College of Engineering and Applied Sciences, State Key Laboratory of Analytical Chemistry for Life Science, Jiangsu Key Laboratory of Artificial Functional Materials, Nanjing University, Nanjing 210023, China.
Laboratory for Microstructures, School of Materials Science and Engineering, Shanghai University, Shanghai 200444, China.
ACS Nano. 2024 Mar 26;18(12):9031-9042. doi: 10.1021/acsnano.3c12796. Epub 2024 Mar 12.
Cuproptosis has drawn enormous attention in antitumor material fields; however, the responsive activation of cuproptosis against tumors using nanomaterials with high atom utilization is still challenging. Herein, a copper-based nanoplatform consisting of acid-degradable copper hydride (CuH) nanoparticles was developed via a microfluidic synthesis. After coating with tumor-targeting hyaluronic acid (HA), the nanoplatform denoted as HA-CuH-PVP (HCP) shows conspicuous damage toward tumor cells by generating Cu and hydrogen (H) simultaneously. Cu can induce apoptosis by relying on Fenton-like reactions and lead to cuproptosis by causing mitochondrial protein aggregation. Besides, the existence of H can enhance both cell death types by causing mitochondrial dysfunction and intracellular redox homeostatic disorders. experimental results further exhibit the desirable potential of HCP for killing tumor cells and inhibiting lung metastases, which will broaden the horizons of designing copper-based materials triggering apoptosis and cuproptosis for better antitumor efficacy.
铜死亡在抗肿瘤材料领域引起了极大关注;然而,利用高原子利用率的纳米材料响应性地激活铜死亡以对抗肿瘤仍然具有挑战性。在此,通过微流控合成开发了一种由可酸降解的氢化铜(CuH)纳米颗粒组成的铜基纳米平台。用肿瘤靶向透明质酸(HA)包覆后,该纳米平台表示为 HA-CuH-PVP(HCP)通过同时生成 Cu 和 H,对肿瘤细胞表现出明显的损伤。Cu 可以通过芬顿样反应诱导细胞凋亡,并通过导致线粒体蛋白聚集导致铜死亡。此外,H 的存在可以通过引起线粒体功能障碍和细胞内氧化还原稳态紊乱来增强这两种细胞死亡类型。实验结果进一步显示了 HCP 杀死肿瘤细胞和抑制肺转移的理想潜力,这将拓宽设计基于铜的材料触发细胞凋亡和铜死亡以提高抗肿瘤疗效的视野。