Department of Pharmacy, University of Pisa, via Bonanno 6, 56126 Pisa, Italy.
Department of Biotechnology, Chemistry and Pharmacy, University of Siena, Via Aldo Moro 2, 53100 Siena, Italy.
Mar Drugs. 2018 May 16;16(5):166. doi: 10.3390/md16050166.
Cutaneous melanoma is the most serious type of skin cancer, so new cytotoxic weapons against novel targets in melanoma are of great interest. Euplotin C (EC), a cytotoxic secondary metabolite of the marine ciliate , was evaluated in the present study on human cutaneous melanoma cells to explore its anti-melanoma activity and to gain more insight into its mechanism of action. EC exerted a marked cytotoxic effect against three different human melanoma cell lines (A375, 501Mel and MeWo) with a potency about 30-fold higher than that observed in non-cancer cells (HDFa cells). A pro-apoptotic activity and a decrease in melanoma cell migration by EC were also observed. At the molecular level, the inhibition of the Erk and Akt pathways, which control many aspects of melanoma aggressiveness, was shown. EC cytotoxicity was antagonized by dantrolene, a ryanodine receptor (RyR) antagonist, in a concentration-dependent manner. A role of RyR as a direct target of EC was also suggested by molecular modelling studies. In conclusion, our data provide the first evidence of the anti-melanoma activity of EC, suggesting it may be a promising new scaffold for the development of selective activators of RyR to be used for the treatment of melanoma and other cancer types.
皮肤黑色素瘤是最严重的皮肤癌类型,因此针对黑色素瘤新型靶点的新型细胞毒性药物具有重要意义。Euplotin C(EC)是一种海洋纤毛虫的细胞毒性次级代谢产物,本研究评估了其对人皮肤黑色素瘤细胞的抗黑色素瘤活性,并深入研究了其作用机制。EC 对三种不同的人黑色素瘤细胞系(A375、501Mel 和 MeWo)具有明显的细胞毒性作用,其效力比非癌细胞(HDFa 细胞)高约 30 倍。EC 还观察到促凋亡活性和黑色素瘤细胞迁移减少。在分子水平上,显示了抑制控制黑色素瘤侵袭性的许多方面的 Erk 和 Akt 通路。丹曲林钠(一种肌浆网钙释放通道(RyR)拮抗剂)以浓度依赖的方式拮抗 EC 的细胞毒性。分子建模研究还提示 RyR 是 EC 的直接作用靶点。总之,我们的数据首次提供了 EC 抗黑色素瘤活性的证据,表明它可能是一种有前途的新型骨架,可用于开发选择性 RyR 激活剂,用于治疗黑色素瘤和其他癌症类型。