Cited 5 times in
1H-[1,2,4]oxadiazolo[4,3-a]quinoxalin-1-one induces cell cycle arrest and apoptosis in HeLa cells by preventing microtubule polymerization
DC Field | Value | Language |
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dc.contributor.author | 김두식 | - |
dc.contributor.author | 김소영 | - |
dc.contributor.author | 서정택 | - |
dc.contributor.author | 안정미 | - |
dc.contributor.author | 이한길 | - |
dc.date.accessioned | 2014-12-20T16:36:28Z | - |
dc.date.available | 2014-12-20T16:36:28Z | - |
dc.date.issued | 2011 | - |
dc.identifier.issn | 0006-291X | - |
dc.identifier.uri | https://ir.ymlib.yonsei.ac.kr/handle/22282913/93036 | - |
dc.description.abstract | 1H-[1,2,4]oxadiazolo[4,3-a]quinoxalin-1-one (ODQ) is known as a specific inhibitor of soluble guanylyl cyclase (sGC). Previously, however, ODQ was reported to induce cell death via sGC-dependent and sGC-independent means in a variety of cell types. The aim of this study was to investigate the mechanism by which ODQ induces cell death in HeLa cells. Treatment of HeLa cells with ODQ induced a concentration-dependent decrease in cell viability over the range from 10 to 100 μM. DNA fragmentation and fluorescence-activated cell sorting analysis using annexin V and propidium iodide staining revealed that ODQ triggered apoptosis at concentrations of 50 and 100 μM within 24 to 48 h. The addition of 8-Br-cGMP in the presence of ODQ failed to rescue HeLa cells from death, suggesting that the inhibition of sGC was not responsible for the pro-apoptotic action of ODQ. ODQ arrested the cell cycle at the G2/M phase and caused disassembly of the microtubule network. This process was reversed by dithiothreitol. In addition, ODQ was shown to inhibit the polymerization of purified tubulin, and this was also prevented by dithiothreitol. These results indicate that ODQ inhibits microtubule assembly by direct oxidation of tubulin, induces cell cycle arrest at the G2/M phase, and triggers apoptosis in HeLa cells. | - |
dc.description.statementOfResponsibility | open | - |
dc.format.extent | 287~292 | - |
dc.relation.isPartOf | BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS | - |
dc.rights | CC BY-NC-ND 2.0 KR | - |
dc.rights.uri | https://creativecommons.org/licenses/by-nc-nd/2.0/kr/ | - |
dc.subject.MESH | Apoptosis/drug effects* | - |
dc.subject.MESH | Cell Cycle/drug effects* | - |
dc.subject.MESH | Enzyme Inhibitors/pharmacology* | - |
dc.subject.MESH | Guanylate Cyclase/antagonists & inhibitors* | - |
dc.subject.MESH | HeLa Cells | - |
dc.subject.MESH | Humans | - |
dc.subject.MESH | Microtubules/drug effects* | - |
dc.subject.MESH | Microtubules/metabolism | - |
dc.subject.MESH | Oxadiazoles/pharmacology* | - |
dc.subject.MESH | Oxidation-Reduction/drug effects | - |
dc.subject.MESH | Quinoxalines/pharmacology* | - |
dc.subject.MESH | Tubulin/metabolism | - |
dc.title | 1H-[1,2,4]oxadiazolo[4,3-a]quinoxalin-1-one induces cell cycle arrest and apoptosis in HeLa cells by preventing microtubule polymerization | - |
dc.type | Article | - |
dc.contributor.college | College of Dentistry (치과대학) | - |
dc.contributor.department | Dept. of Oral Biology (구강생물학) | - |
dc.contributor.googleauthor | So Young Kim | - |
dc.contributor.googleauthor | Jeong Mi An | - |
dc.contributor.googleauthor | Han Gil Lee | - |
dc.contributor.googleauthor | Sik Kim Du | - |
dc.contributor.googleauthor | Chae Uk Cheong | - |
dc.contributor.googleauthor | Jeong Taeg Seo | - |
dc.identifier.doi | 10.1016/j.bbrc.2011.04.018 | - |
dc.admin.author | false | - |
dc.admin.mapping | false | - |
dc.contributor.localId | A00417 | - |
dc.contributor.localId | A01905 | - |
dc.contributor.localId | A02257 | - |
dc.contributor.localId | A03273 | - |
dc.contributor.localId | A00620 | - |
dc.relation.journalcode | J00281 | - |
dc.identifier.eissn | 1090-2104 | - |
dc.identifier.pmid | 21501588 | - |
dc.identifier.url | http://www.sciencedirect.com/science/article/pii/S0006291X1100581X | - |
dc.subject.keyword | ODQ | - |
dc.subject.keyword | Tubulin | - |
dc.subject.keyword | Microtubule | - |
dc.subject.keyword | Cell cycle arrest | - |
dc.subject.keyword | Apoptosis | - |
dc.contributor.alternativeName | Kim, Du Sik | - |
dc.contributor.alternativeName | Kim, So Young | - |
dc.contributor.alternativeName | Seo, Jeong Taeg | - |
dc.contributor.alternativeName | An, Jeong Mi | - |
dc.contributor.alternativeName | Lee, Han Gil | - |
dc.contributor.affiliatedAuthor | Kim, Du Sik | - |
dc.contributor.affiliatedAuthor | Seo, Jeong Taeg | - |
dc.contributor.affiliatedAuthor | An, Jeong Mi | - |
dc.contributor.affiliatedAuthor | Lee, Han Gil | - |
dc.contributor.affiliatedAuthor | Kim, So Young | - |
dc.rights.accessRights | not free | - |
dc.citation.volume | 408 | - |
dc.citation.number | 2 | - |
dc.citation.startPage | 287 | - |
dc.citation.endPage | 292 | - |
dc.identifier.bibliographicCitation | BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, Vol.408(2) : 287-292, 2011 | - |
dc.identifier.rimsid | 27987 | - |
dc.type.rims | ART | - |
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