SIRT2: Controversy and multiple roles in disease and physiology
- PMID: 31505260
- DOI: 10.1016/j.arr.2019.100961
SIRT2: Controversy and multiple roles in disease and physiology
Abstract
Sirtuin 2 (SIRT2) is an NAD+-dependent deacetylase that was under studied compared to other sirtuin family members. SIRT2 is the only sirtuin protein which is predominantly found in the cytoplasm but is also found in the mitochondria and in the nucleus. Recently, accumulating evidence has uncovered a growing number of substrates and additional detailed functions of SIRT2 in a wide range of biological processes, marking its crucial role. Here, we give a comprehensive profile of the crucial physiological functions of SIRT2 and its role in neurological diseases, cancers, and other diseases. This review summarizes the functions of SIRT2 in the nervous system, mitosis regulation, genome integrity, cell differentiation, cell homeostasis, aging, infection, inflammation, oxidative stress, and autophagy. SIRT2 inhibition rescues neurodegenerative disease symptoms and hence SIRT2 is a potential therapeutic target for neurodegenerative disease. SIRT2 is undoubtedly dysfunctional in cancers and plays a dual-faced role in different types of cancers, and although its mechanism is unresolved, SIRT2 remains a promising therapeutic target for certain cancers. In future, the continued rapid growth in SIRT2 research will help clarify its role in human health and disease, and promote the progress of this target in clinical practice.
Keywords: Cancer; Deacetylase; Neurodegeneration; Physiology functions; SIRT2.
Copyright © 2019 Elsevier B.V. All rights reserved.
Similar articles
-
Loss of SIRT2 leads to axonal degeneration and locomotor disability associated with redox and energy imbalance.Aging Cell. 2017 Dec;16(6):1404-1413. doi: 10.1111/acel.12682. Epub 2017 Oct 5. Aging Cell. 2017. PMID: 28984064 Free PMC article.
-
SIRT2 interferes with autophagy-mediated degradation of protein aggregates in neuronal cells under proteasome inhibition.Neurochem Int. 2012 Dec;61(7):992-1000. doi: 10.1016/j.neuint.2012.07.010. Epub 2012 Jul 20. Neurochem Int. 2012. PMID: 22819792
-
Multiple Roles of SIRT2 in Regulating Physiological and Pathological Signal Transduction.Genet Res (Camb). 2022 Aug 29;2022:9282484. doi: 10.1155/2022/9282484. eCollection 2022. Genet Res (Camb). 2022. PMID: 36101744 Free PMC article. Review.
-
The role of Sirtuin 2 in liver - An extensive and complex biological process.Life Sci. 2024 Feb 15;339:122431. doi: 10.1016/j.lfs.2024.122431. Epub 2024 Jan 17. Life Sci. 2024. PMID: 38242495 Review.
-
Sirtuin 2 mutations in human cancers impair its function in genome maintenance.J Biol Chem. 2017 Jun 16;292(24):9919-9931. doi: 10.1074/jbc.M116.772566. Epub 2017 May 1. J Biol Chem. 2017. PMID: 28461331 Free PMC article.
Cited by
-
The NAD-dependent deacetylase SIRT2 regulates T cell differentiation involved in tumor immune response.Int J Biol Sci. 2020 Oct 3;16(15):3075-3084. doi: 10.7150/ijbs.49735. eCollection 2020. Int J Biol Sci. 2020. PMID: 33061819 Free PMC article.
-
Sirtuin modulators: past, present, and future perspectives.Future Med Chem. 2022 Jun;14(12):915-939. doi: 10.4155/fmc-2022-0031. Epub 2022 May 18. Future Med Chem. 2022. PMID: 35583203 Free PMC article. Review.
-
Mammalian Sirtuins and Their Relevance in Vascular Calcification.Front Pharmacol. 2022 May 23;13:907835. doi: 10.3389/fphar.2022.907835. eCollection 2022. Front Pharmacol. 2022. PMID: 35677446 Free PMC article. Review.
-
SIRT2 plays complex roles in neuroinflammation neuroimmunology-associated disorders.Front Immunol. 2023 May 5;14:1174180. doi: 10.3389/fimmu.2023.1174180. eCollection 2023. Front Immunol. 2023. PMID: 37215138 Free PMC article. Review.
-
Sirtuin 2 Exerts Regulatory Functions on Radiation-Induced Myocardial Fibrosis in Mice by Mediating H3K27 Acetylation of Galectin-3 Promoter.Acta Cardiol Sin. 2024 Mar;40(2):214-224. doi: 10.6515/ACS.202403_40(2).20231026B. Acta Cardiol Sin. 2024. PMID: 38532816 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources