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诱导白血病细胞凋亡的增殖抑制型香豆素来源于.的茎干树皮

Apoptosis in Leukemic Cells Induced by Anti-proliferative Coumarin Isolated from the Stem Bark of .

机构信息

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.

出版信息

J Microbiol Biotechnol. 2020 Aug 28;30(8):1214-1221. doi: 10.4014/jmb.2006.06022.

Abstract

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.

摘要

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。

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