Stueven Noah A, Schlaeger Nicholas M, Monte Aaron P, Hwang Sheng-Ping L, Huang Cheng-Chen
Biology Department, University of Wisconsin-River Falls, River Falls, WI 54022, United States.
Department of Chemistry and Biochemistry, University of Wisconsin-La Crosse, La Crosse, WI 54601, United States.
Toxicol Appl Pharmacol. 2017 Dec 15;337:30-38. doi: 10.1016/j.taap.2017.10.008. Epub 2017 Oct 16.
Melanoma is the most aggressive form of skin cancer. Current challenges to melanoma therapy include the adverse effects from immunobiologics, resistance to drugs targeting the MAPK pathway, intricate interaction of many signal pathways, and cancer heterogeneity. Thus combinational therapy with drugs targeting multiple signaling pathways becomes a new promising therapy. Here, we report a family of stilbene-like compounds called A11 that can inhibit melanoma growth in both melanoma-forming zebrafish embryos and mouse melanoma cells. The growth inhibition by A11 is a result of mitosis reduction but not apoptosis enhancement. Meanwhile, A11 activates both MAPK and Akt signaling pathways. Many A11-treated mouse melanoma cells exhibit morphological changes and resemble normal melanocytes. Furthermore, we found that A11 causes down-regulation of melanocyte differentiation genes, including Pax3 and MITF. Together, our results suggest that A11 could be a new melanoma therapeutic agent by inhibiting melanocyte differentiation and proliferation.
黑色素瘤是皮肤癌中最具侵袭性的形式。目前黑色素瘤治疗面临的挑战包括免疫生物制剂的不良反应、对靶向MAPK通路药物的耐药性、众多信号通路的复杂相互作用以及癌症异质性。因此,使用靶向多种信号通路的药物进行联合治疗成为一种新的有前景的治疗方法。在此,我们报告了一类称为A11的芪样化合物,它们能够在形成黑色素瘤的斑马鱼胚胎和小鼠黑色素瘤细胞中抑制黑色素瘤的生长。A11对生长的抑制是有丝分裂减少而非凋亡增强的结果。同时,A11激活MAPK和Akt信号通路。许多经A11处理的小鼠黑色素瘤细胞表现出形态变化,类似于正常黑素细胞。此外,我们发现A11导致黑素细胞分化基因(包括Pax3和MITF)的下调。总之,我们的结果表明,A11可能通过抑制黑素细胞分化和增殖成为一种新的黑色素瘤治疗药物。