体内
声动力疗法
程序性细胞死亡
活性氧
内质网
免疫原性细胞死亡
免疫系统
先天免疫系统
未折叠蛋白反应
细胞凋亡
细胞生物学
化学
免疫疗法
癌症研究
生物物理学
免疫学
生物
生物化学
生物技术
作者
Xiuxin Lu,Kun Qiao,Firdoz Shaik,Yang Zheng,Zhaoyou Chu,Haisheng Qian,Xijun Liu,Weiqing Zhang
出处
期刊:Nano Research
[Springer Science+Business Media]
日期:2023-03-10
卷期号:16 (7): 9730-9742
被引量:35
标识
DOI:10.1007/s12274-023-5562-9
摘要
Facilitated by reactive oxygen species (ROS)-involved therapies, tumor cells undergo immunogenic cell death (ICD) to stimulate long-term immunity response. However, it is hard to trigger abundant and large-scale ICD for satisfactory cancer immunotherapy. Herein, a multifunctional sonosensitizer that consists of Au single atoms and clusters anchored on TiO2 nanosheets (named AuS/C-TiO2) is reported for augmented sonodynamic therapy (SDT) and glucose depletion, which ultimately induce robust ICD due to the improved ROS generation and strong endoplasmic reticulum (ER) stress. The synergy effect between Au cluster/single atom with TiO2 nanosheets intensifies apoptosis and ICD pathways to inhibit 80% of tumor cells through in vivo analyses. Furthermore, immune cells in vivo analyses verify the effectiveness of AuS/C-TiO2 sonosensitizer towards the induction of antitumor immunity. This study thus reveals that simultaneous presence of ROS generation and strong ER stress can efficiently evoke a strong ICD-mediated immune response.
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