Katschnig A M, Kauer M O, Schwentner R, Tomazou E M, Mutz C N, Linder M, Sibilia M, Alonso J, Aryee D N T, Kovar H
Children's Cancer Research Institute, St Anna Kinderkrebsforschung, Vienna, Austria.
Institute of Cancer Research, Medical University Vienna, Vienna, Austria.
Oncogene. 2017 Oct 26;36(43):5995-6005. doi: 10.1038/onc.2017.202. Epub 2017 Jul 3.
Ewing sarcoma (EWS) is a paediatric bone cancer with high metastatic potential. Cellular plasticity resulting from dynamic cytoskeletal reorganization, typically regulated via the Rho pathway, is a prerequisite for metastasis initiation. Here, we interrogated the role of the Ewing sarcoma driver oncogene EWS-FLI1 in cytoskeletal reprogramming. We report that EWS-FLI1 strongly represses the activity of the Rho-F-actin signal pathway transcriptional effector MRTFB, affecting the expression of a large number of EWS-FLI1-anticorrelated genes including structural and regulatory cytoskeletal genes. Consistent with this finding, chromatin immunoprecipitation sequencing (ChIP-seq) revealed strong overlaps in myocardin-related transcription factor B (MRTFB) and EWS-FLI1 chromatin occupation, especially for EWS-FLI1-anticorrelated genes. Binding of the transcriptional co-activator Yes-associated protein (YAP)-1, enrichment of TEAD-binding motifs in these shared genomic binding regions and overlapping transcriptional footprints of MRTFB and TEAD factors led us to propose synergy between MRTFB and the YAP/TEAD complex in the regulation of EWS-FLI1-anticorrelated genes. We propose that EWS-FLI1 suppresses the Rho-actin pathway by perturbation of a MRTFB/YAP-1/TEAD transcriptional module, which directly affects the actin-autoregulatory feedback loop. As spontaneous fluctuations in EWS-FLI1 levels of Ewing sarcoma cells in vitro and in vivo, associated with a switch between a proliferative, non-migratory EWS-FLI1-high and a non-proliferative highly migratory EWS-FLI1-low state, were recently described, our data provide a mechanistic basis for the underlying EWS-FLI1-dependent reversible cytoskeletal reprogramming of Ewing sarcoma cells.
尤因肉瘤(EWS)是一种具有高转移潜能的儿科骨癌。由动态细胞骨架重组导致的细胞可塑性通常通过Rho途径调控,是转移起始的先决条件。在此,我们探究了尤因肉瘤驱动癌基因EWS-FLI1在细胞骨架重编程中的作用。我们报告称,EWS-FLI1强烈抑制Rho-F-肌动蛋白信号通路转录效应因子MRTFB的活性,影响大量与EWS-FLI1呈反相关基因的表达,包括结构和调节性细胞骨架基因。与此发现一致,染色质免疫沉淀测序(ChIP-seq)揭示了心肌素相关转录因子B(MRTFB)和EWS-FLI1在染色质占据上有强烈重叠,特别是对于与EWS-FLI1呈反相关的基因。转录共激活因子Yes相关蛋白(YAP)-1的结合、这些共享基因组结合区域中TEAD结合基序的富集以及MRTFB和TEAD因子重叠的转录足迹,使我们提出MRTFB与YAP/TEAD复合物在调控与EWS-FLI1呈反相关基因方面存在协同作用。我们提出EWS-FLI1通过干扰MRTFB/YAP-1/TEAD转录模块来抑制Rho-肌动蛋白途径,这直接影响肌动蛋白的自调节反馈环。由于最近描述了尤因肉瘤细胞在体外和体内EWS-FLI1水平的自发波动,这与增殖性、非迁移性的EWS-FLI1高状态和非增殖性、高迁移性的EWS-FLI1低状态之间的转换有关,我们的数据为尤因肉瘤细胞潜在的EWS-FLI1依赖性可逆细胞骨架重编程提供了机制基础。