The DOI matches its Crossref record; 30 of the 30 references it cites were found in a registry or an index.
IGF-1 receptor regulates lifespan and resistance to oxidative stress in mice
Open accessAbstract
Studies in invertebrates have led to the identification of a number of genes that regulate lifespan, some of which encode components of the insulin or insulin-like signalling pathways. Examples include the related tyrosine kinase receptors InR (Drosophila melanogaster) and DAF-2 (Caenorhabditis elegans) that are homologues of the mammalian insulin-like growth factor type 1 receptor (IGF-1R). To investigate whether IGF-1R also controls longevity in mammals, we inactivated the IGF-1R gene in mice (Igf1r). Here, using heterozygous knockout mice because null mutants are not viable, we report that Igf1r(+/-) mice live on average 26% longer than their wild-type littermates (P < 0.02). Female Igf1r(+/-) mice live 33% longer than wild-type females (P < 0.001), whereas the equivalent male mice show an increase in lifespan of 16%, which is not statistically significant. Long-lived Igf1r(+/-) mice do not develop dwarfism, their energy metabolism is normal, and their nutrient uptake, physical activity, fertility and reproduction are unaffected. The Igf1r(+/-) mice display greater resistance to oxidative stress, a known determinant of ageing. These results indicate that the IGF-1 receptor may be a central regulator of mammalian lifespan.
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
“Nutrient sensing and energy homeostasis have been implicated as connecting mitochondrial function and longevity104,105.”
From Stem cell aging: mechanisms, regulators and therapeutic opportunities (2014) · cites this paper as [105]
In the citing paper
“Mutations that decrease IGF1 levels or activity cause reduced growth and longer life in mice by up to 65% (Coschigano et al., 2000; Holzenberger et al., 2003).”
From The Search for Antiaging Interventions: From Elixirs to Fasting Regimens (2014) · cites this paper as Holzenberger et al., 2003
Citations
Cites
Oxidants, oxidative stress and the biology of ageing
Finkel, T., & Holbrook, N. J. (2000) · Nature · doi:10.1038/35041687 · Cited by 9,413
Liu, J.-P., Baker, J. C., Perkins, A. S., Robertson, E. J., & Efstratiadis, A. (1993) · Cell · doi:10.1016/s0092-8674(05)80084-4 · Cited by 2,854
Kimura, K. D., Tissenbaum, H. A., Liu, Y., & Ruvkun, G. (1997) · Science · doi:10.1126/science.277.5328.942 · Cited by 2,250
The p66shc adaptor protein controls oxidative stress response and life span in mammals
Migliaccio, E., Giorgio, M., Mele, S., Pelicci, G., Reboldi, P., Pandolfi, P. P., Lanfrancone, L., & Pelicci, P. G. (1999) · Nature · doi:10.1038/46311 · Cited by 1,712
Tatar, M., Kopelman, A. H., Epstein, D., Tu, M., Yin, C. ‐., & Garofalo, R. S. (2001) · Science · doi:10.1126/science.1057987 · Cited by 1,630
Extension of Life-Span by Loss of CHICO, a Drosophila Insulin Receptor Substrate Protein
Clancy, D. J., Gems, D., Harshman, L. G., Oldham, S., Stocker, H., Hafen, E., Leevers, S. J., & Partridge, L. (2001) · Science · doi:10.1126/science.1057991 · Cited by 1,436
Genetic pathways that regulate ageing in model organisms
Guarente, L., & Kenyon, C. J. (2000) · Nature · doi:10.1038/35041700 · Cited by 1,337
Kulkarni, R., Brüning, J. C., Winnay, J. N., Postic, C., Magnuson, M. A., & Kahn, C. R. (1999) · Cell · doi:10.1016/s0092-8674(00)80546-2 · Cited by 1,148
Dwarf mice and the ageing process
Brown‐Borg, H. M., Borg, K. E., Meliska, C. J., & Bartke, A. (1996) · Nature · doi:10.1038/384033a0 · Cited by 1,091
Flurkey, K., Papaconstantinou, J., Miller, R. A., & Harrison, D. E. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.111158898 · Cited by 826
Cited by
Sorted by citations
Items 201–300 of 1,005
Xu, J., & Liao, K. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m402297200 · Cited by 213
Franceschi, C., Olivieri, F., Marchegiani, F., Cardelli, M., Cavallone, L., Capri, M., Salvioli, S., Valensin, S., Benedictis, G. D., Iorio, A. D., et al. (2004) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2004.08.028 · Cited by 211
Impact of genomic damage and ageing on stem cell function
Behrens, A., van Deursen, J. M., Rudolph, K. L., & Schumacher, B. (2014) · Nature Cell Biology · doi:10.1038/ncb2928 · Cited by 207
Analysis of long-lived C. elegans daf-2 mutants using serial analysis of gene expressionPreprint
Halaschek-Wiener, J., Khattra, J. S., McKay, S., Pouzyrev, A. T., Stott, J. M., Yang, G., Holt, R. A., Jones, S. J. M., Marra, M. A., Brooks-Wilson, A. R., et al. (2005) · Genome Research · doi:10.1101/gr.3274805 · Cited by 215
Aging, stress and the hippocampus
Miller, D. B., & O’Callaghan, J. P. (2005) · Ageing Research Reviews · doi:10.1016/j.arr.2005.03.002 · Cited by 206
Remarkable longevity and stress resistance of nematode PI3K‐null mutants
Ayyadevara, S., Alla, R., Thaden, J. J., & Reis, R. J. S. (2007) · Aging Cell · doi:10.1111/j.1474-9726.2007.00348.x · Cited by 205
Altıntaş, Ö., Park, S., & Lee, S. (2016) · BMB Reports · doi:10.5483/bmbrep.2016.49.2.261 · Cited by 217
Gene activities that mediate increased life span of C. elegans insulin-like signaling mutantsPreprint
Samuelson, A. V., Carr, C. E., & Ruvkun, G. (2007) · Genes & Development · doi:10.1101/gad.1588907 · Cited by 206
Evolutionary conservation of regulated longevity assurance mechanisms
McElwee, J. J., Schuster, E. F., Blanc, E., Piper, M. D. W., Thomas, J. H., Patel, D. S., Selman, C., Withers, D. J., Thornton, J. M., Partridge, L., et al. (2007) · Genome biology · doi:10.1186/gb-2007-8-7-r132 · Cited by 201
Overexpression of Mn Superoxide Dismutase Does Not Increase Life Span in Mice
Jang, Y. C., Pérez, V., Song, W. J., Lustgarten, M. S., Salmon, A. B., Mele, J., Qi, W., Liu, Y., Liang, H., Chaudhuri, A. R., et al. (2009) · The Journals of Gerontology Series A · doi:10.1093/gerona/glp100 · Cited by 205
Metabolism and Colorectal Cancer
Sedlak, J. C., Yilmaz, Ö. H., & Roper, J. (2022) · Annual Review of Pathology Mechanisms of Disease · doi:10.1146/annurev-pathmechdis-031521-041113 · Cited by 208
Sharples, A. P., Hughes, D. C., Deane, C. S., Saini, A. S., Selman, C., & Stewart, C. E. (2015) · Aging Cell · doi:10.1111/acel.12342 · Cited by 204
Kim, K. S., Seu, Y. B., Baek, S.-H., Kim, M. J., Kim, K. J., Kim, J. H., & Kim, J.-R. (2007) · Molecular Biology of the Cell · doi:10.1091/mbc.e07-03-0280 · Cited by 199
Effects of oxidative stress on adiponectin secretion and lactate production in 3T3-L1 adipocytes
Soares, A. F., Guichardant, M., Cozzone, D., Bernoud‐Hubac, N., Bouzaïdi-Tiali, N., Lagarde, M., & Géloën, A. (2005) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2004.12.010 · Cited by 198
Self-citationInhibition of the Mechanistic Target of Rapamycin (mTOR)–Rapamycin and BeyondPreprint
Lamming, D. W. (2016) · Cold Spring Harbor Perspectives in Medicine · doi:10.1101/cshperspect.a025924 · Cited by 205
Regulation of growth and metabolism by imprinted genes
Smith, F. M., Garfield, A. S., & Ward, A. (2006) · Cytogenetic and Genome Research · doi:10.1159/000090843 · Cited by 196
IGF1 Shapes Macrophage Activation in Response to Immunometabolic Challenge
Spadaro, O., Camell, C. D., Bosurgi, L., Nguyen, K., Youm, Y., Rothlin, C. V., & Dixit, V. D. (2017) · Cell Reports · doi:10.1016/j.celrep.2017.03.046 · Cited by 201
Reduction in glutathione peroxidase 4 increases life span through increased sensitivity to apoptosis
Ran, Q., Liang, H., Ikeno, Y., Qi, W., Prolla, T. A., Roberts, L. J., Wolf, N., VanRemmen, H., & Richardson, A. (2007) · The Journals of Gerontology Series A: Biological Sciences and Medical Sciences · doi:10.1093/gerona/62.9.932 · Cited by 195
Broughton, S. J., Alic, N., Slack, C., Bass, T. M., Ikeya, T., Vinti, G., Tommasi, A. M., Driege, Y., Hafen, E., & Partridge, L. (2008) · PLoS ONE · doi:10.1371/journal.pone.0003721 · Cited by 194
Development of Calorie Restriction Mimetics as a Prolongevity Strategy
Ingram, D. K., Anson, R. M., de Cabo, R., Mamczarz, J., Zhu, M., Mattison, J. A., Lane, M. A., & Roth, G. S. (2004) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1297.074 · Cited by 194
Biology of insulin‐like growth factors in development
Dupont, J., & Holzenberger, M. (2003) · Birth Defects Research Part C Embryo Today Reviews · doi:10.1002/bdrc.10022 · Cited by 194
Self-citationOlsen, C. P., & Gilst, M. R. V. (2008) · Cell Metabolism · doi:10.1016/j.cmet.2008.08.007 · Cited by 193
Antidepressant action: to the nucleus and beyond
Malberg, J. E., & Blendy, J. A. (2005) · Trends in Pharmacological Sciences · doi:10.1016/j.tips.2005.10.005 · Cited by 193
Aging, Atherosclerosis, and IGF-1
Higashi, Y., Sukhanov, S., Anwar, A., Shai, S., & Delafontaine, P. (2012) · The Journals of Gerontology Series A · doi:10.1093/gerona/gls102 · Cited by 195
Genetics of Aging in Caenorhabditis elegans
Antebi, A. (2007) · PLoS Genetics · doi:10.1371/journal.pgen.0030129 · Cited by 190
Fitness cost of extended lifespan in Caenorhabditis elegans
Jenkins, N. L., McColl, G., & Lithgow, G. J. (2004) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.2004.2897 · Cited by 188
Caenorhabditis elegans: an emerging genetic model for the study of innate immunity
Kurz, C. L., & Ewbank, J. J. (2003) · Nature Reviews Genetics · doi:10.1038/nrg1067 · Cited by 192
Genetics and epigenetics of aging and longevity
Moskalev, A., Aliper, A. M., Smit‐McBride, Z., Buzdin, A. A., & Zhavoronkov, A. A. (2014) · Cell Cycle · doi:10.4161/cc.28433 · Cited by 189
Cai, W., He, C., Zhu, L., Xue, C., Zheng, F., Striker, G. E., & Vlassara, H. (2008) · American Journal Of Pathology · doi:10.2353/ajpath.2008.080152 · Cited by 188
Deletion of the Huntingtin Polyglutamine Stretch Enhances Neuronal Autophagy and Longevity in Mice
Zheng, S., Clabough, E. B. D., Sarkar, S., Futter, M., Rubinsztein, D. C., & Zeitlin, S. O. (2010) · PLoS Genetics · doi:10.1371/journal.pgen.1000838 · Cited by 192
Rizzo, L. B., Costa, L. G., Mansur, R. B., Swardfager, W., Belangero, S. I., Grassi-Oliveira, R., McIntyre, R. S., Bauer, M. E., & Brietzke, E. (2014) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2014.02.004 · Cited by 183
Characterization of the direct targets of FOXO transcription factors throughout evolution
Webb, A. E., Kundaje, A., & Brunet, A. (2016) · Aging Cell · doi:10.1111/acel.12479 · Cited by 182
Endocrine Parameters and Phenotypes of the Growth Hormone Receptor Gene Disrupted (GHR−/−) Mouse
List, E. O., Sackmann‐Sala, L., Berryman, D. E., Funk, K. R., Kelder, B., Sustarsic, E. G., Okada, S., Ding, J., Cruz‐Topete, D., & Kopchick, J. J. (2010) · Endocrine Reviews · doi:10.1210/er.2010-0009 · Cited by 185
Simpson, D. J., & Chandra, T. (2021) · Aging Cell · doi:10.1111/acel.13452 · Cited by 195
Fridell, Y.-W. C., Sánchez-Blanco, A., Silvia, B. A., & Helfand, S. L. (2005) · Cell Metabolism · doi:10.1016/j.cmet.2005.01.005 · Cited by 185
The mouse as a model organism in aging research: Usefulness, pitfalls and possibilities
Vanhooren, V., & Libert, C. (2012) · Ageing Research Reviews · doi:10.1016/j.arr.2012.03.010 · Cited by 190
Can Growth Hormone (GH) Accelerate Aging? Evidence from GH-Transgenic Mice
Bartke, A. (2003) · Neuroendocrinology · doi:10.1159/000073704 · Cited by 180
FOXO transcription factors in ageing and cancer
Greer, E. L., & Brunet, A. (2007) · Acta Physiologica · doi:10.1111/j.1748-1716.2007.01780.x · Cited by 182
González, A., Rota, M., Nurzyńska, D., Misao, Y., Tillmanns, J., Ojaimi, C., Padín-Iruegas, E., Müller, P., Esposito, G., Bearzi, C., et al. (2008) · Circulation Research · doi:10.1161/circresaha.107.165464 · Cited by 182
RetractedNeuronal SIRT1 regulates endocrine and behavioral responses to calorie restrictionPreprint
Cohen, D. E., Supinski, A., Bonkowski, M. S., Dönmez, G., & Guarente, L. (2009) · Genes & Development · doi:10.1101/gad.1839209 · Cited by 182
Insulin/IGF-1 paradox of aging: Regulation via AKT/IKK/NF-κB signaling
Salminen, A., & Kaarniranta, K. (2010) · Cellular Signalling · doi:10.1016/j.cellsig.2009.10.006 · Cited by 177
The Consequences of Altered Somatotropic System on Reproduction1
Chandrashekar, V., Zaczek, D., & Bartke, A. (2004) · Biology of Reproduction · doi:10.1095/biolreprod.103.027060 · Cited by 175
Reduced Oxidant Stress and Extended Lifespan in Mice Exposed to a Low Glycotoxin Diet
Cai, W., He, C., Zhu, L., Chen, X., Wallenstein, S. R., Striker, G. E., & Vlassara, H. (2007) · American Journal Of Pathology · doi:10.2353/ajpath.2007.061281 · Cited by 177
Systemic stress signalling: understanding the cell non-autonomous control of proteostasis
Taylor, R. C., Berendzen, K. M., & Dillin, A. G. (2014) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm3752 · Cited by 178
A disease- and phosphorylation-related nonmechanical function for keratin 8
Ku, N., & Omary, M. B. (2006) · The Journal of Cell Biology · doi:10.1083/jcb.200602146 · Cited by 171
Aging, tumor suppression and cancer: high wire-act!
Campisi, J. (2004) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2004.09.024 · Cited by 176
Meissner, B., Boll, M., Daniel, H., & Baumeister, R. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m403415200 · Cited by 171
Vellai, T. (2008) · Cell Death and Differentiation · doi:10.1038/cdd.2008.126 · Cited by 173
Santos, A. L., Sinha, S., & Lindner, A. B. (2018) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2018/1941285 · Cited by 168
Caloric restriction: From soup to nuts
Spindler, S. R. (2009) · Ageing Research Reviews · doi:10.1016/j.arr.2009.10.003 · Cited by 169
The mitochondrial free radical theory of ageing - Where do we stand?
Gruber, J. (2008) · Frontiers in bioscience · doi:10.2741/3174 · Cited by 171
Late-life targeting of the IGF-1 receptor improves healthspan and lifespan in female mice
Mao, K., Quipildor, G. F., Tabrizian, T., Novaj, A., Guan, F., Walters, R. O., Delahaye, F., Hubbard, G. B., Ikeno, Y., Ejima, K., et al. (2018) · Nature Communications · doi:10.1038/s41467-018-04805-5 · Cited by 167
GSK-3α is a central regulator of age-related pathologies in mice
Zhou, J., Freeman, T. A., Ahmad, F., Shang, X., Mangano, E. N., Gao, E., Farber, J. L., Wang, Y., Ma, X.-L., Woodgett, J. R., et al. (2013) · Journal of Clinical Investigation · doi:10.1172/jci64398 · Cited by 170
Partridge, L. (2009) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2009.0222 · Cited by 174
Local expression of GH and IGF-1 in the hippocampus of GH-deficient long-lived mice
Sun, L. Y., Al-Regaiey, K., Masternak, M. M., Wang, J., & Bartke, A. (2004) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2004.07.010 · Cited by 167
Vitale, G., Pellegrino, G., Vollery, M., & Hofland, L. J. (2019) · Frontiers in Endocrinology · doi:10.3389/fendo.2019.00027 · Cited by 166
Regulation of reproduction and longevity by nutrient-sensing pathways
Templeman, N. M., & Murphy, C. T. (2017) · The Journal of Cell Biology · doi:10.1083/jcb.201707168 · Cited by 175
Neuroendocrine Regulation of Growth Hormone Secretion
Steyn, F. J., Tolle, V., Chen, C., & Epelbaum, J. (2016) · Comprehensive physiology · doi:10.1002/cphy.c150002 · Cited by 173
The evolution of senescence from a comparative perspective
Ricklefs, R. E. (2008) · Functional Ecology · doi:10.1111/j.1365-2435.2008.01420.x · Cited by 174
Chaperone networks: Tipping the balance in protein folding diseases
Voisine, C., Pedersen, J. S., & Morimoto, R. I. (2010) · Neurobiology of Disease · doi:10.1016/j.nbd.2010.05.007 · Cited by 166
Tryptophan metabolism: entering the field of aging and age-related pathologies
van der Goot, A. T., & Nollen, E. A. A. (2013) · Trends in Molecular Medicine · doi:10.1016/j.molmed.2013.02.007 · Cited by 166
A potential link between phosphate and aging—Lessons from Klotho-deficient mice
Kuro‐o, M. (2010) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2010.02.008 · Cited by 166
Autophagy, polyphenols and healthy ageing
Pallauf, K., & Rimbach, G. H. (2012) · Ageing Research Reviews · doi:10.1016/j.arr.2012.03.008 · Cited by 167
Is Older Colder or Colder Older? The Association of Age With Body Temperature in 18,630 Individuals
Waalen, J., & Buxbaum, J. N. (2011) · The Journals of Gerontology Series A · doi:10.1093/gerona/glr001 · Cited by 163
Girnita, L., Shenoy, S. K., Sehat, B., Vasilcanu, R., Girnita, A., Lefkowitz, R. J., & Larsson, O. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m501129200 · Cited by 162
Insulin‐like growth factor‐1 regulates the SIRT 1‐p53 pathway in cellular senescence
Tran, D., Bergholz, J., Zhang, H., He, H., Wang, Y., Zhang, Y., Li, Q., Kirkland, J. L., & Xiao, Z. (2014) · Aging Cell · doi:10.1111/acel.12219 · Cited by 161
“It has been shown that reduced IGF-1 signaling protects against oxidative damage in simple organisms and in mice (Holzenberger et al., 2003), likely through reduced AKT activity, which is known to promote ROS production (Di Segni et al.”
BackgroundSignaling networks determining life span
Riera, C. E., Merkwirth, C., De Magalhaes Filho, C. D., & Dillin, A. (2016) · Annual Review of Biochemistry · doi:10.1146/annurev-biochem-060815-014451 · Cited by 161
The retardation of aging by caloric restriction: its significance in the transgenic era
Barger, J. L., Walford, R. L., & Weindruch, R. (2003) · Experimental Gerontology · doi:10.1016/j.exger.2003.10.017 · Cited by 160
van Heemst, D. (2010) · Europe PMC (PubMed Central) · Cited by 160
The role of insulin and IGF-1 signaling in longevity
Katić, M., & Kahn, C. R. (2005) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-004-4297-y · Cited by 163
Endocrine regulation of aging and reproduction in Drosophila
Toivonen, J. M., & Partridge, L. (2008) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2008.07.005 · Cited by 164
Fasting and Caloric Restriction in Cancer Prevention and Treatment
Brandhorst, S., & Longo, V. D. (2016) · Recent results in cancer research/Recent Results in Cancer Research · doi:10.1007/978-3-319-42118-6_12 · Cited by 166
Ruminations on dietary restriction and aging
Kennedy, B. K., Steffen, K. K., & Kaeberlein, M. R. (2007) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-007-6470-y · Cited by 161
Cohen, A. A. (2017) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2017.05.028 · Cited by 169
Resveratrol is a class IA phosphoinositide 3-kinase inhibitor
Fröjdö, S., Cozzone, D., Vidal, H., & Pirola, L. (2007) · Biochemical Journal · doi:10.1042/bj20070236 · Cited by 158
Butcher, R. A., Ragains, J. R., Kim, E., & Clardy, J. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0806676105 · Cited by 156
Lamitina, S. T., & Strange, K. B. (2004) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00451.2004 · Cited by 155
Piper, M. D. W., Selman, C., McElwee, J. J., & Partridge, L. (2008) · Journal of Internal Medicine · doi:10.1111/j.1365-2796.2007.01906.x · Cited by 159
Isolated Growth Hormone Deficiency (GHD) in Childhood and Adolescence: Recent Advances
Alatzoglou, K. S., Webb, E. A., Tissier, P. L., & Dattani, M. (2014) · Endocrine Reviews · doi:10.1210/er.2013-1067 · Cited by 159
Therapeutic Targeting of the IGF Axis
Osher, E. L., & Macaulay, V. M. (2019) · Cells · doi:10.3390/cells8080895 · Cited by 154
daf-16 Protects the Nematode Caenorhabditis elegans During Food Deprivation
Henderson, S. T., Bonafè, M., & Johnson, T. E. (2006) · The Journals of Gerontology Series A · doi:10.1093/gerona/61.5.444 · Cited by 155
The emerging role of FOXO transcription factors in pancreatic β cells
Glauser, D. A., & Schlegel, W. (2007) · Journal of Endocrinology · doi:10.1677/joe-06-0191 · Cited by 153
Accelerated failure time models provide a useful statistical framework for aging research
Swindell, W. R. (2008) · Experimental Gerontology · doi:10.1016/j.exger.2008.10.005 · Cited by 157
Early diabetic neuropathy: Triggers and mechanisms
Dobretsov, M. G. (2007) · World Journal of Gastroenterology · doi:10.3748/wjg.v13.i2.175 · Cited by 153
Metabolic Syndrome as a Risk Factor for Alzheimer’s Disease: A Focus on Insulin Resistance
Ezkurdia, A., Ramírez, M. J., & Solas, M. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24054354 · Cited by 160
Richard, D. S., Rybczynski, R., Wilson, T. G., Wang, Y., Wayne, M. L., Zhou, Y., Partridge, L., & Harshman, L. G. (2005) · Journal of Insect Physiology · doi:10.1016/j.jinsphys.2004.12.013 · Cited by 153
Adaptive mechanisms to oxidative stress during aging
Yu, B. P., & Chung, H. Y. (2006) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2006.01.023 · Cited by 156
Genetics of Aging in the Fruit Fly,Drosophila melanogaster
Helfand, S. L., & Rogina, B. (2003) · Annual Review of Genetics · doi:10.1146/annurev.genet.37.040103.095211 · Cited by 152
Oxidative damage and age-related functional declines
Martin, I., & Grotewiel, M. S. (2006) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2006.01.008 · Cited by 152
In Vivo Analysis of Growth Hormone Receptor Signaling Domains and Their Associated Transcripts
Rowland, J., Lichanska, A. M., Kerr, L. M., White, M. E., d’Aniello, E., Maher, S., Brown, R. J. P., Teasdale, R. D., Noakes, P. G., & Waters, M. J. (2004) · Molecular and Cellular Biology · doi:10.1128/mcb.25.1.66-77.2005 · Cited by 152
Hormone-Treated Snell Dwarf Mice Regain Fertility But Remain Long Lived and Disease Resistant
Vergara, M., Smith‐Wheelock, M., Harper, J. M., Sigler, R. E., & Miller, R. A. (2004) · The Journals of Gerontology Series A · doi:10.1093/gerona/59.12.1244 · Cited by 151
Milman, S., Huffman, D. M., & Barzilai, N. (2016) · Cell Metabolism · doi:10.1016/j.cmet.2016.05.014 · Cited by 150
Does Reduced IGF-1R Signaling in Igf1r+/− Mice Alter Aging?
Bokov, A. F., Garg, N., Ikeno, Y., Thakur, S., Musi, N., DeFronzo, R. A., Zhang, N., Erickson, R. C., Gelfond, J., Hubbard, G. B., et al. (2011) · PLoS ONE · doi:10.1371/journal.pone.0026891 · Cited by 152
Neuronal protection by sirtuins in Alzheimer's disease
Anekonda, T. S., & Reddy, P. H. (2005) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2005.03492.x · Cited by 152
Branched-chain amino acid catabolism is a conserved regulator of physiological ageing
Mansfeld, J., Urban, N., Priebe, S., Groth, M., Frahm, C., Hartmann, N., Gebauer, J., Ravichandran, M., Dommaschk, A., Schmeisser, S., et al. (2015) · Nature Communications · doi:10.1038/ncomms10043 · Cited by 151
Vascular cell senescence and vascular aging
Minamino, T., Miyauchi, H., Yoshida, T., Tateno, K., Kunieda, T., & Komuro, I. (2003) · Journal of Molecular and Cellular Cardiology · doi:10.1016/j.yjmcc.2003.11.010 · Cited by 153
Sex Differences in Longevity and in Responses to Anti-Aging Interventions: A Mini-Review
Austad, S. N., & Bartke, A. (2015) · Gerontology · doi:10.1159/000381472 · Cited by 153
Chen, W., Müller, D., Richling, E., & Wink, M. (2013) · Journal of Agricultural and Food Chemistry · doi:10.1021/jf3054643 · Cited by 150
Testa, G., Biasi, F., Poli, G., & Chiarpotto, E. (2014) · Current Pharmaceutical Design · doi:10.2174/13816128113196660699 · Cited by 153
Reduced Circulating Insulin Enhances Insulin Sensitivity in Old Mice and Extends Lifespan
Templeman, N. M., Flibotte, S., Chik, J. H. L., Sinha, S., Lim, G. E., Foster, L. J., Nislow, C., & Johnson, J. D. (2017) · Cell Reports · doi:10.1016/j.celrep.2017.06.048 · Cited by 151
Metadata
- Authors
- Holzenberger, M., Dupont, J., Ducos, B., Leneuve, P., Géloën, A., Even, P. C., Cervera, P., & Le Bouc, Y.
- Affiliations
- Inserm (FR)
- Physiologie de la Reproduction et des Comportements (FR)
- Institut National de Recherche pour l'Agriculture, l'Alimentation et l'Environnement (FR)
- Hôpital Saint-Antoine (FR)
- Corresponding author
- Holzenberger, Martin
- ORCID
- Venue
- Nature
- Published
- 2002-12-04
- Volume
- 421
- Issue
- 6919
- Pages
- 182-187
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- OpenAlex
- W1985425785
- Cited by
- 2,109
- References
- 30
- Citations by year
- 2026: 32 · 2025: 41 · 2024: 56 · 2023: 61 · 2022: 84 · 2021: 87 · 2020: 81 · 2019: 73 · 2018: 59 · 2017: 82 · 2016: 84 · 2015: 91 · 2014: 86 · 2013: 87 · 2012: 99
- FWCI
- 29.68
- Type
- journal article
- Language
- en
- Open access
- Licence
- other-oa
- www.springer.com/tdm (tdm)
- Locations
- Nature (publishedVersion)
- PubMed (publishedVersion)
- HAL (submittedVersion, other-oa)
- HAL (submittedVersion)
- RePEc: Research Papers in Economics (submittedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Aging › Genetics, Aging, and Longevity in Model Organisms
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Growth Hormone and Insulin-like Growth Factors
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Metabolism, Diabetes, and Cancer
- Keywords
- IGF-1 receptor, lifespan, longevity, oxidative stress resistance, insulin receptor, daf-2, international normalized ratio, heterozygous knockout mice, aging, sex differences in longevity
- MeSH terms
- Aging, Animals, Blood Glucose, Cells, Cultured, Female, Fertility, Fibroblasts, Glucose Tolerance Test, Ligands, Longevity, Male, Phenotype, Sexual Maturation, Signal Transduction, Gene Deletion, Receptor, IGF Type 1, Mice, Knockout, Oxidative Stress, Mice
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review