Kikuchi Hiroyuki, Ohtsuki Takashi, Koyano Takashi, Kowithayakorn Thaworn, Sakai Toshiyuki, Ishibashi Masami
Graduate School of Pharmaceutical Sciences, Chiba University, 1-33 Yayoi-cho, Inage-ku, Chiba 263-8522, Japan.
Bioorg Med Chem. 2009 Feb 1;17(3):1181-6. doi: 10.1016/j.bmc.2008.12.033. Epub 2008 Dec 24.
Death receptor 5 (DR5) is an apoptosis-inducing membrane receptor for TNF-related apoptosis-inducing ligand (TRAIL). On screening for compounds that enhance DR5 expression using a luciferase assay with DLD-1/SacI, we previously identified 4'-demethyltoxicarol isoflavone (1) isolated from the leaves of Millettia brandisiana. In this study, we revealed that 1 sensitized TRAIL-resistant human gastric adenocarcinoma (AGS) cells to TRAIL-induced apoptosis by up-regulating the expression of DR5. 1 induced DR5 expression at both the mRNA and protein level. A human recombinant DR5/Fc chimera remarkably inhibited 1-induced apoptosis. These results suggest that the enhancement of DR5 expression by 1 was critical to the cell death. Furthermore, a MeOH extract of the bark of Ardisia colorata markedly enhanced DR5 activity in this screening system. Bioassay-guided fractionation of A. colorata led to the isolation and identification of a new isoflavone, coloratanin A (3), together with ten known compounds. The chemical structure of the new compound was elucidated on the basis of a spectroscopic analysis.
死亡受体5(DR5)是肿瘤坏死因子相关凋亡诱导配体(TRAIL)的一种诱导凋亡的膜受体。在使用DLD-1/SacI荧光素酶检测法筛选增强DR5表达的化合物时,我们之前从布兰迪斯崖豆藤的叶子中鉴定出了4'-去甲基毒卡罗异黄酮(1)。在本研究中,我们发现1通过上调DR5的表达使对TRAIL耐药的人胃腺癌(AGS)细胞对TRAIL诱导的凋亡敏感。1在mRNA和蛋白质水平上均诱导了DR5的表达。人重组DR5/Fc嵌合体显著抑制了1诱导的凋亡。这些结果表明1增强DR5表达对细胞死亡至关重要。此外,在该筛选系统中,紫金牛树皮的甲醇提取物显著增强了DR5活性。对紫金牛进行生物活性导向分离,得到并鉴定了一种新的异黄酮,紫金牛素A(3)以及十种已知化合物。基于光谱分析阐明了新化合物的化学结构。