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Reactive oxygen species are generated through a BLT2-linked cascade in Ras-transformed cells

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dc.contributor.authorChoi, Jung-A-
dc.contributor.authorKim, Eun-Young-
dc.contributor.authorSong, Haiwon-
dc.contributor.authorKim, Cheolmin-
dc.contributor.authorKim, Jae-Hong-
dc.date.accessioned2021-09-09T11:10:01Z-
dc.date.available2021-09-09T11:10:01Z-
dc.date.created2021-06-10-
dc.date.issued2008-02-15-
dc.identifier.issn0891-5849-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/124073-
dc.description.abstractAlthough production of reactive oxygen species (ROS) by oncogenic Ras is thought to be crucial for Ras transformation, very little is known about the signaling mechanism involved. In the present study, we investigated whether BLT2, a low-affinity leukotriene 134 receptor, is involved in the generation of ROS in H-Ras(V12)-transformed fibroblasts. We show that downregulation of BLT2 using RNA interference or antisense oligonucleotides inhibits ROS generation, and that Nox1 acts downstream of BLT2. Moreover, BLT2 overexpression caused, increased ROS production and partial transformation. Taken together, our results suggest that a BLT2-Nox1-linked cascade is responsible for the elevated ROS generation in Ras-transformed cells. Our finding may contribute to clarifying the signaling events underlying the enhanced levels of ROS frequently observed in various transformed cells and possibly serve as a basis for developing new therapeutic strategies for human cancers. (c) 2007 Elsevier Inc. All rights reserved.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherELSEVIER SCIENCE INC-
dc.subjectLEUKOTRIENE B-4 RECEPTOR-
dc.subjectMANGANESE SUPEROXIDE-DISMUTASE-
dc.subjectPHOSPHOLIPASE A(2)-
dc.subjectLUNG-CANCER-
dc.subjectCYCLOOXYGENASE-2 COX-2-
dc.subjectMEDIATES CHEMOTAXIS-
dc.subjectSIGNAL-TRANSDUCTION-
dc.subjectPROSTATE-CANCER-
dc.subjectBREAST-CANCER-
dc.subjectOXIDASE NOX1-
dc.titleReactive oxygen species are generated through a BLT2-linked cascade in Ras-transformed cells-
dc.typeArticle-
dc.contributor.affiliatedAuthorKim, Jae-Hong-
dc.identifier.doi10.1016/j.freeradbiomed.2007.10.041-
dc.identifier.scopusid2-s2.0-38649140489-
dc.identifier.wosid000253090200014-
dc.identifier.bibliographicCitationFREE RADICAL BIOLOGY AND MEDICINE, v.44, no.4, pp.624 - 634-
dc.relation.isPartOfFREE RADICAL BIOLOGY AND MEDICINE-
dc.citation.titleFREE RADICAL BIOLOGY AND MEDICINE-
dc.citation.volume44-
dc.citation.number4-
dc.citation.startPage624-
dc.citation.endPage634-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaEndocrinology & Metabolism-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryEndocrinology & Metabolism-
dc.subject.keywordPlusLEUKOTRIENE B-4 RECEPTOR-
dc.subject.keywordPlusMANGANESE SUPEROXIDE-DISMUTASE-
dc.subject.keywordPlusPHOSPHOLIPASE A(2)-
dc.subject.keywordPlusLUNG-CANCER-
dc.subject.keywordPlusCYCLOOXYGENASE-2 COX-2-
dc.subject.keywordPlusMEDIATES CHEMOTAXIS-
dc.subject.keywordPlusSIGNAL-TRANSDUCTION-
dc.subject.keywordPlusPROSTATE-CANCER-
dc.subject.keywordPlusBREAST-CANCER-
dc.subject.keywordPlusOXIDASE NOX1-
dc.subject.keywordAuthorROS-
dc.subject.keywordAuthorleukotriene B-4-
dc.subject.keywordAuthorBLT2-
dc.subject.keywordAuthorNox1-
dc.subject.keywordAuthorRas transformation-
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