Remvikos Y, Gerbault-Seurreau M, Vielh P, Zafrani B, Magdelénat H, Dutrillaux B
Laboratory of Physiopathology, Institut Curie, Paris, France.
Cytometry. 1988 Nov;9(6):612-8. doi: 10.1002/cyto.990090616.
Twenty-five human breast cancers, surgically resected, were studied by cytogenetic analysis and DNA flow cytometry (FCM). The establishment of karyotypes showed that multiple cell populations probably were derived from a single ancestor clone, because common marker chromosomes always could be demonstrated. Differences of up to 30% were observed when the estimates of DNA content by the two methods were compared. A general tendency toward the acquisition of large marker chromosomes should be at the origin of this discordance, as the proportion of markers for each case correlated significantly with the magnitude of the difference. Parallel use of the two methods revealed the existence of tumors with DNA diploid FCM profiles and highly abnormal hypodiploid karyotypes (35-40 chromosomes), which may explain the limited value of DNA ploidy as an independent prognostic factor in breast cancer.
对25例手术切除的人类乳腺癌进行了细胞遗传学分析和DNA流式细胞术(FCM)研究。核型分析表明,多个细胞群体可能源自单个祖先克隆,因为总能发现共同的标记染色体。比较两种方法对DNA含量的估计时,观察到高达30%的差异。这种不一致的根源可能是普遍存在的获得大标记染色体的倾向,因为每个病例中标记染色体的比例与差异大小显著相关。两种方法的并行使用揭示了存在DNA二倍体FCM图谱和高度异常的亚二倍体核型(35 - 40条染色体)的肿瘤,这可能解释了DNA倍性作为乳腺癌独立预后因素的价值有限。