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相当一部分微卫星不稳定的结肠肿瘤携带TP53突变,却未表现出染色体不稳定。

A substantial proportion of microsatellite-unstable colon tumors carry TP53 mutations while not showing chromosomal instability.

作者信息

Westra Jantine L, Boven Ludolf G, van der Vlies Pieter, Faber Hendrika, Sikkema Birgit, Schaapveld Michael, Dijkhuizen Trijnie, Hollema Harry, Buys Charles H C M, Plukker John T M, Kok Klaas, Hofstra Robert M W

机构信息

Department of Medical Genetics, University of Groningen, The Netherlands.

出版信息

Genes Chromosomes Cancer. 2005 Jun;43(2):194-201. doi: 10.1002/gcc.20148.

Abstract

Chromosomal instability in colon tumors implies the presence of numerical and structural chromosome aberrations and is further characterized by the absence of microsatellite instability and the occurrence of KRAS and/or TP53 mutations. In a previous screening of 194 colon tumors for both microsatellite instability and TP53 mutation, we found 25 microsatellite-unstable tumors, in 9 (36%) of which, presumed to be chromosomally stable, there were TP53 mutations. This prompted us to investigate whether a TP53 mutation in these microsatellite-unstable tumors would be an indicator of chromosomal instability, that is, whether this would be a category of tumors showing both microsatellite and chromosomal instability. For chromosomal instability assessment, we performed array-comparative genomic hybridization analysis of tumor and control DNA extracted from formalin-fixed, paraffin-embedded stage III colon tumor specimens. The array consisted of 435 subtelomere-specific BACs. We compared all but one (whose DNA was of bad quality) of the microsatellite-unstable TP53 mutation-containing tumors (8) with a similarly sized group of microsatellite-unstable tumors without TP53 mutation (11). Microsatellite-unstable tumors with a TP53 mutation showed on average 0.9 aberrations (range 0-3) when assessed with this array system. Those without a TP53 mutation showed on average 0.7 aberrations (range 0-2). Thus, microsatellite-unstable tumors showed few chromosomal abnormalities regardless of TP53 mutation status. Because, in our study, the microsatellite-stable tumors had on average 3.4chromosomal abnormalities (range 0-7), a clear difference exists between microsatellite-unstable and -stable tumors. Because a substantial proportion of microsatellite-unstable colon tumors carry a TP53 mutation while showing relativelyfewchromosomal aberrations, a TP53 mutation in these tumors cannot be considered to be an indicator of chromosomal instability.

摘要

结肠肿瘤中的染色体不稳定性意味着存在染色体数目和结构畸变,其进一步特征为无微卫星不稳定性以及KRAS和/或TP53突变的发生。在之前对194例结肠肿瘤进行微卫星不稳定性和TP53突变筛查时,我们发现了25例微卫星不稳定肿瘤,其中9例(36%)被推测为染色体稳定,但存在TP53突变。这促使我们研究这些微卫星不稳定肿瘤中的TP53突变是否会是染色体不稳定性的一个指标,即这是否会是一类同时表现出微卫星和染色体不稳定性的肿瘤。为了评估染色体不稳定性,我们对从福尔马林固定、石蜡包埋的III期结肠肿瘤标本中提取的肿瘤和对照DNA进行了阵列比较基因组杂交分析。该阵列由435个亚端粒特异性BAC组成。我们将除1例(其DNA质量较差)外的所有含TP53突变的微卫星不稳定肿瘤(8例)与一组大小相似但无TP53突变的微卫星不稳定肿瘤(11例)进行了比较。使用该阵列系统评估时,有TP53突变的微卫星不稳定肿瘤平均显示0.9个畸变(范围为0 - 3)。无TP53突变的肿瘤平均显示0.7个畸变(范围为0 - 2)。因此,无论TP53突变状态如何,微卫星不稳定肿瘤显示出的染色体异常都很少。由于在我们的研究中,微卫星稳定肿瘤平均有3.4个染色体异常(范围为0 - 7),微卫星不稳定和稳定肿瘤之间存在明显差异。因为相当一部分微卫星不稳定的结肠肿瘤携带TP53突变,同时显示出相对较少的染色体畸变,所以这些肿瘤中的TP53突变不能被认为是染色体不稳定性的一个指标。

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