The DOI matches its Crossref record, with a small difference in title or year; 71 of the 71 references it cites were found in a registry or an index.
FOXO3: A Major Gene for Human Longevity - A Mini-Review
Open accessAbstract
Background: The gene FOXO3, encoding the transcription factor forkhead box O-3 (FoxO3), is one of only two for which genetic polymorphisms have exhibited consistent associations with longevity in diverse human populations. Objective: Here, we review the multitude of actions of FoxO3 that are relevant to health, and thus healthy ageing and longevity. Methods: The study involved a literature search for articles retrieved from PubMed using FoxO3 as keyword. Results: We review the molecular genetics of FOXO3 in longevity, then current knowledge of FoxO3 function relevant to ageing and lifespan. We describe how FoxOs are involved in energy metabolism, oxidative stress, proteostasis, apoptosis, cell cycle regulation, metabolic processes, immunity, inflammation and stem cell maintenance. The single FoxO in Hydra confers immortality to this fresh water polyp, but as more complex organisms evolved, this role has been usurped by the need for FoxO to control a broader range of specialized pathways across a wide spectrum of tissues assisted by the advent of as many as 4 FoxO subtypes in mammals. The major themes of FoxO3 are similar, but not identical, to other FoxOs and include regulation of cellular homeostasis, particularly of stem cells, and of inflammation, which is a common theme of age-related diseases. Other functions concern metabolism, cell cycle arrest, apoptosis, destruction of potentially damaging reactive oxygen species and proteostasis. Conclusions: The mechanism by which longevity-associated alleles of FOXO3 reduce age-related mortality is currently of great clinical interest. The prospect of optimizing FoxO3 activity in humans to increase lifespan and reduce age-related diseases represents an exciting avenue of clinical investigation. Research strategies directed at developing therapeutic agents that target FoxO3, its gene and proteins in the pathway(s) FoxO3 regulates should be encouraged and supported.
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“The SIRT-1 agonist resveratrol ameliorated ageing pathology, in part by activating FOXO3.33,155”
From Senescence-induced inflammation: an important player and key therapeutic target in atherosclerosis (2020) · cites this paper as [33]
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“Direct FOXO3 agonism is pharmacologically possible.33”
From Senescence-induced inflammation: an important player and key therapeutic target in atherosclerosis (2020) · cites this paper as [33]
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“Combination therapy with dasatinib and quercetin (D+Q) removed senescent cells from the tunica media, but not the intima, improving vascular function parameters, but not arterial compliance and plaque burden.33”
From Senescence-induced inflammation: an important player and key therapeutic target in atherosclerosis (2020) · cites this paper as [33]
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Metadata
- Authors
- Morris, B. J., Willcox, D. C., Donlon, T. A., & Willcox, B. J.
- Affiliations
- University of Hawaiʻi at Mānoa (US)
- Kuakini Medical Center (US)
- Venue
- Gerontology
- Publisher
- S. Karger AG
- Published
- 2015
- Volume
- 61
- Issue
- 6
- Pages
- 515-525
- ISSN
- 0304-324X (ISSN-L)
- 1423-0003
- PMC
- PMC5403515
- OpenAlex
- W2058381071
- Cited by
- 353
- References
- 70
- Citations by year
- 2026: 25 · 2025: 32 · 2024: 44 · 2023: 39 · 2022: 45 · 2021: 34 · 2020: 33 · 2019: 26 · 2018: 22 · 2017: 29 · 2016: 20 · 2015: 4
- FWCI
- 2.42
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Gerontology (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institutes of Health (5r01ag038707-04, 5R01AG038707)
- National Institute on Aging (5R01AG038707, R01-AG-038707, R01AG027060)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › FOXO transcription factor regulation
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Aging › Genetics, Aging, and Longevity in Model Organisms
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Muscle Physiology and Disorders
- Keywords
- FOXO3, human longevity, healthy aging, genetic polymorphism, age-related diseases, oxidative stress, proteostasis, apoptosis, cell cycle regulation, stem cell maintenance, inflammation, energy metabolism, Hydra, lifespan
- MeSH terms
- Forkhead Box Protein O3, Animals, Humans, Longevity, Forkhead Transcription Factors
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Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
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