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The Selective Cyclooxygenase-2 Inhibitor Nimesulide Prevents Helicobacter pylori-Associated Gastric Cancer Development in a Mouse Model

DC Field Value Language
dc.contributor.author남기택-
dc.date.accessioned2015-07-14T17:30:12Z-
dc.date.available2015-07-14T17:30:12Z-
dc.date.issued2004-
dc.identifier.issn1078-0432-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/113013-
dc.description.abstractPURPOSE: Helicobacter pylori infection can lead to gastric cancer, and cyclooxygenase-2 (COX-2) is overexpressed in the stomach during H. pylori infection. Therefore, we investigated whether nonsteroidal anti-inflammatory drugs might protect against this form of cancer. Specifically, we examined the chemopreventive effect of the COX-2 inhibitor nimesulide on H. pylori-associated gastric carcinogenesis in mice. EXPERIMENTAL DESIGN: C57BL/6 mice were treated with the carcinogen N-methyl-N-nitrosourea (MNU) and/or H. pylori. To determine the effect of COX-2 inhibition, nimesulide was mixed with feed pellets and administered for the duration of the experiment. All of the mice were sacrificed 50 weeks after the start of the experiment. Histopathology, immunohistochemistry, and Western blotting for COX-2, Bax and Bcl-2 were performed in stomach tissues. In vitro experiments with the human gastric cancer cell line AGS were also performed to identify mechanisms underlying cancer chemoprevention by nimesulide. RESULTS: Gastric tumors developed in 68.8% of mice that were given both MNU and H. pylori, whereas less than 10% developed gastric tumors when given either MNU or H. pylori alone. These findings indicate that H. pylori promotes carcinogen-induced gastric tumorigenesis. In mice treated with both MNU and H. pylori, nimesulide administration substantially reduced H. pylori-associated gastric tumorigenesis, whereas substantial inductions of apoptosis were observed. In vitro studies demonstrated that nimesulide and H. pylori when combined acted synergistically to induce more apoptosis than either alone. CONCLUSIONS: Our data show that nimesulide prevents H. pylori-associated gastric carcinogenesis, and suggest that COX-2 may be a target for chemoprevention of gastric cancer.-
dc.description.statementOfResponsibilityopen-
dc.format.extent8105~8113-
dc.relation.isPartOfCLINICAL CANCER RESEARCH-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.subject.MESHAnimals-
dc.subject.MESHApoptosis/drug effects-
dc.subject.MESHBlotting, Western-
dc.subject.MESHCyclooxygenase 2-
dc.subject.MESHCyclooxygenase 2 Inhibitors-
dc.subject.MESHCyclooxygenase Inhibitors/therapeutic use*-
dc.subject.MESHGastric Mucosa/microbiology-
dc.subject.MESHHelicobacter Infections/complications*-
dc.subject.MESHHelicobacter Infections/drug therapy-
dc.subject.MESHHelicobacter Infections/pathology-
dc.subject.MESHHelicobacter pylori/pathogenicity*-
dc.subject.MESHIn Situ Nick-End Labeling-
dc.subject.MESHMale-
dc.subject.MESHMethylnitrosourea/toxicity-
dc.subject.MESHMice-
dc.subject.MESHMice, Inbred C57BL-
dc.subject.MESHProstaglandin-Endoperoxide Synthases/chemistry*-
dc.subject.MESHProstaglandin-Endoperoxide Synthases/metabolism-
dc.subject.MESHProto-Oncogene Proteins c-bcl-2/metabolism-
dc.subject.MESHStomach Neoplasms/chemically induced-
dc.subject.MESHStomach Neoplasms/microbiology-
dc.subject.MESHStomach Neoplasms/prevention & control*-
dc.subject.MESHSulfonamides/therapeutic use*-
dc.subject.MESHbcl-2-Associated X Protein-
dc.titleThe Selective Cyclooxygenase-2 Inhibitor Nimesulide Prevents Helicobacter pylori-Associated Gastric Cancer Development in a Mouse Model-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Life Science (의생명과학부)-
dc.contributor.googleauthorKi Taek Nam-
dc.contributor.googleauthorKi-Baik Hahm-
dc.contributor.googleauthorDae-Yong Kim-
dc.contributor.googleauthorKi-Hwa Yang-
dc.contributor.googleauthorDong Deuk Jang-
dc.contributor.googleauthorJin Seok Kang-
dc.contributor.googleauthorYoung-Bae Kim-
dc.contributor.googleauthorByeongwoo Ahn-
dc.contributor.googleauthorSang-Uk Han-
dc.contributor.googleauthorMarie Yeo-
dc.contributor.googleauthorSang-Yeon Oh-
dc.identifier.doi10.1158/1078-0432.CCR-04-0896-
dc.admin.authorfalse-
dc.admin.mappingfalse-
dc.contributor.localIdA01243-
dc.relation.journalcodeJ00564-
dc.identifier.pmid15585646-
dc.contributor.alternativeNameNam, Ki Taek-
dc.contributor.affiliatedAuthorNam, Ki Taek-
dc.rights.accessRightsfree-
dc.citation.volume10-
dc.citation.number23-
dc.citation.startPage8105-
dc.citation.endPage8113-
dc.identifier.bibliographicCitationCLINICAL CANCER RESEARCH, Vol.10(23) : 8105-8113, 2004-
dc.identifier.rimsid36856-
dc.type.rimsART-
Appears in Collections:
1. College of Medicine (의과대학) > BioMedical Science Institute (의생명과학부) > 1. Journal Papers

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