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Arginine-rich manganese silicate nanobubbles as a ferroptosis-inducing agent for tumor-targeted theranostics

Cited 275 time in Web of Science Cited 294 time in Scopus
Authors

Wang, Shuaifei; Li, Fangyuan; Qiao, Ruirui; Hu, Xi; Liao, Honrei; Chen, Lumin; Wu, Jiahe; Wu, Haibin; Zhao, Meng; Liu, Jianan; Chen, Rui; Ma, Xibo; Kim, Dokyoon; Sun, Jihong; Davis, Thomas P.; Chen, Chunying; Tian, Jie; Hyeon, Taeghwan; Ling, Daishun

Issue Date
2018-12
Publisher
American Chemical Society
Citation
ACS Nano, Vol.12 No.12, pp.12380-12392
Abstract
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 T-1-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.
ISSN
1936-0851
URI
https://hdl.handle.net/10371/165825
DOI
https://doi.org/10.1021/acsnano.8b06399
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  • College of Engineering
  • School of Chemical and Biological Engineering
Research Area Chemistry, Materials Science

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