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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量化与分析

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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:我们介绍了一种综合的实验和计算方法,旨在识别与抗癌活动有助于或推动药物组合的治疗协同作用的关键细胞组分。该方法包括(i)在高吞吐量转录组实验中的药物协同作用的定量,(ii)数据驱动的逆向工程和前进仿真技术,开发用于药物协同作用的硅模型,(iii)利用相互作用和功能的数据库在最后一步(iv)中实验验证的假设生成的信息。目标是开发一个综合框架,有助于了解药物协同作用的机制细节,以设计更好的组合药物。我们说明了这种方法,申请分析了暴露于法呢基转移酶抑制剂(FTI)的协同抗癌药物组合(FTI)与紫杉烷的细胞细胞的转录组变化。

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