| Literature DB >> 30797775 |
Christian T Meyer1, David J Wooten2, B Bishal Paudel3, Joshua Bauer4, Keisha N Hardeman3, David Westover5, Christine M Lovly6, Leonard A Harris7, Darren R Tyson7, Vito Quaranta8.
Abstract
Two goals motivate treating diseases with drug combinations: reduce off-target toxicity by minimizing doses (synergistic potency) and improve outcomes by escalating effect (synergistic efficacy). Established drug synergy frameworks obscure such distinction, failing to harness the potential of modern chemical libraries. We therefore developed multi-dimensional synergy of combinations (MuSyC), a formalism based on a generalized, multi-dimensional Hill equation, which decouples synergistic potency and efficacy. In mutant-EGFR-driven lung cancer, MuSyC reveals that combining a mutant-EGFR inhibitor with inhibitors of other kinases may result only in synergistic potency, whereas synergistic efficacy can be achieved by co-targeting mutant-EGFR and epigenetic regulation or microtubule polymerization. In mutant-BRAF melanoma, MuSyC determines whether a molecular correlate of BRAFi insensitivity alters a BRAF inhibitor's potency, efficacy, or both. These findings showcase MuSyC's potential to transform the enterprise of drug-combination screens by precisely guiding translation of combinations toward dose reduction, improved efficacy, or both.Entities:
Keywords: BRAF-mutant melanoma; drug synergy; high-throughput combination drug screens; non-small-cell lung cancer; systems pharmacology
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Year: 2019 PMID: 30797775 PMCID: PMC6675406 DOI: 10.1016/j.cels.2019.01.003
Source DB: PubMed Journal: Cell Syst ISSN: 2405-4712 Impact factor: 10.304