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Value of oligonucleotide-based array comparative genomic hybridization for diagnosis of acute promyelocytic leukemia in a patient negative for t(15;17)(q24.1;q21.2)/promyelocytic leukemia-retinoic acid receptor, alpha by conventional cytogenetics and fluorescence in situ hybridization.

作者信息

Alayed Khaled, Medeiros L Jeffrey, Schultz Roger A, Cortes Jorge, Lu Gary, Bueso-Ramos Carlos E, Konoplev Sergej

机构信息

Department of Hematopathology, The University of Texas M.D. Anderson Cancer Center, Houston, TX, USA.

出版信息

Clin Lymphoma Myeloma Leuk. 2013 Aug;13(4):507-10. doi: 10.1016/j.clml.2013.03.007. Epub 2013 Jun 14.

DOI:10.1016/j.clml.2013.03.007
PMID:23770155
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4259115/
Abstract
摘要

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Value of oligonucleotide-based array comparative genomic hybridization for diagnosis of acute promyelocytic leukemia in a patient negative for t(15;17)(q24.1;q21.2)/promyelocytic leukemia-retinoic acid receptor, alpha by conventional cytogenetics and fluorescence in situ hybridization.基于寡核苷酸的阵列比较基因组杂交技术在一名常规细胞遗传学和荧光原位杂交检测t(15;17)(q24.1;q21.2)/早幼粒细胞白血病-维甲酸受体α阴性的急性早幼粒细胞白血病患者诊断中的价值
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Interstitial insertion of RARα gene into PML gene in a patient with acute promyelocytic leukemia (APL) lacking the classic t(15;17).在一名缺乏典型t(15;17)的急性早幼粒细胞白血病（APL）患者中，RARα基因间质性插入到PML基因中。
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Pulsed-field gel electrophoresis analysis of retinoic acid receptor-alpha and promyelocytic leukemia rearrangements. Detection of the t(15;17) translocation in the diagnosis of acute promyelocytic leukemia.维甲酸受体-α和早幼粒细胞白血病重排的脉冲场凝胶电泳分析。急性早幼粒细胞白血病诊断中t(15;17)易位的检测。
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Interstitial insertion of retinoic acid receptor-alpha gene in acute promyelocytic leukemia with normal chromosomes 15 and 17.维甲酸受体α基因在染色体15和17正常的急性早幼粒细胞白血病中的间质插入。
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Cancer Biol Ther. 2020 Apr 2;21(4):309-314. doi: 10.1080/15384047.2019.1702398. Epub 2020 Jan 20.

本文引用的文献

1
Microarray, gene sequencing, and reverse transcriptase-polymerase chain reaction analyses of a cryptic PML-RARA translocation.隐匿性PML-RARA易位的微阵列、基因测序及逆转录聚合酶链反应分析
Cancer Genet. 2012 Oct;205(10):537-40. doi: 10.1016/j.cancergen.2012.07.017. Epub 2012 Sep 13.
2
Acute promyelocytic leukemia with a STAT5b-RARα fusion transcript defined by array-CGH, FISH, and RT-PCR.通过阵列比较基因组杂交、荧光原位杂交和逆转录聚合酶链反应确定具有STAT5b-RARα融合转录本的急性早幼粒细胞白血病。
Cancer Genet. 2012 Jun;205(6):327-31. doi: 10.1016/j.cancergen.2012.02.007.
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Acute promyelocytic leukemia: four distinct patterns by flow cytometry immunophenotyping.急性早幼粒细胞白血病：流式细胞术免疫表型分析的四种不同模式
Pol J Pathol. 2012 Mar;63(1):8-17.
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Acute promyelocytic leukemia with trisomy 8 showing normal PML-RARA FISH signal patterns: diagnostic application of long-distance polymerase chain reaction in molecularly discrepant leukemia cases.
Ann Hematol. 2012 Oct;91(10):1645-8. doi: 10.1007/s00277-012-1439-9. Epub 2012 Mar 9.
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The use of new technologies in the detection of balanced translocations in hematologic disorders.新技术在血液系统疾病中检测平衡易位的应用。
Curr Opin Genet Dev. 2012 Jun;22(3):264-71. doi: 10.1016/j.gde.2012.01.005. Epub 2012 Feb 13.
6
CD117 expression is a sensitive but nonspecific predictor of FLT3 mutation in T acute lymphoblastic leukemia and T/myeloid acute leukemia.CD117 表达是 T 急性淋巴细胞白血病和 T/髓系急性白血病中 FLT3 突变的一个敏感但非特异性预测指标。
Am J Clin Pathol. 2012 Feb;137(2):213-9. doi: 10.1309/AJCPR3N3JMSYLPFG.
7
Curing all patients with acute promyelocytic leukemia: are we there yet?治愈所有急性早幼粒细胞白血病患者：我们做到了吗？
Hematol Oncol Clin North Am. 2011 Dec;25(6):1215-33, viii. doi: 10.1016/j.hoc.2011.10.002.
8
The pathogenesis and management of the coagulopathy of acute promyelocytic leukaemia.急性早幼粒细胞白血病凝血异常的发病机制与处理。
Br J Haematol. 2012 Jan;156(1):24-36. doi: 10.1111/j.1365-2141.2011.08922.x. Epub 2011 Nov 3.
9
Microgranular variant of acute promyelocytic leukemia with normal conventional cytogenetics, negative PML/RARA FISH and positive PML/RARA transcripts by RT-PCR.急性早幼粒细胞白血病微颗粒变异型，常规细胞遗传学正常，PML/RARA荧光原位杂交阴性，逆转录聚合酶链反应检测PML/RARA转录本阳性
Cancer Genet. 2011 Sep;204(9):522-3. doi: 10.1016/j.cancergen.2011.09.001.
10
Rapid high-resolution mapping of balanced chromosomal rearrangements on tiling CGH arrays.利用平铺 CGH 阵列快速高分辨率映射平衡染色体重排。
J Mol Diagn. 2011 Nov;13(6):621-33. doi: 10.1016/j.jmoldx.2011.07.005. Epub 2011 Sep 9.