自噬
光热治疗
活性氧
化学
癌症研究
肿瘤微环境
体外
细胞内
癌细胞
体内
细胞生物学
癌症
细胞凋亡
材料科学
生物
纳米技术
生物化学
肿瘤细胞
遗传学
生物技术
作者
Ziye Wei,Weili Si,Mengli Huang,Man Lu,Wenjun Wang,Liang Chen,Xiaochen Dong,Yu Cai
标识
DOI:10.1002/adhm.202402367
摘要
Abstract As an intracellular protective mechanism, autophagy has the potential to significantly impair the therapeutic effects of photothermal therapy (PTT) and chemodynamic therapy (CDT), which helps cancer cells survive under harsh conditions, such as high temperature and reactive oxygen species (ROS). In this study, an autophagy blockage enhanced PTT and CDT synergistic therapy nanoplatform is constructed by loading hydroxychloroquine (HCQ) with autophagy inhibitory effect into hollow copper sulfide (HCuS). Specifically, HCuS produces toxic ROS through Fenton‐like reaction in the tumor microenvironment (TME). At the same time, PTT‐mediated temperature elevation of the tumor region accelerates the Fenton‐like reaction and ROS production, enhancing the therapeutic effect of CDT. Furthermore, the internal autophagy inhibitor HCQ significantly blocks the fusion of autophagosomes and lysosomes by deacidifying lysosomes, cutting off the self‐protection mechanism of cancer cells, and amplifying the combined treatment of PTT and CDT. Both in vitro and in vivo results demonstrate that the combination of photothermal‐enhanced chemodynamic therapy with inhibition of autophagy provides new insights into designing multifunctional therapeutic nanoagents.
科研通智能强力驱动
Strongly Powered by AbleSci AI