Kaminskaia E V, Baranov V S, Vakhtin Iu B
Tsitologiia. 1985 Feb;27(2):240-3.
By means of staining procedure which reveals the constitutive heterochromatin (CH), the number of CH-blocks was detected in the nuclei of interphase cells obtained from the subcutaneously growing rhabdomyosarcoma and from its 10 lung colonies. The range of variability of the number of CH-blocks in tumor cell populations was greater than in the populations of normal lung cells and lymphocytes. The mean numbers of CH-blocks varied from 17.8 +/- 0.9 to 28.0 +/- 1.2 in cells of different clones, the mean number of CH-blocks in clones being the same as in the subcutaneously growing uncloned tumor. The coefficient of heritability h2 of character "the number of CH-blocks", calculated on the basis of population and interclonal variances, was equal to 0.15, and that calculated by one-factor dispersional analysis was actually the same (0.16). It is concluded that the high heterogeneity of tumor cells may be conditioned not only by their high phenotypic instability, but also by a high frequency of mutations.
通过一种能显示组成型异染色质(CH)的染色程序,在从皮下生长的横纹肌肉瘤及其10个肺转移瘤中获取的间期细胞核中检测到CH块的数量。肿瘤细胞群体中CH块数量的变异范围大于正常肺细胞和淋巴细胞群体。不同克隆细胞中CH块的平均数量在17.8±0.9至28.0±1.2之间变化,克隆中CH块的平均数量与皮下生长的未克隆肿瘤中的相同。基于群体和克隆间方差计算的“CH块数量”性状的遗传力系数h2等于0.15,通过单因素方差分析计算的结果实际上相同(0.16)。得出的结论是,肿瘤细胞的高度异质性可能不仅由其高表型不稳定性决定,还由高突变频率决定。