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Systematic Analysis of Quantitative Logic Model Ensembles Predicts Drug Combination Effects on Cell Signaling Networks

机译:定量逻辑模型的系统分析可预测药物组合对细胞信号网络的影响

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A major challenge in developing anticancer therapies is determining the efficacies of drugs and their combinations in physiologically relevant microenvironments. We describe here our application of ?¢????constrained fuzzy logic?¢???? (CFL) ensemble modeling of the intracellular signaling network for predicting inhibitor treatments that reduce the phospho?¢????levels of key transcription factors downstream of growth factors and inflammatory cytokines representative of hepatocellular carcinoma (HCC) microenvironments. We observed that the CFL models successfully predicted the effects of several kinase inhibitor combinations. Furthermore, the ensemble predictions revealed ambiguous predictions that could be traced to a specific structural feature of these models, which we resolved with dedicated experiments, finding that IL?¢????1???± activates downstream signals through TAK1 and not MEKK1 in HepG2 cells. We conclude that CFL?¢????Q2LM (Querying Quantitative Logic Models) is a promising approach for predicting effective anticancer drug combinations in cancer?¢????relevant microenvironments.
机译:开发抗癌疗法的主要挑战是确定药物及其组合在生理相关的微环境中的功效。我们在这里描述约束条件模糊逻辑的应用。 (CFL)细胞内信号网络的集成模型,用于预测抑制剂处理,以降低生长因子和肝细胞癌(HCC)微环境代表的炎性细胞因子下游关键转录因子的磷酸化水平。我们观察到CFL模型成功地预测了几种激酶抑制剂组合的作用。此外,整体预测揭示了模棱两可的预测,这些预测可以追溯到这些模型的特定结构特征,我们通过专门的实验对其进行了解析,结果发现IL ???????? 1 ???±通过TAK1而不是MEKK1激活下游信号。在HepG2细胞中我们得出的结论是,CFL Q2LM(查询定量逻辑模型)是预测癌症相关微环境中有效抗癌药物组合的有前途的方法。

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