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Cited 18 time in webofscience Cited 19 time in scopus
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Ursonic acid exerts inhibitory effects on matrix metalloproteinases via ERK signaling pathway

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dc.contributor.authorSon J.-
dc.contributor.authorLee S.Y.-
dc.date.available2020-03-03T06:45:57Z-
dc.date.created2020-02-24-
dc.date.issued2020-01-
dc.identifier.issn0009-2797-
dc.identifier.urihttps://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/17759-
dc.description.abstractUrsonic acid is a pentacyclic triterpenoid compound that can be extracted from Ziziphus jujuba Mill., a traditional medicine. Matrix metalloproteinases (MMPs) are involved in cancer metastasis and skin aging. Regulation of various MMPs is closely associated with mitogen-activated protein kinases (MAPKs), including ERK, p38, and JNK MAPKs. In this study, we investigated the possibility of ursonic acid as an anti-cancer/anti-skin aging agent targeting MMPs. Cytotoxic effects of ursonic acid were analyzed by cell counting kit-8 (CCK-8) assay. Invasive abilities of ursonic acid-treated A549 and H1299 non-small cell lung cancer (NSCLC) cells were tested with Boyden chamber assay. Effects of ursonic acid on MMPs were analyzed by zymography assays and quantitative real time polymerase chain reaction (qRT-PCR). We also conducted flow cytometry and western blot analysis to elucidate the mechanisms of MMP regulation by ursonic acid. Our results revealed that ursonic acid inhibited transcriptional expression of gelatinases (MMP-2 and MMP-9) via inhibition of ERK and CREB signaling pathways in NSCLC cells. Moreover, ursonic acid reduced mRNA levels of collagenase (MMP-1) via suppression of ERK and c-Fos signaling pathways in HaCaT keratinocytes. These results suggest that ursonic acid could be a potential candidate for development of an effective novel anti-cancer and anti-wrinkle agent. © 2019 Elsevier B.V.-
dc.language영어-
dc.language.isoen-
dc.publisherElsevier Ireland Ltd-
dc.relation.isPartOfChemico-Biological Interactions-
dc.titleUrsonic acid exerts inhibitory effects on matrix metalloproteinases via ERK signaling pathway-
dc.typeArticle-
dc.type.rimsART-
dc.description.journalClass1-
dc.identifier.wosid000514572800042-
dc.identifier.doi10.1016/j.cbi.2019.108910-
dc.identifier.bibliographicCitationChemico-Biological Interactions, v.315-
dc.description.isOpenAccessN-
dc.identifier.scopusid2-s2.0-85076716293-
dc.citation.titleChemico-Biological Interactions-
dc.citation.volume315-
dc.contributor.affiliatedAuthorSon J.-
dc.contributor.affiliatedAuthorLee S.Y.-
dc.type.docTypeArticle-
dc.subject.keywordAuthorERK-
dc.subject.keywordAuthorKeratinocyte-
dc.subject.keywordAuthorMAPK-
dc.subject.keywordAuthorMatrix metalloproteinase-
dc.subject.keywordAuthorNon-small cell lung cancer-
dc.subject.keywordAuthorUrsonic acid-
dc.subject.keywordPluscyclic AMP responsive element binding protein-
dc.subject.keywordPlusgelatinase A-
dc.subject.keywordPlusgelatinase B-
dc.subject.keywordPlusinterstitial collagenase-
dc.subject.keywordPlusmatrix metalloproteinase-
dc.subject.keywordPlusmessenger RNA-
dc.subject.keywordPlusmitogen activated protein kinase-
dc.subject.keywordPlusprotein c fos-
dc.subject.keywordPlustriterpenoid-
dc.subject.keywordPlusunclassified drug-
dc.subject.keywordPlusursonic acid-
dc.subject.keywordPlusA-549 cell line-
dc.subject.keywordPlusArticle-
dc.subject.keywordPluscontrolled study-
dc.subject.keywordPlusdrug cytotoxicity-
dc.subject.keywordPlusdrug effect-
dc.subject.keywordPlusenzyme degradation-
dc.subject.keywordPlusenzyme inhibition-
dc.subject.keywordPlusenzyme regulation-
dc.subject.keywordPlusflow cytometry-
dc.subject.keywordPlusHaCat cell line-
dc.subject.keywordPlushuman-
dc.subject.keywordPlushuman cell-
dc.subject.keywordPlusMAPK signaling-
dc.subject.keywordPlusNCI-H1299 cell line-
dc.subject.keywordPlusprotein expression-
dc.subject.keywordPlusreal time polymerase chain reaction-
dc.subject.keywordPlusWestern blotting-
dc.subject.keywordPluszymography-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
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