Drugs That Regulate Local Cell Signaling: AKAP Targeting as a Therapeutic Option

被引:38
作者
Bucko, Paula J. [1 ]
Scott, John D. [1 ]
机构
[1] Univ Washington, Dept Pharmacol, Seattle, WA 98195 USA
来源
ANNUAL REVIEW OF PHARMACOLOGY AND TOXICOLOGY, VOL 61, 2021 | 2021年 / 61卷
基金
美国国家卫生研究院;
关键词
spatial signaling; A-kinase anchoring protein; protein kinase A; anchoring disruptor agents; small-molecule inhibitors; precision pharmacology; PROTEIN-KINASE-A; ANCHORING PROTEIN; CYCLIC-AMP; SYNAPTIC INCORPORATION; SELECTIVE DISRUPTION; PEPTIDE DISRUPTORS; CATALYTIC SUBUNIT; MOLECULAR-CLONING; CA2+ CHANNELS; CAMP;
D O I
10.1146/annurev-pharmtox-022420-112134
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Cells respond to environmental cues by mobilizing signal transduction cascades that engage protein kinases and phosphoprotein phosphatases. Correct organization of these enzymes in space and time enables the efficient and precise transmission of chemical signals. The cyclic AMP-dependent protein kinase A is compartmentalized through its association with A-kinase anchoring proteins (AKAPs). AKAPs are a family of multivalent scaffolds that constrain signaling enzymes and effectors at subcellular locations to drive essential physiological events. More recently, it has been recognized that defective signaling in certain endocrine disorders and cancers proceeds through pathological AKAP complexes. Consequently, pharmacologically targeting these macromolecular complexes unlocks new therapeutic opportunities for a growing number of clinical indications. This review highlights recent findings on AKAP signaling in disease, particularly in certain cancers, and offers an overview of peptides and small molecules that locally regulate AKAP-binding partners.
引用
收藏
页码:361 / 379
页数:19
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