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The SYT-SSX1 fusion type of synovial sarcoma is associated with increased expression of cyclin A and D1. A link between t(X;18)(p11.2; q11.2) and the cell cycle machinery.

Abstract
A recent large multi-centre study convincingly confirmed previous observations that the SYT-SSX1 fusion type, compared to SYT-SSX2, of synovial sarcoma is associated with a worse clinical outcome. Apart from the clinical impact, this fact also suggests (1) that the SYT-SSX fusion gene may influence molecular mechanisms involved in tumour growth and progression; and (2) that the SYT-SSX1 fusion type has a stronger influence on these mechanisms than SYT-SSX2. The nature of the underlying mechanisms is, however, still unknown. In this study we made use of the SYT-SSX1 vs SYT-SSX2 concept to investigate whether major, tumour relevant, and growth regulatory proteins (e.g. cyclins and cyclin-dependent kinases) may be involved. Using Western blotting analysis on 74 fresh, fusion variant-typed, tumour samples from localized synovial sarcoma, we found a significant correlation between SYT-SSX1 and high expression of cyclin A (P=0.003) and D1 (P=0.025). Our data suggest that SYT-SSX may influence the cell cycle machinery, and that the more aggressive phenotype of the SYT-SSX1 variant is due to an accelerated tumour cell proliferation.
AuthorsYuntao Xie, Bjorn Skytting, Gunnar Nilsson, Robert J Grimer, Chas D Mangham, Cyril Fisher, Janet Shipley, Bodil Bjerkehagen, Ola Myklebost, Olle Larsson
JournalOncogene (Oncogene) Vol. 21 Issue 37 Pg. 5791-6 (Aug 22 2002) ISSN: 0950-9232 [Print] England
PMID12173050 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Cyclin A
  • Oncogene Proteins, Fusion
  • Proto-Oncogene Proteins c-bcl-2
  • SYT-SSX fusion protein
  • Cyclin D1
Topics
  • Cell Cycle
  • Chromosomes, Human, Pair 18
  • Cyclin A (analysis)
  • Cyclin D1 (analysis)
  • Humans
  • Oncogene Proteins, Fusion (genetics)
  • Proto-Oncogene Proteins c-bcl-2 (analysis)
  • Sarcoma, Synovial (chemistry, genetics, pathology)
  • Translocation, Genetic
  • X Chromosome

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