鼻咽癌
每1
GPX4
癌症研究
脂质过氧化
生物
化学
内科学
谷胱甘肽过氧化物酶
基因表达
基因
医学
内分泌学
超氧化物歧化酶
氧化应激
生物化学
放射治疗
时钟
作者
Yan Zeng,Ziqi Wang,Feng Jin,Jinhua Long,Yu Chen,Mang Zhang,Hong Tang,Pan Luo,Youn Jin Ye,Wei-Li Wu
标识
DOI:10.1080/09291016.2023.2298024
摘要
Nasopharyngeal carcinoma (NPC) still recurs or leads to distant metastasis in 10%–30% patients after standardized treatment, which increases the serious toxic side effects and treatment difficulty with recourse therapy. In this study, we found that the biological clock gene Period1(PER1) was expressed at low levels in human nasopharyngeal carcinoma cell (CNE2)and NPC tissues, and overexpression of PER1 decreased the invasion and migration ability of NPC cells and increased the expression of lipid peroxidation (LPO), Fe2+ and glutathione (GSH). The expression of glutathione peroxidase (GPX4) and solute carrier family 7 member 11 (SLC7A11) was found to be decreased in CNE2 cells and tissues of NPC. Our results suggest that PER1 may induce ferroptosis in CNE2 by inhibiting the expression of GPX4 and SLC7A11, thereby causing LPO and Fe2+ accumulation in CNE2 and finally inducing ferroptosis in CNE2. This novel mechanism may provide a new direction for the treatment of NPC.
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