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治疗相关性急性非淋巴细胞白血病患者的染色体带型分析

Banded chromosome analysis in patients with treatment-associated acute nonlymphocytic leukemia.

作者信息

Arthur D C, Bloomfield C D

出版信息

Cancer Genet Cytogenet. 1984 Jul;12(3):189-99. doi: 10.1016/0165-4608(84)90030-x.

DOI:10.1016/0165-4608(84)90030-x
PMID:6722761
Abstract

We have analyzed G-banded metaphase chromosomes from 20 patients with treatment-associated acute nonlymphocytic leukemia (t-ANLL). Nine patients were previously treated for hematologic malignancies and 11 for solid tumors. The interval from initial therapy to t-ANLL ranged from 35 to 182 mo (median 75.5 mo). Medial age at diagnosis of t-ANLL was 58.5 years. Clonal chromosome abnormalities were found in 19 patients (95%). Loss or partial deletion of the long arm of chromosomes #5 and/or #7 were most common, occurring in nine patients. These abnormalities were associated with hypodiploid complex karyotypes. Other nonrandom abnormalities recurring among karyotypes with abnormalities of chromosome #5 included loss of one #18, partial deletion of the long arm of chromosome #2, ring chromosomes, and a Philadelphia (Ph1) chromosome. We also identified a group of five patients whose only karyotypic abnormality was addition of whole chromosomes. The remaining five patients had other karyotypic abnormalities, the most common of which were structural rearrangements in a pseudodiploid clone. Combined data from our study and the three previously published large series of patients with t-ANLL studied with banding suggest a relationship between karyotype and intensity of prior therapy, with abnormalities of chromosomes #5 and #7 occurring more often in the intensively treated patients.

摘要

我们分析了20例治疗相关急性非淋巴细胞白血病(t-ANLL)患者的G显带中期染色体。9例患者既往接受过血液系统恶性肿瘤治疗,11例接受过实体瘤治疗。从初始治疗到发生t-ANLL的时间间隔为35至182个月(中位时间75.5个月)。t-ANLL诊断时的中位年龄为58.5岁。19例患者(95%)发现有克隆性染色体异常。5号和/或7号染色体长臂的缺失或部分缺失最为常见,9例患者出现此类情况。这些异常与亚二倍体复杂核型有关。在5号染色体异常的核型中反复出现的其他非随机异常包括18号染色体单体、2号染色体长臂部分缺失、环形染色体和费城(Ph1)染色体。我们还发现一组5例患者,其唯一的核型异常是整条染色体的增加。其余5例患者有其他核型异常,最常见的是假二倍体克隆中的结构重排。我们的研究数据与之前发表的3个用显带技术研究t-ANLL患者的大型系列数据综合分析表明,核型与既往治疗强度之间存在关联,5号和7号染色体异常在接受强化治疗的患者中更常见。

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1
Banded chromosome analysis in patients with treatment-associated acute nonlymphocytic leukemia.治疗相关性急性非淋巴细胞白血病患者的染色体带型分析
Cancer Genet Cytogenet. 1984 Jul;12(3):189-99. doi: 10.1016/0165-4608(84)90030-x.
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All patients with acute nonlymphocytic leukemia may have a chromosomal defect.所有急性非淋巴细胞白血病患者可能都有染色体缺陷。
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引用本文的文献

1
5q deletion in childhood T-acute lymphoblastic leukemia at diagnosis: a case report.儿童T淋巴细胞急性淋巴细胞白血病诊断时5号染色体长臂缺失:一例报告
J Med Case Rep. 2025 Jun 12;19(1):271. doi: 10.1186/s13256-024-04999-x.
2
Chromosomes in acute nonlymphocytic leukemia.
Hum Genet. 1986 Jun;73(2):137-46. doi: 10.1007/BF00291604.
3
Induction of sister chromatid exchanges at common fragile sites.
Am J Hum Genet. 1987 Nov;41(5):882-90.
4
Assignment of CSF-1 to 5q33.1: evidence for clustering of genes regulating hematopoiesis and for their involvement in the deletion of the long arm of chromosome 5 in myeloid disorders.
集落刺激因子-1定位于5q33.1:调控造血的基因成簇存在以及它们参与骨髓疾病中5号染色体长臂缺失的证据。
Proc Natl Acad Sci U S A. 1987 May;84(9):2970-4. doi: 10.1073/pnas.84.9.2970.
5
Genetic markers on chromosome 7.7号染色体上的遗传标记。
J Med Genet. 1988 May;25(5):294-306. doi: 10.1136/jmg.25.5.294.
6
Chromosome breakage and recombination at fragile sites.脆性位点处的染色体断裂与重组。
Am J Hum Genet. 1988 Sep;43(3):265-73.
7
Deletion mapping of human chromosome 5 using chromosome-specific DNA probes.使用染色体特异性DNA探针进行人类5号染色体的缺失图谱分析。
Am J Hum Genet. 1985 Sep;37(5):839-52.
8
Cosegregation of hypertrophic cardiomyopathy and a fragile site on chromosome 16 in a large Italian family.在一个意大利大家庭中肥厚型心肌病与16号染色体上一个脆性位点的共分离。
J Med Genet. 1990 Jun;27(6):363-6. doi: 10.1136/jmg.27.6.363.
9
Loss of both CSF1R (FMS) alleles in patients with myelodysplasia and a chromosome 5 deletion.骨髓增生异常综合征合并5号染色体缺失患者中CSF1R(FMS)两个等位基因的缺失。
Proc Natl Acad Sci U S A. 1991 Jul 15;88(14):6176-80. doi: 10.1073/pnas.88.14.6176.