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National Institute of Environmental Health Sciences

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Publication Detail

Title: The Ews/Fli-1 fusion gene switches the differentiation program of neuroblastomas to Ewing sarcoma/peripheral primitive neuroectodermal tumors.

Authors: Rorie, Checo J; Thomas, Venetia D; Chen, Pengchin; Pierce, Heather Hanson; O'Bryan, John P; Weissman, Bernard E

Published In Cancer Res, (2004 Feb 15)

Abstract: Neuroblastoma (NB) and the Ewing sarcoma (ES)/peripheral primitive neuroectodermal tumor (PNET) family are pediatric cancers derived from neural crest cells. Although NBs display features of the sympathetic nervous system, ES/PNETs express markers consistent with parasympathetic differentiation. To examine the control of these differentiation markers, we generated NB x ES/PNET somatic cell hybrids. NB-specific markers were suppressed in the hybrids, whereas ES/PNET-specific markers were unaffected. These results suggested that the Ews/Fli-1 fusion gene, resulting from a translocation unique to ES/PNETs, might account for the loss of NB-specific markers. To test this hypothesis, we generated two different NB cell lines that stably expressed the Ews/Fli-1 gene. We observed that heterologous expression of the Ews/Fli-1 protein led to the suppression of NB-specific markers and de novo expression of ES/PNET markers. To determine the extent of changes in differentiation, we used the Affymetrix GeneChip Array system to observe global transcriptional changes of genes. This analysis revealed that the gene expression pattern of the Ews/Fli-1-expressing NB cells resembled that observed in pooled ES/PNET cell lines and differed significantly from the NB parental cells. Therefore, we propose that Ews/Fli-1 contributes to the etiology of ES/PNET by subverting the differentiation program of its neural crest precursor cell to a less differentiated and more proliferative state.

PubMed ID: 14973077 Exiting the NIEHS site

MeSH Terms: Adaptor Proteins, Signal Transducing*; Cell Differentiation; Cell Line, Tumor; Humans; Neuroblastoma/pathology*; Neuroectodermal Tumors, Primitive, Peripheral/pathology*; Oligonucleotide Array Sequence Analysis; Oncogene Proteins, Fusion/genetics*; Proteins/genetics; Proto-Oncogene Protein c-fli-1; RNA-Binding Protein EWS; Sarcoma, Ewing/pathology*; Shc Signaling Adaptor Proteins; Src Homology 2 Domain-Containing, Transforming Protein 1; Transcription Factors/genetics*

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