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Network-based analysis of reverse phase protein array data

机译:基于网络的反相蛋白阵列数据分析

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In this paper, we introduce a computational method for constructing networks based on reverse phase protein array (RPPA) data to identify complex patterns in protein signaling. The method is applied to phosphoproteomic profiles of basal expression and activation/phosphorylation of 76 key signaling proteins in three breast cancer cell lines (MCF7, LCC1, and LCC9). Temporal RPPA data are acquired at 48h, 96h, and 144h after knocking down four genes in separate experiments. These genes are selected from a previous study as important determinants for breast cancer survival. Interaction networks between the proteins and phosphorylated proteins are constructed by analyzing the expression levels of protein pairs using a multivariate analysis of variance model. A new scoring criterion is introduced to determine the proteins that changed significantly at each of the three time points. Signaling networks are constructed based on statistically significant protein pairs selected from the RPPA data. Through a topology based analysis, we search for wiring patterns to help identify key network nodes that are associated with protein expression changes in various experimental conditions.
机译:在本文中,我们介绍用于构建基于反相蛋白质阵列(RPPA)数据在蛋白信号以识别复杂的图案网络的计算方法。该方法被应用到基础表达和激活/三种乳腺癌细胞系76个键信号蛋白(MCF7,LCC1,和LCC9)的磷酸化的磷酸化蛋白质组学轮廓。颞RPPA数据被撞倒在单独的实验四个基因后在48h,96h后,和144H获取。这些基因是从以前的研究为乳腺癌生存的重要决定因素选择。蛋白质和磷酸化蛋白之间的相互作用的网络通过使用方差模型的多变量分析分析蛋白对表达水平构成。新的评分标准引入到确定分别在三个时间点的变化显著的蛋白质。信令网络基于从RPPA数据中选择统计学显著蛋白对构成。通过基于拓扑的分析,我们搜索的布线模式,以帮助识别与在不同的实验条件下蛋白表达变化相关的关键网络节点。

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