Detection of SYT-SSX1/2 fusion transcripts by reverse transcriptase- polymerase chain reaction (RT-PCR) is a valuable diagnostic tool in synovial sarcoma
Publikation: Beitrag in Fachzeitschrift › Forschungsartikel › Beigetragen › Begutachtung
Beitragende
Abstract
Cytogenetically, most synovial sarcomas are characterised by a specific chromosomal translocation [(X;18)(p11.2;q11.2)], which results in the generation of fusion transcripts comprising SYT (18q11) and either SSX1 or SSX2 (Xp11) sequences. By using a sensitive reverse transcriptase-polymerase chain reaction (RT-PCR) protocol, specific SYT-SSX1/2 fusion transcripts were detected in 10 histopathologically confirmed synovial sarcomas. Control tumours with morphological spindle cell patterns mimicking monophasic synovial sarcoma tested negative (18/19) in the RT-PCR protocol, with the exception of one spindle cell sarcoma originally classified as a fibrosarcoma. Furthermore, the established RT-PCR protocol was used to evaluate the feasibility of SYT-SSX1/2 fusion transcript detection for minimal residual disease analysis. Analyses of surgical margins revealed a fusion transcript in two of four operations for synovial sarcoma analysed, one of which was diagnosed with turnout free margins by conventional histopathology. These data suggest that the RT-PCR amplification of SYT- SSX1/2 fusion transcripts is a valuable tool in the differentiation of synovial sarcomas, especially in cases of equivocal morphology. Additionally, the RT-PCR approach may be used for the detection of residual tumour cells in synovial sarcoma patients.
Details
Originalsprache | Englisch |
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Seiten (von - bis) | 2087-2093 |
Seitenumfang | 7 |
Fachzeitschrift | European journal of cancer |
Jahrgang | 34 |
Ausgabenummer | 13 |
Publikationsstatus | Veröffentlicht - Dez. 1998 |
Peer-Review-Status | Ja |
Extern publiziert | Ja |
Externe IDs
PubMed | 10070316 |
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Schlagworte
Ziele für nachhaltige Entwicklung
ASJC Scopus Sachgebiete
Schlagwörter
- Minimal residual disease, RT-PCR, Sarcoma, SYT-SSX1/2, Translocation