Publication: Are EWSR1-NFATc2-positive sarcomas really Ewing sarcomas?
dc.contributor.author | Baldauf, Michaela C | |
dc.contributor.author | Gerke, Julia S | |
dc.contributor.author | Orth, Martin F | |
dc.contributor.author | Dallmayer, Marlene | |
dc.contributor.author | Baumhoer, Daniel | |
dc.contributor.author | de-Alava, Enrique | |
dc.contributor.author | Hartmann, Wolfgang | |
dc.contributor.author | Kirchner, Thomas | |
dc.contributor.author | Grünewald, Thomas G P | |
dc.date.accessioned | 2023-01-25T10:11:21Z | |
dc.date.available | 2023-01-25T10:11:21Z | |
dc.date.issued | 2018-06-12 | |
dc.description.abstract | Recently, Charville et al. [1] reported that EWSR1-rearranged fusion proteins mediate the expression of the paired-box transcription factor PAX7 in Ewing sarcoma. Based on an analysis of a published gene expression microarray dataset (accession code GSE60740), they state having identified PAX7 to be significantly overexpressed in Ewing sarcoma in comparison to CIC-DUX4-positive round cell sarcomas [1]. In that microarray analysis they compared CIC-DUX4-positive sarcomas with EWSR1-NFATc2-positive sarcomas, assuming that EWSR1-NFATc2-positive sarcomas belong to the family of Ewing sarcomas [1], which are typically characterized by EWSR1-ETS fusion oncogenes [2]. Accordingly, Charville et al. [1] summarized in a schematic EWSR1-FLI1-, EWSR1-ERG-, and EWSR1-NFATc2-positive sarcomas as “Ewing sarcoma,” referring to Szuhai et al. (2009) [3], and did not take into account more recent reports in the literature that EWSR1-NFATc2-positive sarcomas may constitute an own entity [2]. Comparison of the dataset (GSE60740) used by Charville et al. to a published transcriptome reference dataset of genetically defined EWSR1-ETS-positive Ewing sarcomas (GSE34620) [4] and 13 other malignancies that may constitute morphological mimics [5] shows that EWSR1-NFATc2-positive sarcomas do not cluster with any other analyzed tumor entity including EWSR1-ETS-positive Ewing sarcoma | |
dc.description.version | Si | |
dc.identifier.citation | Baldauf MC, Gerke JS, Orth MF, Dallmayer M, Baumhoer D, de Alava E, et al. Are EWSR1-NFATc2-positive sarcomas really Ewing sarcomas? Mod Pathol. 2018 Jun;31(6):997-999. | |
dc.identifier.doi | 10.1038/s41379-018-0009-7 | |
dc.identifier.essn | 1530-0285 | |
dc.identifier.pmid | 29895896 | |
dc.identifier.unpaywallURL | https://www.nature.com/articles/s41379-018-0009-7.pdf | |
dc.identifier.uri | http://hdl.handle.net/10668/12582 | |
dc.issue.number | 6 | |
dc.journal.title | Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc | |
dc.journal.titleabbreviation | Mod Pathol | |
dc.language.iso | en | |
dc.organization | Instituto de Biomedicina de Sevilla-IBIS | |
dc.organization | Hospital Universitario Virgen del Rocío | |
dc.page.number | 997-999 | |
dc.provenance | Realizada la curación de contenido 13/03/2025 | |
dc.publisher | Elsevier BV | |
dc.pubmedtype | Letter | |
dc.pubmedtype | Comment | |
dc.relation.publisherversion | https://linkinghub.elsevier.com/retrieve/pii/S0893-3952(22)01501-0 | |
dc.rights.accessRights | Restricted Access | |
dc.subject | Transcriptome | |
dc.subject | Neoplasms, Connective Tissue | |
dc.subject | Skin Neoplasms | |
dc.subject | Oncogenes | |
dc.subject | Microarray Analysis | |
dc.subject.decs | Sarcoma | |
dc.subject.decs | Conjunto de datos | |
dc.subject.decs | Neoplasias | |
dc.subject.decs | Informe de investigación | |
dc.subject.decs | Proteínas | |
dc.subject.decs | Oncogenes | |
dc.subject.decs | Análisis por micromatrices | |
dc.subject.decs | Transcriptoma | |
dc.subject.decs | Expresión génica | |
dc.subject.decs | Células | |
dc.subject.mesh | Humans | |
dc.subject.mesh | NFATC Transcription Factors | |
dc.subject.mesh | PAX7 Transcription Factor | |
dc.subject.mesh | RNA-Binding Protein EWS | |
dc.subject.mesh | Sarcoma, Ewing | |
dc.title | Are EWSR1-NFATc2-positive sarcomas really Ewing sarcomas? | |
dc.type | letter | |
dc.type.hasVersion | VoR | |
dc.volume.number | 31 | |
dspace.entity.type | Publication |
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