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A mammalian cell cycle checkpoint pathway utilizing p53 and GADD45 is defective in ataxia-telangiectasia
Abstract
Cell cycle checkpoints can enhance cell survival and limit mutagenic events following DNA damage. Primary murine fibroblasts became deficient in a G1 checkpoint activated by ionizing radiation (IR) when both wild-type p53 alleles were disrupted. In addition, cells from patients with the radiosensitive, cancer-prone disease ataxia-telangiectasia (AT) lacked the IR-induced increase in p53 protein levels seen in normal cells. Finally, IR induction of the human GADD45 gene, an induction that is also defective in AT cells, was dependent on wild-type p53 function. Wild-type but not mutant p53 bound strongly to a conserved element in the GADD45 gene, and a p53-containing nuclear factor, which bound this element, was detected in extracts from irradiated cells. Thus, we identified three participants (AT gene(s), p53, and GADD45) in a signal transduction pathway that controls cell cycle arrest following DNA damage; abnormalities in this pathway probably contribute to tumor development.
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“The p53 target genes BTG236, 154, 155 and GADD45A13, 156 can also induce G1/S and G2/M cell cycle arrest, respectively.”
From Census and evaluation of p53 target genes (2017) · cites this paper as [13]
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Cites
Single-Step Method of RNA Isolation by Acid Guanidinium Thiocyanate–Phenol–Chloroform Extraction
Chomczynski, P., & Sacchi, N. (1987) · Analytical Biochemistry · doi:10.1006/abio.1987.9999 · Cited by 65,515
Dignam, J. D., Lebovitz, R. M., & Roeder, R. G. (1983) · Nucleic Acids Research · doi:10.1093/nar/11.5.1475 · Cited by 11,262
p53 Mutations in Human Cancers
Hollstein, M., Sidransky, D., Vogelstein, B., & Harris, C. C. (1991) · Science · doi:10.1126/science.1905840 · Cited by 8,018
Self-citationMice 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
The E6 oncoprotein encoded by human papillomavirus types 16 and 18 promotes the degradation of p53
Scheffner, M., Werness, B. A., Huibregtse, J. M., Levine, A. J., & Howley, P. M. (1990) · Cell · doi:10.1016/0092-8674(90)90409-8 · Cited by 3,995
The Causes of Cancer: Quantitative Estimates of Avoidable Risks of Cancer in the United States Today
Doll, R., & Peto, R. (1981) · JNCI: Journal of the National Cancer Institute · doi:10.1093/jnci/66.6.1192 · Cited by 3,927 · cited 1×
“Discussion Exposure to DNA-damaging agents probably contributes to the development of a significant percentage of human cancers (Doll and Peto, 1981).”
BackgroundGerm Line p53 Mutations in a Familial Syndrome of Breast Cancer, Sarcomas, and Other Neoplasms
Malkin, D., Li, F. P., Strong, L. C., Fraumeni, J. F., Nelson, C. E., Kim, D. H., Kassel, J., Gryka, M. A., Bischoff, F. Z., Tainsky, M. A., et al. (1990) · Science · doi:10.1126/science.1978757 · Cited by 3,765
Participation of p53 protein in the cellular response to DNA damage.
Kastan, M. B., Onyekwere, O. C., Sidransky, D., Vogelstein, B., & Craig, R. W. (1991) · PubMed · Cited by 3,761
Self-citationThe Causes of Cancer: Quantitative Estimates of Avoidable Risks of Cancer in the United States Today
Peto, R. (1983) · Springer eBooks · doi:10.1007/978-1-4757-1117-2_30 · Cited by 3,504
Momand, J., Zambetti, G. P., Olson, D. C., George, D., & Levine, A. J. (1992) · Cell · doi:10.1016/0092-8674(92)90644-r · Cited by 3,113
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DNA damage response pathway in radioadaptive response
Sasaki, M. S., Ejima, Y., Tachibana, A., Yamada, T., Ishizaki, K., Shimizu, T., & Nomura, T. (2002) · Mutation research. Fundamental and molecular mechanisms of mutagenesis · doi:10.1016/s0027-5107(02)00084-2 · Cited by 166
Bcl-2 and p53 Protein Expression, Apoptosis, and p53 Mutation in Human Epithelial Ovarian Cancers
Chan, W. Y., Cheung, K., Schorge, J. O., Huang, L., Welch, W. R., Bell, D. A., Berkowitz, R. S., & Mok, S. C. (2000) · American Journal Of Pathology · doi:10.1016/s0002-9440(10)64744-x · Cited by 175
Verhaegh, G. W. C. T., Richard, M., & Hainaut, P. L. (1997) · Molecular and Cellular Biology · doi:10.1128/mcb.17.10.5699 · Cited by 168
Cellular radiosensitivity: How much better do we understand it?
Jeggo, P. A., & Lavin, M. F. (2009) · International Journal of Radiation Biology · doi:10.3109/09553000903261263 · Cited by 175
Inhibition of p53 Transactivation Function by the Human T-Cell Lymphotropic Virus Type 1 Tax Protein
Pise-Masison, C. A., Choi, K. S., Radonovich, M. F., Dittmer, J., Kim, S., & Brady, J. N. (1998) · Journal of Virology · doi:10.1128/jvi.72.2.1165-1170.1998 · Cited by 172
Orchestration of DNA Damage Checkpoint Dynamics across the Human Cell Cycle
Chao, H. X., Poovey, C. E., Privette, A. A., Grant, G. D., Chao, H. Y., Cook, J. G., & Purvis, J. E. (2017) · Cell Systems · doi:10.1016/j.cels.2017.09.015 · Cited by 167
Chi, S.-W., Ayed, A., & Arrowsmith, C. H. (1999) · The EMBO Journal · doi:10.1093/emboj/18.16.4438 · Cited by 173
Blagosklonny, M. V. (2000) · The FASEB Journal · doi:10.1096/fj.99-1078rev · Cited by 170
Mammalian GADD34, an Apoptosis- and DNA Damage-inducible Gene
Hollander, M. C., Zhan, Q., Bae, I., & Fornace, A. J. (1997) · Journal of Biological Chemistry · doi:10.1074/jbc.272.21.13731 · Cited by 166
Self-citationMomand, J. A., & Zambetti, G. P. (1997) · Journal of Cellular Biochemistry · doi:10.1002/(sici)1097-4644(19970301)64:3 · Cited by 167
The Secondary Leukemias: Challenges and Research Directions
Smith, M. A., McCaffrey, R. P., & Karp, J. E. (1996) · JNCI Journal of the National Cancer Institute · doi:10.1093/jnci/88.7.407 · Cited by 166
Darnell, G. A., & Richardson, D. R. (1999) · Blood · doi:10.1182/blood.v94.2.781 · Cited by 168
Role for BRG1 in Cell Cycle Control and Tumor Suppression
Hendricks, K. B., Shanahan, F., & Lees, E. M. (2003) · Molecular and Cellular Biology · doi:10.1128/mcb.24.1.362-376.2004 · Cited by 163
Navas, T. A., Sánchez, Y., & Elledge, S. J. (1996) · Genes & Development · doi:10.1101/gad.10.20.2632 · Cited by 167
A multispecialty approach to the diagnosis and management of pancreatic cancer
Hawes, R. H., Xiong, Q., Waxman, I., Chang, K. J., Evans, D. B., & Abbruzzese, J. L. (2000) · The American Journal of Gastroenterology · doi:10.1111/j.1572-0241.2000.01699.x · Cited by 165
Phosphorylation of murine p53 at Ser-18 regulates the p53 responses to DNA damage
Chao, C., Saito, S., Anderson, C. W., Appella, E., & Xu, Y. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.220252297 · Cited by 168
Gottlieb, E., Haffner, R., King, A., Asher, G., Gruss, P., Lonai, P., & Oren, M. (1997) · The EMBO Journal · doi:10.1093/emboj/16.6.1381 · Cited by 165
Calorie restriction delays spontaneous tumorigenesis in p53-knockout transgenic mice.
Hursting, S. D., Perkins, S. N., & Phang, J. M. (1994) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.91.15.7036 · Cited by 166
A DNA End-Binding Factor Involved in Double-Strand Break Repair and V(D)J Recombination
Rathmell, W. K., & Chu, G. (1994) · Molecular and Cellular Biology · doi:10.1128/mcb.14.7.4741 · Cited by 166
p53-dependent repression of CDK4 translation in TGF-beta-induced G1 cell-cycle arrest.Preprint
Ewen, M. E., Oliver, C. J., Sluss, H. K., Miller, S. J., & Peeper, D. S. (1995) · Genes & Development · doi:10.1101/gad.9.2.204 · Cited by 165
Proteolysis by Calpains: a Possible Contribution to Degradation of p53
Pariât, M., Carillo, S., Molinari, M., Salvat, C., Debüssche, L., Bracco, L. P., Milner, J., & Piechaczyk, M. (1997) · Molecular and Cellular Biology · doi:10.1128/mcb.17.5.2806 · Cited by 163
The specificity of p53 mutation spectra in sunlight induced human cancers
Daya–Grosjean, L., Dumaz, N., & Sarasin, A. R. (1995) · Journal of Photochemistry and Photobiology B Biology · doi:10.1016/1011-1344(95)07130-t · Cited by 162
Bakalkin, G. Y., Selivanova, G., Yakovleva, T., Владимировна, К. Е., Kashuba, E., Magnússon, K. P., Székely, L., Klein, G., Terenius, L. Y., & Wiman, K. G. (1995) · Nucleic Acids Research · doi:10.1093/nar/23.3.362 · Cited by 166
The role of DNA damage responses in p53 biology
Speidel, D. (2015) · Archives of Toxicology · doi:10.1007/s00204-015-1459-z · Cited by 172
Thottassery, J. V., Zambetti, G. P., Arimori, K., Schuetz, E. G., & Schuetz, J. D. (1997) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.94.20.11037 · Cited by 161
Amson, R. B., Nemani, M., Roperch, J.-P., Israeli, D., Bougueleret, L., Gall, I. L., Medhioub, M., Linares‐Cruz, G., Lethrosne, F., Pasturaud, P., et al. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.9.3953 · Cited by 165
Gottlieb, E., Haffner, R., von Rüden, T., Wagner, E. F., & Oren, M. (1994) · The EMBO Journal · doi:10.1002/j.1460-2075.1994.tb06390.x · Cited by 163
Bulavin, D. V., Kovalsky, O., Hollander, M. C., & Fornace, A. J. (2003) · Molecular and Cellular Biology · doi:10.1128/mcb.23.11.3859-3871.2003 · Cited by 161
Self-citationCaught in the cross fire: p53 in inflammation
Cooks, T., Harris, C. C., & Oren, M. (2014) · Carcinogenesis · doi:10.1093/carcin/bgu134 · Cited by 162
Involvement of p53 in cell differentiation and development
Almog, N., & Rotter, V. (1997) · Biochimica et Biophysica Acta (BBA) - Reviews on Cancer · doi:10.1016/s0304-419x(97)00012-7 · Cited by 163
Fragments of ATM Which Have Dominant-Negative or Complementing Activity
Morgan, S. E., Lovly, C. M., Pandita, T. K., Shiloh, Y., & Kastan, M. B. (1997) · Molecular and Cellular Biology · doi:10.1128/mcb.17.4.2020 · Cited by 161
Self-citationLu, H., Taya, Y., Ikeda, M., & Levine, A. J. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.11.6399 · Cited by 162
Effects of Radiation on Cerebral Vasculature: A Review
O'Connor, M. M., & Mayberg, M. R. (2000) · Neurosurgery · doi:10.1093/neurosurgery/46.1.138 · Cited by 161
p53 regulation of DNA excision repair pathways
Smith, M. L. (2002) · Mutagenesis · doi:10.1093/mutage/17.2.149 · Cited by 164
Brown, K. D., Ziv, Y., Sadanandan, S., Chessa, L., Collins, F. S., Shiloh, Y., & Tagle, D. A. (1997) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.94.5.1840 · Cited by 161
Responses to DNA damage and regulation of cell cycle checkpoints by the ATM protein kinase family
Hoekstra, M. F. (1997) · Current Opinion in Genetics & Development · doi:10.1016/s0959-437x(97)80125-6 · Cited by 160
The transcription factor p53: Not a repressor, solely an activator.
Fischer, M., Steiner, L., & Engeland, K. (2014) · Cell Cycle · doi:10.4161/15384101.2014.949083 · Cited by 153
MacLachlan, T. K., Takimoto, R., & El‐Deiry, W. S. (2002) · Molecular and Cellular Biology · doi:10.1128/mcb.22.12.4280-4292.2002 · Cited by 160
Self-citationGenetic alterations in adult diffuse glioma: occurrence, significance, and prognostic implications
Justin, S. S. (2000) · Frontiers in bioscience · doi:10.2741/smith · Cited by 160
Knudson, A. G. (2002) · American Journal of Medical Genetics · doi:10.1002/ajmg.10320 · Cited by 160
Ataxia-Telangiectasia: Closer to Unraveling the Mystery
Shiloh, Y. (1995) · European Journal of Human Genetics · doi:10.1159/000472285 · Cited by 159
Regulation and Mechanisms of Mammalian Gene Amplification
Stark, G. R. (1993) · Advances in cancer research · doi:10.1016/s0065-230x(08)60956-2 · Cited by 159
Hypothesis: Ataxia‐telangiectasia: Is ATM a sensor of oxidative damage and stress?
Rotman, G., & Shiloh, Y. (1997) · BioEssays · doi:10.1002/bies.950191011 · Cited by 160
Early stages of p53-induced apoptosis are reversible
Geske, F. J., Lieberman, R., Strange, R., & Gerschenson, L. E. (2001) · Cell Death and Differentiation · doi:10.1038/sj.cdd.4400786 · Cited by 157
Current and potential therapeutic strategies for the treatment of ataxia-telangiectasia
Lavin, M. F., Gueven, N., Bottle, S. E., & Gatti, R. A. (2007) · British Medical Bulletin · doi:10.1093/bmb/ldm012 · Cited by 159
Giladi, M., Munster, M., Schneiderman, R. S., Voloshin, T., Porat, Y., Blat, R., Zielinska-Chomej, K., Hååg, P., Bomzon, Z., Kirson, E. D., et al. (2017) · Radiation Oncology · doi:10.1186/s13014-017-0941-6 · Cited by 160
Koutsodontis, G., Tentes, I. K., Papakosta, P., Moustakas, A., & Kardassis, D. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m104130200 · Cited by 159
Dickkopf-1, an inhibitor of the Wnt signaling pathway, is induced by p53
Wang, J., Shou, J., & Chen, X. (2000) · Oncogene · doi:10.1038/sj.onc.1203503 · Cited by 160
Adenovirus E1B 55K Represses p53 Activation In Vitro
Martin, M. E. D., & Berk, A. J. (1998) · Journal of Virology · doi:10.1128/jvi.72.4.3146-3154.1998 · Cited by 159
p53 Negatively Regulates cdc2 Transcription via the CCAAT-binding NF-Y Transcription Factor
Yun, J., Chae, H., Choy, H. E., Chung, J., Yoo, H., Han, M.-H., & Shin, D. Y. (1999) · Journal of Biological Chemistry · doi:10.1074/jbc.274.42.29677 · Cited by 155
The p53-Binding Protein 53BP2 Also Interacts with Bcl2 and Impedes Cell Cycle Progression at G 2 /M
Naumovski, L., & Cleary, M. L. (1996) · Molecular and Cellular Biology · doi:10.1128/mcb.16.7.3884 · Cited by 156
Inhibitors of the Cip/Kip Family
Hengst, L., & Reed, S. I. (1998) · Current topics in microbiology and immunology · doi:10.1007/978-3-642-71941-7_2 · Cited by 155
Dantzer, F. (1998) · Nucleic Acids Research · doi:10.1093/nar/26.8.1891 · Cited by 155
Cell cycle-dependent expression of the mouseRad51 gene in proliferating cells
Yamamoto, A., Yagi, H., Habu, T., Yoshimura, Y., Matsushiro, A., Nishimune, Y., Morita, T., Taki, T., Yoshida, K., Yamamoto, K., et al. (1996) · Molecular and General Genetics MGG · doi:10.1007/bf02174338 · Cited by 155
Ionizing radiation activates the ATM kinase throughout the cell cycle
Pandita, T. K., Lieberman, H. B., Lim, D., Dhar, S., Zheng, W., Taya, Y., & Kastan, M. B. (2000) · Oncogene · doi:10.1038/sj.onc.1203444 · Cited by 155
Self-citationOkamoto, T., Izumi, H., Imamura, T., Takano, H., Ise, T., Uchiumi, T., Kuwano, M., & Kohno, K. (2000) · Oncogene · doi:10.1038/sj.onc.1204029 · Cited by 159
Splitting the ATM: distinct repair and checkpoint defects in ataxia–telangiectasia
Jeggo, P. A., Carr, A. M., & Lehmann, A. R. (1998) · Trends in Genetics · doi:10.1016/s0168-9525(98)01511-x · Cited by 156
Lu, W.-J., Lee, N. P. Y., Kaul, S. C., Lan, F., Poon, R. T. P., Wadhwa, R., & Luk, J. M. (2011) · Cell Death and Differentiation · doi:10.1038/cdd.2010.177 · Cited by 160
Zhan, Q., Chen, I. T., Antinore, M. J., & Fornace, A. J. (1998) · Molecular and Cellular Biology · doi:10.1128/mcb.18.5.2768 · Cited by 154
Self-citationPhosphorylation of Serine 18 Regulates Distinct p53 Functions in Mice
Sluss, H. K., Armata, H., Gallant, J., & Jones, S. N. (2004) · Molecular and Cellular Biology · doi:10.1128/mcb.24.3.976-984.2004 · Cited by 152
Lu, H., Fisher, R. P., Bailey, P., & Levine, A. J. (1997) · Molecular and Cellular Biology · doi:10.1128/mcb.17.10.5923 · Cited by 156
Ball, K. L., Laı́n, S., Fåhræus, R., Smythe, C., & Lane, D. P. (1997) · Current Biology · doi:10.1016/s0960-9822(06)00029-7 · Cited by 156
Apoptosis, cancer and the p53 tumour suppressor gene
Lee, J. M., & Bernstein, A. (1995) · Cancer and Metastasis Reviews · doi:10.1007/bf00665797 · Cited by 149
Inhibition of DNA Topoisomerase IIα Gene Expression by the p53 Tumor Suppressor
Wang, Q., Zambetti, G. P., & Suttle, D. P. (1997) · Molecular and Cellular Biology · doi:10.1128/mcb.17.1.389 · Cited by 152
E2F1 Uses the ATM Signaling Pathway to Induce p53 and Chk2 Phosphorylation and Apoptosis
Powers, J. T., Hong, S., Mayhew, C. N., Rogers, P. M., Knudsen, E. S., & Johnson, D. G. (2004) · Molecular Cancer Research · doi:10.1158/1541-7786.203.2.4 · Cited by 152
Wickremasinghe, R. G., & Hoffbrand, A. V. (1999) · Blood · doi:10.1182/blood.v93.11.3587 · Cited by 151
Chang, Y., Lee, Y. S., Tejima, T., Tanaka, K., Ōmura, S., Heintz, N. H., Mitsui, Y., & Magae, J. (1998) · PubMed · Cited by 152
p53 stabilization in response to DNA damage requires Akt/PKB and DNA-PK
Boehme, K. A., Kulikov, R., & Blattner, C. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0703423105 · Cited by 152
Human homologue of S. pombe Rad9 interacts with BCL-2/BCL-xL and promotes apoptosis
Komatsu, K., Miyashita, T., Hang, H., Hopkins, K. M., Zheng, W., Cuddeback, S. M., Yamada, M., Lieberman, H. B., & Wang, H. (1999) · Nature Cell Biology · doi:10.1038/71316 · Cited by 151
Cell cycle-dependent and ATM-independent expression of human Chk1 kinase
Kaneko, Y., Watanabe, N., Morisaki, H., Akita, H., Fujimoto, A., Tominaga, K., Terasawa, M., Tachibana, A., Ikeda, K., & Nakanishi, M. (1999) · Oncogene · doi:10.1038/sj.onc.1202706 · Cited by 150
The impact of heterochromatin on DSB repair
Goodarzi, A. A., Noon, A. T., & Jeggo, P. A. (2009) · Biochemical Society Transactions · doi:10.1042/bst0370569 · Cited by 149
Arima, Y., Nitta, M., Kuninaka, S., Zhang, D., Fujiwara, T., Taya, Y., Nakao, M., & Saya, H. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m410691200 · Cited by 149
Epperly, M. W., Gretton, J. E., Sikora, C. A., Jefferson, M., Bernarding, M., Nie, S., & Greenberger, J. S. (2003) · Radiation Research · doi:10.1667/rr3081 · Cited by 150
Apoptosis and protein expression after focal cerebral ischemia in rat
Li, Y., Chopp, M., Powers, C., & Jiang, N. (1997) · Brain Research · doi:10.1016/s0006-8993(97)00524-6 · Cited by 151
The dual role model for p53 in maintaining genomic integrity
Janus, F., Albrechtsen, N. J. W., Dornreiter, I., Wiesmüller, L., Große, F., & Deppert, W. (1999) · Cellular and Molecular Life Sciences · doi:10.1007/s000180050266 · Cited by 154
Cross-Referencing Eukaryotic Genomes: TIGR Orthologous Gene Alignments (TOGA)Preprint
Lee, Y., Sultana, R., Pertea, G. M., Cho, J., Karamycheva, S. A., Tsai, J., Parvizi, B., Cheung, F., Antonescu, V., White, J., et al. (2002) · Genome Research · doi:10.1101/gr.212002 · Cited by 150
Regulation of the Chk2 protein kinase by oligomerization-mediated cis- and trans-phosphorylation.
Schwarz, J. K., Lovly, C. M., & Piwnica-Worms, H. M. (2003) · PubMed · Cited by 147
p53 GENE MUTATIONS AND PHOTOCARCINOGENESIS
Nataraj, A. J., Trent, J. C., & Ananthaswamy, H. N. (1995) · Photochemistry and Photobiology · doi:10.1111/j.1751-1097.1995.tb05262.x · Cited by 147
Cip1 inhibits DNA replication but not PCNA-dependent nucleotide excision—repair
Shivji, M. K. K., Grey, S. J., Strausfeld, U. P., Wood, R. D., & Blow, J. J. (1994) · Current Biology · doi:10.1016/s0960-9822(00)00244-x · Cited by 149
DNA Damages Processed by Base Excision Repair: Biological Consequences
Wallace, S. S. (1994) · International Journal of Radiation Biology · doi:10.1080/09553009414551661 · Cited by 146
Strategies for manipulating the p53 pathway in the treatment of human cancer
Hupp, T. R., Lane, D. P., & Ball, K. L. (2000) · Biochemical Journal · doi:10.1042/bj3520001 · Cited by 148
Roles of Histone Deacetylases and Inhibitors in Anticancer Therapy
Verza, F. A., Das, U., Fachin, A. L., Dimmock, J. R., & Marins, M. (2020) · Cancers · doi:10.3390/cancers12061664 · Cited by 149
McKinney, K. M., & Prives, C. L. (2002) · Molecular and Cellular Biology · doi:10.1128/mcb.22.19.6797-6808.2002 · Cited by 149
Siede, W., Friedberg, A. S., Dianova, I. I., & Friedberg, E. C. (1994) · Genetics · doi:10.1093/genetics/138.2.271 · Cited by 145
Ang, H. C., Joerger, A. C., Mayer, S., & Fersht, A. R. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.m604209200 · Cited by 148
Fisher, C., Gillett, C. E., Vojtěšek, B., Barnes, D. M., & Millis, R. (1994) · British Journal of Cancer · doi:10.1038/bjc.1994.4 · Cited by 145
Kim, J. M., Yoon, Y., & Tsang, B. K. (1999) · Endocrinology · doi:10.1210/en.140.5.2307 · Cited by 147
Baptiste, N., Friedlander, P. A., Chen, X., & Prives, C. L. (2002) · Oncogene · doi:10.1038/sj.onc.1205015 · Cited by 149
PAC1 phosphatase is a transcription target of p53 in signalling apoptosis and growth suppression
Yin, Y., Liu, Y., Jin, Y. J., Hall, E. J., & Barrett, J. C. (2003) · Nature · doi:10.1038/nature01519 · Cited by 145
The regulation of p53 function: Steiner award lecture
Lane, D. P. (1994) · International Journal of Cancer · doi:10.1002/ijc.2910570502 · Cited by 144
p53 Down-regulates Human Matrix Metalloproteinase-1 (Collagenase-1) Gene Expression
Sun, Y., Sun, Y., Wenger, L., Rutter, J. L., Brinckerhoff, C., & Cheung, H. S. (1999) · Journal of Biological Chemistry · doi:10.1074/jbc.274.17.11535 · Cited by 145
Shay, J. W., Tomlinson, G. E., Piatyszek, M. A., & Gollahon, L. (1995) · Molecular and Cellular Biology · doi:10.1128/mcb.15.1.425 · Cited by 145
Molecular mechanisms of photocarcinogenesis
Matsumura, Y. (2002) · Frontiers in bioscience · doi:10.2741/matsumur · Cited by 143
Direct involvement of p53 in the base excision repair pathway of the DNA repair machinery
Offer, H., Wolkowicz, R., Matas, D., Blumenstein, S., Livneh, Z., & Rotter, V. (1999) · FEBS Letters · doi:10.1016/s0014-5793(99)00505-0 · Cited by 150
The Role of p53 in Cell Cycle Regulation
Shaw, P. H. (1996) · Pathology - Research and Practice · doi:10.1016/s0344-0338(96)80088-4 · Cited by 150
Pise-Masison, C. A., Mahieux, R., Jiang, H., Ashcroft, M. A., Radonovich, M. F., Duvall, J. F., Guillerm, C., & Brady, J. N. (2000) · Molecular and Cellular Biology · doi:10.1128/.20.10.3377-3386.2000 · Cited by 148
Defective G2 checkpoint function in cells from individuals with familial cancer syndromes.
Paules, R. S., Levedakou, E. N., Wilson, S. J., Innes, C. L., Rhodes, N., Tlsty, T. D., Galloway, D. A., Donehower, L. A., Tainsky, M. A., & Kaufmann, W. K. (1995) · PubMed · Cited by 143
Dirmeier, U., Hoffmann, R. F. G., Kilger, E., Schultheiß, U., Briseño, C., Gires, O., Kieser, A., Eick, D., Sugden, B., & Hammerschmidt, W. (2005) · Oncogene · doi:10.1038/sj.onc.1208367 · Cited by 143
The loss of mdm2 induces p53 mediated apoptosis
de Rozìeres, S., Maya, R. B.-Y., Oren, M., & Lozano, G. (2000) · Oncogene · doi:10.1038/sj.onc.1203468 · Cited by 146
p53 Mutations in Barrett's adenocarcinoma and high-grade dysplasia
Neshat, K., Sanchez, C. A., Galipeau, P. C., Blount, P. L., Levine, D. S., Joslyn, G., & Reid, B. J. (1994) · Gastroenterology · doi:10.1016/0016-5085(94)90415-4 · Cited by 143
Metadata
- Authors
- Kastan, M. B., Zhan, Q., El-Deiry, W. S., Carrier, F., Jacks, T., Walsh, W. V., Plunkett, B. S., Vogelstein, B., & Fornace, A. J.
- Affiliations
- Johns Hopkins University (US)
- National Cancer Institute (US)
- Massachusetts Institute of Technology (US)
- Venue
- Cell
- Publisher
- Elsevier BV
- Published
- 1992-11
- Volume
- 71
- Issue
- 4
- Pages
- 587-597
- ISSN
- 0092-8674 (ISSN-L)
- OpenAlex
- W1986179131
- Cited by
- 3,047
- References
- 64
- Citations by year
- 2026: 11 · 2025: 16 · 2024: 17 · 2023: 20 · 2022: 23 · 2021: 23 · 2020: 24 · 2019: 16 · 2018: 31 · 2017: 34 · 2016: 35 · 2015: 43 · 2014: 44 · 2013: 30 · 2012: 48
- FWCI
- 86.58
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Cell (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Cancer Institute (CA 09071, CA43460, T32CA009071)
- National Institute of Environmental Health Sciences (ES05777)
- Topics
- Health Sciences › Medicine › Oncology › Cancer-related Molecular Pathways
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › DNA Repair Mechanisms
- Health Sciences › Medicine › Radiology, Nuclear Medicine and Imaging › Effects of Radiation Exposure
- Keywords
- ataxia telangiectasia, p53, GADD45, cell cycle checkpoints, G1/S checkpoint, ionizing radiation, DNA damage response, cell cycle arrest, signal transduction, cancer susceptibility, radiosensitivity
- MeSH terms
- Amino Acid Sequence, Animals, Ataxia Telangiectasia, Base Sequence, Cell Cycle, Cell Line, Cloning, Molecular, DNA Damage, DNA Repair, Gene Expression Regulation, Humans, Molecular Sequence Data, Genes, p53, Mutagenesis, Mice
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