Abstract
Recent cytogenetical and molecular studies have indicated that synovial sarcoma harbors a t(X;18)(p11.2;q11.2) translocation, resulting in the formation of a hybrid SYT/SSX (SSX1 or SSX2) gene. We newly established a human cell line, HS-SY-3, from a synovial sarcoma. HS-SY-3 cells were shown to harbor the pathognomonic t(X;18)(p11.2;q11.2) translocation by chromosome analysis but not to exhibit the classical hybrid SYT/SSX transcripts induced by this translocation, using RTPCR. To determine the reason for this discrepancy, we analyzed cDNA from HS-SY-3 cells, as well as the original sarcoma tissue by the rapid amplification of cDNA 3' end assay, and found that the chimaeric cDNA was 240 bp shorter than the previously established SYT/SSX1 cDNA due to truncation of the 3' side of SSX1. The HS-SY-3 cells should be useful for future functional studies of the SYT/SSX chimeric gene.
| Original language | English |
|---|---|
| Pages (from-to) | 459-464 |
| Number of pages | 6 |
| Journal | International Journal of Cancer |
| Volume | 82 |
| Issue number | 3 |
| DOIs | |
| State | Published - 1999 |
Keywords
- Aged
- Aged, 80 and over
- Female
- Gene Amplification
- Humans
- Hybridization, Genetic
- In Situ Hybridization, Fluorescence
- Karyotyping
- Reverse Transcriptase Polymerase Chain Reaction
- Sarcoma, Synovial/genetics
- Translocation, Genetic
- Tumor Cells, Cultured
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