Gebhart E, Brüderlein S, Tulusan A H, von Maillot K, Birkmann J
Int J Cancer. 1984 Sep 15;34(3):369-73. doi: 10.1002/ijc.2910340313.
Screening of the occurrence of double minutes (DM) was performed in more than 1,000 metaphases obtained from a total of 22 solid human breast tumours and more than 3,600 metaphases from a total of 55 malignant effusions (45 patients with different types of carcinomas). DM were observed in 15 of these breast tumor cases and in 34 of the effusions (obtained from 29 cancer patients). The percentage of cells exhibiting DM as well as the number of DM per respective cell varied widely. It could be seen that metastatic cells from malignant effusions exhibited on the average more DM per cell than did cells of primary breast carcinomas. Differences in the incidence of DM could be observed between different carcinomas as well as between different age groups. In addition, it did not appear that DM could be induced by mutagenic tumor therapy. DM are thus not a rare finding in human solid tumors but, as cytogenetic equivalents of gene amplification, they rather represent a fundamental biological characteristic of tumor development.
对从总共22例人类实体乳腺肿瘤中获取的1000多个中期细胞以及从总共55例恶性积液(45例患有不同类型癌症的患者)中获取的3600多个中期细胞进行了双微体(DM)出现情况的筛查。在这些乳腺肿瘤病例中有15例观察到了DM,在积液中有34例观察到了DM(来自29例癌症患者)。显示出DM的细胞百分比以及每个相应细胞中的DM数量差异很大。可以看出,来自恶性积液的转移细胞平均每个细胞中的DM比原发性乳腺癌细胞更多。在不同癌症之间以及不同年龄组之间可以观察到DM发生率的差异。此外,似乎DM不会由诱变肿瘤治疗诱导产生。因此,DM在人类实体肿瘤中并非罕见发现,而是作为基因扩增的细胞遗传学等效物,它们更代表了肿瘤发展的一种基本生物学特征。