Cited by 217Sirtuins and Resveratrol in MedicineMitochondrial Function and PathologyGenetics, Aging, and Longevity in Model Organisms

SIRT3 regulates progression and development of diseases of aging

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McDonnell, Eoin, Peterson, Brett S., Bomze, Howard M., Hirschey, Matthew D.·2015·Trends in Endocrinology & Metabolism

Abstract

The mitochondrial sirtuin SIRT3 is a protein deacylase that influences almost every major aspect of mitochondrial biology, including nutrient oxidation, ATP generation, reactive oxygen species (ROS) detoxification, mitochondrial dynamics, and the mitochondrial unfolded protein response (UPR). Interestingly, mice lacking SIRT3 (SIRT3KO), either spontaneously or when crossed with mouse models of disease, develop several diseases of aging at an accelerated pace, such as cancer, metabolic syndrome, cardiovascular disease, and neurodegenerative diseases, and, thus, might be a valuable model of accelerated aging. In this review, we discuss functions of SIRT3 in pathways involved in diseases of aging and how the lack of SIRT3 might accelerate the aging process. We also suggest that further studies on SIRT3 will help uncover important new pathways driving the aging process.

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Crossref · 10.1016/j.tem.2015.06.001

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  • SIRT3 is involved in cancer progression, neurodegenerative and cardiovascular disease as well as metabolic syndromes, and is likely a critical participant in many age-related disease processes.

    “SIRT3 is involved in cancer progression, neurodegenerative and cardiovascular disease as well as metabolic syndromes [212], and is likely a critical participant in many age-related disease processes.”

    From Redox control of senescence and age-related disease. (2017) · cites this paper as [212]

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  1. [18]Altekruse S SEER Cancer Statistics Review 1975 2007 National Cancer Institute Bethesda, MD
  2. [44]Federation ID IDF Diabetes Atlas 6th Edition

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Authors
McDonnell, E., Peterson, B. S., Bomze, H. M., & Hirschey, M. D.
Affiliations
Duke University (US)
Corresponding author
Hirschey, Matthew D.
Venue
Trends in Endocrinology & Metabolism
Publisher
Elsevier BV
Published
2015-09
Volume
26
Issue
9
Pages
486-492
ISSN
1043-2760 (ISSN-L)
OpenAlex
W1491563504
Cited by
217
References
97
Citations by year
2026: 11 · 2025: 16 · 2024: 18 · 2023: 21 · 2022: 31 · 2021: 21 · 2020: 17 · 2019: 22 · 2018: 16 · 2017: 23 · 2016: 18 · 2015: 2
FWCI
2.05
Type
journal article
Language
en
Open access
Locations
  • Trends in Endocrinology and Metabolism (publishedVersion)
  • PubMed (publishedVersion)
  • PubMed Central (acceptedVersion)
Funders
  • National Institute on Alcohol Abuse and Alcoholism (R01AA022146)
  • National Institute on Aging (R01AG045351, P30AG028716)
  • National Cancer Institute (T32CA059365)
  • National Institute of General Medical Sciences (T32GM007184, T32GM007105)
  • National Institute of Diabetes and Digestive and Kidney Diseases (R24DK085610)
Topics
  • Health Sciences › Medicine › Geriatrics and Gerontology › Sirtuins and Resveratrol in Medicine
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Mitochondrial Function and Pathology
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Aging › Genetics, Aging, and Longevity in Model Organisms
Keywords
SIRT3, mitochondrial sirtuins, aging, age-related diseases, SIRT3 knockout mice, accelerated aging, mitochondrial dynamics, mitochondrial unfolded protein response, reactive oxygen species scavenging, cancer, metabolic syndrome, cardiovascular disease, neurodegenerative diseases
MeSH terms
Aging, Animals, Disease, Humans, Longevity, Mice, Sirtuin 3

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