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代表性差异分析和杂合性缺失研究检测到神经母细胞瘤中的3p缺失。

Representational difference analysis and loss of heterozygosity studies detect 3p deletions in neuroblastoma.

作者信息

Hallstensson K, Thulin S, Aburatani H, Hippo Y, Martinsson T

机构信息

Department of Clinical Genetics, University of Gothenburg, East Hospital, Sweden.

出版信息

Eur J Cancer. 1997 Oct;33(12):1966-70. doi: 10.1016/s0959-8049(97)00228-1.

Abstract

In an attempt to identify genes involved in neuroblastoma, we scanned neuroblastoma tumour DNAs for homozygous deletions by representational difference analysis (RDA). The RDA produced several difference products, nine of which represented hemizygous deletions located on chromosome 1 or 3. In order to detect deletions, a genomewide loss of heterozygosity (LOH) screening with polymorphic markers was performed. Allelic losses on a number of different chromosomes were detected, mainly in favourable neuroblastomas (stage 1, 2 and 4S). The most frequently deleted region, apart from 1p, was chromosomal region 3p. A more detailed study was made in this region, which showed that 9 out of 58 (16%) tested neuroblastoma tumours showed allelic loss in the same region on chromosome 3p, i.e. 3pter-14.2. Thus, both RDA and LOH studies showed chromosome region 3p as being frequently involved in deletions and/or rearrangements in neuroblastoma tumours. Therefore, it is possible that one or more of the 3p genes implicated in the development of other cancers also play a role in neuroblastoma development and/or progression.

摘要

为了鉴定与神经母细胞瘤相关的基因,我们通过代表性差异分析(RDA)扫描神经母细胞瘤肿瘤DNA以寻找纯合缺失。RDA产生了几个差异产物,其中9个代表位于1号或3号染色体上的半合子缺失。为了检测缺失,我们使用多态性标记进行了全基因组杂合性缺失(LOH)筛查。在许多不同染色体上检测到了等位基因缺失,主要见于预后良好的神经母细胞瘤(1期、2期和4S期)。除了1p之外,最常发生缺失的区域是染色体区域3p。我们对该区域进行了更详细的研究,结果显示,在58个检测的神经母细胞瘤肿瘤中,有9个(16%)在3号染色体p臂的同一区域(即3pter-14.2)出现了等位基因缺失。因此,RDA和LOH研究均表明,染色体区域3p经常参与神经母细胞瘤肿瘤的缺失和/或重排。所以,在其他癌症发生过程中涉及的3p基因中的一个或多个,也有可能在神经母细胞瘤的发生和/或进展中发挥作用。

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