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Cyclooxygenase inhibitors induce apoptosis in oral cavity cancer cells by increased expression of nonsteroidal anti-inflammatory drug-activated gene

DC Field Value Language
dc.contributor.author김경수-
dc.contributor.author윤주헌-
dc.contributor.author이정권-
dc.date.accessioned2015-07-14T16:46:12Z-
dc.date.available2015-07-14T16:46:12Z-
dc.date.issued2004-
dc.identifier.issn0006-291X-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/111553-
dc.description.abstractWe have investigated whether NAG-1 is induced in oral cavity cancer cells by various NSAIDs and if apoptosis induced by NSAIDs can be linked directly with the induction of NAG-1. NAG-1 expression was increased by diclofenac, aceclofenac, indomethacin, ibuprofen, and sulindac sulfide, in the order of NAG-1 induction, but not by acetaminophen, piroxicam or NS-398. Diclofenac was the most effective NAG-1 inducer. Incubation with diclofenac inhibited cell proliferation and induced apoptosis. The expression of NAG-1 was observed in advance of the induction of apoptosis. Conditioned medium from NAG-1-overexpressing Drosophila cells inhibited SCC 1483 cells proliferation and induced apoptosis. In summary, some NSAIDs induce NAG-1 expression in oral cavity cancer cells and the induced NAG-1 protein appears to mediate apoptosis. Therefore, NSAIDs may be considered as a possible chemopreventive agent against oral cavity cancer.-
dc.description.statementOfResponsibilityopen-
dc.format.extent1298~1303-
dc.relation.isPartOfBIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.subject.MESHAnti-Inflammatory Agents, Non-Steroidal/pharmacology*-
dc.subject.MESHAntineoplastic Agents/pharmacology-
dc.subject.MESHApoptosis/drug effects*-
dc.subject.MESHCell Line, Tumor-
dc.subject.MESHCell Proliferation/drug effects-
dc.subject.MESHCyclooxygenase Inhibitors/pharmacology*-
dc.subject.MESHCytokines/metabolism*-
dc.subject.MESHCytokines/pharmacology*-
dc.subject.MESHDose-Response Relationship, Drug-
dc.subject.MESHGrowth Differentiation Factor 15-
dc.subject.MESHHumans-
dc.subject.MESHMouth/drug effects-
dc.subject.MESHMouth/pathology-
dc.subject.MESHMouth Neoplasms/metabolism*-
dc.subject.MESHMouth Neoplasms/pathology*-
dc.subject.MESHRecombinant Proteins/metabolism-
dc.subject.MESHRecombinant Proteins/pharmacology-
dc.titleCyclooxygenase inhibitors induce apoptosis in oral cavity cancer cells by increased expression of nonsteroidal anti-inflammatory drug-activated gene-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Otorhinolaryngology (이비인후과학)-
dc.contributor.googleauthorKyung-Su Kim-
dc.contributor.googleauthorJoo-Heon Yoon-
dc.contributor.googleauthorJong-Bum Yoo-
dc.contributor.googleauthorJoo-Hwan Lee-
dc.contributor.googleauthorJeung Gweon Lee-
dc.contributor.googleauthorJi-Hwan Ryu-
dc.contributor.googleauthorWon Jae Lee-
dc.contributor.googleauthorThomas E. Eling-
dc.contributor.googleauthorSeung Joon Baek-
dc.contributor.googleauthorJin Kook Kim-
dc.identifier.doi10.1016/j.bbrc.2004.10.176-
dc.admin.authorfalse-
dc.admin.mappingfalse-
dc.relation.journalcodeJ00281-
dc.identifier.eissn1090-2104-
dc.identifier.pmid15555568-
dc.identifier.urlhttp://www.sciencedirect.com/science/article/pii/S0006291X04025082-
dc.subject.keywordNonsteroidal anti-inflammatory drugs-
dc.subject.keywordOral cavity cancer-
dc.subject.keywordApoptosis-
dc.subject.keywordNSAID-activated gene-1-
dc.subject.keywordDrosophila-
dc.contributor.alternativeNameKim, Kyung Su-
dc.contributor.alternativeNameYoon, Joo Heon-
dc.contributor.alternativeNameLee, Jeung Gweon-
dc.rights.accessRightsnot free-
dc.citation.volume325-
dc.citation.number4-
dc.citation.startPage1298-
dc.citation.endPage1303-
dc.identifier.bibliographicCitationBIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, Vol.325(4) : 1298-1303, 2004-
dc.identifier.rimsid34915-
dc.type.rimsART-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Otorhinolaryngology (이비인후과학교실) > 1. Journal Papers

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