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急性淋巴细胞白血病中的微小21号染色体着丝粒。

A diminutive chromosome 21 centromere in acute lymphoblastic leukemia.

作者信息

Roberts Kathryn A, Martineau Mary, Broadfield Zoë J, Gibson Brenda E S, Harewood Louise, Stewart Janet, Harrison Christine J

机构信息

LRF Cytogenetics Group, Cancer Sciences Division, University of Southampton, MP 822, Duthie Building, Southampton General Hospital, Tremona Road, Southampton, SO16 6YD, UK.

出版信息

Cancer Genet Cytogenet. 2006 May;167(1):78-81. doi: 10.1016/j.cancergencyto.2005.10.010.

Abstract

A chance observation of a tiny constitutional variant for the centromere of chromosome 21 in two patients with acute lymphoblastic leukemia (ALL), suggested a possible correlation with the cytogenetic findings in their leukemic cells. Interphase FISH revealed three 13/21 centromeric signals and a single MLL signal in the blast cells of each patient. Metaphase FISH with dual-color application of whole-chromosome paint (wcp) and centromeric probes for chromosome 21 showed two copies of chromosome 21, one with a tiny centromeric signal which corresponded to the invisible centromere in the interphase cells. Patient 2700 had a normal karyotype in his bone marrow at diagnosis. All metaphases from his stimulated peripheral blood also had the tiny chromosome 21 centromere, proving it to be a constitutional variant. Patient 3314 showed the abnormal karyotype 46,XY,inv(1)(p?q?),del(11)(q?),del(12)(p?),inc in his bone marrow. Interphase FISH revealed only one copy each of the ABL and ETV6 genes, in addition to the loss of the MLL signal. The question arises, is there an association between the diminutive centromeric signals for chromosome 21 and the chromosomal instability demonstrated by the deletions of key genes from the leukemic blasts of these two patients?

摘要

在两名急性淋巴细胞白血病(ALL)患者中偶然观察到21号染色体着丝粒的一个微小的体质性变异,提示其可能与白血病细胞中的细胞遗传学发现相关。间期荧光原位杂交(FISH)显示,每名患者的原始细胞中有三个13/21着丝粒信号和一个单一的混合系白血病(MLL)信号。用全染色体涂染探针(wcp)和21号染色体着丝粒探针进行双色应用的中期FISH显示有两条21号染色体,其中一条有着丝粒微小信号,这与间期细胞中不可见的着丝粒相对应。患者2700诊断时骨髓核型正常。其刺激外周血的所有中期细胞也都有21号染色体着丝粒微小信号,证明这是一种体质性变异。患者3314骨髓中显示异常核型46,XY,inv(1)(p?q?),del(11)(q?),del(12)(p?),inc。间期FISH显示,除MLL信号缺失外,ABL和ETV6基因各只有一个拷贝。问题来了,这两名患者白血病原始细胞中关键基因缺失所显示的染色体不稳定性与21号染色体着丝粒微小信号之间是否存在关联?

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