7-Diethylamino-3(2 '-benzoxazolyl)-coumarin is a novel microtubule inhibitor with antimitotic activity in multidrug resistant cancer cells
- Authors
- Kim, Su-Nam; Kim, Nam Hyun; Park, Yeon Sook; Kim, Hanna; Lee, Seokjoon; Wang, Qian; Kim, Yong Kee
- Issue Date
- 2009-06-15
- Publisher
- PERGAMON-ELSEVIER SCIENCE LTD
- Citation
- BIOCHEMICAL PHARMACOLOGY, v.77, no.12, pp.1773 - 1779
- Abstract
- Microtubules are a proven target for anticancer drug development because they are critical for mitotic spindle formation and the separation of chromosomes at mitosis. We here report a novel synthetic microtubule inhibitor 7-diethylamino-3(2'-benzoxazolyl)-coumarin (DBC). DBC causes destabilization of microtubules, leading to a cell cycle arrest at G(2)/M stage. In addition, human cancer cells are more sensitive to DBC (IC50 44.8-475.2 nM) than human normal fibroblast (IC50 7.9 mu M), and DBC induces apoptotic cell death of cancer cells. Furthermore, our data show that DBC is a poor substrate of drug efflux pumps and effective against multidrug resistant (MDR) cancer cells. Taken together, these results describe a novel pharmacological property of DBC as a microtubule inhibitor, which may make it an attractive new agent for treatment of MDR cancer. (c) 2009 Elsevier Inc. All rights reserved.
- Keywords
- AURORA KINASES; P-GLYCOPROTEIN; AGENTS; DRUGS; TARGETS; MITOSIS; AURORA KINASES; P-GLYCOPROTEIN; AGENTS; DRUGS; TARGETS; MITOSIS; 7-Diethylamino-3(2 ' -benzoxazolyl)-coumarin; Microtubule; Multidrug resistance
- ISSN
- 0006-2952
- URI
- https://pubs.kist.re.kr/handle/201004/132389
- DOI
- 10.1016/j.bcp.2009.03.007
- Appears in Collections:
- KIST Article > 2009
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