Key result
Loss of chromosome 3p was the most frequent alteration in monophasic synovial sarcomas but did not involve RASSF1 and MLH1 promoter regions, suggesting post-transcriptional deregulation.
Observational (n=15)
Monophasic synovial sarcomas exhibit genetic complexity with frequent 3p loss, but RASSF1 and MLH1 appear to be deregulated post-transcriptionally rather than through promoter loss.
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3p loss without RASSF1/MLH1 promoter involvement may refine synovial sarcoma subtyping; leaves open post-transcriptional mechanisms for future mechanistic studies.
Differential diagnosis of monophasic synovial sarcoma requires the detection of specific biological markers. In this study we evaluated the presence of molecular alterations in 15 monophasic synovial sarcomas. Multiple changes affecting chromosome arms were detected by CGH-array in all microdissected cases available, and an association between gain or loss of specific regions harbouring cancer progression-associated genes and aneuploid status was found. The most frequent alteration was loss of 3p including 3p21.3-p23 region that, however, did not involve the promoter regions of the corresponding genes, RASSF1 and MLH1. Using Real-Time PCR, mRNA levels of both resulted moderately high compared to normal tissue; however, the weak to absent protein expression suggests RASSF1 and MLH1 post-transcription deregulation. Moreover, immunohistochemical analysis revealed that both mesenchymal and epithelial antigens were present in diploid tumours. These findings confirm the genetic complexity of monophasic synovial sarcoma and underline the need to integrate different analyses for a better knowledge of this tumour, essential to investigate new diagnostic and prognostic markers.
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Pazzaglia et al. (2006) conducted an observational in monophasic synovial sarcoma (n=15). Loss of chromosome 3p was evaluated on Molecular alterations and RASSF1/MLH1 transcriptional activity. Loss of chromosome 3p was the most frequent alteration in monophasic synovial sarcomas but did not involve RASSF1 and MLH1 promoter regions, suggesting post-transcriptional deregulation.
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