脂质过氧化
甲状腺间变性癌
铁蛋白
维生素C
GPX4
化学
癌变
癌症研究
癌症
甲状腺
活性氧
抗氧化剂
内科学
甲状腺癌
癌细胞
药理学
生物化学
内分泌学
医学
过氧化氢酶
谷胱甘肽过氧化物酶
作者
Xiaowen Wang,Shichen Xu,Li Zhang,Xian Cheng,Huixin Yu,Jiandong Bao,Rongrong Lu
标识
DOI:10.1016/j.bbrc.2021.02.126
摘要
Anaplastic thyroid cancer (ATC) is a rare but highly lethal disease. So far, there is no available established treatment which can prolong its survival. In this regard, effective therapies are urgently needed. Vitamin C widely serves as an anti-cancer agent. However, the potential effects of vitamin C against thyroid tumorigenesis remained unclear. The present study demonstrated that vitamin C could significantly inhibit ATC cells growth through ferroptosis activation, evidenced by the GPX4 inactivation, ROS accumulation and iron-dependent lipid peroxidation. Our results demonstrated that vitamin C treatment induced ferritinophagy and subsequent degradation of ferritin, leading to the release of free iron. Excessive iron further triggered ROS generation via Fenton reaction. The positive feedback mediated by ROS and iron sustained lipid peroxidation and further resulted in ferroptosis of ATC cells. The better understanding of the anti-cancer mechanisms of vitamin C provides a potential strategy for ATC therapy.
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