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

Author:

Song Yong Jin1,Lee Dae Young1,Kang Dong-Won1,Kim Yong Kee1,Kim Su-Nam2,Lee Kang Ro2,Lee Hyang Woo2,Han Jeung-Whan2,Lee Hoi Young3

Affiliation:

1. College of Medicine, Kwandong University, Gangneung 210–701, Korea

2. College of Pharmacy, Sungkyunkwan University, Suwon 440–746, Korea

3. College of Medicine, Konyang University, Nonsan 320–711, Korea

Abstract

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.

Publisher

Oxford University Press (OUP)

Subject

Pharmaceutical Science,Pharmacology

Reference26 articles.

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