Multiscale Modeling to Optimize Inhibition of Oncogenic ERK Pathway Signaling

多尺度建模优化致癌 ERK 通路信号传导的抑制

• 批准号: 10337242
• 负责人: William S Hlavacek
• 金额: $ 67.44万
• 依托单位: YALE UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2020
• 资助国家: 美国
• 起止时间: 2020-02-07 至 2025-01-31
• 项目状态: 未结题
• 来源: https://reporter.nih.gov/project-details/10337242
• 关键词: Accounting; Affect; BAY 54-9085; BRAF gene; Behavior; Binding; Biochemical; Biological Models; Caco-2 Cells; Cancer cell line; Cell Line; Cell Proliferation; Cell model; Cells; Clinic; Clinical; Colorectal Cancer; Complex; Computer Models; Coupled; Data; Drug Combinations; Drug Controls; Drug Targeting; Drug resistance; Effectiveness; Feedback; Foundations; Free Energy; Genetic; Genetically Engineered Mouse; Goals; Growth; In Vitro; KSR gene; Kinetics; Knock-out; Link; MAP Kinase Gene; MEKs; Malignant Neoplasms; Melanoma Cell; Modeling; Molecular; Molecular Biology; Molecular Conformation; Mutate; Mutation; Oncogenic; Pathway interactions; Pharmaceutical Preparations; Phosphotransferases; Positioning Attribute; Property; Protein Isoforms; Protein Kinase; Proteins; Recovery; Regulation; Resistance; Scaffolding Protein; Signal Pathway; Signal Transduction; Signaling Protein; Specificity; System; Systems Biology; Testing; Therapeutic; Thermodynamics; Time; Validation; Work; Xenograft procedure; base; cell transformation; clinical efficacy; dimer; drug efficacy; drug sensitivity; experimental study; in vivo; inhibitor; kinase inhibitor; knock-down; mathematical model; melanoma; molecular dynamics; molecular scale; multi-scale modeling; next generation; novel; novel strategies; overexpression; patient derived xenograft model; precision medicine; predictive modeling; prevent; protein expression; response; scaffold; small molecule inhibitor; standard of care; success; targeted treatment; therapy resistant; tool; tumor

PROJECT SUMMARY/ABSTRACT Small molecule inhibitors targeting the RAF/MEK/ERK pathway have become potent tools in precision medicine, but their clinical efficacy is highly variable across the diversity of RAS- and BRAF-mutated cancers. Even in susceptible cancers, these inhibitors rarely give durable responses. Studying the causes of resistance, which include ‘paradoxical’ ERK pathway activation by RAF inhibitors, has revealed complex molecular adaptations in the complicated networks comprised of RAF and ERK pathway kinases. These complexities limit our ability to understand and predict effectiveness of targeted therapies, especially in combination – despite decades of intense study, including mathematical modeling. Accurate predictions require understanding not only of the molecular complexities of protein kinase regulation and the intricate systems-level behavior of the networks that kinase constitute, but also of how these two levels of control are coupled. The challenge of accurately predicting effectiveness of targeted therapies and their combinations therefore demands an amalgamation of molecular and systems biology approaches. The systems biology project proposed here aims to identify optimal combinations of kinase inhibitors through mechanistic models that integrate understanding of both: 1) Conformation selectivity of kinase inhibitors – affecting structural, thermodynamic and kinetic properties of the targeted kinase(s); and 2) Systems-level network properties, including feedback loops, mutations and kinase/scaffold abundances, which can modify feedback loops and allow normally inconsequential kinase isoforms to compensate for isoform-specific kinase inhibition. Combining these features necessitates novel approaches to modeling cell signaling that directly link molecular/structural and network facets to predict which inhibitors and their combinations can efficiently suppress oncogenic signaling while disabling or delaying signal recovery, growth, and drug resistance. We propose to develop such next-generation multiscale models of oncogenic ERK signaling and drug responses, and to establish a new conceptual foundation for discovering effective drug combinations by integrating structural, thermodynamic and kinetic information – and combining short time-scale molecular dynamics (MD) with long time-scale modeling of systems-level dynamics. We will test our model predictions rigorously by integrating and iterating modeling and experimental studies. Experimental studies will begin in paired isogenic cancer cell lines with defined mutational differences. Once model predictions are suitably robust, we will progress to panels of cancer cell lines, then to cell line-derived xenografts in vivo, and then to patient-derived xenografts and genetically engineered mouse models (GEMMs) of melanoma – as a presage to clinically integrated predictions. We will determine if the strategy of hitting a kinase by two (or more) inhibitors with distinct conformation selectivity – as appears promising in our preliminary data – is generally applicable, can be combined with inhibition of different targets within a pathway, and can be understood at a detailed mechanistic level using our multiscale models.

项目概要/摘要 针对 RAF/MEK/ERK 通路的小分子抑制剂已成为精准医疗的有力工具， 但它们的临床疗效在不同的 RAS 和 BRAF 突变癌症中差异很大。 对于易感癌症，这些抑制剂很少能产生持久的反应，而研究耐药性的原因。 包括 RAF 抑制剂“矛盾的”ERK 通路激活，揭示了复杂的分子适应 由 RAF 和 ERK 通路激酶组成的复杂网络限制了我们的能力。 了解并预测靶向治疗的有效性，尤其是联合治疗——尽管几十年来 深入的研究，包括数学建模，不仅需要理解。 蛋白激酶调节的分子复杂性和网络的复杂系统级行为 激酶的构成，以及这两个控制水平如何耦合的挑战。 因此，靶向治疗及其组合的有效性需要分子融合 这里提出的系统生物学项目旨在最佳地识别。 通过整合对以下两者的理解的机制模型来组合激酶抑制剂： 1) 激酶抑制剂的构象选择性——影响其结构、热力学和动力学特性 目标激酶；和 2) 系统级网络特性，包括反馈循环、突变和 激酶/支架丰度，可以修改反馈环并允许通常无关紧要的激酶 结合这些特征需要新的异构体来补偿异构体特异性激酶抑制。 细胞信号传导建模方法直接连接分子/结构和网络方面以预测哪些 抑制剂及其组合可以有效抑制致癌信号，同时禁用或延迟信号 我们建议开发此类下一代多尺度模型。 致癌 ERK 信号传导和药物反应，并为发现建立新的概念基础 通过整合结构、热力学和动力学信息并结合起来有效的药物组合 我们将测试短时标分子动力学（MD）和长时标系统级动力学建模。 我们的模型通过整合和迭代建模和实验研究进行了严格的预测。 研究将在具有明确突变差异的配对同基因癌细胞系中开始。 足够强大，我们将进展到癌细胞系组，然后是细胞系衍生的体内异种移植物， 然后是源自患者的黑色素瘤异种移植物和基因工程小鼠模型 (GEMM)——如 我们将确定是否采用两次（或更多）击中激酶的策略。 具有独特构象选择性的抑制剂——正如我们的初步数据中显示的那样——通常是 适用，可以与途径内不同靶标的抑制相结合，并且可以在一定程度上理解 使用我们的多尺度模型详细的机械水平。