Li Xiaofan, Ohtsuki Takashi, Koyano Takashi, Kowithayakorn Thaworn, Ishibashi Masami
Graduate School of Pharmaceutical Sciences, Chiba University, 1-33 Yayoi-cho, Inage-ku, Chiba 263-8522, Japan.
Chem Asian J. 2009 Apr 6;4(4):540-7. doi: 10.1002/asia.200800354.
Aberrant Wnt/beta-catenin signaling has recently been implicated in tumorigenesis. On the basis of our screening program targeting inhibition of TCF/beta-catenin transcriptional activity, a plant extract of Eleutherine palmifolia was selected as a hit sample. Activity-guided fractionations led to the isolation of 15 naphthalene derivatives (1-15), including 4 new glucosides, eleutherinosides B-E (1-4), and 10 of the 15 compounds showed strong activities with high viability among 293T cells. Our data showed that 2 and 9 inhibited the transcription of TCF/beta-catenin in SW480 colon cancer cells in a dose-dependent manner. These two compounds also showed selective cytotoxicity against three colorectal cancer cell lines. In addition, treatment with 9 led to a significant decrease in the level of nuclear beta-catenin protein, suggesting this reduction to have resulted in the inhibitory effect of 9 on the transcription of TCF/beta-catenin.
异常的Wnt/β-连环蛋白信号通路最近被认为与肿瘤发生有关。基于我们针对抑制TCF/β-连环蛋白转录活性的筛选程序,伞莎草的一种植物提取物被选为阳性样本。活性导向分级分离导致分离出15种萘衍生物(1-15),包括4种新的糖苷,刺蒺藜皂甙B-E(1-4),并且这15种化合物中的10种在293T细胞中表现出具有高活力的强活性。我们的数据表明,化合物2和9以剂量依赖性方式抑制SW480结肠癌细胞中TCF/β-连环蛋白的转录。这两种化合物还对三种结肠癌细胞系表现出选择性细胞毒性。此外,用化合物9处理导致核β-连环蛋白水平显著降低,表明这种降低导致了化合物9对TCF/β-连环蛋白转录的抑制作用。