Department of Pharmacology, University of Washington, Seattle, Washington 98195, USA; email:
Annu Rev Pharmacol Toxicol. 2021 Jan 6;61:361-379. doi: 10.1146/annurev-pharmtox-022420-112134. Epub 2020 Jul 6.
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.
细胞通过动员信号转导级联来响应环境线索,该级联涉及蛋白激酶和磷酸蛋白磷酸酶。这些酶在空间和时间上的正确组织能够实现化学信号的高效和精确传递。环腺苷酸依赖性蛋白激酶 A 通过与 A 激酶锚定蛋白(AKAP)的关联而分隔。AKAP 是一类多功能支架,可将信号酶和效应物约束在亚细胞位置,以驱动基本的生理事件。最近,人们已经认识到,某些内分泌疾病和癌症中的信号转导缺陷是通过病理性 AKAP 复合物进行的。因此,针对这些大分子复合物进行药理学靶向治疗为越来越多的临床适应症开辟了新的治疗机会。这篇综述强调了 AKAP 信号在疾病中的最新发现,特别是在某些癌症中,并概述了局部调节 AKAP 结合伴侣的肽和小分子。