Extraskeletal myxoid chondrosarcoma (EMC) is a very rare sarcoma most often arising in the soft tissue. Rare EMC of the bone have been reported. EMC exhibits distinctive clinico-pathological and genetic features; however, despite the name, it lacks any feature of cartilaginous differentiation. EMC is characterized by the rearrangement of the NR4A3, which, in most cases (about 62-75%), is fused with EWSR1 and less frequently with other partners, including TAF15 (27%), TCF12 (4%), TFG, and FUS. We herein report the identification by whole-transcriptome sequencing of HSPA8 as a novel fusion partner of NR4A3 in a case of EMC. FISH analysis confirmed the presence of a genomic HSPA8-NR4A3 translocation in the vast majority of tumor cells. Our findings expand the spectrum of NR4A3 fusion partners involved in EMC pathobiology.

HSPA8 as a novel fusion partner of NR4A3 in extraskeletal myxoid chondrosarcoma / M. Urbini, A. Astolfi, M.A. Pantaleo, S. Serravalle, A.P. Dei Tos, P. Picci, V. Indio, M. Sbaraglia, S. Benini, A. Righi, M. Gambarotti, A. Gronchi, C. Colombo, G.P. Dagrada, S. Pilotti, R. Maestro, M. Polano, M. Saponara, G. Tarantino, A. Pession, G. Biasco, P.G. Casali, S. Stacchiotti. - In: GENES, CHROMOSOMES & CANCER. - ISSN 1045-2257. - 56:7(2017), pp. 582-586. [10.1002/gcc.22462]

HSPA8 as a novel fusion partner of NR4A3 in extraskeletal myxoid chondrosarcoma

P.G. Casali;S. Stacchiotti
2017

Abstract

Extraskeletal myxoid chondrosarcoma (EMC) is a very rare sarcoma most often arising in the soft tissue. Rare EMC of the bone have been reported. EMC exhibits distinctive clinico-pathological and genetic features; however, despite the name, it lacks any feature of cartilaginous differentiation. EMC is characterized by the rearrangement of the NR4A3, which, in most cases (about 62-75%), is fused with EWSR1 and less frequently with other partners, including TAF15 (27%), TCF12 (4%), TFG, and FUS. We herein report the identification by whole-transcriptome sequencing of HSPA8 as a novel fusion partner of NR4A3 in a case of EMC. FISH analysis confirmed the presence of a genomic HSPA8-NR4A3 translocation in the vast majority of tumor cells. Our findings expand the spectrum of NR4A3 fusion partners involved in EMC pathobiology.
Chondrosarcoma; DNA-Binding Proteins; Female; Groin; HSC70 Heat-Shock Proteins; Humans; In Situ Hybridization, Fluorescence; Middle Aged; Neoplasms, Connective and Soft Tissue; Oncogene Proteins, Fusion; Receptors, Steroid; Receptors, Thyroid Hormone; Tomography, X-Ray Computed; Genetics; Cancer Research
Settore MED/06 - Oncologia Medica
2017
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/555614
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