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
Flagged first, then by citations
Cited by
Sorted by citations
Items 701–800 of 1,019
Aliper, A. M., Belikov, A. V., Garazha, A., Jellen, L. C., Artemov, A. V., Suntsova, M., Ivanova, A., Venkova, L. S., Borisov, N. M., Buzdin, A. A., et al. (2016) · Aging · doi:10.18632/aging.101047 · Cited by 67
Mechanisms, pathways and strategies for rejuvenation through epigenetic reprogramming
Cipriano, A., Moqri, M., Maybury-Lewis, S. Y., Rogers-Hammond, R., de Jong, T. A., Parker, A., Rasouli, S., Schöler, H. R., Sinclair, D. A., & Sebastiano, V. (2023) · Nature Aging · doi:10.1038/s43587-023-00539-2 · Cited by 66
Cui, M., Yu, H. K., Wang, J., Gao, J., & Li, J. (2013) · Journal of Diabetes Research · doi:10.1155/2013/852754 · Cited by 65
Amino Acid Sensing via General Control Nonderepressible-2 Kinase and Immunological Programming
Battu, S., Minhas, G., Mishra, A., & Khan, N. (2017) · Frontiers in Immunology · doi:10.3389/fimmu.2017.01719 · Cited by 69
Nutritional Regulation of Intestinal Stem Cells
Alonso, S., & Yilmaz, Ö. H. (2018) · Annual Review of Nutrition · doi:10.1146/annurev-nutr-082117-051644 · Cited by 66
Nutrients and Pathways that Regulate Health Span and Life Span
Pignatti, C., D’Adamo, S., Stefanelli, C., Flamigni, F., & Cetrullo, S. (2020) · Geriatrics · doi:10.3390/geriatrics5040095 · Cited by 68
Bitter Taste Receptor Polymorphisms and Human Aging
Campa, D., Rango, F. D., Carrai, M., Crocco, P., Montesanto, A., Canzian, F., Rose, G., Rizzato, C., Passarino, G., & Barale, R. (2012) · PLoS ONE · doi:10.1371/journal.pone.0045232 · Cited by 66
The effect of resveratrol on longevity across species: a meta-analysis
Hector, K. L., Lagisz, M., & Nakagawa, S. (2012) · Biology Letters · doi:10.1098/rsbl.2012.0316 · Cited by 65
Lithium as a Treatment for Alzheimer’s Disease: The Systems Pharmacology Perspective
Hampel, H. J., Lista, S., Mango, D., Nisticò, R., Perry, G. L., Ávila, J., Hernández, F., Geerts, H., Vergallo, A., (APMI), A. P. M. I., et al. (2019) · Journal of Alzheimer s Disease · doi:10.3233/jad-190197 · Cited by 67
The untapped potential of reptile biodiversity for understanding how and why animals age
Hoekstra, L. A., Schwartz, T. S., Sparkman, A. M., Miller, D. A. W., & Bronikowski, A. M. (2019) · Functional Ecology · doi:10.1111/1365-2435.13450 · Cited by 69
Tain, L. S., Jain, C., Nespital, T., Fröhlich, J., Hinze, Y., Grönke, S., & Partridge, L. (2019) · Aging Cell · doi:10.1111/acel.13043 · Cited by 64
Self-citationRuple, A., MacLean, E. L., Snyder‐Mackler, N., Creevy, K. E., & Promislow, D. (2021) · Annual Review of Animal Biosciences · doi:10.1146/annurev-animal-051021-080937 · Cited by 77
Pharmaceutical and nutraceutical activation of FOXO3 for healthy longevity
McIntyre, R. L., Liu, Y. J., Hu, I. M., Morris, B. J., Willcox, B. J., Donlon, T. A., Houtkooper, R. H., & Janssens, G. E. (2022) · Ageing Research Reviews · doi:10.1016/j.arr.2022.101621 · Cited by 68
Interaction between Insulin-Like Growth Factor-1 and Atherosclerosis and Vascular Aging
Higashi, Y., Quevedo, H. C., Tiwari, S., Sukhanov, S., Shai, S., Anwar, A., & Delafontaine, P. (2014) · Frontiers of hormone research · doi:10.1159/000360571 · Cited by 65
Ye, F., Zhang, Y., Liu, Y., Yamada, K., Tso, J. L., Menjivar, J. C., Tian, J. Y., Yong, W. H., Schaue, D., Mischel, P. S., et al. (2013) · PLoS ONE · doi:10.1371/journal.pone.0080397 · Cited by 63
Chaudhari, A. B., Gupta, R., Patel, S. A., Velingkaar, N., & Kondratov, R. V. (2017) · Molecular Biology of the Cell · doi:10.1091/mbc.e16-08-0624 · Cited by 65
Protective effects of short-term dietary restriction in surgical stress and chemotherapy
Brandhorst, S., Harputlugil, E., Mitchell, J. R., & Longo, V. D. (2017) · Ageing Research Reviews · doi:10.1016/j.arr.2017.02.001 · Cited by 67
Self-citationRas signaling in aging and metabolic regulation
Slack, C. (2017) · Nutrition and Healthy Aging · doi:10.3233/nha-160021 · Cited by 63
Conformational Restriction and Steric Hindrance in Medicinal Chemistry
Wipf, P., Skoda, E. M., & Mann, A. (2015) · Elsevier eBooks · doi:10.1016/b978-0-12-417205-0.00011-0 · Cited by 64
Centenarian Studies: Important Contributors to Our Understanding of the Aging Process and Longevity
Willcox, D. C., Willcox, B. J., & Poon, L. W. (2010) · Current Gerontology and Geriatrics Research · doi:10.1155/2010/484529 · Cited by 70
Caloric restriction and longevity: Effects of reduced body temperature
Carrillo, A. E., & Flouris, A. D. (2010) · Ageing Research Reviews · doi:10.1016/j.arr.2010.10.001 · Cited by 64
de Cavanagh, E. M. V., Inserra, F., & Ferder, L. (2015) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.00459.2014 · Cited by 66
Nectarine promotes longevity in Drosophila melanogaster
Boyd, O., Weng, P., Sun, X., Alberico, T., Laslo, M., Obenland, D., Kern, B., & Zou, S. (2011) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2011.03.011 · Cited by 63
MicroRNAs and the metabolic hallmarks of aging
Victoria, B., López, Y. O. N., & Masternak, M. M. (2017) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2016.12.021 · Cited by 64
Adipose tissue aging is regulated by an altered immune system
Zhang, Y.-X., Ou, M.-Y., Yang, Z.-H., Sun, Y., Li, Q.-F., & Zhou, S.-B. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1125395 · Cited by 62
Genetics of extreme human longevity to guide drug discovery for healthy ageing
Zhang, Z. D., Milman, S., Lin, J.-R., Wierbowski, S. D., Yu, H., Barzilai, N., Gorbunova, V. A., Ladiges, W., Niedernhofer, L. J., Suh, Y., et al. (2020) · Nature Metabolism · doi:10.1038/s42255-020-0247-0 · Cited by 63
Paton, B., Suárez, M., Herrero, P., & Canela-Canela, N. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22115788 · Cited by 61
Serotonin and dopamine modulate aging in response to food odor and availability
Miller, H. A., Huang, S., Dean, E. S., Schaller, M. L., Tuckowski, A. M., Munneke, A. S., Beydoun, S., Pletcher, S. D., & Leiser, S. F. (2022) · Nature Communications · doi:10.1038/s41467-022-30869-5 · Cited by 68
Liver-Derived IGF-I Regulates Mean Life Span in Mice
Svensson, J., Sjögren, K., Fäldt, J., Andersson, N., Isaksson, O. G. P., Jansson, J., & Ohlsson, C. (2011) · PLoS ONE · doi:10.1371/journal.pone.0022640 · Cited by 63
Metabotropic GABA signalling modulates longevity in C. elegans
Chun, L., Gong, J., Yuan, F., Zhang, B., Liu, H., Zheng, T., Yu, T., Xu, X. Z. S., & Liu, J. (2015) · Nature Communications · doi:10.1038/ncomms9828 · Cited by 62
High‐resolution mapping of cancer cell networks using co‐functional interactions
Boyle, E. A., Pritchard, J. K., & Greenleaf, W. J. (2018) · Molecular Systems Biology · doi:10.15252/msb.20188594 · Cited by 63
Akami, M., Ren, X., Qi, X., Mansour, A., Gao, B., Cao, S., & Niu, C. (2019) · BMC Microbiology · doi:10.1186/s12866-019-1607-3 · Cited by 62
Divergent Aging of Isogenic Yeast Cells Revealed through Single-Cell Phenotypic Dynamics
Jin, M., Li, Y., O’Laughlin, R., Bittihn, P., Pillus, L., Tsimring, L. S., Hasty, J., & Hao, N. (2019) · Cell Systems · doi:10.1016/j.cels.2019.02.002 · Cited by 61
Polyphenols against Skin Aging
Menaa, F., Menaa, A., & Tréton, J. (2013) · Polyphenols in Human Health and Disease · doi:10.1016/b978-0-12-398456-2.00063-3 · Cited by 62
Signaling and Damaging Functions of Free Radicals in Aging-Free Radical Theory, Hormesis, and TOR.
Afanasʹev, I. B. (2010) · Europe PMC (PubMed Central) · Cited by 61
miR-184 Regulates Pancreatic β-Cell Function According to Glucose Metabolism
Tattikota, S. G., Rathjen, T., Hausser, J., Khedkar, A., Kabra, U. D., Pandey, V., Sury, M. D., Wessels, H., Mollet, I. G., Eliasson, L., et al. (2015) · Journal of Biological Chemistry · doi:10.1074/jbc.m115.658625 · Cited by 59
Ageing and the small, non-coding RNA world
Kato, M., & Slack, F. J. (2012) · Ageing Research Reviews · doi:10.1016/j.arr.2012.03.012 · Cited by 61
Starvation, detoxification, and multidrug resistance in cancer therapy
Lee, C. D., Raffaghello, L., & Longo, V. D. (2012) · Drug Resistance Updates · doi:10.1016/j.drup.2012.01.004 · Cited by 64
Self-citationBriga, M., & Verhulst, S. (2015) · Experimental Gerontology · doi:10.1016/j.exger.2015.09.002 · Cited by 61
Hipkiss, A. R. (2017) · Aging and Disease · doi:10.14336/ad.2016.1030 · Cited by 61
Aruoma, O. I., Hausman-Cohen, S., Pizano, J. M., Schmidt, M. A., Minich, D. M., Joffe, Y. T., Brandhorst, S., Evans, S. J., & Brady, D. M. (2019) · Journal of the American College of Nutrition · doi:10.1080/07315724.2019.1582980 · Cited by 61
Le, K. N., Zhan, M., Cho, Y., Wan, J., Patel, D. S., & Lu, H. (2020) · Communications Biology · doi:10.1038/s42003-020-1013-2 · Cited by 61
Kitada, M., Kume, S., Takeda-Watanabe, A., Tsuda, S.-I., Kanasaki, K., & Koya, D. (2013) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2013.06.014 · Cited by 60
Sirtuins and Renal Oxidative Stress
Ogura, Y., Kitada, M., & Koya, D. (2021) · Antioxidants · doi:10.3390/antiox10081198 · Cited by 61
Glycine and aging: Evidence and mechanisms
Johnson, A. A., & Cuellar, T. L. (2023) · Ageing Research Reviews · doi:10.1016/j.arr.2023.101922 · Cited by 65
Metabotyping of Long-Lived Mice using 1H NMR Spectroscopy
Wijeyesekera, A., Selman, C., Barton, R. H., Holmes, E. C., Nicholson, J. K., & Withers, D. J. (2012) · Journal of Proteome Research · doi:10.1021/pr2010154 · Cited by 65
Ethanol and Acetate Acting as Carbon/Energy Sources Negatively Affect Yeast Chronological Aging
Orlandi, I., Ronzulli, R., Casatta, N., & Vai, M. (2013) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2013/802870 · Cited by 60
Zajitschek, F., Zajitschek, S. R. K., Friberg, U., & Maklakov, A. A. (2012) · AGE · doi:10.1007/s11357-012-9445-3 · Cited by 60
Finckenberg, P., Eriksson, O., Baumann, M., Merasto, S., Lalowski, M. M., Levijoki, J. M., Haasio, K., Kytö, V., Müller, D. N., Luft, F. C., et al. (2011) · Hypertension · doi:10.1161/hypertensionaha.111.179457 · Cited by 59
Aging Biology and Novel Targets for Drug Discovery
Couteur, D. G. L., McLachlan, A. J., Quinn, R. J., Simpson, S. J., & de Cabo, R. (2011) · The Journals of Gerontology Series A · doi:10.1093/gerona/glr095 · Cited by 61
Kim, G.-D., Cho, Y.-H., & Yoo, S.-D. (2017) · Scientific Reports · doi:10.1038/s41598-017-03506-1 · Cited by 59
Hine, C., Zhu, Y., Hollenberg, A. N., & Mitchell, J. R. (2018) · Antioxidants and Redox Signaling · doi:10.1089/ars.2017.7434 · Cited by 63
Health Benefits of Anti-aging Drugs
Piskovatska, V., Strilbytska, O. M., Koliada, A. K., Vaiserman, A. M., & Lushchak, O. V. (2019) · Sub-cellular biochemistry/Subcellular biochemistry · doi:10.1007/978-981-13-3681-2_13 · Cited by 62
Quick and reliable assessment of chronological life span in yeast cell populations by flow cytometry
Ocampo, A., & Barrientos, A. (2011) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2011.06.007 · Cited by 61
Death and dessert: nutrient signalling pathways and ageing
Alic, N., & Partridge, L. (2011) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2011.07.006 · Cited by 60
Self-citationCao, L., Tang, Y., Quan, Z., Zhang, Z., Oliver, S. G., & Zhang, N. (2016) · PLoS Genetics · doi:10.1371/journal.pgen.1006458 · Cited by 64
Opposing effects on cardiac function by calorie restriction in different‐aged mice
Sheng, Y., Lv, S., Huang, M., Lv, Y., Yu, J., Liu, J., Tang, T., Qi, H., Di, W., & Ding, G. (2017) · Aging Cell · doi:10.1111/acel.12652 · Cited by 59
The flight response impairs cytoprotective mechanisms by activating the insulin pathway
Rosa, M. J. D., Veuthey, T., Florman, J., Grant, J., Blanco, M. G., Andersen, N., Donnelly, J. L., Rayes, D., & Alkema, M. J. (2019) · Nature · doi:10.1038/s41586-019-1524-5 · Cited by 58
Wilson, K. A., Beck, J. N., Nelson, C. S., Hilsabeck, T. A. U., Promislow, D., Brem, R. B., & Kapahi, P. (2020) · Current Biology · doi:10.1016/j.cub.2020.05.020 · Cited by 63
Hydrogen sulfide in ageing, longevity and disease
Wilkie, S. E., Borland, G., Carter, R. N., Morton, N. M., & Selman, C. (2021) · Biochemical Journal · doi:10.1042/bcj20210517 · Cited by 58
Traditional and Medical Applications of Fasting
Visioli, F., Mucignat‐Caretta, C., Anile, F., & Panaite, S.-A. (2022) · Nutrients · doi:10.3390/nu14030433 · Cited by 63
Mechanisms Underlying Brain Aging Under Normal and Pathological Conditions
Jin, M., & Cai, S. (2022) · Neuroscience Bulletin · doi:10.1007/s12264-022-00969-9 · Cited by 61
Dietary Restriction and Nutrient Balance in Aging
Santos, J., Leitão-Correia, F., Sousa, M. J., & Leão, C. (2015) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2016/4010357 · Cited by 61
Baker, N., & Tuan, R. S. (2013) · Stem Cell Research & Therapy · doi:10.1186/scrt276 · Cited by 62
Caloric restriction - A promising anti-cancer approach: From molecular mechanisms to clinical trials
Kopeina, G. S., Senichkin, V. V., & Zhivotovsky, B. (2016) · Biochimica et Biophysica Acta (BBA) - Reviews on Cancer · doi:10.1016/j.bbcan.2016.11.002 · Cited by 59
Centenarians as a model to discover genetic and epigenetic signatures of healthy ageing
Puca, A. A., Spinelli, C., Accardi, G., Villa, F., & Caruso, C. (2017) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2017.10.004 · Cited by 60
Pushing the Limits of Cancer Therapy: The Nutrient Game
Lettieri‐Barbato, D., & Aquilano, K. (2018) · Frontiers in Oncology · doi:10.3389/fonc.2018.00148 · Cited by 58
Deprez, M.-A., Eskes, E., Winderickx, J., & Wilms, T. (2018) · FEMS Yeast Research · doi:10.1093/femsyr/foy048 · Cited by 62
Arpón, A., Milagro, F. I., Santos, J. L., García‐Granero, M., Riezu‐Boj, J. I., & Martínez, J. A. (2019) · Frontiers in Endocrinology · doi:10.3389/fendo.2019.00496 · Cited by 56
Lang, S., Bose, N., Wilson, K. A., Brackman, D. J., Hilsabeck, T. A. U., Watson, M., Beck, J. N., Sharma, A., Chen, L., Killilea, D. W., et al. (2019) · PLoS Genetics · doi:10.1371/journal.pgen.1008318 · Cited by 57
Tissue-Specific Coupling between Insulin/IGF and TORC1 Signaling via PRAS40 in Drosophila
Pallares-Cartes, C., Cakan‐Akdogan, G., & Teleman, A. A. (2012) · Developmental Cell · doi:10.1016/j.devcel.2011.10.029 · Cited by 57
Why the disposable soma theory cannot explain why women live longer and why we age
Blagosklonny, M. V. (2010) · Aging · doi:10.18632/aging.100253 · Cited by 56
Agephagy – Adapting Autophagy for Health During Aging
Stead, E. R., Castillo-Quan, J. I., Martinez-Miguel, V. E., Lujan, C., Ketteler, R., Kinghorn, K. J., & Bjedov, I. (2019) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2019.00308 · Cited by 61
Black chokeberry (Aronia melanocarpa) extracts in terms of geroprotector criteria
Platonova, E. Y., Shaposhnikov, M. V., Lee, H., Lee, J.-H., Min, K., & Moskalev, A. (2021) · Trends in Food Science & Technology · doi:10.1016/j.tifs.2021.06.020 · Cited by 60
Yin, J., Liu, X., Yuan, J., Jiang, J. S., & Cai, S. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.4013-13.2014 · Cited by 57
Dietary restriction in cerebral bioenergetics and redox state
Amigo, I., & Kowaltowski, A. J. (2014) · Redox Biology · doi:10.1016/j.redox.2013.12.021 · Cited by 59
Harputlugil, E., Hine, C., Vargas, D., Robertson, L. T., Manning, B. D., & Mitchell, J. R. (2014) · Cell Reports · doi:10.1016/j.celrep.2014.07.018 · Cited by 57
Chronic caloric restriction partially protects against age-related alteration in serum metabolome
Guzman, J. M. D., Ku, G., Fahey, R., Youm, Y., Kass, I. J., Ingram, D. K., Dixit, V. D., & Kheterpal, I. (2012) · AGE · doi:10.1007/s11357-012-9430-x · Cited by 57
Wuttke, D., Connor, R. A., Vora, C., Craig, T., Li, Y., Wood, S. H., Vasieva, O., Reis, R. J. S., Tang, F., & de Magalhães, J. P. (2012) · PLoS Genetics · doi:10.1371/journal.pgen.1002834 · Cited by 55
Predicting Successful Aging in a Population-Based Sample of Georgia Centenarians
Arnold, J., Dai, J., Nahapetyan, L., Arte, A., Johnson, M. A., Hausman, D. B., Rodgers, W. L., Hensley, R. B., Martin, P., MacDonald, M. M., et al. (2010) · Current Gerontology and Geriatrics Research · doi:10.1155/2010/989315 · Cited by 57
Emran, S., Yang, M., He, X., Zandveld, J., & Piper, M. D. W. (2014) · Aging · doi:10.18632/aging.100665 · Cited by 55
Afschar, S., Toivonen, J. M., Hoffmann, J. M., Tain, L. S., Wieser, D., Finlayson, A., Driege, Y., Alic, N., Emran, S., Stinn, J., et al. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1515137113 · Cited by 60
Self-citationÁlvarez-García, Ó., Olmer, M., Akagi, R., Akasaki, Y., Fisch, K. M., Shen, T., Su, A. I., & Lotz, M. (2016) · Osteoarthritis and Cartilage · doi:10.1016/j.joca.2016.04.015 · Cited by 60
SIRT6 Overexpression Improves Various Aspects of Mouse Healthspan
Roichman, A., Kanfi, Y., Glazz, R., Naiman, S., Amit, U., Landa, N., Tinman, S., Stein, I., Pikarsky, E., Leor, J., et al. (2016) · The Journals of Gerontology Series A · doi:10.1093/gerona/glw152 · Cited by 56
Use of Caenorhabditis elegans To Study the Potential Bioactivity of Natural Compounds
Liao, V. H. (2018) · Journal of Agricultural and Food Chemistry · doi:10.1021/acs.jafc.7b05700 · Cited by 57
Which is the most significant cause of aging?
Liochev, S. (2015) · Antioxidants · doi:10.3390/antiox4040793 · Cited by 56
Imbalance of ER and Mitochondria Interactions: Prelude to Cardiac Ageing and Disease?
Li, J., Zhang, D., Brundel, B. J. J. M., & Wiersma, M. (2019) · Cells · doi:10.3390/cells8121617 · Cited by 55
Prolonged fasting drives a program of metabolic inflammation in human adipose tissue
Fazeli, P. K., Zhang, Y., O’Keefe, J., Pesaresi, T., Lun, M., Lawney, B. P., & Steinhauser, M. L. (2020) · Molecular Metabolism · doi:10.1016/j.molmet.2020.101082 · Cited by 56
The Naked Mole-Rat as a Model for Healthy Aging
Oka, K., Yamakawa, M., Kawamura, Y., Kutsukake, N., & Miura, K. (2022) · Annual Review of Animal Biosciences · doi:10.1146/annurev-animal-050322-074744 · Cited by 59
Bailey, R. L., & Stover, P. J. (2023) · Annual Review of Nutrition · doi:10.1146/annurev-nutr-061021-025153 · Cited by 61
Biomarkers of aging: from molecules and surrogates to physiology and function
Furrer, R., & Handschin, C. (2025) · Physiological Reviews · doi:10.1152/physrev.00045.2024 · Cited by 68
Liao, C., & Kennedy, B. K. (2014) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/b978-0-12-397920-9.00003-2 · Cited by 59
Wu, Z., Liu, S., & Huang, D. (2013) · PLoS ONE · doi:10.1371/journal.pone.0064448 · Cited by 55
Moore, M. N. (2015) · Environmental Research · doi:10.1016/j.envres.2015.03.015 · Cited by 59
The zebrafish as a gerontology model in nervous system aging, disease, and repair
houcke, J. V., Groef, L. D., Dekeyster, E., & Moons, L. (2015) · Ageing Research Reviews · doi:10.1016/j.arr.2015.10.004 · Cited by 59
Han, C. J., Linser, P. J., Park, H.-J., Kim, M., White, K., Vann, J. M., Ding, D., Prolla, T. A., & Someya, S. (2016) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2016.03.023 · Cited by 56
Saldivia, M., Ceballos-Pérez, G., Bart, J.-M., & Navarro, M. (2016) · Cell Reports · doi:10.1016/j.celrep.2016.09.041 · Cited by 54
Peixoto, H. S., Roxo, M., Röhrig, T., Richling, E., Wang, X., & Wink, M. (2017) · Medicines · doi:10.3390/medicines4030061 · Cited by 59
Serine-Dependent Sphingolipid Synthesis Is a Metabolic Liability of Aneuploid Cells
Hwang, S., Gustafsson, H. T., O’Sullivan, C., Bisceglia, G., Huang, X., Klose, C. D., Schevchenko, A., Dickson, R. C., Cavaliere, P., Dephoure, N., et al. (2017) · Cell Reports · doi:10.1016/j.celrep.2017.11.103 · Cited by 55
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