Calotropis gigantea extract induces apoptosis through extrinsic/intrinsic pathways and reactive oxygen species generation in A549 and NCI-H1299 non-small cell lung cancer cells

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dc.contributor.authorJ Lee-
dc.contributor.authorH J Jang-
dc.contributor.authorH Chun-
dc.contributor.authorT H Pham-
dc.contributor.authorY Bak-
dc.contributor.authorJ W Shin-
dc.contributor.authorH Jin-
dc.contributor.authorYong In Kim-
dc.contributor.authorHyung Won Ryu-
dc.contributor.authorSei-Ryang Oh-
dc.contributor.authorD Y Yoon-
dc.date.accessioned2019-07-10T01:23:37Z-
dc.date.available2019-07-10T01:23:37Z-
dc.date.issued2019-
dc.identifier.issn1472-6882-
dc.identifier.uri10.1186/s12906-019-2561-1ko
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/18828-
dc.description.abstractBackground: Calotropis gigantea (CG) is a tall and waxy flower that is used as a traditional remedy for fever, indigestion, rheumatism, leprosy, and leukoderma. However, the precise mechanisms of its anticancer effects have not yet been examined in human non-small cell lung cancer (NSCLC) cells. In this study, we investigated whether CG extract exerted an apoptotic effect in A549 and NCI-H1299 NSCLC cells. Methods: The ethanol extract of CG was prepared, and its apoptotic effects on A549 and NCI-H1299 NSCLC cells were assessed by using the 3-(4,5-dimethylthiazol-2-yl)-5-(3-carboxy methoxyphenyl)-2-(4-sulfophenyl)-2Htetrazolium (MTS) assay, annexin V-fluorescein isothiocyanate/propidium iodide (PI) staining, cell cycle analysis, realtime polymerase chain reaction (RT-PCR), western blotting, JC-1 staining, and ROS detection assay. Results: The CG extract induced apoptosis through the stimulation of intrinsic and extrinsic signaling pathways in A549 and NCI-H1299 lung cancer cells. Cell cycle arrest was induced by the CG extract in both cell lines. Reactive oxygen species (ROS), which can induce cell death, were also generated in the CG-treated A549 and NCI-H1299 cells. Conclusions: These data confirmed that CG caused apoptosis through the activation of extrinsic and intrinsic pathways, cell cycle arrest, and ROS generation in A549 and NCI-H1299 lung cancer cells. Thus, CG can be suggested as a potential agent for lung cancer therapy.-
dc.publisherSpringer-BMC-
dc.titleCalotropis gigantea extract induces apoptosis through extrinsic/intrinsic pathways and reactive oxygen species generation in A549 and NCI-H1299 non-small cell lung cancer cells-
dc.title.alternativeCalotropis gigantea extract induces apoptosis through extrinsic/intrinsic pathways and reactive oxygen species generation in A549 and NCI-H1299 non-small cell lung cancer cells-
dc.typeArticle-
dc.citation.titleBMC Complementary and Alternative Medicine-
dc.citation.number0-
dc.citation.endPage134-
dc.citation.startPage134-
dc.citation.volume19-
dc.contributor.affiliatedAuthorYong In Kim-
dc.contributor.affiliatedAuthorHyung Won Ryu-
dc.contributor.affiliatedAuthorSei-Ryang Oh-
dc.contributor.alternativeName이지연-
dc.contributor.alternativeName장희주-
dc.contributor.alternativeName천현우-
dc.contributor.alternativeNamePham-
dc.contributor.alternativeName박예솔-
dc.contributor.alternativeName신종운-
dc.contributor.alternativeName진항-
dc.contributor.alternativeName김용인-
dc.contributor.alternativeName류형원-
dc.contributor.alternativeName오세량-
dc.contributor.alternativeName윤도영-
dc.identifier.bibliographicCitationBMC Complementary and Alternative Medicine, vol. 19, pp. 134-134-
dc.identifier.doi10.1186/s12906-019-2561-1-
dc.subject.keywordCalotropis gigantea-
dc.subject.keywordNon-small cell lung cancer cell-
dc.subject.keywordAnti-cancer-
dc.subject.keywordApoptosis-
dc.subject.keywordROS-
dc.subject.localCalotropis gigantea-
dc.subject.localNon-small cell lung cancer cell-
dc.subject.localAnti-cancer-
dc.subject.localAnticancer-
dc.subject.localanti-cancer-
dc.subject.localanticancer-
dc.subject.localAnti-Cancer-
dc.subject.localapoptosis-
dc.subject.localApoptosis-
dc.subject.localReactive oxidative 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.localROS-
dc.subject.localReactive oxygen species (ROS)-
dc.subject.localreactive oxygen species-
dc.subject.localreactive oxygen species (ROS)-
dc.description.journalClassY-
Appears in Collections:
Ochang Branch Institute > Natural Product Research Center > 1. Journal Articles
Ochang Branch Institute > 1. Journal Articles
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