Tissue microarray profiling of primary and xenotransplanted synovial sarcomas demonstrates the immunophenotypic similarities existing between SYT-SSX fusion gene confirmed, biphasic, and monophasic fibrous variants
| Autor: | Samuel Navarro, Jose Antonio Heredia Alvaro, Carmen Carda, Pau Lluís Gozalbo Sabater, José Antonio López-Guerrero, Manish Mani Subramaniam, Antonio Pellín, Antonio Llombart-Bosch |
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| Rok vydání: | 2006 |
| Předmět: |
Male
Pathology medicine.medical_specialty Mitotic index Oncogene Proteins Fusion Molecular Sequence Data Mice Nude Soft Tissue Neoplasms Biology Pathology and Forensic Medicine Fusion gene Mice Sarcoma Synovial Cytokeratin Immunophenotyping Biomarkers Tumor medicine Animals Cluster Analysis Humans RNA Messenger RNA Neoplasm Molecular Biology Mice Inbred BALB C Tissue microarray Base Sequence Reverse Transcriptase Polymerase Chain Reaction Gene Expression Profiling Cell Biology General Medicine medicine.disease Immunohistochemistry Xenograft Model Antitumor Assays Primary tumor Synovial sarcoma Phenotype Tissue Array Analysis Immunostaining |
| Zdroj: | Virchows Archiv. 449:435-447 |
| ISSN: | 1432-2307 0945-6317 |
| DOI: | 10.1007/s00428-006-0271-9 |
| Popis: | This paper discusses the diversity of synovial sarcomas (SSs) [biphasic (BSS), monophasic fibrous (MFSS), and poorly differentiated (PDSS)] and tissue microarray (TMA) evaluation of the immunophenotypic and histological progression of SSs in nude mice using three TMAs comprising 11 primary SSs (8 MFSSs, 2 BSSs, and 1 PDSS) and their xenografts. BSS and MFSS progressively transformed to a similar undifferentiated phenotype with loss of glandular component in the xenografts. Epidermal growth factor receptor and SALL2 were expressed in primary tumors and xenografts. Enhanced bcl-2 and bax expression were noted in xenografts. Ki-67 overexpression in xenografts correlated with high mitotic index. Epithelial membrane antigen (EMA) and cytokeratin AE1/AE3 were detected in all original and xenografted SSs. Hierarchical clustering differentiated original MFSS and BSS, but their xenografts clustered together due to similar immunoexpression profile. Our study demonstrates definite phenotypic variability of BSS and MFSS in the xenografts. Differences in immunoexpression for various markers existed between primary tumor and xenografts but not between subtypes. Hierarchical clustering grouped TMA immunostaining data and confirmed immunophenotypic variability; however, it failed to reveal any immunophenotypic differences between SYT-SSX1 and SYT-SSX2 type tumors. Nonetheless, reverse-transcriptase-polymerase chain reaction detected SYT-SSX transcripts in all primary SSs and their xenografts, thereby demonstrating their genetic stability. |
| Databáze: | OpenAIRE |
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