| Literature DB >> 25948588 |
Jong-Eun Kim1,2,3, Joe Eun Son1,4, Hyein Jeong4, Dong Joon Kim3, Sang Kwon Seo4, Eunjung Lee4,5, Tae Gyu Lim1,2,3, Jong Rhan Kim1,2,4, Hanyong Chen3, Ann M Bode3, Ki Won Lee1,2,4, Zigang Dong3.
Abstract
The Pim-1 kinase regulates cell survival, proliferation, and differentiation and is overexpressed frequently in many malignancies, including leukemia and skin cancer. In this study, we used kinase profiling analysis to demonstrate that 2'-hydroxycinnamicaldehyde (2'-HCA), a compound found in cinnamon, specifically inhibits Pim-1 activity. Cocrystallography studies determined the hydrogen bonding pattern between 2'-HCA and Pim-1. Notably, 2'-HCA binding altered the apo kinase structure in a manner that shielded the ligand from solvent, thereby acting as a gatekeeper loop. Biologically, 2'-HCA inhibited the growth of human erythroleukemia or squamous epidermoid carcinoma cells by inducing apoptosis. The compound was also effective as a chemopreventive agent against EGF-mediated neoplastic transformation. Finally, 2'-HCA potently suppressed the growth of mouse xenografts representing human leukemia or skin cancer. Overall, our results offered preclinical proof of concept for 2'-HCA as a potent anticancer principle arising from direct targeting of the Pim-1 kinase. ©2015 American Association for Cancer Research.Entities:
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Year: 2015 PMID: 25948588 PMCID: PMC4490130 DOI: 10.1158/0008-5472.CAN-14-3655
Source DB: PubMed Journal: Cancer Res ISSN: 0008-5472 Impact factor: 12.701