Department of Clinical Pharmacology, Faculty of Medical Sciences, Kyushu University, Fukuoka, Japan.
J Pharmacol Sci. 2013;121(2):103-9. doi: 10.1254/jphs.12204fp. Epub 2013 Jan 25.
Differentiation-inducing factor-1 (DIF-1), a morphogen for Dictyostelium discoideum, inhibits the proliferation of human cancer cell lines by suppressing the Wnt/β-catenin signaling pathway. In this study, we examined the effect of DIF-1 on c-Myc, a target gene product of the Wnt/β-catenin signaling pathway, mainly using HCT-116 colon cancer cells. DIF-1 strongly reduced the amount of c-Myc protein in time- and concentration-dependent manners and reduced c-Myc mRNA expression by inhibiting promoter activity through the TCF binding sites. The effect of DIF-1 on c-Myc was also confirmed using the human cervical cell line HeLa. Pretreatment with the proteasome inhibitor MG132 or glycogen synthase kinase-3β (GSK-3β) inhibitors (LiCl and SB216763) attenuated the effect of DIF-1, suggesting that DIF-1 induced c-Myc protein degradation through GSK-3β activation. Furthermore, we examined whether c-Myc was involved in the anti-proliferative effect of DIF-1 using c-Myc-overexpressing cells and found that c-Myc was associated with the anti-proliferative effect of this compound. These results suggest that DIF-1 inhibits c-Myc expression by inhibiting promoter activity and inducing protein degradation via GSK-3β activation, resulting in the inhibition of cell proliferation. Since c-Myc seems to be profoundly involved in accelerated proliferation of various malignant tumors, DIF-1 may have a potential to develop into a novel anti-cancer agent.
分化诱导因子-1(DIF-1)是一种盘基网柄菌的形态发生因子,通过抑制 Wnt/β-连环蛋白信号通路来抑制人类癌细胞系的增殖。在这项研究中,我们主要使用 HCT-116 结肠癌细胞来研究 DIF-1 对 Wnt/β-连环蛋白信号通路靶基因产物 c-Myc 的影响。DIF-1 以时间和浓度依赖性方式强烈降低 c-Myc 蛋白的量,并通过抑制 TCF 结合位点的启动子活性来降低 c-Myc mRNA 表达。在人宫颈癌细胞系 HeLa 中也证实了 DIF-1 对 c-Myc 的作用。用蛋白酶体抑制剂 MG132 或糖原合酶激酶-3β(GSK-3β)抑制剂(LiCl 和 SB216763)预处理可减弱 DIF-1 的作用,表明 DIF-1 通过激活 GSK-3β 诱导 c-Myc 蛋白降解。此外,我们使用 c-Myc 过表达细胞检查了 c-Myc 是否参与 DIF-1 的抗增殖作用,发现 c-Myc 与该化合物的抗增殖作用有关。这些结果表明,DIF-1 通过抑制启动子活性和通过 GSK-3β 激活诱导蛋白降解来抑制 c-Myc 表达,从而抑制细胞增殖。由于 c-Myc 似乎在各种恶性肿瘤的加速增殖中起着重要作用,因此 DIF-1 可能具有开发成新型抗癌剂的潜力。