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Undifferentiated small round cell sarcoma in a young male: a case report.
Ricker, Cora A; Berlow, Noah E; Crawford, Kenneth A; Georgopapadakos, Todd; Huelskamp, Audrey N; Woods, Andrew D; Dhimolea, Eugen; Ramkissoon, Shakti H; Spunt, Sheri L; Rudzinski, Erin R; Keller, Charles.
Afiliação
  • Ricker CA; Children's Cancer Therapy Development Institute, Beaverton, Oregon 97005, USA.
  • Berlow NE; Children's Cancer Therapy Development Institute, Beaverton, Oregon 97005, USA.
  • Crawford KA; Children's Cancer Therapy Development Institute, Beaverton, Oregon 97005, USA.
  • Georgopapadakos T; Children's Cancer Therapy Development Institute, Beaverton, Oregon 97005, USA.
  • Huelskamp AN; Children's Cancer Therapy Development Institute, Beaverton, Oregon 97005, USA.
  • Woods AD; Children's Cancer Therapy Development Institute, Beaverton, Oregon 97005, USA.
  • Dhimolea E; Dana-Farber Cancer Institute, Boston, Massachusetts 02215, USA.
  • Ramkissoon SH; Foundation Medicine Inc., Cambridge, Massachusetts 02141, USA.
  • Spunt SL; Department of Pediatrics, Stanford University School of Medicine, Palo Alto, California 94304, USA.
  • Rudzinski ER; Seattle Children's Hospital, Seattle, Washington 98105, USA.
  • Keller C; Children's Cancer Therapy Development Institute, Beaverton, Oregon 97005, USA.
Article em En | MEDLINE | ID: mdl-32014859
CIC-rearranged sarcomas (CRSs) have recently been characterized as a distinct sarcoma subgroup with a less favorable prognosis compared to other small round cell sarcomas. CRSs share morphologic features with Ewing's sarcoma and prior to 2013 were grouped under undifferentiated sarcomas with round cell phenotype by the WHO classification. In this report, whole-genome sequencing and RNA sequencing were performed for an adolescent male patient with CRS who was diagnosed with undifferentiated pleomorphic sarcoma (UPS) by three contemporary institutions. Somatic mutation analysis identified mutations in IQGAP1, CCNC, and ATXN1L in pre- and post-treatment tissue samples, as well as a CIC-DUX4 fusion that was confirmed by qPCR and DUX4 immunohistochemistry. Of particular interest was the overexpression of the translation factor eEF1A1, which has oncogenic properties and has recently been identified as a target of the investigational agent plitidepsin. This case may provide a valuable waypoint in the understanding and classification of CRSs and may provide a rationale for targeting eEF1A1 in similar soft tissue sarcoma cases.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Sarcoma de Células Pequenas Tipo de estudo: Etiology_studies / Prognostic_studies Limite: Child / Humans / Male Idioma: En Revista: Cold Spring Harb Mol Case Stud Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Sarcoma de Células Pequenas Tipo de estudo: Etiology_studies / Prognostic_studies Limite: Child / Humans / Male Idioma: En Revista: Cold Spring Harb Mol Case Stud Ano de publicação: 2020 Tipo de documento: Article