芬戈莫德
河马信号通路
肝细胞癌
癌症研究
医学
背景(考古学)
效应器
药理学
细胞生长
药品
多发性硬化
生物
免疫学
古生物学
遗传学
作者
Jiamin Du,Meijia Qian,Tao Yuan,Bo Zhang,Xueqin Chen,Ning An,Qiaojun He,Bo Yang,Song Ye,Hong Zhu
标识
DOI:10.2478/acph-2022-0029
摘要
Hepatocellular carcinoma (HCC) remains a notably global health challenge with high mortality rates and poor prognosis. The deregulation of the Hippo signalling pathway, especially the overexpression and activation of downstream effector Yes-associated protein (YAP), has been demonstrated to result in the rapid malignant evolution of HCC. In this context, multiple efforts have been dedicated to targeting YAP for HCC therapy, but effective YAP inhibitors are still lacking. In this study, through a YAP-TEAD (8×GTIIC) luciferase reporter assay, we identified fingolimod, an immunomodulatory drug approved for the treatment of multiple sclerosis, as a novel YAP inhibitor. Fingolimod suppressed the proliferation of HCC cell lines by downregulating the protein levels as well as the trans-activating function of YAP. Overall, our current study not only identifies fingolimod as a novel YAP-targeting in hibitor, but also indicates that this clinically-approved drug could be utilized as a potential and feasible therapeutic drug for HCC.
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