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Global Stabilization of Boolean Networks to Control the Heterogeneity of Cellular Responses

机译:布尔网络的全局稳定性以控制细胞反应的异质性

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摘要

Boolean networks (BNs) have been widely used as a useful model for molecular regulatory networks in systems biology. In the state space of BNs, attractors represent particular cell phenotypes. For targeted therapy of cancer, there is a pressing need to control the heterogeneity of cellular responses to the targeted drug by reducing the number of attractors associated with the ill phenotypes of cancer cells. Here, we present a novel control scheme for global stabilization of BNs to a unique fixed point. Using a sufficient condition of global stabilization with respect to the adjacency matrix, we can determine a set of constant controls so that the controlled BN is steered toward an unspecified fixed point which can then be further transformed to a desired attractor by subsequent control. Our method is efficient in that it has polynomial complexity with respect to the number of state variables, while having exponential complexity with respect to in-degree of BNs. To demonstrate the applicability of the proposed control scheme, we conduct simulation studies using a regulation influence network describing the metastatic process of cells and the Mitogen-activated protein kinase (MAPK) signaling network that is crucial in cancer cell fate determination.
机译:布尔网络(BN)已被广泛用作系统生物学中分子调控网络的有用模型。在BN的状态空间中,吸引子代表特定的细胞表型。对于癌症的靶向治疗,迫切需要通过减少与癌细胞的不良表型有关的吸引子的数量来控制对靶向药物的细胞应答的异质性。在这里,我们提出了一种新颖的控制方案,用于将BN全局稳定到唯一的固定点。使用关于邻接矩阵的全局稳定的充分条件,我们可以确定一组恒定控制,以便将受控BN导向未指定的固定点,然后可以通过后续控制将其进一步转换为所需的吸引子。我们的方法之所以有效,是因为它相对于状态变量的数量具有多项式复杂性,而相对于BN的度数则具有指数复杂性。为了证明所提出的控制方案的适用性,我们使用描述细胞转移过程的调节影响网络和对癌细胞命运决定至关重要的丝裂原活化蛋白激酶(MAPK)信号网络进行模拟研究。

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