Loss of SS18-SSX1 Inhibits Viability and Induces Apoptosis in Synovial Sarcoma

• Published in: Clinical orthopaedics and related research Vol. 472; no. 3; pp. 874 - 882
• Main Authors: Carmody Soni, Emily E., Schlottman, Silke, Erkizan, Hayriye V., Uren, Aykut, Toretsky, Jeffrey A.
• Format: Journal Article
• Language: English
• Published: Boston Springer US 01.03.2014; Lippincott Williams & Wilkins Ovid Technologies
• Subjects: Adult; Apoptosis; Basic Research; Caspase 3 - metabolism; Cell Line, Tumor; Cell Survival; Child; Conservative Orthopedics; Down-Regulation; Female; Gene Expression Regulation, Neoplastic; Gene Knockdown Techniques; Humans; Male; Medicine; Medicine & Public Health; Middle Aged; Neoplasm Proteins - genetics; Neoplasm Proteins - metabolism; Oncogene Proteins, Fusion - genetics; Oncogene Proteins, Fusion - metabolism; Orthopedics; Proto-Oncogene Proteins - genetics; Proto-Oncogene Proteins - metabolism; Repressor Proteins - genetics; Repressor Proteins - metabolism; RNA Interference; Sarcoma, Synovial - genetics; Sarcoma, Synovial - metabolism; Sarcoma, Synovial - pathology; Signal Transduction; Sports Medicine; Surgery; Surgical Orthopedics; Symposium: Musculoskeletal Tumor Society 2012 Symposium; Translocation, Genetic; Synovial Sarcoma Cell; Protein Partner; Splice Variant; Synovial Sarcoma; shRNA Construct
• ISSN: 0009-921X; 1528-1132
• DOI: 10.1007/s11999-013-3065-9

Background Most synovial sarcomas contain a chromosomal translocation t(X;18), which results in the formation of an oncoprotein SS18-SSX critical to the viability of synovial sarcoma. Questions/purposes We (1) established and characterized three novel synovial sarcoma cell lines and asked (2) whether inhibition of SS18-SSX1 decreases cell viability in these cell lines; and (3) whether reduction in viability after SS18-SSX1 knockdown is caused by apoptosis. After identifying a specific posttranscriptional splice variant in our cell lines, we asked (4) whether this provides a survival benefit in synovial sarcoma. Methods Cells lines were characterized. SS18-SSX1 knockdown was achieved using a shRNA system. Cell viability was assessed by WST-1 analysis and apoptosis examined by caspase-3 activity. Results We confirmed the SS18-SSX1 translocation in all cell lines and identified a consistent splicing variant. We achieved successful knockdown of SS18-SSX1 and with this saw a significant reduction in cell viability. Decreased viability was a result of increased apoptosis. Reintroduction of the exon 8 sequence into cells reduced cell viability in all cell lines. Conclusions We confirmed the presence of the SS18-SSX1 translocation in our cell lines and its importance in the survival of synovial sarcoma. We have also demonstrated that reduction in cell viability is related to an increase in apoptosis. In addition, we have identified a potential mediator of SS18-SSX function in exon 8. Clinical Relevance SS18-SSX represents a tumor-specific target in synovial sarcoma. Exploitation of SS18-SSX and its protein partners will allow us to develop potent tumor-specific therapeutic agents.