谷胱甘肽
活性氧
葡萄糖氧化酶
阿霉素
化学
化疗
体内
多重耐药
药理学
氧化应激
氧化还原
NADPH氧化酶
生物化学
癌症研究
医学
生物
酶
内科学
有机化学
生物技术
抗生素
作者
Jinzhi Xu,Yan Xu,Lixin Sun,Bei Lü,Yan Xi,Zhonghao Wang,Tong Zhang
标识
DOI:10.1016/j.biopha.2021.111606
摘要
The development of multidrug resistance (MDR) is a major cause for the failure of chemotherapy, which requires the aid of nanomedicine.Here in our study, a Cu2+ based metal-organic framework (COF) was firstly developed and employed as a carrier for the delivery of glucose oxidase (GOx) and doxorubicin (Dox) (COF/GOx/Dox) for the therapy of MDR lung cancers.Our results showed that the GOx can catalyze glucose and produce H2O2. In the mean time, the Cu2+ can react with GSH and then transform into Cu+, which resulted in GSH depletion. Afterwards, the produced Cu+ and H2O2 trigger Fenton reaction to generate ROS to damage the redox equilibrium of cancer cells. Both effects contributed to the reverse of MDR in A549/Dox cells and finally resulted in significantly enhanced in vitro/in vivo anticancer performance.The combination of glutathione depletion/reactive oxygen species elevation might be a promising strategy to enhance the efficacy of chemotherapy and reverse MDR in cancers.
科研通智能强力驱动
Strongly Powered by AbleSci AI