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MLL-AF9阳性急性单核细胞白血病中一种新的AF9断点。

A novel AF9 breakpoint in MLL-AF9-positive acute monoblastic leukemia.

作者信息

Alonso Cristina N, Longo Patricia L Rubio, Gallego Marta S, Medina Adriana, Felice María S

机构信息

Molecular Biology Laboratory, Department of Hematology-Oncology, Hospital de Pediatría SAMIC "Prof. Dr. J. P. Garrahan", Buenos Aires, Argentina.

出版信息

Pediatr Blood Cancer. 2008 Apr;50(4):869-71. doi: 10.1002/pbc.21393.

Abstract

MLL-AF9 is the most frequent MLL rearrangement in childhood acute myeloid leukemia (AML) and it may be also found in acute lymphoblastic leukemia (ALL) of patients younger than 1-year-old (infants). We report a novel AF9 breakpoint site, located between previously reported sites A and B, detected in an infant who was diagnosed with AML-FAB M5. The occurrence of this new breakpoint should be considered when designing RT-PCR assays for the screening of MLL abnormalities. The precise characterization of the MLL-AF9 transcript is important to carry out the minimal residual disease analysis during the follow-up of the patients.

摘要

MLL-AF9是儿童急性髓系白血病(AML)中最常见的MLL重排,在1岁以下(婴儿)患者的急性淋巴细胞白血病(ALL)中也可能发现。我们报告了一个新的AF9断点位点,位于先前报道的A和B位点之间,在一名被诊断为AML-FAB M5的婴儿中检测到。在设计用于筛查MLL异常的RT-PCR检测方法时,应考虑这个新断点的出现。MLL-AF9转录本的精确特征对于在患者随访期间进行微小残留病分析很重要。

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