The DOI matches its Crossref record; 132 of the 132 references it cites were found in a registry or an index.
DNA double-strand break repair: From mechanistic understanding to cancer treatment
Abstract
Accurate repair of DNA double-strand breaks is essential to life. Indeed, defective DNA double-strand break repair can lead to toxicity and large scale sequence rearrangements that cause cancer and promote premature aging. Here, we highlight the two major repair systems for handling DNA double-strand breaks: homologous recombination and non-homologous end joining. To clarify recombination mechanisms, we present animations that illustrate DNA strand movements. In addition to describing how these pathways operate, we also describe why appropriate pathway choice is critical to genomic stability, and we summarize key pathway control features related to cell cycle checkpoint and apoptosis signaling. Importantly, recent progress in delineating the effects of specific defects in repair and checkpoint control has helped to explain several disease phenotypes, including cancer and premature aging. Improved understanding of these pathways has also sparked development of novel chemotherapeutic strategies that kill tumors with increased specificity and efficacy. This review aims to provide a foundational understanding of how the homologous recombination and non-homologous end joining pathways operate, and to demonstrate how a better understanding of these processes has advanced both our understanding of the underlying causes of cancer and our ability to innovate novel cancer treatment strategies.
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
“In this step, RAD51 works together with BRCA2 to allow the strand invasion onto undamaged DNA duplex [119,120].”
From Focus on UV-Induced DNA Damage and Repair—Disease Relevance and Protective Strategies (2020) · cites this paper as [119]
Citations
Cites
Targeting the DNA repair defect in BRCA mutant cells as a therapeutic strategy
Farmer, H., McCabe, N., Lord, C. J., Tutt, A. N. J., Johnson, D. A., Richardson, T. B., Santarosa, M., Dillon, K. J., Hickson, I., Knights, C., et al. (2005) · Nature · doi:10.1038/nature03445 · Cited by 6,683
Instability and decay of the primary structure of DNA
Lindahl, T. (1993) · Nature · doi:10.1038/362709a0 · Cited by 5,679
Specific killing of BRCA2-deficient tumours with inhibitors of poly(ADP-ribose) polymerase
Bryant, H. E., Schultz, N., Thomas, H. D., Parker, K. M., Flower, D., Lopez, E., Kyle, S., Meuth, M., Curtin, N. J., & Helleday, T. (2005) · Nature · doi:10.1038/nature03443 · Cited by 5,198
Self-citationThe double-strand-break repair model for recombination
Szostak, J. W., Orr-Weaver, T. L., Rothstein, R. J., & Stahl, F. W. (1983) · Cell · doi:10.1016/0092-8674(83)90331-8 · Cited by 2,437
Alu repeats and human genomic diversity
Batzer, M., & Deininger, P. (2002) · Nature reviews genetics · doi:10.1038/nrg798 · Cited by 1,522
Brca1 Controls Homology-Directed DNA Repair
Moynahan, M. E., Chiu, J. W., Koller, B. H., & Jasin, M. (1999) · Molecular Cell · doi:10.1016/s1097-2765(00)80202-6 · Cited by 1,245
Chromosomal stability and the DNA double-stranded break connection
van Gent, D. C., Hoeijmakers, J. H. J., & Kanaar, R. (2001) · Nature Reviews Genetics · doi:10.1038/35056049 · Cited by 1,219
Structure of the Ku heterodimer bound to DNA and its implications for double-strand break repair
Walker, J. R., Corpina, R. A., & Goldberg, J. D. (2001) · Nature · doi:10.1038/35088000 · Cited by 1,216
Pathways of DNA Double-Strand Break Repair during the Mammalian Cell Cycle
Rothkamm, K., Krüger, I., Thompson, L. H., & Lübrich, M. (2003) · Molecular and Cellular Biology · doi:10.1128/mcb.23.16.5706-5715.2003 · Cited by 1,187
Ma, Y., Pannicke, U., Schwarz, K., & Lieber, M. R. (2002) · Cell · doi:10.1016/s0092-8674(02)00671-2 · Cited by 1,166
A mechanism for gene conversion in fungi
Holliday, R. (2007) · Genetics Research · doi:10.1017/s0016672308009476 · Cited by 1,144
The Bloom's syndrome helicase suppresses crossing over during homologous recombination
Wu, L., & Hickson, I. D. (2003) · Nature · doi:10.1038/nature02253 · Cited by 1,087
The ATM-Chk2-Cdc25A checkpoint pathway guards against radioresistant DNA synthesis
Falck, J., Mailand, N., Syljuåsen, R. G., Bartek, J., & Lukas, J. (2001) · Nature · doi:10.1038/35071124 · Cited by 1,085
Requirement of the MRN complex for ATM activation by DNA damage
Uziel, T., Lerenthal, Y., Moyal, L., Andegeko, Y., Mittelman, L., & Shiloh, Y. (2003) · The EMBO Journal · doi:10.1093/emboj/cdg541 · Cited by 1,075
Requirement of poly(ADP-ribose) polymerase in recovery from DNA damage in mice and in cells
Murcia, J. M., Niedergang, C., Trucco, C., Ricoul, M., Dutrillaux, B., Mark, M. P., Oliver, F. J., Masson, M., Dierich, A., LeMeur, M., et al. (1997) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.94.14.7303 · Cited by 1,058
The importance of repairing stalled replication forks
Cox, M. M., Goodman, M. F., Kreuzer, K. N., Sherratt, D. J., Sandler, S. J., & Marians, K. J. (2000) · Nature · doi:10.1038/35003501 · Cited by 1,044
BRCA2 Is Required for Homology-Directed Repair of Chromosomal Breaks
Moynahan, M. E., Pierce, A. J., & Jasin, M. (2001) · Molecular Cell · doi:10.1016/s1097-2765(01)00174-5 · Cited by 1,007
A Manyfold Increase in Sister Chromatid Exchanges in Bloom's Syndrome Lymphocytes
Chaganti, R. S. K., Schonberg, S. A., & GERMAN, J. L. (1974) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.71.11.4508 · Cited by 941
The 3′ to 5′ Exonuclease Activity of Mre11 Facilitates Repair of DNA Double-Strand Breaks
Paull, T. T., & Gellert, M. F. (1998) · Molecular Cell · doi:10.1016/s1097-2765(00)80097-0 · Cited by 919
Moshous, D., Callebaut, I., de Chasseval, R., Corneo, B., Cavazzana, M., Deist, F. L., Tezcan, İ., Sanal, Ö., Bertrand, Y., Philippe, N., et al. (2001) · Cell · doi:10.1016/s0092-8674(01)00309-9 · Cited by 912
Rad51‐deficient vertebrate cells accumulate chromosomal breaks prior to cell death
Sonoda, E., Sasaki, M., Buerstedde, J., Bezzubova, O., Shinohara, A., Ogawa, H., Takata, M., Yamaguchi-Iwai, Y., & Takeda, S. (1998) · EMBO Journal · doi:10.1093/emboj/17.2.598 · Cited by 860
Riballo, E., Kühne, M., Rief, N., Doherty, A., Smith, G. C. M., Recio, M.-J., Reis, C., Dahm, K., Fricke, A., Krempler, A., et al. (2004) · Molecular Cell · doi:10.1016/j.molcel.2004.10.029 · Cited by 837
The Fanconi anaemia/BRCA pathway
D'Andrea, A. D., & Grompe, M. (2003) · Nature Reviews Cancer · doi:10.1038/nrc970 · Cited by 822
XLF Interacts with the XRCC4-DNA Ligase IV Complex to Promote DNA Nonhomologous End-Joining
Ahnesorg, P., Smith, P., & Jackson, S. P. (2006) · Cell · doi:10.1016/j.cell.2005.12.031 · Cited by 794
Targeted disruption of the Rad51 gene leads to lethality in embryonic mice.
Tsuzuki, T., Fujii, Y., Sakumi, K., Tominaga, Y., Nakao, K., Sekiguchi, M., Matsushiro, A., Yoshimura, Y., & MoritaT (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.13.6236 · Cited by 792
DNA end resection, homologous recombination and DNA damage checkpoint activation require CDK1
Ira, G., Pellicioli, A., Balijja, A., Wang, X., Fiorani, S., Carotenuto, W., Liberi, G., Bressan, D., Wan, L., Hollingsworth, N. M., et al. (2004) · Nature · doi:10.1038/nature02964 · Cited by 722
Buck, D., Malivert, L., de Chasseval, R., Barraud, A., Fondanèche, M.-C., Sanal, O., Plebani, A., Stéphan, J.-L., Hufnagel, M., le Deist, F., et al. (2006) · Cell · doi:10.1016/j.cell.2005.12.030 · Cited by 722
Role of BRCA2 in Control of the RAD51 Recombination and DNA Repair Protein
Davies, A. A., Masson, J., McIlwraith, M. J., Stasiak, A. Z., Stasiak, A., Venkitaraman, A. R., & West, S. C. (2001) · Molecular Cell · doi:10.1016/s1097-2765(01)00175-7 · Cited by 720
Lim, D., & Hasty, P. (1996) · Molecular and Cellular Biology · doi:10.1128/mcb.16.12.7133 · Cited by 703
Human Rad51 Protein Promotes ATP-Dependent Homologous Pairing and Strand Transfer Reactions In Vitro
Baumann, P., Benson, F. E., & West, S. C. (1996) · Cell · doi:10.1016/s0092-8674(00)81394-x · Cited by 689
Involvement of Brca2 in DNA Repair
Patel, K. J., Yu, V. P. C. C., Lee, H., Corcoran, A. E., Thistlethwaite, F. C., Evans, M. J., Colledge, W. H., Friedman, L. S., Ponder, B. A. J., & Venkitaraman, A. R. (1998) · Molecular Cell · doi:10.1016/s1097-2765(00)80035-0 · Cited by 646
The Bloom's and Werner's syndrome proteins are DNA structure-specific helicases
Mohaghegh, P. (2001) · Nucleic Acids Research · doi:10.1093/nar/29.13.2843 · Cited by 617
The origin of interspersed repeats in the human genome
Smit, A. F. A. (1996) · Current Opinion in Genetics & Development · doi:10.1016/s0959-437x(96)80030-x · Cited by 611
A loss-of-function RNA interference screen for molecular targets in cancer
Ngo, V. N., Davis, R. E., Lamy, L., Yu, X., Zhao, H. G., Lenz, G., Lam, L. T., Davé, S. S., Yang, L., Powell, J. I., et al. (2006) · Nature · doi:10.1038/nature04687 · Cited by 606
The role of double-strand break repair — insights from human genetics
O’Driscoll, M., & Jeggo, P. A. (2005) · Nature Reviews Genetics · doi:10.1038/nrg1746 · Cited by 600
Johnson, R. D., & Jasin, M. (2000) · The EMBO Journal · doi:10.1093/emboj/19.13.3398 · Cited by 590
Rad52 protein stimulates DNA strand exchange by Rad51 and replication protein A
New, J. H., Sugiyama, T., Zaitseva, E., & Kowalczykowski, S. C. (1998) · Nature · doi:10.1038/34950 · Cited by 589
The Rad50 zinc-hook is a structure joining Mre11 complexes in DNA recombination and repair
Hopfner, K., Craig, L., Moncalián, G., Zinkel, R. A., Usui, T., Owen, B. A. L., Kärcher, A., Henderson, B., Bodmer, J.-L., McMurray, C. T., et al. (2002) · Nature · doi:10.1038/nature00922 · Cited by 571
Syljuåsen, R. G., Sørensen, C. S., Hansen, L. T., Fugger, K., Lundin, C., Johansson, F., Helleday, T., Sehested, M., Lukas, J., & Bártek, J. (2005) · Molecular and Cellular Biology · doi:10.1128/mcb.25.9.3553-3562.2005 · Cited by 562
Self-citationPARP is important for genomic stability but dispensable in apoptosisPreprint
Wang, Z., Stingl, L., Morrison, C. G., Jantsch, M. F., Łoś, M., Schulze‐Osthoff, K., & Wagner, E. F. (1997) · Genes & Development · doi:10.1101/gad.11.18.2347 · Cited by 557
Frequent chromosomal translocations induced by DNA double-strand breaks
Richardson, C., & Jasin, M. (2000) · Nature · doi:10.1038/35015097 · Cited by 517
Human Rad50/Mre11 Is a Flexible Complex that Can Tether DNA Ends
de Jager, M., van Noort, J., van Gent, D. C., Dekker, C., Kanaar, R., & Wyman, C. (2001) · Molecular Cell · doi:10.1016/s1097-2765(01)00381-1 · Cited by 512
The Bloom's syndrome gene product promotes branch migration of Holliday junctions
Karow, J., Constantinou, A., Li, J., West, S. C., & Hickson, I. D. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.100448097 · Cited by 502
Niedernhofer, L. J., Odijk, H., Budzowska, M., van Drunen, E., Maas, A., Theil, A. F., de Wit, J., Jaspers, N. G. J., Beverloo, H. B., Hoeijmakers, J. H. J., et al. (2004) · Molecular and Cellular Biology · doi:10.1128/mcb.24.13.5776-5787.2004 · Cited by 493
Dynamic assembly of end-joining complexes requires interaction between Ku70/80 and XRCC4
Mari, P., Florea, B. I., Persengiev, S. P., Verkaik, N. S., Brüggenwirth, H. T., Modesti, M., Giglia‐Mari, G., Bezstarosti, K., Demmers, J., Luider, T. M., et al. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0609061103 · Cited by 461
Catalysis of homologous DNA pairing by yeast Rad51 and Rad54 proteins
Petukhova, G. D., Stratton, S. A., & Sung, P. (1998) · Nature · doi:10.1038/30037 · Cited by 445
Richardson, C. A., Moynahan, M. E., & Jasin, M. (1998) · Genes & Development · doi:10.1101/gad.12.24.3831 · Cited by 442
Recombinational DNA repair and human disease
Thompson, L. H., & Schild, D. (2002) · Mutation Research - Fundamental and Molecular Mechanisms of Mutagenesis · doi:10.1016/s0027-5107(02)00224-5 · Cited by 417
Clarifying the mechanics of DNA strand exchange in meiotic recombination
Neale, M. J., & Keeney, S. (2006) · Nature · doi:10.1038/nature04885 · Cited by 417
Ku Recruits the XRCC4-Ligase IV Complex to DNA Ends
McElhinny, S. A. N., McCarville, J., Snowden, C. M., & Ramsden, D. A. (2020) · PubMed Central · doi:10.17615/5hds-gb46 · Cited by 402
Identification and purification of two distinct complexes containing the five RAD51 paralogsPreprint
Masson, J., Tarsounas, M., Stasiak, A. Z., Stasiak, A., Punatar, R. S., McIlwraith, M. J., Benson, F. E., & West, S. C. (2001) · Genes & Development · doi:10.1101/gad.947001 · Cited by 395
The CDK regulates repair of double‐strand breaks by homologous recombination during the cell cycle
Aylon, Y., Liefshitz, B., & Kupiec, M. (2004) · The EMBO Journal · doi:10.1038/sj.emboj.7600469 · Cited by 387
Arnaudeau, C., Lundin, C., & Helleday, T. (2001) · Journal of Molecular Biology · doi:10.1006/jmbi.2001.4564 · Cited by 387
Self-citationConstantinou, A., Tarsounas, M., Karow, J., Brosh, R. M., Bohr, V. A., Hickson, I. D., & West, S. C. (2000) · EMBO Reports · doi:10.1093/embo-reports/kvd004 · Cited by 387
ATR and ATM regulate the timing of DNA replication origin firing
Shechter, D., Costanzo, V., & Gautier, J. (2004) · Nature Cell Biology · doi:10.1038/ncb1145 · Cited by 383
Cancer predisposition caused by elevated mitotic recombination in Bloom mice
Luo, G., Santoro, I. Μ., McDaniel, L. D., Nishijima, I., Mills, M., Youssoufian, H., Vogel, H. S., Schultz, R. A., & Bradley, A. (2000) · Nature Genetics · doi:10.1038/82548 · Cited by 372
Strumberg, D., Pilon, A. A., Smith, M. W., Hickey, R. J., Malkas, L. H., & Pommier, Y. G. (2000) · Molecular and Cellular Biology · doi:10.1128/mcb.20.11.3977-3987.2000 · Cited by 367
The exaptive excellence of spandrels as a term and prototype
Gould, S. J. (1997) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.94.20.10750 · Cited by 346
Shao, R.-G., Cao, C., Zhang, H., Kohn, K. W., Wold, M. S., & Pommier, Y. (1999) · The EMBO Journal · doi:10.1093/emboj/18.5.1397 · Cited by 345
Saleh-Gohari, N., Bryant, H. E., Schultz, N., Parker, K. M., Cassel, T. N., & Helleday, T. (2005) · Molecular and Cellular Biology · doi:10.1128/mcb.25.16.7158-7169.2005 · Cited by 339
Self-citationMcElhinny, S. A. N., Havener, J. M., García–Díaz, M., Juárez, R., Bębenek, K., Kee, B. L., Blanco, L., Kunkel, T. A., & Ramsden, D. A. (2005) · Molecular Cell · doi:10.1016/j.molcel.2005.06.012 · Cited by 327
Ding, Q., Reddy, Y. V. R., Wang, W., Woods, T. L., Douglas, P., Ramsden, D. A., Lees‐Miller, S. P., & Meek, K. (2003) · Molecular and Cellular Biology · doi:10.1128/mcb.23.16.5836-5848.2003 · Cited by 324
Thompson, L. H., Brookman, K. W., Dillehay, L. E., Carrano, A. V., Mazrimas, J. A., Mooney, C. L., & Minkler, J. L. (1982) · Mutation research. Fundamental and molecular mechanisms of mutagenesis · doi:10.1016/0027-5107(82)90276-7 · Cited by 321
Poly(ADP-ribose) polymerase (PARP-1) has a controlling role in homologous recombination
Schultz, N. D. (2003) · Nucleic Acids Research · doi:10.1093/nar/gkg703 · Cited by 314
Gene Conversion Tracts from Double-Strand Break Repair in Mammalian Cells
Elliott, B., Richardson, C. A., Winderbaum, J., Nickoloff, J. A., & Jasin, M. (1998) · Molecular and Cellular Biology · doi:10.1128/mcb.18.1.93 · Cited by 305
McIlwraith, M. J., Vaisman, A., Liu, Y., Fanning, E., Woodgate, R., & West, S. C. (2005) · Molecular Cell · doi:10.1016/j.molcel.2005.10.001 · Cited by 304
Damage recognition in nucleotide excision repair of DNA
Batty, D. P., & Wood, R. D. (2000) · Gene · doi:10.1016/s0378-1119(99)00489-8 · Cited by 298
Rescue of arrested replication forks by homologous recombination
Michel, B., Flores, M. J., Viguera, E., Grompone, G., Seigneur, M., & Bidnenko, V. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.111008798 · Cited by 292
Mesoscale conformational changes in the DNA-repair complex Rad50/Mre11/Nbs1 upon binding DNA
Moreno‐Herrero, F., de Jager, M., Dekker, N. H., Kanaar, R., Wyman, C., & Dekker, C. (2005) · Nature · doi:10.1038/nature03927 · Cited by 278
Chappell, C., Hanakahi, L. A., Karimi‐Busheri, F., Weinfeld, M., & West, S. C. (2002) · The EMBO Journal · doi:10.1093/emboj/21.11.2827 · Cited by 275
Sargent, R. G., Brenneman, M. A., & Wilson, J. H. (1997) · Molecular and Cellular Biology · doi:10.1128/mcb.17.1.267 · Cited by 271
der Zwet, M. K.-V., Overkamp, W. J., van Lange, R. E. E., Essers, J., van Duijn-Goedhart, A., Wiggers, I., Swaminathan, S., van Buul, P. V., Errami, A., Tan, R., et al. (2002) · Molecular and Cellular Biology · doi:10.1128/mcb.22.2.669-679.2002 · Cited by 267
Independent and sequential recruitment of NHEJ and HR factors to DNA damage sites in mammalian cells
Kim, J. S., Krasieva, T. B., Kurumizaka, H., Chen, D. J., Taylor, A. M. R., & Yokomori, K. (2005) · The Journal of Cell Biology · doi:10.1083/jcb.200411083 · Cited by 261
Mediator function of the human Rad51B–Rad51C complex in Rad51/RPA-catalyzed DNA strand exchangePreprint
Sigurðsson, S., Komen, S. V., Bussen, W., Schild, D., Albala, J. S., & Sung, P. (2001) · Genes & Development · doi:10.1101/gad.935501 · Cited by 257
Homologous Recombination Resolution Defect in Werner Syndrome
Saintigny, Y., Makienko, K., Swanson, C. L., Emond, M. J., & Monnat, R. J. (2002) · Molecular and Cellular Biology · doi:10.1128/mcb.22.20.6971-6978.2002 · Cited by 257
Sugiyama, T., & Kowalczykowski, S. C. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m203494200 · Cited by 251
The mechanism of non-homologous end-joining: a synopsis of synapsis
Weterings, E., & van Gent, D. C. (2004) · DNA repair · doi:10.1016/j.dnarep.2004.06.003 · Cited by 247
Mre11 Protein Complex Prevents Double-Strand Break Accumulation during Chromosomal DNA Replication
Costanzo, V., Robertson, K., Bibikova, M., Kim, E., Grieco, D., Gottesman, M., Carroll, D., & Gautier, J. (2001) · Molecular Cell · doi:10.1016/s1097-2765(01)00294-5 · Cited by 239
Break-induced replication: A review and an example in budding yeast
Kraus, E., Leung, W.-Y., & Haber, J. E. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.151008198 · Cited by 239
Xrcc4 physically links DNA end processing by polynucleotide kinase to DNA ligation by DNA ligase IV
Koch, C. A., Agyei, R., Galicia, S., Metalnikov, P. S., O’Donnell, E., Starostine, A., Weinfeld, M., & Durocher, D. (2004) · The EMBO Journal · doi:10.1038/sj.emboj.7600375 · Cited by 237
Li, G. C., Ouyang, H., Li, X., Nagasawa, H., Little, J. B., Chen, D. J., Ling, C., FUKS, Z. Y., & Cordon-Cardo, C. (1998) · Molecular Cell · doi:10.1016/s1097-2765(00)80108-2 · Cited by 235
Dual Roles for DNA Polymerase η in Homologous DNA Recombination and Translesion DNA Synthesis
Kawamoto, T., Araki, K., Sonoda, E., Yamashita, Y. M., Harada, K. H., Kikuchi, K., Masutani, C., Hanaoka, F., Nozaki, K., Hashimoto, N., et al. (2005) · Molecular Cell · doi:10.1016/j.molcel.2005.10.016 · Cited by 231
Visualization of Altered Replication Dynamics after DNA Damage in Human Cells
Merrick, C. J., Jackson, D. A., & Diffley, J. F. X. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m400022200 · Cited by 228
Moshous, D., Pannetier, C., de Chasseval, R., Deist, F. L., Cavazzana, M., Romana, S. P., Macintyre, E. A., Canioni, D., Brousse, N., Fischer, A., et al. (2003) · Journal of Clinical Investigation · doi:10.1172/jci16774 · Cited by 228
A Double Holliday Junction Dissolvasome Comprising BLM, Topoisomerase IIIα, and BLAP75
Raynard, S. J., Bussen, W., & Sung, P. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.c600051200 · Cited by 227
Methylation-induced blocks to in vitro DNA replication
Larson, K. L., Sahm, J., Shenkar, R., & Bs, S. (1985) · Mutation research. Fundamental and molecular mechanisms of mutagenesis · doi:10.1016/0027-5107(85)90103-4 · Cited by 223
p53‐catalyzed annealing of complementary single‐stranded nucleic acids.
Oberosler, P., Hloch, P., Ramsperger, U., & Stahl, H. D. (1993) · The EMBO Journal · doi:10.1002/j.1460-2075.1993.tb05893.x · Cited by 222
BRCA2-dependent and independent formation of RAD51 nuclear foci
Tarsounas, M., Davies, D. C., & West, S. C. (2003) · Oncogene · doi:10.1038/sj.onc.1206263 · Cited by 214
Schreiber, V., Hunting, D. J., Trucco, C., Gowans, B. J., Grünwald, D., de MURCIA, G., & Murcia, J. M. (1995) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.92.11.4753 · Cited by 203
Specific Interactions between the Human RAD51 and RAD52 Proteins
Shen, Z., Cloud, K. G., Chen, D. J., & Park, M. S. (1996) · Journal of Biological Chemistry · doi:10.1074/jbc.271.1.148 · Cited by 200
Rad54 protein promotes branch migration of Holliday junctions
Bugreev, D. V., Mazina, O. M., & Mazin, A. V. (2006) · Nature · doi:10.1038/nature04889 · Cited by 195
Alu: Structure, Origin, Evolution, Significance, and Function of One-Tenth of Human DNA
Schmid, C. W. (1996) · Progress in nucleic acid research and molecular biology · doi:10.1016/s0079-6603(08)60148-8 · Cited by 193
Chromatin structural elements and chromosomal translocations in leukemia
Zhang, Y., & Rowley, J. D. (2006) · DNA repair · doi:10.1016/j.dnarep.2006.05.020 · Cited by 188
Petermann, E., Maya‐Mendoza, A., Zachos, G., Gillespie, D. A., Jackson, D. A., & Caldecott, K. W. (2006) · Molecular and Cellular Biology · doi:10.1128/mcb.26.8.3319-3326.2006 · Cited by 181
Chromosomal Translocation Mechanisms at Intronic Alu Elements in Mammalian Cells
Elliott, B., Richardson, C. A., & Jasin, M. (2005) · Molecular Cell · doi:10.1016/j.molcel.2005.02.028 · Cited by 175
Sharpless, N. E., Ferguson, D. O., O’Hagan, R. C., Castrillón, D. H., Lee, C., Farazi, P. A., Alson, S., Fleming, J., Morton, C. C., Frank, K. M., et al. (2001) · Molecular Cell · doi:10.1016/s1097-2765(01)00425-7 · Cited by 173
Petermann, E., & Caldecott, K. W. (2006) · Cell Cycle · doi:10.4161/cc.5.19.3256 · Cited by 170
WRN exonuclease structure and molecular mechanism imply an editing role in DNA end processing
Perry, J. J. P., Yannone, S. M., Holden, L. G., Hitomi, C., Asaithamby, A., Han, S., Cooper, P. K., Chen, D. J., & Tainer, J. A. (2006) · Nature Structural & Molecular Biology · doi:10.1038/nsmb1088 · Cited by 166
Human p53 Binds Holliday Junctions Strongly and Facilitates Their Cleavage
Lee, S., Cavallo, L. M., & Griffith, J. D. (1997) · Journal of Biological Chemistry · doi:10.1074/jbc.272.11.7532 · Cited by 152
Reddy, Y. V. R., Ding, Q., Lees‐Miller, S. P., Meek, K., & Ramsden, D. A. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m406432200 · Cited by 136
Prado, F., & Aguilera, A. (1995) · Genetics · doi:10.1093/genetics/139.1.109 · Cited by 128
Engelward, B. P., Allan, J. M., Dreslin, A. J., Kelly, J. D., Wu, M. M., Gold, B. I., & Samson, L. D. (1998) · Journal of Biological Chemistry · doi:10.1074/jbc.273.9.5412 · Cited by 128
Self-citationRole of ERCC1 in removal of long non‐homologous tails during targeted homologous recombination
Adair, G. M., Rolig, R. L., Moore‐Faver, D., Zabelshansky, M., Wilson, J. H., & Nairn, R. S. (2000) · The EMBO Journal · doi:10.1093/emboj/19.20.5552 · Cited by 125
Evidence for intrachromosomal gene conversion in cultured mouse cells
Liskay, R. M., & Stachelek, J. L. (1983) · Cell · doi:10.1016/0092-8674(83)90218-0 · Cited by 125
The role of DNA dependent protein kinase in synapsis of DNA ends
Weterings, E. (2003) · Nucleic Acids Research · doi:10.1093/nar/gkg889 · Cited by 125
Extensive Loss of Heterozygosity Is Suppressed during Homologous Repair of Chromosomal Breaks
Stark, J. M., & Jasin, M. (2002) · Molecular and Cellular Biology · doi:10.1128/mcb.23.2.733-743.2003 · Cited by 122
High frequency in vivo loss of heterozygosity is primarily a consequence of mitotic recombination.
Gupta, P. K., Sahota, A. S., Boyadjiev, S. A., Bye, S., Shao, C., O’Neill, J. P., Hunter, T., Albertini, R. J., Stambrook, P. J., & Tischfield, J. A. (1997) · PubMed · Cited by 117
RAD51 is involved in repair of damage associated with DNA replication in mammalian cells
Lundin, C., Schultz, N., Arnaudeau, C., Mohindra, A., Hansen, L. T., & Helleday, T. (2003) · Journal of Molecular Biology · doi:10.1016/s0022-2836(03)00313-9 · Cited by 113
Self-citationBerger, J. M., & Schoeffler, A. J. (2005) · Biochemical Society Transactions · doi:10.1042/bst20051465 · Cited by 112
Simbulan-Rosenthal, C. M., Haddad, B. R., Rosenthal, D. S., Ohler, Z. W., Coleman, A., Luo, R., Young, H. M., Wang, Z., Ried, T., & Smulson, M. E. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.23.13191 · Cited by 105
Mechanisms of loss of heterozygosity in retinoblastoma
Zhu, X., Dunn, J. M., Goddard, A. D., Squire, J. A., Becker, A., Phillips, R. A., & Gallie, B. L. (2008) · Cytogenetics and Cell Genetics · doi:10.1159/000133261 · Cited by 105
The incidence of sister chromatid exchanges in cultured human lymphocytes
Morgan, W. F., & Crossen, P. E. (1977) · Mutation research. Fundamental and molecular mechanisms of mutagenesis · doi:10.1016/s0027-5107(77)80032-8 · Cited by 104
Gebow, D., Miselis, N. R., & Liber, H. L. (2000) · Molecular and Cellular Biology · doi:10.1128/mcb.20.11.4028-4035.2000 · Cited by 98
ATM is required for the cellular response to thymidine induced replication fork stress
Bolderson, E., Scorah, J., Helleday, T., Smythe, C., & Meuth, M. (2004) · Human Molecular Genetics · doi:10.1093/hmg/ddh316 · Cited by 86
Self-citationvan Heemst, D., Brugmans, L., Verkaik, N. S., & van Gent, D. C. (2003) · DNA repair · doi:10.1016/j.dnarep.2003.09.004 · Cited by 83
Radiation effects on DNA synthesis in a defined chromosomal replicon.
Larner, J. M., Lee, H., & Hamlin, J. L. (1994) · Molecular and Cellular Biology · doi:10.1128/mcb.14.3.1901 · Cited by 79
Analysis of mouse Rad54 expression and its implications for homologous recombination
Essers, J., Hendriks, R. W., Wesoły, J., Beerens, C. E. M. T., Smit, B., Hoeijmakers, J. H. J., Wyman, C., Dronkert, M. L. G., & Kanaar, R. (2002) · DNA repair · doi:10.1016/s1568-7864(02)00110-6 · Cited by 79
Visualization of recombination intermediates produced by RAD52‐mediated single‐strand annealing
Dyck, E. V., Stasiak, A. Z., Stasiak, A., & West, S. C. (2001) · EMBO Reports · doi:10.1093/embo-reports/kve201 · Cited by 78
Lucky breaks: analysis of recombination in Saccharomyces
Haber, J. E. (2000) · Mutation research. Fundamental and molecular mechanisms of mutagenesis · doi:10.1016/s0027-5107(00)00040-3 · Cited by 77
Molecular nature of in vivo mutations in human cells at the autosomal HLA-A locus.
Morley, A. A., Grist, S. A., Turner, D. R., Kutlaca, A., & Bennett, G. (1990) · PubMed · Cited by 72
Transpositions and translocations induced by site-specific double-strand breaks in budding yeast
Haber, J. E. (2006) · DNA repair · doi:10.1016/j.dnarep.2006.05.025 · Cited by 70
Holmquist, G. P. (1998) · Mutation research. Fundamental and molecular mechanisms of mutagenesis · doi:10.1016/s0027-5107(98)00051-7 · Cited by 64
Rad52 and Ku bind to different DNA structures produced early in double-strand break repair
Ristić, D. (2003) · Nucleic Acids Research · doi:10.1093/nar/gkg729 · Cited by 58
Interactions between p53, hMSH2-hMSH6 and HMG I(Y) on Holliday junctions and bulged bases
Subramanian, D. (2002) · Nucleic Acids Research · doi:10.1093/nar/30.11.2427 · Cited by 47
Construction of humanXRCC1minigenes that fully correct the CHO DNA repair mutant EM9
Caldecott, K. W., Tucker, J. D., & Thompson, L. H. (1992) · Nucleic Acids Research · doi:10.1093/nar/20.17.4575 · Cited by 46
Lebel, M. (2002) · Carcinogenesis · doi:10.1093/carcin/23.1.213 · Cited by 39
Wiktor‐Brown, D. M., Hendricks, C. A., Olipitz, W., & Engelward, B. P. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0604943103 · Cited by 38
Self-citationOverkamp, W. J. I., Rooimans, M. A., Neuteboom, I., Telleman, P., Arwert, F., & Zdzienicka, M. Z. (1993) · Somatic Cell and Molecular Genetics · doi:10.1007/bf01233248 · Cited by 35
The genetics of pancreatic adenocarcinoma: a roadmap for a mouse model
Bardeesy, N. M., Sharpless, N. E., DePinho, R. A., & Merlino, G. T. (2001) · Seminars in Cancer Biology · doi:10.1006/scbi.2000.0371 · Cited by 35
Jonnalagadda, V. S., Matsuguchi, T., & Engelward, B. P. (2005) · DNA repair · doi:10.1016/j.dnarep.2005.02.002 · Cited by 28
Self-citationV(D)J Recombination: Links to Transposition and Double-strand Break RepairPreprint
Gellert, M. F., Hesse, J. E., Hiom, K. J., Melek, M., Modesti, M., Paull, T. T., Ramsden, D. A., & van Gent, D. C. (1999) · Cold Spring Harbor Symposia on Quantitative Biology · doi:10.1101/sqb.1999.64.161 · Cited by 27
Saleh-Gohari, N., & Helleday, T. (2004) · Oncogene · doi:10.1038/sj.onc.1208178 · Cited by 17
Self-citation
Cited by
Sorted by citations
DNA repair pathways as targets for cancer therapy
Helleday, T., Petermann, E., Lundin, C., Hodgson, B., & Sharma, R. A. (2008) · Nature Reviews Cancer · doi:10.1038/nrc2342 · Cited by 1,666
Self-citationHypoxic microenvironment in cancer: molecular mechanisms and therapeutic interventions
Chen, Z., Han, F., Du, Y., Shi, H., & Zhou, W. (2023) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-023-01332-8 · Cited by 1,612
Hypoxia, DNA repair and genetic instability
Bristow, R. G., & Hill, R. P. (2008) · Nature Reviews Cancer · doi:10.1038/nrc2344 · Cited by 1,140
Repair of ionizing radiation-induced DNA double-strand breaks by non-homologous end-joining
Mahaney, B. L., Meek, K., & Lees‐Miller, S. P. (2009) · Biochemical Journal · doi:10.1042/bj20080413 · Cited by 722
Base excision repair of oxidative DNA damage and association with cancer and aging
Maynard, S., Schurman, S. H., Harboe, C., de Souza-Pinto, N. C., & Bohr, V. A. (2008) · Carcinogenesis · doi:10.1093/carcin/bgn250 · Cited by 712
Metadata
- Authors
- HELLEDAY, T., LO, J., VANGENT, D., & ENGELWARD, B.
- Affiliations
- Stockholm University (SE)
- Massachusetts Institute of Technology (US)
- Venue
- DNA Repair
- Publisher
- Elsevier BV
- Published
- 2007-07-01
- Volume
- 6
- Issue
- 7
- Pages
- 923-935
- ISSN
- 1568-7856 (ISSN-L)
- 1568-7864
- OpenAlex
- W2077892030
- Cited by
- 640
- References
- 132
- Citations by year
- 2026: 5 · 2025: 8 · 2024: 9 · 2023: 10 · 2022: 22 · 2021: 23 · 2020: 32 · 2019: 29 · 2018: 22 · 2017: 22 · 2016: 36 · 2015: 42 · 2014: 52 · 2013: 60 · 2012: 53
- FWCI
- 19.06
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- DNA repair (publishedVersion)
- PubMed (publishedVersion)
- EUR Research Repository (Erasmus University Rotterdam) (submittedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › DNA Repair Mechanisms
- Health Sciences › Medicine › Oncology › PARP inhibition in cancer therapy
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › DNA and Nucleic Acid Chemistry
- Keywords
- DNA double-strand break repair, homologous recombination, non-homologous end joining, genome stability, cell cycle checkpoints, apoptosis signaling, premature aging, cancer, targeted cancer therapy
- MeSH terms
- Animals, Cell Cycle, Cell Transformation, Neoplastic, DNA Repair, DNA Replication, Humans, Neoplasms, Recombination, Genetic, Gene Rearrangement, Genomic Instability, DNA Repair Enzymes, DNA Breaks, Double-Stranded
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