Monpezat J P, Delattre O, Bernard A, Grunwald D, Remvikos Y, Muleris M, Salmon R J, Frelat G, Dutrillaux B, Thomas G
Génétique des Tumeurs, Institut Curie, Paris, France.
Int J Cancer. 1988 Mar 15;41(3):404-8. doi: 10.1002/ijc.2910410315.
The zygosity of 19 colorectal carcinomas (either near-diploid or polyploid) from patients known to be heterozygous for RFLPs located on chromosome 18 or on the short arm of chromosome 17 has been examined. In most cases, at least one allele was significantly under-represented. The reason for the absence of complete loss of heterozygosity was investigated for 5 polyploid tumors. It was shown that the diploid component which, in these tumors, is essentially composed of non-neoplastic cells, remains heterozygous as the polyploid component invariably loses heterozygosity. The results strongly suggest that many colorectal carcinomas originate from a single cell which had lost at least part of either chromosome 18 or of one short arm of chromosome 17, or both.
对已知在18号染色体或17号染色体短臂上存在RFLP杂合性的患者的19例结肠直肠癌(近二倍体或多倍体)的纯合性进行了检测。在大多数情况下,至少有一个等位基因明显代表性不足。对5例多倍体肿瘤缺失杂合性完全丧失的原因进行了研究。结果表明,在这些肿瘤中,二倍体成分主要由非肿瘤细胞组成,仍保持杂合性,而多倍体成分总是失去杂合性。结果强烈提示,许多结肠直肠癌起源于一个至少丢失了18号染色体部分或17号染色体一条短臂部分或两者均丢失的单个细胞。