The DOI matches its Crossref record; 275 of the 275 references it cites were found in a registry or an index.
Spermidine in health and disease
Abstract
Having your longevity and eating too: Although caloric restriction has clear benefits for maximizing health span and life span, it is sufficiently unpleasant that few humans stick to it. Madeo et al. review evidence that increased intake of the polyamine spermidine appears to reproduce many of the healthful effects of caloric restriction, and they explain its cellular actions, which include enhancement of autophagy and protein deacetylation. Spermidine is found in foods such as wheat germ, soybeans, nuts, and some fruits and vegetables and produced by the microbiota. Increased uptake of spermidine has protective effects against cancer, metabolic disease, heart disease, and neurodegeneration. Science , this issue p. eaan2788
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
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?
In the citing paper
“Several CR-associated genes, including GPX3, HMGN2, NQO1 and ODC1 (encoding a rate-limiting enzyme of polyamine biosynthesis), possess or promote antioxidant activities61–66 (Fig. 5c–f and Supplementary Fig. 43a–d).”
From Single-cell multiregion dissection of Alzheimer’s disease (2024) · cites this paper as [66]
In the citing paper
“Similarly, dietary supplementation with the polyamine spermidine prolongs life span and health span in several animal models66, and spermidine has also been shown to enhance memory performance and counteract age-related cognitive decline79–81.”
From Single-cell multiregion dissection of Alzheimer’s disease (2024) · cites this paper as [66]
In the citing paper
“Polyamines are autophagy inducers33 that are implicated in immune regulation and have been shown to improve anti-cancer immunity in mice, synergizing with anti-PD ligand 1 immunotherapy22,34.”
From Longitudinal gut microbiome changes in immune checkpoint blockade-treated advanced melanoma (2024) · cites this paper as [33]
In the citing paper
“Thus, aging is linked to the decline of circulating spermidine and a-ketoglutarate, which are both endowed with anti-aging and anticancer properties.233,234”
From Meta-hallmarks of aging and cancer (2023) · cites this paper as [233]
In the citing paper
“Disabled autophagy due to progressive depletion of spermidine in aging tissues 233 can be expected to interfere with the immune recognition of cancer cells due the incapacity of dendritic cells to recognize autophagy-deficient cancer cells, as well as due to defective T lymphocyte and NK cell responses.163,252”
From Meta-hallmarks of aging and cancer (2023) · cites this paper as [233]
In the citing paper
“In particular, metabolites of the spermidine and kynurenine pathways are associated with the gut microbiota as well as the physiology of the host231,232.”
From The gut microbiota and the brain–gut–kidney axis in hypertension and chronic kidney disease (2018) · cites this paper as [232]
Citations
Cites
López-Otín, C., Blasco, M. A., Partridge, L., Serrano, M., & Kroemer, G. (2013) · Cell · doi:10.1016/j.cell.2013.05.039 · Cited by 14,982
Self-citationMitochondrial Dysfunction and Oxidative Stress in Neurodegenerative Diseases
Lin, M. T., & Beal, M. F. (2006) · Nature · doi:10.1038/nature05292 · Cited by 6,455
Inflamm‐aging: An Evolutionary Perspective on Immunosenescence
FRANCESCHI, C., BONAFÈ, M., VALENSIN, S., OLIVIERI, F., DE LUCA, M., OTTAVIANI, E., & DE BENEDICTIS, G. (2000) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2000.tb06651.x · Cited by 5,358
Resveratrol improves health and survival of mice on a high-calorie diet
Baur, J. A., Pearson, K. J., Price, N. L., Jamieson, H. A., Lerin, C., Kalra, A., Prabhu, V. V., Allard, J. S., Lopez-Lluch, G., Lewis, K., et al. (2006) · Nature · doi:10.1038/nature05354 · Cited by 4,290
Rapamycin 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
Immunogenic cell death in cancer and infectious disease
Galluzzi, L., Buqué, A., Kepp, O., Zitvogel, L., & Kroemer, G. (2017) · Nature Reviews Immunology · doi:10.1038/nri.2016.107 · Cited by 3,119
Self-citationExtending Healthy Life Span—From Yeast to Humans
Fontana, L., Partridge, L., & Longo, V. D. (2010) · Science · doi:10.1126/science.1172539 · Cited by 3,023
Autophagy in Human Health and Disease
Choi, A. M. K., Ryter, S. W., & Levine, B. (2013) · New England Journal of Medicine · doi:10.1056/nejmra1205406 · Cited by 2,583
Rubinsztein, D. C., Mariño, G., & Kroemer, G. (2011) · Cell · doi:10.1016/j.cell.2011.07.030 · Cited by 2,107
Self-citationFoxO3 Controls Autophagy in Skeletal Muscle In Vivo
Mammucari, C., Milan, G., Romanello, V., Masiero, E., Rudolf, R., Del Piccolo, P., Burden, S. J., Di Lisi, R., Sandri, C., Zhao, J., et al. (2007) · Cell Metabolism · doi:10.1016/j.cmet.2007.11.001 · Cited by 1,953
Long-term weight loss maintenance
Wing, R. R., & Phelan, S. (2005) · The American Journal of Clinical Nutrition · doi:10.1093/ajcn/82.1.222s · Cited by 1,941 · cited 1×
“Moreover, only few people seem capable of changing their dietary routines for extended periods (6).”
BackgroundSirtuin activators mimic caloric restriction and delay ageing in metazoans
Wood, J. G., Rogina, B., Lavu, S., Howitz, K., Helfand, S. L., Tatar, M., & Sinclair, D. (2004) · Nature · doi:10.1038/nature02789 · Cited by 1,868
Small molecule activators of SIRT1 as therapeutics for the treatment of type 2 diabetes
Milne, J. C., Lambert, P. D., Schenk, S., Carney, D. P., Smith, J. J., Gagne, D. J., Jin, L., Boss, O., Perni, R. B., Vu, C. B., et al. (2007) · Nature · doi:10.1038/nature06261 · Cited by 1,707
Induction of autophagy by spermidine promotes longevity
Eisenberg, T., Knauer, H., Schauer, A., Büttner, S., Ruckenstuhl, C., Carmona-Gutierrez, D., Ring, J., Schroeder, S., Magnes, C., Antonacci, L., et al. (2009) · Nature Cell Biology · doi:10.1038/ncb1975 · Cited by 1,680
Self-citationThe anti-inflammatory agents aspirin and salicylate inhibit the activity of IκB kinase-β
Yin, M.-J., Yamamoto, Y., & Gaynor, R. B. (1998) · Nature · doi:10.1038/23948 · Cited by 1,596
mTOR regulates memory CD8 T-cell differentiation
Araki, K., Turner, A. P., Shaffer, V. O., Gangappa, S., Keller, S. A., Bachmann, M. F., Larsen, C. P., & Ahmed, R. (2009) · Nature · doi:10.1038/nature08155 · Cited by 1,575
Enhancing CD8 T-cell memory by modulating fatty acid metabolism
Pearce, E. L., Walsh, M. C., Cejas, P. J., Harms, G. M., Shen, H., Wang, L.-S., Jones, R. G., & Choi, Y. (2009) · Nature · doi:10.1038/nature08097 · Cited by 1,559
Immunological effects of conventional chemotherapy and targeted anticancer agents
Galluzzi, L., Buqué, A., Kepp, O., Zitvogel, L., & Kroemer, G. (2015) · Cancer Cell · doi:10.1016/j.ccell.2015.10.012 · Cited by 1,530
Self-citationRothwell, P. M., Fowkes, F. G. R., Belch, J. F., Ogawa, H., Warlow, C. P., & Meade, T. W. (2011) · The Lancet · doi:10.1016/s0140-6736(10)62110-1 · Cited by 1,497
Gomes, A. P., Price, N. L., Ling, A. J. Y., Moslehi, J. J., Montgomery, M. K., Rajman, L., White, J. P., Teodoro, J. S., Wrann, C. D., Hubbard, B. P., et al. (2013) · Cell · doi:10.1016/j.cell.2013.11.037 · Cited by 1,482
Metformin improves healthspan and lifespan in mice
Martin-Montalvo, A., Mercken, E. M., Mitchell, S. J., Palacios, H. H., Mote, P. L., Scheibye-Knudsen, M., Gomes, A. P., Ward, T. M., Minor, R. K., Blouin, M.-J., et al. (2013) · Nature Communications · doi:10.1038/ncomms3192 · Cited by 1,445
Acetyl coenzyme A: a central metabolite and second messenger
Pietrocola, F., Galluzzi, L., Bravo-San Pedro, J. M., Madeo, F., & Kroemer, G. (2015) · Cell Metabolism · doi:10.1016/j.cmet.2015.05.014 · Cited by 1,378
Self-citationAutophagy-Dependent Anticancer Immune Responses Induced by Chemotherapeutic Agents in Mice
Michaud, M., Martins, I., Sukkurwala, A. Q., Adjemian, S., Ma, Y., Pellegatti, P., Shen, S., Kepp, O., Scoazec, M., Mignot, G., et al. (2011) · Science · doi:10.1126/science.1208347 · Cited by 1,377
Self-citationResveratrol Ameliorates Aging-Related Metabolic Phenotypes by Inhibiting cAMP Phosphodiesterases
Park, S. J., Ahmad, F., Philp, A., Baar, K., Williams, T., Luo, H., Ke, H., Rehmann, H., Taussig, R., Brown, A. L., et al. (2012) · Cell · doi:10.1016/j.cell.2012.01.017 · Cited by 1,370
Autophagy maintains stemness by preventing senescence
García-Prat, L., Martínez-Vicente, M., Perdiguero, E., Ortet, L., Rodríguez-Ubreva, J., Rebollo, E., Ruiz-Bonilla, V., Gutarra, S., Ballestar, E., Serrano, A. L., et al. (2016) · Nature · doi:10.1038/nature16187 · Cited by 1,355
NAD + repletion improves mitochondrial and stem cell function and enhances life span in mice
Zhang, H., Ryu, D., Wu, Y., Gariani, K., Wang, X., Luan, P., D’Amico, D., Ropelle, E. R., Lutolf, M. P., Aebersold, R., et al. (2016) · Science · doi:10.1126/science.aaf2693 · Cited by 1,255
Cantó, C., Houtkooper, R. H., Pirinen, E., Youn, D. Y., Oosterveer, M. H., Cen, Y., Fernandez-Marcos, P. J., Yamamoto, H., Andreux, P. A., Cettour-Rose, P., et al. (2012) · Cell Metabolism · doi:10.1016/j.cmet.2012.04.022 · Cited by 1,238
Mouchiroud, L., Houtkooper, R. H., Moullan, N., Katsyuba, E., Ryu, D., Cantó, C., Mottis, A., Jo, Y.-S., Viswanathan, M., Schoonjans, K., et al. (2013) · Cell · doi:10.1016/j.cell.2013.06.016 · Cited by 1,210
Schulz, T. J., Zarse, K., Voigt, A., Urban, N., Birringer, M., & Ristow, M. (2007) · Cell Metabolism · doi:10.1016/j.cmet.2007.08.011 · Cited by 1,209
Cardioprotection and lifespan extension by the natural polyamine spermidine
Eisenberg, T., Abdellatif, M., Schroeder, S., Primessnig, U., Stekovic, S., Pendl, T., Harger, A., Schipke, J., Zimmermann, A., Schmidt, A., et al. (2016) · Nature Medicine · doi:10.1038/nm.4222 · Cited by 1,168
Self-citationPolyamines and cancer: old molecules, new understanding
Gerner, E. W., & Meyskens, F. L. (2004) · Nature reviews. Cancer · doi:10.1038/nrc1454 · Cited by 1,163
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
Metformin as a tool to target aging
Barzilai, N., Crandall, J. P., Kritchevsky, S. B., & Espeland, M. A. (2016) · Cell Metabolism · doi:10.1016/j.cmet.2016.05.011 · Cited by 1,096
Mechanisms 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
Fasting, Circadian Rhythms, and Time-Restricted Feeding in Healthy Lifespan
Longo, V. D., & Panda, S. (2016) · Cell Metabolism · doi:10.1016/j.cmet.2016.06.001 · Cited by 1,013
Metformin retards aging in C. elegans by altering microbial folate and methionine metabolism
Cabreiro, F., Au, C., Leung, K.-Y., Vergara-Irigaray, N., Cochemé, H. M., Noori, T., Weinkove, D., Schuster, E., Greene, N. D. E., & Gems, D. (2013) · Cell · doi:10.1016/j.cell.2013.02.035 · Cited by 967
Mills, K. F., Yoshida, S., Stein, L. R., Grozio, A., Kubota, S., Sasaki, Y., Redpath, P., Migaud, M. E., Apte, R. S., Uchida, K., et al. (2016) · Cell Metabolism · doi:10.1016/j.cmet.2016.09.013 · Cited by 930
Modulation of cellular function by polyamines
Igarashi, K., & Kashiwagi, K. (2009) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2009.07.009 · Cited by 852
Mammalian polyamine metabolism and function
Pegg, A. E. (2009) · IUBMB Life · doi:10.1002/iub.230 · Cited by 786
GABA from reactive astrocytes impairs memory in mouse models of Alzheimer's disease
Jo, S., Yarishkin, O., Hwang, Y. J., Chun, Y. E., Park, M., Woo, D. H., Bae, J. Y., Kim, T., Lee, J., Chun, H., et al. (2014) · Nature Medicine · doi:10.1038/nm.3639 · Cited by 783
The Ancient Drug Salicylate Directly Activates AMP-Activated Protein Kinase
Hawley, S. A., Fullerton, M. D., Ross, F. A., Schertzer, J. D., Chevtzoff, C., Walker, K. J., Peggie, M. W., Zibrova, D., Green, K. A., Mustard, K. J., et al. (2012) · Science · doi:10.1126/science.1215327 · Cited by 760
Metabolic Control of Longevity
López-Otín, C., Galluzzi, L., Freije, J. M. P., Madeo, F., & Kroemer, G. (2016) · Cell · doi:10.1016/j.cell.2016.07.031 · Cited by 753
Self-citationFasting Cycles Retard Growth of Tumors and Sensitize a Range of Cancer Cell Types to Chemotherapy
Lee, C. D., Raffaghello, L., Brandhorst, S., Safdie, F. M., Bianchi, G., Martín‐Montalvo, A., Pistoia, V., Wei, M., Hwang, S., Merlino, A., et al. (2012) · Science Translational Medicine · doi:10.1126/scitranslmed.3003293 · Cited by 734
Anson, R. M., Guo, Z., de Cabo, R., Iyun, T., Rios, M., Hagepanos, A., Ingram, D. K., Lane, M. A., & Mattson, M. P. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1035720100 · Cited by 732
Ma, Y., Adjemian, S., Mattarollo, S. R., Yamazaki, T., Aymeric, L., Yang, H., Catani, J. P. P., Hannani, D., Duret, H., Steegh, K., et al. (2013) · Immunity · doi:10.1016/j.immuni.2013.03.003 · Cited by 727
Self-citationFunctions of Polyamines in Mammals
Pegg, A. E. (2016) · Journal of Biological Chemistry · doi:10.1074/jbc.r116.731661 · Cited by 720
TOR Signaling and Rapamycin Influence Longevity by Regulating SKN-1/Nrf and DAF-16/FoxO
Robida-Stubbs, S., Glover-Cutter, K., Lamming, D. W., Mizunuma, M., Narasimhan, S. D., Neumann-Haefelin, E., Sabatini, D. M., & Blackwell, T. K. (2012) · Cell Metabolism · doi:10.1016/j.cmet.2012.04.007 · Cited by 648
Miller, R. A., Harrison, D. E., Astle, C. M., Fernández, E., Flurkey, K., Han, M. L., Javors, M. A., Li, X., Nadon, N. L., Nelson, J. F., et al. (2013) · Aging Cell · doi:10.1111/acel.12194 · Cited by 625
PINK1/Parkin-mediated mitophagy in mammalian cells
Eiyama, A., & Okamoto, K. (2015) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2015.01.002 · Cited by 603
Association of Coffee Drinking with Total and Cause-Specific Mortality
Freedman, N. D., Park, Y., Abnet, C. C., Hollenbeck, A. R., & Sinha, R. R. (2012) · New England Journal of Medicine · doi:10.1056/nejmoa1112010 · Cited by 597
The GH/IGF-1 axis in ageing and longevity
Junnila, R. K., List, E. O., Berryman, D. E., Murrey, J. W., & Kopchick, J. J. (2013) · Nature Reviews Endocrinology · doi:10.1038/nrendo.2013.67 · Cited by 574
Polyamines: Natural and engineered abiotic and biotic stress tolerance in plants
Hussain, S. S., Ali, M., Ahmad, M., & Siddique, K. H. M. (2011) · Biotechnology Advances · doi:10.1016/j.biotechadv.2011.01.003 · Cited by 564
Caloric restriction mimetics enhance anticancer immunosurveillance
Pietrocola, F., Pol, J., Vacchelli, E., Rao, S., Enot, D. P., Baracco, E. E., Levesque, S., Castoldi, F., Jacquelot, N., Yamazaki, T., et al. (2016) · Cancer Cell · doi:10.1016/j.ccell.2016.05.016 · Cited by 542
Self-citationZhang, C., & Cuervo, A. M. (2008) · Nature Medicine · doi:10.1038/nm.1851 · Cited by 520
Critical role of acetylation in tau-mediated neurodegeneration and cognitive deficits
Min, S.-W., Chen, X., Tracy, T. E., Li, Y., Zhou, Y., Wang, C., Shirakawa, K., Minami, S. S., Defensor, E., Mok, S. A., et al. (2015) · Nature Medicine · doi:10.1038/nm.3951 · Cited by 516
Spermidine and resveratrol induce autophagy by distinct pathways converging on the acetylproteome
Morselli, E., Mariño, G., Bennetzen, M. V., Eisenberg, T., Megalou, E. V., Schroeder, S., Cabrera, S., Bénit, P., Rustin, P., Criollo, A., et al. (2011) · The Journal of Cell Biology · doi:10.1083/jcb.201008167 · Cited by 509
Self-citationRegulation of autophagy by cytosolic acetyl-coenzyme A
Mariño, G., Pietrocola, F., Eisenberg, T., Kong, Y., Malik, S. A., Andryushkova, A., Schroeder, S., Pendl, T., Harger, A., Niso-Santano, M., et al. (2014) · Molecular Cell · doi:10.1016/j.molcel.2014.01.016 · Cited by 500
Self-citationNicotinamide N-methyltransferase knockdown protects against diet-induced obesity
Kraus, D., Yang, Q., Kong, D., Banks, A. S., Zhang, L., Rodgers, J. T., Pirinen, E., Pulinilkunnil, T., Gong, F., Wang, Y.-C., et al. (2014) · Nature · doi:10.1038/nature13198 · Cited by 495
A dual role for autophagy in a murine model of lung cancer
Rao, S., Tortola, L., Perlot, T., Wirnsberger, G., Novatchkova, M., Nitsch, R., Sykacek, P., Frank, L., Schramek, D., Komnenovic, V., et al. (2014) · Nature Communications · doi:10.1038/ncomms4056 · Cited by 453
Self-citationChemotherapy-induced antitumor immunity requires formyl peptide receptor 1
Vacchelli, E., Ma, Y., Baracco, E. E., Sistigu, A., Enot, D. P., Pietrocola, F., Yang, H., Adjemian, S., Chaba, K., Semeraro, M., et al. (2015) · Science · doi:10.1126/science.aad0779 · Cited by 452
Self-citationHarrison, D. E., Strong, R., Allison, D. B., Ames, B. N., Astle, C. M., Atamna, H., Fernandez, E., Flurkey, K., Javors, M. A., Nadon, N. L., et al. (2014) · Aging Cell · doi:10.1111/acel.12170 · Cited by 445
Fasting-Mimicking Diet Reduces HO-1 to Promote T Cell-Mediated Tumor Cytotoxicity
Biase, S. D., Lee, C. D., Brandhorst, S., Manes, B., Buono, R., Cheng, C., Cacciottolo, M., Martín‐Montalvo, A., de Cabo, R., Wei, M., et al. (2016) · Cancer Cell · doi:10.1016/j.ccell.2016.06.005 · Cited by 418
Howell, J. J., Hellberg, K., Turner, M., Talbott, G., Kolar, M. J., Ross, D. S., Hoxhaj, G., Saghatelian, A., Shaw, R. J., & Manning, B. D. (2017) · Cell Metabolism · doi:10.1016/j.cmet.2016.12.009 · Cited by 408
Mehta, R. A., Cassol, T., Li, N., Ali, N., Handa, A. K., & Mattoo, A. K. (2002) · Nature Biotechnology · doi:10.1038/nbt0602-613 · Cited by 407
The SIRT1 Activator SRT1720 Extends Lifespan and Improves Health of Mice Fed a Standard Diet
Mitchell, S. J., Martín‐Montalvo, A., Mercken, E. M., Palacios, H. H., Ward, T. M., Abulwerdi, G. A., Minor, R. K., Vlasuk, G. P., Ellis, J. L., Sinclair, D. A., et al. (2014) · Cell Reports · doi:10.1016/j.celrep.2014.01.031 · Cited by 402
SIRT1 Negatively Regulates the Mammalian Target of Rapamycin
Ghosh, H. S., McBurney, M., & Robbins, P. D. (2010) · PLoS ONE · doi:10.1371/journal.pone.0009199 · Cited by 397
Yoshino, J., Conte, C., Fontana, L., Mittendorfer, B., Imai, S., Schechtman, K. B., Gu, C. C., Kunz, I., Fanelli, F. R., Patterson, B. W., et al. (2012) · Cell Metabolism · doi:10.1016/j.cmet.2012.09.015 · Cited by 389
Saura, J., Luque, J. M., Cesura, A. M., Prada, M. D., Chan‐Palay, V., Huber, G., Löffler, J., & Richards, J. G. (1994) · Neuroscience · doi:10.1016/0306-4522(94)90311-5 · Cited by 385
Wang, I.-F., Guo, B.-S., Liu, Y.-C., Wu, C.-C., Yang, C.-H., Tsai, K.-J., & Shen, C.-K. J. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1206362109 · Cited by 377
Restoring polyamines protects from age-induced memory impairment in an autophagy-dependent manner
Gupta, V., Scheunemann, L., Eisenberg, T., Mertel, S., Bhukel, A., Koemans, T. S., Kramer, J. M., Liu, K. S. Y., Schroeder, S., Stunnenberg, H. G., et al. (2013) · Nature Neuroscience · doi:10.1038/nn.3512 · Cited by 376
Self-citationRapamycin extends murine lifespan but has limited effects on aging
Neff, F., Flores-Dominguez, D., Ryan, D. P., Horsch, M., Schröder, S., Adler, T., Afonso, L. C., Aguilar-Pimentel, J. A., Becker, L., Garrett, L., et al. (2013) · Journal of Clinical Investigation · doi:10.1172/jci67674 · Cited by 374
Amyloid-binding compounds maintain protein homeostasis during ageing and extend lifespan
Alavez, S., Vantipalli, M. C., Zucker, D. J. S., Klang, I. M., & Lithgow, G. J. (2011) · Nature · doi:10.1038/nature09873 · Cited by 361
Autophagy is a critical regulator of memory CD8+ T cell formation
Puleston, D. J., Zhang, H., Powell, T. J., Lipina, E., Sims, S., Panse, I., Watson, A. S., Cerundolo, V., Townsend, A. R., Klenerman, P., et al. (2014) · eLife · doi:10.7554/elife.03706 · Cited by 360
Spermidine induces autophagy by inhibiting the acetyltransferase EP300
Pietrocola, F., Lachkar, S., Enot, D. P., Niso-Santano, M., Bravo-San Pedro, J. M., Sica, V, Izzo, V, Maiuri, M. C., Madeo, F., Mariño, G., et al. (2015) · Cell Death & Differentiation · doi:10.1038/cdd.2014.215 · Cited by 357
Self-citationNordihydroguaiaretic acid and aspirin increase lifespan of genetically heterogeneous male mice
Strong, R., Miller, R. A., Astle, C. M., Floyd, R. A., Flurkey, K., Hensley, K. L., Javors, M. A., Leeuwenburgh, C., Nelson, J. F., Ongini, E., et al. (2008) · Aging Cell · doi:10.1111/j.1474-9726.2008.00414.x · Cited by 349
The Search for Antiaging Interventions: From Elixirs to Fasting Regimens
de Cabo, R., Carmona-Gutierrez, D., Bernier, M., Hall, M. N., & Madeo, F. (2014) · Cell · doi:10.1016/j.cell.2014.05.031 · Cited by 345
Self-citationImpact of intestinal microbiota on intestinal luminal metabolome
Matsumoto, M., Kibe, R., Ooga, T., Aiba, Y., Kurihara, S., Sawaki, E., Koga, Y., & Benno, Y. (2012) · Scientific Reports · doi:10.1038/srep00233 · Cited by 334
Autophagy and neurodegeneration
Frake, R. A., Ricketts, T., Menzies, F. M., & Rubinsztein, D. C. (2015) · Journal of Clinical Investigation · doi:10.1172/jci73944 · Cited by 332
Lee, C. D., Safdie, F. M., Raffaghello, L., Wei, M., Madia, F., Parrella, E., Hwang, D., Cohen, P., Bianchi, G., & Longo, V. D. (2010) · Cancer Research · doi:10.1158/0008-5472.can-09-3228 · Cited by 326
Zhang, M., Caragine, T., Wang, H., Cohen, P. S., Botchkina, G., Soda, K., Bianchi, M., Ulrich, P., Cerami, A., Sherry, B., et al. (1997) · The Journal of Experimental Medicine · doi:10.1084/jem.185.10.1759 · Cited by 317
Spermine and spermidine mediate protection against oxidative damage caused by hydrogen peroxide
Rider, J. E., Hacker, A., Mackintosh, C. A., Pegg, A. E., Woster, P. M., & Casero, R. A. (2007) · Amino Acids · doi:10.1007/s00726-007-0513-4 · Cited by 308
SRT1720 improves survival and healthspan of obese mice
Minor, R. K., Baur, J. A., Gomes, A. P., Ward, T. M., Csiszár, A., Mercken, E. M., Abdelmohsen, K., Shin, Y., Cantó, C., Scheibye‐Knudsen, M., et al. (2011) · Scientific Reports · doi:10.1038/srep00070 · Cited by 306
Polyamines and cancer: implications for chemotherapy and chemoprevention
Nowotarski, S. L., Woster, P. M., & Casero, R. A. (2013) · Expert Reviews in Molecular Medicine · doi:10.1017/erm.2013.3 · Cited by 306
Cheng, M., Wang, C., Shiao, M., Liu, M., Huang, Y.-Y., Huang, C.-Y., Mao, C., Lin, J., Ho, H., & Yang, N. (2015) · Journal of the American College of Cardiology · doi:10.1016/j.jacc.2015.02.018 · Cited by 298
Decrease in Polyamines with Aging and Their Ingestion from Food and Drink
Nishimura, K., Shiina, R., Kashiwagi, K., & Igarashi, K. (2006) · The Journal of Biochemistry · doi:10.1093/jb/mvj003 · Cited by 295
Matsumoto, M., Kurihara, S., Kibe, R., Ashida, H., & Benno, Y. (2011) · PLoS ONE · doi:10.1371/journal.pone.0023652 · Cited by 290 · cited 3×
“Supplementation of the polyamine precursor arginine (alone or in combination with probiotics) may also suffice to increase spermidine concentrations in the colon and blood (46, 47).”
BackgroundInfluentialResveratrol induces autophagy by directly inhibiting mTOR through ATP competition
Park, D., Jeong, H., Lee, M. N., Koh, A., Kwon, O., Yang, Y. R., Noh, J., Suh, P., Park, H., & Ryu, S. H. (2016) · Scientific Reports · doi:10.1038/srep21772 · Cited by 287
Anisimov, V. N., Berstein, L. M., Popovich, I. G., Zabezhinski, M. A., Egormin, P. A., Piskunova, T. S., Semenchenko, A. V., Tyndyk, M. L., Yurova, M. N., Kovalenko, I. G., et al. (2011) · Aging · doi:10.18632/aging.100273 · Cited by 285
Kumar, M., Bijo, A. J., Baghel, R. S., Reddy, C. R. K., & Jha, B. (2011) · Plant Physiology and Biochemistry · doi:10.1016/j.plaphy.2011.10.016 · Cited by 278
Regulation of Autophagy by the p300 Acetyltransferase
Lee, I. H., & Finkel, T. (2009) · Journal of Biological Chemistry · doi:10.1074/jbc.m807135200 · Cited by 277
Shi, J., Fu, X., Peng, T., Huang, X.-S., Fan, Q.-J., & Liu, J.-H. (2010) · Tree Physiology · doi:10.1093/treephys/tpq030 · Cited by 275
Kibe, R., Kurihara, S., Sakai, Y., Suzuki, H., Ooga, T., Sawaki, E., Muramatsu, K., Nakamura, A., Yamashita, A., Kitada, Y., et al. (2014) · Scientific Reports · doi:10.1038/srep04548 · Cited by 273
The importance of dietary polyamines in cell regeneration and growth
Bardócz, S., Duguid, T. J., Brown, D. S., Grant, G., Pusztai, A. J., White, A. L., & Ralph, A. (1995) · British Journal Of Nutrition · doi:10.1079/bjn19950087 · Cited by 269
Curcumin-mediated lifespan extension in Caenorhabditis elegans
Liao, V. H., Yu, C., Chu, Y.-J., Li, W.-H., Hsieh, Y., & Wang, T.-T. (2011) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2011.07.008 · Cited by 266
Eisenberg, T., Schroeder, S., Andryushkova, A., Pendl, T., Küttner, V., Bhukel, A., Mariño, G., Pietrocola, F., Harger, A., Zimmermann, A., et al. (2014) · Cell Metabolism · doi:10.1016/j.cmet.2014.02.010 · Cited by 256
Self-citationRoychoudhury, A., Basu, S., & Sengupta, D. N. (2010) · Journal of Plant Physiology · doi:10.1016/j.jplph.2010.07.009 · Cited by 254
Jiménez, Y., Mattison, J. A., Pearson, K. J., Martín‐Montalvo, A., Palacios, H. H., Sossong, A. M., Ward, T. M., Younts, C. M., Lewis, K. N., Allard, J. S., et al. (2013) · Cell Metabolism · doi:10.1016/j.cmet.2013.09.004 · Cited by 247
Caloric restriction mimetics: towards a molecular definition
Madeo, F., Pietrocola, F., Eisenberg, T., & Kroemer, G. (2014) · Nature Reviews Drug Discovery · doi:10.1038/nrd4391 · Cited by 245
Self-citationD-Glucosamine supplementation extends life span of nematodes and of ageing mice
Weimer, S., Priebs, J., Kuhlow, D., Groth, M., Priebe, S., Mansfeld, J., Merry, T. L., Dubuis, S., Laube, B., Pfeiffer, A. F. H., et al. (2014) · Nature Communications · doi:10.1038/ncomms4563 · Cited by 245
Metabolomic Analysis of Pressure-Overloaded and Infarcted Mouse Hearts
Sansbury, B. E., DeMartino, A. M., Xie, Z., Brooks, A. C., Brainard, R. E., Watson, L. J., DeFilippis, A. P., Cummins, T. D., Harbeson, M. A., Brittian, K. R., et al. (2014) · Circulation Heart Failure · doi:10.1161/circheartfailure.114.001151 · Cited by 234
Huang, Y., Lin, C., He, F., Li, Z., Guan, Y., Hu, Q., & Hu, J. (2017) · BMC Plant Biology · doi:10.1186/s12870-016-0951-9 · Cited by 228
An Ancient, Unified Mechanism for Metformin Growth Inhibition in C. Elegans and Cancer
Wu, L., Zhou, B., Oshiro-Rapley, N., Li, M., Paulo, J. A., Webster, C. M., Mou, F., Kacergis, M. C., Talkowski, M. E., Carr, C. E., et al. (2016) · Cell · doi:10.1016/j.cell.2016.11.055 · Cited by 227
Nahar, K., Hasanuzzaman, M., Rahman, A., Alam, M. M., Mahmud, J.-A., Suzuki, T., & Fujita, M. (2016) · Frontiers in Plant Science · doi:10.3389/fpls.2016.01104 · Cited by 226
Shu, S., Yuan, L., Guo, S., Sun, J., & Yuan, Y. (2012) · Plant Physiology and Biochemistry · doi:10.1016/j.plaphy.2012.11.028 · Cited by 222
Histone deacetylase 10 promotes autophagy-mediated cell survival
Oehme, I., Linke, J.-P., Böck, B. C., Milde, T., Lodrini, M., Hartenstein, B., Wiegand, I., Eckert, C., Roth, W., Kool, M., et al. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1300113110 · Cited by 221
Gupta, S., Hastak, K., Afaq, F., Ahmad, N., & Mukhtar, H. (2003) · Oncogene · doi:10.1038/sj.onc.1207353 · Cited by 218
The autophagy enhancer spermidine reverses arterial aging
LaRocca, T. J., Gioscia‐Ryan, R. A., Hearon, C. M., & Seals, D. R. (2013) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2013.04.004 · Cited by 216
Yin, L., Wang, S., Tanaka, K., Fujihara, S., Itai, A., Den, X., & Zhang, S. (2015) · Plant Cell & Environment · doi:10.1111/pce.12521 · Cited by 214
Mattison, J. A., Wang, M., Bernier, M., Zhang, J., Park, S. S., Maudsley, S. R., An, S. S., Santhanam, L., Martin, B., Faulkner, S., et al. (2014) · Cell Metabolism · doi:10.1016/j.cmet.2014.04.018 · Cited by 206
Chen, T., Shen, L., Yu, J., Wan, H., Guo, A., Chen, J., Long, Y., Zhao, J., & Pei, G. (2011) · Aging Cell · doi:10.1111/j.1474-9726.2011.00722.x · Cited by 204
Histone deacetylase 10 structure and molecular function as a polyamine deacetylase
Hai, Y., Shinsky, S. A., Porter, N. J., & Christianson, D. W. (2017) · Nature Communications · doi:10.1038/ncomms15368 · Cited by 200
Polyamine-rich food decreases age-associated pathology and mortality in aged mice
Soda, K., Dobashi, Y., Kano, Y., Tsujinaka, S., & Konishi, F. (2009) · Experimental Gerontology · doi:10.1016/j.exger.2009.08.013 · Cited by 190
Graham, S. F., Chevallier, O. P., Elliott, C. T., Hölscher, C., Johnston, J. A., McGuinness, B., Kehoe, P. G., Passmore, A. P., & Green, B. D. (2015) · PLoS ONE · doi:10.1371/journal.pone.0119452 · Cited by 188
Abbas, S., & Wink, M. (2008) · Planta Medica · doi:10.1055/s-0028-1088378 · Cited by 184
Fan, J., Yang, X., Li, J., Shu, Z., Dai, J., Liu, X., Li, B., Jia, S., Kou, X., Yang, Y., et al. (2017) · Oncotarget · doi:10.18632/oncotarget.15728 · Cited by 183
Yang, Q., Zheng, C., Cao, J., Cao, G., Shou, P., Lin, L., Velletri, T., Jiang, M., Chen, Q., Han, Y., et al. (2016) · Cell Death and Differentiation · doi:10.1038/cdd.2016.71 · Cited by 182
Spermine prevents endonuclease activation and apoptosis in thymocytes*1
Brüne, B. (1991) · Experimental Cell Research · doi:10.1016/0014-4827(91)90380-d · Cited by 178
Yue, F., Li, W., Zou, J., Jiang, X., Xu, G., Huang, H. W., & Liu, L. (2017) · Cancer Research · doi:10.1158/0008-5472.can-16-3462 · Cited by 178
Minois, N. (2014) · Gerontology · doi:10.1159/000356748 · Cited by 176
Anti-inflammatory effects of spermidine in lipopolysaccharide-stimulated BV2 microglial cells
Choi, Y. H., & Park, H. M. (2012) · Journal of Biomedical Science · doi:10.1186/1423-0127-19-31 · Cited by 174
Schwarz, C., Stekovic, S., Wirth, M., Benson, G. S., Royer, P., Sigrist, S. J., Pieber, T. R., Dammbrueck, C., Magnes, C., Eisenberg, T., et al. (2018) · Aging · doi:10.18632/aging.101354 · Cited by 164
Self-citationNiu, Y., Na, L., Feng, R., Gong, L., Zhao, Y., Li, Q., Li, Y., & Sun, C. (2013) · Aging Cell · doi:10.1111/acel.12133 · Cited by 163
Polyamines in foods: development of a food database
Ali, M. A., Poortvliet, E., Strömberg, R., & Yngve, A. (2011) · Food & Nutrition Research · doi:10.3402/fnr.v55i0.5572 · Cited by 163
Circadian Clock Control by Polyamine Levels through a Mechanism that Declines with Age
Zwighaft, Z., Aviram, R., Shalev, M., Rousso-Noori, L., Kraut‐Cohen, J., Golik, M., Brandis, A. S., Reinke, H., Aharoni, A., Kahana, C., et al. (2015) · Cell Metabolism · doi:10.1016/j.cmet.2015.09.011 · Cited by 162
Polyamines and Their Metabolites as Diagnostic Markers of Human Diseases
Park, M. H., & Igarashi, K. (2013) · Biomolecules & Therapeutics · doi:10.4062/biomolther.2012.097 · Cited by 162
Polyamines in the gut lumen: bioavailability and biodistribution
Milović, V. (2001) · European Journal of Gastroenterology & Hepatology · doi:10.1097/00042737-200109000-00004 · Cited by 159
Sahin, E., Haubenwallner, S., Kuttke, M., Kollmann, I., Halfmann, A., Dohnal, A. M., Chen, L., Cheng, P. P., Hoesel, B., Einwallner, E., et al. (2014) · The Journal of Immunology · doi:10.4049/jimmunol.1302167 · Cited by 159
Mostofa, M. G., Yoshida, N., & Fujita, M. (2013) · Plant Growth Regulation · doi:10.1007/s10725-013-9865-9 · Cited by 158
Spermidine protects against α-synuclein neurotoxicity
Büttner, S., Broeskamp, F., Sommer, C., Markaki, M., Habernig, L., Alavian‐Ghavanini, A., Carmona‐Gutiérrez, D., Eisenberg, T., Michael, E., Kroemer, G., et al. (2014) · Cell Cycle · doi:10.4161/15384101.2014.973309 · Cited by 157
Self-citationAutophagy, NLRP3 inflammasome and auto-inflammatory/immune diseases.
Zhong, Z., Sánchez‐López, E., & Karin, M. (2016) · PubMed · Cited by 156
Phadwal, K., Alegre-Abarrategui, J., Watson, A. S., Pike, L., Anbalagan, S., Hammond, E. M., Wade-Martins, R., McMichael, A., Klenerman, P., & Simon, A. K. (2012) · Autophagy · doi:10.4161/auto.18935 · Cited by 155
Rady, M. M., & Hemida, K. A. (2015) · Ecotoxicology and Environmental Safety · doi:10.1016/j.ecoenv.2015.05.008 · Cited by 154
Long-Term Oral Polyamine Intake Increases Blood Polyamine Concentrations
Soda, K., Kano, Y., SAKURAGI, M., Takao, K., Lefor, A. K., & Konishi, F. (2009) · Journal of Nutritional Science and Vitaminology · doi:10.3177/jnsv.55.361 · Cited by 153
Spermidine and spermine are enriched in whole blood of nona/centenarians
Pucciarelli, S., Moreschini, B., Micozzi, D., De Fronzo, G. S., Carpi, F. M., Polzonetti, V., Vincenzetti, S., Mignini, F., & Napolioni, V. (2012) · Rejuvenation Research · doi:10.1089/rej.2012.1349 · Cited by 144
Jell, J., Merali, S., Hensen, M. L., Mazurchuk, R. V., Spernyak, J. A., Diegelman, P., Kisiel, N. D., Barrero, C. A., Deeb, K. K., Alhonen, L. I., et al. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.m610265200 · Cited by 136
Matsumoto, M., & Benno, Y. (2007) · Microbiology and Immunology · doi:10.1111/j.1348-0421.2007.tb03887.x · Cited by 129
Spermidine Protects against Oxidative Stress in Inflammation Models Using Macrophages and Zebrafish
Jeong, J., Cha, H., Han, M. H., Hwang, S. J., Lee, D.-S., Yoo, J. S., Choi, I., Kim, S., Kim, H., Kim, G., et al. (2017) · Biomolecules & Therapeutics · doi:10.4062/biomolther.2016.272 · Cited by 125
ATM mediates spermidine-induced mitophagy via PINK1 and Parkin regulation in human fibroblasts
Qi, Y., Qiu, Q., Gu, X., Tian, Y., & Zhang, Y. (2016) · Scientific Reports · doi:10.1038/srep24700 · Cited by 123
Puyang, X., An, M., Han, L., & Zhang, X. (2015) · Ecotoxicology and Environmental Safety · doi:10.1016/j.ecoenv.2015.03.023 · Cited by 120
Zhou, Z.-Q., Fan, H., He, R., Xiao, J., Tsoi, B., Lan, K.-H., Kurihara, H., So, K., Yao, X., & Gao, H. (2016) · Journal of Agricultural and Food Chemistry · doi:10.1021/acs.jafc.5b05274 · Cited by 120
Loss of the RNA polymerase III repressor MAF1 confers obesity resistancePreprint
Bonhoure, N., Byrnes, A., Moir, R. D., Hodroj, W., Preitner, F., Praz, V., Marcelin, G., Chua, S. C., Martínez-López, N., Singh, R., et al. (2015) · Genes & Development · doi:10.1101/gad.258350.115 · Cited by 119
Alzheimer's disease–like pathology has transient effects on the brain and blood metabolome
Pan, X., Nasaruddin, M. L., Elliott, C. T., McGuinness, B., Passmore, A. P., Kehoe, P. G., Hölscher, C., McClean, P. L., Graham, S. F., & Green, B. D. (2015) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2015.11.014 · Cited by 118
Igarashi, K., Ueda, S., Yoshida, K., & Kashiwagi, K. (2006) · Amino Acids · doi:10.1007/s00726-006-0264-7 · Cited by 116
Radhakrishnan, R., & Lee, I.-J. (2012) · Journal of Plant Growth Regulation · doi:10.1007/s00344-012-9274-8 · Cited by 116
Gupta, V., Pech, U., Bhukel, A., Fulterer, A., Ender, A., Mauermann, S. F., Andlauer, T. F. M., Antwi-Adjei, E., Beuschel, C. B., Thriene, K., et al. (2016) · PLoS Biology · doi:10.1371/journal.pbio.1002563 · Cited by 114
Self-citationYang, Y., Chen, S., Zhang, Y., Lin, X., YiYin, S., Xue, Z., Qian, H., Wang, S., Wan, G., Zheng, X., et al. (2017) · Cell Death and Disease · doi:10.1038/cddis.2017.161 · Cited by 114
Exploring the therapeutic space around NAD+
Houtkooper, R. H., & Auwerx, J. H. (2012) · The Journal of Cell Biology · doi:10.1083/jcb.201207019 · Cited by 113
Caloric restriction mimetics: natural/physiological pharmacological autophagy inducers
Mariño, G., Pietrocola, F., Madeo, F., & Kroemer, G. (2014) · Autophagy · doi:10.4161/auto.36413 · Cited by 112
Self-citationSpermine protects mice against lethal sepsis partly by attenuating surrogate inflammatory markers
Zhu, S., Ashok, M., Li, J., Li, W., Yang, H., Wang, P., Tracey, K. J., Sama, A. E., & Wang, H. (2009) · Molecular Medicine · doi:10.2119/molmed.2009.00062 · Cited by 109
Yamamoto, T. M., Hinoi, E., Fujita, H., Iezaki, T., Takahata, Y., Takamori, M., & Yoneda, Y. (2012) · British Journal of Pharmacology · doi:10.1111/j.1476-5381.2012.01856.x · Cited by 109
Identification of a mammalian vesicular polyamine transporter
Hiasa, M., Miyaji, T., Haruna, Y., Takeuchi, T., Harada, Y., Moriyama, S., Yamamoto, A., Omote, H., & Moriyama, Y. (2014) · Scientific Reports · doi:10.1038/srep06836 · Cited by 109
Minois, N., Carmona‐Gutiérrez, D., Bauer, M. A., Rockenfeller, P., Eisenberg, T., Brandhorst, S., Sigrist, S. J., Kroemer, G., & Madeo, F. (2012) · Cell Death and Disease · doi:10.1038/cddis.2012.139 · Cited by 109
Self-citationFernández, Á. F., Bárcena, C., Martínez-García, G. G., Tamargo-Gómez, I., Suárez, M. F., Pietrocola, F., Castoldi, F., Esteban, L., Sierra-Filardi, E., Boya, P., et al. (2017) · Cell Death & Disease · doi:10.1038/cddis.2017.373 · Cited by 109
Self-citationGonzalez, M. E., Marco, F., Minguet, E. G., Carrasco, P., Blázquez, M. A., Carbonell, J., RUIZ, O. A., & Pieckenstain, F. L. (2011) · PLANT PHYSIOLOGY · doi:10.1104/pp.110.171413 · Cited by 108
Nahar, K., Hasanuzzaman, M., Suzuki, T., & Fujita, M. (2016) · Ecotoxicology · doi:10.1007/s10646-016-1740-9 · Cited by 108
Soda, K., Kano, Y., Chiba, F., Koizumi, K., & Miyaki, Y. (2013) · PLoS ONE · doi:10.1371/journal.pone.0064357 · Cited by 107
Yiu, J., Liu, C., Fang, D. Y.-T., & Lai, Y. (2009) · Plant Physiology and Biochemistry · doi:10.1016/j.plaphy.2009.03.007 · Cited by 104
Mackeh, R., Lorin, S., Ratier, A., Mejdoubi‐Charef, N., Baillet, A., Bruneel, A., Hamaï, A., Codogno, P., Poüs, C., & Perdiz, D. (2014) · Journal of Biological Chemistry · doi:10.1074/jbc.m113.507400 · Cited by 104
Modulation of learning and memory by natural polyamines
Guerra, G. P., Rubin, M. A., & Mello, C. F. (2016) · Pharmacological Research · doi:10.1016/j.phrs.2016.03.023 · Cited by 103
Jamwal, S., & Kumar, P. (2015) · Physiology & Behavior · doi:10.1016/j.physbeh.2015.12.015 · Cited by 102
Michiels, C. F., Kurdi, A., Timmermans, J., Meyer, G. R. Y. D., & Martinet, W. (2016) · Atherosclerosis · doi:10.1016/j.atherosclerosis.2016.07.899 · Cited by 102
Parvin, S., Lee, O. R., Sathiyaraj, G., Khorolragchaa, A., Kim, Y., & Yang, D. (2013) · Gene · doi:10.1016/j.gene.2013.12.021 · Cited by 101
Reactivation of autophagy by spermidine ameliorates the myopathic defects of collagen VI-null mice
Chrisam, M., Pirozzi, M., Castagnaro, S., Blaauw, B., Polishchuck, R., Cecconi, F., Grumati, P., & Bonaldo, P. (2015) · Autophagy · doi:10.1080/15548627.2015.1108508 · Cited by 101
Magnes, C., Fauland, A., Gander, E., Narath, S. H., Ratzer, M., Eisenberg, T., Madeo, F., Pieber, T. R., & Sinner, F. M. (2014) · Journal of Chromatography A · doi:10.1016/j.chroma.2013.12.061 · Cited by 100
Self-citationMacrophage ABHD5 promotes colorectal cancer growth by suppressing spermidine production by SRM
Miao, H., Ou, J., Peng, Y., Zhang, X., Chen, Y., Hao, L., Xie, G., Wang, Z., Pang, X., Ruan, Z., et al. (2016) · Nature Communications · doi:10.1038/ncomms11716 · Cited by 100
Li, S., Jin, H., & Zhang, Q. (2016) · Frontiers in Plant Science · doi:10.3389/fpls.2016.01221 · Cited by 99
Nahar, K., Hasanuzzaman, M., Alam, M., & Fujita, M. (2015) · International Journal of Molecular Sciences · doi:10.3390/ijms161226220 · Cited by 98
Rojas, F., González, D., Cortés, N., Ampuero, E., Hernández, D. E., Fritz, E., Abarzúa, S., Martinez, A. N., Elorza, Á. A., Alvarez, A. R., et al. (2015) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2015.00203 · Cited by 97
Spermine reverses lipopolysaccharide-induced memory deficit in mice
Frühauf, P. K. S., Ineu, R. P., Tomazi, L., Duarte, T., Mello, C. F., & Rubin, M. A. (2015) · Journal of Neuroinflammation · doi:10.1186/s12974-014-0220-5 · Cited by 97
Development of a Polyamine Database for Assessing Dietary Intake
Zoumas‐Morse, C., Rock, C. L., Quintana, E. L., Neuhouser, M. L., Gerner, E. W., & Meyskens, F. L. (2007) · Journal of the American Dietetic Association · doi:10.1016/j.jada.2007.03.012 · Cited by 97
Kee, K., Foster, B. A., Merali, S., Kramer, D. L., Hensen, M. L., Diegelman, P., Kisiel, N. D., Vujcic, S., Mazurchuk, R. V., & Porter, C. W. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m406002200 · Cited by 94
Noro, T., Namekata, K., Kimura, A. K., Guo, X., Azuchi, Y., Harada, C., Nakano, T., Tsuneoka, H., & Harada, T. (2015) · Cell Death and Disease · doi:10.1038/cddis.2015.93 · Cited by 93
Polyamine transport, accumulation, and release in brain
Masuko, T., Kusama‐Eguchi, K., Sakata, K., Kusama, T., Chaki, S., Okuyama, S., Williams, K. L., Kashiwagi, K., & Igarashi, K. (2003) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.2003.01558.x · Cited by 92
Wen, X., Ban, Y., Inoue, H., Matsuda, N., & Moriguchi, T. (2009) · Transgenic Research · doi:10.1007/s11248-009-9296-6 · Cited by 91
Polyamines in mammalian ageing: An oncological problem, too? A review
Scalabrino, G., & Ferioli, M. E. (1984) · Mechanisms of Ageing and Development · doi:10.1016/0047-6374(84)90090-3 · Cited by 91
Spermine, a Natural Polyamine, Suppresses LFA-1 Expression on Human Lymphocyte
Soda, K., Kano, Y., Nakamura, T., Kasono, K., Kawakami, M., & Konishi, F. (2005) · The Journal of Immunology · doi:10.4049/jimmunol.175.1.237 · Cited by 89
Sebti, S., Prébois, C., Pérez-Gracia, E., Bauvy, C., Desmots, F., Pirot, N., Gongora, C., Bach, A.-S., Hubberstey, A. V., Palissot, V., et al. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1313618111 · Cited by 88
Wagner, A. E., Piegholdt, S., Rabe, D., Baenas, N., Schloesser, A., Eggersdorfer, M. L., Stocker, A., & Rimbach, G. H. (2015) · Oncotarget · doi:10.18632/oncotarget.5215 · Cited by 88
Age-related changes in polyamines in memory-associated brain structures in rats
Liu, P., Gupta, N. K., Jing, Y., & Zhang, H. (2008) · Neuroscience · doi:10.1016/j.neuroscience.2008.06.033 · Cited by 85
Limited Blood‐Brain Barrier Transport of Polyamines
Shin, W. ‐., Fong, W. F., Pang, S., & Wong, P. C. L. (1985) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.1985.tb08724.x · Cited by 84
Chen, L., Liu, Y., Wu, G., Zhang, N., Shen, Q., & Zhang, R. (2017) · Molecular Plant-Microbe Interactions · doi:10.1094/mpmi-02-17-0027-r · Cited by 84
Zhou, X., Xu, J., Ni, Y.-H., Chen, X., Zhang, H., Zhang, X., Liu, W.-J., Luo, L., & Fu, Y. (2014) · Journal of Ovarian Research · doi:10.1186/s13048-014-0097-z · Cited by 82
Wan, Q.-L., Zheng, S., Wu, G.-S., & Luo, H. (2013) · Experimental Gerontology · doi:10.1016/j.exger.2013.02.020 · Cited by 81
Asghar, M., Monjok, E. M., Kouamou, G., Ohia, S. E., Bagchi, D., & Lokhandwala, M. F. (2007) · Molecular and Cellular Biochemistry · doi:10.1007/s11010-007-9489-3 · Cited by 81
Exogenous administration of spermine improves glucose utilization and decreases bodyweight in mice
Sadasivan, S. K., Vasamsetti, B. M. K., Singh, J. K., Marikunte, V. V., Oommen, A. M., Jagannath, M. R., & Rao, R. P. (2014) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2014.01.073 · Cited by 79
Are milk polyamines preventive agents against food allergy?
Dandrifosse, G., Peulen, O., Khefif, N. E. E., Deloyer, P., Dandrifosse, A.-C., & Grandfils, C. (2000) · Proceedings of The Nutrition Society · doi:10.1017/s0029665100000100 · Cited by 78
Serafini‐Fracassini, D., Duca, S. D., Monti, F., Poli, F., Sacchetti, G., Bregoli, A. M., Biondi, S., & Mea, M. D. (2002) · Cell Death and Differentiation · doi:10.1038/sj.cdd.4400954 · Cited by 78
Kamiab, F., Talaie, A., Khezri, M., & Javanshah, A. (2013) · Plant Growth Regulation · doi:10.1007/s10725-013-9857-9 · Cited by 76
Shu, S., Chen, L., Lu, W., Sun, J., Guo, S., Yuan, Y., & Li, J. (2014) · Journal of Plant Research · doi:10.1007/s10265-014-0653-z · Cited by 75
Deng, K., He, H., Qiu, J. J., Lorber, B., Bryson, J. B., & Filbin, M. T. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.1175-09.2009 · Cited by 74
Ramot, Y., Tiede, S., Bı́ró, T., Bakar, M. H. A., Sugawara, K., Philpott, M. P., Harrison, W. J., Pietilä, M., & Paus, R. (2011) · PLoS ONE · doi:10.1371/journal.pone.0022564 · Cited by 73
Impact of nitric oxide on metabolism in health and age‐related disease
Knott, A. B., & Bossy‐Wetzel, E. (2010) · Diabetes Obesity and Metabolism · doi:10.1111/j.1463-1326.2010.01267.x · Cited by 73
Jamwal, S., Singh, S., Kaur, N., & Kumar, P. (2015) · Neurotoxicity Research · doi:10.1007/s12640-015-9535-y · Cited by 72
Spermidine Alleviates Severity of Murine Experimental Autoimmune Encephalomyelitis
Guo, X., Harada, C., Namekata, K., Kimura, A. K., Mitamura, Y., Yoshida, H., Matsumoto, Y., & Harada, T. (2011) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.10-6015 · Cited by 72
Gong, X., Liu, Y., Huang, D., Zeng, G., Liu, S., Tang, H., Zhou, L., Hu, X., Zhou, Y., & Tan, X. (2016) · Environmental Science and Pollution Research · doi:10.1007/s11356-016-6122-6 · Cited by 72
Salicylate, diflunisal and their metabolites inhibit CBP/p300 and exhibit anticancer activity
Shirakawa, K., Wang, L., Man, N., Maksimoska, J., Sorum, A. W., Lim, H. W., Lee, I. S., Shimazu, T., Newman, J. C., Schröder, S., et al. (2016) · eLife · doi:10.7554/elife.11156 · Cited by 72
Muscle mitohormesis promotes cellular survival via serine/glycine pathway flux
Ost, M., Keipert, S., van Schothorst, E. M., Donner, V., van der Stelt, I., Kipp, A. P., Petzke, K., Jové, M., Pamplona, R., Portero‐Otín, M., et al. (2014) · The FASEB Journal · doi:10.1096/fj.14-261503 · Cited by 69
Coffee induces autophagy in vivo
Pietrocola, F., Malik, S. A., Mariño, G., Vacchelli, E., Senovilla, L., Chaba, K., Niso‐Santano, M., Maiuri, M. C., Madeo, F., & Kroemer, G. (2014) · Cell Cycle · doi:10.4161/cc.28929 · Cited by 68
Self-citationHu, L., Xiang, L., ShuTing, L., Zou, Z., & Hu, X. (2015) · Physiologia Plantarum · doi:10.1111/ppl.12398 · Cited by 67
Spermine delays leaf senescence in Lactuca sativa and prevents the decay of chloroplast photosystems
Serafini‐Fracassini, D., Sandro, A. D., & Duca, S. D. (2010) · Plant Physiology and Biochemistry · doi:10.1016/j.plaphy.2010.03.005 · Cited by 65
Cited by
Sorted by citations
Hallmarks of aging: An expanding universe
López-Otín, C., Blasco, M. A., Partridge, L., Serrano, M., & Kroemer, G. (2023) · Cell · doi:10.1016/j.cell.2022.11.001 · Cited by 6,549
Self-citationBiological Functions of Autophagy Genes: A Disease Perspective
Levine, B., & Kroemer, G. (2019) · Cell · doi:10.1016/j.cell.2018.09.048 · Cited by 2,832
Self-citationAutophagy in healthy aging and disease
Aman, Y., Schmauck-Medina, T., Hansen, M., Morimoto, R. I., Simon, A. K., Bjedov, I., Palikaras, K., Simonsen, A., Johansen, T., Tavernarakis, N., et al. (2021) · Nature Aging · doi:10.1038/s43587-021-00098-4 · Cited by 1,313
Self-citationPolyamine metabolism and cancer: treatments, challenges and opportunities
Casero, R. A., Stewart, T. M., & Pegg, A. E. (2018) · Nature reviews. Cancer · doi:10.1038/s41568-018-0050-3 · Cited by 826
Measuring biological aging in humans: a quest
Ferrucci, L., Gonzalez‐Freire, M., Fabbri, E., Simonsick, E., Tanaka, T., Moore, Z., Salimi, S., Sierra, F., & de Cabo, R. (2020) · Aging Cell · doi:10.1111/acel.13080 · Cited by 781
Metadata
- Authors
- Madeo, F., Eisenberg, T., Pietrocola, F., & Kroemer, G.
- Affiliations
- University of Graz (AT)
- Inserm (FR)
- Karolinska University Hospital (SE)
- Corresponding author
- Madeo, Frank
- Eisenberg, Tobias
- Kroemer, Guido
- Venue
- Science
- Published
- 2018-01-26
- Volume
- 359
- Issue
- 6374
- ISSN
- 0036-8075 (ISSN-L)
- 1095-9203
- OpenAlex
- W2784734859
- Cited by
- 1,154
- References
- 275
- Citations by year
- 2026: 179 · 2025: 179 · 2024: 154 · 2023: 132 · 2022: 150 · 2021: 113 · 2020: 122 · 2019: 74 · 2018: 50
- FWCI
- 6.03
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Science (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Association pour la Recherche sur le Cancer
- European Commission (ERA-Net for Research on Rare Diseases)
- European Research Council
- Agence Nationale de la Recherche (Projets blancs)
- Fondation Leducq
- Austrian Science Fund (P23490-B20, P29262, P24381, P29203 P27893, I1000, W1226, and ‘SFB Lipotox’ (F3012))
- FFG Austria (COIN-project 855987)
- RHU Torino Lumière
- SIRIC Cancer Research and Personalized Medicine
- Fondation pour la Recherche Médicale
- Ligue Contre le Cancer
- Labex
- Institut Universitaire de France
- Institut National Du Cancer
- Cancéropôle Île-de-France
- BMWFW Austria and the Karl-Franzens University
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Aging › Genetics, Aging, and Longevity in Model Organisms
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Polyamine Metabolism and Applications
- Health Sciences › Medicine › Geriatrics and Gerontology › Sirtuins and Resveratrol in Medicine
- Keywords
- spermidine, polyamines, caloric restriction mimetics, aging, age-related diseases, cardioprotection, neuroprotection, mitochondrial function, anti-inflammatory activity, stem cell senescence, protein deacetylation, autophagy, cardiovascular mortality, cancer mortality
- MeSH terms
- Aging, Animals, Anti-Inflammatory Agents, Non-Steroidal, Autophagy, Biological Transport, Cardiovascular Diseases, Humans, Spermidine, Neuroprotective Agents, Dietary Supplements, Metabolic Syndrome, Caloric Restriction, Carcinogenesis
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