Satya-Prakash K L, Pathak S, Hsu T C, Olivé M, Cailleau R
Cancer Genet Cytogenet. 1981 Jan;3(1):61-73. doi: 10.1016/0165-4608(81)90057-1.
The chromosomal constitution of 8 human breast tumor cell lines has been analyzed by conventional staining and G-banding methods. The stem line number was established in each case. In all cell lines, a large number of marker chromosomes have been identified. In addition to the 1q marker chromosome, previously reported to be present in several breast tumors from this laboratory, we also found marker chromosomes involving the 11q segment in all 8 cases, and markers resembling some of those found in the Hela cells in 6 out of 8 lines. It appears that the primary genetic (and cytogenetic) changes are specific for each type of target cell and are not shared by other neoplasms. Marker chromosomes found in different types of tumors may represent genetic changes associated with cancer progression, which may be the result of a multitude of genetic alterations.
采用传统染色和G显带方法分析了8个人类乳腺肿瘤细胞系的染色体组成。在每种情况下都确定了干系数目。在所有细胞系中,均鉴定出大量标记染色体。除了本实验室先前报道的存在于几例乳腺肿瘤中的1q标记染色体外,我们还在所有8例中发现了涉及11q区段的标记染色体,并且在8个细胞系中的6个中发现了类似于在Hela细胞中发现的一些标记。看来,原发性遗传(和细胞遗传学)变化对于每种靶细胞类型都是特异的,并且其他肿瘤并不共有。在不同类型肿瘤中发现的标记染色体可能代表与癌症进展相关的遗传变化,这可能是多种遗传改变的结果。