Abstract

Abstract Ginkgetin, isolated from herbal medicines, has been reported to play a role in antitumor activity. However, the relevant pathway integrating cell cycle regulation and signaling pathways involved in growth inhibition in cancer cells remains to be identified. In the present study, ginkgetin treatment of colon cancer cells resulted in significant dose-dependent growth inhibition together with apoptosis, G2-phase cell cycle arrest at a 5 μM (IC50) dose in HCT116colon cancer cells and ginkgetin also inhibits tumor growth in a mouse xenograft model of HCT116 cells. We found that ginkgetin regulated the expression of genes which are critically involved in cell cycle, cell signaling transduction, and cell proliferation using DNA microarray analysis. Furthermore, we provided evidence that ginkgetin inhibited BUB3, cyclin B, CDC2, and b-Myb expression. Especially ginkgetin induced G2-phase arrest by down-regulates expression of b-Myb Our data have suggested that ginkgetin exerts its anticancer effects through induction of cell cycle arrest at G2 phase as well as inhibition cell proliferation. Note: This abstract was not presented at the meeting. Citation Format: Byoung-Mog Kwon, Yu-Jin Lee. Ginkgetin inhibits the growth of cancer cells via the cell cycle arrest at G2-phase. [abstract]. In: Proceedings of the 105th Annual Meeting of the American Association for Cancer Research; 2014 Apr 5-9; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2014;74(19 Suppl):Abstract nr 4562. doi:10.1158/1538-7445.AM2014-4562

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