Fisetin inhibits TNF-α/NF-κB-induced IL-8 expression by targeting PKCδ in human airway epithelial cells

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dc.contributor.authorSeoghyun Lee-
dc.contributor.authorH Ro-
dc.contributor.authorH J In-
dc.contributor.authorJi Hee Choi-
dc.contributor.authorMun-Ock Kim-
dc.contributor.authorJinhyuk Lee-
dc.contributor.authorS T Hong-
dc.contributor.authorSu Ui Lee-
dc.date.accessioned2018-07-19T16:30:42Z-
dc.date.available2018-07-19T16:30:42Z-
dc.date.issued2018-
dc.identifier.issn1043-4666-
dc.identifier.uri10.1016/j.cyto.2018.01.004ko
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/17943-
dc.description.abstractFisetin (3,7,3′,4′-tetrahydroxyflavone), a natural flavonoid, is a therapeutic agent for respiratory inflammatory diseases such as chronic obstructive pulmonary disease (COPD). However, detailed molecular mechanisms regarding the target protein of fisetin remain unknown. Fisetin significantly reduces tumour necrosis factor alpha (TNF-α)-induced interleukin (IL)-8 levels by inhibiting both nuclear factor kappa B (NF-κB) transcriptional activity and the phosphorylation of its upstream effectors. We show that fisetin prevents interactions between protein kinase C (PKC)δ and TNF receptor-associated factor 2 (TRAF2), thereby inhibiting the inhibitor of kappa B kinase (IKK)/NF-κB downstream signalling cascade. Furthermore, we found that fisetin directly binds to PKCδ in vitro. Our findings provide evidence that fisetin inhibits the TNF-α-activated IKK/NF-κB cascade by targeting PKCδ thereby mediating inflammatory diseases such as COPD. These data suggest that fisetin is a good therapeutic drug for the treatment of inflammatory lung diseases, such as COPD, by inhibiting the TNF-α/NF-κB signalling pathway-
dc.publisherElsevier-
dc.titleFisetin inhibits TNF-α/NF-κB-induced IL-8 expression by targeting PKCδ in human airway epithelial cells-
dc.title.alternativeFisetin inhibits TNF-α/NF-κB-induced IL-8 expression by targeting PKCδ in human airway epithelial cells-
dc.typeArticle-
dc.citation.titleCytokine-
dc.citation.number0-
dc.citation.endPage254-
dc.citation.startPage247-
dc.citation.volume108-
dc.contributor.affiliatedAuthorSeoghyun Lee-
dc.contributor.affiliatedAuthorJi Hee Choi-
dc.contributor.affiliatedAuthorMun-Ock Kim-
dc.contributor.affiliatedAuthorJinhyuk Lee-
dc.contributor.affiliatedAuthorSu Ui Lee-
dc.contributor.alternativeName이석현-
dc.contributor.alternativeName노현주-
dc.contributor.alternativeName이현주-
dc.contributor.alternativeName최지희-
dc.contributor.alternativeName김문옥-
dc.contributor.alternativeName이진혁-
dc.contributor.alternativeName홍성태-
dc.contributor.alternativeName이수의-
dc.identifier.bibliographicCitationCytokine, vol. 108, pp. 247-254-
dc.identifier.doi10.1016/j.cyto.2018.01.004-
dc.subject.keywordChronic obstructive pulmonary disease (COPD)-
dc.subject.keywordFisetin-
dc.subject.keywordIL-8-
dc.subject.keywordPKCδ-
dc.subject.keywordTNF-α/NF-κB pathway-
dc.subject.localChronic obstructive pulmonary disease-
dc.subject.localChronic obstructive pulmonary disease (COPD)-
dc.subject.localchronic obstructive pulmonary disease-
dc.subject.localPulmonary disease, chronic obstructive-
dc.subject.localFisetin-
dc.subject.localfisetin-
dc.subject.localIL-8-
dc.subject.localPKCδ-
dc.subject.localTNF-α/NF-κB pathway-
dc.description.journalClassY-
Appears in Collections:
Ochang Branch Institute > Natural Product Research Center > 1. Journal Articles
Synthetic Biology and Bioengineering Research Institute > Genome Editing Research Center > 1. Journal Articles
Center for Gene & Cell Theraphy > 1. Journal Articles
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