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在慢性髓性白血病中检测到典型的费城阳性急性淋巴细胞白血病的mRNA异常表达。

Unusual expression of mRNA typical of Philadelphia positive acute lymphoblastic leukemia detected in chronic myeloid leukemia.

作者信息

Kirk J A, Radich J, Edmands S, Lee A, VanDevanter D R, Reems J A, Bryant E M

机构信息

Fred Hutchinson Cancer Research Center, Seattle, WA 98104, USA.

出版信息

Am J Hematol. 1996 Jul;52(3):129-34. doi: 10.1002/(SICI)1096-8652(199607)52:3<129::AID-AJH1>3.0.CO;2-V.

DOI:10.1002/(SICI)1096-8652(199607)52:3<129::AID-AJH1>3.0.CO;2-V
PMID:8756076
Abstract

The Philadelphia chromosome (Ph) is found in both chronic myeloid leukemia (CML) and acute lymphoblastic leukemia (ALL). The Ph translocation, t(9;22)(q34;q11), can disrupt the BCR gene on chromosome 22 in one to two areas called the major (Mbcr1) and minor (mbcr1) breakpoint cluster regions. In CML the breakpoint has been mapped almost exclusively to Mbcr1, whereas in Ph positive ALL both Mbcr1 and the upstream mbcr1 breakpoints have been described. In this communication we describe an unusual patient with typical chronic phase Ph positive CML and evidence of the uncharacteristic mbcr1 breakpoint, predicting expression of the ALL-type p190 fusion protein. Fluorescence in situ hybridization demonstrated BCR gene rearrangement, the reverse transcription polymerase chain reaction detected the BCR-ABL fusion mRNA characteristic of the mbcr1 breakpoint, and failed to detect BCR-ABL mRNA characteristic of the Mbcr1 breakpoint. Southern blot analysis revealed no rearrangement in Mbcr1, and direct sequencing of the PCR product confirmed it to be the ALL-type mbcr1 fusion mRNA with the first exon of the BCR gene fused to ABL exon a2. This case differs from the previously reported cases of "p190" CML in that the patient presented without abnormal hematopoietic features other than those found in typical CML and provides further evidence that the p190 mRNA is not sufficient to cause an acute rather than chronic leukemia.

摘要

费城染色体(Ph)见于慢性髓性白血病(CML)和急性淋巴细胞白血病(ALL)。Ph易位,t(9;22)(q34;q11),可在22号染色体上的一到两个区域破坏BCR基因,这两个区域称为主要(Mbcr1)和次要(mbcr1)断点簇区域。在CML中,断点几乎完全定位于Mbcr1,而在Ph阳性ALL中,Mbcr1和上游mbcr1断点均有描述。在本报告中,我们描述了一名不寻常的患者,其患有典型慢性期Ph阳性CML,并存在非典型mbcr1断点的证据,提示表达ALL型p190融合蛋白。荧光原位杂交显示BCR基因重排,逆转录聚合酶链反应检测到mbcr1断点特征性的BCR-ABL融合mRNA,而未检测到Mbcr1断点特征性的BCR-ABL mRNA。Southern印迹分析显示Mbcr1无重排,PCR产物直接测序证实其为ALL型mbcr1融合mRNA,BCR基因的第一个外显子与ABL外显子a2融合。该病例与先前报道的“p190”CML病例不同,该患者除了典型CML中发现的异常造血特征外,无其他异常造血特征,进一步证明p190 mRNA不足以导致急性而非慢性白血病。

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