Abstract

BackgroundTransfection of NF κB synthetic decoy Oligodeoxynucleotides (ODNs) has been proposed as a promising therapeutic strategy for a variety of diseases arising from constitutive activation of the eukaryotic transcription factor NF κB. The decoy approach faces some limitations under physiological conditions notably nuclease-induced degradation.ResultsIn this work, we show how a systems pharmacology model of NF κB regulatory networks displaying oscillatory temporal dynamics, can be used to predict quantitatively the dependence of therapeutic efficacy of NF κB synthetic decoy ODNs on dose, unbinding kinetic rates and nuclease-induced degradation rates. Both deterministic mass action simulations and stochastic simulations of the systems biology model show that the therapeutic efficacy of synthetic decoy ODNs is inversely correlated with unbinding kinetic rates, nuclease-induced degradation rates and molecular stripping rates, but is positively correlated with dose. We show that the temporal coherence of the stochastic dynamics of NF κB regulatory networks is most sensitive to adding NF κB synthetic decoy ODNs having unbinding time-scales that are in-resonance with the time-scale of the limit cycle of the network.ConclusionsThe pharmacokinetics/pharmacodynamics (PK/PD) predicted by the systems-level model should provide quantitative guidance for in-depth translational research of optimizing the thermodynamics/kinetic properties of synthetic decoy ODNs.

Highlights

  • Transfection of NFκB synthetic decoy Oligodeoxynucleotides (ODNs) has been proposed as a promising therapeutic strategy for a variety of diseases arising from constitutive activation of the eukaryotic transcription factor NFκB

  • The model does not account for the effect of the degradation of NFκB synthetic decoy ODNs, which is reported later

  • Drug development needs to take into account the negative influence on therapeutic efficacy of active-dissociation processes such as molecular stripping when tailoring dose and unbinding kinetic rates of drugs to achieve optimal efficacy

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Summary

Introduction

Transfection of NFκB synthetic decoy Oligodeoxynucleotides (ODNs) has been proposed as a promising therapeutic strategy for a variety of diseases arising from constitutive activation of the eukaryotic transcription factor NFκB. While induced activation of NFκB plays a pivotal role in regulating immune and inflammatory responses, constitutive NFκB activation is observed in many pathologies [2, 4]. Such constitutive activity is widely considered as a major causal event for many human diseases, including chronic inflammation, auto-immune diseases and cancer etc [5,6,7,8]. We aim to understand how NFκB synthetic decoy ODNs affect the systems biology of the entire biological network of NFκB signaling, and if network models

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