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IL-18 enhances ULBP2 expression through the MAPK pathway in leukemia cells

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dc.contributor.authorSong, Hyunkeun-
dc.contributor.authorKim, Kyung-Eun-
dc.contributor.authorHur, Daeyoung-
dc.contributor.authorLim, Jong-Seok-
dc.contributor.authorYang, Young-
dc.contributor.authorCho, Byung Joo-
dc.contributor.authorKim, Cherl-hyun-
dc.contributor.authorKim, Taesung-
dc.contributor.authorBang, Saic-
dc.contributor.authorLee, Wang Jae-
dc.contributor.authorPark, Hyunjeong-
dc.contributor.authorCho, DaeHo-
dc.date.available2021-02-22T14:32:54Z-
dc.date.issued2008-09-
dc.identifier.issn0165-2478-
dc.identifier.issn1879-0542-
dc.identifier.urihttps://scholarworks.sookmyung.ac.kr/handle/2020.sw.sookmyung/14176-
dc.description.abstractExpression of UL16-binding proteins (ULBPs) has been reported in various cancers, such as leukemia and melanoma, and also in some other cancer cell lines. However, the factors that modulate the expression of ULBPs are not well defined. In this study, we investigated the effects of IL-18 on the expression of NKG2D ligands in leukemia cells. IL-18 treatment increased ULBP2 expression in leukemia cells at the mRNA and protein levels. In addition, PD98059 (an ERK1/2 MAPK inhibitor) and SP600125 (a JNK inhibitor) attenuated IL-18-induced ULBP2 expression in a dose-dependent manner. We observed that ERK1/2 and JNK MAPK phosphorylation increased upon treatment with IL-18. IL-18 elevated CD107a expression in cancer cells and increased the cytotoxic activity of NK cells; therefore, we propose that IL-18 increases the susceptibility of target cells by inducing surface expression of ULBP2. Taken together, these findings suggest that IL-18 may play a critical role in regulating ULBP2 expression via the ERK1/2 and JNK MAPK pathways in leukemia cells. (C) 2008 Elsevier B.V. All rights reserved.-
dc.format.extent5-
dc.language영어-
dc.language.isoENG-
dc.publisherELSEVIER SCIENCE BV-
dc.titleIL-18 enhances ULBP2 expression through the MAPK pathway in leukemia cells-
dc.typeArticle-
dc.publisher.location네델란드-
dc.identifier.doi10.1016/j.imlet.2008.07.007-
dc.identifier.scopusid2-s2.0-50449084622-
dc.identifier.wosid000260160800015-
dc.identifier.bibliographicCitationIMMUNOLOGY LETTERS, v.120, no.1-2, pp 103 - 107-
dc.citation.titleIMMUNOLOGY LETTERS-
dc.citation.volume120-
dc.citation.number1-2-
dc.citation.startPage103-
dc.citation.endPage107-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaImmunology-
dc.relation.journalWebOfScienceCategoryImmunology-
dc.subject.keywordPlusNATURAL-KILLER-CELLS-
dc.subject.keywordPlusI-RELATED MOLECULES-
dc.subject.keywordPlusNKG2D RECEPTOR-
dc.subject.keywordPlusT-CELLS-
dc.subject.keywordPlusGLYCOPROTEIN UL16-
dc.subject.keywordPlusGAMMA PRODUCTION-
dc.subject.keywordPlusNK CELLS-
dc.subject.keywordPlusCYTOTOXICITY-
dc.subject.keywordPlusLIGANDS-
dc.subject.keywordPlusSUSCEPTIBILITY-
dc.subject.keywordAuthorIL-18-
dc.subject.keywordAuthorNatural killer cells-
dc.subject.keywordAuthorTumor immunity-
dc.subject.keywordAuthorULBP-
dc.subject.keywordAuthorNKG2D-
dc.identifier.urlhttps://www.sciencedirect.com/science/article/abs/pii/S0165247808001867?via%3Dihub-
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대학 > 기초교양대학 > 기초교양학부 > 1. Journal Articles
이과대학 > 생명시스템학부 > 1. Journal Articles
원격대학원 > 향장미용학과 > 1. Journal Articles

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