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pubmed-article:9247632pubmed:abstractTextClear cell sarcoma (CCS), a rare tumour of deep soft tissues, often has a t(12; 22) (q13; q12) translocation that induces the formation of a hybrid EWS/ATF-1 gene. To investigate these alterations further, we established a new continuous cell line directly from a CCS taken from a 9-year-old girl. The cultures were characterized with respect to morphological, ultrastructural, immunohistochemical and karyotypical features and were tested by reverse transcription PCR (RT-PCR) for chimaeric EWS/ATF-1 transcripts. The continuous cell line, designated KAO, is tumorigenic in nude mice, and the resultant tumours resemble the primary CCS. The tumour cells and the cultured cells have melanosomes in their cytoplasm and are immunoreactive with the melanoma-specific antibody HMB45, but do not express S-100 protein. The cultured CCS cells have the t(12; 22)(q13; q12) translocation and express the hybrid EWS/ATF-1 gene. No transcripts of the hybrid gene were detected in a malignant cutaneous melanoma tested simultaneously. Although CCS and malignant melanoma are morphologically related, the present results suggest that their geneses differ at the chromosome and molecular levels. They also indicate that chromosome analysis and detection of fusion EWS/ATF-1 transcripts may be useful adjuvant tools for the diagnosis of CCS.lld:pubmed
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pubmed-article:9247632pubmed:articleTitleEstablishment of a new continuous clear cell sarcoma cell line. Morphological and cytogenetic characterization and detection of chimaeric EWS/ATF-1 transcripts.lld:pubmed
pubmed-article:9247632pubmed:affiliationDepartment of Pathology, Hokkaido University School of Medicine, Sapporo, Japan.lld:pubmed
pubmed-article:9247632pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:9247632pubmed:publicationTypeCase Reportslld:pubmed
pubmed-article:9247632pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed
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