癌细胞
RNA解旋酶A
癌变
癌症
癌症研究
生物
体内
体外
核糖核酸
解旋酶
细胞生物学
化学
基因
生物化学
遗传学
作者
Xiyu Tang,Yuanlian Deng,Yingying Liang,D. Liao,Fuyu Wen,Yandong Zhang
出处
期刊:ACS omega
[American Chemical Society]
日期:2024-06-17
卷期号:9 (26): 28372-28384
标识
DOI:10.1021/acsomega.4c02265
摘要
RNA helicase DHX33 has been identified as a critical factor promoting cancer development. In the present study, a previously developed small molecule inhibitor for DHX33, KY386, was found to robustly kill cancer cells via a new path, the ferroptosis pathway. Mechanistically, DHX33 promotes the expression of critical players in lipid metabolism including FADS1, FADS2, and SCD1 genes, thereby sensitizing cancer cells to ferroptosis mediated cell death. Our study reveals a novel mechanism of DHX33 in promoting tumorigenesis and highlights that pharmacological targeting DHX33 can be a feasible option in human cancers. Normally differentiated cells are insensitive to DHX33 inhibition, and DHX33 inhibitors have little cellular toxicity in vitro and in vivo. Our studies demonstrated that DHX33 inhibitors can be promising anticancer agents with great potential for cancer treatment.
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