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首页> 外文期刊>Brazilian Journal of Medical and Biological Research >Acute promyelocytic leukemia: the study of t(15;17) translocation by fluorescent in situ hybridization, reverse transcriptase-polymerase chain reaction and cytogenetic techniques
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Acute promyelocytic leukemia: the study of t(15;17) translocation by fluorescent in situ hybridization, reverse transcriptase-polymerase chain reaction and cytogenetic techniques

机译:急性早幼粒细胞白血病:通过荧光原位杂交,逆转录酶-聚合酶链反应和细胞遗传学技术研究t(15; 17)易位

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摘要

Acute promyelocytic leukemia (AML M3) is a well-defined subtype of leukemia with specific and peculiar characteristics. Immediate identification of t(15;17) or the PML/RARA gene rearrangement is fundamental for treatment. The objective of the present study was to compare fluorescent in situ hybridization (FISH), reverse transcriptase-polymerase chain reaction (RT-PCR) and karyotyping in 18 samples (12 at diagnosis and 6 after treatment) from 13 AML M3 patients. Bone marrow samples were submitted to karyotype G-banding, FISH and RT-PCR. At diagnosis, cytogenetics was successful in 10 of 12 samples, 8 with t(15;17) and 2 without. FISH was positive in 11/12 cases (one had no cells for analysis) and positivity varied from 25 to 93% (mean: 56%). RT-PCR was done in 6/12 cases and all were positive. Four of 8 patients with t(15;17) presented positive RT-PCR as well as 2 without metaphases. The lack of RT-PCR results in the other samples was due to poor quality RNA. When the three tests were compared at diagnosis, karyotyping presented the translocation in 80% of the tested samples while FISH and RT-PCR showed the PML/RARA rearrangement in 100% of them. Of 6 samples evaluated after treatment, 3 showed a normal karyotype, 1 persistence of an abnormal clone and 2 no metaphases. FISH was negative in 4 samples studied and 2 had no material for analysis. RT-PCR was positive in 4 (2 of which showed negative FISH, indicating residual disease) and negative in 2. When the three tests were compared after treatment, they showed concordance in 2 of 6 samples or, when there were not enough cells for all tests, concordance between karyotype and RT-PCR in one. At remission, RT-PCR was the most sensitive test in detecting residual disease, as expected (positive in 4/6 samples). An incidence of about 40% of 5' breaks and 60% of 3' breaks, i.e., bcr3 and bcr1/bcr2, respectively, was observed.
机译:急性早幼粒细胞白血病(AML M3)是具有特定和特殊特征的明确定义的白血病亚型。立即鉴定t(15; 17)或PML / RARA基因重排对于治疗至关重要。本研究的目的是比较13例AML M3患者的18个样本(诊断时为12个,治疗后为6个)的荧光原位杂交(FISH),逆转录酶-聚合酶链反应(RT-PCR)和核型分析。骨髓样品进行了核型G谱带,FISH和RT-PCR。在诊断时,细胞遗传学在12个样品中的10个中成功进行,其中8个具有t(15; 17),两个没有。 FISH在11/12例中为阳性(一个没有用于分析的细胞),阳性率为25%至93%(平均:56%)。 RT-PCR在6/12例中进行,均为阳性。 t(15; 17)的8例患者中有4例呈现RT-PCR阳性,而2例没有中期。其他样品中缺乏RT-PCR结果的原因是RNA质量较差。在诊断中比较这三个测试时,核型分析显示80%的测试样品发生易位,而FISH和RT-PCR显示100%的PML / RARA重排。在处理后评估的6个样品中,有3个显示出正常的核型,1个持续存在异常克隆和2个没有中期。在所研究的4个样品中FISH呈阴性,而2个没有分析材料。 RT-PCR在4份中呈阳性(其中2份FISH阴性,表明残留病),在2份中阴性。当对三种测试进行处理后进行比较时,它们在6个样品中的2个中显示出一致性,或者在没有足够的细胞用于检测时所有测试中,核型与RT-PCR的一致性都在其中。在缓解时,RT-PCR是检测残留疾病中最灵敏的测试,与预期的一样(4/6个样本呈阳性)。观察到大约40%的5'断裂和60%的3'断裂的发生率,即bcr3和bcr1 / bcr2。

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