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Cited 7 time in webofscience Cited 7 time in scopus
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Apoptosis in Leukemic Cells Induced by Anti-Proliferative Coumarin Isolated from the Stem Bark of Fraxinus rhynchophyllaopen access

Authors
Lee, Beom ZooLee, Ik SooChau Ha PhamJeong, Soon-KyuLee, SulhaeHong, KwangWonYoo, Hee Min
Issue Date
Aug-2020
Publisher
KOREAN SOC MICROBIOLOGY & BIOTECHNOLOGY
Keywords
Fraxinus rhynchophylla; coumarin; leukemia; apoptosis; ROS; cytotoxicity
Citation
JOURNAL OF MICROBIOLOGY AND BIOTECHNOLOGY, v.30, no.8, pp 1214 - 1221
Pages
8
Indexed
SCIE
SCOPUS
KCI
Journal Title
JOURNAL OF MICROBIOLOGY AND BIOTECHNOLOGY
Volume
30
Number
8
Start Page
1214
End Page
1221
URI
https://scholarworks.dongguk.edu/handle/sw.dongguk/6368
DOI
10.4014/jmb.2006.06022
ISSN
1017-7825
1738-8872
Abstract
Esculetin 6-O-beta-D-arabinofuranosyl-(1 -> 6)-beta-D-glucopyranoside (EAG) is a coumarin glycoside isolated from the stem bark of Fraxinus rhynchophylla. This study scrutinized the anti-proliferative activity of EAG on blood cancer-derived Jurkat leukemic cells. Cell viability assays in leukemic cancer cells determined that EAG possesses potent anti-proliferative effects. Moreover, treatment with EAG increased the proportion of apoptotic cells, resulted in cell cycle arrest being induced at the subG0/G1 phase, and reduced the proportion of cells present in the S phase. In addition, mitochondrial membrane potential was reduced by EAG in Jurkat cells. Additionally, EAG triggered apoptosis that was mediated by the downregulation of BCL-XL, p-I kappa Ba, and p-p65 expressions in addition to the upregulation of cleaved Caspase 3 and BAX expressions. These findings revealed that the toxic effect of EAG was mediated by intracellular signal transduction pathways that involved a mechanism in which reactive oxygen species (ROS) were upregulated. Thus, this study concludes that EAG could potentially serve as a therapeutic agent for leukemia.
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