K Tanaka, M Takechi, J Hong, C Shigeta, N Oguma, N Kamada, Y Takimoto, A Kuramoto, H Okita
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引用次数: 0
摘要
我们报告了两例双分钟(DMs)染色体白血病患者。两例患者均被诊断为急性髓细胞白血病(AML) FAB M2。细胞遗传学分析显示,1例患者染色体核型正常,1-53条DMs染色体;2例患者在白血病发生前8年有喉癌广泛放疗史,8号染色体8q24区缺失,1-84条DMs染色体复杂畸变。对两名患者的DNA分析显示,癌基因c-myc在白血病细胞中扩增了约5至10倍。c-myc的其他14个致癌基因为c-myb、c-abl和N-myc,基因含量没有增加。此外,通过体内选择法在第一例患者中检测到一种转化基因N-ras。这是关于c-myc基因扩增和DMs染色体的AML患者的第二篇报道。
[c-myc gene amplification and N-ras transforming gene in two cases of acute myelocytic leukemia with double minute chromosomes].
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.