Tanaka K, Takechi M, Hong J, Shigeta C, Oguma N, Kamada N, Takimoto Y, Kuramoto A, Okita H
Nihon Ketsueki Gakkai Zasshi. 1989 Nov;52(7):1137-46.
We report two leukemia patients with double minutes (DMs) chromosomes. Both patients were diagnosed as having acute myelocytic leukemia (AML) FAB M2. Cytogenetic analysis showed normal chromosome karyotype with 1-53 DMs chromosomes in the first patient, and complex chromosome aberrations including deletion of chromosome 8 at 8q24 region and 1-84 DMs chromosomes in the second patient who had a history of extensive radiotherapy for laryngeal cancer 8 years prior to the development of leukemia. Analysis of DNA from the two patients revealed that oncogene of c-myc was amplified about 5 to 10 folds in the leukemic cells. The other fourteen oncogene of c-myc was c-myb, c-abl and N-myc, showed no increases of gene content. Furthermore, a transforming gene, N-ras was detected in the first patient by in vivo selection assay method. This is the second report on AML patients with c-myc gene amplification and DMs chromosomes.
我们报告了两名患有双微体(DMs)染色体的白血病患者。两名患者均被诊断为急性髓细胞白血病(AML)FAB M2型。细胞遗传学分析显示,第一名患者染色体核型正常,但有1 - 53条双微体染色体;第二名患者有复杂的染色体畸变,包括8号染色体8q24区域缺失以及1 - 84条双微体染色体,该患者在患白血病8年前有喉癌广泛放疗史。对两名患者的DNA分析显示,白血病细胞中c - myc癌基因扩增了约5至10倍。其他14个癌基因,即c - myb、c - abl和N - myc,基因含量未增加。此外,通过体内选择测定法在第一名患者中检测到一个转化基因N - ras。这是关于伴有c - myc基因扩增和双微体染色体的AML患者的第二篇报道。