Journal
ACS NANO
Volume 16, Issue 1, Pages 855-868Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acsnano.1c08464
Keywords
single-atom catalysis; selective ferroptosis; self-adaptive; DNA modulation; ROS regulation; activated GSH-consuming
Categories
Funding
- National Key R&D Program of China [2021YFF1200700, 2019YFA0709202]
- Natural Science Foundation of China [21871249, 91856205, 21820102009]
- Jilin Province Science and Technology Development Plan Project [20190701028GH, 20200201420JC, CAS QYZDJ-SSW-SLH052]
Ask authors/readers for more resources
A self-adaptive ferroptosis platform has been developed by engineering a DNA modulator onto the surface of single-atom nanozymes, enabling selective and safe antitumor response and promoting the development of selective cancer therapy.
Ferroptosis, resulting from the catastrophic accumulation of lipid reactive oxygen species (ROS) and the inactivation of glutathione (GSH)-dependent peroxidase 4 (GPX4), has emerged as a form of regulated cell death for cancer therapy. Despite progress made with current ferroptosis inducers, efficient systems to trigger ferroptosis remain challenging, owing largely to their low activity, uncontrollable behavior, and even nonselective interactions. Here, we report a self-adaptive ferroptosis platform by engineering a DNA modulator onto the surface of single-atom nanozymes (SA-zymes). The modulator could not only specifically intensify the ROS-generating activity but also endow the SAzymes with on-demand GSH-consuming ability in tumor cells, accelerating selective and safe ferroptosis. The self-adaptive antitumor response has been demonstrated in colon cancer and breast cancer, promoting the development of selective cancer therapy.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available