The DOI matches its Crossref record; 64 of the 64 references it cites were found in a registry or an index.
Common mechanisms of PIKK regulation
Open accessAbstract
Kinases in the phosphoinositide three-kinase-related kinase (PIKK) family include ATM (ataxia-telangiectasia mutated), ATR (ATM- and Rad3-related), DNA-PKcs (DNA-dependent protein kinase catalytic subunit), mTOR (mammalian target of rapamycin), and SMG1 (suppressor with morphological effect on genitalia family member). These atypical protein kinases regulate DNA damage responses, nutrient-dependent signaling, and nonsense-mediated mRNA decay. This review focuses on the mechanisms regulating the PIKK family with a strong emphasis on the DNA damage regulated kinases. We outline common regulatory themes and suggest how discoveries about the regulation of one PIKK can be informative for the other family members.
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?
In the citing paper
“In fact, ATM (Ataxia Telangiectasia Mutated) is activated by double-strand breaks (DSBs) caused, for example, by ionizing radiation (IR), while ATR (ATM and Rad3-Related) is activated by ssDNA coated with the RPA heterotrimeric complex and mainly triggers checkpoint activation after UV irradiation or replication-stress.”
From Mind the gap: keeping UV lesions in check (2011) · cites this paper as [40]
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
DNA damage activates ATM through intermolecular autophosphorylation and dimer dissociation
Bakkenist, C. J., & Kastan, M. B. (2003) · Nature · doi:10.1038/nature01368 · Cited by 3,466
Kim, D., Sarbassov, D. D., Ali, S. M., King, J. E., Latek, R. R., Erdjument‐Bromage, H., Tempst, P., & Sabatini, D. M. (2002) · Cell · doi:10.1016/s0092-8674(02)00808-5 · Cited by 3,051
The Rag GTPases Bind Raptor and Mediate Amino Acid Signaling to mTORC1
Sancak, Y., Peterson, T. R., Shaul, Y. D., Lindquist, R. A., Thoreen, C. C., Bar-Peled, L., & Sabatini, D. M. (2008) · Science · doi:10.1126/science.1157535 · Cited by 2,773
Sensing DNA Damage Through ATRIP Recognition of RPA-ssDNA Complexes
Zou, L., & Elledge, S. J. (2003) · Science · doi:10.1126/science.1083430 · Cited by 2,693
Sarbassov, D. D., Ali, S. M., Kim, D.-H., Guertin, D. A., Latek, R. R., Erdjument-Bromage, H., Tempst, P., & Sabatini, D. M. (2004) · Current Biology · doi:10.1016/j.cub.2004.06.054 · Cited by 2,665
ATR: an essential regulator of genome integrity
Cimprich, K. A., & Cortez, D. (2008) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm2450 · Cited by 1,798
Self-citationATM Activation by DNA Double-Strand Breaks Through the Mre11-Rad50-Nbs1 Complex
Lee, J.-H., & Paull, T. T. (2005) · Science · doi:10.1126/science.1108297 · Cited by 1,424
Conserved modes of recruitment of ATM, ATR and DNA-PKcs to sites of DNA damage
Falck, J., Coates, J., & Jackson, S. P. (2005) · Nature · doi:10.1038/nature03442 · Cited by 1,304
The DNA-dependent protein kinase: Requirement for DNA ends and association with Ku antigen
Gottlieb, T. M., & Jackson, S. P. (1993) · Cell · doi:10.1016/0092-8674(93)90057-w · Cited by 1,233
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
Cited by
Sorted by citations
The ATM protein kinase: regulating the cellular response to genotoxic stress, and more
Shiloh, Y., & Ziv, Y. (2013) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm3546 · Cited by 1,649
DNA Damage Sensing by the ATM and ATR Kinases
Marechal, A., & Zou, L. (2013) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a012716 · Cited by 1,514
mTOR kinase structure, mechanism and regulation
Yang, H., Rudge, D. G., Koos, J. D., Vaidialingam, B., Yang, H. J., & Pavletich, N. P. (2013) · Nature · doi:10.1038/nature12122 · Cited by 1,075
Paull, T. T. (2015) · Annual Review of Biochemistry · doi:10.1146/annurev-biochem-060614-034335 · Cited by 492
Replication stress induces 53BP1-containing OPT domains in G1 cells
Harrigan, J. A., Belotserkovskaya, R., Coates, J., Dimitrova, D. S., Polo, S. E., Bradshaw, C. R., Fraser, P., & Jackson, S. P. (2011) · The Journal of Cell Biology · doi:10.1083/jcb.201011083 · Cited by 357
ATR signalling: more than meeting at the fork
Nam, E. A., & Cortez, D. (2011) · Biochemical Journal · doi:10.1042/bj20102162 · Cited by 316
Self-citationDNA mismatch repair and the DNA damage response
Li, Z., Pearlman, A. H., & Hsieh, P. (2015) · DNA repair · doi:10.1016/j.dnarep.2015.11.019 · Cited by 323
Platinum Resistance in Ovarian Cancer: Role of DNA Repair
Damia, G. L. M., & Broggini, M. (2019) · Cancers · doi:10.3390/cancers11010119 · Cited by 304
Cellular functions of the protein kinase ATM and their relevance to human disease
Lee, J., & Paull, T. T. (2021) · Nature Reviews Molecular Cell Biology · doi:10.1038/s41580-021-00394-2 · Cited by 303
ATM and ATR signaling at a glance
Awasthi, P., Foiani, M., & Kumar, A. (2015) · Journal of Cell Science · doi:10.1242/jcs.169730 · Cited by 292
ATM-Dependent and -Independent Dynamics of the Nuclear Phosphoproteome After DNA Damage
Bensimon, A., Schmidt, A., Ziv, Y., Elkon, R., Wang, S., Chen, D. J., Aebersold, R. H., & Shiloh, Y. (2010) · Science Signaling · doi:10.1126/scisignal.2001034 · Cited by 290
The Ku heterodimer: Function in DNA repair and beyond
Fell, V. L., & Schild‐Poulter, C. (2014) · Mutation Research/Reviews in Mutation Research · doi:10.1016/j.mrrev.2014.06.002 · Cited by 297
DNA Damage Response: Three Levels of DNA Repair Regulation
Sirbu, B. M., & Cortez, D. (2013) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a012724 · Cited by 272
Self-citationMultiple roles of ATM in monitoring and maintaining DNA integrity
Derheimer, F. A., & Kastan, M. B. (2010) · FEBS Letters · doi:10.1016/j.febslet.2010.05.031 · Cited by 265
Inositol pyrophosphates: between signalling and metabolism
Wilson, M. S. C., Livermore, T. M., & Saiardi, A. (2013) · Biochemical Journal · doi:10.1042/bj20130118 · Cited by 256
Tti1 and Tel2 Are Critical Factors in Mammalian Target of Rapamycin Complex Assembly
Kaizuka, T., Hara, T., Oshiro, N., Kikkawa, U., Yonezawa, K., Takehana, K., Iemura, S.-I., Natsume, T., & Mizushima, N. (2010) · Journal of Biological Chemistry · doi:10.1074/jbc.m110.121699 · Cited by 255
The ubiquitous role of ubiquitin in the DNA damage response
Al-Hakim, A., Escribano‐Diaz, C., Landry, M.-C., O’Donnell, L., Panier, S., Szilard, R. K., & Durocher, D. (2010) · DNA repair · doi:10.1016/j.dnarep.2010.09.011 · Cited by 240
Roitinger, E., Hofer, M., Köcher, T., Pichler, P., Novatchkova, M., Yang, J., Schlögelhofer, P., & Mechtler, K. (2015) · Molecular & Cellular Proteomics · doi:10.1074/mcp.m114.040352 · Cited by 224
Involvement of Matrin 3 and SFPQ/NONO in the DNA damage response
Salton, M., Lerenthal, Y., Wang, S., Chen, D. J., & Shiloh, Y. (2010) · Cell Cycle · doi:10.4161/cc.9.8.11298 · Cited by 218
Beyond ATM: The protein kinase landscape of the DNA damage response
Bensimon, A., Aebersold, R. H., & Shiloh, Y. (2011) · FEBS Letters · doi:10.1016/j.febslet.2011.05.013 · Cited by 214
Autophosphorylation and ATM Activation
Kozlov, S., Graham, M. E., Jakob, B., Tobias, F., Kijas, A. W., Tanuji, M., Chen, P., Robinson, P. J., Taucher-Scholz, G., Suzuki, K., et al. (2010) · Journal of Biological Chemistry · doi:10.1074/jbc.m110.204065 · Cited by 221
McIlwain, D. R., Pan, Q., Reilly, P. T., Elia, A., McCracken, S. A., Wakeham, A. C., Itie-YouTen, A., Blencowe, B. J., & Mak, T. W. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1007336107 · Cited by 197
The Meiotic Checkpoint Network: Step-by-Step through Meiotic ProphasePreprint
Subramanian, V. V., & Hochwagen, A. (2014) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a016675 · Cited by 188
DNA damage response in cisplatin-induced nephrotoxicity
Zhu, S., Pabla, N., Tang, C., He, L., & Dong, Z. (2015) · Archives of Toxicology · doi:10.1007/s00204-015-1633-3 · Cited by 183
Senescence in Post-Mitotic Cells: A Driver of Aging?
von Zglinicki, T., Wan, T., & Miwa, S. (2021) · Antioxidants & Redox Signaling · doi:10.1089/ars.2020.8048 · Cited by 170
Jarvis, I. W. H., Dreij, K., Mattsson, Å., Jernström, B., & Stenius, U. (2014) · Toxicology · doi:10.1016/j.tox.2014.03.012 · Cited by 163
The R2TP complex: Discovery and functions
Kakihara, Y., & Houry, W. A. (2011) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2011.08.016 · Cited by 157
Hwang, J., & Maquat, L. E. (2011) · Current Opinion in Genetics & Development · doi:10.1016/j.gde.2011.03.008 · Cited by 149
Trial Watch: Targeting ATM–CHK2 and ATR–CHK1 pathways for anticancer therapy
Manic, G., Obrist, F., Sistigu, A., & Vitale, I. (2015) · Molecular & Cellular Oncology · doi:10.1080/23723556.2015.1012976 · Cited by 152
Kiss, R. C., Xia, F., & Acklin, S. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22158199 · Cited by 150
ATM and ATR Signaling Regulate the Recruitment of Human Telomerase to Telomeres
Tong, A. S., Stern, J. L., Sfeir, A. J., Kartawinata, M., de Lange, T., Zhu, X., & Bryan, T. M. (2015) · Cell Reports · doi:10.1016/j.celrep.2015.10.041 · Cited by 138
Functions of SMARCAL1, ZRANB3, and HLTF in maintaining genome stability
Poole, L. A., & Cortez, D. (2017) · Critical Reviews in Biochemistry and Molecular Biology · doi:10.1080/10409238.2017.1380597 · Cited by 142
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
Cerboni, C., Fionda, C., Soriani, A., Zingoni, A., Doria, M., Cippitelli, M., & Santoni, A. (2014) · Frontiers in Immunology · doi:10.3389/fimmu.2013.00508 · Cited by 141
Rao, F., Cha, J., Xu, J., Xu, R., Vandiver, M. S., Tyagi, R., Tokhunts, R. A., Koldobskiy, M. A., Fu, C., Barrow, R. K., et al. (2014) · Molecular Cell · doi:10.1016/j.molcel.2014.02.020 · Cited by 126
Nam, E. A., Zhao, R., Glick, G. G., Bansbach, C. E., Friedman, D. B., & Cortez, D. (2011) · Journal of Biological Chemistry · doi:10.1074/jbc.m111.248914 · Cited by 129
Self-citationEukaryotic DNA damage checkpoint activation in response to double-strand breaks
Finn, K., Lowndes, N. F., & Grenon, M. (2012) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-011-0875-3 · Cited by 127
Structures of closed and open conformations of dimeric human ATM
Baretić, D., Pollard, H., Fisher, D. I., Johnson, C. M., Santhanam, B., Truman, C., Kouba, T., Fersht, A. R., Phillips, C., & Williams, R. L. (2017) · Science Advances · doi:10.1126/sciadv.1700933 · Cited by 132
ATM, ATR, CHK1, CHK2 and WEE1 inhibitors in cancer and cancer stem cells
Ronco, C., Martin, A. R., Demange, L., & Benhida, R. (2016) · MedChemComm · doi:10.1039/c6md00439c · Cited by 131
Checkpoint mechanisms: the puppet masters of meiotic prophase
MacQueen, A. J., & Hochwagen, A. (2011) · Trends in Cell Biology · doi:10.1016/j.tcb.2011.03.004 · Cited by 125
Liu, P., Xu, Z., Lu, P., Hu, D., Chen, M., Li, L., & Ma, Y. (2013) · Journal of Experimental Botany · doi:10.1093/jxb/ert133 · Cited by 113
Systemic DNA damage responses in aging and diseases
Ribezzo, F., Shiloh, Y., & Schumacher, B. (2016) · Seminars in Cancer Biology · doi:10.1016/j.semcancer.2015.12.005 · Cited by 116
ATM protein kinase: the linchpin of cellular defenses to stress
Bhatti, S., Kozlov, S., Farooqi, A. A., Naqi, A., Lavin, M., & Khanna, K. K. (2011) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-011-0683-9 · Cited by 116
Maciejczyk, M., Mikołuć, B., Pietrucha, B. M., Heropolitańska–Pliszka, E., Pac, M., Motkowski, R., & Car, H. (2016) · Redox Biology · doi:10.1016/j.redox.2016.12.030 · Cited by 114
Dealing with DNA damage: Relationships between checkpoint and repair pathways
Warmerdam, D. O., & Kanaar, R. (2009) · Mutation Research/Reviews in Mutation Research · doi:10.1016/j.mrrev.2009.12.001 · Cited by 122
Ataxia-telangiectasia (A-T): An emerging dimension of premature ageing
Shiloh, Y., & Lederman, H. M. (2016) · Ageing Research Reviews · doi:10.1016/j.arr.2016.05.002 · Cited by 115
ATM: Expanding roles as a chief guardian of genome stability
Shiloh, Y. (2014) · Experimental Cell Research · doi:10.1016/j.yexcr.2014.09.002 · Cited by 111
Parvovirus Minute Virus of Mice Induces a DNA Damage Response That Facilitates Viral Replication
Adeyemi, R. O., Landry, S., Davis-Gardner, M. E., Weitzman, M. D., & Pintel, D. J. (2010) · PLoS Pathogens · doi:10.1371/journal.ppat.1001141 · Cited by 105
The Cross Talk Between p53 and mTOR Pathways in Response to Physiological and Genotoxic Stresses
Cui, D., Qu, R., Liu, D., Xiong, X., Liang, T., & Zhao, Y. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.775507 · Cited by 112
Phan, L. M., & Rezaeian, A.-H. (2021) · Genes · doi:10.3390/genes12060845 · Cited by 113
Suppression of nonsense mutations as a therapeutic approach to treat genetic diseases
Keeling, K. M., & Bedwell, D. M. (2011) · Wiley Interdisciplinary Reviews - RNA · doi:10.1002/wrna.95 · Cited by 106
Identification of pyrimidine derivatives as hSMG-1 inhibitors
Gopalsamy, A., Bennett, E. M., Shi, M., Zhang, W., Bard, J., & Yu, K. (2012) · Bioorganic & Medicinal Chemistry Letters · doi:10.1016/j.bmcl.2012.08.107 · Cited by 104
Moon, S.-H., Lin, L., Zhang, X., Nguyen, T., Darlington, Y. F., Waldman, A. S., Lu, X., & Donehower, L. A. (2010) · Journal of Biological Chemistry · doi:10.1074/jbc.m109.071696 · Cited by 108
Chaperone-like activity of the AAA+ proteins Rvb1 and Rvb2 in the assembly of various complexes
Nano, N., & Houry, W. A. (2013) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2011.0399 · Cited by 111
Clinical Candidates Targeting the ATR–CHK1–WEE1 Axis in Cancer
Górecki, L., Andrš, M., & Korábečný, J. (2021) · Cancers · doi:10.3390/cancers13040795 · Cited by 107
Consensus, debate, and prospective on pancreatic cancer treatments
Wang, J., Yang, J., Narang, A. K., He, J., Wolfgang, C. L., Li, K., & Zheng, L. (2024) · Journal of Hematology & Oncology · doi:10.1186/s13045-024-01613-x · Cited by 104
Baritaud, M., Cabon, L., Delavallée, L., Galán‐Malo, P., Me, G., Brunelle-Navas, M.-N., & Susín, S. A. (2012) · Cell Death and Disease · doi:10.1038/cddis.2012.120 · Cited by 98
TORC2 Signaling Pathway Guarantees Genome Stability in the Face of DNA Strand Breaks
Shimada, K., Filipuzzi, I., Ståhl, M., Helliwell, S. B., Studer, C., Hoepfner, D., Seeber, A., Loewith, R., Movva, N. R., & Gasser, S. M. (2013) · Molecular Cell · doi:10.1016/j.molcel.2013.08.019 · Cited by 89
New insights into the roles of ATM and DNA-PKcs in the cellular response to oxidative stress
Chen, B. P. C., Li, M., & Asaithamby, A. (2012) · Cancer Letters · doi:10.1016/j.canlet.2011.12.004 · Cited by 84
DNA-PKcs promotes chromatin decondensation to facilitate initiation of the DNA damage response
Lu, H., Saha, J., Beckmann, P. J., Hendrickson, E. A., & Davis, A. J. (2019) · Nucleic Acids Research · doi:10.1093/nar/gkz694 · Cited by 90
Zhang, H., Xu, J., Long, Y., Maimaitijiang, A., Su, Z., Li, W., & Li, J. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms252312928 · Cited by 97
Menéndez, J. A., Cufí, S., Oliveras‐Ferraros, C., Martı́n-Castillo, B., Joven, J., Vellón, L., & Vázquez‐Martín, A. (2011) · Aging · doi:10.18632/aging.100407 · Cited by 84
Paull, T. T. (2010) · DNA repair · doi:10.1016/j.dnarep.2010.09.015 · Cited by 90
FOXOs: masters of the equilibrium
Gui, T., & Burgering, B. M. T. (2021) · FEBS Journal · doi:10.1111/febs.16221 · Cited by 86
The kinomes of apicomplexan parasites
Miranda‐Saavedra, D., Gabaldón, T., Barton, G. J., Langsley, G., & Doerig, C. (2012) · Microbes and Infection · doi:10.1016/j.micinf.2012.04.007 · Cited by 82
The DNA damage checkpoint response to replication stress: A Game of Forks
Jossen, R., & Bermejo, R. (2013) · Frontiers in Genetics · doi:10.3389/fgene.2013.00026 · Cited by 88
PIKKs — the solenoid nest where partners and kinases meet
Baretić, D., & Williams, R. L. (2014) · Current Opinion in Structural Biology · doi:10.1016/j.sbi.2014.11.003 · Cited by 85
Mammalian TOR signaling to the AGC kinases
Su, B., & Jacinto, E. (2011) · Critical Reviews in Biochemistry and Molecular Biology · doi:10.3109/10409238.2011.618113 · Cited by 79
DNA damage, metabolism and aging in pro-inflammatory T cells
Li, Y., Goronzy, J. J., & Weyand, C. M. (2017) · Experimental Gerontology · doi:10.1016/j.exger.2017.10.027 · Cited by 80
ATM and ATR signaling at a glance
Awasthi, P., Foiani, M., & Kumar, A. (2016) · Journal of Cell Science · doi:10.1242/jcs.188631 · Cited by 78
RNF20–RNF40: A ubiquitin‐driven link between gene expression and the DNA damage response
Shiloh, Y., Shema, E., Moyal, L., & Oren, M. (2011) · FEBS Letters · doi:10.1016/j.febslet.2011.07.034 · Cited by 77
Targeting ATM and ATR for cancer therapeutics: Inhibitors in clinic
Priya, B., Ravi, S., & Kirubakaran, S. (2023) · Drug Discovery Today · doi:10.1016/j.drudis.2023.103662 · Cited by 77
Compromised genomic integrity impedes muscle growth after Atrx inactivation
Huh, M. S., O’Dea, T. P., Ouazia, D., McKay, B. C., Parise, G., Parks, R. J., Rudnicki, M. A., & Picketts, D. J. (2012) · Journal of Clinical Investigation · doi:10.1172/jci63765 · Cited by 71
Molecular basis of human ATM kinase inhibition
Stakyte, K., Rotheneder, M., Lammens, K., Bartho, J. D., Grädler, U., Fuchß, T., Pehl, U., Alt, A., van de Logt, E., & Hopfner, K. (2021) · Nature Structural & Molecular Biology · doi:10.1038/s41594-021-00654-x · Cited by 66
Chromatin: Receiver and Quarterback for Cellular Signals
Johnson, D. G., & Dent, S. (2013) · Cell · doi:10.1016/j.cell.2013.01.017 · Cited by 70
Architecture of the Saccharomyces cerevisiae NuA4/TIP60 complex
Wang, X., Ahmad, S., Zhang, Z., Côté, J., & Cai, G. (2018) · Nature Communications · doi:10.1038/s41467-018-03504-5 · Cited by 71
DNA repair as a shared hallmark in cancer and ageing
Clarke, T. L., & Mostoslavsky, R. (2022) · Molecular Oncology · doi:10.1002/1878-0261.13285 · Cited by 74
Levy‐Barda, A., Lerenthal, Y., Davis, A. J., Chung, Y. M., Essers, J., Shao, Z., van Vliet, N., Chen, D. J., Hu, M. C. ‐., Kanaar, R., et al. (2011) · Cell Cycle · doi:10.4161/cc.10.24.18642 · Cited by 66
Cheruiyot, A., Li, S., Srivatsan, S. N., Ahmed, T., Chen, Y., Lemacon, D. S., Li, Y., Yang, Z., Wadugu, B. A., Warner, W. A., et al. (2021) · Cancer Research · doi:10.1158/0008-5472.can-20-4016 · Cited by 61
Structure of the intact ATM/Tel1 kinase
Wang, X., Chu, H., Lv, M., Zhang, Z., Qiu, S., Liu, H., Shen, X., Wang, W., & Cai, G. (2016) · Nature Communications · doi:10.1038/ncomms11655 · Cited by 65
The activating transcription factor 2: an influencer of cancer progression
Huebner, K., Procházka, J., Monteiro, A. C., Mahadevan, V., & Schneider‐Stock, R. (2019) · Mutagenesis · doi:10.1093/mutage/gez041 · Cited by 61
Ataxia-telangiectasia: future prospects
Albaradie, R., & Chaudhary, M. (2014) · The Application of Clinical Genetics · doi:10.2147/tacg.s35759 · Cited by 60
Zimmermann, M., Don, A. S. A., Donaldson, M. S., Dallapiazza, R. F., Cowan, C. E., & Horne, M. C. (2012) · Journal of Biological Chemistry · doi:10.1074/jbc.m112.376855 · Cited by 63
Simioni, C., Cani, A., Martelli, A. M., Zauli, G., Tabellini, G., McCubrey, J. A., Capitani, S., & Neri, L. M. (2014) · Oncotarget · doi:10.18632/oncotarget.2490 · Cited by 60
Fallone, F., Britton, S., Nieto, L., Salles, B., & Muller, C. (2012) · Oncogene · doi:10.1038/onc.2012.462 · Cited by 56
Structure of the human ATM kinase and mechanism of Nbs1 binding
Warren, C., & Pavletich, N. P. (2022) · eLife · doi:10.7554/elife.74218 · Cited by 57
Structure of the human dimeric ATM kinase
Lau, W. C. Y., Li, Y., Liu, Z., Gao, Y., Zhang, Q., & Huen, M. S. Y. (2016) · Cell Cycle · doi:10.1080/15384101.2016.1158362 · Cited by 58
ATR inhibition enables complete tumour regression in ALK-driven NB mouse models
Szydzik, J., Lind, D. E., Arefin, B., Kurhe, Y., Umapathy, G., Siaw, J. T., Claeys, A., Gabre, J. L., den Eynden, J. V., Hallberg, B., et al. (2021) · Nature Communications · doi:10.1038/s41467-021-27057-2 · Cited by 51
DNA damage‐induced CHK1 autophosphorylation at Ser296 is regulated by an intramolecular mechanism
Okita, N., Minato, S., 近江恵理, Tanuma, S.-I., & Higami, Y. (2012) · FEBS Letters · doi:10.1016/j.febslet.2012.09.048 · Cited by 51
The Intersection of DNA Damage Response and Ferroptosis—A Rationale for Combination Therapeutics
Chen, P., Tseng, W. H.-S., & Chi, J. (2020) · Biology · doi:10.3390/biology9080187 · Cited by 51
Darżynkiewicz, Z., Zhao, H. L., Halicka, H. D., Rybak, P., Dobrucki, J. W., & Włodkowic, D. (2012) · Critical Reviews in Clinical Laboratory Sciences · doi:10.3109/10408363.2012.738808 · Cited by 50
Zhao, H. L., Rybak, P., Dobrucki, J. W., Traganos, F., & Darżynkiewicz, Z. (2011) · Cytometry Part A · doi:10.1002/cyto.a.21172 · Cited by 51
Lang, P. Y., Nanjangud, G. J., Sokolsky‐Papkov, M., Shaw, C., Hwang, D., Parker, J. S., Kabanov, A. V., & Gershon, T. R. (2016) · Development · doi:10.1242/dev.139022 · Cited by 46
Oxidative stress and cell senescence as drivers of ageing: Chicken and egg
von Zglinicki, T. (2024) · Ageing Research Reviews · doi:10.1016/j.arr.2024.102558 · Cited by 57
Schlam‐Babayov, S., Bensimon, A., Harel, M., Geiger, T., Aebersold, R. H., Ziv, Y., & Shiloh, Y. (2020) · The EMBO Journal · doi:10.15252/embj.2020104400 · Cited by 48
Aquarius is required for proper CtIP expression and homologous recombination repair
Sakasai, R., Isono, M., Wakasugi, M., HASHIMOTO, M. W., Sunatani, Y., Matsui, T., Shibata, A., Matsunaga, T., & Iwabuchi, K. (2017) · Scientific Reports · doi:10.1038/s41598-017-13695-4 · Cited by 45
Take your PIKK: tumour viruses and DNA damage response pathways
Pancholi, N. J., Price, A. M., & Weitzman, M. D. (2017) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2016.0269 · Cited by 44
Bhattacharjee, S., & Nandi, S. (2018) · Cancers · doi:10.3390/cancers10090298 · Cited by 44
ATR-mediated regulation of nuclear and cellular plasticity
Kidiyoor, G. R., Kumar, A., & Foiani, M. (2016) · DNA repair · doi:10.1016/j.dnarep.2016.05.020 · Cited by 45
Mind the gap: keeping UV lesions in check
Novarina, D., Amara, F., Lazzaro, F., Plevani, P., & Muzi-Falconi, M. (2011) · DNA Repair · doi:10.1016/j.dnarep.2011.04.030 · Cited by 43
Metadata
- Authors
- Lovejoy, C. A., & Cortez, D.
- Affiliations
- Vanderbilt University (US)
- Corresponding author
- Cortez, David
- Venue
- DNA Repair
- Publisher
- Elsevier BV
- Published
- 2009-09-02
- Volume
- 8
- Issue
- 9
- Pages
- 1004-1008
- ISSN
- 1568-7856 (ISSN-L)
- 1568-7864
- PMC
- PMC2725225
- OpenAlex
- W2023620387
- Cited by
- 277
- References
- 64
- Citations by year
- 2026: 11 · 2025: 3 · 2024: 14 · 2023: 12 · 2022: 9 · 2021: 23 · 2020: 15 · 2019: 22 · 2018: 16 · 2017: 16 · 2016: 19 · 2015: 15 · 2014: 16 · 2013: 22 · 2012: 17
- FWCI
- 8.60
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- DNA repair (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Cancer Institute (R01CA102729)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › DNA Repair Mechanisms
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › PI3K/AKT/mTOR signaling in cancer
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Protein Kinase Regulation and GTPase Signaling
- Keywords
- ATM, ATR, DNA-PKcs, mTOR, SMG1, kinase regulation, DNA damage response, nutrient signaling, nonsense-mediated mRNA decay, protein kinase signaling
- MeSH terms
- Animals, Humans, Protein Kinases, Protein Processing, Post-Translational, Enzyme Activators, Protein Transport
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