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

Authors
Kim, Su-NamKim, Nam HyunPark, Yeon SookKim, HannaLee, SeokjoonWang, QianKim, 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
Files in This Item:
There are no files associated with this item.
Export
RIS (EndNote)
XLS (Excel)
XML

qrcode

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.

BROWSE