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
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Several CR-associated genes, including GPX3, HMGN2, NQO1 and ODC1 (encoding a rate-limiting enzyme of polyamine biosynthesis), possess or promote antioxidant activities.
“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]
Dietary supplementation with the polyamine spermidine prolongs life span and health span in several animal models, and spermidine has also been shown to enhance memory performance and counteract age-related cognitive decline.
“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]
Polyamines are autophagy inducers implicated in immune regulation and have been shown to improve anti-cancer immunity in mice, synergizing with anti-PD ligand 1 immunotherapy.
“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]
Aging is linked to decline of circulating spermidine and alpha-ketoglutarate, which both have anti-aging and anticancer properties.
“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]
Progressive loss of spermidine in aging tissues disables autophagy, which is expected to impair immune recognition of cancer cells because dendritic cells cannot recognize autophagy-deficient cancer cells and because T lymphocyte and NK cell responses are defective.
“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]
Metabolites of the spermidine and kynurenine pathways are associated with the gut microbiota as well as the physiology of the host.
“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]
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 · see citing works
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 · see citing works
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 · see citing works
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 · see citing works
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 · see citing works
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 · see citing works
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 · see citing works
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 · see citing works
Rubinsztein, D. C., Mariño, G., & Kroemer, G. (2011) · Cell · doi:10.1016/j.cell.2011.07.030 · Cited by 2,107 · see citing works
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 · see citing works
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× · see citing works
“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 · see citing works
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 · see citing works
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 · see citing works
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 · see citing works
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 · see citing works
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 · see citing works
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 · see citing works
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 · see citing works
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 · see citing works
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 · see citing works
Autophagy-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 · see citing works
Self-citationAutophagy 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 · see citing works
Resveratrol 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 1,352 · see citing works
Acetyl Coenzyme A: A Central Metabolite and Second Messenger
Pietrocola, F., Galluzzi, L., Pedro, J. M. B., Madeo, F., & Kroemer, G. (2015) · Cell Metabolism · doi:10.1016/j.cmet.2015.05.014 · Cited by 1,349 · see citing works
Self-citationZhang, 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 · see citing works
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 · see citing works
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 · see citing works
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 · see citing works
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 · see citing works
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 · see citing works
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 · see citing works
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 · see citing works
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 · see citing works
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 · see citing works
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 · see citing works
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 · see citing works
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 · see citing works
Mammalian polyamine metabolism and function
Pegg, A. E. (2009) · IUBMB Life · doi:10.1002/iub.230 · Cited by 786 · see citing works
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 · see citing works
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 · see citing works
Self-citationThe 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 745 · see citing works
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 · see citing works
Functions of Polyamines in Mammals
Pegg, A. E. (2016) · Journal of Biological Chemistry · doi:10.1074/jbc.r116.731661 · Cited by 720 · see citing works
Fasting 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 715 · see citing works
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 698 · see citing works
Self-citationTOR 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 · see citing works
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 624 · see citing works
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 · see citing works
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 · see citing works
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 · see citing works
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 559 · see citing works
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 · see citing works
Self-citationZhang, C., & Cuervo, A. M. (2008) · Nature Medicine · doi:10.1038/nm.1851 · Cited by 520 · see citing works
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 · see citing works
Regulation 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 · see citing works
Self-citationSpermidine 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 495 · see citing works
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 487 · see citing works
Chemotherapy-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 · see citing works
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 · see citing works
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 444 · see citing works
Self-citationHowell, 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 · see citing works
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 · see citing works
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 405 · see citing works
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 399 · see citing works
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 · see citing works
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 · see citing works
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 381 · see citing works
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 · see citing works
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 374 · see citing works
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 · see citing works
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 370 · see citing works
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 · see citing works
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 · see citing works
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 · see citing works
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 · see citing works
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 · see citing works
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 · see citing works
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 322 · see citing works
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 · see citing works
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 · see citing works
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 304 · see citing works
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 · see citing works
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 297 · see citing works
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 · see citing works
Matsumoto, M., Kurihara, S., Kibe, R., Ashida, H., & Benno, Y. (2011) · PLoS ONE · doi:10.1371/journal.pone.0023652 · Cited by 290 · cited 3× · see citing works
“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).”
BackgroundInfluentialAnisimov, 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 · see citing works
Resveratrol 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 281 · see citing works
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 · see citing works
Regulation of Autophagy by the p300 Acetyltransferase
Lee, I. H., & Finkel, T. (2009) · Journal of Biological Chemistry · doi:10.1074/jbc.m807135200 · Cited by 276 · see citing works
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 · see citing works
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 271 · see citing works
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 · see citing works
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 264 · see citing works
Self-citationCurcumin-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 259 · see citing works
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 · see citing works
Self-citationRoychoudhury, A., Basu, S., & Sengupta, D. N. (2010) · Journal of Plant Physiology · doi:10.1016/j.jplph.2010.07.009 · Cited by 254 · see citing works
D-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 241 · see citing works
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 240 · see citing works
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 · see citing works
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 · see citing works
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 · see citing works
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 224 · see citing works
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 · see citing works
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 · see citing works
Gupta, S., Hastak, K., Afaq, F., Ahmad, N., & Mukhtar, H. (2003) · Oncogene · doi:10.1038/sj.onc.1207353 · Cited by 218 · see citing works
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 216 · see citing works
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 · see citing works
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 207 · see citing works
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 · see citing works
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 · see citing works
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 · see citing works
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 184 · see citing works
Abbas, S., & Wink, M. (2008) · Planta Medica · doi:10.1055/s-0028-1088378 · Cited by 184 · see citing works
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 179 · see citing works
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 · see citing works
Minois, N. (2014) · Gerontology · doi:10.1159/000356748 · Cited by 176 · see citing works
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 176 · see citing works
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 · see citing works
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 165 · see citing works
Self-citationPolyamines 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 · see citing works
Niu, 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 162 · see citing works
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 · see citing works
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 161 · see citing works
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 · see citing works
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 159 · see citing works
Mostofa, M. G., Yoshida, N., & Fujita, M. (2013) · Plant Growth Regulation · doi:10.1007/s10725-013-9865-9 · Cited by 158 · see citing works
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 · see citing works
Self-citationAutophagy, NLRP3 inflammasome and auto-inflammatory/immune diseases.
Zhong, Z., Sánchez‐López, E., & Karin, M. (2016) · PubMed · Cited by 156 · see citing works
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 · see citing works
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 155 · see citing works
Rady, M. M., & Hemida, K. A. (2015) · Ecotoxicology and Environmental Safety · doi:10.1016/j.ecoenv.2015.05.008 · Cited by 154 · see citing works
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 · see citing works
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 · see citing works
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 138 · see citing works
Matsumoto, M., & Benno, Y. (2007) · Microbiology and Immunology · doi:10.1111/j.1348-0421.2007.tb03887.x · Cited by 129 · see citing works
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 · see citing works
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 122 · see citing works
Puyang, X., An, M., Han, L., & Zhang, X. (2015) · Ecotoxicology and Environmental Safety · doi:10.1016/j.ecoenv.2015.03.023 · Cited by 120 · see citing works
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 · see citing works
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 117 · see citing works
Igarashi, K., Ueda, S., Yoshida, K., & Kashiwagi, K. (2006) · Amino Acids · doi:10.1007/s00726-006-0264-7 · Cited by 116 · see citing works
Radhakrishnan, R., & Lee, I.-J. (2012) · Journal of Plant Growth Regulation · doi:10.1007/s00344-012-9274-8 · Cited by 116 · see citing works
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 115 · see citing works
Yang, 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 · see citing works
Spermine 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 · see citing works
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 · see citing works
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 109 · see citing works
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 109 · see citing works
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 · see citing works
Self-citationYamamoto, 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 108 · see citing works
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 108 · see citing works
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 · see citing works
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 107 · see citing works
Self-citationSoda, K., Kano, Y., Chiba, F., Koizumi, K., & Miyaki, Y. (2013) · PLoS ONE · doi:10.1371/journal.pone.0064357 · Cited by 107 · see citing works
Nahar, K., Hasanuzzaman, M., Suzuki, T., & Fujita, M. (2016) · Ecotoxicology · doi:10.1007/s10646-016-1740-9 · Cited by 106 · see citing works
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 · see citing works
Jamwal, S., & Kumar, P. (2015) · Physiology & Behavior · doi:10.1016/j.physbeh.2015.12.015 · Cited by 102 · see citing works
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 · see citing works
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 · see citing works
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 · see citing works
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 · see citing works
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 100 · see citing works
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 99 · see citing works
Li, S., Jin, H., & Zhang, Q. (2016) · Frontiers in Plant Science · doi:10.3389/fpls.2016.01221 · Cited by 99 · see citing works
Nahar, K., Hasanuzzaman, M., Alam, M., & Fujita, M. (2015) · International Journal of Molecular Sciences · doi:10.3390/ijms161226220 · Cited by 98 · see citing works
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 97 · see citing works
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 · see citing works
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 96 · see citing works
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 95 · see citing works
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 · see citing works
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 · see citing works
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 · see citing works
Wen, X., Ban, Y., Inoue, H., Matsuda, N., & Moriguchi, T. (2009) · Transgenic Research · doi:10.1007/s11248-009-9296-6 · Cited by 91 · see citing works
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 · see citing works
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 · see citing works
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 · see citing works
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 85 · see citing works
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 · see citing works
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 84 · see citing works
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 · see citing works
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 · see citing works
Wan, Q.-L., Zheng, S., Wu, G.-S., & Luo, H. (2013) · Experimental Gerontology · doi:10.1016/j.exger.2013.02.020 · Cited by 80 · see citing works
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 80 · see citing works
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 · see citing works
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 · see citing works
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 · see citing works
Kamiab, F., Talaie, A., Khezri, M., & Javanshah, A. (2013) · Plant Growth Regulation · doi:10.1007/s10725-013-9857-9 · Cited by 76 · see citing works
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 · see citing works
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 · see citing works
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 · see citing works
Jamwal, S., Singh, S., Kaur, N., & Kumar, P. (2015) · Neurotoxicity Research · doi:10.1007/s12640-015-9535-y · Cited by 72 · see citing works
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 · see citing works
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 · see citing works
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 · see citing works
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 70 · see citing works
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 · see citing works
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 · see citing works
Self-citationHu, L., Xiang, L., ShuTing, L., Zou, Z., & Hu, X. (2015) · Physiologia Plantarum · doi:10.1111/ppl.12398 · Cited by 67 · see citing works
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 · see citing works
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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 · see citing works
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 · see citing works
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 · see citing works
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 824 · see citing works
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 · see citing works
Autophagy as a promoter of longevity: insights from model organisms
Hansen, M., Rubinsztein, D. C., & Walker, D. W. (2018) · Nature Reviews Molecular Cell Biology · doi:10.1038/s41580-018-0033-y · Cited by 754 · see citing works
The gut microbiota and the brain–gut–kidney axis in hypertension and chronic kidney disease
Yang, T., Richards, E. M., Pepine, C. J., & Raizada, M. K. (2018) · Nature Reviews Nephrology · doi:10.1038/s41581-018-0018-2 · Cited by 753 · see citing works
Mittelbrunn, M., & Kroemer, G. (2021) · Nature Immunology · doi:10.1038/s41590-021-00927-z · Cited by 702 · see citing works
Self-citationMadeo, F., Carmona-Gutierrez, D., Hofer, S. J., & Kroemer, G. (2019) · Cell Metabolism · doi:10.1016/j.cmet.2019.01.018 · Cited by 630 · see citing works
Self-citationSpermidine improves gut barrier integrity and gut microbiota function in diet-induced obese mice
Ma, L., Ni, Y., Wang, Z., Tu, W., Ni, L., Zhuge, F., Zheng, A., Hu, L., Zhao, Y., Zheng, L., et al. (2020) · Gut Microbes · doi:10.1080/19490976.2020.1832857 · Cited by 596 · see citing works
Promoting the clearance of neurotoxic proteins in neurodegenerative disorders of ageing
Boland, B., Yu, W. H., Corti, O., Mollereau, B., Henriques, A., Bézard, E., Pastores, G., Rubinsztein, D. C., Nixon, R. A., Duchen, M. R., et al. (2018) · Nature Reviews Drug Discovery · doi:10.1038/nrd.2018.109 · Cited by 552 · see citing works
Self-citationMeta-hallmarks of aging and cancer
López-Otín, C., Pietrocola, F., Roiz-Valle, D., Galluzzi, L., & Kroemer, G. (2023) · Cell Metabolism · doi:10.1016/j.cmet.2022.11.001 · Cited by 529 · see citing works
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Medina, C. B., Mehrotra, P., Arandjelovic, S., Perry, J. S. A., Guo, Y., Morioka, S., Barron, B. J., Walk, S. F., Ghesquière, B., Krupnick, A. S., et al. (2020) · Nature · doi:10.1038/s41586-020-2121-3 · Cited by 513 · see citing works
The quest to slow ageing through drug discovery
Partridge, L., Fuentealba, M., & Kennedy, B. K. (2020) · Nature Reviews Drug Discovery · doi:10.1038/s41573-020-0067-7 · Cited by 468 · see citing works
Mitophagy in degenerative joint diseases
Sun, K., Jing, X., Guo, J., Yao, X., & Guo, F. (2020) · Autophagy · doi:10.1080/15548627.2020.1822097 · Cited by 464 · see citing works
Lou, G., Palikaras, K., Lautrup, S., Scheibye‐Knudsen, M., Tavernarakis, N., & Fang, E. F. (2019) · Trends in Molecular Medicine · doi:10.1016/j.molmed.2019.07.002 · Cited by 449 · see citing works
Krämer, J., Kang, R., Grimm, L., Cola, L. D., Picchetti, P., & Biedermann, F. (2022) · Chemical Reviews · doi:10.1021/acs.chemrev.1c00746 · Cited by 455 · see citing works
Autophagy in metabolic disease and ageing
Kitada, M., & Koya, D. (2021) · Nature Reviews Endocrinology · doi:10.1038/s41574-021-00551-9 · Cited by 413 · see citing works
PINK1/Parkin-mediated mitophagy in neurodegenerative diseases
Li, J., Yang, D., Li, Z., Zhao, M., Wang, D., Sun, Z., Wen, P., Dai, Y., Gou, F., Ji, Y., et al. (2022) · Ageing Research Reviews · doi:10.1016/j.arr.2022.101817 · Cited by 388 · see citing works
Autophagy in liver diseases: Time for translation?
Allaire, M., Rautou, P.-E., Codogno, P., & Lotersztajn, S. (2019) · Journal of Hepatology · doi:10.1016/j.jhep.2019.01.026 · Cited by 378 · see citing works
Mitophagy: An Emerging Role in Aging and Age-Associated Diseases
Chen, G., Kroemer, G., & Kepp, O. (2020) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2020.00200 · Cited by 359 · see citing works
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Holbert, C. E., Cullen, M., Casero, R. A., & Stewart, T. M. (2022) · Nature reviews. Cancer · doi:10.1038/s41568-022-00473-2 · Cited by 370 · see citing works
Sun, C., Wang, A., Zhou, Y., Chen, P., Wang, X., Huang, J., Gao, J., Wang, X. D., Shu, L., Lu, J., et al. (2023) · Nature Communications · doi:10.1038/s41467-023-38360-5 · Cited by 347 · see citing works
Single-cell multiregion dissection of Alzheimer’s disease
Mathys, H., Boix, C. A., Akay, L. A., Xia, Z., Davila-Velderrain, J., Ng, A. P., Jiang, X., Abdelhady, G., Galani, K., Mantero, J., et al. (2024) · Nature · doi:10.1038/s41586-024-07606-7 · Cited by 343 · see citing works
Polyamines control eIF5A hypusination, TFEB translation, and autophagy to reverse B cell senescence
Zhang, H., Alsaleh, G., Feltham, J., Sun, Y., Napolitano, G., Riffelmacher, T., Charles, P., Frau, L., Hublitz, P., Yu, Z., et al. (2019) · Molecular Cell · doi:10.1016/j.molcel.2019.08.005 · Cited by 341 · see citing works
ATP13A2 deficiency disrupts lysosomal polyamine export
van Veen, S., Martin, S., den Haute, C. V., Benoy, V., Lyons, J. A., Vanhoutte, R., Kahler, J. P., Decuypere, J.-P., Gelders, G., Lambie, E. J., et al. (2020) · Nature · doi:10.1038/s41586-020-1968-7 · Cited by 335 · see citing works
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Stark, S. M., Kirwan, C. B., & Stark, C. E. L. (2019) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2019.08.003 · Cited by 326 · see citing works
Intermittent and periodic fasting, longevity and disease
Longo, V. D., Tano, M. D., Mattson, M. P., & Guidi, N. (2021) · Nature Aging · doi:10.1038/s43587-020-00013-3 · Cited by 288 · see citing works
Epigenetic changes during aging and their reprogramming potential
Kane, A. E., & Sinclair, D. A. (2019) · Critical Reviews in Biochemistry and Molecular Biology · doi:10.1080/10409238.2019.1570075 · Cited by 283 · see citing works
Autophagy and the hallmarks of aging
Kaushik, S., Tasset, I., Arias, E., Pampliega, O., Wong, E., Martinez-Vicente, M., & Cuervo, A. M. (2021) · Ageing Research Reviews · doi:10.1016/j.arr.2021.101468 · Cited by 285 · see citing works
Hallmarks of cardiovascular ageing
Abdellatif, M., Rainer, P. P., Sedej, S., & Kroemer, G. (2023) · Nature Reviews Cardiology · doi:10.1038/s41569-023-00881-3 · Cited by 285 · see citing works
Self-citationMuñoz‐Esparza, N., Latorre‐Moratalla, M. L., Comas-Basté, O., Toro-Funes, N., Veciana-Nogués, M. T., & Vidal‐Carou, M. C. (2019) · Frontiers in Nutrition · doi:10.3389/fnut.2019.00108 · Cited by 275 · see citing works
Making sense of the ageing methylome
Seale, K., Horvath, S., Teschendorff, A., Eynon, N., & Voisin, S. (2022) · Nature Reviews Genetics · doi:10.1038/s41576-022-00477-6 · Cited by 274 · see citing works
Polyamine catabolism and oxidative damage
Stewart, T. M., Dunston, T. T., Woster, P. M., & Casero, R. A. (2018) · Journal of Biological Chemistry · doi:10.1074/jbc.tm118.003337 · Cited by 269 · see citing works
Targeting Autophagy in Aging and Aging-Related Cardiovascular Diseases
Ren, J. T., & Zhang, Y. (2018) · Trends in Pharmacological Sciences · doi:10.1016/j.tips.2018.10.005 · Cited by 269 · see citing works
Mitophagy in Alzheimer’s Disease and Other Age-Related Neurodegenerative Diseases
Cai, Q., & Jeong, Y. Y. (2020) · Cells · doi:10.3390/cells9010150 · Cited by 263 · see citing works
Pleiotropic effects of mitochondria in aging
de Lima, T. I., Li, T. Y., Mottis, A., & Auwerx, J. H. (2022) · Nature Aging · doi:10.1038/s43587-022-00191-2 · Cited by 242 · see citing works
Chang, X., Lochner, A., Wang, H.-H., Wang, S., Zhu, H., Ren, J. T., & Zhou, H. (2021) · Theranostics · doi:10.7150/thno.60143 · Cited by 231 · see citing works
Dietary and Gut Microbiota Polyamines in Obesity- and Age-Related Diseases
Ramos-Molina, B., Queipo-Ortuño, M. I., Lambertos, A., Tinahones, F. J., & Peñafiel, R. (2019) · Frontiers in Nutrition · doi:10.3389/fnut.2019.00024 · Cited by 226 · see citing works
Age-Associated Mitochondrial Dysfunction Accelerates Atherogenesis
Tyrrell, D. J., Blin, M. G., Song, J., Wood, S. C., Zhang, M., Beard, D. A., & Goldstein, D. R. (2019) · Circulation Research · doi:10.1161/circresaha.119.315644 · Cited by 226 · see citing works
Spermidine activates mitochondrial trifunctional protein and improves antitumor immunity in mice
Al-Habsi, M., Chamoto, K., Matsumoto, K., Nomura, N., Zhang, B., Sugiura, Y., Sonomura, K., Maharani, A., Nakajima, Y., Wu, Y., et al. (2022) · Science · doi:10.1126/science.abj3510 · Cited by 223 · see citing works
Spermidine: A physiological autophagy inducer acting as an anti-aging vitamin in humans?
Madeo, F., Bauer, M. A., Carmona-Gutierrez, D., & Kroemer, G. (2019) · Autophagy · doi:10.1080/15548627.2018.1530929 · Cited by 212 · see citing works
Self-citationMicrobial-derived metabolites as a risk factor of age-related cognitive decline and dementia
Connell, E., Le Gall, G., Pontifex, M. G., Sami, S., Cryan, J. F., Clarke, G., Müller, M., & Vauzour, D. (2022) · Molecular Neurodegeneration · doi:10.1186/s13024-022-00548-6 · Cited by 208 · see citing works
Mechanisms of spermidine-induced autophagy and geroprotection
Hofer, S. J., Simon, A. K., Bergmann, M., Eisenberg, T., Kroemer, G., & Madeo, F. (2022) · Nature Aging · doi:10.1038/s43587-022-00322-9 · Cited by 205 · see citing works
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Zhang, T., Liu, Q., Gao, W., Sehgal, S. A., & Wu, H. (2021) · Autophagy · doi:10.1080/15548627.2021.1975914 · Cited by 207 · see citing works
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Carriche, G. M., Almeida, L., Stüve, P., Velásquez, L. N., Dhillon-LaBrooy, A., Roy, U., Lindenberg, M., Strowig, T., Plaza‐Sirvent, C., Schmitz, I., et al. (2020) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2020.04.037 · Cited by 199 · see citing works
The Lichens’ Microbiota, Still a Mystery?
Grimm, M., Grube, M., Schiefelbein, U., Zühlke, D., Bernhardt, J., & Riedel, K. (2021) · Frontiers in Microbiology · doi:10.3389/fmicb.2021.623839 · Cited by 191 · see citing works
Dietary regulation in health and disease
Wu, Q., Gao, Z., Yu, X., & Wang, P. (2022) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-022-01104-w · Cited by 182 · see citing works
S‐adenosylmethionine: A metabolite critical to the regulation of autophagy
Ouyang, Y., Wu, Q., Li, J., Sun, S., & Sun, S. (2020) · Cell Proliferation · doi:10.1111/cpr.12891 · Cited by 176 · see citing works
Metabolomic analyses of COVID-19 patients unravel stage-dependent and prognostic biomarkers
Danlos, F., Grajeda‐Iglesias, C., Durand, S., Sauvat, A., Roumier, M., Cantin, D., Colomba, É., Rohmer, J., Pommeret, F., Baciarello, G., et al. (2021) · Cell Death and Disease · doi:10.1038/s41419-021-03540-y · Cited by 168 · see citing works
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Martel, J., Ojcius, D. M., Ko, Y., Ke, P., Wu, C.-Y., Peng, H., & Young, J. D. (2019) · Trends in Endocrinology and Metabolism · doi:10.1016/j.tem.2019.04.001 · Cited by 163 · see citing works
Wirth, M., Benson, G. S., Schwarz, C., Köbe, T., Grittner, U., Schmitz, D., Sigrist, S. J., Bohlken, J., Stekovic, S., Madeo, F., et al. (2018) · Cortex · doi:10.1016/j.cortex.2018.09.014 · Cited by 163 · see citing works
Self-citationGaitán, J. M., Moon, H. Y., Stremlau, M., Dubal, D. B., Cook, D. B., Okonkwo, O. C., & van Praag, H. (2021) · Frontiers in Endocrinology · doi:10.3389/fendo.2021.660181 · Cited by 160 · see citing works
van Vliet, S., Bain, J. R., Muehlbauer, M. J., Provenza, F. D., Kronberg, S. L., Pieper, C. F., & Huffman, K. M. (2021) · Scientific Reports · doi:10.1038/s41598-021-93100-3 · Cited by 160 · see citing works
Mahajan, U. V., Varma, V., Griswold, M., Blackshear, C., An, Y., Oommen, A., Varma, S., Troncoso, J., Pletnikova, O., O'Brien, R., et al. (2020) · PLoS Medicine · doi:10.1371/journal.pmed.1003012 · Cited by 144 · see citing works
Liu, R., Li, X., Ma, H., Yang, Q., Shang, Q., Song, L., Zheng, Z., Zhang, S., Pan, Y., Huang, P., et al. (2020) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2020.10.029 · Cited by 159 · see citing works
Longitudinal gut microbiome changes in immune checkpoint blockade-treated advanced melanoma
Björk, J. R., Bolte, L. A., Maltez Thomas, A., Lee, K. A., Rossi, N., Wind, T. T., Smit, L. M., Armanini, F., Asnicar, F., Blanco-Miguez, A., et al. (2024) · Nature Medicine · doi:10.1038/s41591-024-02803-3 · Cited by 156 · see citing works
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Gobert, A. P., Latour, Y. L., Asim, M., Barry, D. P., Allaman, M. M., Finley, J. L., Smith, T. M., McNamara, K. M., Singh, K., Sierra, J. C., et al. (2021) · Gastroenterology · doi:10.1053/j.gastro.2021.11.005 · Cited by 154 · see citing works
Polyamine synthesis as a target of MYC oncogenes
Bachmann, A. S., & Geerts, D. (2018) · Journal of Biological Chemistry · doi:10.1074/jbc.tm118.003336 · Cited by 148 · see citing works
Polyamines: their significance for maintaining health and contributing to diseases
Xuan, M., Gu, X., Li, J., Huang, D., Chen, X., & He, Y. (2023) · Cell Communication and Signaling · doi:10.1186/s12964-023-01373-0 · Cited by 159 · see citing works
MitophAging: Mitophagy in Aging and Disease
Bakula, D., & Scheibye‐Knudsen, M. (2020) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2020.00239 · Cited by 150 · see citing works
Kirkman, D. L., Robinson, A. T., Rossman, M. J., Seals, D. R., & Edwards, D. G. (2021) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.00917.2020 · Cited by 146 · see citing works
Polyamines and Kynurenines at the Intersection of Immune Modulation
Proietti, E., Rossini, S., Grohmann, U., & Mondanelli, G. (2020) · Trends in Immunology · doi:10.1016/j.it.2020.09.007 · Cited by 141 · see citing works
Cross-species metabolomic analysis identifies uridine as a potent regeneration promoting factor
Liu, Z., Li, W., Geng, L., Sun, L., Wang, Q., Yu, Y., Yan, P., Liang, C., Ren, J., Song, M., et al. (2022) · Cell Discovery · doi:10.1038/s41421-021-00361-3 · Cited by 135 · see citing works
Liang, Y., Piao, C., Beuschel, C. B., Toppe, D., Kollipara, L., Bogdanow, B., Maglione, M., Lützkendorf, J., See, J. C. K., Huang, S., et al. (2021) · Cell Reports · doi:10.1016/j.celrep.2021.108941 · Cited by 131 · see citing works
Self-citationThe roles of arginases and arginine in immunity
Canè, S., Geiger, R., & Bronte, V. (2024) · Nature reviews. Immunology · doi:10.1038/s41577-024-01098-2 · Cited by 135 · see citing works
Yeast as a tool to identify anti-aging compounds
Zimmermann, A., Hofer, S. J., Pendl, T., Kainz, K., Madeo, F., & Carmona‐Gutiérrez, D. (2018) · FEMS Yeast Research · doi:10.1093/femsyr/foy020 · Cited by 124 · see citing works
Self-citationAutophagy in health and disease: From molecular mechanisms to therapeutic target
Lu, G. X., Wang, Y., Shi, Y. P., Zhang, Z., Huang, C., He, W., Wang, C., & Shen, H. (2022) · MedComm · doi:10.1002/mco2.150 · Cited by 127 · see citing works
Zhu, G., Xie, Y., Wang, J., Wang, M., Qian, Y., Sun, Q., Dai, Y., & Li, C. (2024) · Advanced Materials · doi:10.1002/adma.202409066 · Cited by 126 · see citing works
A metabolic profile of polyamines in parkinson disease: A promising biomarker
Saiki, S., Sasazawa, Y., Fujimaki, M., Kamagata, K., Kaga, N., Taka, H., Li, Y., Souma, S., Hatano, T., Imamichi, Y., et al. (2019) · Annals of Neurology · doi:10.1002/ana.25516 · Cited by 123 · see citing works
The path toward using microbial metabolites as therapies
Descamps, H. C., Herrmann, B. I., Wiredu, D., & Thaiss, C. A. (2019) · EBioMedicine · doi:10.1016/j.ebiom.2019.05.063 · Cited by 121 · see citing works
Baek, A.-R., Hong, J., Song, K. S., Jang, A., Kim, D.-J., Chin, S., & Park, S. (2020) · Experimental & Molecular Medicine · doi:10.1038/s12276-020-00545-z · Cited by 122 · see citing works
New Insights into the Roles and Mechanisms of Spermidine in Aging and Age-Related Diseases
Ni, Y., & Liu, Y. (2021) · Aging and Disease · doi:10.14336/ad.2021.0603 · Cited by 121 · see citing works
Alsaleh, G., Panse, I., Swadling, L., Zhang, H., Richter, F. C., Meyer, A., Lord, J., Barnes, E., Klenerman, P., Green, C., et al. (2020) · eLife · doi:10.7554/elife.57950 · Cited by 120 · see citing works
The road ahead for health and lifespan interventions
Gonzalez-Freire, M., Diaz-Ruiz, A., Hauser, D., Martinez-Romero, J., Ferrucci, L., Bernier, M., & de Cabo, R. (2020) · Ageing Research Reviews · doi:10.1016/j.arr.2020.101037 · Cited by 118 · see citing works
Zhou, S., Gu, J. H., Liu, R., Song, W., Wang, Q., Shen, H., Dai, Y., Zhou, H., Zhang, F., & Lü, L. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.00948 · Cited by 120 · see citing works
Carbotoxicity—Noxious Effects of Carbohydrates
Kroemer, G., López-Otı́n, C., Madeo, F., & de Cabo, R. (2018) · Cell · doi:10.1016/j.cell.2018.07.044 · Cited by 117 · see citing works
Self-citationAlmeida, L., Dhillon-LaBrooy, A., Carriche, G. M., Berod, L., & Sparwasser, T. D. (2021) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2021.03.033 · Cited by 112 · see citing works
Spermidine reduces neuroinflammation and soluble amyloid beta in an Alzheimer’s disease mouse model
Freitag, K., Sterczyk, N., Wendlinger, S., Obermayer, B., Schulz, J., Farztdinov, V. M., Mülleder, M., Ralser, M., Houtman, J., Fleck, L., et al. (2022) · Journal of Neuroinflammation · doi:10.1186/s12974-022-02534-7 · Cited by 122 · see citing works
Hou, Y., Chen, M., Bian, Y., Hu, Y., Chuan, J., Zhong, L., Zhu, Y., & Tong, R. (2024) · npj Vaccines · doi:10.1038/s41541-024-00874-4 · Cited by 116 · see citing works
Guo, Y., Ye, Q., Deng, P., Cao, Y., He, D., Zhou, Z., Wang, C., Zaytseva, Y. Y., Schwartz, C. E., Lee, E. Y., et al. (2020) · Nature Communications · doi:10.1038/s41467-020-17067-x · Cited by 114 · see citing works
Spermidine alleviates cardiac aging by improving mitochondrial biogenesis and function
Wang, J., Li, S., Wang, J., Wu, F., Chen, Y., Zhang, H., Guo, Y., Yan, L., Li, L., Yu, X., et al. (2020) · Aging · doi:10.18632/aging.102647 · Cited by 113 · see citing works
Nutritional Aspects of Spermidine
Madeo, F., Hofer, S. J., Pendl, T., Bauer, M. A., Eisenberg, T., Carmona‐Gutiérrez, D., & Kroemer, G. (2020) · Annual Review of Nutrition · doi:10.1146/annurev-nutr-120419-015419 · Cited by 114 · see citing works
Self-citationEffects of anti-aging interventions on intestinal microbiota
Du, Y., Gao, Y., Zeng, B., Fan, X., Yang, D., & Yang, M. (2021) · Gut Microbes · doi:10.1080/19490976.2021.1994835 · Cited by 115 · see citing works
Fine-Tuning Cardiac Insulin-Like Growth Factor 1 Receptor Signaling to Promote Health and Longevity
Abdellatif, M., Trummer-Herbst, V., Heberle, A. M., Humnig, A., Pendl, T., Durand, S., Cerrato, G., Hofer, S. J., Islam, M., Voglhuber, J., et al. (2022) · Circulation · doi:10.1161/circulationaha.122.059863 · Cited by 108 · see citing works
Self-citationCaloric Restriction Mimetics in Nutrition and Clinical Trials
Hofer, S. J., Davinelli, S., Bergmann, M., Scapagnini, G., & Madeo, F. (2021) · Frontiers in Nutrition · doi:10.3389/fnut.2021.717343 · Cited by 109 · see citing works
Self-citationYan, J., Yan, J., Wang, Y., Ling, Y., Song, X., Wang, S., Liu, H., Liu, Q., Zhang, Y., Yang, P., et al. (2019) · British Journal of Pharmacology · doi:10.1111/bph.14706 · Cited by 108 · see citing works
Increased immunosuppression impairs tissue homeostasis with aging and age-related diseases
Salminen, A. (2020) · Journal of Molecular Medicine · doi:10.1007/s00109-020-01988-7 · Cited by 110 · see citing works
D'Arcy, M. (2024) · APOPTOSIS · doi:10.1007/s10495-024-01977-y · Cited by 113 · see citing works
Schwarz, C., Benson, G. S., Horn, N., Wurdack, K., Grittner, U., Schilling, R., Märschenz, S., Köbe, T., Hofer, S. J., Magnes, C., et al. (2022) · JAMA Network Open · doi:10.1001/jamanetworkopen.2022.13875 · Cited by 106 · see citing works
Self-citationIturria-Medina, Y., Adewale, Q., Khan, A. F., Ducharme, S., Rosa-Neto, P., O’Donnell, K., Petyuk, V. A., Gauthier, S., De Jager, P. L., Breitner, J., et al. (2022) · Science Advances · doi:10.1126/sciadv.abo6764 · Cited by 100 · see citing works
Antiaging agents: safe interventions to slow aging and healthy life span extension
Liu, J. (2022) · Natural Products and Bioprospecting · doi:10.1007/s13659-022-00339-y · Cited by 107 · see citing works
Liu, X., Chen, A., Liang, Q., Yang, X., Dong, Q., Fu, M., Wang, S., Li, Y., Ye, Y., Lan, Z., et al. (2021) · Aging Cell · doi:10.1111/acel.13377 · Cited by 104 · see citing works
First we eat, then we do everything else: The dynamic metabolic regulation of efferocytosis
Trzeciak, A. J., Wang, Y., & Perry, J. S. A. (2021) · Cell Metabolism · doi:10.1016/j.cmet.2021.08.001 · Cited by 107 · see citing works
Wirth, M., Schwarz, C., Benson, G. S., Horn, N., Buchert, R., Lange, C., Köbe, T., Hetzer, S., Maglione, M., Michael, E., et al. (2019) · Alzheimer s Research & Therapy · doi:10.1186/s13195-019-0484-1 · Cited by 105 · see citing works
Self-citationYAP/TAZ drives cell proliferation and tumour growth via a polyamine–eIF5A hypusination–LSD1 axis
Li, H., Wu, B.-K., Kanchwala, M., Cai, J., Wang, L., Xing, C., Zheng, Y., & Pan, D. (2022) · Nature Cell Biology · doi:10.1038/s41556-022-00848-5 · Cited by 102 · see citing works
Mitophagy in the pathogenesis and management of disease
Wang, Q., Sun, Y., Li, T. Y., & Auwerx, J. (2026) · Cell Research · doi:10.1038/s41422-025-01203-7 · Cited by 103 · see citing works
Tabone, M., Bressa, C., García-Merino, J. A., Moreno‐Pérez, D., Chu‐Van, E., Castelli, F. A., Fenaille, F., & Larrosa, M. (2021) · Scientific Reports · doi:10.1038/s41598-021-82947-1 · Cited by 100 · see citing works
Metabolic Stress, Autophagy, and Cardiovascular Aging: from Pathophysiology to Therapeutics
Ren, J. T., Sowers, J. R., & Zhang, Y. (2018) · Trends in Endocrinology and Metabolism · doi:10.1016/j.tem.2018.08.001 · Cited by 99 · see citing works
Spermidine delays aging in humans
Madeo, F., Carmona‐Gutiérrez, D., Kepp, O., & Kroemer, G. (2018) · Aging · doi:10.18632/aging.101517 · Cited by 95 · see citing works
Self-citation
- 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
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