Arif M, Tanaka K, Damodaran C, Asou H, Kyo T, Dohy H, Kamada N
Department of Cancer Cytogenetics, Hiroshima University, Japan.
Leuk Res. 1996 Sep;20(9):709-16. doi: 10.1016/0145-2126(96)00018-5.
Fifty patients [25 acute myeloid leukemia (AML) and 25 myelodysplastic syndrome (MDS)], without monosomy 7 according to conventional cytogenetics, were re-examined by fluorescence in situ hybridization (FISH). Eleven (44.0%) patients with AML and nine (36.0%) with MDS showed hidden monosomy 7. Two samples who had both monosomy 7 and iso chromosome 17 were analyzed by dual color FISH to identify their clonal origin, and showed that these two abnormalities can occur together or independently. Only one of 16 MDS patients without monosomy 7 transformed into AML whereas four of eight MDS patients with the hidden monosomy 7 transformed into AML, suggesting patients with this abnormality are more likely to undergo transformation to AML.
根据传统细胞遗传学检查没有7号染色体单体的50例患者(25例急性髓系白血病患者和25例骨髓增生异常综合征患者),通过荧光原位杂交(FISH)技术进行了重新检查。11例(44.0%)急性髓系白血病患者和9例(36.0%)骨髓增生异常综合征患者显示存在隐匿性7号染色体单体。对2例同时存在7号染色体单体和17号等臂染色体的样本进行双色FISH分析以确定其克隆起源,结果显示这两种异常可能同时出现或独立出现。16例没有7号染色体单体的骨髓增生异常综合征患者中只有1例转化为急性髓系白血病,而8例存在隐匿性7号染色体单体的骨髓增生异常综合征患者中有4例转化为急性髓系白血病,提示存在这种异常的患者更有可能转化为急性髓系白血病。