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Inference of Disease-Related Molecular Logic from Systems-Based Microarray Analysis

机译:基于系统的微阵列分析推论疾病相关的分子逻辑

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摘要

Computational analysis of gene expression data from microarrays has been useful for medical diagnosis and prognosis. The ability to analyze such data at the level of biological modules, rather than individual genes, has been recognized as important for improving our understanding of disease-related pathways. It has proved difficult, however, to infer pathways from microarray data by deriving modules of multiple synergistically interrelated genes, rather than individual genes. Here we propose a systems-based approach called Entropy Minimization and Boolean Parsimony (EMBP) that identifies, directly from gene expression data, modules of genes that are jointly associated with disease. Furthermore, the technique provides insight into the underlying biomolecular logic by inferring a logic function connecting the joint expression levels in a gene module with the outcome of disease. Coupled with biological knowledge, this information can be useful for identifying disease-related pathways, suggesting potential therapeutic approaches for interfering with the functions of such pathways. We present an example providing such gene modules associated with prostate cancer from publicly available gene expression data, and we successfully validate the results on additional independently derived data. Our results indicate a link between prostate cancer and cellular damage from oxidative stress combined with inhibition of apoptotic mechanisms normally triggered by such damage.
机译:来自微阵列的基因表达数据的计算分析已用于医学诊断和预后。在生物学模块而不是单个基因的水平上分析此类数据的能力已被认为对增进我们对疾病相关途径的了解很重要。然而,已经证明很难通过衍生多个协同相关基因而不是单个基因的模块来从微阵列数据推断途径。在这里,我们提出了一种称为熵最小化和布尔简约性(EMBP)的基于系统的方法,该方法直接从基因表达数据中识别与疾病联合的基因模块。此外,该技术通过推断将基因模块中关节表达水平与疾病结果联系起来的逻辑功能,从而洞察了潜在的生物分子逻辑。结合生物学知识,此信息可用于识别与疾病相关的途径,提示潜在的治疗方法可干扰此类途径的功能。我们提供了一个示例,提供了从公开可用的基因表达数据中与前列腺癌相关的此类基因模块,并且我们在其他独立衍生的数据上成功验证了结果。我们的结果表明,前列腺癌与氧化应激引起的细胞损伤以及通常由这种损伤引发的凋亡机制的抑制相联系。

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