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17号染色体短臂缺失及p53基因突变在慢性髓性白血病急变期的预后意义

Prognostic significance of loss of a chromosome 17p and p53 gene mutations in blast crisis of chronic myelogenous leukaemia.

作者信息

Nakai H, Misawa S, Taniwaki M, Horiike S, Takashima T, Seriu T, Nakagawa H, Fujii H, Shimazaki C, Maruo N

机构信息

Department of Medicine, Kyoto Prefectural University of Medicine, Japan.

出版信息

Br J Haematol. 1994 Jun;87(2):425-7. doi: 10.1111/j.1365-2141.1994.tb04938.x.

DOI:10.1111/j.1365-2141.1994.tb04938.x
PMID:7947294
Abstract

In 31 cases of chronic myelogenous leukaemia (CML) we examined the prognostic significance of chromosomal loss of a 17p and p53 mutations at the onset of blast crisis (BC). p53 mutations were closely related to a shortened survival in CML-BC (P < 0.005 by the logrank test), whereas loss of a 17p by itself was not a poor prognostic indicator. The prognostic significance of loss of a 17p, however, emerged when combined with its predominance in the metaphases analysed. This predominance might easily and rapidly be screened by polymerase chain reaction-based analysis in about half of the cases.

摘要

在31例慢性粒细胞白血病(CML)患者中,我们研究了急变期(BC)开始时17号染色体短臂缺失及p53突变的预后意义。p53突变与CML-BC患者生存期缩短密切相关(对数秩检验P<0.005),而单纯17号染色体短臂缺失并非不良预后指标。然而,当17号染色体短臂缺失与分析中期相中其优势存在相结合时,其预后意义显现出来。在约半数病例中,基于聚合酶链反应的分析可轻松快速筛查出这种优势存在。

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Prognostic significance of loss of a chromosome 17p and p53 gene mutations in blast crisis of chronic myelogenous leukaemia.17号染色体短臂缺失及p53基因突变在慢性髓性白血病急变期的预后意义
Br J Haematol. 1994 Jun;87(2):425-7. doi: 10.1111/j.1365-2141.1994.tb04938.x.
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Genetic alterations in the p53 gene in the blast crisis of chronic myelogenous leukemia: analysis by polymerase chain reaction based techniques.慢性粒细胞白血病急变期p53基因的遗传改变:基于聚合酶链反应技术的分析
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Multiple aberrant splicing of the p53 transcript without genomic mutations around exon-intron junctions in a case of chronic myelogenous leukaemia in blast crisis: a possible novel mechanism of p53 inactivation.一例慢性髓性白血病急变期患者中,p53转录本存在多个异常剪接,而外显子-内含子连接处周围无基因组突变:p53失活的一种可能新机制。
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Involvement of the cyclin-dependent kinase-4 inhibitor (CDKN2) gene in the pathogenesis of lymphoid blast crisis of chronic myelogenous leukaemia.细胞周期蛋白依赖性激酶4抑制剂(CDKN2)基因在慢性粒细胞白血病淋巴母细胞危象发病机制中的作用。
Br J Haematol. 1995 Nov;91(3):625-9. doi: 10.1111/j.1365-2141.1995.tb05358.x.

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