Bereich Organische Chemie, Martin-Luther-Universität Halle-Wittenberg, Kurt-Mothes-Str. 2, D-06120 Halle, Saale, Germany.
Bioorg Med Chem. 2010 Nov 1;18(21):7458-74. doi: 10.1016/j.bmc.2010.08.054. Epub 2010 Sep 18.
Glycyrrhetinic acid (GA) is one of many interesting triterpenoic acids showing anticancerogenic potential. GA is known to trigger apoptosis in tumour cell lines, although GA has a low cytotoxicity. In our study we were able to prepare derivatives of GA that show lowered the IC(50) values as determined by a sulforhodamine B (SRB) assay using 15 different human tumour cell lines. Thus, combining an ester group combined with the presence of an amino acid moiety led to a ca. 60-fold improved antitumor activity. Experiments on mouse embryonic fibroblasts (NiH3T3) revealed that these compounds showed a better selectivity for tumour cells compared to the parent compound GA. An apoptotic effect of some of these compounds was determined using an acridine orange/ethidium bromide (AO/EB) test and DNA laddering experiments.
甘草次酸(GA)是一种具有抗癌潜力的有趣的三萜烯酸之一。GA 已知能在肿瘤细胞系中引发细胞凋亡,尽管 GA 的细胞毒性较低。在我们的研究中,我们能够制备 GA 的衍生物,这些衍生物通过使用 15 种不同的人肿瘤细胞系的磺基罗丹明 B(SRB)测定法显示出降低的 IC 50 值。因此,将酯基与氨基酸部分结合在一起导致抗肿瘤活性提高约 60 倍。在小鼠胚胎成纤维细胞(NiH3T3)上的实验表明,与母体化合物 GA 相比,这些化合物对肿瘤细胞具有更好的选择性。使用吖啶橙/溴化乙锭(AO/EB)试验和 DNA 梯段实验确定了其中一些化合物的凋亡作用。