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7号染色体单体与Ph阳性急性淋巴细胞白血病:细胞遗传学和分子学方面

Monosomy 7 and Ph-positive acute lymphoblastic leukaemia: cytogenetic and molecular aspects.

作者信息

Eridani S, Gorman P, Sheer D, Duncombe A S, Glass U H, Shivji M K

机构信息

Division of Haematology, United Medical School, Guy's Hospital, London, U.K.

出版信息

Leuk Res. 1987;11(11):965-9. doi: 10.1016/0145-2126(87)90114-7.

Abstract

A combination of monosomy 7 and translocation t(9;22) (q34;q11), rarely observed in acute lymphoblastic leukaemia (ALL), is here reported: a peculiarity of this case was that the "breakpoint cluster region" on chromosome 22 was not rearranged, as demonstrated by molecular analysis, and a new c-abl protein (p190) was found, instead of the usual p210 protein usually associated with the Ph chromosome; moreover a rearrangement of c-abl oncogene was found. The clinical course of this patient was, as expected, unfavorable: a few normal metaphases were observed during a short partial remission.

摘要

本文报告了一种急性淋巴细胞白血病(ALL)中罕见的7号染色体单体与t(9;22)(q34;q11)易位的组合:该病例的一个特殊之处在于,经分子分析证实,22号染色体上的“断点簇区域”未发生重排,并且发现了一种新的c-abl蛋白(p190),而非通常与费城染色体相关的p210蛋白;此外,还发现了c-abl癌基因的重排。正如预期的那样,该患者的临床病程不佳:在短期部分缓解期观察到少数正常中期分裂相。

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