A review study on the modulation of SIRT1 expression by miRNAs in aging and age-associated diseases

被引:30
|
作者
Zia, Aliabbas [1 ]
Sahebdel, Faezeh [2 ]
Farkhondeh, Tahereh [3 ,4 ]
Ashrafizadeh, Milad [5 ,6 ]
Zarrabi, Ali [5 ]
Hushmandi, Kiavash [7 ]
Samarghandian, Saeed [8 ]
机构
[1] Univ Tehran, Inst Biochem & Biophys IBB, Dept Biochem, Tehran, Iran
[2] Univ Minnesota, Med Sch, Dept Rehabil Med, Minneapolis, MN USA
[3] Birjand Univ Med Sci, Cardiovasc Dis Res Ctr, Birjand, Iran
[4] Birjand Univ Med Sci, Fac Pharm, Birjand, Iran
[5] Sabanci Univ, Fac Engn & Nat Sci, Univ Caddesi 27, Istanbul, Turkey
[6] Sabanci Univ Nanotechnol Res & Applicat Ctr SUNUM, Istanbul, Turkey
[7] Univ Tehran, Div Epidemiol, Dept Food Hyg & Qual Control, Fac Vet Med, Tehran, Iran
[8] Neyshabur Univ Med Sci, Noncommunicable Dis Res Ctr, Neyshabur, Iran
关键词
SIRT1; microRNAs; Aging; Age-associated diseases; FARNESOID X RECEPTOR; EPITHELIAL-MESENCHYMAL TRANSITION; SMALL HETERODIMER PARTNER; GRANULOSA-CELL APOPTOSIS; MIR-200; FAMILY; TUMOR-SUPPRESSOR; DOWN-REGULATION; FOLLICULAR ATRESIA; CIRCULATING LEVELS; NAD(+) METABOLISM;
D O I
10.1016/j.ijbiomac.2021.08.013
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
Sirtuin-1 (SIRT1) as a NAD + -dependent Class III protein deacetylase, involves in longevity and various cellular physiological processes. SIRT1 via deacetylating transcription factors regulates cell growth, inflammation, metabolism, hypoxic responses, cell survival, senescence, and aging. MicroRNAs (miRNAs) are short non-coding RNAs that modulate the expression of target genes in a post-transcriptional manner. Recent investigations have exhibited that miRNAs have an important role in regulating cell growth, development, stress responses, tumor formation and suppression, cell death, and aging. In the present review, we summarize recent findings about the roles of miRNAs in regulating SIRT1 and SIRT1-associated signaling cascade and downstream effects, like apoptosis and aging. Here we introduce and discuss how activity and expression of SIRT1 are modulated by miRNAs and further review the therapeutic potential of targeting miRNAs for age-associated diseases that involve SIRT1 dysfunction. Although at its infancy, research on the roles of miRNAs in aging and their function through modulating SIRT1 may provide new insights in deciphering the key molecular pathways related to aging and age-associated disorders.
引用
收藏
页码:52 / 61
页数:10
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