Knight J C, Renwick P J, Dal Cin P, Van den Berghe H, Fletcher C D
Department of Histopathology, U.M.D.S. St. Thomas' Hospital, London, United Kingdom.
Cancer Res. 1995 Jan 1;55(1):24-7.
Translocation t(12;16)(q13;p11) is regarded as a diagnostic marker for myxoid liposarcoma. Cytogenetic data on round cell liposarcomas and combined myxoid and round cell tumors is scarce, and the genetic basis of progression of myxoid tumors to high grade, round cell lesions is unknown. We have accumulated six round cell, four combined myxoid and round cell, and three myxoid liposarcomas for analysis. t(12;16)(q13;p11) was present in three round cell lesions and was detectable in all of the tumors by DNA analysis. In each tumor type, the CHOP gene in 12q13 was rearranged and fused to the TLS gene in 16p11. A variant TLS-CHOP RNA transcript was detected by polymerase chain reaction but did not correlate with clinicopathological data. No distinguishing cytogenetic or molecular markers for round cell or mixed lesions were found. The histogenic and genetic relatedness of myxoid and round cell liposarcomas is apparent from these data.
易位t(12;16)(q13;p11)被视为黏液样脂肪肉瘤的诊断标志物。关于圆形细胞脂肪肉瘤以及黏液样和圆形细胞混合型肿瘤的细胞遗传学数据匮乏,且黏液样肿瘤进展为高级别圆形细胞病变的遗传基础尚不清楚。我们已收集了6例圆形细胞脂肪肉瘤、4例黏液样和圆形细胞混合型脂肪肉瘤以及3例黏液样脂肪肉瘤用于分析。t(12;16)(q13;p11)存在于3例圆形细胞病变中,通过DNA分析在所有肿瘤中均可检测到。在每种肿瘤类型中,12q13上的CHOP基因发生重排并与16p11上的TLS基因融合。通过聚合酶链反应检测到一种变异的TLS-CHOP RNA转录本,但它与临床病理数据无关。未发现圆形细胞或混合型病变的特异性细胞遗传学或分子标志物。从这些数据可以看出黏液样和圆形细胞脂肪肉瘤在组织发生和遗传上的相关性。