Mitochondrial sirtuins in stem cells and cancer

被引:23
|
作者
Jaiswal, Amit [1 ,2 ]
Xudong, Zhu [2 ]
Zhenyu, Ju [1 ,3 ]
Saretzki, Gabriele [4 ]
机构
[1] Hangzhou Normal Univ, Inst Ageing Res, Sch Med, Hangzhou, Zhejiang, Peoples R China
[2] Friedrich Schiller Univ, Fac Biol Sci, Jena, Germany
[3] Jinan Univ, Inst Ageing & Regenerat Med, Key Lab Regenerat Med, Minist Educ, Guangzhou, Guangdong, Peoples R China
[4] Newcastle Univ, Biosci Inst, Campus Ageing & Vital, Newcastle Upon Tyne, Tyne & Wear, England
关键词
cancer; mitochondria; sirtuins; SIRT3; SIRT4; SIRT5; stem cells; INHIBITS PROSTATE-CANCER; TUMOR-SUPPRESSIVE FUNCTION; HEPATOCELLULAR-CARCINOMA; SIRT3; EXPRESSION; DOWN-REGULATION; GASTRIC-CANCER; OXIDATIVE-PHOSPHORYLATION; POOR-PROGNOSIS; POSTTRANSLATIONAL MODIFICATIONS; CALORIE RESTRICTION;
D O I
10.1111/febs.15879
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The mammalian sirtuin family consists of seven proteins, three of which (SIRT3, SIRT4, and SIRT5) localise specifically within mitochondria and preserve mitochondrial function and homeostasis. Mitochondrial sirtuins are involved in diverse functions such as deacetylation, ADP-ribosylation, demalonylation and desuccinylation, thus affecting various aspects of cell fate. Intriguingly, mitochondrial sirtuins are able to manage these delicate processes with accuracy mediated by crosstalk between the nucleus and mitochondria. Previous studies have provided ample information about their substrates and targets, whereas less is known about their role in cancer and stem cells. Here, we review and discuss recent advances in our understanding of the structural and functional properties of mitochondrial sirtuins, including their targets in cancer and stem cells. These advances could help to improve the understanding of their interplay with signalling cascades and pathways, leading to new avenues for developing novel drugs for sirtuin-related disease treatments. We also highlight the complex network of mitochondrial sirtuins in cancer and stem cells, which may be important in deciphering the molecular mechanism for their activation and inhibition.
引用
收藏
页码:3393 / 3415
页数:23
相关论文
共 50 条
  • [41] Decreased mitochondrial priming determines chemoresistance of colon cancer stem cells
    S Colak
    C D Zimberlin
    E Fessler
    L Hogdal
    P R Prasetyanti
    C M Grandela
    A Letai
    J P Medema
    Cell Death & Differentiation, 2014, 21 : 1170 - 1177
  • [42] Mitochondrial membrane potential and reactive oxygen species in cancer stem cells
    Zhang, Bei-bei
    Wang, Dao-gang
    Guo, Fen-fen
    Xuan, Chao
    FAMILIAL CANCER, 2015, 14 (01) : 19 - 23
  • [43] Adipose Stem Cells and Their Interplay with Cancer Cells and Mitochondrial Reservoir: A New Promising Target
    Rehman, Ayesha
    Marigliano, Martina
    Torsiello, Martina
    La Noce, Marcella
    Papaccio, Gianpaolo
    Tirino, Virginia
    Del Vecchio, Vitale
    Papaccio, Federica
    CANCERS, 2024, 16 (15)
  • [44] Mitochondrial functions in stem cells
    Margineantu, Daciana H.
    Hockenbery, David M.
    CURRENT OPINION IN GENETICS & DEVELOPMENT, 2016, 38 : 110 - 117
  • [45] Mitochondrial regulation in stem cells
    Wang, Yifei
    Barthez, Marine
    Chen, Danica
    TRENDS IN CELL BIOLOGY, 2024, 34 (08) : 685 - 694
  • [46] Mitochondrial Heterogeneity in Stem Cells
    Naik, Prajna Paramita
    Praharaj, Prakash P.
    Bhol, Chandra S.
    Panigrahi, Debasna P.
    Mahapatra, Kewal K.
    Patra, Srimanta
    Saha, Sarbari
    Bhutia, Sujit K.
    STEM CELLS HETEROGENEITY - NOVEL CONCEPTS, 2019, 1123 : 179 - 194
  • [47] The sirtuins in the pathogenesis of cancer
    Susanne Voelter-Mahlknecht
    Ulrich Mahlknecht
    Clinical Epigenetics, 2010, 1 : 71 - 83
  • [48] The sirtuins in the pathogenesis of cancer
    Voelter-Mahlknecht, Susanne
    Mahlknecht, Ulrich
    CLINICAL EPIGENETICS, 2010, 1 : 71 - 83
  • [49] Sirtuins, metabolism, and cancer
    Martinez-Pastor, Barbara
    Mostoslavsky, Raul
    FRONTIERS IN PHARMACOLOGY, 2012, 3
  • [50] Stem Cells, Cancer, and Cancer Stem Cells.
    Wahl, G. M.
    CANCER RESEARCH, 2011, 71