Pacific Institute of Bioorganic Chemistry, 159 Prospect 100-Let Vladivostoku, Vladivostok 690022, Russian Federation.
Bioorg Med Chem. 2010 Jun 1;18(11):3834-40. doi: 10.1016/j.bmc.2010.04.043. Epub 2010 Apr 21.
3- and 10-Bromofascaplysins was previously found to possess cytotoxic activity. In this study, we investigated their cancer preventive and proapoptotic properties. These effects were tested on mouse skin epidermal JB6 P(+) Cl41 cell line, its stable transfectants, and human tumor HL-60, THP-1, SNU-C4, SK-MEL-28, DLD-1, MDA-MB-231, and HeLa cells using a variety of assessments, including a cell viability (MTS) assay, flow cytometry, anchorage-independent soft agar assay, luciferase assay, mitochondrial permeability assay, and Western blotting. 3- and 10-Bromofascaplysins were effective at submicromolar concentrations as the anticancer agents, which exerted their action, at least in part, through the induction of caspase-8, -9, -3-dependent apoptosis.
3- 和 10-溴菲斯卡斯林先前被发现具有细胞毒性活性。在这项研究中,我们研究了它们的防癌和促凋亡特性。这些效应在小鼠皮肤表皮 JB6 P(+) Cl41 细胞系及其稳定转染子、人肿瘤 HL-60、THP-1、SNU-C4、SK-MEL-28、DLD-1、MDA-MB-231 和 HeLa 细胞上进行了测试,使用了多种评估方法,包括细胞活力 (MTS) 测定、流式细胞术、非锚定依赖性软琼脂测定、荧光素酶测定、线粒体通透性测定和 Western blot 分析。3- 和 10-溴菲斯卡斯林在亚微摩尔浓度下作为抗癌剂有效,其作用至少部分是通过诱导 caspase-8、-9、-3 依赖性凋亡来发挥的。