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EWSR1-The Most Common Rearranged Gene in Soft Tissue Lesions, Which Also Occurs in Different Bone Lesions: An Updated Review.
Flucke, Uta; van Noesel, Max M; Siozopoulou, Vasiliki; Creytens, David; Tops, Bastiaan B J; van Gorp, Joost M; Hiemcke-Jiwa, Laura S.
Afiliação
  • Flucke U; Department of Pathology, Radboud University Medical Center, 6525 GA Nijmegen, The Netherlands.
  • van Noesel MM; Princess Máxima Center for Pediatric Oncology, 3584 CS Utrecht, The Netherlands.
  • Siozopoulou V; Princess Máxima Center for Pediatric Oncology, 3584 CS Utrecht, The Netherlands.
  • Creytens D; Division Cancer & Imaging, University Medical Center Utrecht, 3584 CX Utrecht, The Netherlands.
  • Tops BBJ; Department of Pathology, Antwerp University Hospital, 2650 Edegem, Belgium.
  • van Gorp JM; Department of Pathology, Ghent University Hospital, Ghent University, 9000 Ghent, Belgium.
  • Hiemcke-Jiwa LS; Princess Máxima Center for Pediatric Oncology, 3584 CS Utrecht, The Netherlands.
Diagnostics (Basel) ; 11(6)2021 Jun 15.
Article em En | MEDLINE | ID: mdl-34203801
ABSTRACT
EWSR1 belongs to the FET family of RNA-binding proteins including also Fused in Sarcoma (FUS), and TATA-box binding protein Associated Factor 15 (TAF15). As consequence of the multifunctional role of EWSR1 leading to a high frequency of transcription of the chromosomal region where the gene is located, EWSR1 is exposed to aberrations such as rearrangements. Consecutive binding to other genes leads to chimeric proteins inducing oncogenesis. The other TET family members are homologous. With the advent of widely used modern molecular techniques during the last decades, it has become obvious that EWSR1 is involved in the development of diverse benign and malignant tumors with mesenchymal, neuroectodermal, and epithelial/myoepithelial features. As oncogenic transformation mediated by EWSR1-fusion proteins leads to such diverse tumor types, there must be a selection on the multipotent stem cell level. In this review, we will focus on the wide variety of soft tissue and bone entities, including benign and malignant lesions, harboring EWSR1 rearrangement. Fusion gene analysis is the diagnostic gold standard in most of these tumors. We present clinicopathologic, immunohistochemical, and molecular features and discuss differential diagnoses.
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Texto completo: 1 Coleções: 01-internacional Temas: Geral Base de dados: MEDLINE Idioma: En Revista: Diagnostics (Basel) Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Holanda

Texto completo: 1 Coleções: 01-internacional Temas: Geral Base de dados: MEDLINE Idioma: En Revista: Diagnostics (Basel) Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Holanda