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Network analysis of genes regulated in renal diseases: implications for a molecular-based classification

机译:肾脏疾病中调控基因的网络分析:对基于分子的分类的启示

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Background Chronic renal diseases are currently classified based on morphological similarities such as whether they produce predominantly inflammatory or non-inflammatory responses. However, such classifications do not reliably predict the course of the disease and its response to therapy. In contrast, recent studies in diseases such as breast cancer suggest that a classification which includes molecular information could lead to more accurate diagnoses and prediction of treatment response. This article describes how we extracted gene expression profiles from biopsies of patients with chronic renal diseases, and used network visualizations and associated quantitative measures to rapidly analyze similarities and differences between the diseases. Results The analysis revealed three main regularities: (1) Many genes associated with a single disease, and fewer genes associated with many diseases. (2) Unexpected combinations of renal diseases that share relatively large numbers of genes. (3) Uniform concordance in the regulation of all genes in the network. Conclusion The overall results suggest the need to define a molecular-based classification of renal diseases, in addition to hypotheses for the unexpected patterns of shared genes and the uniformity in gene concordance. Furthermore, the results demonstrate the utility of network analyses to rapidly understand complex relationships between diseases and regulated genes.
机译:背景技术目前,慢性肾脏疾病是根据形态相似性进行分类的,例如它们主要产生炎症反应还是非炎症反应。但是,这样的分类不能可靠地预测疾病的进程及其对治疗的反应。相反,最近在诸如乳腺癌的疾病中的研究表明,包括分子信息的分类可以导致更准确的诊断和治疗反应的预测。本文介绍了我们如何从慢性肾脏疾病患者的活组织检查中提取基因表达谱,并使用网络可视化和相关的定量方法快速分析了疾病之间的异同。结果分析揭示了三个主要规律:(1)与一种疾病有关的基因很多,而与多种疾病有关的基因更少。 (2)共享大量基因的肾脏疾病的意外组合。 (3)在网络中所有基因的调节中具有一致的一致性。结论总体结果表明,除了假设共享基因的意外模式和基因一致性的假设外,还需要定义基于肾脏疾病的分子分类。此外,结果表明网络分析可用于快速了解疾病和受调控基因之间的复杂关系。

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