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Undifferentiated small round cell sarcoma in a young male: a case report
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 ro...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6996518/ https://www.ncbi.nlm.nih.gov/pubmed/32014859 http://dx.doi.org/10.1101/mcs.a004812 |
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author | 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 |
author_facet | 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 |
author_sort | Ricker, Cora A. |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-6996518 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Cold Spring Harbor Laboratory Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-69965182020-02-14 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 Cold Spring Harb Mol Case Stud Research Article 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. Cold Spring Harbor Laboratory Press 2020-02 /pmc/articles/PMC6996518/ /pubmed/32014859 http://dx.doi.org/10.1101/mcs.a004812 Text en © 2020 Ricker et al.; Published by Cold Spring Harbor Laboratory Press http://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial License (http://creativecommons.org/licenses/by-nc/4.0/) , which permits reuse and redistribution, except for commercial purposes, provided that the original author and source are credited. |
spellingShingle | Research Article 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 Undifferentiated small round cell sarcoma in a young male: a case report |
title | Undifferentiated small round cell sarcoma in a young male: a case report |
title_full | Undifferentiated small round cell sarcoma in a young male: a case report |
title_fullStr | Undifferentiated small round cell sarcoma in a young male: a case report |
title_full_unstemmed | Undifferentiated small round cell sarcoma in a young male: a case report |
title_short | Undifferentiated small round cell sarcoma in a young male: a case report |
title_sort | undifferentiated small round cell sarcoma in a young male: a case report |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6996518/ https://www.ncbi.nlm.nih.gov/pubmed/32014859 http://dx.doi.org/10.1101/mcs.a004812 |
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