过氧化氢
化学
癌症治疗
脱氧核酶
癌细胞
过氧化氢酶
诱导剂
谷胱甘肽
细胞内
纳米技术
癌症
生物物理学
DNA
组合化学
生物化学
材料科学
生物
酶
医学
内科学
基因
作者
Qiao Yu,Jie Zhou,Yong Liu,Xiao Qiong Li,Shan Li,Hong Zhou,Bin Kang,Hong‐Yuan Chen,Jing‐Juan Xu
标识
DOI:10.1002/adhm.202301429
摘要
Abstract Cuproptosis, a kind of newly recognized cell death modality, shows enormous prospect in cancer treatment. The inducer of cuproptosis has more advantages in tumor therapy, especially that can trigger cuproptosis and chemodynamic therapy (CDT) simultaneously. However, cuproptosis is restricted to the deficiency of intracellular copper ions and the nonspecific delivery of copper‐based ionophores. Therefore, high level delivery, responsive release, and utilizing synergistic‐function of inducer become the key on cuproptosis‐based oncotherapy. In this work, a cascade nanosystem is constructed for enhanced cuproptosis and CDT. In the weak acidic environment of tumor cells, DNA, zinc ions, and Cu + can release from the nanosystem. Since Cu + having superior performance in mediating both Fenton‐like reaction and cuproptosis, the released Cu + induces cuproptosis and CDT efficiently, accompanied by Cu 2+ generation. Then Cu 2+ can be converted into Cu + partially by glutathione (GSH) to from a Cu + supply loop and ensure the synergistic action. Meanwhile, the consumption of GSH also contributes to cuproptosis and CDT in return. Finally, DNA and Zn 2+ form DNAzyme to shear catalase‐related RNA, resulting in the accumulation of hydrogen peroxide and further enhancing combination therapy. These results provide a promising nanotherapeutic platform and may inspire the design for potential cancer treatment based on cuproptosis.
科研通智能强力驱动
Strongly Powered by AbleSci AI