Rotundifuran induces ferroptotic cell death and mitochondria permeability transition in lung cancer cells

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dc.contributor.authorMyung Ji Kang-
dc.contributor.authorD O Moon-
dc.contributor.authorJi-Yoon Park-
dc.contributor.authorNamho Kim-
dc.contributor.authorSu Hyeon Lee-
dc.contributor.authorHyung Won Ryu-
dc.contributor.authorY H Huh-
dc.contributor.authorHyun Sun Lee-
dc.contributor.authorMun-Ock Kim-
dc.date.accessioned2024-03-06T16:36:23Z-
dc.date.available2024-03-06T16:36:23Z-
dc.date.issued2024-
dc.identifier.issn2227-9059-
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/33781-
dc.description.abstractRotundifuran (RF), a potent anti-inflammatory and anti-cancer compound, is a natural compound predominantly present in Vitex Rotundifolia. Herein, we investigated the effects of RF on the growth of lung cancer cells. Our findings suggested that RF inhibits cell growth, highlighting its potential as a therapeutic agent for cancer treatment. Interestingly, we observed that cell growth inhibition was not due to apoptosis, as caspases were not activated and DNA fragmentation did not occur. Furthermore, we found that intracellular vacuoles and autophagy were induced, but RF-induced cell death was not affected when autophagy was inhibited. This prompted us to investigate other possible mechanisms underlying cell growth inhibition. Through a cDNA chip analysis, we confirmed changes in the expression of ferroptosis-related genes and observed lipid peroxidation. We further examined the effect of ferroptosis inhibitors and found that they alleviated cell growth inhibition induced by RF. We also observed the involvement of calcium signaling, ROS accumulation, and JNK signaling in the induction of ferroptosis. Our findings suggested that RF is a potent anti-cancer drug and further studies are needed to validate its clinal use.-
dc.publisherMDPI-
dc.titleRotundifuran induces ferroptotic cell death and mitochondria permeability transition in lung cancer cells-
dc.title.alternativeRotundifuran induces ferroptotic cell death and mitochondria permeability transition in lung cancer cells-
dc.typeArticle-
dc.citation.titleBiomedicines-
dc.citation.number3-
dc.citation.endPage576-
dc.citation.startPage576-
dc.citation.volume12-
dc.contributor.affiliatedAuthorMyung Ji Kang-
dc.contributor.affiliatedAuthorJi-Yoon Park-
dc.contributor.affiliatedAuthorNamho Kim-
dc.contributor.affiliatedAuthorSu Hyeon Lee-
dc.contributor.affiliatedAuthorHyung Won Ryu-
dc.contributor.affiliatedAuthorHyun Sun Lee-
dc.contributor.affiliatedAuthorMun-Ock Kim-
dc.contributor.alternativeName강명지-
dc.contributor.alternativeName문동오-
dc.contributor.alternativeName박지윤-
dc.contributor.alternativeName김남호-
dc.contributor.alternativeName이수현-
dc.contributor.alternativeName류형원-
dc.contributor.alternativeName허양훈-
dc.contributor.alternativeName이현선-
dc.contributor.alternativeName김문옥-
dc.identifier.bibliographicCitationBiomedicines, vol. 12, no. 3, pp. 576-576-
dc.identifier.doi10.3390/biomedicines12030576-
dc.subject.keywordRotundifuran-
dc.subject.keywordFerroptosis-
dc.subject.keywordReactive oxygen species (ROS)-
dc.subject.keywordMitochondria permeability transition (MPT)-
dc.subject.localFerroptosis-
dc.subject.localferroptosis-
dc.subject.localROS-
dc.subject.localReactive Oxygen Species (ROS)-
dc.subject.localReactive oxidative species-
dc.subject.localReactive oxygen species-
dc.subject.localReactive oxygen species (ROS)-
dc.subject.localreactive oxygen species-
dc.subject.localreactive oxygen species (ROS)-
dc.subject.localReactive Oxygen Species-
dc.subject.localReactive oxygen species(ROS)-
dc.subject.localMitochondria permeability transition (MPT)-
dc.description.journalClassY-
Appears in Collections:
Ochang Branch Institute > Natural Product Research Center > 1. Journal Articles
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