Institute of Functional Nano and Soft Materials (FUNSOM), Jiangsu Key Laboratory for Carbon-Based Functional Materials and Devices, Soochow University, Suzhou, 215123, China.
Angew Chem Int Ed Engl. 2022 Sep 26;61(39):e202208849. doi: 10.1002/anie.202208849. Epub 2022 Aug 25.
Multiple amplification of tumor oxidative stress has been demonstrated as efficient strategy to enhance the reactive oxygen species (ROS)-mediated cancer therapy. Herein, vanadium-based nanocatalysts, hydrogen vanadium bronzes (H V O , for short HVO), were constructed and employed as novel biocatalysts for amplifying tumor oxidative stress and enhancing cancer catalytic therapy. Such HVO nanocatalysts harboring multivalent V element possessed multi-functional catalytic activity in decomposing H O into ⋅OH and depleting endogenous glutathione (GSH) to dually amplify tumor oxidative stress. Meanwhile, HVO nanocatalysts could also be activated by ultrasound to further triply amplify oxidative stress. The massive intracellular ROS caused mitochondrial dysfunction, DNA damage, cell cycle arrest, and cell proliferation inhibition, further realizing cancer cell death and tumor growth inhibition. Collectively, HVO nanocatalysts highlight the remarkable value of ROS-mediated cancer therapies.
已证实,肿瘤氧化应激的多重扩增是增强活性氧(ROS)介导的癌症治疗的有效策略。在此,构建了基于钒的纳米催化剂-氢钒青铜(HVO,简称 HVO),并将其用作新型生物催化剂,以放大肿瘤氧化应激并增强癌症催化治疗。这种含有多价 V 元素的 HVO 纳米催化剂具有将 H2O2 分解为 ⋅OH 和耗尽内源性谷胱甘肽(GSH)的多功能催化活性,从而双重放大肿瘤氧化应激。同时,HVO 纳米催化剂也可以被超声激活,进一步三重放大氧化应激。大量的细胞内 ROS 导致线粒体功能障碍、DNA 损伤、细胞周期停滞和细胞增殖抑制,从而实现癌细胞死亡和肿瘤生长抑制。总之,HVO 纳米催化剂突出了 ROS 介导的癌症治疗的显著价值。