催化作用
氧化还原
癌细胞
化学
癌症治疗
组合化学
基因沉默
肿瘤微环境
癌症研究
癌症
生物物理学
材料科学
纳米技术
生物化学
肿瘤细胞
生物
基因
有机化学
遗传学
作者
Xiaowen Guan,Xiyang Ge,Hongliang Dong,Juanjuan Wei,Jin Ouyang,Na Na
标识
DOI:10.1002/adhm.202301853
摘要
Abstract Single‐atom nanozymes (SAzymes) have obtained increasing interest to mimic natural enzymes for efficient cancer therapy, while challenged by chemoresistance from cellular redox homeostasis and the interface of reductive species in tumor microenvironment (TME). Herein, a dual single‐atomic ultrathin 2D metal organic framework (MOF) nanosheet of multienzyme (Pd/Cu SAzyme@Dzy) is prepared to synergistically overcome chemoresistance for multienzyme enhanced cancer catalytic therapy. The Pd SAzyme exhibits peroxidase (POD)‐like catalytic activity for overcoming chemoresistance via disturbing cellular redox balance. This is further enhanced by cascade generation of more ∙OH via Cu + ‐catalyzed POD‐like reactions, initiated by in situ‐reduction of Cu 2+ into Cu + upon GSH depletion. This process can also avoid the consumption of ∙OH by endogenous reductive GSH in TME, ensuring the adequate amount of ∙OH for highly efficient therapy. Besides, the DNAzyme is also delivered for gene therapy of silencing cancer‐cell‐targeting VEGFR2 protein to further enhance the therapy. Based on both experiments and theoretical calculations, the synergetic multienzyme‐based cancer therapy is examined and the enhancement by the cascade tumor antichemoresistance is revealed.
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