Hypoxia-induced IL-18 increases hypoxia-inducible factor-1α expression through a Rac1-dependent NF-κB pathway

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dc.contributor.authorJ Kim-
dc.contributor.authorY Shao-
dc.contributor.authorS Y Kim-
dc.contributor.authorS Kim-
dc.contributor.authorH K Song-
dc.contributor.authorJ H Jeon-
dc.contributor.authorHyun Woo Suh-
dc.contributor.authorJin Woong Chung-
dc.contributor.authorSuk Ran Yoon-
dc.contributor.authorY S Kim-
dc.contributor.authorIn Pyo Choi-
dc.date.accessioned2017-04-19T09:09:04Z-
dc.date.available2017-04-19T09:09:04Z-
dc.date.issued2008-
dc.identifier.issn1059-1524-
dc.identifier.uri10.1091/mbc.E07-02-0182ko
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/8289-
dc.description.abstractInterleukin-18 (IL-18) plays pivotal roles in linking inflammatory immune responses and tumor progression and metastasis, yet the manner in which this occurs remains to be sufficiently clarified. Here we report that hypoxia induces the transcription and secretion of IL-18, which subsequently induces the expression of hypoxia-inducible factor-1α (HIF-1α). Mechanistically, IL-18 induces HIF-1α through the activity of the GTPase Rac1, which inducibly associates with the IL-18 receptor β (IL-18Rβ) subunit, via a PI3K-AKT-NF-κB-dependent pathway. Importantly, the knockdown of the IL-18Rβ subunit inhibited IL-18-driven tumor cell metastasis. Collectively, these findings demonstrate a feed-forward pathway in HIF-1α-mediated tumor progression, in which the induction of IL-18 by hypoxia or inflammatory cells augments the expression of both HIF-1α and tumor cell metastasis.-
dc.publisherAmer Soc Cell Biology-
dc.titleHypoxia-induced IL-18 increases hypoxia-inducible factor-1α expression through a Rac1-dependent NF-κB pathway-
dc.title.alternativeHypoxia-induced IL-18 increases hypoxia-inducible factor-1α expression through a Rac1-dependent NF-κB pathway-
dc.typeArticle-
dc.citation.titleMolecular Biology of Cell-
dc.citation.number2-
dc.citation.endPage444-
dc.citation.startPage433-
dc.citation.volume19-
dc.contributor.affiliatedAuthorHyun Woo Suh-
dc.contributor.affiliatedAuthorJin Woong Chung-
dc.contributor.affiliatedAuthorSuk Ran Yoon-
dc.contributor.affiliatedAuthorIn Pyo Choi-
dc.contributor.alternativeName김정기-
dc.contributor.alternativeNameShao-
dc.contributor.alternativeName김상용-
dc.contributor.alternativeName김세일-
dc.contributor.alternativeName송현근-
dc.contributor.alternativeName전준호-
dc.contributor.alternativeName서현우-
dc.contributor.alternativeName정진웅-
dc.contributor.alternativeName윤석란-
dc.contributor.alternativeName김영상-
dc.contributor.alternativeName최인표-
dc.identifier.bibliographicCitationMolecular Biology of Cell, vol. 19, no. 2, pp. 433-444-
dc.identifier.doi10.1091/mbc.E07-02-0182-
dc.description.journalClassY-
Appears in Collections:
Division of A.I. & Biomedical Research > Immunotherapy Research Center > 1. Journal Articles
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