谷胱甘肽
糖酵解
肿瘤微环境
纳米载体
癌细胞
化学
癌症研究
生物化学
细胞生物学
肿瘤细胞
癌症
新陈代谢
药理学
生物
医学
酶
药品
内科学
作者
Ying Huang,Si Wu,Lu Zhang,Qingqing Deng,Jinsong Ren,Xiaogang Qu
出处
期刊:ACS Nano
[American Chemical Society]
日期:2022-02-25
卷期号:16 (3): 4228-4238
被引量:113
标识
DOI:10.1021/acsnano.1c10231
摘要
The high glutathione (GSH) content in tumor cells strongly affects the efficiency of chemodynamic therapy (CDT). Despite devoted efforts, it still remains a formidable challenge for manufacturing a tumor-specific CDT with rapid and thorough depletion of GSH. Herein, a multistage GSH-consuming and tumor-specific CDT is presented. By consuming the reserved GSH and inhibiting both the raw materials and energy supply of GSH synthesis in cancer cells, it achieves highly potent GSH exhaustion. Our used glycolysis inhibitor cuts off the specific glycolysis of tumor cells to increase the sensitivity to CDT. Furthermore, the starvation effect of glycolysis inhibitor can stimulate the protective mode of normal cells. Since the glycolysis inhibitor and nanocarrier are responsive to tumor microenvironment, this makes CDT more selective to tumor cells. Our work not only fabricates nanomedicine with GSH exhausted function for highly potent CDT but also uses metabolic differences to achieve tumor-specific therapy.
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