Fingolimod exerts in vitro anticancer activity against hepatocellular carcinoma cell lines via YAP/TAZ suppression

Author:

Du Jiamin1,Qian Meijia1,Yuan Tao1,Zhang Bo2,Chen Xueqin3,An Ning4,He Qiaojun1,Yang Bo1,Ye Song5,Zhu Hong126

Affiliation:

1. Zhejiang Province Key Laboratory of Anticancer Drug Research , College of Pharmaceutical Sciences, Zhejiang University , Hangzhou , China

2. Key Laboratory of Clinical Cancer Pharmacology and Toxicology Research of Zhejiang Province , Affiliated Hangzhou First People’s Hospital, Zhejiang University School of Medicine , Hangzhou , China

3. Department of Oncology, Key Laboratory of Clinical Cancer Pharmacology and Toxicology Research of Zhejiang Province , Affiliated Hangzhou First People´s Hospital, Zhejiang University School of Medicine , Hangzhou China

4. Department of Pharmacy , Ningbo Medical Center Lihuili Hospital , Ningbo , China

5. Division of Hepatobiliary and Pancreatic Surgery, Department of Surgery , The Second Affiliated Hospital, School of Medicine Zhejiang University , Hangzhou , China

6. The Westlake Laboratory of Life Sciences and Biomedicine , Hangzhou , China

Abstract

Abstract 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.

Publisher

Walter de Gruyter GmbH

Subject

Pharmaceutical Science,Pharmacology,General Medicine

Cited by 3 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Targeting the Hippo/YAP1 signaling pathway in hepatocellular carcinoma: From mechanisms to therapeutic drugs (Review);International Journal of Oncology;2024-07-31

2. Pharmacological Effects of FTY720 and its Derivatives;Current Topics in Medicinal Chemistry;2024-01

3. Complex roles of Hippo-YAP/TAZ signaling in hepatocellular carcinoma;Journal of Cancer Research and Clinical Oncology;2023-08-22

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