| Literature DB >> 33772996 |
Mengyu Chang1,2, Zhiyao Hou3,4, Man Wang5, Chunzheng Yang1,2, Ruifeng Wang1, Fang Li1, Donglian Liu3, Tieli Peng3, Chunxia Li5, Jun Lin1,2.
Abstract
Photothermal therapy (PTT) is an extremely promising tumor therapeutic modality. However, excessive heat inevitably injures normal tissues near tumors, and the damage to cancer cells caused by mild hyperthermia is easily repaired by stress-induced heat shock proteins (HSPs). Thus, maximizing the PTT efficiency and minimizing the damage to healthy tissues simultaneously by adopting appropriate therapeutic temperatures is imperative. Herein, an innovative strategy is reported: ferroptosis-boosted mild PTT based on a single-atom nanozyme (SAzyme). The Pd SAzyme with atom-economical utilization of catalytic centers exhibits peroxidase (POD) and glutathione oxidase (GSHOx) mimicking activities, and photothermal conversion performance, which can result in ferroptosis featuring the up-regulation of lipid peroxides (LPO) and reactive oxygen species (ROS). The accumulation of LPO and ROS provides a powerful approach for cleaving HSPs, which enables Pd SAzyme-mediated mild-temperature PTT.Entities:
Keywords: Pd SAzyme; ferroptosis; heat shock proteins; nanozymes; photothermal therapy
Year: 2021 PMID: 33772996 DOI: 10.1002/anie.202101924
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336