## Abstract Synovial sarcoma is an aggressive soft tissue tumor that is characterized cytogenetically by the t(X;18)(p11;q11) translocation, resulting in fusion between the __SS18__ gene on chromosome 18 and one of the __SSX__ genes on the X chromosome. The three fusion genes that have been detecte
Gene expression profiles relate to SS18/SSX fusion type in synovial sarcoma
✍ Scribed by Josefin Fernebro; Princy Francis; Patrik Edén; Åke Borg; Ioannis Panagopoulos; Fredrik Mertens; Johan Vallon-Christersson; Måns Åkerman; Anders Rydholm; Henrik CF Bauer; Nils Mandahl; Mef Nilbert
- Publisher
- John Wiley and Sons
- Year
- 2005
- Tongue
- French
- Weight
- 301 KB
- Volume
- 118
- Category
- Article
- ISSN
- 0020-7136
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✦ Synopsis
Abstract
We applied 27k spotted cDNA microarray slides to assess gene expression profiles in 26 samples from 24 patients with synovial sarcomas (SS). The data were analyzed in relation to histopathologic type, cytogenetic aberrations, gene fusion type and development of distant metastases. Supervised analysis based on gene fusion type in 12 SS with SS18/SSX1 and 9 with SS18/SSX2 revealed significant differences in gene expression profiles. Among the discriminators were several genes that have previously been found to be upregulated in SS, including AXL, ZIC2, SPAG7, AGRN, FOXC1, NCAM1 and multiple metallothioneins. Histopathology and degree of cytogenetic complexity did not significantly influence expression, whereas a genetic signature that related to development of metastases could be discerned, albeit with a high false‐positive rate. In conclusion, our findings demonstrate differentially expressed genes for the 2 major gene fusion variants in SS, SS18/SSX1 and SS18/SSX2, and thereby suggest that these result in different downstream effects. © 2005 Wiley‐Liss, Inc.
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