Watanabe M, Suzuki K, Kodama S
Division of Radiation Biology, School of Medicine, Yokohama City University, Japan.
Cancer Res. 1990 Feb 1;50(3):760-5.
Chromosomes from nine morphologically transformed (MT) cell lines (designated MT14 to MT22) of Golden hamster embryo cells induced by X-rays and from tumor-derived cell lines (MT14T to MT22T), obtained after injection of MT cells, were analyzed by the Giemsa banding method. MT cell lines showed a variety of numerical abnormalities. All of the MT cell lines involved trisomy of chromosomes 11 (80 to 100% of cells in each cell line) and 3 (8% of MT22 cells and 100% in other cell lines). Although the latent period for tumor growth differed greatly, eight of nine MT cell lines (MT14 to MT21) produced tumors at the site of injection. All tumor-derived cell lines involved trisomy of chromosome 3 at a 100% rate of incidence. Seven of nine tumor-derived cell lines (MT15T to MT18T, MT20T to MT22T) lost one chromosome 11 from the trisomic condition, resulting in disomy of chromosome 11. These results suggest that trisomies of chromosomes 11 and 3 may play a role in X-ray-induced neoplastic progression.
用吉姆萨显带法分析了经X射线诱导的金黄仓鼠胚胎细胞的9个形态转化(MT)细胞系(命名为MT14至MT22)以及注射MT细胞后获得的肿瘤衍生细胞系(MT14T至MT22T)的染色体。MT细胞系表现出多种数量异常。所有MT细胞系均涉及11号染色体三体(每个细胞系中80%至100%的细胞)和3号染色体三体(MT22细胞中的8%以及其他细胞系中的100%)。尽管肿瘤生长的潜伏期差异很大,但9个MT细胞系中的8个(MT14至MT21)在注射部位产生了肿瘤。所有肿瘤衍生细胞系均以100%的发生率涉及3号染色体三体。9个肿瘤衍生细胞系中的7个(MT15T至MT18T,MT20T至MT22T)从三体状态丢失了一条11号染色体,导致11号染色体二体。这些结果表明,11号和3号染色体三体可能在X射线诱导的肿瘤进展中起作用。