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Validation of an interphase fluorescence in situ hybridization approach for the detection of MLL gene rearrangements and of the MLL/AF9 fusion in acute myeloid leukemia | Haematologica

机译:间相荧光原位杂交方法在急性髓细胞白血病中检测MLL基因重排和MLL / AF9融合的验证血液学

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To validate a 2-step FISH assay for the identification of the t(9;11)(p22;q23), 96 acute myeloid leukemias were studied by cytogenetic analysis, FISH and molecular biology. After a first FISH step using an MLL probe, 24/27 cases with 11q23 break showed MLL rearrangement. Southern blotting confirmed FISH data. In the second step, 24 cases with MLL rearrangement were studied using MLL and AF9 probes: 17/18 cases with t(9;11) showed MLL/AF9 fusion. In 6 patients with 11q23/MLL rearrangements other than t(9;11), FISH confirmed MLL involvement and excluded AF9 involvement. This is a reliable method for the identification of MLL/AF9 fusion in interphase cells, allowing for a reclassification of cases with suboptimal chromosome morphology. The frequency of deletion surrounding MLL and AF9 breakpoint is low.
机译:为了验证用于鉴定t(9; 11)(p22; q23)的两步FISH分析,通过细胞遗传学分析,FISH和分子生物学研究了96种急性髓细胞白血病。在使用MLL探针进行FISH的第一步之后,有24/27例11q23断裂的病例显示了MLL重排。 Southern印迹证实了FISH数据。第二步,使用MLL和AF9探针研究了24例MLL重排患者:17/18例t(9; 11)患者显​​示MLL / AF9融合。在6例tq(9; 11)以外的11q23 / MLL重排患者中,FISH确诊MLL受累,AF9受累。这是鉴定间期细胞中MLL / AF9融合的可靠方法,可对染色体形态欠佳的病例进行重新分类。 MLL和AF9断点周围的删除频率很低。

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