| Literature DB >> 30495919 |
Shuaifei Wang, Fangyuan Li, Ruirui Qiao1, Xi Hu, Hongwei Liao, Lumin Chen2, Jiahe Wu, Haibin Wu, Meng Zhao, Jianan Liu3, Rui Chen4, Xibo Ma5, Dokyoon Kim3, Jihong Sun2, Thomas P Davis1,6, Chunying Chen4, Jie Tian5, Taeghwan Hyeon3,7, Daishun Ling8.
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 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.Entities:
Keywords: GPX4; ferroptosis; glutathione; nanobubbles; theranostics
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Year: 2018 PMID: 30495919 DOI: 10.1021/acsnano.8b06399
Source DB: PubMed Journal: ACS Nano ISSN: 1936-0851 Impact factor: 15.881