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一例急性未分化白血病中SET-NUP214可变融合转录本的分子特征分析

Molecular characterization of alternative SET-NUP214 fusion transcripts in a case of acute undifferentiated leukemia.

作者信息

Kim Juwon, Lee Sang-Guk, Song Jaewoo, Kim Soo Jeong, Rha Sun Young, Lee Kyung-A, Park Tae Sung, Choi Jong Rak

机构信息

Department of Laboratory Medicine, Yonsei University College of Medicine, Seodaemun-gu, Seoul, Korea.

出版信息

Cancer Genet Cytogenet. 2010 Sep;201(2):73-80. doi: 10.1016/j.cancergencyto.2010.05.010.

Abstract

Cryptic deletions are occasionally reported in hematologic malignancies. The SET-NUP214 fusion gene has been rarely reported in acute myeloid leukemia, acute undifferentiated leukemia, and recurrently in T-cell acute lymphoblastic leukemia. The fusion product is generated by a submicroscopic deletion in the vicinity of 9q34. Herein we present a novel case of acute undifferentiated leukemia with SET-NUP214 rearrangement due to the cryptic deletion of the 9q34 region producing two different types of fusion transcripts by alternative splicing and molecular characterization of the fusion transcripts by fluorescence in situ hybridization, reverse transcriptase-polymerase chain reaction, and array comparative genomic hybridization analyses.

摘要

隐匿性缺失在血液系统恶性肿瘤中偶尔会有报道。SET-NUP214融合基因在急性髓系白血病、急性未分化白血病中鲜有报道,而在T细胞急性淋巴细胞白血病中则反复出现。该融合产物是由9q34附近的亚显微缺失产生的。在此,我们报告一例新型急性未分化白血病病例,其因9q34区域的隐匿性缺失导致SET-NUP214重排,通过可变剪接产生两种不同类型的融合转录本,并通过荧光原位杂交、逆转录-聚合酶链反应和阵列比较基因组杂交分析对融合转录本进行分子特征分析。

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