Department of Food Science and Biotechnology, College of Life Science and Biotechnology, Dongguk University, Goyang 10326, Republic of Korea.
Chemland Co., Ltd., Gunpo IT Valley, Gunpo 15850, Republic of Korea.
J Microbiol Biotechnol. 2020 Aug 28;30(8):1214-1221. doi: 10.4014/jmb.2006.06022.
Esculetin 6-O-β-D-arabinofuranosyl-(1→6)-β-D-glucopyranoside (EAG) is a coumarin glycoside isolated from the stem bark of . 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-IκBα, 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.
秦皮素 6-O-β-D-阿拉伯呋喃糖基-(1→6)-β-D-吡喃葡萄糖苷(EAG)是从白皮科茎皮中分离得到的香豆素糖苷。本研究探讨了 EAG 对血液癌源性 Jurkat 白血病细胞的抗增殖活性。在白血病癌细胞中的细胞活力测定表明,EAG 具有很强的抗增殖作用。此外,EAG 处理增加了凋亡细胞的比例,导致细胞周期阻滞在亚 G0/G1 期,并降低了 S 期细胞的比例。此外,EAG 还降低了 Jurkat 细胞中的线粒体膜电位。此外,EAG 通过下调 BCL-XL、p-IκBα 和 p-p65 的表达以及上调 cleaved Caspase 3 和 BAX 的表达,触发了凋亡。这些发现表明,EAG 的毒性作用是通过涉及活性氧(ROS)上调的细胞内信号转导途径介导的。因此,本研究得出结论,EAG 可能是治疗白血病的潜在药物。