粘液样脂肪肉瘤
染色体易位
生物
脂肪肉瘤
病理
细胞遗传学
聚合酶链反应
细胞
基因
切碎
癌症研究
分子生物学
肉瘤
遗传学
医学
染色体
化疗
作者
JC Knight,Pamela Renwick,Paola Dal Cin,Herman Van den Berghe,Christopher D.�M. Fletcher
出处
期刊:PubMed
日期:1995-01-01
卷期号:55 (1): 24-7
被引量:57
摘要
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.
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