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Boolean modeling and fault diagnosis in oxidative stress response

机译:氧化应激反应的布尔建模和故障诊断

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摘要

BackgroundOxidative stress is a consequence of normal and abnormal cellular metabolism and is linked to the development of human diseases. The effective functioning of the pathway responding to oxidative stress protects the cellular DNA against oxidative damage; conversely the failure of the oxidative stress response mechanism can induce aberrant cellular behavior leading to diseases such as neurodegenerative disorders and cancer. Thus, understanding the normal signaling present in oxidative stress response pathways and determining possible signaling alterations leading to disease could provide us with useful pointers for therapeutic purposes. Using knowledge of oxidative stress response pathways from the literature, we developed a Boolean network model whose simulated behavior is consistent with earlier experimental observations from the literature. Concatenating the oxidative stress response pathways with the PI3-Kinase-Akt pathway, the oxidative stress is linked to the phenotype of apoptosis, once again through a Boolean network model. Furthermore, we present an approach for pinpointing possible fault locations by using temporal variations in the oxidative stress input and observing the resulting deviations in the apoptotic signature from the normally predicted pathway. Such an approach could potentially form the basis for designing more effective combination therapies against complex diseases such as cancer.
机译:背景氧化应激是正常和异常细胞代谢的结果,并与人类疾病的发展有关。响应氧化应激的途径的有效功能可以保护细胞DNA免受氧化损伤。相反,氧化应激反应机制的失败会诱导异常的细胞行为,从而导致诸如神经退行性疾病和癌症的疾病。因此,了解氧化应激反应途径中存在的正常信号传导并确定可能导致疾病的信号传导改变可能为我们提供治疗目的的有用指示。利用文献中对氧化应激反应途径的了解,我们开发了布尔网络模型,其模拟行为与文献中较早的实验观察结果一致。将氧化应激反应途径与PI3-激酶-Akt途径联系起来,再次通过布尔网络模型将氧化应激与细胞凋亡的表型联系起来。此外,我们提出了一种通过使用氧化应力输入中的时间变化并观察凋亡标记与正常预测途径的偏离而确定可能的故障位置的方法。这种方法可能会为设计针对复杂疾病(例如癌症)的更有效的联合疗法奠定基础。

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