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Inhibition of protein kinase CK2 expression and activity blocks tumor cell growth
Authors:Dan Zhu  Jennifer Hensel  Robert Hilgraf  Mahan Abbasian  Owen Pornillos  Gordafaried Deyanat-Yazdi  Xuequn Helen Hua  Sarah Cox
Affiliation:1. Celgene Corporation, 4550 Towne Centre Court, San Diego, CA, 92121, USA
2. Department of Molecular Physiology & Biological Physics, University of Virginia, Charlottesville, VA, 22908, USA
3. Ambit Biosciences, 4215 Sorrento Valley Boulevard, San Diego, CA, 92121, USA
4. Genomics Institute of the Novartis Research Foundation, 10675 John Jay Hopkins Drive, San Diego, CA, 92121, USA
Abstract:Protein kinase CK2 (CK2) is a highly conserved and ubiquitous serine/threonine kinase. It is a multifunctional and pleiotropic protein kinase implicated in the regulation of cell proliferation, survival, and differentiation. Deregulation of CK2 is observed in a wide variety of tumors. It has been the focus of intensive research efforts to establish the cause–effect relationship between CK2 and neoplastic growth. Here, we further validate the role of CK2 in cancer cell growth using siRNA approach. We also screened a library of more than 200,000 compounds and identified several molecules, which inhibit CK2 with IC50 < 1 μM. The binding mode of a representative compound with maize CK2 was determined. In addition, the cellular activity of the compounds was demonstrated by their inhibition of phosphorylation of PTEN Ser370 in HCT116 cells. Treatment of a variety of cancer cell lines with the newly identified CK2 inhibitor significantly blocked cell growth with IC50s as low as 300 nM.
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