肝细胞癌
可药性
脆弱性(计算)
医学
癌症研究
基因缺失
生物
生物信息学
免疫学
乙型肝炎病毒
靶向治疗
内科学
肝癌
基因沉默
病毒性肝炎
小RNA
癌
癌症
平衡
肿瘤科
临床实习
作者
Yiming Zhang,Yushan Hou,Xinxin Wang,Kaikun Xu,Pei Jiang,Siqi Wang,Huimin Kang,Hu Zhang,Jingzhuo Jin,Xiaofen Huang,Zifeng Liu,Songpeng Yang,Jiaqi Liu,Lingqiang Zhang,Fuchu HE,Chunyan Tian,Aihua Sun
标识
DOI:10.3350/cmh.2025.1157
摘要
ERLIN1 represents a druggable metabolic vulnerability in cholesterol-dysregulated HCC. Targeting the ASB11-ERLIN1 axis with the clinically approved ZoA reestablishes cholesterol homeostasis and offers a promising therapeutic strategy to overcome the current limitations of cholesterol-targeted HCC therapies.
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