Kurzrock R, Blick M B, Talpaz M, Velasquez W S, Trujillo J M, Kouttab N M, Kloetzer W S, Arlinghaus R B, Gutterman J U
Ann Intern Med. 1986 Nov;105(5):673-9. doi: 10.7326/0003-4819-105-5-673.
We have followed one patient with Philadelphia (Ph)-negative chronic myelogenous leukemia and identified an additional four patients from the literature who showed the rearrangement in the breakpoint cluster region (bcr) on chromosome 22 characteristic of Ph-positive chronic myelogenous leukemia. The clinical course of these five patients was similar to that of Ph-positive patients, with easily controlled leukocyte counts, a prolonged benign phase, and prolonged survival. Furthermore, we have shown, for the first time, that bcr rearrangement in Ph-negative chronic myelogenous leukemia can result in expression of the aberrant 210-kilodalton bcr-abl fusion protein, which has been strongly implicated in Ph-positive leukemogenesis. Research data pertaining to possible cytogenetic mechanisms leading to production of p210bcr-abl in the absence of the Ph chromosome are reviewed. Molecular analysis provides an important tool for classifying and predicting prognosis of some patients with Ph-negative chronic myelogenous leukemia.
我们对一名费城(Ph)阴性慢性粒细胞白血病患者进行了跟踪,并从文献中另外确定了4名患者,他们在22号染色体上的断裂点簇区域(bcr)出现了重排,这是Ph阳性慢性粒细胞白血病的特征。这5名患者的临床病程与Ph阳性患者相似,白细胞计数易于控制,良性期延长,生存期延长。此外,我们首次表明,Ph阴性慢性粒细胞白血病中的bcr重排可导致异常的210千道尔顿bcr-abl融合蛋白表达,该蛋白与Ph阳性白血病的发生密切相关。本文综述了有关在无Ph染色体情况下导致p210bcr-abl产生的可能细胞遗传学机制的研究数据。分子分析为一些Ph阴性慢性粒细胞白血病患者的分类和预后预测提供了重要工具。