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Apoptotic cell death of human leukaemia U937 cells by ubiquinone-9 purified from Pleurotus eryngii

Authors
Bae, Jeen-SooPark, Jin WookPark, So HyunPark, Jung BinRho, Yoon-HwaRyu, Young BaeLee, Kun-SikPark, Ki-HunBae, Young-Seuk
Issue Date
2009
Publisher
TAYLOR & FRANCIS LTD
Keywords
Pleurotus eryngii; ubiquinone-9; DNA topoisomerase I inhibitor; apoptosis; human leukaemia cells; anticancer drug
Citation
NATURAL PRODUCT RESEARCH, v.23, no.12, pp 1112 - 1119
Pages
8
Indexed
SCIE
SCOPUS
Journal Title
NATURAL PRODUCT RESEARCH
Volume
23
Number
12
Start Page
1112
End Page
1119
URI
https://scholarworks.gnu.ac.kr/handle/sw.gnu/27156
DOI
10.1080/14786410802417107
ISSN
1478-6419
1478-6427
Abstract
A chloroform extract of the edible mushroom Pleurotus eryngii showed an inhibitory effect on mammalian DNA topoisomerase I. The topoisomerase I inhibitory compound was purified and identified as ubiquinone-9. Ubiquinone-9 was shown to inhibit the activity of topoisomerase I with IC50 of about 50 mu M. Concentration of 110 mu M ubiquinone-9 caused 50% growth inhibition of human leukaemia U937 cells, but not that of normal fibroblast NIH3T3 and 3Y1 cells. Ubiquinone-9-induced cell death was characterised with the cleavage of poly (ADP-ribose) polymerase and pro-caspase 3. Furthermore, ubiquinone-9 induced the fragmentation of DNA into an apoptotic DNA ladder, indicating that the inhibitor triggered apoptosis. The induction of apoptosis by ubiquinone-9 was also confirmed using flow cytometry analysis. Taken together, these results suggest that ubiquinone-9 may function by inhibiting oncogenic disease, at least in part, through the inhibition of topoisomerase I activity.
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