首页> 外文期刊>Haematologica >Dual-color split signal fluorescence in situ hybridization assays for the detection of CALM/AF10 in t(10;11)(p13;q14-q21)-positive acute leukemia | Haematologica
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Dual-color split signal fluorescence in situ hybridization assays for the detection of CALM/AF10 in t(10;11)(p13;q14-q21)-positive acute leukemia | Haematologica

机译:双色分裂信号荧光原位杂交测定可检测t(10; 11)(p13; q14-q21)阳性急性白血病中的CALM / AF10 |血液学

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We developed dual-color split fluorescence in situ hybridization (FISH) assays to detect AF10 and/or CALM rearrangements. Among nine cases of acute leukemia with translocation breakpoints at 10p13 and 11q14-21, a CALM/AF10 rearrangement was found in seven and was confirmed by reverse transcriptase polymerase chain reaction (RT-PCR) in all. In 2/7 cases, FISH detected CALM/AF10 in extramedullary leukemic infiltrations in the mediastinum and breast. As expected, FISH was less sensitive than RT-PCR for disease monitoring of CALM-AF10 positive cases. This new FISH assay reliably discriminates between MLL/AF10 and CALM/AF10 genomic rearrangements, identifies variant and complex CALM/AF10 translocations and detects the CALM/AF10 rearrangement in extramedullary leukemic infiltrations.
机译:我们开发了双色拆分式荧光原位杂交(FISH)分析方法来检测AF10和/或CALM重排。在9例转位点分别在10p13和11q14-21的急性白血病中,在7例中发现了CALM / AF10重排,并且全部通过逆转录酶聚合酶链反应(RT-PCR)得以证实。在2/7例病例中,FISH在纵隔和乳房的髓外白血病浸润中检测到了CALM / AF10。不出所料,对于ISHM-AF10阳性病例的疾病监测,FISH不如RT-PCR敏感。这种新的FISH分析可可靠地区分MLL / AF10和CALM / AF10基因组重排,识别变异和复杂的CALM / AF10易位,并检测髓外白血病浸润中的CALM / AF10重排。

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