Apoptosis in Leukemic Cells Induced by Anti-Proliferative Coumarin Isolated from the Stem Bark of Fraxinus rhynchophylla

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...

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Veröffentlicht in:Journal of microbiology and biotechnology 2020, 30(8), , pp.1214-1221
Hauptverfasser: Lee, Beom Zoo, Lee, Ik Soo, Chau Ha Pham, Jeong, Soon-Kyu, Lee, Sulhae, Hong, KwangWon, Yoo, Hee Min
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Sprache:eng
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Zusammenfassung: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.
ISSN:1017-7825
1738-8872
DOI:10.4014/jmb.2006.06022