡。我们的体外和体内实验揭示了这些前药的优异抗癌疗效,突显了这种策略用于有效癌症治疗的令人鼓舞的前景。