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DNA damage and ageing: new-age ideas for an age-old problem
Open accessAbstract
Loss of genome maintenance may causally contribute to ageing, as exemplified by the premature appearance of multiple symptoms of ageing in a growing family of human syndromes and in mice with genetic defects in genome maintenance pathways. Recent evidence revealed a similarity between such prematurely ageing mutants and long-lived mice harbouring mutations in growth signalling pathways. At first sight this seems paradoxical as they represent both extremes of ageing yet show a similar 'survival' response that is capable of delaying age-related pathology and extending lifespan. Understanding the mechanistic basis of this response and its connection with genome maintenance would open exciting possibilities for counteracting cancer or age-related diseases, and for promoting longevity.
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“IIS down-modulation reflects a defensive response aimed at minimizing cell growth and metabolism in the context of systemic damage”
From The Hallmarks of Aging (2013) · cites this paper as Garinis et al., 2008
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“Late-generation telomerase-knockout mice exhibit a premature aging syndrome characterized by hair graying, shortened survival and impaired responses to acute and chronic stress (63,77).”
From Telomeres and telomerase in cancer (2010) · cites this paper as [77]
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Cites
Friedberg, E. C., Walker, G. C., Siede, W., Wood, R. D., Schultz, R. A., & Ellenberger, T. (2005) · doi:10.1128/9781555816704 · Cited by 5,683
Instability and decay of the primary structure of DNA
Lindahl, T. (1993) · Nature · doi:10.1038/362709a0 · Cited by 5,679
Genome maintenance mechanisms for preventing cancer
Hoeijmakers, J. H. J. (2001) · Nature · doi:10.1038/35077232 · Cited by 3,939
Self-citationLiu, 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
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
The Effect of Retarded Growth Upon the Length of Life Span and Upon the Ultimate Body Size
McCay, C. M., Crowell, M. F., & Maynard, L. A. (1935) · The Journal of Nutrition · doi:10.1093/jn/10.1.63 · Cited by 2,264
IGF-1 receptor regulates lifespan and resistance to oxidative stress in mice
Holzenberger, M., Dupont, J., Ducos, B., Leneuve, P., Géloën, A., Even, P. C., Cervera, P., & Le Bouc, Y. (2003) · Nature · doi:10.1038/nature01298 · Cited by 2,109
Understanding the odd science of aging
Kirkwood, T. B. L. (2005) · Cell · doi:10.1016/j.cell.2005.01.027 · Cited by 1,984
Suppression of Aging in Mice by the Hormone Klotho
Kurosu, H., Yamamoto, M., Clark, J. D., Pastor, J. V., Nandi, A., Gurnani, P., McGuinness, O. P., Chikuda, H., Yamaguchi, M., Kawaguchi, H., et al. (2005) · Science · doi:10.1126/science.1112766 · Cited by 1,935
Harman, D. (1981) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.78.11.7124 · Cited by 1,915
Research works printed but not linked: 3
- Vilhem Bohr, D. W., de Souza Pinto, N. C., van der Pluijm, I. & Hoeijmakers, J. H. DNA Repair and Aging, (Cold Spring Harbor Laboratory Press, New York, 2008).
- Bootsma, D. K., K. H., Cleaver, J. E. & Hoeijmakers, J. H. J. The Metabolic and Molecular Basis of inherited Disease, 677–703 (McGraw-Hill, New York, 2001).
- der Pluijm I, G. G. et al. Impaired genome maintenance suppresses the growth hormone–insulin-like growth factor 1 axis in mice with cockayne syndrome. PLoS Biol. 5, 23–38 (2006).
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van Deursen, J. M. (2014) · Nature · doi:10.1038/nature13193 · Cited by 2,623
Hoeijmakers, J. H. J. (2009) · New England Journal of Medicine · doi:10.1056/nejmra0804615 · Cited by 2,239
Understanding nucleotide excision repair and its roles in cancer and ageing
Marteijn, J. A., Lans, H., Vermeulen, W., & Hoeijmakers, J. H. J. (2014) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm3822 · Cited by 1,192
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Weidner, C. I., Lin, Q., Koch, C. M., Eisele, L., Beier, F., Ziegler, P., Bauerschlag, D. O., Jöckel, K.-H., Erbel, R., Mühleisen, T. W., et al. (2014) · Genome Biology · doi:10.1186/gb-2014-15-2-r24 · Cited by 837
Telomeres and telomerase in cancer
Artandi, S. E., & DePinho, R. A. (2010) · Carcinogenesis · doi:10.1093/carcin/bgp268 · Cited by 823
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Walter, D., Lier, A., Geiselhart, A., Thalheimer, F. B., Huntscha, S., Sobotta, M. C., Moehrle, B., Brocks, D., Bayindir, I., Kaschutnig, P., et al. (2015) · Nature · doi:10.1038/nature14131 · Cited by 619
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Campbell, J. M., Bellman, S. M., Stephenson, M. D., & Lisy., K. (2017) · Ageing Research Reviews · doi:10.1016/j.arr.2017.08.003 · Cited by 455
Coppé, J.-P., Patil, C. K., Rodier, F., Krtolica, A., Beauséjour, C. M., Parrinello, S., Hodgson, J. G., Chin, K., Desprez, P.-Y., & Campisi, J. (2010) · PLoS ONE · doi:10.1371/journal.pone.0009188 · Cited by 455
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Maynard, S., Fang, E. F., Scheibye‐Knudsen, M., Croteau, D. L., & Bohr, V. A. (2015) · Cold Spring Harbor Perspectives in Medicine · doi:10.1101/cshperspect.a025130 · Cited by 454
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Matsumura, H., Mohri, Y., Binh, N. T., Morinaga, H., Fukuda, M., Ito, M., Kurata, S., Hoeijmakers, J., & Nishimura, E. K. (2016) · Science · doi:10.1126/science.aad4395 · Cited by 416
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Picca, A., Mankowski, R. T., Burman, J. L., Donisi, L., Js, K., Marzetti, E., & Leeuwenburgh, C. (2018) · Nature Reviews Cardiology · doi:10.1038/s41569-018-0059-z · Cited by 399
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Burtner, C. R., & Kennedy, B. K. (2010) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm2944 · Cited by 386
Fransquet, P. D., Wrigglesworth, J., Woods, R. L., Ernst, M. E., & Ryan, J. (2019) · Clinical Epigenetics · doi:10.1186/s13148-019-0656-7 · Cited by 369
Meiners, S., Eickelberg, O., & Königshoff, M. (2015) · European Respiratory Journal · doi:10.1183/09031936.00186914 · Cited by 340
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McCord, R. A., Michishita, E., Hong, T., Berber, E., Boxer, L. D., Kusumoto, R., Guan, S., Shi, X., Gozani, O., Burlingame, A. L., et al. (2009) · Aging · doi:10.18632/aging.100011 · Cited by 313
Cellular stress response pathways and ageing: intricate molecular relationships
Kourtis, N., & Tavernarakis, N. (2011) · The EMBO Journal · doi:10.1038/emboj.2011.162 · Cited by 312
Yahata, T., Takanashi, T., Muguruma, Y., Ibrahim, A. A., Matsuzawa, H., Uno, T., Sheng, Y., Onizuka, M., Ito, M., Kato, S., et al. (2011) · Blood · doi:10.1182/blood-2011-01-330050 · Cited by 313
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Yoshihara, M., Hayashizaki, Y., & Murakawa, Y. (2017) · Stem Cell Reviews and Reports · doi:10.1007/s12015-016-9680-6 · Cited by 283
Hinz, M., Stilmann, M., Arslan, S. Ç., Khanna, K. K., Dittmar, G., & Scheidereit, C. (2010) · Molecular Cell · doi:10.1016/j.molcel.2010.09.008 · Cited by 280
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Yu, Q., Katlinskaya, Y. V., Carbone, C. J., Zhao, B., Katlinski, K. V., Zheng, H., Guha, M., Li, N., Chen, Q., Yang, T., et al. (2015) · Cell Reports · doi:10.1016/j.celrep.2015.03.069 · Cited by 260
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Rebelo-Marques, A., De Sousa Lages, A., Andrade, R., Ribeiro, C. F., Mota-Pinto, A., Carrilho, F., & Espregueira-Mendes, J. (2018) · Frontiers in Endocrinology · doi:10.3389/fendo.2018.00258 · Cited by 246
Sotiropoulou, P. A., Candi, A., Mascré, G., Clercq, S. D., Youssef, K. K., Lapouge, G., Dahl, E., Semeraro, C., Denecker, G., Marine, J., et al. (2010) · Nature Cell Biology · doi:10.1038/ncb2059 · Cited by 252
Park, Y.-Y., Lee, S., Karbowski, M., Neutzner, A., Youle, R. J., & Cho, H. (2010) · Journal of Cell Science · doi:10.1242/jcs.061481 · Cited by 244
Krishnan, V., Chow, M. Z. Y., Wang, Z., Zhang, L., Liu, B., Liu, X., & Zhou, Z. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1102789108 · Cited by 236
Do DNA Double-Strand Breaks Drive Aging?
White, R. R., & Vijg, J. (2016) · Molecular Cell · doi:10.1016/j.molcel.2016.08.004 · Cited by 232
Self-citationA nuclear poly(ADP-Ribose)-dependent signalosome confers DNA damage-induced IκB kinase activation.
Stilmann, M., Hinz, M., Arslan, S. Ç., Zimmer, A., Schreiber, V., & Scheidereit, C. (2009) · Molecular Cell · doi:10.1016/j.molcel.2009.09.032 · Cited by 232
Maintaining genome stability in the nervous system
McKinnon, P. J. (2013) · Nature Neuroscience · doi:10.1038/nn.3537 · Cited by 229
Age-Related Accumulation of Somatic Mitochondrial DNA Mutations in Adult-Derived Human iPSCs
Kang, E., Wang, X., Tippner-Hedges, R., Ma, H., Folmes, C. D. L., Gutiérrez, N. M., Lee, Y., Dyken, C. V., Ahmed, R., Li, Y., et al. (2016) · Cell stem cell · doi:10.1016/j.stem.2016.02.005 · Cited by 216
Determinants of accelerated metabolomic and epigenetic aging in a UK cohort
Robinson, O., Chadeau Hyam, M., Karaman, I., Climaco Pinto, R., Ala-Korpela, M., Handakas, E., Fiorito, G., Gao, H., Heard, A., Jarvelin, M., et al. (2020) · Aging Cell · doi:10.1111/acel.13149 · Cited by 205
Yang, J., Huang, T., Petralia, F., Long, Q., Zhang, B., Argmann, C., Zhao, Y. B., Mobbs, C. V., Schadt, E. E., Zhu, J., et al. (2015) · Scientific Reports · doi:10.1038/srep15145 · Cited by 200
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Raamsdonk, J. M. V., & Hekimi, S. (2010) · Antioxidants and Redox Signaling · doi:10.1089/ars.2010.3215 · Cited by 186
Gao, X., Yu, X., Zhang, C., Wang, Y., Sun, Y., Sun, H., Zhang, H., Shi, Y., & He, X. (2022) · Stem Cell Reviews and Reports · doi:10.1007/s12015-022-10370-8 · Cited by 180
Aging and reprogramming: a two-way street
Mahmoudi, S., & Brunet, A. (2012) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2012.10.004 · Cited by 171
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Barbosa, J. D. S., Cabral, T. M., Ferreira, D. N., Agnez‐Lima, L. F., & de Medeiros, S. R. B. (2009) · Ecotoxicology and Environmental Safety · doi:10.1016/j.ecoenv.2009.10.008 · Cited by 153
Marangos, P., Stevense, M., Niaka, K., Lagoudaki, M., Nabti, I., Jessberger, R., & Carroll, J. (2015) · Nature Communications · doi:10.1038/ncomms9706 · Cited by 156
Mariño, G., Ugalde, A. P., Fernández, Á. F., Osorio, F. G., Fueyo, A., Freije, J. M. P., & López-Otín, C. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1002696107 · Cited by 131
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Lee, H. Y., Jung, S.-E., Oh, Y. N., Choi, A., Yang, W. I., & Shin, K. (2015) · Forensic Science International Genetics · doi:10.1016/j.fsigen.2015.05.014 · Cited by 148
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Self-citationThe ATR barrier to replication-born DNA damage
Lopez-Contreras, A. J., & Fernández-Capetillo, Ó. (2010) · DNA repair · doi:10.1016/j.dnarep.2010.09.012 · Cited by 148
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Monnat, R. J. (2010) · Seminars in Cancer Biology · doi:10.1016/j.semcancer.2010.10.002 · Cited by 127
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Parascandolo, A., & Laukkanen, M. O. (2018) · Antioxidants and Redox Signaling · doi:10.1089/ars.2017.7268 · Cited by 119
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Treiber, N., Maity, P., Singh, K., Kohn, M., Keist, A. F., Ferchiu, F., Sante, L., Frese, S., Bloch, W., Kreppel, F., et al. (2011) · Aging Cell · doi:10.1111/j.1474-9726.2010.00658.x · Cited by 109
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Maskey, R. S., Kim, M. S., Baker, D. J., Childs, B. G., Malureanu, L. A., Jeganathan, K. B., Machida, Y., van Deursen, J. M., & Machida, Y. (2014) · Nature Communications · doi:10.1038/ncomms6744 · Cited by 106
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Mano, T., Nagata, K., Nonaka, T., Tarutani, A., Imamura, T., Hashimoto, T., Bannai, T., Mano, K. K., Tsuchida, T., Ohtomo, R., et al. (2017) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1707151114 · Cited by 105
Mihalas, B. P., Redgrove, K. A., McLaughlin, E. A., & Nixon, B. (2017) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2017/4015874 · Cited by 109
Nie, Y., Zheng, Y., Ogawa, M., Miyagi, E., & Taniguchi, H. (2018) · Stem Cell Research & Therapy · doi:10.1186/s13287-017-0749-1 · Cited by 102
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Vo, N. N., Seo, H.-Y., Robinson, A. R., Sowa, G., Bentley, D. R., Taylor, L. N., Studer, R., Ūsas, A., Huard, J., Alber, S. M., et al. (2010) · Journal of Orthopaedic Research® · doi:10.1002/jor.21153 · Cited by 99
Promoting longevity by maintaining metabolic and proliferative homeostasis
Wang, L., Karpac, J., & Jasper, H. (2013) · Journal of Experimental Biology · doi:10.1242/jeb.089920 · Cited by 91
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Kinoshita, P. F., Leite, J. A., Orellana, A. M., Vasconcelos, A. R., Quintas, L. E. M., Kawamoto, E. M., & Scavone, C. (2016) · Frontiers in Physiology · doi:10.3389/fphys.2016.00195 · Cited by 93
PCNA promotes processive DNA end resection by Exo1
Chen, X., Paudyal, S. C., Chin, R.-I., & You, Z. (2013) · Nucleic Acids Research · doi:10.1093/nar/gkt672 · Cited by 86
Li, J., Cai, D., Yao, X., Zhang, Y., Chen, L., Jing, P., Wang, L., & Wang, Y. (2016) · International Journal of Molecular Sciences · doi:10.3390/ijms17060849 · Cited by 90
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Agrawal, A., Tay, J., Yang, G., Agrawal, S., & Gupta, S. (2010) · Aging · doi:10.18632/aging.100121 · Cited by 84
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Andreo-López, M. C., Contreras-Bolívar, V., Muñoz‐Torres, M., García-Fontana, B., & García‐Fontana, C. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24054491 · Cited by 94
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Ahmad, A., Banerjee, S., Wang, Z. P., Kong, D., Majumdar, A. P. N., & Sarkar, F. H. (2009) · Current Aging Science · doi:10.2174/1874609810902030174 · Cited by 83
The ageing epigenome: Damaged beyond repair?
Sinclair, D. A., & Oberdoerffer, P. (2009) · Ageing Research Reviews · doi:10.1016/j.arr.2009.04.004 · Cited by 86
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Visser, W. E., Bombardieri, C. R., Zevenbergen, C., Barnhoorn, S., Ottaviani, A., van der Pluijm, I., Brandt, R., Kaptein, E., van Heerebeek, R., van Toor, H., et al. (2016) · PLOS ONE · doi:10.1371/journal.pone.0149941 · Cited by 82
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Cortat, B., Garcia, C. C. M., Quinet, A., Schuch, A. P., de Lima-Bessa, K. M., & Menck, C. F. M. (2013) · Photochemical & Photobiological Sciences · doi:10.1039/c3pp50023c · Cited by 80
Otterbein, L. E., Hedblom, A., Harris, C. E., Csizmadia, E., Gallo, D. J., & Wegiel, B. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1102295108 · Cited by 79
R-loops trigger the release of cytoplasmic ssDNAs leading to chronic inflammation upon DNA damage
Chatzidoukaki, O., Stratigi, K., Goulielmaki, E., Niotis, G., Akalestou-Clocher, A., Gkirtzimanaki, K., Zafeiropoulos, A., Altmüller, J., Topalis, P., & Garinis, G. A. (2021) · Science Advances · doi:10.1126/sciadv.abj5769 · Cited by 79
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Metadata
- Authors
- Garinis, G. A., van der Horst, G. T. J., Vijg, J., & H.J. Hoeijmakers, J.
- Affiliations
- Erasmus MC (NL)
- Venue
- Nature Cell Biology
- Published
- 2008-11
- Volume
- 10
- Issue
- 11
- Pages
- 1241-1247
- ISSN
- 1465-7392 (ISSN-L)
- 1476-4679
- PMC
- PMC4351702
- OpenAlex
- W2077496230
- Cited by
- 366
- References
- 63
- Citations by year
- 2026: 4 · 2025: 6 · 2024: 13 · 2023: 7 · 2022: 14 · 2021: 24 · 2020: 21 · 2019: 19 · 2018: 24 · 2017: 27 · 2016: 33 · 2015: 25 · 2014: 21 · 2013: 31 · 2012: 24
- FWCI
- 2.05
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature Cell Biology (publishedVersion)
- PubMed (publishedVersion)
- EUR Research Repository (Erasmus University Rotterdam) (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- EUR Research Repository (Erasmus University Rotterdam) (submittedVersion)
- RePub (Erasmus University Rotterdam) (submittedVersion, other-oa)
- Funders
- National Institute on Aging (1P01 AG‑17242‑02, P01AG017242)
- National Institute of Environmental Health Sciences (U01ES011044)
- 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 › DNA Repair Mechanisms
- Keywords
- DNA damage, aging, genome maintenance, lifespan extension, longevity, age-related diseases, cancer prevention
- MeSH terms
- Aging, Animals, DNA Damage, Humans, Longevity, Aging, Premature, Mice
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