Description
Clear cell sarcoma (CCS) is an aggressive soft tissue malignant tumor characterized by a unique t(12; 22) translocation, leading to the expression of a chimeric EWS/ATF1 fusion gene.  However, little is known about the mechanisms underlying how EWS/ATF1 is involved in the development of CCSs.  In addition, the cells of origin for CCSs remain to be determined.  We generated EWS/ATF1-inducible mice, and examined the effects of EWS/ATF1 expression in adult cells.  We show that the forced expression of EWS/ATF1 results in the development of EWS/ATF1-dependent sarcomas in mice.  The histology of EWS/ATF1-induced sarcomas resembles that of CCSs and EWS/ATF1-induced tumor cells express CCS-markers, such as S100, Sox10, and Mitf.  A lineage tracing experiment revealed that such sarcomas are derived from neural crest-lineage cells.  Finally, we found that EWS/ATF1 directly induces Fos in an ERK-independent manner, and demonstrated that the increased Fos expression is important for the active cell proliferation in not only EWS/ATF1-induced sarcomas, but also in human CCSs.  Our results indicate that FOS, as well as EWS/ATF1 itself, could be a promising therapeutic target for the treatment of EWS/ATF1-related sarcomas.