Dasabuvir suppresses esophageal squamous cell carcinoma growth in vitro and in vivo through targeting ROCK1.
Xinning LiuYanan JiangHao ZhouXiaokun ZhaoMingzhu LiZhuo BaoZitong WangChenyang ZhangZhenliang XieJimin ZhaoZigang DongKangdong LiuZhiping GuoPublished in: Cell death & disease (2023)
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.
Keyphrases
- hepatitis c virus
- cell cycle
- signaling pathway
- protein kinase
- induced apoptosis
- cell proliferation
- pi k akt
- human immunodeficiency virus
- cell cycle arrest
- epithelial mesenchymal transition
- end stage renal disease
- chronic kidney disease
- ejection fraction
- peritoneal dialysis
- free survival
- young adults
- long non coding rna
- binding protein
- drug induced