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iTReX:单药和联合治疗剂量反应分析数据的交互式探索。

iTReX: Interactive exploration of mono- and combination therapy dose response profiling data.

机构信息

Bioinformatics and Omics Data Analytics, German Cancer Research Center (DKFZ), Heidelberg, Germany; Hopp Children's Cancer Center (KiTZ), Heidelberg, Germany; Division of Pediatric Neurooncology, German Cancer Research Center (DKFZ) and German Cancer Consortium (DKTK), Heidelberg, Germany; Faculty of Biosciences, Heidelberg University, Heidelberg, Germany.

Hopp Children's Cancer Center (KiTZ), Heidelberg, Germany; Clinical Cooperation Unit Pediatric Oncology, German Cancer Research Center (DKFZ) and German Cancer Consortium (DKTK), Heidelberg, Germany.

出版信息

Pharmacol Res. 2022 Jan;175:105996. doi: 10.1016/j.phrs.2021.105996. Epub 2021 Nov 27.

Abstract

High throughput screening methods, measuring the sensitivity and resistance of tumor cells to drug treatments have been rapidly evolving. Not only do these screens allow correlating response profiles to tumor genomic features for developing novel predictors of treatment response, but they can also add evidence for therapy decision making in precision oncology. Recent analysis methods developed for either assessing single agents or combination drug efficacies enable quantification of dose-response curves with restricted symmetric fit settings. Here, we introduce iTReX, a user-friendly and interactive Shiny/R application, for both the analysis of mono- and combination therapy responses. The application features an extended version of the drug sensitivity score (DSS) based on the integral of an advanced five-parameter dose-response curve model and a differential DSS for combination therapy profiling. Additionally, iTReX includes modules that visualize drug target interaction networks and support the detection of matches between top therapy hits and the sample omics features to enable the identification of druggable targets and biomarkers. iTReX enables the analysis of various quantitative drug or therapy response readouts (e.g. luminescence, fluorescence microscopy) and multiple treatment strategies (drug treatments, radiation). Using iTReX we validate a cost-effective drug combination screening approach and reveal the application's ability to identify potential sample-specific biomarkers based on drug target interaction networks. The iTReX web application is accessible at https://itrex.kitz-heidelberg.de.

摘要

高通量筛选方法,用于测量肿瘤细胞对药物治疗的敏感性和耐药性,正在迅速发展。这些筛选方法不仅可以将反应谱与肿瘤基因组特征相关联,从而开发出新的治疗反应预测因子,还可以为精准肿瘤学中的治疗决策提供依据。最近开发的用于评估单一药物或联合药物疗效的分析方法,可以在受限的对称拟合设置下定量剂量反应曲线。在这里,我们介绍了 iTReX,这是一个用户友好且互动的 Shiny/R 应用程序,用于分析单药和联合治疗反应。该应用程序具有基于高级五参数剂量反应曲线模型的积分的扩展版药物敏感性评分 (DSS),以及用于联合治疗分析的差分 DSS。此外,iTReX 还包括可视化药物靶标相互作用网络的模块,并支持检测顶级治疗靶点与样本组学特征之间的匹配,从而能够识别可用药靶标和生物标志物。iTReX 可以分析各种定量药物或治疗反应读数(例如发光、荧光显微镜)和多种治疗策略(药物治疗、放射治疗)。使用 iTReX,我们验证了一种具有成本效益的药物联合筛选方法,并揭示了该应用程序基于药物靶标相互作用网络识别潜在样本特异性生物标志物的能力。iTReX 网络应用程序可在 https://itrex.kitz-heidelberg.de 访问。

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