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Chromosomal Regions in Prostatic Carcinomas Studied by Comparative Genomic Hybridization, Hierarchical Cluster Analysis and Self-Organizing Feature Maps

机译:通过比较基因组杂交,分层聚类分析和自组织特征图研究前列腺癌中的染色体区域

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摘要

Comparative genomic hybridization (CGH) is an established genetic method which enables a genome‐wide survey of chromosomal imbalances. For each chromosome region, one obtains the information whether there is a loss or gain of genetic material, or whether there is no change at that place. Therefore, large amounts of data quickly accumulate which must be put into a logical order. Cluster analysis can be used to assign individual cases (samples) to different clusters of cases, which are similar and where each cluster may be related to a different tumour biology. Another approach consists in a clustering of chromosomal regions by rewriting the original data matrix, where the cases are written as rows and the chromosomal regions as columns, in a transposed form. In this paper we applied hierarchical cluster analysis as well as two implementations of self‐organizing feature maps as classical and neuronal tools for cluster analysis of CGH data from prostatic carcinomas to such transposed data sets. Self‐organizing maps are artificial neural networks with the capability to form clusters on the basis of an unsupervised learning rule. We studied a group of 48 cases of incidental carcinomas, a tumour category which has not been evaluated by CGH before. In addition we studied a group of 50 cases of pT2N0‐tumours and a group of 20 pT3N0‐carcinomas. The results show in all case groups three clusters of chromosomal regions, which are (i) normal or minimally affected by losses and gains, (ii) regions with many losses and few gains and (iii) regions with many gains and few losses. Moreover, for the pT2N0‐ and pT3N0‐groups, it could be shown that the regions 6q, 8p and 13q lay all on the same cluster (associated with losses), and that the regions 9q and 20q belonged to the same cluster (associated with gains). For the incidental cancers such clear correlations could not be demonstrated.
机译:比较基因组杂交(CGH)是一种建立的遗传方法,其能够进行基因组的染色体失衡调查。对于每个染色体区域,获得信息是否存在遗传物质的损失或增益,或者在该地方是否没有变化。因此,大量数据迅速累积,必须放入逻辑顺序。聚类分析可用于将单个情况(样本)分配给不同的病例簇,它们类似,并且每个群集可能与不同的肿瘤生物学有关。另一种方法在于通过重写原始数据矩阵来组成染色体区域的聚类,其中案例以转置形式被写为作为列的行和染色体区域。在本文中,我们应用了分层集群分析以及自组织特征映射的两种实现,作为CGH数据从前列腺癌到这种转换数据集的CGH数据的聚类和神经元工具。自组织地图是人工神经网络,具有基于无监督的学习规则形成群集的能力。我们研究了一组48例偶然癌,一种肿瘤类别,尚未通过CGH评估。此外,我们研究了一组50例PT2N0-肿瘤和一组20pt3N0-癌。结果表明,在所有情况下都显示了三种染色体区域簇,这是(i)正常或最小地受损和收益影响,(ii)具有许多损失的地区,并且(iii)地区的损失和(iii)地区有许多收益和损失很少。此外,对于PT2N0和PT3N0组,可以示出区域6Q,8P和13Q在同一群集中(与损耗相关联),并且区域9Q和20Q属于同一群集(与之相关联收益)。对于偶然的癌症,不能证明这种明确的相关性。

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