Activation of Wnt/β-Catenin in Ewing Sarcoma Cells Antagonizes EWS/ETS Function and Promotes Phenotypic Transition to More Metastatic Cell States

Cancer Res. 2016 Sep 1;76(17):5040-53. doi: 10.1158/0008-5472.CAN-15-3422. Epub 2016 Jun 30.

Abstract

Ewing sarcomas are characterized by the presence of EWS/ETS fusion genes in the absence of other recurrent genetic alterations and mechanisms of tumor heterogeneity that contribute to disease progression remain unclear. Mutations in the Wnt/β-catenin pathway are rare in Ewing sarcoma but the Wnt pathway modulator LGR5 is often highly expressed, suggesting a potential role for the axis in tumor pathogenesis. We evaluated β-catenin and LGR5 expression in Ewing sarcoma cell lines and tumors and noted marked intra- and inter-tumor heterogeneity. Tumors with evidence of active Wnt/β-catenin signaling were associated with increased incidence of tumor relapse and worse overall survival. Paradoxically, RNA sequencing revealed a marked antagonism of EWS/ETS transcriptional activity in Wnt/β-catenin-activated tumor cells. Consistent with this, Wnt/β-catenin-activated cells displayed a phenotype that was reminiscent of Ewing sarcoma cells with partial EWS/ETS loss of function. Specifically, activation of Wnt/β-catenin induced alterations to the actin cytoskeleton, acquisition of a migratory phenotype, and upregulation of EWS/ETS-repressed genes. Notably, activation of Wnt/β-catenin signaling led to marked induction of tenascin C (TNC), an established promoter of cancer metastasis, and an EWS/ETS-repressed target gene. Loss of TNC function in Ewing sarcoma cells profoundly inhibited their migratory and metastatic potential. Our studies reveal that heterogeneous activation of Wnt/β-catenin signaling in subpopulations of tumor cells contributes to phenotypic heterogeneity and disease progression in Ewing sarcoma. Significantly, this is mediated, at least in part, by inhibition of EWS/ETS fusion protein function that results in derepression of metastasis-associated gene programs. Cancer Res; 76(17); 5040-53. ©2016 AACR.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Blotting, Western
  • Bone Neoplasms / metabolism
  • Bone Neoplasms / pathology*
  • Calmodulin-Binding Proteins / metabolism
  • Cell Line, Tumor
  • Flow Cytometry
  • Heterografts
  • Humans
  • Immunohistochemistry
  • In Situ Hybridization
  • Mice
  • Mice, Inbred NOD
  • Mice, SCID
  • Oncogene Proteins, Fusion / metabolism
  • Phenotype
  • Polymerase Chain Reaction
  • Proto-Oncogene Protein c-ets-1 / metabolism
  • RNA-Binding Protein EWS
  • RNA-Binding Proteins / metabolism
  • Sarcoma, Ewing / metabolism
  • Sarcoma, Ewing / pathology*
  • Tissue Array Analysis
  • Transcriptome
  • Wnt Signaling Pathway / physiology*

Substances

  • Calmodulin-Binding Proteins
  • EWSR1 protein, human
  • Oncogene Proteins, Fusion
  • Proto-Oncogene Protein c-ets-1
  • RNA-Binding Protein EWS
  • RNA-Binding Proteins