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RanBPM inhibits BLT2-mediated IL-8 production and invasiveness in aggressive breast cancer cells

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dc.contributor.authorWei, Jun-Dong-
dc.contributor.authorJang, Jae-Hyun-
dc.contributor.authorKim, Jae-Hong-
dc.date.accessioned2021-09-03T10:43:10Z-
dc.date.available2021-09-03T10:43:10Z-
dc.date.created2021-06-16-
dc.date.issued2017-01-29-
dc.identifier.issn0006-291X-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/84864-
dc.description.abstractRanBPM is a scaffolding protein that regulates several cellular processes by interacting with various proteins. Previously, we reported that RanBPM acts as a negative regulator of BLT2, a low-affinity leukotriene B4 receptor; thus, it interferes with BLT2-mediated cell motility. In the present study, we observed that the expression levels of RanBPM were markedly reduced in the highly aggressive MDAMB- 435 and MDA-MB-231 human breast cancer cell lines compared with those in non-invasive MCF7 cells. Additionally, we found that the restoration of RanBPM levels suppressed the invasiveness of these aggressive breast cancer cells in a manner dependent on BLT2 activation. In contrast, the knockdown of endogenous RanBPM by shRNA strongly promoted invasiveness in non-invasive MCF-7 cells. We also observed that RanBPM suppressed the invasiveness of aggressive breast cancer cells by inhibiting BLT2mediated reactive oxygen species (ROS) generation and IL-8 production. Taken together, our results suggest that RanBPM acts as a negative regulator of BLT2, thus attenuating the invasiveness of aggressive breast cancer cells. (C) 2016 Elsevier Inc. All rights reserved.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherACADEMIC PRESS INC ELSEVIER SCIENCE-
dc.subjectBLT2-LINKED PATHWAY-
dc.subjectANDROGEN RECEPTOR-
dc.subjectCARCINOMA CELLS-
dc.subjectOVARIAN-CANCER-
dc.subjectUP-REGULATION-
dc.subjectLUNG-CANCER-
dc.subjectIN-VITRO-
dc.subjectEXPRESSION-
dc.subjectPROTEIN-
dc.subjectINTERLEUKIN-8-
dc.titleRanBPM inhibits BLT2-mediated IL-8 production and invasiveness in aggressive breast cancer cells-
dc.typeArticle-
dc.contributor.affiliatedAuthorKim, Jae-Hong-
dc.identifier.doi10.1016/j.bbrc.2016.12.147-
dc.identifier.scopusid2-s2.0-85009259968-
dc.identifier.wosid000397259000048-
dc.identifier.bibliographicCitationBIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, v.483, no.1, pp.305 - 311-
dc.relation.isPartOfBIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS-
dc.citation.titleBIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS-
dc.citation.volume483-
dc.citation.number1-
dc.citation.startPage305-
dc.citation.endPage311-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaBiophysics-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryBiophysics-
dc.subject.keywordPlusBLT2-LINKED PATHWAY-
dc.subject.keywordPlusANDROGEN RECEPTOR-
dc.subject.keywordPlusCARCINOMA CELLS-
dc.subject.keywordPlusOVARIAN-CANCER-
dc.subject.keywordPlusUP-REGULATION-
dc.subject.keywordPlusLUNG-CANCER-
dc.subject.keywordPlusIN-VITRO-
dc.subject.keywordPlusEXPRESSION-
dc.subject.keywordPlusPROTEIN-
dc.subject.keywordPlusINTERLEUKIN-8-
dc.subject.keywordAuthorBreast cancer-
dc.subject.keywordAuthorBLT2-
dc.subject.keywordAuthorRanBPM-
dc.subject.keywordAuthorInvasiveness-
dc.subject.keywordAuthorIL-8-
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