Abstract

Numerous molecular abnormalities contribute to the genetic derangements involved in tumorigenesis. Chromosomal translocations are a frequent source of these derangements, producing unique fusion proteins with novel oncogenic properties. EWS/ETS fusions in Ewing sarcoma are a prime example of this, resulting in potent chimeric oncoproteins with novel biological properties and a unique transcriptional signature essential for oncogenesis. Recent evidence demonstrates that EWS/FLI, the most common EWS/ETS fusion in Ewing sarcoma, upregulates gene expression using a GGAA microsatellite response element dispersed throughout the human genome. These GGAA microsatellites function as enhancer elements, are sites of epigenetic regulation and are necessary for EWS/FLI DNA binding and upregulation of principal oncogenic targets. An increasing number of GGAA motifs appear to substantially enhance EWS/FLI-mediated gene expression, which has compelling biological implications as these GGAA microsatellites are highly polymorphic within and between ethnically distinct populations. Historically regarded as junk DNA, this emerging evidence clearly demonstrates that microsatellite DNA plays an instrumental role in EWS/FLI-mediated transcriptional regulation and oncogenesis in Ewing sarcoma. This unprecedented role of GGAA microsatellite DNA in Ewing sarcoma provides a unique opportunity to expand our mechanistic understanding of how EWS/ETS fusions influence cancer susceptibility, prognosis and transcriptional regulation.

Highlights

  • Aberrant chromosomal translocations are common observations in cancer and in many instances these events give rise to chimeric fusion products with novel biological and cellular functions

  • Given the mechanistic importance of GGAA microsatellites in EWS/FLI-mediated gene regulation, we hypothesized that polymorphic GGAA microsatellites within and between ethnically distinct human populations may exist, providing a potential explanation for the aforementioned patterns of Ewing sarcoma susceptibility and prognosis

  • Results from this study demonstrated that the NR0B1 and CAV1 GGAA microsatellites were highly polymorphic in both European and African populations

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Summary

Introduction

Aberrant chromosomal translocations are common observations in cancer and in many instances these events give rise to chimeric fusion products with novel biological and cellular functions. Many of these chimeric fusion proteins function as oncogenic transcription factors, essential for cellular transformation and/or critical malignant cellular phenotypes [1,2]. All Ewing sarcoma tumors harbor a somatic translocation, fusing the EWSR1 gene (encoding the EWS protein) on chromosome 22 with a member of the ETS family of transcription factors, most commonly FLI1 (encoding the FLI protein), located on chromosome 11 [t(11;22)(q24;q12)]. ¶-EWSR1 SUREHV UHG DQG¶-EWSR1 probes (green) detect the presence of a chromosomal rearrangement; when the red and green probes are split into two distinct signals (white arrows) a chromosomal rearrangement is identified, whereas an orange signal indicates an intact EWSR1 locus

ETS Family of Transcription Factors
Microsatellite DNA in Cancer Pathogenesis
Findings
10. Conclusions
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