Shuo Chen1, Xue Guan2, Li-Li Wang3, Bo Li4, Xiu-Bo Sang5, Yao Liu6, Yang Zhao7. 1. Department of Gynecology, The First Affiliated Hospital of China Medical University, Shenyang 110001, China. Electronic address: chenshuo077003@163.com. 2. Department of Gynecology, The First Affiliated Hospital of China Medical University, Shenyang 110001, China. Electronic address: guanxue_guanguan@163.com. 3. Department of Gynecology, The First Affiliated Hospital of China Medical University, Shenyang 110001, China. Electronic address: wly117422@163.com. 4. Surgery Department, Northwestern Memorial Hospital, United States; Feinberg School of Medicine, Northwestern University, United States. Electronic address: boli@northwestern.edu. 5. Department of Gynecology, The First Affiliated Hospital of China Medical University, Shenyang 110001, China. Electronic address: 18202417055@163.com. 6. Department of Gynecology, The First Affiliated Hospital of China Medical University, Shenyang 110001, China. Electronic address: 13654030896@163.com. 7. Department of Gynecology, The First Affiliated Hospital of China Medical University, Shenyang 110001, China. Electronic address: yida.zhaoyang@163.com.
Abstract
OBJECTIVE: Cyclin-dependent kinases (CDKs) are important regulators of the cell cycle; previous studies have shown that misregulation of CDK4 (cyclin-dependent kinase 4) activity can lead to cancer. The present study investigated the anti-tumor effects of a highly selective CDK4 inhibitor fascaplysin in ovarian carcinoma cell lines. MATERIALS AND METHODS: In our study, cell proliferation, cell cycle, cell apoptosis, cell invasion, and cell migration relative assays were performed in ovarian cancer cell lines A2780 and OVCAR3 in the presence of different concentrations of fascaplysin. The protein expression levels of CDK4, cyclin D1, Bcl-2 (B-cell lymphoma-2), and VEGFA (vascular endothelial growth factor A) were determined by western blot. RESULTS: Our results showed that fascaplysin inhibited ovarian cancer cell proliferation, invasion and migration, as well as inducing S arrest and cell apoptosis. Treatment with fascaplysin also suppressed CDK4, cyclin D1, Bcl-2, and VEGFA expression at protein levels. CONCLUSIONS: Above all, our results showed that fascaplysin has anti-tumor activity against ovarian cancer cell lines through inhibiting CDK4, and may be a therapeutic target for the treatment of ovarian carcinomas.
OBJECTIVE: Cyclin-dependent kinases (CDKs) are important regulators of the cell cycle; previous studies have shown that misregulation of CDK4 (cyclin-dependent kinase 4) activity can lead to cancer. The present study investigated the anti-tumor effects of a highly selective CDK4 inhibitor fascaplysin in ovarian carcinoma cell lines. MATERIALS AND METHODS: In our study, cell proliferation, cell cycle, cell apoptosis, cell invasion, and cell migration relative assays were performed in ovarian cancer cell lines A2780 and OVCAR3 in the presence of different concentrations of fascaplysin. The protein expression levels of CDK4, cyclin D1, Bcl-2 (B-cell lymphoma-2), and VEGFA (vascular endothelial growth factor A) were determined by western blot. RESULTS: Our results showed that fascaplysin inhibited ovarian cancer cell proliferation, invasion and migration, as well as inducing S arrest and cell apoptosis. Treatment with fascaplysin also suppressed CDK4, cyclin D1, Bcl-2, and VEGFA expression at protein levels. CONCLUSIONS: Above all, our results showed that fascaplysin has anti-tumor activity against ovarian cancer cell lines through inhibiting CDK4, and may be a therapeutic target for the treatment of ovarian carcinomas.
Authors: Adelina Plangger; Barbara Rath; Maximilian Hochmair; Martin Funovics; Christoph Neumayer; Robert Zeillinger; Gerhard Hamilton Journal: Invest New Drugs Date: 2021-10-01 Impact factor: 3.651