癌细胞
电压依赖性阴离子通道
活性氧
脂质过氧化
细胞凋亡
癌症研究
癌症
癌症治疗
细胞内
细胞生物学
化学
医学
生物
生物化学
氧化应激
内科学
基因
细菌外膜
大肠杆菌
作者
Yongming Zhao,Yanqing Li,Ruifeng Zhang,Feng Wang,Zhihui Wang,Yan Jiao
摘要
Erastin was initially discovered as a small molecule compound that selectively kills tumor cells expressing ST and RASV12 and was later widely investigated as an inducer of ferroptosis. Ferroptosis is a recently discovered form of cell death caused by peroxidation induced by the accumulation of intracellular lipid reactive oxygen species (L-ROS) in an iron-dependent manner. Erastin can mediate ferroptosis through a variety of molecules including the cystine-glutamate transport receptor (system XC-), the voltage-dependent anion channel (VDAC), and p53. Erastin is able to enhance the sensitivity of chemotherapy and radiotherapy, suggesting a promising future in cancer therapy. We hope that this review will help to better understand the role of erastin in ferroptosis and lay the foundation for further research and the development of erastin-based cancer therapies in the future.
科研通智能强力驱动
Strongly Powered by AbleSci AI