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bcr-abl mRNA lacking abl exon a2 detected by polymerase chain reaction in a chronic myelogeneous leukemia patient.

作者信息

van der Plas D C, Soekarman D, van Gent A M, Grosveld G, Hagemeijer A

机构信息

Department of Cell Biology and Genetics, Erasmus University, Rotterdam, The Netherlands.

出版信息

Leukemia. 1991 Jun;5(6):457-61.

PMID:2056770
Abstract

Using the polymerase chain reaction and Southern blot analysis the expression was detected of a bcr-abl mRNA lacking abl exon a2. This was due to a corresponding unusual localization of the breakpoint in the c-abl gene and was seen in a patient with Philadelphia (Ph) chromosome positive chronic myelogeneous leukemia in chronic phase. This type of mRNA has been described only once before in two Ph-positive acute lymphoblastic leukemia patients, by Soekarman et al. (1). The abl exon a2 sequences, which are missing in the three reported patients, code for a part of the SH3 region of the abl protein, which is supposed to be involved in negative regulation of the kinase domain. The clinical significance of this finding is discussed.

摘要

相似文献

1
bcr-abl mRNA lacking abl exon a2 detected by polymerase chain reaction in a chronic myelogeneous leukemia patient.
Leukemia. 1991 Jun;5(6):457-61.
2
Heterogeneity of the breakpoint in the ABL gene in cases with BCR/ABL transcript lacking ABL exon a2.缺乏ABL外显子a2的BCR/ABL转录本病例中ABL基因断点的异质性
Leukemia. 1994 Oct;8(10):1696-702.
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Leukemia. 1992 Sep;6(9):948-51.
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Acute lymphoid leukemia molecular phenotype in a patient with benign-phase chronic myelogenous leukemia.一名处于良性期慢性粒细胞白血病患者的急性淋巴细胞白血病分子表型
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Two patients with novel BCR/ABL fusion transcripts (e8/a2 and e13/a2) resulting from translocation breakpoints within BCR exons.两名患者因BCR外显子内的易位断点产生了新的BCR/ABL融合转录本(e8/a2和e13/a2)。
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Unusual expression of mRNA typical of Philadelphia positive acute lymphoblastic leukemia detected in chronic myeloid leukemia.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。
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Alu and translisin recognition site sequences flanking translocation sites in a novel type of chimeric bcr-abl transcript suggest a possible general mechanism for bcr-abl breakpoints.一种新型嵌合bcr-abl转录本中易位位点侧翼的Alu和转座酶识别位点序列提示了bcr-abl断点的一种可能的普遍机制。
Haematologica. 2000 Jan;85(1):40-6.

引用本文的文献

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Chronic myeloid leukemia with two rare fusion gene transcripts of atypical BCR::ABL: A case report and literature review.慢性髓性白血病伴两种罕见非典型 BCR::ABL 融合基因转录本:病例报告及文献复习。
Medicine (Baltimore). 2024 Jan 19;103(3):e36728. doi: 10.1097/MD.0000000000036728.
2
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3
A variant transcript, e1a3, of the minor BCR-ABL fusion gene in acute lymphoblastic leukemia: case report and review of the literature.
急性淋巴细胞白血病中次要BCR-ABL融合基因的一种变异转录本e1a3:病例报告及文献复习
Int J Hematol. 2008 Mar;87(2):184-188. doi: 10.1007/s12185-008-0031-5. Epub 2008 Feb 6.
4
Monitoring bcr-abl by polymerase chain reaction in the treatment of chronic myeloid leukemia.在慢性髓性白血病治疗中通过聚合酶链反应监测bcr-abl
Curr Oncol Rep. 2003 Sep;5(5):426-35. doi: 10.1007/s11912-003-0030-x.