The DOI matches its Crossref record; 70 of the 70 references it cites were found in a registry or an index.
Cellular senescence and apoptosis: how cellular responses might influence aging phenotypes
Open accessAbstract
Aging in complex multi-cellular organisms such as mammals entails distinctive changes in cells and molecules that ultimately compromise the fitness of adult organisms. These cellular and molecular changes lead to the phenotypes we recognize as aging. This review discusses some of the cellular and molecular changes that occur with age, specifically changes that occur as a result of cellular responses that evolved to ameliorate the inevitable damage that is caused by endogenous and environmental insults. Because the force of natural selection declines with age, it is likely that these processes were never optimized during their evolution to benefit old organisms. That is, some age-related changes may be the result of gene activities that were selected for their beneficial effects in young organisms, but the same gene activities may have unselected, deleterious effects in old organisms, a phenomenon termed antagonistic pleiotropy. Two cellular processes, apoptosis and cellular senescence, may be examples of antagonistic pleiotropy. Both processes are essential for the viability and fitness of young organisms, but may contribute to aging phenotypes, including certain age-related diseases.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
The check wasn’t confident either way, so it gives no verdict — never disputed.
In the citing paper
“magnetic resonance imaging (MRI) studies have shown that normal aging is associated with gray matter volume reductions and functional alterations in several regions critical for higher cognitive function: prefrontal, medial temporal and parietal cortices.21–24”
From Maintenance, reserve and compensation: the cognitive neuroscience of healthy ageing (2018) · cites this paper as [24]
Experimental — accuracy not yet measuredThe check wasn’t confident either way, so it gives no verdict — never disputed.
In the citing paper
“It is worth noting that young adults may also upregulate activity in response to increased task demands, but that the demand threshold for upregulation may be higher in young, compared to older adults24,36.”
From Maintenance, reserve and compensation: the cognitive neuroscience of healthy ageing (2018) · cites this paper as [24]
Experimental — accuracy not yet measured
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Hanahan, D., & Weinberg, R. A. (2000) · Cell · doi:10.1016/s0092-8674(00)81683-9 · Cited by 29,219
Apoptosis in the Pathogenesis and Treatment of Disease
Thompson, C. B. (1995) · Science · doi:10.1126/science.7878464 · Cited by 6,524
Extension of Life-Span by Introduction of Telomerase into Normal Human Cells
Bodnar, A. G., Ouellette, M., Frolkis, M., Holt, S. E., Chiu, C.-P., Morin, G. B., Harley, C. B., Shay, J. W., Lichtsteiner, S., & Wright, W. E. (1998) · Science · doi:10.1126/science.279.5349.349 · Cited by 4,975
Mice deficient for p53 are developmentally normal but susceptible to spontaneous tumours
Donehower, L. A., Harvey, M., Slagle, B. L., McArthur, M. J., Montgomery, C. A., Butel, J. S., & Bradley, A. (1992) · Nature · doi:10.1038/356215a0 · Cited by 4,649
Mechanisms And Functions Of Cell Death
Ellis, R. E., Yuan, J., & Horvitz, H. R. (1991) · Annual Review of Cell Biology · doi:10.1146/annurev.cb.07.110191.003311 · Cited by 2,088
Tumor spectrum analysis in p53-mutant mice
Jacks, T., Remington, L., Williams, B. O., Schmitt, E. M., Halachmi, S., Bronson, R. T., & Weinberg, R. A. (1994) · Current Biology · doi:10.1016/s0960-9822(00)00002-6 · Cited by 2,051
Kirkwood, T. B. L., & Austad, S. N. (2000) · Nature · doi:10.1038/35041682 · Cited by 1,774
Krtolica, A., Parrinello, S., Lockett, S., Desprez, P.-Y., & Campisi, J. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.211053698 · Cited by 1,730
Self-citationVaux, D. L., & Korsmeyer, S. J. (1999) · Cell · doi:10.1016/s0092-8674(00)80564-4 · Cited by 1,564
p53 mutant mice that display early ageing-associated phenotypes
Tyner, S. D., Venkatachalam, S., Choi, J., Jones, S., Ghebranious, N., Igelmann, H., Lu, X., Soron, G., Cooper, B., Brayton, C., et al. (2002) · Nature · doi:10.1038/415045a · Cited by 1,459 · cited 1×
“Strikingly, it also accelerated aging in some tissues, and modestly decreased the life span (Tyner et al., 2002).”
Background
Research works printed but not linked: 1
- Dimri, G. P., Lee, X., Basile, G., Acosta, M., Scott, G., Roskelley, C., Medrano, E. E., Linskens, M., Rubelj, I., Pereira-Smith, O. M., Peacocke, M., Campisi, J. 1995. A novel biomarker identifies senescent human cells in culture and in aging skin in vivo. Proc. Natl. Acad. Sci. USA 92, 9363-9367.
Cited by
Sorted by citations
Senescent cells, tumor suppression, and organismal aging: good citizens, bad neighbors
Campisi, J. (2005) · Cell · doi:10.1016/j.cell.2005.02.003 · Cited by 2,379
Self-citationCellular senescence in ageing: from mechanisms to therapeutic opportunities
Di Micco, R., Krizhanovsky, V., Baker, D., & d’Adda di Fagagna, F. (2021) · Nature Reviews Molecular Cell Biology · doi:10.1038/s41580-020-00314-w · Cited by 2,277
Calorie restriction promotes mammalian cell survival by inducing the SIRT1 deacetylase
Cohen, H. Y., Miller, C., Bitterman, K. J., Wall, N. R., Hekking, B., Kessler, B., Howitz, K. T., Gorospe, M., de Cabo, R., & Sinclair, D. A. (2004) · Science · doi:10.1126/science.1099196 · Cited by 1,924
Walston, J., Hadley, E. C., Ferrucci, L., Guralnik, J. M., Newman, A. B., Studenski, S. A., Ershler, W. B., Harris, T., & Fried, L. P. (2006) · Journal of the American Geriatrics Society · doi:10.1111/j.1532-5415.2006.00745.x · Cited by 1,605
Maintenance, reserve and compensation: the cognitive neuroscience of healthy ageing
Cabeza, R., Albert, M., Belleville, S., Craik, F. I. M., Duarte, A., Grady, C. L., Lindenberger, U., Nyberg, L., Park, D. C., Reuter-Lorenz, P. A., et al. (2018) · Nature Reviews Neuroscience · doi:10.1038/s41583-018-0068-2 · Cited by 1,298
Fat tissue, aging, and cellular senescence
Tchkonia, T., Morbeck, D. E., Von Zglinicki, T., Van Deursen, J., Lustgarten, J., Scrable, H., Khosla, S., Jensen, M. D., & Kirkland, J. L. (2010) · Aging Cell · doi:10.1111/j.1474-9726.2010.00608.x · Cited by 1,094
Nutrient-Sensitive Mitochondrial NAD+ Levels Dictate Cell Survival
Yang, H., Yang, T., Baur, J. A., Perez, E., Matsui, T., Carmona, J. J., Lamming, D. W., Souza-Pinto, N. C., Bohr, V. A., Rosenzweig, A., et al. (2007) · Cell · doi:10.1016/j.cell.2007.07.035 · Cited by 950
TGF-β1 Signaling and Tissue Fibrosis
Kim, K. K., Sheppard, D., & Chapman, H. A. (2018) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a022293 · Cited by 800
DNA damage response and cellular senescence in tissues of aging mice
Wang, C., Jurk, D., Maddick, M., Nelson, G., Martin‐Ruiz, C., & Von Zglinicki, T. (2009) · Aging Cell · doi:10.1111/j.1474-9726.2009.00481.x · Cited by 696
Cardiac Stem Cell and Myocyte Aging, Heart Failure, and Insulin-Like Growth Factor-1 Overexpression
Torella, D., Rota, M., Nurzyńska, D., Musso, E., Monsen, A., Shiraishi, I., Zias, E. A., Walsh, K. X., Rosenzweig, A., Sussman, M. A., et al. (2004) · Circulation Research · doi:10.1161/01.res.0000117306.10142.50 · Cited by 538
When drug therapy gets old: pharmacokinetics and pharmacodynamics in the elderly
Turnheim, K. (2003) · Experimental Gerontology · doi:10.1016/s0531-5565(03)00133-5 · Cited by 531
Rajah, M. N., & D'Esposito, M. (2005) · Brain · doi:10.1093/brain/awh608 · Cited by 513
p53-dependent release of Alarmin HMGB1 is a central mediator of senescent phenotypes
Davalos, A. R., Kawahara, M., Malhotra, G. K., Schaum, N., Huang, J., Ved, U., Beausejour, C. M., Coppe, J.-P., Rodier, F., & Campisi, J. (2013) · Journal of Cell Biology · doi:10.1083/jcb.201206006 · Cited by 439
Self-citationCD28 extinction in human T cells: altered functions and the program of T‐cell senescence
Vallejo, A. N. (2005) · Immunological Reviews · doi:10.1111/j.0105-2896.2005.00256.x · Cited by 446
Human cell senescence as a DNA damage response
Zglinicki, T. V., Saretzki, G., Ladhoff, J., Fagagna, F. D. D., & Jackson, S. P. (2005) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2004.09.034 · Cited by 419
Genotoxic Stress Abrogates Renewal of Melanocyte Stem Cells by Triggering Their Differentiation
Inomata, K., Aoto, T., Binh, N. T., Okamoto, N., Tanimura, S., Wakayama, T., Iseki, S., Hara, E., Masunaga, T., Shimizu, H., et al. (2009) · Cell · doi:10.1016/j.cell.2009.03.037 · Cited by 368
Mechanisms of cellular senescence in human and mouse cells.
Itahana, K., Campisi, J., & Dimri, G. P. (2004) · Biogerontology · doi:10.1023/b:bgen.0000017682.96395.10 · Cited by 338
Self-citationThe Biology of Aging and Frailty
Fedarko, N. S. (2010) · Clinics in Geriatric Medicine · doi:10.1016/j.cger.2010.08.006 · Cited by 359
From Bedside to Bench: Research Agenda for Frailty
Fried, L. P., Hadley, E. C., Walston, J. D., Newman, A. B., Guralnik, J. M., Studenski, S. A., Harris, T. B., Ershler, W. B., & Ferrucci, L. (2005) · Science of Aging Knowledge Environment · doi:10.1126/sageke.2005.31.pe24 · Cited by 307
Cellular senescence and the aging brain
Chinta, S. J., Woods, G., Rane, A., Demaria, M., Campisi, J., & Andersen, J. K. (2015) · Experimental Gerontology · doi:10.1016/j.exger.2014.09.018 · Cited by 282
Self-citationReplicative senescence: a critical review
Cristofalo, V. J., Lorenzini, A., Allen, R. G., Torres, C. A., & Tresini, M. (2004) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2004.07.010 · Cited by 285
Oxidative Stress Damage as a Detrimental Factor in Preterm Birth Pathology
Menon, R. (2014) · Frontiers in Immunology · doi:10.3389/fimmu.2014.00567 · Cited by 249
Life history trade-offs in cancer evolution
Aktipis, A., Boddy, A. M., Gatenby, R. A., Brown, J. S., & Maley, C. C. (2013) · Nature reviews. Cancer · doi:10.1038/nrc3606 · Cited by 237
Vallejo, A. N., Weyand, C. M., & Goronzy, J. J. (2004) · Trends in Molecular Medicine · doi:10.1016/j.molmed.2004.01.002 · Cited by 223
Telomere length and dynamics predict mortality in a wild longitudinal study
Barrett, E. L. B., Burke, T. A., Hammers, M., Komdeur, J., & Richardson, D. S. (2012) · Molecular Ecology · doi:10.1111/mec.12110 · Cited by 221
Cellular responses to reactive oxygen species-induced DNA damage and aging
Bertram, C., & Hass, R. (2008) · Biological Chemistry · doi:10.1515/bc.2008.031 · Cited by 217
SIRT1 regulation of apoptosis of human chondrocytes
Takayama, K., Ishida, K., Matsushita, T., Fujita, N., Hayashi, S., Sasaki, K., Tei, K., Kubo, S., Matsumoto, T., Fujioka, H., et al. (2009) · Arthritis & Rheumatism · doi:10.1002/art.24864 · Cited by 210
The impact of cerebrovascular aging on vascular cognitive impairment and dementia
Yang, T., Sun, Y., Lu, Z., Leak, R. K., & Zhang, F. (2016) · Ageing Research Reviews · doi:10.1016/j.arr.2016.09.007 · Cited by 214
The Immune System in the Elderly: Activation-Induced and Damage-Induced Apoptosis
Ginaldi, L., Martinis, M. D., Monti, D., & Franceschi, C. (2004) · Immunologic Research · doi:10.1385/ir:30:1:081 · Cited by 202
Menon, R., Boldogh, I. R., Hawkins, H. K., Woodson, M., Polettini, J., Syed, T. A., Fortunato, S. J., Saade, G. R., Papaconstantinou, J., & Taylor, R. N. (2014) · American Journal Of Pathology · doi:10.1016/j.ajpath.2014.02.011 · Cited by 202
Telomeres: Linking stress and survival, ecology and evolution
Haussmann, M. F., & Marchetto, N. M. (2010) · Current Zoology · doi:10.1093/czoolo/56.6.714 · Cited by 204
Knudson, C. B., & Knudson, W. (2004) · Clinical Orthopaedics and Related Research · doi:10.1097/01.blo.0000143804.26638.82 · Cited by 180
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
Self-citationTelomere Attrition Due to Infection
Ilmonen, P., Kotrschal, A., & Penn, D. J. (2008) · PLoS ONE · doi:10.1371/journal.pone.0002143 · Cited by 174
Tamori, Y., & Deng, W. (2013) · Developmental Cell · doi:10.1016/j.devcel.2013.04.013 · Cited by 154
Quirici, V., Guerrero, C. J., Krause, J. S., Wingfield, J. C., & Vásquez, R. A. (2016) · Frontiers in Zoology · doi:10.1186/s12983-016-0133-5 · Cited by 145
Chien, K. R., & Karsenty, G. (2005) · Cell · doi:10.1016/j.cell.2005.02.006 · Cited by 143
Histone Modifications in Senescence-Associated Resistance to Apoptosis by Oxidative Stress
Sanders, Y. Y., Liu, H., Zhang, X., Hecker, L., Bernard, K., Desai, L., Liu, G., & Thannickal, V. J. (2013) · Redox Biology · doi:10.1016/j.redox.2012.11.004 · Cited by 138
Martin-Ruiz, C. M., Saretzki, G. C., Petrie, J., Ladhoff, J., Jeyapalan, J. C., Wei, W., Sedivy, J. M., & von Zglinicki, T. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m311980200 · Cited by 134
Cancer and aging: the importance of telomeres in genome maintenance
Rodier, F., Kim, S.-H., Nijjar, T., Yaswen, P., & Campisi, J. (2005) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2004.10.012 · Cited by 132
Self-citationOvarian cancer: pathology, biology, and disease models
Daniel, G. R. (2009) · Frontiers in bioscience · doi:10.2741/3364 · Cited by 133
LEARNING ABILITY AND LONGEVITY: A SYMMETRICAL EVOLUTIONARY TRADE-OFF IN DROSOPHILA
Burger, J. M. S., Kolß, M., Pont, J., & Kawecki, T. J. (2008) · Evolution · doi:10.1111/j.1558-5646.2008.00376.x · Cited by 126
Biological, Clinical, and Psychosocial Correlates at the Interface of Cancer and Aging Research
Dale, W., Mohile, S. G., Eldadah, B. A., Trimble, E. L., Schilsky, R. L., Cohen, H. J., Muss, H. B., Schmader, K. E., FERRELL, B. R., Extermann, M., et al. (2012) · JNCI Journal of the National Cancer Institute · doi:10.1093/jnci/djs145 · Cited by 114
Anisimov, V. N. (2007) · Cancer Control · doi:10.1177/107327480701400104 · Cited by 114
Expression of SUMO-2/3 Induced Senescence through p53- and pRB-mediated Pathways
Li, T., Santockyte, R., Shen, R., Tekle, E., Wang, G., Yang, D. C. H., & Chock, P. B. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.m608236200 · Cited by 107
Puterman, E., & Epel, E. (2012) · Social and Personality Psychology Compass · doi:10.1111/j.1751-9004.2012.00465.x · Cited by 106
de Magalhães, J. P. (2004) · Experimental Cell Research · doi:10.1016/j.yexcr.2004.07.006 · Cited by 108
Molecular mechanisms of cardiomyocyte aging
Sheydina, A., Riordon, D. R., & Boheler, K. R. (2011) · Clinical Science · doi:10.1042/cs20110115 · Cited by 102
Differential patterns of apoptosis in response to aging in Drosophila
Zheng, J., Edelman, S. W., Tharmarajah, G., Walker, D. W., Pletcher, S. D., & Seroude, L. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0503374102 · Cited by 100
Male age, germline mutations and the benefits of polyandry
Radwan, J. (2003) · Ecology Letters · doi:10.1046/j.1461-0248.2003.00484.x · Cited by 99
Proteasome inhibition by chronic oxidative stress in human trabecular meshwork cells
Caballero, M., Liton, P. B., Epstein, D. L., & González, P. (2003) · Biochemical and Biophysical Research Communications · doi:10.1016/s0006-291x(03)01385-8 · Cited by 98
Wu, L. W., Wang, Y.-L., Christensen, J. M., Khalifian, S., Schneeberger, S., Raimondi, G., Cooney, D. S., Lee, W. P. A., & Brandacher, G. (2014) · Transplant Immunology · doi:10.1016/j.trim.2014.03.001 · Cited by 100
Spatio‐temporal variation in lifelong telomere dynamics in a long‐term ecological study
Spurgin, L. G., Bebbington, K., Fairfield, E. A., Hammers, M., Komdeur, J., Burke, T. A., Dugdale, H. L., & Richardson, D. S. (2017) · Journal of Animal Ecology · doi:10.1111/1365-2656.12741 · Cited by 94
Iron Accumulation During Cellular Senescence in Human Fibroblasts In Vitro
Killilea, D. W., Atamna, H., Liao, C., & Ames, B. N. (2003) · Antioxidants & Redox Signaling · doi:10.1089/152308603770310158 · Cited by 92
Comparative aspects of zebrafish (Danio rerio) as a model for aging research
Gerhard, G. S. (2003) · Experimental Gerontology · doi:10.1016/j.exger.2003.10.022 · Cited by 89
Analysis of age-related changes in the functional morphologies of salivary glands in mice
Choi, J., Park, I. S., Kim, S.-K., Lim, J., & Kim, Y. (2013) · Archives of Oral Biology · doi:10.1016/j.archoralbio.2013.07.008 · Cited by 83
Correction of cellular phenotypes of Hutchinson-Gilford Progeria cells by RNA interference
Huang, S., Chen, L., Libina, N., Janes, J. H., Martin, G. M., Campisi, J., & Oshima, J. (2005) · Human Genetics · doi:10.1007/s00439-005-0051-7 · Cited by 82
Self-citationManagement of multicellular senescence and oxidative stress
Haines, D. D., Juhász, B., & Tósaki, Á. (2013) · Journal of Cellular and Molecular Medicine · doi:10.1111/jcmm.12074 · Cited by 81
Pearce, D. J., Anjos‐Afonso, F., Ridler, C. M., Eddaoudi, A., & Bonnet, D. A. (2006) · Stem Cells · doi:10.1634/stemcells.2006-0405 · Cited by 77
Ravelojaona, V., Robert, A. M., & Robert, L. (2008) · Archives of Gerontology and Geriatrics · doi:10.1016/j.archger.2007.12.004 · Cited by 73
Relationships between cancer and aging: a multilevel approach
Anisimov, V. N., Sikora, E., & Pawelec, G. (2009) · Biogerontology · doi:10.1007/s10522-008-9209-8 · Cited by 73
Replicative senescence and the art of counting
von Zglinicki, T. (2003) · Experimental Gerontology · doi:10.1016/j.exger.2003.09.015 · Cited by 69
Chronic antigenic load and apoptosis in immunosenescence
Ginaldi, L., Martinis, M. D., Monti, D., & Franceschi, C. (2004) · Trends in Immunology · doi:10.1016/j.it.2004.11.005 · Cited by 65
Exterkate, L., Slegtenhorst, B. R., Kelm, M., Seyda, M., Schuitenmaker, J. M., Quante, M., Uehara, H., Elkhal, A., & Tullius, S. G. (2015) · Transplantation · doi:10.1097/tp.0000000000001003 · Cited by 64
Adipose tissue, immune aging, and cellular senescence
Frasca, D., & Blomberg, B. B. (2020) · Seminars in Immunopathology · doi:10.1007/s00281-020-00812-1 · Cited by 72
Liu, M., Gu, L., Zhang, Y., Li, Y., Zhang, L., Xin, Y., Wang, Y., & Xu, Z. (2024) · Cancer Letters · doi:10.1016/j.canlet.2024.217025 · Cited by 62
Balancing DNA repair to prevent ageing and cancer
Stead, E. R., & Bjedov, I. (2021) · Experimental Cell Research · doi:10.1016/j.yexcr.2021.112679 · Cited by 62
Identification of evolutionarily conserved genetic regulators of cellular aging
Laschober, G. T., Ruli, D., Hofer, E., Mück, C., Carmona‐Gutiérrez, D., Ring, J., Hütter, E., Ruckenstuhl, C., Mičutková, L., Brunauer, R., et al. (2010) · Aging Cell · doi:10.1111/j.1474-9726.2010.00637.x · Cited by 54
Bullón, P., Battino, M. A., Varela‐López, A., Pérez-López, P., Granados-Principal, S. M., Ramírez-Tortosa, M. C., Ochoa, J. J., Cordero, M. D., González-Alonso, A., Ramírez-Tortosa, C. L., et al. (2013) · PLoS ONE · doi:10.1371/journal.pone.0074234 · Cited by 54
A polymorphism in the tumor suppressor p53 affects aging and longevity in mouse models
Zhao, Y., Wu, L., Yue, X., Zhang, C., Wang, J., Li, J., Sun, X., Zhu, Y., Feng, Z., & Hu, W. (2018) · eLife · doi:10.7554/elife.34701 · Cited by 54
Increased Arf/p53 activity in stem cells, aging and cancer
Carrasco‐García, E., Moreno, M., Moreno‐Cugnon, L., & Matheu, A. (2017) · Aging Cell · doi:10.1111/acel.12574 · Cited by 52
Signaling pathway requirements for induction of senescence by telomere homolog oligonucleotides
Li, G., Eller, M. S., Hanna, K., & Gilchrest, B. A. (2004) · Experimental Cell Research · doi:10.1016/j.yexcr.2004.08.019 · Cited by 49
Mather, K. A., Jorm, A. F., Milburn, P. J., Tan, X., Easteal, S., & Christensen, H. M. (2010) · The Journals of Gerontology Series A · doi:10.1093/gerona/glq050 · Cited by 48
Kajstura, J., Bolli, R., Sonnenblick, E. H., Anversa, P., & Leri, A. (2006) · Journal of Molecular and Cellular Cardiology · doi:10.1016/j.yjmcc.2005.12.013 · Cited by 49
Moh, M. C., Zhang, T., Lee, L. H., & Shen, S. (2008) · Carcinogenesis · doi:10.1093/carcin/bgn226 · Cited by 48
Age dependence of male mating ability and sperm competition success in the bulb mite
Radwan, J., Michalczyk, Ł., & Prokop, Z. M. (2005) · Animal Behaviour · doi:10.1016/j.anbehav.2004.09.006 · Cited by 47
Frasca, D., Romero, M., Diaz, A., Garcia, D., Thaller, S. R., & Blomberg, B. B. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22041839 · Cited by 43
Nikitakis, N. G., Sauk, J. J., & Papanicolaou, S. I. (2004) · Oral Surgery Oral Medicine Oral Pathology Oral Radiology and Endodontology · doi:10.1016/j.tripleo.2003.12.032 · Cited by 42
Aging stem cells, latexin, and longevity
Liang, Y., & Zant, G. E. V. (2008) · Experimental Cell Research · doi:10.1016/j.yexcr.2008.01.032 · Cited by 42
Transgenic expression of cyclooxygenase-2 (COX2) causes premature aging phenotypes in mice
Kim, J., Vaish, V., Feng, M., Field, K., Chatzistamou, I., & Shim, M. (2016) · Aging · doi:10.18632/aging.101060 · Cited by 41
Atamna, H., Atamna, W., Al-Eyd, G., Shanower, G., & Dhahbi, J. M. (2015) · Redox Biology · doi:10.1016/j.redox.2015.09.004 · Cited by 40
Senescent cells at the crossroads of aging, disease, and tissue homeostasis
Kuehnemann, C., & Wiley, C. D. (2023) · Aging Cell · doi:10.1111/acel.13988 · Cited by 44
New Insights on Molecular Mechanisms of Renal Aging
Schmitt, R., & Melk, A. (2012) · American Journal of Transplantation · doi:10.1111/j.1600-6143.2012.04214.x · Cited by 39
Genomic regulation of senescence and innate immunity signaling in the retinal pigment epithelium
Chaum, E., Winborn, C. S., & Bhattacharya, S. (2015) · Mammalian Genome · doi:10.1007/s00335-015-9568-9 · Cited by 40
Aging, Senescence, and Human Variation
Crews, D. E., & Ice, G. H. (2012) · Human Biology · doi:10.1002/9781118108062.ch13 · Cited by 39
miR-290 acts as a physiological effector of senescence in mouse embryo fibroblasts
Pitto, L., Rizzo, M., Simili, M., Colligiani, D., Evangelista, M., Mercatanti, A., Mariani, L., Cremisi, F., & Rainaldi, G. (2009) · Physiological Genomics · doi:10.1152/physiolgenomics.00085.2009 · Cited by 38
Increased ROS generation in subsets of OGG1 knockout fibroblast cells
Bácsi, A., Chodaczek, G., Hazra, T. K., Konkel, D. A., & Boldogh, I. R. (2007) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2007.09.005 · Cited by 38
Causes and consequences of telomere lengthening in a wild vertebrate population
Brown, T. J., Spurgin, L. G., Dugdale, H. L., Komdeur, J., Burke, T. A., & Richardson, D. S. (2021) · Molecular Ecology · doi:10.1111/mec.16059 · Cited by 42
Boehm, A. K., Seth, M., Mayr, K. G., & Fortier, L. A. (2007) · Arthritis & Rheumatism · doi:10.1002/art.22664 · Cited by 37
Aging and the programmed death phenomena
Skulachev, V. P. (2003) · Topics in current genetics · doi:10.1007/978-3-540-37005-5_8 · Cited by 36
Histone demethylase JMJD3 at the intersection of cellular senescence and cancer
Perrigue, P. M., Najbauer, J., & Barciszewski, J. (2016) · Biochimica et Biophysica Acta (BBA) - Reviews on Cancer · doi:10.1016/j.bbcan.2016.03.002 · Cited by 35
Wang, F., Deng, A., Li, M., Wei, J., Qin, H., & Wang, A. (2012) · Molecules · doi:10.3390/molecules18010418 · Cited by 33
Wang, X., Brégégère, F. M., Soroka, Y., Frušić‐Zlotkin, M., & Milner, Y. (2004) · FEBS Letters · doi:10.1016/j.febslet.2004.04.083 · Cited by 33
Li, L.-H., Wu, L.-J., Tashiro, S., Onodera, S., Uchiumi, F., & Ikejima, T. (2007) · Journal of Asian Natural Products Research · doi:10.1080/10286020600604260 · Cited by 31
Targeting DNA damage in ageing: towards supercharging DNA repair
Bujarrabal-Dueso, A., Garinis, G. A., Robbins, P. D., Vijg, J., & Schumacher, B. (2025) · Nature Reviews Drug Discovery · doi:10.1038/s41573-025-01212-6 · Cited by 32
Involvement of IL‐1 family proteins in p38 linked cellular senescence of mouse embryonic fibroblasts
Uekawa, N., Nishikimi, A., Isobe, K.-I., Iwakura, Y., & Maruyama, M. (2004) · FEBS Letters · doi:10.1016/j.febslet.2004.08.033 · Cited by 29
Telomere dynamics in the first year of life, but not later in life, predict lifespan in a wild bird
Sheldon, E. L., Eastwood, J. R., Teunissen, N., Roast, M. J., Aranzamendi, N. H., Fan, M., Hall, M. L., Kingma, S. A., Verhulst, S., & Peters, A. (2021) · Molecular Ecology · doi:10.1111/mec.16296 · Cited by 28
Positive Selection and Enhancer Evolution Shaped Lifespan and Body Mass in Great Apes
Tejada-Martínez, D., Avelar, R. A., Lopes, I., Zhang, B., Novoa, G., de Magalhães, J. P., & Trizzino, M. (2021) · Molecular Biology and Evolution · doi:10.1093/molbev/msab369 · Cited by 30
Analysis of Cellular Senescence in Culture In Vivo: The Senescence‐Associated β‐Galactosidase Assay
Bandyopadhyay, D., Gatza, C. E., Donehower, L. A., & Medrano, E. E. (2005) · Current Protocols in Cell Biology · doi:10.1002/0471143030.cb1809s27 · Cited by 29
Enoki, N., Kiyoshima, T., Sakai, T., Kobayashi, I., Takahashi, K., Terada, Y., & Sakai, H. (2007) · Journal of Molecular Histology · doi:10.1007/s10735-007-9105-6 · Cited by 27
Metadata
- Authors
- Campisi, J.
- Affiliations
- Buck Institute for Research on Aging (US)
- Corresponding author
- Campisi, J
- ORCID
- Campisi, J
- Venue
- Experimental Gerontology
- Publisher
- Elsevier BV
- Published
- 2003-01
- Volume
- 38
- Issue
- 1-2
- Pages
- 5-11
- ISSN
- 0531-5565 (ISSN-L)
- OpenAlex
- W1973723400
- Cited by
- 218
- References
- 70
- Citations by year
- 2026: 1 · 2025: 8 · 2024: 5 · 2023: 7 · 2022: 4 · 2021: 8 · 2020: 6 · 2019: 2 · 2018: 8 · 2017: 6 · 2016: 4 · 2015: 5 · 2014: 10 · 2013: 11 · 2012: 11
- FWCI
- 6.17
- Type
- journal article
- Language
- en
- Open access
- green
- www.escholarship.org
- Locations
- Experimental Gerontology (publishedVersion)
- PubMed (publishedVersion)
- eScholarship (California Digital Library) (submittedVersion)
- Funders
- U.S. Department of Energy
- Ellison Medical Foundation
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Aging › Genetics, Aging, and Longevity in Model Organisms
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Telomeres, Telomerase, and Senescence
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Cell death mechanisms and regulation
- Keywords
- cellular senescence, apoptosis, aging, antagonistic pleiotropy, age-related diseases, natural selection, evolutionary trade-offs, aging phenotypes
- MeSH terms
- Aged, Aging, Animals, Gene Expression Regulation, Humans, Mammals, Neoplasms, Genes, Tumor Suppressor, Cellular Senescence, Apoptosis, Multifactorial Inheritance
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