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成人急性髓细胞白血病中获得性基因组拷贝数异常与生存。

Acquired genomic copy number aberrations and survival in adult acute myelogenous leukemia.

机构信息

Division of Hematology and Oncology, Department of Internal Medicine, University of Michigan, Ann Arbor, MI 48109-0936, USA.

出版信息

Blood. 2010 Dec 2;116(23):4958-67. doi: 10.1182/blood-2010-01-266999. Epub 2010 Aug 20.

DOI:10.1182/blood-2010-01-266999
PMID:20729466
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3012590/
Abstract

Genomic aberrations are of predominant importance to the biology and clinical outcome of patients with acute myelogenous leukemia (AML), and conventional karyotype-based risk classifications are routinely used in clinical decision making in AML. One of the known limitations of cytogenetic analysis is the inability to detect genomic abnormalities less than 5 Mb in size, and it is currently unclear whether overcoming this limitation with high-resolution genomic single-nucleotide polymorphism (SNP) array analysis would be clinically relevant. Furthermore, given the heterogeneity of molecular mechanisms/aberrations that underlie the conventional karyotype-based risk classifications, it is likely that further refinements in genomic risk prognostication can be achieved. In this study, we analyzed flow cytometer-sorted, AML blast-derived, and paired, buccal DNA from 114 previously untreated prospectively enrolled AML patients for acquired genomic copy number changes and loss of heterozygosity using Affymetrix SNP 6.0 arrays, and we correlated genomic lesion load and specific chromosomal abnormalities with patient survival. Using multivariate analyses, we found that having ≥ 2 genomic lesions detected through SNP 6.0 array profiling approximately doubles the risk of death when controlling for age- and karyotype-based risk. Finally, we identified an independent negative prognostic impact of p53 mutations, or p53 mutations and 17p-loss of heterozygosity combined on survival in AML.

摘要

基因组异常对于急性髓系白血病 (AML) 患者的生物学和临床结局具有重要意义,基于常规核型的风险分类在 AML 的临床决策中被常规使用。细胞遗传学分析的一个已知局限性是无法检测小于 5Mb 的基因组异常,目前尚不清楚使用高分辨率基因组单核苷酸多态性 (SNP) 阵列分析是否能克服这一局限性。此外,鉴于构成基于常规核型的风险分类的分子机制/异常的异质性,在基因组风险预测方面可能会有进一步的改进。在这项研究中,我们使用 Affymetrix SNP 6.0 阵列分析了 114 名以前未经治疗的前瞻性入组的 AML 患者的流式细胞仪分选的 AML 原始细胞衍生的和配对的口腔 DNA,以获得获得性基因组拷贝数变化和杂合性丢失,并将基因组病变负荷和特定染色体异常与患者生存相关联。通过多变量分析,我们发现 SNP 6.0 阵列分析检测到的≥2 个基因组病变时,在控制年龄和核型风险后,死亡风险大约增加一倍。最后,我们确定了 p53 突变或 p53 突变和 17p 杂合性丢失在 AML 患者生存中的独立负预后影响。

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本文引用的文献

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Clin Cancer Res. 2010 Aug 15;16(16):4135-47. doi: 10.1158/1078-0432.CCR-09-2639. Epub 2010 May 26.
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Multiple distinct molecular mechanisms influence sensitivity and resistance to MDM2 inhibitors in adult acute myelogenous leukemia.多种不同的分子机制影响成人急性髓系白血病对 MDM2 抑制剂的敏感性和耐药性。
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New lesions detected by single nucleotide polymorphism array-based chromosomal analysis have important clinical impact in acute myeloid leukemia.基于单核苷酸多态性阵列的染色体分析检测到的新病变对急性髓系白血病具有重要的临床影响。
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Mutation in TET2 in myeloid cancers.髓系癌症中TET2基因的突变。
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