Full metadata record
DC Field | Value | Language |
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dc.contributor.author | Kim, Su-Nam | - |
dc.contributor.author | Kim, Nam Hyun | - |
dc.contributor.author | Park, Yeon Sook | - |
dc.contributor.author | Kim, Hanna | - |
dc.contributor.author | Lee, Seokjoon | - |
dc.contributor.author | Wang, Qian | - |
dc.contributor.author | Kim, Yong Kee | - |
dc.date.accessioned | 2024-01-20T21:05:21Z | - |
dc.date.available | 2024-01-20T21:05:21Z | - |
dc.date.created | 2021-09-03 | - |
dc.date.issued | 2009-06-15 | - |
dc.identifier.issn | 0006-2952 | - |
dc.identifier.uri | https://pubs.kist.re.kr/handle/201004/132389 | - |
dc.description.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. | - |
dc.language | English | - |
dc.publisher | PERGAMON-ELSEVIER SCIENCE LTD | - |
dc.subject | AURORA KINASES | - |
dc.subject | P-GLYCOPROTEIN | - |
dc.subject | AGENTS | - |
dc.subject | DRUGS | - |
dc.subject | TARGETS | - |
dc.subject | MITOSIS | - |
dc.title | 7-Diethylamino-3(2 '-benzoxazolyl)-coumarin is a novel microtubule inhibitor with antimitotic activity in multidrug resistant cancer cells | - |
dc.type | Article | - |
dc.identifier.doi | 10.1016/j.bcp.2009.03.007 | - |
dc.description.journalClass | 1 | - |
dc.identifier.bibliographicCitation | BIOCHEMICAL PHARMACOLOGY, v.77, no.12, pp.1773 - 1779 | - |
dc.citation.title | BIOCHEMICAL PHARMACOLOGY | - |
dc.citation.volume | 77 | - |
dc.citation.number | 12 | - |
dc.citation.startPage | 1773 | - |
dc.citation.endPage | 1779 | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.identifier.wosid | 000266084600003 | - |
dc.identifier.scopusid | 2-s2.0-67349212426 | - |
dc.relation.journalWebOfScienceCategory | Pharmacology & Pharmacy | - |
dc.relation.journalResearchArea | Pharmacology & Pharmacy | - |
dc.type.docType | Article | - |
dc.subject.keywordPlus | AURORA KINASES | - |
dc.subject.keywordPlus | P-GLYCOPROTEIN | - |
dc.subject.keywordPlus | AGENTS | - |
dc.subject.keywordPlus | DRUGS | - |
dc.subject.keywordPlus | TARGETS | - |
dc.subject.keywordPlus | MITOSIS | - |
dc.subject.keywordAuthor | 7-Diethylamino-3(2 &apos | - |
dc.subject.keywordAuthor | -benzoxazolyl)-coumarin | - |
dc.subject.keywordAuthor | Microtubule | - |
dc.subject.keywordAuthor | Multidrug resistance | - |
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