Dose-response prediction for in-vitro drug combination datasets: a probabilistic approach

被引:2
|
作者
Ronneberg, Leiv [1 ,2 ]
Kirk, Paul D. W. [2 ,3 ,4 ]
Zucknick, Manuela [1 ]
机构
[1] Univ Oslo, Oslo Ctr Biostat & Epidemiol, Oslo, Norway
[2] Univ Cambridge, MRC Biostat Unit, Cambridge, England
[3] Univ Cambridge, Cambridge Inst Therapeut Immunol & Infect Dis, Cambridge, England
[4] Canc Res UK Cambridge Ctr, Ovarian Canc Programme, Cambridge, England
基金
欧盟地平线“2020”; 英国医学研究理事会;
关键词
Gaussian process regression; Bayesian inference; Cell viability assay; Drug synergy; CANCER; SYNERGY; VORINOSTAT; TOXICITY; THERAPY;
D O I
10.1186/s12859-023-05256-6
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
In this paper we propose PIICM, a probabilistic framework for dose-response prediction in high-throughput drug combination datasets. PIICM utilizes a permutation invariant version of the intrinsic co-regionalization model for multi-output Gaussian process regression, to predict dose-response surfaces in untested drug combination experiments. Coupled with an observation model that incorporates experimental uncertainty, PIICM is able to learn from noisily observed cell-viability measurements in settings where the underlying dose-response experiments are of varying quality, utilize different experimental designs, and the resulting training dataset is sparsely observed. We show that the model can accurately predict dose-response in held out experiments, and the resulting function captures relevant features indicating synergistic interaction between drugs.
引用
收藏
页数:31
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