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A novel fusion gene, SS18L1/SSX1, in synovial sarcoma

Storlazzi, Tiziana LU ; Mertens, Fredrik LU ; Mandahl, Nils LU ; Gisselsson, David LU ; Isaksson, Margareth LU ; Gustafson, Pelle LU ; Domanski, Henryk A LU and Panagopoulos, Ioannis LU (2003) In Genes, Chromosomes and Cancer 37(2). p.195-200
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 detected thus far, SS18/SSX1, SS18/SSX2, and SS18/SSX4, account for more than 95% of the synovial sarcomas. Because SS18/SSX fusions do not seem to occur in other tumor types, and because synovial sarcomas may sometimes be difficult to distinguish from other spindle cell tumors, molecular genetic analysis has become established as an important diagnostic tool. Upon cytogenetic analysis of a soft-tissue tumor that showed classic synovial sarcoma morphology, we detected... (More)

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 detected thus far, SS18/SSX1, SS18/SSX2, and SS18/SSX4, account for more than 95% of the synovial sarcomas. Because SS18/SSX fusions do not seem to occur in other tumor types, and because synovial sarcomas may sometimes be difficult to distinguish from other spindle cell tumors, molecular genetic analysis has become established as an important diagnostic tool. Upon cytogenetic analysis of a soft-tissue tumor that showed classic synovial sarcoma morphology, we detected two supernumerary marker chromosomes but no rearrangement of chromosomes X or 18. By fluorescence in situ hybridization, the marker chromosomes were shown to contain material from chromosomes X and 20, including the SSX gene cluster on the X chromosome and the SS18L1 gene, which shows strong homology with the SS18 gene, on chromosome 20. Further RT-PCR analysis and sequencing of the amplified products revealed a novel SS18L1/SSX1 fusion transcript in which nucleotide 1216 (exon 10) of SS18L1 was fused in-frame with nucleotide 422 (exon 6) of SSX1. Thus, the existence of genetic heterogeneity has to be taken into account when RT-PCR is used for the diagnosis of synovial sarcoma.

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published
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keywords
Adult, Amino Acid Sequence, Base Sequence, Chromosomes, Human, Pair 20, Chromosomes, Human, X, Humans, Leg, Male, Molecular Sequence Data, Neoplasm Proteins, Oncogene Proteins, Fusion, Proteins, Proto-Oncogene Proteins, Repressor Proteins, Sarcoma, Synovial, Sequence Homology, Nucleic Acid, Translocation, Genetic, Tumor Cells, Cultured, Case Reports, Journal Article, Research Support, Non-U.S. Gov't
in
Genes, Chromosomes and Cancer
volume
37
issue
2
pages
6 pages
publisher
John Wiley & Sons Inc.
external identifiers
  • pmid:12696068
  • wos:000182648800010
  • scopus:0037732860
  • pmid:12696068
ISSN
1045-2257
DOI
10.1002/gcc.10210
language
English
LU publication?
yes
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The information about affiliations in this record was updated in December 2015. The record was previously connected to the following departments: Department of Orthopaedics (Lund) (013028000), Division of Clinical Genetics (013022003), Pathology, (Lund) (013030000)
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d2586c7c-9a79-4d2d-82ac-a16780b18dcf (old id 113382)
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http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=12696068&dopt=Abstract
date added to LUP
2016-04-01 12:10:24
date last changed
2022-02-18 18:55:15
@article{d2586c7c-9a79-4d2d-82ac-a16780b18dcf,
  abstract     = {{<p>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 detected thus far, SS18/SSX1, SS18/SSX2, and SS18/SSX4, account for more than 95% of the synovial sarcomas. Because SS18/SSX fusions do not seem to occur in other tumor types, and because synovial sarcomas may sometimes be difficult to distinguish from other spindle cell tumors, molecular genetic analysis has become established as an important diagnostic tool. Upon cytogenetic analysis of a soft-tissue tumor that showed classic synovial sarcoma morphology, we detected two supernumerary marker chromosomes but no rearrangement of chromosomes X or 18. By fluorescence in situ hybridization, the marker chromosomes were shown to contain material from chromosomes X and 20, including the SSX gene cluster on the X chromosome and the SS18L1 gene, which shows strong homology with the SS18 gene, on chromosome 20. Further RT-PCR analysis and sequencing of the amplified products revealed a novel SS18L1/SSX1 fusion transcript in which nucleotide 1216 (exon 10) of SS18L1 was fused in-frame with nucleotide 422 (exon 6) of SSX1. Thus, the existence of genetic heterogeneity has to be taken into account when RT-PCR is used for the diagnosis of synovial sarcoma.</p>}},
  author       = {{Storlazzi, Tiziana and Mertens, Fredrik and Mandahl, Nils and Gisselsson, David and Isaksson, Margareth and Gustafson, Pelle and Domanski, Henryk A and Panagopoulos, Ioannis}},
  issn         = {{1045-2257}},
  keywords     = {{Adult; Amino Acid Sequence; Base Sequence; Chromosomes, Human, Pair 20; Chromosomes, Human, X; Humans; Leg; Male; Molecular Sequence Data; Neoplasm Proteins; Oncogene Proteins, Fusion; Proteins; Proto-Oncogene Proteins; Repressor Proteins; Sarcoma, Synovial; Sequence Homology, Nucleic Acid; Translocation, Genetic; Tumor Cells, Cultured; Case Reports; Journal Article; Research Support, Non-U.S. Gov't}},
  language     = {{eng}},
  number       = {{2}},
  pages        = {{195--200}},
  publisher    = {{John Wiley & Sons Inc.}},
  series       = {{Genes, Chromosomes and Cancer}},
  title        = {{A novel fusion gene, SS18L1/SSX1, in synovial sarcoma}},
  url          = {{http://dx.doi.org/10.1002/gcc.10210}},
  doi          = {{10.1002/gcc.10210}},
  volume       = {{37}},
  year         = {{2003}},
}