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Genome maintenance mechanisms for preventing cancer
Abstract
The early notion that cancer is caused by mutations in genes critical for the control of cell growth implied that genome stability is important for preventing oncogenesis. During the past decade, knowledge about the mechanisms by which genes erode and the molecular machinery designed to counteract this time-dependent genetic degeneration has increased markedly. At the same time, it has become apparent that inherited or acquired deficiencies in genome maintenance systems contribute significantly to the onset of cancer. This review summarizes the main DNA caretaking systems and their impact on genome stability and carcinogenesis.
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“CS patients, defective in the TCR branch of NER (1, 27), present a very different clinical picture, one of developmental defects and neurodegeneration; many but not all patients are also photosensitive, some developing blistering sunburns (5, 28).”
From Why Cockayne syndrome patients do not get cancer despite their DNA repair deficiency (2016) · cites this paper as [27]
In the citing paper
“Both XP and CS patients have defects in NER.”
From Why Cockayne syndrome patients do not get cancer despite their DNA repair deficiency (2016) · cites this paper as [27]
In the citing paper
“Ultraviolet (UV) light induces DNA damage that blocks replication and transcription [1][2][3] triggering either cell death or genetic instability.”
From Gap-filling and bypass at the replication fork are both active mechanisms for tolerance of low-dose ultraviolet-induced DNA damage in the human genome (2014) · cites this paper as [1]
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2 retracted
RETRACTED: Transcription-Coupled Repair of 8-oxoGuanine
Page, F. L., Kwoh, E. E., Avrutskaya, A. V., Gentil, A., Leadon, S. A., Sarasin, A. R., & Cooper, P. K. (2000) · Cell · doi:10.1016/s0092-8674(00)80827-2 · Cited by 280
RetractedPage, F. L., Kwoh, E. E., Avrutskaya, A. V., Gentil, A., Leadon, S. A., Sarasin, A. R., & Cooper, P. K. (2005) · Cell · doi:10.1016/j.cell.2005.11.005 · Cited by 271
RetractedOxidants, oxidative stress and the biology of ageing
Finkel, T., & Holbrook, N. J. (2000) · Nature · doi:10.1038/35041687 · Cited by 9,413
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
The DNA damage response: putting checkpoints in perspective
Zhou, B.-B. S., & Elledge, S. J. (2000) · Nature · doi:10.1038/35044005 · Cited by 3,213
A survey of telomerase activity in human cancer
Shay, J. W., & Bacchetti, S. (1997) · European Journal of Cancer · doi:10.1016/s0959-8049(97)00062-2 · Cited by 2,794
DNA double-strand breaks: signaling, repair and the cancer connection
Khanna, K. K., & Jackson, S. P. (2001) · Nature Genetics · doi:10.1038/85798 · Cited by 2,455
Cancer-epigenetics comes of age
Jones, P. A., & Laird, P. W. (1999) · Nature Genetics · doi:10.1038/5947 · Cited by 2,358
Bootsma, D., & Hoeijmakers, J. H. J. (1996) · Trends in Genetics · doi:10.1016/0168-9525(96)81408-9 · Cited by 2,285
Self-citation
Research works printed but not linked: 2
- Bootsma, D., Kraemer, K. H., Cleaver, J. & Hoeijmakers, J. H. J. in The Metabolic and Molecular Basis of Inherited Disease Vol. 1 (eds Scriver, C. R., Beaudet, A. L., Sly, W. S. & Valle, D.) 677–703 (McGraw-Hill, New York, 2001).
- Digweed, M., Reis, A. & Sperling, K. Nijmegen breakage syndrome: consequences of defective DNA double strand break repair. BioEssays 21, 649–656 (1999). · DOI
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Eker, A. P. M., Quayle, C., Chaves, I., & van der Horst, G. T. J. (2009) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-009-8735-0 · Cited by 72
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Groth, P., Orta, M. L., Elvers, I., Majumder, M. M., Lagerqvist, A., & Helleday, T. (2012) · Nucleic Acids Research · doi:10.1093/nar/gks315 · Cited by 75
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Ramadan, K., Shevelev, I., & Hübscher, U. (2004) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm1530 · Cited by 75
SMIRNOVA, E., TOUEILLE, M., MARKKANEN, E., & HÜBSCHER, U. (2005) · Biochemical Journal · doi:10.1042/bj20050211 · Cited by 74
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Guan, X., Bai, H., Shi, G., Theriot, C. A., Hazra, T. K., Mitra, S., & Lu, A.-L. (2007) · Nucleic Acids Research · doi:10.1093/nar/gkm075 · Cited by 74
Gembka, A., Toueille, M., Smirnova, E., Poltz, R., Ferrari, E., Villani, G., & Hubscher, U. (2007) · Nucleic Acids Research · doi:10.1093/nar/gkl1139 · Cited by 74
Tornaletti, S. (2009) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-009-8738-x · Cited by 74
Hu, J., Liu, M.-H., Li, Y., Tang, B., & Zhang, C. (2017) · Chemical Science · doi:10.1039/c7sc04296e · Cited by 73
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Su, M., Wang, H., Wang, W., Wang, Y., Ouyang, L., Chen, P., Xia, L., Cao, D., & Liao, Q. (2018) · Acta Biochimica et Biophysica Sinica · doi:10.1093/abbs/gmy022 · Cited by 72
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CanProVar: a human cancer proteome variation database
Li, J., Duncan, D. T., & Zhang, B. (2010) · Human Mutation · doi:10.1002/humu.21176 · Cited by 72
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Li, H., Mitchell, J. R., & Hasty, P. (2008) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2008.02.002 · Cited by 76
Okuda, Y., Nishi, R., Ng, J. M. Y., Vermeulen, W., van der Horst, G. T. J., Mori, T., Hoeijmakers, J. H. J., Hanaoka, F., & Sugasawa, K. (2004) · DNA repair · doi:10.1016/j.dnarep.2004.06.010 · Cited by 74
Self-citationChang, C. H., Chiu, C. F., Wang, H.-C., Wu, H. C., Tsai, R.-Y., Tsai, C. W., Wang, R. F., Wang, C.-H., Tsou, Y.-A., & Bau, D. T. (2009) · PubMed · Cited by 73
Dahm‐Daphi, J., Hubbe, P., Horvath, F., El‐Awady, R., Bouffard, K. E., Powell, S. N., & Willers, H. (2005) · Oncogene · doi:10.1038/sj.onc.1208396 · Cited by 74
Watanabe, S., Ichimura, T., Fujita, N., Tsuruzoe, S., Ohki, I., Shirakawa, M., Kawasuji, M., & Nakao, M. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2131819100 · Cited by 76
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Li, C., Hu, Z., Lü, J., Liu, Z., Wang, L., El‐Naggar, A. K., Sturgis, E. M., Spitz, M. R., & Wei, Q. (2007) · Cancer · doi:10.1002/cncr.22861 · Cited by 73
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Jiang, X., Chen, C., Zhao, W., & Zhang, Z. (2013) · Environmental Toxicology and Pharmacology · doi:10.1016/j.etap.2013.08.002 · Cited by 73
Dietlein, F., Thelen, L., Jokić, M., Jachimowicz, R. D., Ivan, L., Knittel, G., Leeser, U., van Oers, J., Edelmann, W., Heukamp, L. C., et al. (2014) · Cancer Discovery · doi:10.1158/2159-8290.cd-13-0907 · Cited by 70
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Thompson, L., Jeusset, L. M., Lepage, C. C., & McManus, K. J. (2017) · Cancers · doi:10.3390/cancers9110151 · Cited by 80
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Loree, J. M., Koturbash, I., Kutanzi, K. R., Baker, M., Pogribny, I. P., & Kovalchuk, O. (2006) · International Journal of Radiation Biology · doi:10.1080/09553000600960027 · Cited by 72
Chang, M., Wang, W.-N., Wang, A., Tian, T., Wang, P., Zheng, Y., & Liu, Y. (2009) · Comparative Biochemistry and Physiology Part C Toxicology & Pharmacology · doi:10.1016/j.cbpc.2008.12.011 · Cited by 72
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Ray, A., Mir, S. N., Wani, G., Zhao, Q., Battu, A., Zhu, Q., Wang, Q.-E., & Wani, A. A. (2009) · Molecular and Cellular Biology · doi:10.1128/mcb.00503-09 · Cited by 71
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Thoma, F. (2005) · DNA repair · doi:10.1016/j.dnarep.2005.04.005 · Cited by 71
Toussaint, M., & Conconi, A. (2006) · Nature Protocols · doi:10.1038/nprot.2006.304 · Cited by 71
Uchida, F., Uzawa, K., Kasamatsu, A., Takatori, H., Sakamoto, Y., Ogawara, K., Shiiba, M., Bukawa, H., & Tanzawa, H. (2013) · PLoS ONE · doi:10.1371/journal.pone.0056381 · Cited by 71
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Holme, J. A., Gorria, M., Arlt, V. M., Øvrebø, S., Solhaug, A., Tekpli, X., Landvik, N. E., Laurence Therese, H. U. C., Fardel, O., & Lagadic‐Gossmann, D. (2007) · Chemico-Biological Interactions · doi:10.1016/j.cbi.2007.01.008 · Cited by 71
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Kim, M. K., Cho, K.-J., Kwon, G. Y., Park, S.-I., Kim, Y., Kim, J. H., Song, H.-Y., Shin, J. H., Jung, H., Lee, G. H., et al. (2007) · European Journal of Cancer · doi:10.1016/j.ejca.2007.09.006 · Cited by 70
Chen, Y.-R., Liu, M., Chang, Y., Wu, C.-C., Hu, C.-Y., & Chen, J. (2008) · Journal of Virology · doi:10.1128/jvi.00430-08 · Cited by 71
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Wijnhoven, S., Beems, R. B., Roodbergen, M., van den Berg, J., Lohman, P. H. M., Diderich, K. E. M., van der Horst, G. T. J., Vijg, J., Hoeijmakers, J. H. J., & STEEG, H. V. (2005) · DNA repair · doi:10.1016/j.dnarep.2005.07.002 · Cited by 72
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Vijg, J., Busuttil, R. A., Bahar, R., & Dollé, M. E. T. (2005) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1323.007 · Cited by 68
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Yu, D., Zhang, X., Liu, J., Yuan, P., Tan, W., Guo, Y., Sun, T., Zhao, D., Yang, M., Liu, J., et al. (2008) · Clinical Cancer Research · doi:10.1158/1078-0432.ccr-07-1612 · Cited by 69
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Conde, J., Silva, S., Azevedo, A. P., Teixeira, V., Pina, J. E., Rueff, J., & Gaspar, J. (2009) · BMC Cancer · doi:10.1186/1471-2407-9-344 · Cited by 68
Sakano, S., Wada, T., Matsumoto, H., Sugiyama, S., Inoue, R., Eguchi, S., Ito, H., Ohmi, C., Matsuyama, H., & Naito, K. (2006) · British Journal of Cancer · doi:10.1038/sj.bjc.6603290 · Cited by 68
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Zhang, L., Zhao, J., Zhang, H., Jiang, J., & Yu, R. (2013) · Biosensors and Bioelectronics · doi:10.1016/j.bios.2012.12.037 · Cited by 68
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Vermeij, W. P., Hoeijmakers, J. H. J., & Pothof, J. (2014) · Current Opinion in Genetics & Development · doi:10.1016/j.gde.2014.06.006 · Cited by 70
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Zawahir, Z., Dayam, R., Deng, J. N., Pereira, C., & Neamati, N. (2008) · Journal of Medicinal Chemistry · doi:10.1021/jm800739m · Cited by 68
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Cotto-Rios, X. M., Jones, M. V., Busino, L., Pagano, M., & Huang, T. T. (2011) · The Journal of Cell Biology · doi:10.1083/jcb.201101062 · Cited by 69
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Metadata
- Authors
- Hoeijmakers, J. H. J.
- Affiliations
- Erasmus University Rotterdam (NL)
- Corresponding author
- Hoeijmakers, Jan H. J.
- Venue
- Nature
- Published
- 2001-05-01
- Volume
- 411
- Issue
- 6835
- Pages
- 366-374
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- OpenAlex
- W2096136751
- Semantic Scholar
- d0f61e028e7f97375defc2b754e37345af93b400
- Cited by
- 3,939
- References
- 68
- Citations by year
- 2026: 48 · 2025: 65 · 2024: 70 · 2023: 118 · 2022: 99 · 2021: 143 · 2020: 137 · 2019: 146 · 2018: 156 · 2017: 138 · 2016: 179 · 2015: 189 · 2014: 189 · 2013: 201 · 2012: 217
- FWCI
- 11.16
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Nature (publishedVersion)
- PubMed (publishedVersion)
- EUR Research Repository (Erasmus University Rotterdam) (submittedVersion)
- RePEc: Research Papers in Economics (submittedVersion)
- Funders
- KWF Kankerbestrijding
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › DNA Repair Mechanisms
- Health Sciences › Medicine › Oncology › Cancer-related Molecular Pathways
- Health Sciences › Medicine › Pathology and Forensic Medicine › Genetic factors in colorectal cancer
- Keywords
- genome maintenance, genome stability, carcinogenesis, DNA repair, DNA damage response, mutagenesis, cancer prevention
- MeSH terms
- Animals, DNA Damage, DNA Repair, Humans, Models, Genetic, Neoplasms, Recombination, Genetic, Syndrome, Transcription, Genetic, Telomere, Genome, Base Pair Mismatch
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