Author ORCID Identifier
Document Type
Article
Publication Date
9-5-2015
Abstract
IKKα has been implicated as a key regulator of oncogenesis and driver of the metastatic process; therefore is regarded as a promising therapeutic target in anticancer drug development. In spite of the progress made in the development of IKK inhibitors, no potent IKKa inhibitor(s) have been identified. Our multistep approach of molecular modeling and direct binding has led to the identification of plant flavone apigenin as a specific IKKa inhibitor. Here we report apigenin, in micro molar range, inhibits IKKa kinase activity, demonstrates anti-proliferative and anti-invasive activities in functional cell based assays and exhibits anticancer efficacy in experimental tumor model. We found that apigenin directly binds with IKKa, attenuates IKKa kinase activity and suppresses NF-κB/p65 activation in human prostate cancer PC-3 and 22Rv1 cells much more effectively than IKK inhibitor, PS1145. We also showed that apigenin caused cell cycle arrest similar to knockdown of IKKa in prostate cancer cells. Studies in xenograft mouse model indicate that apigenin feeding suppresses tumor growth, lowers proliferation and enhances apoptosis. These effects correlated with inhibition of p-IKKa, NF-κB/p65, proliferating cell nuclear antigen and increase in cleaved caspase 3 expression in a dose-dependent manner. Overall, our results suggest that inhibition of cell proliferation, invasiveness and decrease in tumor growth by apigenin are mediated by its ability to suppress IKKa and downstream targets affecting NF-κB signaling pathways.
Keywords
apigenin, cell cycle, NF-κB signaling, prostate cancer, therapeutic target
Publication Title
Oncotarget
Rights
© 2015 The Author(s).
Creative Commons License
This work is licensed under a Creative Commons Attribution 4.0 International License.
Recommended Citation
Shukla S., Kanwal R., Shankar E., Datt M., Chance M. R., Fu P., MacLennan G. T., Gupta S. Apigenin blocks IKKα activation and suppresses prostate cancer progression. Oncotarget. 2015; 6: 31216-31232. Retrieved from https://www.oncotarget.com/article/5157/text/