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Quantification and Analysis of Combination Drug Synergy in High-Throughput Transcriptome Studies

机译:高通量转录组研究中组合药物协同作用的定量和分析

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We present an integrated experimental and computational approach designed to identify the key cellular components that either contribute to or drive therapeutic synergy of drug combinations with anticancer activity. The approach includes (i) quantification of drug synergy in high throughput transcriptome experiments, (ii) data-driven reverse engineering and forward simulation technology to develop an in silico model predictive of drug synergy, and (iii) utilization of databases of interaction and functional information in hypothesis generation that are validated experimentally in a final step (iv). The goal is to develop an integrated framework that aids in understanding the mechanistic details of drug synergy to design better combination drugs. We illustrate this approach with an application to the analysis of transcriptome changes in cells exposed to the synergistic anticancer drug combination of farnesyl transferase inhibitors (FTIs) combined with taxanes.
机译:我们提出了一种集成的实验和计算方法,旨在识别有助于或驱动具有抗癌活性的药物组合的治疗协同作用的关键细胞成分。该方法包括(i)在高通量转录组实验中量化药物协同作用,(ii)数据驱动的逆向工程和正向仿真技术,以开发可预测药物协同作用的计算机模拟模型,以及(iii)利用相互作用和功能数据库在最后一步(iv)中通过实验验证的假设生成中的信息。目的是开发一个集成的框架,以帮助理解药物协同作用的机械细节,从而设计出更好的组合药物。我们举例说明了这种方法的应用,用于分析暴露于法呢基转移酶抑制剂(FTIs)与紫杉烷类的协同抗癌药物组合的细胞中的转录组变化。

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