A GSH-depleted platinum(IV) prodrug triggers ferroptotic cell death in breast cancer

被引:22
|
作者
Qi, Dachuan [1 ]
Xing, Lei [2 ]
Shen, Lijun [2 ]
Sun, Wenshuang [4 ]
Cai, Cheng [1 ]
Xue, Chunhua [1 ]
Song, Xuwei [1 ]
Yu, Hua [1 ]
Jiang, Hulin [2 ]
Li, Chengjun [4 ]
Jin, Qingri [3 ]
Zhang, Zhiqi [1 ]
机构
[1] Tongji Univ, Shanghai Peoples Hosp 4, Sch Med, Dept Gen Surg, Shanghai 200434, Peoples R China
[2] China Pharmaceut Univ, Dept Pharmaceut, Nanjing 210009, Peoples R China
[3] Zhejiang A&F Univ, Coll Anim Sci & Technol, Coll Vet Med, Key Lab Appl Technol Green Ecohlth Anim Husb Zhej, Linan 311300, Peoples R China
[4] Nanjing Univ, Jinling Hosp, Sch Med, Dept Orthoped, Nanjing 210002, Peoples R China
关键词
Cisplatin; Ferroptosis; Cancer therapy; Glutathione depletion; Tetravalent platinum prodrug; CISPLATIN; NANOPRODRUG; DRUGS;
D O I
10.1016/j.cclet.2022.03.105
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Cisplatin is the first-line drug for treatment of various solid tumors including breast cancer due to the broad anti-tumor spectrum and strong anti-tumor effect. However, serious side effects and long-term medication of reduced sensitivity by high GSH in tumor cells have severely restricted its further clinical application. Herein, a GSH-depleted Pt(IV) prodrug (Platin B) based on cisplatin and 4-carboxylphenylboronic acid pinacol ester was prepared to solve the problems. As an excellent GSH scavenger, 4-carboxylphenylboronic acid pinacol ester could be activated by intracellular redox reactions to release quinone methide, thereby amplifying oxidative stress and leading to breast cancer ferroptosis therapy. Interestingly, the consumption of GSH can also reduce cisplatin inactivation, enhance the sensitivity of tumor cells to cisplatin and efficiently induce apoptosis/ferroptosis. This work highlights the use of GSH scavenger for triggering ferroptotic cell death in breast cancer. (C) 2022 Published by Elsevier B.V. on behalf of Chinese Chemical Society and Institute of Materia Medica, Chinese Academy of Medical Sciences.
引用
收藏
页码:4595 / 4599
页数:5
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