Department of Human Genetics and Biochemistry, Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv 69978, Israel.
Rappaport Faculty of Medicine and Research Institute, Technion-Israel Institute of Technology, Haifa 31096, Israel.
Mol Cell. 2015 Aug 20;59(4):664-76. doi: 10.1016/j.molcel.2015.06.028. Epub 2015 Jul 30.
The most critical stage in initiation of melanoma metastasis is the radial to vertical growth transition, yet the triggers of this transition remain elusive. We suggest that the microenvironment drives melanoma metastasis independently of mutation acquisition. Here we examined the changes in microenvironment that occur during melanoma radial growth. We show that direct contact of melanoma cells with the remote epidermal layer triggers vertical invasion via Notch signaling activation, the latter serving to inhibit MITF function. Briefly, within the native Notch ligand-free microenvironment, MITF, the melanocyte lineage master regulator, binds and represses miR-222/221 promoter in an RBPJK-dependent manner. However, when radial growth brings melanoma cells into contact with distal differentiated keratinocytes that express Notch ligands, the activated Notch intracellular domain impairs MITF binding to miR-222/221 promoter. This de-repression of miR-222/221 expression triggers initiation of invasion. Our findings may direct melanoma prevention opportunities via targeting specific microenvironments.
黑色素瘤转移启动的最关键阶段是横向到垂直生长的转变,但这一转变的触发因素仍难以捉摸。我们认为,微环境独立于突变的获取驱动黑色素瘤转移。在这里,我们检查了黑色素瘤横向生长过程中微环境的变化。我们发现,黑色素瘤细胞与远处表皮层的直接接触通过 Notch 信号激活触发垂直入侵,后者用于抑制 MITF 功能。简而言之,在天然的 Notch 配体缺乏的微环境中,黑素细胞谱系主调控因子 MITF 通过 RBPJK 依赖性方式结合并抑制 miR-222/221 启动子。然而,当横向生长使黑色素瘤细胞与表达 Notch 配体的远端分化角蛋白细胞接触时,激活的 Notch 细胞内结构域会损害 MITF 与 miR-222/221 启动子的结合。miR-222/221 表达的这种去抑制触发了入侵的开始。我们的发现可能通过靶向特定的微环境为黑色素瘤预防提供机会。