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慢性髓性白血病急变期克隆起源的分子证据。

Molecular evidence for the clonal origin of blast crisis in chronic myeloid leukaemia.

作者信息

Zalcberg J R, Friedlander M L, Minden M D

出版信息

Br J Cancer. 1986 Apr;53(4):459-64. doi: 10.1038/bjc.1986.73.

Abstract

Cytogenetic and enzymatic studies have shown that chronic myeloid leukemia (CML) represents the clonal proliferation of a pluripotent stem cell. The Philadelphia chromosome (Ph') is the characteristic karyotypic abnormality seen in this disease, although the exact role of this clonal marker in the pathogenesis of CML is uncertain. At a molecular level, the Ph' has recently been shown to represent the translocation of c-abl to a limited (breakpoint cluster region, bcr) on chromosome 22. We have used probes for the bcr gene to obtain molecular evidence for the clonal origin of blast crisis in 2 patient with CML. In both cases, the first with myeloid and the second with lymphoid blast crisis, there was rearrangement of the bcr gene. The patterns of rearrangement varied between patients but were identical when comparing acute and chronic phases within the same individual. As the Ph' translocation is thought to represent a random recombination event these data not only provide further evidence for the clonal origin of blast crisis in CML, but also suggest that in the second patient this translocation event had already occurred at the pluripotent stem cell.

摘要

细胞遗传学和酶学研究表明,慢性粒细胞白血病(CML)代表多能干细胞的克隆性增殖。费城染色体(Ph')是该疾病中可见的特征性核型异常,尽管这种克隆标记在CML发病机制中的确切作用尚不确定。在分子水平上,最近已证明Ph'代表c-abl基因易位至22号染色体上的一个有限区域(断裂点簇区域,bcr)。我们使用bcr基因探针,为2例CML患者急变期的克隆起源获取分子证据。在这两例患者中,第一例为髓系急变,第二例为淋巴系急变,均存在bcr基因重排。患者之间重排模式有所不同,但在同一个体的急性期和慢性期进行比较时则是相同的。由于Ph'易位被认为是一个随机重组事件,这些数据不仅为CML急变期的克隆起源提供了进一步证据,还表明在第二例患者中,这种易位事件在多能干细胞阶段就已经发生。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9909/2001434/40e225c537f4/brjcancer00528-0011-a.jpg

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