上皮样肉瘤
滑膜肉瘤
生物
融合基因
肉瘤
组织发生
病理
免疫分型
癌症研究
软组织肉瘤
基因
免疫组织化学
分子生物学
免疫学
遗传学
医学
流式细胞术
作者
Carmen de Torres,Teresa Cardesa,Sandra Rodríguez,Juan C. Cigudosa,Jaume Mora
出处
期刊:Cancer genetics and cytogenetics
[Elsevier]
日期:2005-10-01
卷期号:162 (1): 50-56
被引量:11
标识
DOI:10.1016/j.cancergencyto.2005.03.009
摘要
Epithelioid sarcoma is a rare malignant soft tissue tumor of unknown histogenesis, characterized by the epithelioid morphology of tumor cells and co-expression of epithelial and mesenchymal lineage proteins. A common epithelial and mesenchymal immunophenotype is also found in another soft tissue tumor, the biphasic subtype of synovial sarcoma. Furthermore, the presence of a breakpoint at 18q11 in epithelioid sarcoma, similar to that found in synovial sarcoma, has been reported. These facts would support the hypothesis that both tumors may share a common histogenetic background. However, expression of the SYT-SSX fusion genes has been investigated in epithelioid sarcoma with negative results. We report, to our knowledge, the first epithelioid sarcoma in which the presence of SYT-SSX1 fusion gene has been detected by means of conventional RT-PCR analysis and sequencing, real-time RT-PCR and FISH. The SYT-SSX1 gene fusion was identified in a small proportion of tumoral cells. This finding supports a likely common histogenetic background for both epithelioid sarcoma and synovial sarcoma.
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