GPX4
谷胱甘肽
活性氧
癌细胞
纳米技术
材料科学
癌症研究
化学
细胞生物学
生物化学
生物物理学
癌症
谷胱甘肽过氧化物酶
生物
酶
遗传学
作者
Shuaifei Wang,Fangyuan Li,Ruirui Qiao,Xi Hu,Hongwei Liao,Lumin Chen,Jiahe Wu,Haibin Wu,Meng Zhao,Jianan Liu,Rui Chen,Xibo Ma,Dokyoon Kim,Jihong Sun,Thomas P. Davis,Chunying Chen,Jie Tian,Taeghwan Hyeon,Daishun Ling
出处
期刊:ACS Nano
[American Chemical Society]
日期:2018-11-29
卷期号:12 (12): 12380-12392
被引量:321
标识
DOI:10.1021/acsnano.8b06399
摘要
Ferroptosis, an iron-based cell-death pathway, has recently attracted great attention owing to its effectiveness in killing cancer cells. Previous investigations focused on the development of iron-based nanomaterials to induce ferroptosis in cancer cells by the up-regulation of reactive oxygen species (ROS) generated by the well-known Fenton reaction. Herein, we report a ferroptosis-inducing agent based on arginine-rich manganese silicate nanobubbles (AMSNs) that possess highly efficient glutathione (GSH) depletion ability and thereby induce ferroptosis by the inactivation of glutathione-dependent peroxidases 4 (GPX4). The AMSNs were synthesized via a one-pot reaction with arginine (Arg) as the surface ligand for tumor homing. Subsequently, a significant tumor suppression effect can be achieved by GSH depletion-induced ferroptosis. Moreover, the degradation of AMSNs during the GSH depletion contributed to T1-weighted magnetic resonance imaging (MRI) enhancement as well as on-demand chemotherapeutic drug release for synergistic cancer therapy. We anticipate that the GSH-depletion-induced ferroptosis strategy by using manganese-based nanomaterials would provide insights in designing nanomedicines for tumor-targeted theranostics.
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