Author:
Isenberg Natalie M.,Mertins Susan D.,Yoon Byung-Jun,Reyes Kristofer G.,Urban Nathan M.
Abstract
AbstractPharmacodynamic (PD) models are mathematical models of cellular reaction networks that include drug mechanisms of action. These models are useful for studying predictive therapeutic outcomes of novel drug therapies in silico. However, PD models are known to possess significant uncertainty with respect to constituent parameter data, leading to uncertainty in the model predictions. Furthermore, experimental data to calibrate these models is often limited or unavailable for novel pathways. In this study, we present a Bayesian optimal experimental design approach for improving PD model prediction accuracy. We then apply our method using simulated experimental data to account for uncertainty in hypothetical laboratory measurements. This leads to a probabilistic prediction of drug performance and a quantitative measure of which prospective laboratory experiment will optimally reduce prediction uncertainty in the PD model. The methods proposed here provide a way forward for uncertainty quantification and guided experimental design for models of novel biological pathways.
Funder
Advanced Scientific Computing Research
DOE Office of Biological and Environmental Research
Empire State Development Corporation
Brookhaven National Laboratory
National Cancer Institute
Publisher
Springer Science and Business Media LLC