| Literature DB >> 34851608 |
Weiyun Zhang1,2, Jiawei Liu3, Xuyu Li2, Yue Zheng4, Lianfu Chen5, Dongdong Wang3, Mohamed Frahat Foda1,6, Zhaoyu Ma1,3, Yanli Zhao3, Heyou Han1,2.
Abstract
Chemodynamic therapy (CDT) destroys cancer cells by converting H2O2 or O2 into reactive oxygen species (ROS), but its therapeutic efficacy is restricted by the antioxidant capacity of tumor. Previous solutions focused on strengthening the nanodrugs with the ability to increase ROS production or weaken the antioxidant capacity of cancer cells. Conversely, we here develop a mild nanodrug with negligible side effects. Specifically, the Au@Pt nanozyme decorated on a bacterial surface (Bac-Au@Pt) is reported to achieve precise CDT. Due to the tumor targeting ability of bacteria and catalytic property of Au@Pt nanozyme under acidic conditions, this nanosystem can release ROS to tumor cells effectively. In addition, the interferon gamma released by T cells specifically decreases the intracellular reductants in tumor cells, while having no obvious effect on normal cells. Therefore, a low dose of Bac-Au@Pt achieves a satisfactory therapeutic efficacy to tumor cells and is nontoxic to normal cells even at their acidic components. This nanosystem enables CDT and immunotherapy to mutually benefit and improve by each other, providing a promising strategy to achieve high anticancer efficacy even with a low dose usage.Entities:
Keywords: ferroptosis; immunotherapy; microbial synthesis; nanozyme; precise chemodynamic therapy
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Year: 2021 PMID: 34851608 DOI: 10.1021/acsnano.1c05605
Source DB: PubMed Journal: ACS Nano ISSN: 1936-0851 Impact factor: 15.881