GPX4
脂质过氧化
活性氧
化学
谷胱甘肽
光热治疗
抗氧化剂
单线态氧
癌细胞
细胞生物学
声动力疗法
生物化学
癌症治疗
磷脂过氧化氢谷胱甘肽过氧化物酶
生物物理学
血卟啉
谷胱甘肽过氧化物酶
下调和上调
细胞凋亡
氧化应激
过氧化脂质
癌症
过氧化物酶
癌症研究
姜黄素
氧气
荧光素酶
过氧化氢
脂滴
细胞
细胞损伤
作者
Yafei Lin,Xue Han,Lei Wang,Zhuoran Li,Wenting Zhang,Xuening Zhang,Yueyang Yao,Yonghao Gai,Xi Zhu,Yang Zhang
摘要
-glutathione (GSH)-GPX4 route, and hematoporphyrin monomethyl ether (HMME) enables SDT to generate ROS and lipid peroxides and eliminate heat resistance. This provides a novel strategy to address the self-hypoxic characteristics of tumor microenvironments, antioxidant defenses, and laser-responsive heat tolerance issues. In addition, it lays theoretical and experimental foundations for the application of iridium-based nano-drugs in cancer therapy enhanced by ferroptosis through amplified GSH depletion.
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