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成年费城染色体阴性急性淋巴细胞白血病患者BCR-ABL序列的聚合酶链反应分析

Polymerase chain reaction analysis of BCR-ABL sequences in adult Philadelphia chromosome-negative acute lymphoblastic leukemia patients.

作者信息

Janssen J W, Fonatsch C, Ludwig W D, Rieder H, Maurer J, Bartram C R

机构信息

Department of Pediatrics II, University of Ulm, Germany.

出版信息

Leukemia. 1992 May;6(5):463-4.

PMID:1593911
Abstract

The Philadelphia (Ph) translocation is the most common cytogenetic abnormality in adult acute lymphoblastic leukemia (ALL) and is associated with an adverse prognosis. Using polymerase chain reaction (PCR) technology we recently observed a remarkably high incidence (55%) of BCR-ABL rearrangements in adult common ALL patients. In the present study we asked whether a subset of Ph-negative cALL, similarly to Ph-negative chronic myelocytic leukemia (CML) patients, exhibit BCR-ABL transcripts. PCR analysis of 58 adult Ph-negative cALL patients, including 47 cases with a normal karyotype revealed no evidence of chimeric BCR-ABL genes. We conclude that Ph-negative BCR/ABL-positive ALL is very rare entity if existing at all.

摘要

费城(Ph)染色体易位是成人急性淋巴细胞白血病(ALL)中最常见的细胞遗传学异常,与不良预后相关。我们最近使用聚合酶链反应(PCR)技术观察到成人普通ALL患者中BCR-ABL重排的发生率非常高(55%)。在本研究中,我们探讨了一部分Ph阴性的普通ALL患者是否与Ph阴性慢性髓性白血病(CML)患者类似,存在BCR-ABL转录本。对58例成人Ph阴性普通ALL患者进行PCR分析,其中包括47例核型正常的患者,结果未发现嵌合BCR-ABL基因的证据。我们得出结论,Ph阴性BCR/ABL阳性ALL即便存在,也是非常罕见的实体。

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