The Role of Sirtuins in Cellular Senescence and the Development of Age-Associated Diseases

被引:0
作者
Markelov, V. A. [1 ,2 ]
Akhmadishina, L. Z. [1 ,3 ]
Kochetova, O. V. [1 ,2 ]
Erdman, V. V. [1 ,2 ]
Korytina, G. F. [1 ,2 ]
机构
[1] Russian Acad Sci, Inst Biochem & Genet, Subdiv Ufa Fed Res Ctr, Ufa 450054, Russia
[2] Bashkir State Med Univ, Ufa 450000, Russia
[3] Ufa State Petr Technol Univ, Ufa 450064, Russia
基金
俄罗斯科学基金会;
关键词
sirtuins; cellular senescence; cell cycle; repair; age associated diseases; longevity; SIRT2 POLYMORPHISM RS10410544; OBSTRUCTIVE PULMONARY-DISEASE; DNA-DAMAGE; REPLICATIVE SENESCENCE; HETEROCHROMATIN FOCI; CALORIE RESTRICTION; ALZHEIMERS-DISEASE; GENE POLYMORPHISMS; OXIDATIVE STRESS; CELLS;
D O I
10.1134/S1022795425700152
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The increasing number of people aged 65 and older is an irreversible global trend. The growing number of studies increase confidence that classical age-associated diseases and geriatric conditions share a common set of basic biological mechanisms. Many endogenous molecules counteract the mechanisms of cellular senescence. To date, a number of anti-aging molecules have been identified, the role of which has been assessed in the pathophysiology of different diseases. NAD-dependent protein deacetylases and ADP-ribosyltransferases from the sirtuin family are considered as potential factors that slow down aging. Sirtuins are associated with antioxidant and oxidative stress reactions, regulation of mitochondrial function, repair of DNA damage and metabolism. Sirtuins and associated signaling cascades of cellular senescence regulatory network have a considerable impact on the development of age-associated diseases. The review presents a comprehensive analysis of the results of basic and clinical studies to shed the newlight on the role of sirtuins in the processes of cellular senescence and in the development of age-associated diseases. The data on the mechanisms of cellular senescence, the function of sirtuins (SIRT1-7), their interaction with key regulators of signaling cascades of cellular senescence and data on the association of polymorphic variants of sirtuin genes with the development of multifactorial diseases and longevity are presented.
引用
收藏
页码:613 / 633
页数:21
相关论文
共 212 条
[1]   Chemokine signaling via the CXCR2 receptor reinforces senescence [J].
Acosta, Juan C. ;
O'Loghlen, Ana ;
Banito, Ana ;
Guijarro, Maria V. ;
Augert, Arnaud ;
Raguz, Selina ;
Fumagalli, Marzia ;
Da Costa, Marco ;
Brown, Celia ;
Popov, Nikolay ;
Takatsu, Yoshihiro ;
Melamed, Jonathan ;
di Fagagna, Fabrizio d'Adda ;
Bernard, David ;
Hernando, Eva ;
Gil, Jesus .
CELL, 2008, 133 (06) :1006-1018
[2]  
Albani D, 2015, INT J MOL EPIDEMIOL, V6, P20
[3]   Modulation of human longevity by SIRT3 single nucleotide polymorphisms in the prospective study "Treviso Longeva (TRELONG)" [J].
Albani, Diego ;
Ateri, Eleonora ;
Mazzuco, Stefano ;
Ghilardi, Alice ;
Rodilossi, Serena ;
Biella, Gloria ;
Ongaro, Fausta ;
Antuono, Piero ;
Boldrini, Paolo ;
Di Giorgi, Enrico ;
Frigato, Andrea ;
Durante, Elisabetta ;
Caberlotto, Livio ;
Zanardo, Andrea ;
Siculi, Marinella ;
Gallucci, Maurizio ;
Forloni, Gianluigi .
AGE, 2014, 36 (01) :469-478
[4]   Autophagy prevents microglial senescence [J].
Amin, Sadaf ;
Liu, Bangyan ;
Gan, Li .
NATURE CELL BIOLOGY, 2023, 25 (07) :923-925
[5]   Naturally occurring p16Ink4a-positive cells shorten healthy lifespan [J].
Baker, Darren J. ;
Childs, Bennett G. ;
Durik, Matej ;
Wijers, Melinde E. ;
Sieben, Cynthia J. ;
Zhong, Jian ;
Saltness, Rachel A. ;
Jeganathan, Karthik B. ;
Verzosa, Grace Casaclang ;
Pezeshki, Abdulmohammad ;
Khazaie, Khashayarsha ;
Miller, Jordan D. ;
van Deursen, Jan M. .
NATURE, 2016, 530 (7589) :184-+
[6]   Combined loss of Cdk2 and Cdk4 results in embryonic lethality and Rb hypophosphorylation [J].
Berthet, Cyril ;
Klarmann, Kimberly D. ;
Hilton, Mary Beth ;
Suh, Hyung Chan ;
Keller, Jonathan R. ;
Kiyokawa, Hiroaki ;
Kaldis, Philipp .
DEVELOPMENTAL CELL, 2006, 10 (05) :563-573
[7]   Deglutarylation of glutaryl-CoA dehydrogenase by deacylating enzyme SIRT5 promotes lysine oxidation in mice [J].
Bhatt, Dhaval P. ;
Mills, C. Allie ;
Anderson, Kristin A. ;
Henriques, Barbara J. ;
Lucas, Tania G. ;
Francisco, Sara ;
Liu, Juan ;
Ilkayeva, Olga R. ;
Adams, Alexander E. ;
Kulkarni, Shreyas R. ;
Backos, Donald S. ;
Major, Michael B. ;
Grimsrud, Paul A. ;
Gomes, Claudio M. ;
Hirschey, Matthew D. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2022, 298 (04)
[8]   SIRT7 antagonizes human stem cell aging as a heterochromatin stabilizer [J].
Bi, Shijia ;
Liu, Zunpeng ;
Wu, Zeming ;
Wang, Zehua ;
Liu, Xiaoqian ;
Wang, Si ;
Ren, Jie ;
Yao, Yan ;
Zhang, Weiqi ;
Song, Moshi ;
Liu, Guang-Hui ;
Qu, Jing .
PROTEIN & CELL, 2020, 11 (07) :483-504
[9]   Aging results in DNA damage and telomere dysfunction that is greater in endothelial versus vascular smooth muscle cells and is exacerbated in atheroprone regions [J].
Bloom, Samuel, I ;
Tucker, Jordan R. ;
Lim, Jisok ;
Thomas, Tyler G. ;
Stoddard, Gregory J. ;
Lesniewski, Lisa A. ;
Donato, Anthony J. .
GEROSCIENCE, 2022, 44 (06) :2741-2755
[10]   Sirtuins in Alzheimer's Disease: SIRT2-Related GenoPhenotypes and Implications for PharmacoEpiGenetics [J].
Cacabelos, Ramon ;
Carril, Juan C. ;
Cacabelos, Natalia ;
Kazantsev, Aleksey G. ;
Vostrov, Alex V. ;
Corzo, Lola ;
Cacabelos, Pablo ;
Goldgaber, Dmitry .
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2019, 20 (05)