Biased signaling in drug discovery and precision medicine

被引:0
|
作者
Ji, Ren-Lei [1 ]
Tao, Ya-Xiong [1 ]
机构
[1] Auburn Univ, Coll Vet Med, Dept Anat Physiol & Pharmacol, Auburn, AL 36849 USA
关键词
Biased signaling; Biased ligand; G protein-coupled receptor; Ion channel; Receptor tyrosine kinase; Nuclear receptor; PROTEIN-COUPLED-RECEPTORS; II TYPE-1 RECEPTOR; MU-OPIOID RECEPTOR; POSITIVE ALLOSTERIC MODULATORS; NATURALLY-OCCURRING MUTATIONS; PARATHYROID-HORMONE RECEPTOR; STABILIZED ACTIVE STATE; BETA-ARRESTIN; MELANOCORTIN-4; RECEPTOR; FUNCTIONAL SELECTIVITY;
D O I
10.1016/j.pharmthera.2025.108804
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Receptors are crucial for converting chemical and environmental signals into cellular responses, making them prime targets in drug discovery, with about 70% of drugs targeting these receptors. Biased signaling, or functional selectivity, has revolutionized drug development by enabling precise modulation of receptor signaling pathways. This concept is more firmly established in G protein-coupled receptor and has now been applied to other receptor types, including ion channels, receptor tyrosine kinases, and nuclear receptors. Advances in structural biology have further refined our understanding of biased signaling. This targeted approach enhances therapeutic efficacy and potentially reduces side effects. Numerous biased drugs have been developed and approved as therapeutics to treat various diseases, demonstrating their significant therapeutic potential. This review provides a comprehensive overview of biased signaling in drug discovery and disease treatment, highlighting recent advancements and exploring the therapeutic potential of these innovative modulators across various diseases. (c) 2025 Elsevier Inc. All rights are reserved, including those for text and data mining, AI training, and similar technologies.
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页数:30
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