Department of Drug Chemistry & Technologies, Sapienza University of Rome, P. le A. Moro 5, Rome, 00185, Italy.
Institute of Biological Systems (ISB), Italian National Research Council (CNR), Sezione Meccanismi di Reazione, c/o Department of Chemistry, Sapienza University of Rome, P. le A. Moro 5, Rome, 00185, Italy.
Future Med Chem. 2022 Jun;14(12):915-939. doi: 10.4155/fmc-2022-0031. Epub 2022 May 18.
Sirtuins are NAD-dependent protein lysine deacylase and mono-ADP ribosylases present in both prokaryotes and eukaryotes. The sirtuin family comprises seven isoforms in mammals, each possessing different subcellular localization and biological functions. Sirtuins have received increasing attention in the past two decades given their pivotal functions in a variety of biological contexts, including cytodifferentiation, transcriptional regulation, cell cycle progression, apoptosis, inflammation, metabolism, neurological and cardiovascular physiology and cancer. Consequently, modulation of sirtuin activity has been regarded as a promising therapeutic option for many pathologies. In this review, we provide an up-to-date overview of sirtuin biology and pharmacology. We examine the main features of the most relevant inhibitors and activators, analyzing their structure-activity relationships, applications in biology, and therapeutic potential.
Sirtuins 是 NAD 依赖性蛋白赖氨酸脱酰基酶和单 ADP 核糖基转移酶,存在于原核生物和真核生物中。在哺乳动物中,sirtuin 家族包括七种同工酶,每种同工酶都具有不同的亚细胞定位和生物学功能。在过去的二十年中,由于 sirtuins 在多种生物背景下具有关键作用,包括细胞分化、转录调控、细胞周期进程、细胞凋亡、炎症、代谢、神经和心血管生理学以及癌症等,它们受到了越来越多的关注。因此,调节 sirtuins 的活性被认为是许多病理学的一种有前途的治疗选择。在这篇综述中,我们提供了 sirtuins 生物学和药理学的最新概述。我们检查了最相关的抑制剂和激活剂的主要特征,分析了它们的结构-活性关系、在生物学中的应用和治疗潜力。