A morphologic and molecular reappraisal of myoepithelial tumors of soft tissue, bone, and viscera with EWSR1 and FUS gene rearrangements.


Journal

Genes, chromosomes & cancer
ISSN: 1098-2264
Titre abrégé: Genes Chromosomes Cancer
Pays: United States
ID NLM: 9007329

Informations de publication

Date de publication:
06 2020
Historique:
received: 18 01 2020
revised: 21 01 2020
accepted: 22 01 2020
pubmed: 30 1 2020
medline: 9 2 2021
entrez: 30 1 2020
Statut: ppublish

Résumé

Myoepithelial tumors (MET) represent a clinicopathologically heterogeneous group of tumors, ranging from benign to highly aggressive lesions. Although MET arising in soft tissue, bone, or viscera share morphologic and immunophenotypic overlap with their salivary gland and cutaneous counterparts, there is still controversy regarding their genetic relationship. Half of MET of soft tissue and bone harbor EWSR1 or FUS related fusions, while MET arising in the salivary gland and skin often show PLAG1 and HMGA2 gene rearrangements. Regardless of the site of origin, the gold standard in diagnosing a MET relies on demonstrating its "myoepithelial immunophenotype" of positivity for EMA/CK and S100 protein or GFAP. However, the morphologic spectrum of MET in soft tissue and bone is quite broad and the above immunoprofile is nonspecific, being shared by other pathogenetically unrelated neoplasms. Moreover, rare MET lack a diagnostic immunoprofile but shows instead the characteristic gene fusions. In this study, we analyzed a large cohort of 66 MET with EWSR1 and FUS gene rearrangements spanning various clinical presentations, to better define their morphologic spectrum and establish relevant pathologic-molecular correlations. Genetic analysis was carried out by FISH for EWSR1/FUS rearrangements and potential partners, and/or by targeted RNA sequencing. Then, 82% showed EWSR1 rearrangement, while 18% had FUS abnormalities. EWSR1-POU5F1 occurred with predilection in malignant MET in children and young adults and these tumors had nested epithelioid morphology and clear cytoplasm. In contrast, EWSR1/FUS-PBX1/3 fusions were associated with benign and sclerotic spindle cell morphology. Tumors with EWSR1-KLF17 showed chordoma-like morphology. Our results demonstrate striking morphologic-molecular correlations in MET of bone, soft tissue and viscera, which might have implications in their clinical behavior.

Identifiants

pubmed: 31994243
doi: 10.1002/gcc.22835
pmc: PMC7170037
mid: NIHMS1578502
doi:

Substances chimiques

EWSR1 protein, human 0
FUS protein, human 0
KLF17 protein, human 0
Octamer Transcription Factor-3 0
POU5F1 protein, human 0
RNA-Binding Protein EWS 0
RNA-Binding Protein FUS 0
Transcription Factors 0

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

348-356

Subventions

Organisme : National Cancer Institute (Cycle for Survival)
ID : P50 CA140146-01
Pays : International
Organisme : NCI NIH HHS
ID : P30 CA008748
Pays : United States
Organisme : NCI NIH HHS
ID : P50 CA217694
Pays : United States
Organisme : NCI NIH HHS
ID : P50 CA140146
Pays : United States

Informations de copyright

© 2020 Wiley Periodicals, Inc.

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Auteurs

Albert J H Suurmeijer (AJH)

Department of Pathology and Medical Biology, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.

Brendan C Dickson (BC)

Department of Pathology & Laboratory Medicine, Mount Sinai Hospital, Toronto, Canada.

David Swanson (D)

Department of Pathology & Laboratory Medicine, Mount Sinai Hospital, Toronto, Canada.

Lei Zhang (L)

Department of Pathology, Memorial Sloan Kettering Cancer Center, New York, New York.

Yun-Shao Sung (YS)

Department of Pathology, Memorial Sloan Kettering Cancer Center, New York, New York.

Christopher D Fletcher (CD)

Department of Pathology, Brigham and Women's Hospital, Boston, Massachusetts.

Cristina R Antonescu (CR)

Department of Pathology, Memorial Sloan Kettering Cancer Center, New York, New York.

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Classifications MeSH