The DOI matches its Crossref record; 75 of the 75 references it cites were found in a registry or an index.
Extending Healthy Life Span—From Yeast to Humans
Open accessAbstract
Eat Less, Live Long: Studies in several model organisms have shown that dietary restriction without malnutrition, or manipulation of nutrient-sensing pathways through mutations or drugs, can increase life span and reduce age-related disease. Fontana et al. (p. 321 ) review the ways in which nutrient-sensing pathways are central to aging. Studies of yeast, worms, rodents, and primates show that these pathways are conserved during evolution. Although data on the effects of dietary restriction in primates are very limited, in humans, the protective effects of dietary restriction against cancer, cardiovascular disease, and diabetes must be judged against potentially negative long-term effects. More work is needed to determine whether dietary restriction and the modulation of anti-aging pathways through drugs can extend life span and reduce pathologies in humans.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
The source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“Caloric restriction has been demonstrated to be the most effective strategy to lengthen healthspan and lifespan, and is efficacious in a range of species from yeast to primates255.”
From Cellular senescence in ageing: from mechanisms to therapeutic opportunities (2021) · cites this paper as [255]
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“dietary restriction has been the most effective strategy to demonstrate an increase in lifespan across a whole range of investigated species, including nonhuman primates”
From The Microbiota-Gut-Brain Axis (2019) · cites this paper as Fontana et al., 2010
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“dietary restriction (DR) increases lifespan or healthspan in all investigated eukaryote species, including unicellular and multicellular organisms of several distinct phyla, including non-human primates”
From The Hallmarks of Aging (2013) · cites this paper as Fontana et al., 2010
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“Genetic polymorphisms or mutations that reduce the functions of GH, IGF-1 receptor, insulin receptor or downstream intracellular effectors such as AKT, mTOR and FOXO, have been linked to longevity, both in humans and in model organisms”
From The Hallmarks of Aging (2013) · cites this paper as Fontana et al., 2010
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“Multiple genetic manipulations that attenuate signaling intensity at different levels of the IIS pathway consistently extend the lifespan of worms, flies and mice”
From The Hallmarks of Aging (2013) · cites this paper as Fontana et al., 2010
Experimental — accuracy not yet measured
The source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“Remarkably, the IIS pathway is the most conserved aging-controlling pathway in evolution”
From The Hallmarks of Aging (2013) · cites this paper as Fontana et al., 2010
Experimental — accuracy not yet measuredThe cited source says what the claim attributes to it.
In the citing paper
“Collectively, current available evidence strongly supports the idea that anabolic signaling accelerates aging, and decreased nutrient signaling extends longevity”
From The Hallmarks of Aging (2013) · cites this paper as Fontana et al., 2010
The cited source says what the claim attributes to it.
In the citing paper
“Genetic analyses indicate that this pathway mediates part of the beneficial effects of DR on longevity in worms and flies”
From The Hallmarks of Aging (2013) · cites this paper as Fontana et al., 2010
In the citing paper
“Dietary, genetic, and pharmacological (rapamycin) inhibition of mTOR extends life span in multiple model organisms (83).”
From Health Benefits of the Mediterranean Diet: Metabolic and Molecular Mechanisms (2018) · cites this paper as [83]
In the citing paper
“The IIS pathway informs cells of glucose levels and is the most conserved aging-controlling pathway in evolution.207”
From Meta-hallmarks of aging and cancer (2023) · cites this paper as [207]
In the citing paper
“Suppression of the insulin–insulin-like growth factor 1 (IGF1) signalling (IIS) pathway dramatically extends lifespan in multiple organisms, which suggests that it is an evolutionarily conserved mechanism16.”
From Mitochondrial and metabolic dysfunction in ageing and age-related diseases (2022) · cites this paper as [16]
In the citing paper
“Additional interest on how nutrient scarcity modulates mitochondrial function comes from the fact that CR is the most consistent physiological intervention to improve health and extend lifespan across a wide range of organisms (Fontana et al, 2010; Houtkooper et al, 2010b).”
From Mitochondrial response to nutrient availability and its role in metabolic disease (2014) · cites this paper as Fontana et al, 2010
In the citing paper
“The data infer the mutations cause a physiological state similar to that experienced during periods of reduced calorie intake (206).”
From A Critical Review of the Evidence That Metformin Is a Putative Anti-Aging Drug That Enhances Healthspan and Extends Lifespan (2021) · cites this paper as [206]
In the citing paper
“Caloric restriction reduces the generation of growth hormone, insulin, IGF1, and other growth factors, all of which have been shown to hasten aging and increase mortality in a number of species (see Figure 3) (206).”
From A Critical Review of the Evidence That Metformin Is a Putative Anti-Aging Drug That Enhances Healthspan and Extends Lifespan (2021) · cites this paper as [206]
In the citing paper
“Several genetic mutations, such as in the C. elegans DAF-16 transcription signaling pathway, involving nutrient-sensing pathways have been described and linked to a role in extending lifespan.”
From A Critical Review of the Evidence That Metformin Is a Putative Anti-Aging Drug That Enhances Healthspan and Extends Lifespan (2021) · cites this paper as [206]
In the citing paper
“Furthermore, caloric restriction has been found to extend the life span of several organisms including S. cerevisiae (yeast), C. elegans, fish, rodents, and rhesus monkeys (206, 207).”
From A Critical Review of the Evidence That Metformin Is a Putative Anti-Aging Drug That Enhances Healthspan and Extends Lifespan (2021) · cites this paper as [206]
In the citing paper
“Importantly, CR-mediated longevity in eukaryotes seems to be governed by a set of conserved nutrient signaling pathways (Fontana et al., 2010).”
From The Search for Antiaging Interventions: From Elixirs to Fasting Regimens (2014) · cites this paper as Fontana et al., 2010
In the citing paper
“Among them are the insulin and the TOR/S6K pathways, whose inhibition upon CR eventually confer stress resistance and promote survival during aging.”
From The Search for Antiaging Interventions: From Elixirs to Fasting Regimens (2014) · cites this paper as Fontana et al., 2010
In the citing paper
“Since then, CR has been shown to prolong mean and maximum lifespan in dogs, rodents, worms, flies, yeasts, and prokaryotes (Fontana et al., 2010).”
From The Search for Antiaging Interventions: From Elixirs to Fasting Regimens (2014) · cites this paper as Fontana et al., 2010
In the citing paper
“CR reduces the release of growth factors like growth hormone, insulin and insulin-like growth factor 1 (IGF1), which have been shown to accelerate aging and increase mortality in many organisms (Fontana et al., 2010).”
From The Search for Antiaging Interventions: From Elixirs to Fasting Regimens (2014) · cites this paper as Fontana et al., 2010
In the citing paper
“Stress-related transcription factors represent the common effectors in yeast, flies, worms, and mammals (Fontana et al., 2010).”
From The Search for Antiaging Interventions: From Elixirs to Fasting Regimens (2014) · cites this paper as Fontana et al., 2010
In the citing paper
“Accumulating evidence suggests that protein restriction is necessary and sufficient for depletion of serum IGF1 in humans (Fontana et al., 2010).”
From The Search for Antiaging Interventions: From Elixirs to Fasting Regimens (2014) · cites this paper as Fontana et al., 2010
In the citing paper
“Female rats subjected to prolonged CR become infertile in a reversible fashion (Martin et al., 2007), and moderate CR may be harmful to lean human beings (Fontana et al., 2010).”
From The Search for Antiaging Interventions: From Elixirs to Fasting Regimens (2014) · cites this paper as Fontana et al., 2010
In the citing paper
“CR changes many parameters in the aging human body, including the transcriptome, the hormonal status (in particular the serum concentration of IGF-1 and thyroid hormones), oxidative stress, inflammation, mitochondrial function, and glucose homeostasis (Fontana et al., 2010).”
From The Search for Antiaging Interventions: From Elixirs to Fasting Regimens (2014) · cites this paper as Fontana et al., 2010
In the citing paper
“Hence, exercise training can have a beneficial impact against diseases and metabolic disorders that typically accompany aging, notably cardiovascular diseases, diabetes and osteoporosis (Fontana et al., 2010).”
From The Search for Antiaging Interventions: From Elixirs to Fasting Regimens (2014) · cites this paper as Fontana et al., 2010
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
1 retracted
Bonkowski, M. S., Dominici, F. P., Arum, O., Rocha, J. S., Al-Regaiey, K., Westbrook, R., Spong, A., Panici, J. A., Masternak, M. M., Kopchick, J. J., et al. (2009) · PLoS ONE · doi:10.1371/journal.pone.0004567 · Cited by 125
RetractedRapamycin fed late in life extends lifespan in genetically heterogeneous mice
Harrison, D. E., Strong, R., Sharp, Z. D., Nelson, J. F., Astle, C. M., Flurkey, K., Nadon, N. L., Wilkinson, J. E., Frenkel, K., Carter, C. S., et al. (2009) · Nature · doi:10.1038/nature08221 · Cited by 3,766
Caloric Restriction Delays Disease Onset and Mortality in Rhesus Monkeys
Colman, R. J., Anderson, R. M., Johnson, S. C., Kastman, E. K., Kosmatka, K. J., Beasley, T. M., Allison, D. B., Cruzen, C., Simmons, H. A., Kemnitz, J. W., et al. (2009) · Science · doi:10.1126/science.1173635 · Cited by 2,277
Lin, S.-J., Defossez, P.-A., & Guarente, L. (2000) · Science · doi:10.1126/science.289.5487.2126 · Cited by 1,775
Regulation of lifespan in Drosophila by modulation of genes in the TOR signaling pathway
Kapahi, P., Zid, B. M., Harper, T., Koslover, D., Sapin, V., & Benzer, S. (2004) · Current Biology · doi:10.1016/j.cub.2004.03.059 · Cited by 1,293
Regulation of Yeast Replicative Life Span by TOR and Sch9 in Response to Nutrients
Kaeberlein, M., Powers, R. W., Steffen, K. K., Westman, E. A., Hu, D., Dang, N., Kerr, E. O., Kirkland, K. T., Fields, S., & Kennedy, B. K. (2005) · Science · doi:10.1126/science.1115535 · Cited by 1,293
Pearson, K. J., Baur, J. A., Lewis, K. N., Peshkin, L., Price, N. L., Labinskyy, N., Swindell, W. R., Kamara, D., Minor, R. K., Perez, E., et al. (2008) · Cell Metabolism · doi:10.1016/j.cmet.2008.06.011 · Cited by 1,162
Ribosomal Protein S6 Kinase 1 Signaling Regulates Mammalian Life Span
Selman, C., Tullet, J. M. A., Wieser, D., Irvine, E., Lingard, S. J., Choudhury, A. I., Claret, M., Al-Qassab, H., Carmignac, D., Ramadani, F., et al. (2009) · Science · doi:10.1126/science.1177221 · Cited by 1,120
Self-citationMechanisms of Life Span Extension by Rapamycin in the Fruit Fly Drosophila Melanogaster
Bjedov, I., Toivonen, J. M., Kerr, F., Slack, C., Jacobson, J., Foley, A., & Partridge, L. (2010) · Cell Metabolism · doi:10.1016/j.cmet.2009.11.010 · Cited by 1,057
Self-citationExtension of Chronological Life Span in Yeast by Decreased TOR Pathway Signaling
Powers, R. W., Kaeberlein, M., Caldwell, S. D., Kennedy, B. K., & Fields, S. (2006) · Genes & Development · doi:10.1101/gad.1381406 · Cited by 982
Cited by
Sorted by citations
Items 901–1,000 of 1,019
Green, C. D., Huang, Y., Dou, X., Liu, Y., Liu, Y., & Han, J. J. (2017) · Cell Reports · doi:10.1016/j.celrep.2017.03.001 · Cited by 48
Green coffee extract enhances oxidative stress resistance and delays aging in Caenorhabditis elegans
Amigoni, L., Stuknytė, M., Ciaramelli, C., Magoni, C., Bruni, I., Noni, I. D., Airoldi, C., Regonesi, M. E., & Palmioli, A. (2017) · Journal of Functional Foods · doi:10.1016/j.jff.2017.03.056 · Cited by 50
The role of autophagy in the regulation of yeast life span
Tyler, J. K., & Johnson, J. E. (2018) · Annals of the New York Academy of Sciences · doi:10.1111/nyas.13549 · Cited by 49
Multisite Phosphorylation of S6K1 Directs a Kinase Phospho-code that Determines Substrate Selection
Arif, A., Jia, J., Willard, B. B., Li, X., & Fox, P. L. (2019) · Molecular Cell · doi:10.1016/j.molcel.2018.11.017 · Cited by 50
Chen, C., Liao, Y., Tsai, S.-C., & Thompson, L. V. (2019) · GeroScience · doi:10.1007/s11357-019-00109-8 · Cited by 50
Caloric restriction: implications for sarcopenia and potential mechanisms
Xie, W.-Q., Xiao, W.-F., Tang, K., Wu, Y.-X., Hu, P.-W., Li, Y.-S., Duan, Y., & Lv, S. (2020) · Aging · doi:10.18632/aging.103987 · Cited by 46
M(o)TOR of pseudo-hypoxic state in aging: Rapamycin to the rescue
Leontieva, O. V., & Blagosklonny, M. V. (2014) · Cell Cycle · doi:10.4161/cc.27973 · Cited by 46
Feeding the gut microbiome: impact on multiple sclerosis
Bronzini, M., Maglione, A., Rosso, R., Matta, M., Masuzzo, F., Rolla, S., & Clerico, M. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1176016 · Cited by 49
Manipulation of health span and function by dietary caloric restriction mimetics
Roth, G. S., & Ingram, D. K. (2015) · Annals of the New York Academy of Sciences · doi:10.1111/nyas.12834 · Cited by 46
Uncoupling reproduction from metabolism extends chronological lifespan in yeast
Nagarajan, S., Kruckeberg, A. L., Schmidt, K. H., Kroll, E., Hamilton, M., McInnerney, K., Summers, R., Taylor, T. S., & Rosenzweig, F. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1323918111 · Cited by 46
Mooney, S. M., Rajagopalan, K., Williams, B. H., Zeng, Y., Christudass, C. S., Li, Y., Yin, B., Kulkarni, P., & Getzenberg, R. H. (2011) · Journal of Cellular Biochemistry · doi:10.1002/jcb.23020 · Cited by 44
Nutraceutical Interventions for Promoting Healthy Aging in Invertebrate Models
Dong, Y., Guha, S., Sun, X., Cao, M., Wang, X., & Zou, S. (2012) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2012/718491 · Cited by 48
Detection of early locomotor abnormalities in a Drosophila model of Alzheimer's disease
Jahn, T. R., Kohlhoff, K., Scott, M., Tartaglia, G. G., Lomas, D. A., Dobson, C. M., Vendruscolo, M., & Crowther, D. C. (2011) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2011.01.026 · Cited by 46
Fong, Y., Lin, Y.-C., Wu, C., Wang, H., Lin, L., Chou, H. L., Teng, Y., Yuan, S. F., & Chiu, C. (2014) · The Scientific World JOURNAL · doi:10.1155/2014/937051 · Cited by 46
Exploring the power of yeast to model aging and age-related neurodegenerative disorders
Oliveira, A. V., Vilaça, R., dos Santos, C. N., Costa, V., & Menezes, R. (2016) · Biogerontology · doi:10.1007/s10522-016-9666-4 · Cited by 50
Fasting and fasting-mimicking diets for chemotherapy augmentation
Brandhorst, S. (2021) · GeroScience · doi:10.1007/s11357-020-00317-7 · Cited by 50
Ho, E., Qualls, C., & Villareal, D. T. (2022) · The Journal of nutrition, health and aging · doi:10.1007/s12603-022-1812-x · Cited by 45
Abdallah, H. M., Mohamed, G. A., & Ibrahim, S. R. M. (2022) · Nutrients · doi:10.3390/nu14071531 · Cited by 54
An integrative approach to dietary balance across the life course
Raubenheimer, D., Senior, A. M., Mirth, C. K., Cui, Z., Hou, R., Couteur, D. G. L., Solon‐Biet, S. M., Léopold, P., & Simpson, S. J. (2022) · iScience · doi:10.1016/j.isci.2022.104315 · Cited by 50
Ubiquitin Ligases in Longevity and Aging Skeletal Muscle
Hughes, D. C., Baehr, L. M., Waddell, D. S., Sharples, A. P., & Bodine, S. C. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23147602 · Cited by 45
Park, S.-H., & Park, S.-K. (2022) · Antioxidants · doi:10.3390/antiox11101996 · Cited by 45
Genome-Wide RNAi Longevity Screens in Caenorhabditis elegans
Yanos, M. E., Bennett, C. F., & Kaeberlein, M. R. (2012) · Current Genomics · doi:10.2174/138920212803251391 · Cited by 45
The roles of FoxOs in modulation of aging by calorie restriction
Kim, D. H., Park, M. H., Lee, E. K., Choi, Y. J., Chung, K. W., Moon, K. M., Kim, M. J., An, H. J., Park, J. W., Kim, N. D., et al. (2014) · Biogerontology · doi:10.1007/s10522-014-9519-y · Cited by 47
An Engineering Approach to Extending Lifespan in C. elegans
Sagi, D., & Kim, S. K. (2012) · PLoS Genetics · doi:10.1371/journal.pgen.1002780 · Cited by 47
Sun, X., Wheeler, C. T., Yolitz, J., Laslo, M., Alberico, T., Sun, Y., Song, Q., & Zou, S. (2014) · Cell Reports · doi:10.1016/j.celrep.2014.08.022 · Cited by 45
Shi, F., Nie, B., Gan, W., Zhou, X. ‐., Takagi, Y., Hayakawa, H., Sekiguchi, M., & Cai, J. (2012) · Free Radical Research · doi:10.3109/10715762.2012.689428 · Cited by 45
Good Ol’ Fat: Links between Lipid Signaling and Longevity
Bustos, V., & Partridge, L. (2017) · Trends in Biochemical Sciences · doi:10.1016/j.tibs.2017.07.001 · Cited by 48
Self-citationA proteomic atlas of insulin signalling reveals tissue‐specific mechanisms of longevity assurance
Tain, L. S., Sehlke, R., Jain, C., Chokkalingam, M., Nagaraj, N., Essers, P., Rassner, M., Grönke, S., Froelich, J., Dieterich, C., et al. (2017) · Molecular Systems Biology · doi:10.15252/msb.20177663 · Cited by 44
Self-citationEffect of Caloric Restriction on the in vivo Functional Properties of Aging Microglia
Olmedillas, M., Fröhlich, N. T., Figarella, K., Mojtahedi, N., & Garaschuk, O. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.00750 · Cited by 46
Intracellular amino acid sensing and mTORC1-regulated growth: new ways to block an old target?
Goberdhan, D. C. I. (2010) · PubMed · Cited by 45
Dabour, N. A., Bando, T., Nakamura, T., Miyawaki, K., Mito, T., Ohuchi, H., & Noji, S. (2011) · Development Growth & Differentiation · doi:10.1111/j.1440-169x.2011.01291.x · Cited by 45
Kumar, A., Christian, P. K., Panchal, K., Guruprasad, B. R., & Tiwari, A. K. (2017) · Journal of Dietary Supplements · doi:10.1080/19390211.2016.1275917 · Cited by 44
Long Range Interactions Regulate Igf2 Gene Transcription during Skeletal Muscle Differentiation
Alzhanov, D. T., McInerney, S. F., & Rotwein, P. (2010) · Journal of Biological Chemistry · doi:10.1074/jbc.m110.160986 · Cited by 44
Beaudoin‐Chabot, C., Wang, L., Celik, C., Khalid, A. T.-F. A., Thalappilly, S., Xu, S., Koh, J. H., Lim, V. W. X., Low, A. D., & Thibault, G. (2022) · Nature Communications · doi:10.1038/s41467-022-33630-0 · Cited by 41
Maintaining good hearing: Calorie restriction, Sirt3, and glutathione
Han, C. J., & Someya, S. (2013) · Experimental Gerontology · doi:10.1016/j.exger.2013.02.014 · Cited by 45
Sensory Perception and Aging in Model Systems: From the Outside In
Linford, N. J., Kuo, T.-H., Chan, T. P., & Pletcher, S. D. (2011) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev-cellbio-092910-154240 · Cited by 45
Xu, X., Cai, G., Bu, R., Wang, W., Bai, X., Sun, X., & Chen, X. (2015) · PLoS ONE · doi:10.1371/journal.pone.0144442 · Cited by 44
Changes of telomere status with aging: An update
Ishikawa, N., Nakamura, K., Izumiyama‐Shimomura, N., Aida, J., Matsuda, Y., Arai, T., & Takubo, K. (2016) · Geriatrics and gerontology international/Geriatrics & gerontology international · doi:10.1111/ggi.12772 · Cited by 45
Peixoto, H. S., Roxo, M., Krstin, S., Wang, X., & Wink, M. (2016) · Journal of Functional Foods · doi:10.1016/j.jff.2016.08.012 · Cited by 45
Mitchell, S. E., Tang, Z., Kerbois, C., Delville, C., Derous, D., Green, C. L., Wang, Y., Han, J., Chen, L., Douglas, A., et al. (2017) · Oncotarget · doi:10.18632/oncotarget.15294 · Cited by 45
Yang, S., Pascual-Guiral, S., Landete, R. P., Giménez‐Llort, L., Baltrons, M. A., Arancio, O., Palacio, J. R., Clos, M. V., Yuste, V. J., & Bayascas, J. R. (2018) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2017.00435 · Cited by 46
Tissue-Specific Profiling of Oxidative Stress-Associated Transcriptome in a Healthy Mouse Model
Kim, J. M., Kim, H.-G., & Son, C. (2018) · International Journal of Molecular Sciences · doi:10.3390/ijms19103174 · Cited by 45
The functional changes of the circadian system organization in aging
Zhao, J., Warman, G. R., & Cheeseman, J. F. (2019) · Ageing Research Reviews · doi:10.1016/j.arr.2019.04.006 · Cited by 46
Prostaglandin signals from adult germline stem cells delay somatic ageing of Caenorhabditis elegans
Lee, H. J., Noormohammadi, A., Koyuncu, S., Calculli, G., Simic, M., Herholz, M., Trifunović, A., & Vílchez, D. (2019) · Nature Metabolism · doi:10.1038/s42255-019-0097-9 · Cited by 47
Why and how do termite kings and queens live so long?
Tasaki, E., Takata, M., & Matsuura, K. (2021) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2019.0740 · Cited by 40
Dietary protein and amino acid restriction: Roles in metabolic health and aging-related diseases
Wang, D., Ye, J., Shi, R., Zhao, B., Liu, Z., Lin, W. J., & Liu, X. (2021) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2021.12.009 · Cited by 46
Should animal fats be back on the table? A critical review of the human health effects of animal fat
Barendse, W. (2014) · Animal Production Science · doi:10.1071/an13536 · Cited by 44
An energetics perspective on geroscience: mitochondrial protonmotive force and aging
Berry, B. J., & Kaeberlein, M. R. (2021) · GeroScience · doi:10.1007/s11357-021-00365-7 · Cited by 44
Does diet influence aging? Evidence from animal studies
Couteur, D. G. L., Raubenheimer, D., Solon‐Biet, S. M., de Cabo, R., & Simpson, S. J. (2022) · Journal of Internal Medicine · doi:10.1111/joim.13530 · Cited by 46
Aiello, G., Sabino, C., Pernici, D., Audano, M., Antonica, F., Gianesello, M., Ballabio, C., Quattrone, A., Mitro, N., Romanel, A., et al. (2022) · EMBO Reports · doi:10.15252/embr.202255299 · Cited by 43
Astre, G., Atlan, T., Goshtchevsky, U., Oron-Gottesman, A., Smirnov, M., Shapira, K., Velan, A., Deelen, J., Levy, T., Levanon, E. Y., et al. (2023) · Developmental Cell · doi:10.1016/j.devcel.2023.05.015 · Cited by 44
Dietary and metabolic effects on intestinal stem cells in health and disease
Shay, J. E. S., & Yilmaz, Ö. H. (2024) · Nature Reviews Gastroenterology & Hepatology · doi:10.1038/s41575-024-00980-7 · Cited by 47
Systemic aging and aging‐related diseases
Li, Q., Xiao, N., Zhang, H., Liang, G., Lin, Y., Qian, Z., Yang, X. Y., Yang, J., Fu, Y., Zhang, C., et al. (2025) · The FASEB Journal · doi:10.1096/fj.202402479rrr · Cited by 45
Shushimita, S., de Bruijn, M. J. W., de Bruin, R. W. F., IJzermans, J. N. M., Hendriks, R. W., & Dor, F. J. M. F. (2014) · PLoS ONE · doi:10.1371/journal.pone.0087772 · Cited by 43
Scheiner, R., Steinbach, A., Claßen, G., Strudthoff, N., & Scholz, H. (2014) · Journal of Insect Physiology · doi:10.1016/j.jinsphys.2014.03.011 · Cited by 40
Dietary restriction and the pursuit of effective mimetics
Selman, C. (2014) · Proceedings of The Nutrition Society · doi:10.1017/s0029665113003832 · Cited by 44
Rhie, B., Song, Y.-H., Ryu, H., & Ahn, S. (2013) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2013.09.017 · Cited by 45
Energy restriction and potential energy restriction mimetics
Nikolai, S., Pallauf, K., Huebbe, P., & Rimbach, G. H. (2015) · Nutrition Research Reviews · doi:10.1017/s0954422415000062 · Cited by 43
Mitchell, S. E., Delville, C., Konstantopedos, P., Derous, D., Green, C. L., Wang, Y., Han, J. J., Promislow, D., Douglas, A., Chen, L., et al. (2016) · Oncotarget · doi:10.18632/oncotarget.8158 · Cited by 44
Kitaoka, Y., Nakazato, K., & Ogasawara, R. (2016) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00465.2016 · Cited by 43
Jongbloed, F., Saat, T. C., Verweij, M., Payán‐Gómez, C., Hoeijmakers, J. H. J., van den Engel, S., van Oostrom, C. T., Ambagtsheer, G., Imholz, S., Pennings, J. L. A., et al. (2017) · Scientific Reports · doi:10.1038/srep40901 · Cited by 43
Premature Brain Aging in Baboons Resulting from Moderate Fetal Undernutrition
Franke, K., Clarke, G. D., Dahnke, R., Christian Gaser, B., Kuo, A. H., Li, C., Schwab, M. G., & Nathanielsz, P. W. (2017) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2017.00092 · Cited by 43
Studies on the regulatory mechanism of isocitrate dehydrogenase 2 using acetylation mimics
Xu, Y., Liu, L., Nakamura, A., Someya, S., Miyakawa, T., & Tanokura, M. (2017) · Scientific Reports · doi:10.1038/s41598-017-10337-7 · Cited by 47
Fang, J., Gao, L., Ma, H., Wu, Q., Wu, T., Wu, J., Wang, Q., & Cheng, F. (2017) · Frontiers in Pharmacology · doi:10.3389/fphar.2017.00747 · Cited by 43
Griffin, E. F., Scopel, S. E., Stephen, C. A., Holzhauer, A. C., Vaji, M. A., Tuckey, R. A., Berkowitz, L. A., Caldwell, K. A., & Caldwell, G. A. (2019) · Disease Models & Mechanisms · doi:10.1242/dmm.037218 · Cited by 48
Camberos-Luna, L., & Massieu, L. (2019) · Neurochemistry International · doi:10.1016/j.neuint.2019.104614 · Cited by 44
Kurauti, M. A., Soares, G. M., Marmentini, C., Bronczek, G. A., Branco, R. C. S., & Boschero, A. C. (2021) · Vitamins and hormones · doi:10.1016/bs.vh.2020.12.010 · Cited by 47
Li, H., Yu, X., Meng, F., Zhao, Z., Guan, S., & Wang, L. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22084279 · Cited by 43
Lack of Sir2 increases acetate consumption and decreases extracellular pro-aging factors
Casatta, N., Porro, A., Orlandi, I., Brambilla, L., & Vai, M. (2012) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2012.11.008 · Cited by 43
Parkhitko, A. A., Favorova, O. O., Khabibullin, D., Anisimov, V. N., & Henske, E. P. (2014) · Biochemistry (Moscow) · doi:10.1134/s0006297914020023 · Cited by 44
Facts and controversies in our understanding of how caloric restriction impacts the mitochondrion
Gouspillou, G., & Hepple, R. T. (2013) · Experimental Gerontology · doi:10.1016/j.exger.2013.03.004 · Cited by 42
Park, S.-H., Kim, B.-K., & Park, S.-K. (2022) · Pharmaceuticals · doi:10.3390/ph15121528 · Cited by 43
Wang, J., Shao, F., Yu, Q., Ye, L., Wusiman, D., Wu, R., Tuo, Z., Wang, Z., Li, D., Cho, W. C. S., et al. (2025) · Research · doi:10.34133/research.0612 · Cited by 45
Lavington, E., Cogni, R., Kuczynski, C. A., Koury, S. A., Behrman, E. L., O’Brien, K. R., SCHMIDT, P. S., & Eanes, W. F. (2014) · Molecular Biology and Evolution · doi:10.1093/molbev/msu146 · Cited by 40
Gil-Bona, A., Reales‐Calderón, J. A., Parra‐Giraldo, C. M., Martínez‐López, R., Monteoliva, L., & Gil, C. (2016) · Frontiers in Microbiology · doi:10.3389/fmicb.2016.00064 · Cited by 41
Mechanisms of aging-related proteinopathies in Caenorhabditis elegans
Kim, D., Kim, T. H., & Lee, S. (2016) · Experimental & Molecular Medicine · doi:10.1038/emm.2016.109 · Cited by 42
Foss, E. J., Lao, U., Dalrymple, E., Adrianse, R. L., Loe, T. K., & Bedalov, A. (2017) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1614781114 · Cited by 41
Ratajczak, M. Z., Bartke, A., & Darżynkiewicz, Z. (2017) · Stem Cell Reviews and Reports · doi:10.1007/s12015-017-9728-2 · Cited by 42
The Energy Maintenance Theory of Aging: Maintaining Energy Metabolism to Allow Longevity
Chaudhari, S. N., & Kipreos, E. T. (2018) · BioEssays · doi:10.1002/bies.201800005 · Cited by 42
Lifespan Extension Via Dietary Restriction: Time to Reconsider the Evolutionary Mechanisms?
Moatt, J. P., Savola, E., Regan, J. C., Nussey, D. H., & Walling, C. A. (2020) · BioEssays · doi:10.1002/bies.201900241 · Cited by 45
Giacomello, E., & Toniolo, L. (2021) · Nutrients · doi:10.3390/nu13072346 · Cited by 45
Unified theory of Alzheimer’s disease (UTAD): implications for prevention and curative therapy
Nehls, M. (2016) · Journal of Molecular Psychiatry · doi:10.1186/s40303-016-0018-8 · Cited by 41
He, Y., Liu, Y., & Zhang, M. (2025) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2025.1533963 · Cited by 44
Recent Advances in Aging and Immunosenescence: Mechanisms and Therapeutic Strategies
Wang, S., Huo, T., Lu, M., Zhao, Y., Zhang, J., He, W., & Chen, H. (2025) · Cells · doi:10.3390/cells14070499 · Cited by 47
Mitochondrial dysfunction in cellular senescence: a bridge to neurodegenerative disease
Hruby, A. J., & Higuchi‐Sanabria, R. (2025) · npj Aging · doi:10.1038/s41514-025-00291-4 · Cited by 52
Anti-oxidative cellular protection effect of fasting-induced autophagy as a mechanism for hormesis
Moore, M. N., Shaw, J. P., Adams, D. R. F., & Viarengo, A. (2015) · Marine Environmental Research · doi:10.1016/j.marenvres.2015.04.001 · Cited by 41
Kamei, Y., Tamura, T., Yoshida, R., Ohta, S., Fukusaki, E., & Mukai, Y. (2011) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2011.02.136 · Cited by 43
Snell, T. W., Johnston, R. K., Rabeneck, B., Zipperer, C., & Teat, S. (2014) · Experimental Gerontology · doi:10.1016/j.exger.2014.01.022 · Cited by 41
Koschei the immortal and anti-aging drugs
Blagosklonny, M. V. (2014) · Cell Death and Disease · doi:10.1038/cddis.2014.520 · Cited by 41
How to save Medicare: the anti-aging remedy
Blagosklonny, M. V. (2012) · Aging · doi:10.18632/aging.100479 · Cited by 41
P66SHC and Ageing: ROS and TOR?
Pani, G. (2010) · Aging · doi:10.18632/aging.100182 · Cited by 41
Giller, K., Huebbe, P., Doering, F., Pallauf, K., & Rimbach, G. H. (2013) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.2013.0101 · Cited by 42
Runagall-McNaull, A., Russell Bonduriansky, A., & Crean, A. J. (2015) · Scientific Reports · doi:10.1038/srep11783 · Cited by 41
Dakik, P., & Titorenko, V. I. (2016) · Frontiers in Genetics · doi:10.3389/fgene.2016.00177 · Cited by 41
AMPK as a Pro-longevity Target
Burkewitz, K., Weir, H. J. M., & Mair, W. B. (2016) · Proceedings of the Fourth International Symposium on Polarization Phenomena in Nuclear Reactions · doi:10.1007/978-3-319-43589-3_10 · Cited by 42
Lee, S., Choi, E.-Y., Yang, S.-M., Ryoo, R., Moon, E., Kim, S., & Kim, K. H. (2018) · Bioorganic Chemistry · doi:10.1016/j.bioorg.2018.07.031 · Cited by 41
de Lucia, C., Murphy, T., Steves, C. J., Dobson, R., Proitsi, P., & Thuret, S. (2020) · Communications Biology · doi:10.1038/s42003-020-0844-1 · Cited by 42
A review of nutrition and dietary interventions in oncology
Gray, A., Dang, B. N., Moore, T. B., Clemens, R., & Pressman, P. (2020) · SAGE Open Medicine · doi:10.1177/2050312120926877 · Cited by 49
Translational control in aging and neurodegeneration
Skariah, G., & Todd, P. K. (2020) · Wiley Interdisciplinary Reviews - RNA · doi:10.1002/wrna.1628 · Cited by 42
HLH-11 modulates lipid metabolism in response to nutrient availability
Li, Y., Ding, W., Li, C., & Liu, Y. (2020) · Nature Communications · doi:10.1038/s41467-020-19754-1 · Cited by 40
Metadata
- Authors
- Fontana, L., Partridge, L., & Longo, V. D.
- Affiliations
- Washington University in St. Louis (US)
- University College London (GB)
- University of Southern California (US)
- Corresponding author
- Fontana, Luigi
- Partridge, Linda
- Longo, Valter D.
- Venue
- Science
- Published
- 2010-04-16
- Volume
- 328
- Issue
- 5976
- Pages
- 321-326
- ISSN
- 0036-8075 (ISSN-L)
- 1095-9203
- PMC
- PMC3607354
- OpenAlex
- W2080094749
- Cited by
- 3,023
- References
- 75
- Citations by year
- 2026: 135 · 2025: 168 · 2024: 160 · 2023: 145 · 2022: 194 · 2021: 221 · 2020: 229 · 2019: 194 · 2018: 191 · 2017: 213 · 2016: 174 · 2015: 197 · 2014: 195 · 2013: 207 · 2012: 188
- FWCI
- 16.85
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Science (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- UCL Discovery (University College London) (submittedVersion)
- Institutional Research Information System (Università degli Studi di Brescia) (submittedVersion)
- Funders
- National Institute on Aging (AG20642, R01AG020642, AG025135, R01AG025135)
- National Institute of General Medical Sciences (R01GM075308, GM075308)
- National Institute of Diabetes and Digestive and Kidney Diseases (P30DK056341)
- National Center for Research Resources (UL1RR024992)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Aging › Genetics, Aging, and Longevity in Model Organisms
- Health Sciences › Medicine › Physiology (medical) › Dietary Effects on Health
- Health Sciences › Medicine › Geriatrics and Gerontology › Sirtuins and Resveratrol in Medicine
- Keywords
- dietary restriction, healthspan, aging, nutrient-sensing pathways, growth hormone receptor, age-related diseases, cancer, neurodegeneration, diabetes mellitus, rhesus monkeys, evolution of aging, healthy aging
- MeSH terms
- Aging, Animals, Haplorhini, Drosophila, Eating, Humans, Longevity, Saccharomyces cerevisiae, Signal Transduction, Caenorhabditis elegans, Caloric Restriction, Mice
About these checks
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 ›
Are you an author, or do you see a problem with this page? Request a review