In Vitro and in Silico Evaluation of Bikaverin as a Potent Inhibitor of Human Protein Kinase CK2

• Published in: Molecules (Basel, Switzerland) Switzerland), 2019-04, Vol.24 (7), p.1380
• Main Authors: Haidar, Samer, Aichele, Dagmar, Birus, Robin, Hielscher, Janine, Laitinen, Tuomo, Poso, Antti, Jose, Joachim
• Format: Article
• Language: English
• Subjects: Acids; antiproliferation; Apoptosis; Assaying; bikaverin; Caco-2 Cells; Cancer; Casein kinase II; Casein Kinase II - antagonists & inhibitors; Casein Kinase II - chemistry; Cell cycle; Cell division; Cell growth; Cell Line, Tumor; Cell permeability; Cell proliferation; Cell Proliferation - drug effects; Cell Survival - drug effects; Cell viability; Clinical trials; Computer Simulation; Cytotoxicity; Drug Screening Assays, Antitumor; Enzyme inhibitors; Enzymes; Humans; Inhibitory Concentration 50; Kinases; MCF-7 Cells; Models, Molecular; Molecular dynamics; Molecular Dynamics Simulation; Permeability; Protein kinase C; Protein Kinase Inhibitors - chemistry; Protein Kinase Inhibitors - pharmacology; Proteins; Tumor cell lines; Xanthones - chemistry; Xanthones - pharmacology
• ISSN: 1420-3049; 1420-3049
• DOI: 10.3390/molecules24071380

Protein kinase CK2 is an emerging target for therapeutic intervention in human diseases, particularly in cancer. Inhibitors of this enzyme are currently in clinical trials, indicating the druggability of human CK2. By virtual screening of the ZINC database, we found that the natural compound bikaverin can fit well in the ATP binding site of the target enzyme CK2. By further in vitro evaluation using CK2 holoenzyme, bikaverin turned to be a potent inhibitor with an IC value of 1.24 µM. In this work, the cell permeability of bikaverin was determined using a Caco-2 cell permeability assay as a prerequisite for cellular evaluation and the compound turned out to be cell permeable with a P - value of 4.46 × 10 cm/s. Bikaverin was tested for its effect on cell viability using a MTT assay and cell proliferation using an EdU assay in different cancer cell lines (MCF7, A427 and A431 cells). Cell viability and cell proliferation were reduced dramatically after treatment with 10 µM bikaverin for 24 h. Additionally the IncuCyte live-cell imaging system was applied for monitoring the cytotoxicity of bikaverin in the three tested cancer cell lines. Finally, molecular dynamic studies were performed to clarify the ligand binding mode of bikaverin at the ATP binding site of CK2 and to identify the amino acids involved.