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Eupatilin, a pharmacologically active flavone derived from Artemisia plants, induces apoptosis in human promyelocytic leukemia cells

Cited 85 time in Web of Science Cited 92 time in Scopus
Authors

Seo, Hyo-Joung; Surh, Young-Joon

Issue Date
2001-09
Publisher
Elsevier BV
Citation
Mutation Research - Genetic Toxicology and Environmental Mutagenesis, Vol.496 No.1-2, pp.191-198
Abstract
Extracts of the whole herb of Artemisia asiatica Nakai (Asteraceae) have been used in traditional oriental medicine for the treatment of inflammation, cancer and other disorders. In the present work, we have evaluated the apoptosis-inducing capability of eupatilin (5,7-dihydroxy-3,4,6-trimethoxyflavone), a pharmacologically active ingredient of A. asiatica, in cultured human promyelocytic leukemia (HL-60) cells. Thus, eupatilin exhibited concentration-dependent inhibitory effects on viability and DNA synthesis capability of BL-60 cells. The anti-proliferative effect of eupatilin was attributable to its apoptosis-inducing activity as determined by characteristic nuclear condensation, in situ terminal end-labeling of fragmented DNA (TUNEL), release of mitochondrial cytochrome c into cytoplasm, proteolytic activation of caspases-9, -3, and -7, and cleavage of poly(ADP-ribose)polymerase. Eupatilin-induced BL-60 cell apoptosis does not appear to be mediated via alteration in Bcl-2/Bax-2. Taken together, the above findings suggest that eupatilin has chemopreventive and cytotoxic effects. (C) 2001 Elsevier Science B.V. All rights reserved.
ISSN
1383-5718
URI
https://hdl.handle.net/10371/172863
DOI
https://doi.org/10.1016/S1383-5718(01)00234-0
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  • College of Pharmacy
  • Department of Pharmacy
Research Area Agricultural Sciences

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