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Apoptotic potential of sesquiterpene lactone ergolide through the inhibition of NF-κB signaling pathway

Authors
Yong Jin SongDae Young LeeSu-Nam KimKang Ro LeeHyang Woo LeeJeung-Whan HanDong-Won KangHoi Young Lee김용기
Issue Date
Dec-2005
Publisher
Pharmaceutical Press
Citation
Journal of Pharmacy and Pharmacology, v.57, no.12, pp 1591 - 1597
Pages
7
Journal Title
Journal of Pharmacy and Pharmacology
Volume
57
Number
12
Start Page
1591
End Page
1597
URI
https://scholarworks.sookmyung.ac.kr/handle/2020.sw.sookmyung/148709
DOI
10.1211/jpp.57.12.0009
ISSN
0022-3573
2042-7158
Abstract
Treatment with ergolide, a sesquiterpene lactone from Inula britannica var chinensis, caused the induction of apoptosis in Jurkat T cells, which was confirmed by DNA fragmentation, caspase-3 activation and cleavage of poly(ADP-ribose) polymerase in response to ergolide. Furthermore, mitochondrial dysfunction appeared to be associated with ergolide-induced apoptosis, because Bax translocation and cytochrome c release were stimulated by ergolide. In parallel, the nuclear factor-κB (NF-κB) signaling pathway was significantly inhibited by ergolide, which was accompanied by down-regulation of cell survival molecules, such as X-chromosome-linked inhibitor of apoptosis and Bcl-2. In addition, the JNK signaling pathway was involved in ergolide-induced apoptosis. Collectively, our results identified a new mechanism for the anti-cancer property of ergolide, attributable to the induction of apoptosis through down-regulation of cell survival signal molecules resulting from inhibition of the NF-κB signaling pathway.
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