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Knowledge-guided fuzzy logic modeling to infer cellular signaling networks from proteomic data

机译:知识指导的模糊逻辑建模可从蛋白质组学数据推断细胞信号网络

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摘要

Modeling of signaling pathways is crucial for understanding and predicting cellular responses to drug treatments. However, canonical signaling pathways curated from literature are seldom context-specific and thus can hardly predict cell type-specific response to external perturbations; purely data-driven methods also have drawbacks such as limited biological interpretability. Therefore, hybrid methods that can integrate prior knowledge and real data for network inference are highly desirable. In this paper, we propose a knowledge-guided fuzzy logic network model to infer signaling pathways by exploiting both prior knowledge and time-series data. In particular, the dynamic time warping algorithm is employed to measure the goodness of fit between experimental and predicted data, so that our method can model temporally-ordered experimental observations. We evaluated the proposed method on a synthetic dataset and two real phosphoproteomic datasets. The experimental results demonstrate that our model can uncover drug-induced alterations in signaling pathways in cancer cells. Compared with existing hybrid models, our method can model feedback loops so that the dynamical mechanisms of signaling networks can be uncovered from time-series data. By calibrating generic models of signaling pathways against real data, our method supports precise predictions of context-specific anticancer drug effects, which is an important step towards precision medicine.
机译:信号通路的建模对于理解和预测细胞对药物治疗的反应至关重要。然而,从文献中选择的规范信号通路很少是特定于上下文的,因此很难预测细胞对外部扰动的特定类型的响应。纯粹由数据驱动的方法还具有诸如生物学解释性有限的缺点。因此,非常需要能够集成先验知识和真实数据以进行网络推断的混合方法。在本文中,我们提出了一种知识导向的模糊逻辑网络模型,通过利用先验知识和时间序列数据来推断信号通路。特别是,动态时间规整算法用于测量实验数据与预测数据之间的拟合优度,因此我们的方法可以对按时间顺序排列的实验观测值进行建模。我们在合成数据集和两个真实的磷酸蛋白质组数据集上评估了该方法。实验结果表明,我们的模型可以揭示药物诱导的癌细胞信号通路变化。与现有的混合模型相比,我们的方法可以对反馈回路进行建模,从而可以从时序数据中揭示信令网络的动态机制。通过针对真实数据校准信号通路的通用模型,我们的方法支持对特定背景抗癌药物作用的精确预测,这是迈向精密医学的重要一步。

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