Nanoscale dual-enzyme cascade metal-organic frameworks through biomimetic mineralization as ROS generators for synergistic cancer therapy
- PMID: 32373876
- DOI: 10.1039/d0tb00357c
Nanoscale dual-enzyme cascade metal-organic frameworks through biomimetic mineralization as ROS generators for synergistic cancer therapy
Abstract
Chemodynamic therapy (CDT) has been critically challenged by insufficient H2O2 in cancer tissues and inefficient reactive oxygen species (ROS) production. Herein, we have reported the facile synthesis of an efficient ROS generator (GOx@Pd@ZIF-8) that exerts synergistic anticancer activity by blocking glucose metabolism and producing ROS. Glucose oxidase (GOx) and palladium (Pd) cube nanozymes were incorporated in zeolitic imidazolate framework-8 (ZIF-8) by biomimetic mineralization. Systematic characterization indicated the successful entrapment and embedding of GOx and Pd during ZIF-8 crystal growth. The GOx@Pd@ZIF-8 composite showed favorable catalytic glucose activity and stable ROS production. In vitro experiments showed that the GOx@Pd@ZIF-8 composite effectively inhibited cancer cell proliferation, invasion, and migration and promoted apoptosis through the ROS-mediated signaling pathway, which was further confirmed by bioinformatics analyses of RNA-seq data obtained from in vitro experiments. Furthermore, the GOx@Pd@ZIF-8 composite inhibited tumor growth with few to no side effects on other tissues in vivo. This work provides a novel antitumor strategy involving the construction of a stable and highly active ROS generator that shows promise for the treatment of solid cancers.
Similar articles
-
A cascade-reaction enabled synergistic cancer starvation/ROS-mediated/chemo-therapy with an enzyme modified Fe-based MOF.Biomater Sci. 2019 Aug 20;7(9):3683-3692. doi: 10.1039/c9bm00641a. Biomater Sci. 2019. PMID: 31361291
-
GOx@ZIF-8(NiPd) Nanoflower: An Artificial Enzyme System for Tandem Catalysis.Angew Chem Int Ed Engl. 2017 Dec 11;56(50):16082-16085. doi: 10.1002/anie.201710418. Epub 2017 Nov 20. Angew Chem Int Ed Engl. 2017. PMID: 29119659
-
Erythrocyte Membrane Cloaked Metal-Organic Framework Nanoparticle as Biomimetic Nanoreactor for Starvation-Activated Colon Cancer Therapy.ACS Nano. 2018 Oct 23;12(10):10201-10211. doi: 10.1021/acsnano.8b05200. Epub 2018 Oct 3. ACS Nano. 2018. PMID: 30265804
-
Recent Advances in Emerging Metal- and Covalent-Organic Frameworks for Enzyme Encapsulation.ACS Appl Mater Interfaces. 2021 Dec 8;13(48):56752-56776. doi: 10.1021/acsami.1c13408. Epub 2021 Nov 22. ACS Appl Mater Interfaces. 2021. PMID: 34809426 Review.
-
Dual Enzyme-Encapsulated Materials for Biological Cascade Chemistry and Synergistic Tumor Starvation.Chemistry. 2024 Jun 3;30(31):e202400195. doi: 10.1002/chem.202400195. Epub 2024 May 2. Chemistry. 2024. PMID: 38563653 Review.
Cited by
-
Explaining chemical clues of metal organic framework-nanozyme nano-/micro-motors in targeted treatment of cancers: benchmarks and challenges.J Nanobiotechnology. 2022 Mar 24;20(1):153. doi: 10.1186/s12951-022-01375-z. J Nanobiotechnology. 2022. PMID: 35331244 Free PMC article. Review.
-
Smart Nanozymes for Cancer Therapy: The Next Frontier in Oncology.Adv Healthc Mater. 2023 Oct;12(25):e2300768. doi: 10.1002/adhm.202300768. Epub 2023 Jul 20. Adv Healthc Mater. 2023. PMID: 37392379 Free PMC article. Review.
-
Metal-organic framework-mediated antioxidant enzyme delivery in disease treatment.Redox Biol. 2025 Jul 18;85:103778. doi: 10.1016/j.redox.2025.103778. Online ahead of print. Redox Biol. 2025. PMID: 40714403 Free PMC article. Review.
-
Cyclodextrin metal-organic framework-based protein biocomposites.Biomater Sci. 2022 Nov 22;10(23):6749-6754. doi: 10.1039/d2bm01240e. Biomater Sci. 2022. PMID: 36286095 Free PMC article.
-
Recent Trends in Composite Nanozymes and Their Pro-Oxidative Role in Therapeutics.Front Bioeng Biotechnol. 2022 May 30;10:880214. doi: 10.3389/fbioe.2022.880214. eCollection 2022. Front Bioeng Biotechnol. 2022. PMID: 35711631 Free PMC article. Review.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources