7-Diethylamino-3(2′-benzoxazolyl)-coumarin is a novel microtubule inhibitor with antimitotic activity in multidrug resistant cancer cells

被引:80
作者
Kim, Su-Nam [2 ]
Kim, Nam Hyun [1 ]
Park, Yeon Sook [1 ]
Kim, Hanna [1 ]
Lee, Seokjoon [3 ]
Wang, Qian [4 ]
Kim, Yong Kee [1 ]
机构
[1] Kwandong Univ, Coll Med, Dept Pharmacol, Gangneung Si 210701, Gangwon Do, South Korea
[2] KIST Gangneung Inst, Kangnung 210340, South Korea
[3] Kwandong Univ, Coll Med, Dept Basic Sci, Kangnung 210701, South Korea
[4] Univ S Carolina, Dept Chem & Biochem, Columbia, SC 29203 USA
关键词
7-Diethylamino-3(2 '-benzoxazolyl)-coumarin; Microtubule; Multidrug resistance; AURORA KINASES; P-GLYCOPROTEIN; AGENTS; DRUGS; TARGETS; MITOSIS;
D O I
10.1016/j.bcp.2009.03.007
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
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.
引用
收藏
页码:1773 / 1779
页数:7
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