Graduate School of Pharmaceutical Sciences, Chiba University, 1-8-1 Inohana, Chuo-ku, Chiba, 260-8675, Japan.
Temko Corporation, Tokyo, Japan.
J Nat Med. 2020 Sep;74(4):758-766. doi: 10.1007/s11418-020-01432-7. Epub 2020 Jul 9.
Since Notch signaling plays important roles in cell proliferation and differentiation, aberrant activation of this signaling contributes to cancer progression. In neural stem cells, Notch signaling inhibits differentiation by activating HES1 expression. Therefore, Notch signaling inhibitors may be candidates for new anticancer drugs or have applications in neural regenerative medicine. In this study, six naturally occurring Notch inhibitors were isolated from the methanol (MeOH) extract of Lansium domesticum using our novel cell-based assay. Hongherin (2), a cardiac glycoside, demonstrated potent Notch inhibitory activity with an IC of 0.62 μM and was found to be cytotoxic in HPB-ALL human T cell acute lymphoblastic leukemia cells. Hongherin (2) also induced the differentiation of C17.2 neural stem cells to neurons, causing a 65% increase in differentiation compared to the control. Mechanistically, hongherin (2) reduced the amount of Notch1 (full length) and mastermind-like protein (MAML). This indicates that hongherin (2) inhibits Notch signaling through a dual mechanism involving the reduction of both Notch1 and MAML protein levels.
由于 Notch 信号通路在细胞增殖和分化中发挥着重要作用,因此该信号通路的异常激活会促进癌症的进展。在神经干细胞中,Notch 信号通路通过激活 HES1 的表达来抑制分化。因此,Notch 信号通路抑制剂可能成为新型抗癌药物的候选物,或在神经再生医学中有应用前景。在这项研究中,我们使用新型基于细胞的测定法,从地石榴甲醇提取物中分离出六种天然存在的 Notch 抑制剂。海洋苷(2)是一种强心苷,具有很强的 Notch 抑制活性,IC 为 0.62 μM,并且在 HPB-ALL 人类 T 细胞急性淋巴细胞白血病细胞中具有细胞毒性。海洋苷(2)还能诱导 C17.2 神经干细胞向神经元分化,与对照组相比,分化率增加了 65%。从机制上讲,海洋苷(2)降低了 Notch1(全长)和类脑蛋白(MAML)的含量。这表明海洋苷(2)通过减少 Notch1 和 MAML 蛋白水平的双重机制来抑制 Notch 信号通路。