Zia, Aliabbas and Sahebdel, Faezeh and Farkhondeh, Tahereh and Ashrafizadeh, Milad and Zarrabi, Ali and Hushmandi, Kiavash and Samarghandian, Saeed (2021) A review study on the modulation of SIRT1 expression by miRNAs in aging and age-associated diseases. International Journal of Biological Macromolecules, 188 . pp. 52-61. ISSN 0141-8130 (Print) 1879-0003 (Online)
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Official URL: https://dx.doi.org/10.1016/j.ijbiomac.2021.08.013
Abstract
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.
Item Type: | Article |
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Uncontrolled Keywords: | Age-associated diseases; Aging; microRNAs; SIRT1 |
Divisions: | Faculty of Engineering and Natural Sciences Sabancı University Nanotechnology Research and Application Center |
Depositing User: | Ali Zarrabi |
Date Deposited: | 30 Aug 2022 12:41 |
Last Modified: | 30 Aug 2022 12:41 |
URI: | https://research.sabanciuniv.edu/id/eprint/43708 |