Multiplex PCR of bcr-abl fusion transcripts in Philadelphia positive acute lymphoblastic leukemia.

A Lee, J Kirk, S Edmands, J Radich
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引用次数: 18

Abstract

We describe a multiplex PCR assay for the detection of bcr-abl fusion mRNA in Philadelphia chromosome positive acute lymphoblastic leukemia (Ph + ALL). The assay provides a quick method for screening p190 (e1:a2) and p210 (b2:a2 or b3:a2) bcr-abl mRNAs simultaneously. The assay proves to be highly sensitive with detection of as little as one positive bcr-abl-expressing cell in a background of 10(5) negative bcr-abl cells. Bone marrow and peripheral blood specimens from six patients were in total accordance when run by multiplex PCR and by the single primer PCR approach. The multiplex bcr-abl assay may prove to be highly useful for screening newly diagnosed patients with ALL for the bcr-abl fusion transcript and in following the course of disease during therapy.

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费城阳性急性淋巴细胞白血病中bcr-abl融合转录物的多重PCR分析。
我们描述了一种多重PCR检测费城染色体阳性急性淋巴细胞白血病(Ph + ALL)中bcr-abl融合mRNA的方法。该试验提供了一种同时筛选p190 (e1:a2)和p210 (b2:a2或b3:a2) bcr-abl mrna的快速方法。实验证明,在10(5)个bcr-abl阴性细胞的背景下,检测到一个bcr-abl阳性表达细胞是高度敏感的。6例患者骨髓与外周血标本多重PCR与单引物PCR完全一致。多重bcr-abl测定可能被证明对筛查新诊断的ALL患者的bcr-abl融合转录物和在治疗期间跟踪疾病进程非常有用。
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Rapid and sensitive analysis of mRNA polyadenylation states by PCR. Identification of 3'-terminal exons from yeast artificial chromosomes. Quantitative analysis of specific mRNA transcripts using a competitive PCR assay with electrochemiluminescent detection. Batched analysis of genotypes. A one-step coupled amplification and oligonucleotide ligation procedure for multiplex genetic typing.
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