Bey E, Bernstein R
Cytogenet Cell Genet. 1979;24(3):143-9. doi: 10.1159/000131370.
Numerical and structural chromosome analysis of a human retroperitoneal liposarcoma cell line maintained under standard cell culture conditions revealed a very stable hypodiploid mode. If the cells were not trypsinized for several generations, a near-triploid stemline, which was generally a duplication of the hypodiploid mode, emerged. Some chromosomes appeared to be relatively stable pairs (1, 2, 7, 9, and 12), but most had "lost" one homolog or both (4 and 21) or were rearranged into "new" marker chromosomes. Quantitation of the genetic material showed a loss of 12.0 +/- 3.7% per spread. Only one characteristically long marker chromosome, which is present in every cell, could be identified with certainty as a translocation between chromosomes 4 and 11. Several of the marker chromosomes showed interstitial negatively staining regions with the trypsin-Giemsa method.
在标准细胞培养条件下维持的人腹膜后脂肪肉瘤细胞系的染色体数值和结构分析显示出非常稳定的亚二倍体模式。如果细胞几代不进行胰蛋白酶处理,就会出现一个近三倍体主干系,它通常是亚二倍体模式的重复。一些染色体似乎是相对稳定的配对(1、2、7、9和12号染色体),但大多数染色体“丢失”了一条同源染色体或两条同源染色体(4号和21号染色体),或者重排形成“新”的标记染色体。遗传物质的定量分析显示,每个涂片损失12.0±3.7%。只有一条特征性的长标记染色体,存在于每个细胞中,可以确定它是4号和11号染色体之间的易位。用胰蛋白酶-吉姆萨方法对几条标记染色体进行检测,发现有间质负染区。