Publication | Closed Access
Specific “Unlocking” of a Nanozyme‐Based Butterfly Effect To Break the Evolutionary Fitness of Chaotic Tumors
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Citations
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References
2020
Year
Nanozyme‐based Butterfly EffectMolecular BiologyRedox BiologyTumor BiologyOxidative StressRedox RegulatorCancer Cell BiologyRedox ChemistryChaotic MixingCancer MetabolismBiophysicsRedox SignalingIridium Oxide NanoparticlesBiochemistryChaos TheoryGod CatalysisCancer CellsReactive Oxygen SpecieChaotic TumorsBiomolecular EngineeringPattern FormationNatural SciencesMedicineEvolutionary Fitness
Abstract Chaos and the natural evolution of tumor systems can lead to the failure of tumor therapies. Herein, we demonstrate that iridium oxide nanoparticles (IrO x ) possess acid‐activated oxidase and peroxidase‐like functions and wide pH‐dependent catalase‐like properties. The integration of glucose oxidase (GOD) unlocked the oxidase and peroxidase activities of IrO x by the production of gluconic acid from glucose by GOD catalysis in cancer cells, and the produced H 2 O 2 was converted into O 2 to compensate its consumption in GOD catalysis owing to the catalase‐like function of the nanozyme, thus resulting in the continual consumption of glucose and the self‐supply of substrates to generate superoxide anion and hydroxyl radical. Moreover, IrO x can constantly consume glutathione (GSH) by self‐cyclic valence alternation of Ir IV and Ir III . These cascade reactions lead to a “butterfly effect” of initial starvation therapy and the subsequent pressure of multiple reactive oxygen species (ROS) to completely break the self‐adaption of cancer cells.
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