IL-18 enhances SCF production of melanoma cells by regulating ROI and p38 MAPK activity

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dc.contributor.authorJ Hue-
dc.contributor.authorA Kim-
dc.contributor.authorH Song-
dc.contributor.authorIn Pyo Choi-
dc.contributor.authorH Park-
dc.contributor.authorT Kim-
dc.contributor.authorW J Lee-
dc.contributor.authorH Kang-
dc.contributor.authorD Cho-
dc.date.accessioned2017-04-19T09:02:18Z-
dc.date.available2017-04-19T09:02:18Z-
dc.date.issued2005-
dc.identifier.issn0165-2478-
dc.identifier.uri10.1016/j.imlet.2004.08.008ko
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/6824-
dc.description.abstractIt has been reported that interleukin-18 (IL-18) is secreted by B16 murine melanoma cells and that this endogenous IL-18 is involved in the immune escape of murine melanoma cells. The present study investigated whether interleukin (IL)-18 can regulate stem cell factor (SCF) expression, known to be associated with melanocyte proliferation, in B16F10 murine melanoma cells. SCF expression was examined by RT-PCR, intracellular FACS analysis, and ELISA in IL-18 antisense transfectants. Transfection with IL-18 antisense cDNA reduced SCF expression and the expression was enhanced by addition of exogenous IL-18. In addition, the effect of IL-18 was blocked by the antioxidant, N-acetyl-l-cysteine (NAC), indicating that IL-18 regulates ROI production, which is involved in SCF production. Furthermore, inhibitors of p38 mitogen-activated protein kinase (MAPK), such as SB203580, blocked enhanced SCF expression, indicating that p38 MAPK activity is required for IL-18-enhanced SCF production. Taken together, these results suggest that IL-18 plays a critical role as a regulatory factor of SCF expression via ROI and p38 MAPK activity in B16F10 murine melanoma cells.-
dc.publisherElsevier-
dc.titleIL-18 enhances SCF production of melanoma cells by regulating ROI and p38 MAPK activity-
dc.title.alternativeIL-18 enhances SCF production of melanoma cells by regulating ROI and p38 MAPK activity-
dc.typeArticle-
dc.citation.titleImmunology Letters-
dc.citation.number2-
dc.citation.endPage217-
dc.citation.startPage211-
dc.citation.volume96-
dc.contributor.affiliatedAuthorIn Pyo Choi-
dc.contributor.alternativeName허정심-
dc.contributor.alternativeName김안근-
dc.contributor.alternativeName송현근-
dc.contributor.alternativeName최인표-
dc.contributor.alternativeName박현정-
dc.contributor.alternativeName김태성-
dc.contributor.alternativeName이왕재-
dc.contributor.alternativeName강형식-
dc.contributor.alternativeName조대호-
dc.identifier.bibliographicCitationImmunology Letters, vol. 96, no. 2, pp. 211-217-
dc.identifier.doi10.1016/j.imlet.2004.08.008-
dc.subject.keywordIL-18-
dc.subject.keywordMelanoma-
dc.subject.keywordp38 MAPK-
dc.subject.keywordROI-
dc.subject.keywordSCF-
dc.subject.localIL-18-
dc.subject.localMelanoma-
dc.subject.localmelanoma-
dc.subject.localp38 MAP kinase-
dc.subject.localp38 mitogen-activated protein kinase (p38 MARK)-
dc.subject.localP38 MAPK-
dc.subject.localp38 mitogen-activated protein kinase-
dc.subject.localp38 MAPK-
dc.subject.localp38MAPK-
dc.subject.localROI-
dc.subject.localSCF-
dc.description.journalClassY-
Appears in Collections:
Division of A.I. & Biomedical Research > Immunotherapy Research Center > 1. Journal Articles
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