Suppr超能文献

Sirtuin 调节剂:过去、现在和未来的展望。

Sirtuin modulators: past, present, and future perspectives.

机构信息

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.

出版信息

Future Med Chem. 2022 Jun;14(12):915-939. doi: 10.4155/fmc-2022-0031. Epub 2022 May 18.

Abstract

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.

摘要

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。

相似文献

1
Sirtuin modulators: past, present, and future perspectives.Sirtuin 调节剂:过去、现在和未来的展望。
Future Med Chem. 2022 Jun;14(12):915-939. doi: 10.4155/fmc-2022-0031. Epub 2022 May 18.
5
The role of structural biology in the design of sirtuin activators.结构生物学在 sirtuin 激活剂设计中的作用。
Curr Opin Struct Biol. 2023 Oct;82:102666. doi: 10.1016/j.sbi.2023.102666. Epub 2023 Aug 4.
6
Sirtuin functions and modulation: from chemistry to the clinic.沉默调节蛋白的功能与调控:从化学到临床
Clin Epigenetics. 2016 May 25;8:61. doi: 10.1186/s13148-016-0224-3. eCollection 2016.
9
New assays and approaches for discovery and design of Sirtuin modulators.新型 Sirtuin 调节剂的发现和设计的检测方法和手段。
Expert Opin Drug Discov. 2014 Feb;9(2):183-99. doi: 10.1517/17460441.2014.875526. Epub 2014 Jan 2.
10
A mini-review on Sirtuin activity assays.关于沉默调节蛋白活性检测的小型综述。
Biochem Biophys Res Commun. 2015 Nov 20;467(3):459-66. doi: 10.1016/j.bbrc.2015.09.172. Epub 2015 Oct 9.

引用本文的文献

4
Novel Anti-Cancer Stem Cell Compounds: A Comprehensive Review.新型抗癌干细胞化合物:全面综述
Pharmaceutics. 2024 Aug 1;16(8):1024. doi: 10.3390/pharmaceutics16081024.
7
SIRT1, resveratrol and aging.沉默调节蛋白1、白藜芦醇与衰老
Front Genet. 2024 May 9;15:1393181. doi: 10.3389/fgene.2024.1393181. eCollection 2024.

本文引用的文献

1
Human Sirtuin Regulators: The "Success" Stories.人类沉默调节蛋白调节剂:“成功”故事
Front Physiol. 2021 Oct 21;12:752117. doi: 10.3389/fphys.2021.752117. eCollection 2021.
4
Emerging Therapeutic Potential of SIRT6 Modulators.SIRT6 调节剂的新兴治疗潜力。
J Med Chem. 2021 Jul 22;64(14):9732-9758. doi: 10.1021/acs.jmedchem.1c00601. Epub 2021 Jul 2.
6
SIRT5 IS A DRUGGABLE METABOLIC VULNERABILITY IN ACUTE MYELOID LEUKEMIA.SIRT5 是急性髓系白血病的可靶向代谢脆弱性。
Blood Cancer Discov. 2021 May;2(3):266-287. doi: 10.1158/2643-3230.BCD-20-0168. Epub 2019 Dec 2.
8
The Two-Faced Role of SIRT6 in Cancer.SIRT6在癌症中的双面角色。
Cancers (Basel). 2021 Mar 8;13(5):1156. doi: 10.3390/cancers13051156.
9
Reply to: Binding site for MDL-801 on SIRT6.回复:MDL-801在SIRT6上的结合位点。
Nat Chem Biol. 2021 May;17(5):522-523. doi: 10.1038/s41589-021-00750-5. Epub 2021 Mar 1.
10
Binding site for activator MDL-801 on SIRT6.激活剂MDL-801在SIRT6上的结合位点。
Nat Chem Biol. 2021 May;17(5):519-521. doi: 10.1038/s41589-021-00749-y. Epub 2021 Mar 1.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验