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Mol. Cells 2013; 36(5): 385-392

Published online November 6, 2013

https://doi.org/10.1007/s10059-013-0297-1

© The Korean Society for Molecular and Cellular Biology

Regulation of SIRT1 by MicroRNAs

Sung-E Choi, and Jongsook Kim Kemper

1Department of Molecular and Integrative Physiology, University of Illinois at Urbana, IL 61801, USA, 2Chronic Inflammatory Disease Research Center, Ajou University, Suwon 442-749, Korea

Received: September 30, 2013; Accepted: October 3, 2013

Abstract

Sirtuin 1 (SIRT1) is an NAD+-dependent deacetylase that connects cellular energy levels to homeostatic responses by deacetylating and modulating the activities of many transcriptional regulators. Discovered as a longevity protein in yeast, the mammalian SIRT1 has been intensively studied because of its great potential as a therapeutic target to benefit human health by preventing and improving many age-related diseases. There has been, therefore, substantial interest in developing agents that upregulate SIRT1 expression and activity. SIRT1 is regulated at multiple levels, including post-transcriptionally by microRNAs (miRs), powerful regulators of diverse biological pathways. Here we discuss how expression and activity of SIRT1 and other sirtuins are inhibited by miRs and further discuss the therapeutic potential of targeting miRs for age-related diseases that involve SIRT1 dysfunction, focusing on obesityrelated diseases.

Keywords aging, deacetylase, NAD, NAMPT, obesity, therapeutics

Article

Minireview

Mol. Cells 2013; 36(5): 385-392

Published online November 30, 2013 https://doi.org/10.1007/s10059-013-0297-1

Copyright © The Korean Society for Molecular and Cellular Biology.

Regulation of SIRT1 by MicroRNAs

Sung-E Choi, and Jongsook Kim Kemper

1Department of Molecular and Integrative Physiology, University of Illinois at Urbana, IL 61801, USA, 2Chronic Inflammatory Disease Research Center, Ajou University, Suwon 442-749, Korea

Received: September 30, 2013; Accepted: October 3, 2013

Abstract

Sirtuin 1 (SIRT1) is an NAD+-dependent deacetylase that connects cellular energy levels to homeostatic responses by deacetylating and modulating the activities of many transcriptional regulators. Discovered as a longevity protein in yeast, the mammalian SIRT1 has been intensively studied because of its great potential as a therapeutic target to benefit human health by preventing and improving many age-related diseases. There has been, therefore, substantial interest in developing agents that upregulate SIRT1 expression and activity. SIRT1 is regulated at multiple levels, including post-transcriptionally by microRNAs (miRs), powerful regulators of diverse biological pathways. Here we discuss how expression and activity of SIRT1 and other sirtuins are inhibited by miRs and further discuss the therapeutic potential of targeting miRs for age-related diseases that involve SIRT1 dysfunction, focusing on obesityrelated diseases.

Keywords: aging, deacetylase, NAD, NAMPT, obesity, therapeutics

Mol. Cells
Sep 30, 2023 Vol.46 No.9, pp. 527~572
COVER PICTURE
Chronic obstructive pulmonary disease (COPD) is marked by airspace enlargement (emphysema) and small airway fibrosis, leading to airflow obstruction and eventual respiratory failure. Shown is a microphotograph of hematoxylin and eosin (H&E)-stained histological sections of the enlarged alveoli as an indicator of emphysema. Piao et al. (pp. 558-572) demonstrate that recombinant human hyaluronan and proteoglycan link protein 1 (rhHAPLN1) significantly reduces the extended airspaces of the emphysematous alveoli by increasing the levels of TGF-β receptor I and SIRT1/6, as a previously unrecognized mechanism in human alveolar epithelial cells, and consequently mitigates COPD.

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