Dasabuvir suppresses esophageal squamous cell carcinoma growth in vitro and in vivo through targeting ROCK1

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作者
Xinning Liu
Yanan Jiang
Hao Zhou
Xiaokun Zhao
Mingzhu Li
Zhuo Bao
Zitong Wang
Chenyang Zhang
Zhenliang Xie
Jimin Zhao
Zigang Dong
Kangdong Liu
Zhiping Guo
机构
[1] Zhengzhou University,Department of Pathophysiology, School of Basic Medical Sciences
[2] China-US Hormel (Henan) Cancer Institute,Department of Pulmonary and Critical Care Medicine, Huashan Hospital
[3] Fudan University,State Key Laboratory of Esophageal Cancer Prevention and Treatment
[4] Zhengzhou University,Research Center of Basic Medicine, Academy of Medical Sciences
[5] Henan Provincial Cooperative Innovation Center for Cancer Chemoprevention,Fuwai Central China Cardiovascular Hospital
[6] Zhengzhou University,undefined
[7] Cancer Chemoprevention International Collaboration Laboratory,undefined
[8] Zhengzhou University,undefined
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摘要
Esophageal squamous cell carcinoma (ESCC) is an upper gastrointestinal cancer with high morbidity and mortality. New strategies are urgently needed to prolong patients’ survival. Through screening FDA-approved drugs, we found dasabuvir, a drug approved for hepatitis C virus (HCV) treatment, suppressed ESCC proliferation. Dasabuvir could inhibit the growth of ESCC cells in a time and dose-dependent manner and arrested cell cycle at the G0/G1 phase. The antitumor activity was further validated in vivo using patient-derived xenograft tumor models. In terms of mechanism, we unveil that dasabuvir is a Rho-associated protein kinase 1 (ROCK1) inhibitor. Dasabuvir can bind to ROCK1 and suppress its kinase activity, thus downregulating the phosphorylation of ERK1/2 by ROCK1 and the expression of cyclin-dependent kinase 4 (CDK4) and cyclin D1. These results provide evidence that dasabuvir suppresses ESCC growth in vivo and in vitro through blocking ROCK1/ERK signaling pathway.
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