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首页> 外文期刊>Genes, Chromosomes and Cancer >A substantial proportion of microsatellite-unstable colon tumors carry TP53 mutations while not showing chromosomal instability.
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A substantial proportion of microsatellite-unstable colon tumors carry TP53 mutations while not showing chromosomal instability.

机译:大部分微卫星不稳定的结肠肿瘤带有TP53突变,但未显示染色体不稳定。

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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.
机译:结肠肿瘤中的染色体不稳定表示存在数字和结构染色体畸变,其特征还在于不存在微卫星不稳定以及出现KRAS和/或TP53突变。在先前对194例结肠癌的微卫星不稳定性和TP53突变筛查中,我们发现了25例微卫星不稳定的肿瘤,其中9例(36%)被认为是染色体稳定的,存在TP53突变。这促使我们调查这些微卫星不稳定肿瘤中的TP53突变是否会指示染色体不稳定,即是否属于一类同时显示微卫星和染色体不稳定的肿瘤。对于染色体不稳定性评估,我们对福尔马林固定,石蜡包埋的III期结肠肿瘤标本提取的肿瘤和对照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。我们将包含一个微卫星不稳定的TP53突变的肿瘤(8个除外)(其DNA质量较差)与没有TP53突变的大小相似的一组微卫星不稳定的肿瘤进行了比较(11)。用该阵列系统评估时,具有TP53突变的微卫星不稳定肿瘤平均显示0.9像差(范围0-3)。没有TP53突变的人显示平均0.7像差(范围0-2)。因此,无论TP53突变状态如何,微卫星不稳定肿瘤均显示很少的染色体异常。因为在我们的研究中,微卫星稳定的肿瘤平均存在3.4个染色体异常(范围为0-7),所以微卫星不稳定的肿瘤与稳定的肿瘤之间存在明显的差异。由于相当一部分微卫星不稳定的结肠肿瘤携带TP53突变,但显示出相对很少的染色体畸变,因此不能将这些肿瘤中的TP53突变视为染色体不稳定的指标。

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