TY - JOUR
T1 - Gene expression profiling of synovial sarcoma
T2 - Distinct signature of poorly differentiated type
AU - Nakayama, Robert
AU - Mitani, Sachiyo
AU - Nakagawa, Takeshi
AU - Hasegawa, Tadashi
AU - Kawai, Akira
AU - Morioka, Hideo
AU - Yabe, Hiroo
AU - Toyama, Yoshiaki
AU - Ogose, Akira
AU - Toguchida, Junya
AU - Nakayama, Tomitaka
AU - Yoshida, Teruhiko
AU - Ichikawa, Hitoshi
PY - 2010/11
Y1 - 2010/11
N2 - Poorly differentiated type synovial sarcoma (PDSS) is a variant of synovial sarcoma characterized by predominantly round or short-spindled cell morphology. Although accumulating evidence from clinicopathologic studies suggests a strong association between this variant of synovial sarcoma and poor prognosis, little has been reported on the molecular basis of PDSS. To gain insights into the mechanism(s) that underlie the emergence of PDSS, we analyzed the gene expression profiles of 34 synovial sarcoma clinical samples, including 5 cases of PDSS, using an oligonucleotide microarray. In an unsupervised analysis, the 34 samples fell into 3 groups that correlate closely with histologic subtypes: monophasic, biphasic, and poorly differentiated types. PDSS was characterized by down-regulation of genes associated with neuronal and skeletal development and cell adhesion. Moreover, upregulation of genes on a specific chromosomal locus, 8q21.11, was identified. This locus-specific transcriptional activation in PDSS was confirmed by reverse transcriptase-PCR analysis of 9 additional synovial sarcoma samples. Our results indicate that PDSS tumors constitute a distinct group based on expression profiles.
AB - Poorly differentiated type synovial sarcoma (PDSS) is a variant of synovial sarcoma characterized by predominantly round or short-spindled cell morphology. Although accumulating evidence from clinicopathologic studies suggests a strong association between this variant of synovial sarcoma and poor prognosis, little has been reported on the molecular basis of PDSS. To gain insights into the mechanism(s) that underlie the emergence of PDSS, we analyzed the gene expression profiles of 34 synovial sarcoma clinical samples, including 5 cases of PDSS, using an oligonucleotide microarray. In an unsupervised analysis, the 34 samples fell into 3 groups that correlate closely with histologic subtypes: monophasic, biphasic, and poorly differentiated types. PDSS was characterized by down-regulation of genes associated with neuronal and skeletal development and cell adhesion. Moreover, upregulation of genes on a specific chromosomal locus, 8q21.11, was identified. This locus-specific transcriptional activation in PDSS was confirmed by reverse transcriptase-PCR analysis of 9 additional synovial sarcoma samples. Our results indicate that PDSS tumors constitute a distinct group based on expression profiles.
KW - gene expression profiling
KW - poorly differentiated type
KW - synovial sarcoma
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U2 - 10.1097/PAS.0b013e3181f7ce2c
DO - 10.1097/PAS.0b013e3181f7ce2c
M3 - Article
C2 - 20975339
AN - SCOPUS:78049527531
SN - 0147-5185
VL - 34
SP - 1599
EP - 1607
JO - American Journal of Surgical Pathology
JF - American Journal of Surgical Pathology
IS - 11
ER -