索拉非尼
肝癌
肝细胞癌
基因敲除
癌症研究
癌症
癌细胞
生物
内科学
药理学
细胞凋亡
医学
生物化学
作者
Lingxi Chen,Hanxi Xiao,Yaran Wu,Dongjing Yan,Meihua Shan,Liangbo Sun,Xiaojing Yan,Dong Liu,Tao Li,Yang Zhang,Li Xiang,An Chen,Shuhui Li,Wei Xiang,Zhenhong Ni,Fengtian He,Mingzhen Yang,Jiqin Lian
出处
期刊:Genomics
[Elsevier]
日期:2024-01-01
卷期号:116 (1): 110764-110764
被引量:1
标识
DOI:10.1016/j.ygeno.2023.110764
摘要
Sorafenib is currently the first-line treatment for patients with advanced liver cancer, but its therapeutic efficacy declines significantly after a few months of treatment. Therefore, it is of great importance to investigate the regulatory mechanisms of sorafenib sensitivity in liver cancer cells. In this study, we provided initial evidence demonstrating that circPHKB, a novel circRNA markedly overexpressed in sorafenib-treated liver cancer cells, attenuated the sensitivity of liver cancer cells to sorafenib. Mechanically, circPHKB sequestered miR-1234-3p, resulting in the up-regulation of cytochrome P450 family 2 subfamily W member 1 (CYP2W1), thereby reducing the killing effect of sorafenib on liver cancer cells. Moreover, knockdown of circPHKB sensitized liver cancer cells to sorafenib in vivo. The findings reveal a novel circPHKB/miR-1234-3p/CYP2W1 pathway that decreases the sensitivity of liver cancer cells to sorafenib, suggesting that circPHKB and the axis may serve as promising targets to improve the therapeutic efficacy of sorafenib against liver cancer.
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