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Review
. 2018 Feb;13(2):179-192.
doi: 10.1080/17460441.2018.1413089. Epub 2017 Dec 12.

Improving the efficacy-safety balance of polypharmacology in multi-target drug discovery

Affiliations
Review

Improving the efficacy-safety balance of polypharmacology in multi-target drug discovery

Balaguru Ravikumar et al. Expert Opin Drug Discov. 2018 Feb.

Abstract

Polypharmacology has emerged as an essential paradigm for modern drug discovery process. Multiple lines of evidence suggest that agents capable of modulating multiple targets in a selective manner may offer also improved balance between therapeutic efficacy and safety compared to single-targeted agents. Areas covered: Herein, the authors review the recent progress made in experimental and computational strategies for addressing the critical challenges with rational discovery of selective multi-targeted agents within the context of polypharmacological modelling. Specific focus is placed on multi-targeted mono-therapies, although examples of combinatorial polytherapies are also covered as an important part of the polypharmacology paradigm. The authors focus mainly on anti-cancer treatment applications, where polypharmacology is playing a key role in determining the efficacy-toxicity trade-off of multi-targeting strategies. Expert opinion: Even though it is widely appreciated that complex polypharmacological interactions can contribute both to therapeutic and adverse side-effects, systematic approaches for improving this balance by means of integrated experimental-computational strategies are still lacking. Future developments will be needed for comprehensive collection and harmonization of systems-wide target selectivity data, enabling better utilization and control for multi-targeted activities in the drug development process. Additional areas of future developments include model-based strategies for drug combination screening and improved pre-clinical validation options with animal models.

Keywords: Polypharmacology; computational models; data resources; drug combination therapies; drug repositioning; efficacy-toxicity ratio; multi-target drug design; profiling strategies; screening libraries; web-tools.

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