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The Ink4a tumor suppressor gene product, p19Arf, interacts with MDM2 and neutralizes MDM2’s inhibition of p53
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The INK4a gene encodes two distinct growth inhibitors--the cyclin-dependent kinase inhibitor p16Ink4a, which is a component of the Rb pathway, and the tumor suppressor p19Arf, which has been functionally linked to p53. Here we show that p19Arf potently suppresses oncogenic transformation in primary cells and that this function is abrogated when p53 is neutralized by viral oncoproteins and dominant-negative mutants but not by the p53 antagonist MDM2. This finding, coupled with the observations that p19Arf and MDM2 physically interact and that p19Rrf blocks MDM2-induced p53 degradation and transactivational silencing, suggests that p19Arf functions mechanistically to prevent MDM2's neutralization of p53. Together, our findings ascribe INK4a's potent tumor suppressor activity to the cooperative actions of its two protein products and their relation to the two central growth control pathways, Rb and p53.
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“p19 Arf has been shown to inhibit Mdm2-mediated degradation of p53 (19-21) and is clearly required for activation of p53 in response to aberrant cell cycle entry (19) and oncogene activation (22-24).”
From Ink4a / Arf tumor suppressor does not modulate the degenerative conditions or tumor spectrum of the telomerase-deficient mouse (2007) · cites this paper as [19]
In the citing paper
“Under most conditions ARF functions as a tumor suppressor by binding and inhibiting Mdm2 activity [47–49].”
From Integration of DNA damage and repair with murine double-minute 2 (Mdm2) in tumorigenesis (2012) · cites this paper as [48]
Citations
Cites
WAF1, a potential mediator of p53 tumor suppression
El-Deiry, W. S., Tokino, T., Velculescu, V. E., Levy, D. B., Parsons, R., Trent, J. M., Lin, D., Mercer, W. E., Kinzler, K. W., & Vogelstein, B. (1993) · Cell · doi:10.1016/0092-8674(93)90500-p · Cited by 8,321
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
p53, the cellular gatekeeper for growth and division
Levine, A. J. (1997) · Cell · doi:10.1016/s0092-8674(00)81871-1 · Cited by 7,693
Recombinant Genomes Which Express Chloramphenicol Acetyltransferase in Mammalian Cells
Gorman, C., Moffat, L. F., & Howard, B. H. (1982) · Molecular and Cellular Biology · doi:10.1128/mcb.2.9.1044 · Cited by 7,674
Sherr, C. J. (1996) · Science · doi:10.1126/science.274.5293.1672 · Cited by 5,379
The retinoblastoma protein and cell cycle control
Weinberg, R. A. (1995) · Cell · doi:10.1016/0092-8674(95)90385-2 · Cited by 4,862
Mdm2 promotes the rapid degradation of p53
Haupt, Y., Maya, R., Kazaz, A., & Oren, M. (1997) · Nature · doi:10.1038/387296a0 · Cited by 4,506
The p53 tumour suppressor gene
Levine, A. J., Momand, J. A., & Finlay, C. A. (1991) · Nature · doi:10.1038/351453a0 · Cited by 3,785
A new regulatory motif in cell-cycle control causing specific inhibition of cyclin D/CDK4.
Serrano, M., Hannon, G. J., & Beach, D. (1993) · Nature · doi:10.1038/366704a0 · Cited by 3,650
Regulation of p53 stability by Mdm2
Kubbutat, M. H. G., Jones, S. N., & Vousden, K. H. (1997) · Nature · doi:10.1038/387299a0 · Cited by 3,312
Research works printed but not linked: 6
- Brenner, 1996, Preferential loss of expression of p16INK4a rather than p19ARF in breast cancer, Clin. Cancer Res., 2, 1993
- Elledge, 1996, A question of balance, Trends Biochem. Sci., 6, 388
- Kinoshita, 1996, Altered p16INK4 and retinoblastoma protein status in non-small cell lung cancer, Cancer Res., 56, 5557
- Quelle, 1995, Cloning and characterization of murine p16INK4a and p15INK4b genes, Oncogene, 11, 635
- Schreiber-Agus, 1994, Evolutionary relationships and functional conservation among vertebrate Max-associated proteins, Oncogene, 9, 3167
- Schreiber-Agus, 1997, An amino-terminal domain of Mxi1 mediates anti-Myc oncogenic activity and interacts with a homolog of the yeast transcriptional repressor SIN3, Cell, 80, 777, 10.1016/0092-8674(95)90356-9 · DOI
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RetractedHorie, S., Endo, K., Kawasaki, H., & Terada, T. (2000) · Archiv für Pathologische Anatomie und Physiologie und für Klinische Medicin · doi:10.1007/s004280000201 · Cited by 44
Kral, B. G., Mathias, R. A., Suktitipat, B., Ruczinski, I., Vaidya, D. M., Yanek, L. R., Quyyumi, A. A., Patel, R. S., Zafari, A. M., Vaccarino, V., et al. (2011) · Journal of Human Genetics · doi:10.1038/jhg.2010.171 · Cited by 44
Lassman, A. B. (2004) · Current Neurology and Neuroscience Reports · doi:10.1007/s11910-004-0043-3 · Cited by 44
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Royds, J. A., Hibma, M. H., Dix, B. R., Hananeia, L., Russell, I. A., Wiles, A. K., Wynford‐Thomas, D., & Braithwaite, A. W. (2005) · Oncogene · doi:10.1038/sj.onc.1209185 · Cited by 44
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Modestou, M., Puig-Antich, V., Korgaonkar, C. K., Eapen, A. K., & Quelle, D. E. (2001) · PubMed · Cited by 44
Ayrault, O., Andrique, L., Larsen, C., & Seité, P. (2004) · Oncogene · doi:10.1038/sj.onc.1207968 · Cited by 44
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Pollice, A., Nasti, V., Ronca, R., Vivo, M., Iacono, M. L., Calogero, R., Calabrò, V., & Mantia, G. L. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m310957200 · Cited by 46
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Neilsen, P. M., Pishas, K. I., Callen, D. F., & Thomas, D. M. (2010) · Sarcoma · doi:10.1155/2011/746939 · Cited by 43
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Feng, M.-Y., Wang, K., Song, H., Yu, H., Yu, Q., Shi, Q., & Geng, J. (2009) · Clinical & Experimental Metastasis · doi:10.1007/s10585-009-9291-6 · Cited by 43
Identification of Novel ARF Binding Proteins by Two-Hybrid Screening
Tompkins, V. S., Hagen, J., Zediak, V. P., & Quelle, D. E. (2006) · Cell Cycle · doi:10.4161/cc.5.6.2560 · Cited by 43
ARF mutation accelerates pituitary tumor development in Rb +/− mice
Tsai, K. Y., MacPherson, D. P., Rubinson, D. A., Nikitin, A. Y., Bronson, R. T., Mercer, K. L., Crowley, D. G., & Jacks, T. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.262499599 · Cited by 43
Ferrigno, P. K., & Silver, P. A. (1999) · Oncogene · doi:10.1038/sj.onc.1203132 · Cited by 43
Liu, Y., & Zacksenhaus, E. (2000) · Oncogene · doi:10.1038/sj.onc.1203996 · Cited by 43
Gillett, C., & Barnes, D. M. (1998) · Molecular Pathology · doi:10.1136/mp.51.6.310 · Cited by 43
Chen, J., Riazifar, H., Guan, M., & Huang, T. (2016) · Stem Cell Research & Therapy · doi:10.1186/s13287-015-0264-1 · Cited by 42
Fan, S., Yuan, R., Ma, Y. X., Xiong, J., Meng, Q., Erdos, M. R., Zhao, J.-N., Goldberg, I. D., Pestell, R. G., & Rosen, E. M. (2001) · Oncogene · doi:10.1038/sj.onc.1204666 · Cited by 42
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Bardeesy, N. M., Wong, K., DePinho, R. A., & Chin, L. (2000) · Advances in cancer research · doi:10.1016/s0065-230x(00)79004-x · Cited by 43
Self-citationRole of Retinoblastoma Tumor Suppressor Protein in DNA Damage Response
Wang, S. N. J. Y. J. (2001) · Acta Oncologica · doi:10.1080/02841860152619098 · Cited by 42
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Kumari, R., Kohli, S., & Das, S. (2014) · Molecular & Cellular Oncology · doi:10.4161/23723548.2014.969653 · Cited by 41
Mo, Q., Li, R., Adeegbe, D. O., Peng, G., & Chan, K. S. (2020) · Communications Biology · doi:10.1038/s42003-020-01491-2 · Cited by 41
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MDM2 expression during mouse embryogenesis and the requirement of p53
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Shah, N., Oseth, L., & LeBien, T. W. (1998) · Blood · doi:10.1182/blood.v92.10.3817 · Cited by 41
Bergsmedh, A., Szeles, A., Spetz, A., & Holmgren, L. (2002) · PubMed · Cited by 41
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Tam, A. S. M., Foley, J. F., Devereux, T. R., Maronpot, R. R., & Massey, T. E. (1999) · PubMed · Cited by 40
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Koch, P., Gatfield, J., Löber, C., Hobom, U., Lenz-Stöppler, C., Roth, J., & Dobbelstein, M. (2001) · PubMed · Cited by 40
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Kotsinas, A., Evangelou, K., Zacharatos, P., Kittas, C. N., & Gorgoulis, V. G. (2002) · American Journal Of Pathology · doi:10.1016/s0002-9440(10)64440-9 · Cited by 40
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Pfister, C., LaRue, H., Moore, L., Lacombe, L., Veilleux, C., Têtu, B., Meyer, F., & Fradet, Y. (2000) · International Journal of Cancer · doi:10.1002/(sici)1097-0215(20000120)89:1 · Cited by 30
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Lv, H., Liu, R., Fu, J., Yang, Q., Shi, J., Chen, P., Ji, M., Shi, B., & Hou, P. (2014) · Cell Cycle · doi:10.4161/15384101.2014.947203 · Cited by 39
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Baithun, S. I., Naase, M., Blanes, A., & Díaz‐Cano, S. J. (2001) · Archiv für Pathologische Anatomie und Physiologie und für Klinische Medicin · doi:10.1007/s004280000289 · Cited by 39
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Benanti, J. A., Wang, M. L., Myers, H. E., Robinson, K. L., Grandori, C., & Galloway, D. A. (2007) · Molecular Cancer Research · doi:10.1158/1541-7786.mcr-06-0372 · Cited by 39
Discrete signaling pathways participate in RB-dependent responses to chemotherapeutic agents
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Stadler, W. M., Steinberg, G. D., Yang, X. J., Hagos, F., Turner, C., & Olopade, O. I. (2001) · PubMed · Cited by 39
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van Schanke, A., van Venrooij, G. M. C. A. L., Jongsma, M. J., Banus, H. A., Mullenders, L. H. F., van Kranen, H. J., & de Gruijl, F. R. (2006) · Cancer Research · doi:10.1158/0008-5472.can-05-2476 · Cited by 38
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Willmer, T., Hare, S., Peres, J., & Prince, S. (2016) · Cell Division · doi:10.1186/s13008-016-0019-0 · Cited by 40
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Lecane, P. S., Kiviharju, T. M., Sellers, R. G., & Peehl, D. M. (2003) · The Prostate · doi:10.1002/pros.10197 · Cited by 38
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The Structure of the Vertebrate Lens
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Nakazawa, Y., Kamijo, T., Koike, K., & Noda, T. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m300510200 · Cited by 38
Itoshima, T., Fujiwara, T., Waku, T., Shao, J., Kataoka, M., Yarbrough, W. G., Liu, T.-J., Roth, J., Tanaka, N., & Kodama, M. (2000) · PubMed · Cited by 38
Gorgoulis, V. G., Zacharatos, P., Kotsinas, A., Mariatos, G., Liloglou, T., Vogiatzi, T., Foukas, P., Rassidakis, G. Z., Garinis, G. A., Ioannides, T., et al. (2000) · Molecular Medicine · doi:10.1007/bf03402115 · Cited by 38
Ågesen, T. H., Flørenes, V. A., Molenaar, W. M., Lind, G. E., Berner, J., Plaat, B. E. C., Komdeur, R., Myklebost, O., van den Berg, E., & Lothe, R. A. (2005) · Journal of Neuropathology & Experimental Neurology · doi:10.1093/jnen/64.1.74 · Cited by 38
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Ono, W., Hayashi, Y., Yokoyama, W., Kuroda, T., Kishimoto, H., Ito, I., Kimura, K., Akaogi, K., Waku, T., & Yanagisawa, J. (2013) · Journal of Biological Chemistry · doi:10.1074/jbc.m113.474049 · Cited by 39
Walter, G., & Ruediger, R. (2012) · Cell Cycle · doi:10.4161/cc.11.3.19057 · Cited by 38
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Role for PP2A in ARF signaling to p53
Moule, M. G., Collins, C. H., McCormick, F. P., & Fried, M. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0405533101 · Cited by 37
Role of the alternating reading frame (P19)-p53 pathway in an in vivo murine colon tumor model.
Nambiar, P. R., Giardina, C. A., Guda, K., Aizu, W., Raja, R. G., & Rosenberg, D. W. (2002) · PubMed · Cited by 37
Inhibition of v-Abl transformation by p53 and p19ARF
Cong, F., Zou, X., Hinrichs, K., Calame, K. L., & Goff, S. P. (1999) · Oncogene · doi:10.1038/sj.onc.1203290 · Cited by 38
E2F-1 induces the stabilization of p53 but blocks p53-mediated transactivation
Nip, J., Strom, D. K., Eischen, C. M., Cleveland, J. L., Zambetti, G. P., & Hiebert, S. W. (2001) · Oncogene · doi:10.1038/sj.onc.1204171 · Cited by 37
Kurokawa, K., Tanaka, T., & Kato, J. (1999) · Oncogene · doi:10.1038/sj.onc.1202628 · Cited by 37
Soufir, N., Lacapère, J.-J., Bertrand, G., Matichard, E., Meziani, R., Mirebeau‐Prunier, D., Descamps, V., Gérard, B., Archimbaud, A., Ollivaud, L., et al. (2004) · British Journal of Cancer · doi:10.1038/sj.bjc.6601503 · Cited by 37
Anticancer Drug Toxicity: Prevention, Management, and Clinical Pharmacokinetics
Damjanov, N. (2000) · Modern Pathology · doi:10.1038/modpathol.3880173 · Cited by 37
Apoptosis induced by 1,3,6,7-tetrahydroxyxanthone in Hepatocellular carcinoma and proteomic analysis
Fu, W.-M., Zhang, J.-F., Wang, H., Tan, H., Wang, W.-M., Chen, S., Zhu, X. M., Chan, T.-M., Tse, C.-M., Leung, K., et al. (2012) · APOPTOSIS · doi:10.1007/s10495-012-0729-y · Cited by 36
Merkel, C. A., Medrano, R. F. V., Baraúna, V. G., & Strauss, B. E. (2013) · Cancer Gene Therapy · doi:10.1038/cgt.2013.23 · Cited by 36
Zhu, Z., Luo, Z., Li, Y., Ni, C.-R., Li, H., & Zhu, M.-H. (2008) · Hepatology · doi:10.1002/hep.22675 · Cited by 36
Valente, L. J., Grabow, S., Vandenberg, C. J., Strasser, A., & Janic, A. (2015) · Oncogene · doi:10.1038/onc.2015.457 · Cited by 37
Qu, K., Lin, T. Y., Wei, J., Meng, F., Wang, Z., Huang, Z., Wan, Y., Song, S., Liu, S., Chang, H., et al. (2013) · PubMed · Cited by 36
Negative auto-regulators trap p53 in their web
Zhou, X. Y., Cao, B., & Lu, H. (2017) · Journal of Molecular Cell Biology · doi:10.1093/jmcb/mjx001 · Cited by 37
Expression of p14, MDM2, and MDM4 in human retinoblastoma
Guo, Y., Pajovic, S., & Gallie, B. L. (2008) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2008.07.055 · Cited by 36
D’Amico, M., Wu, K., Fu, M., Rao, M., Albanese, C., Russell, R. G., Lian, H., Bregman, D. B., White, M. A., & Pestell, R. G. (2004) · Cancer Research · doi:10.1158/0008-5472.can-03-2519 · Cited by 38
Metadata
- Authors
- Pomerantz, J., Schreiber-Agus, N., Liégeois, N. J., Silverman, A., Alland, L., Chin, L., Potes, J., Chen, K., Orlow, I., Lee, H.-W., Cordon-Cardo, C., & DePinho, R. A.
- Affiliations
- Albert Einstein College of Medicine (US)
- Memorial Sloan Kettering Cancer Center (US)
- Corresponding author
- DePinho, Ronald A
- Venue
- Cell
- Publisher
- Elsevier BV
- Published
- 1998-03
- Volume
- 92
- Issue
- 6
- Pages
- 713-723
- ISSN
- 0092-8674 (ISSN-L)
- OpenAlex
- W2039463309
- Cited by
- 1,521
- References
- 72
- Citations by year
- 2026: 4 · 2025: 10 · 2024: 6 · 2023: 23 · 2022: 19 · 2021: 23 · 2020: 19 · 2019: 16 · 2018: 12 · 2017: 24 · 2016: 27 · 2015: 32 · 2014: 44 · 2013: 44 · 2012: 47
- FWCI
- 64.86
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Cell (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Cancer Institute (CA 47179, CA 47538, CADK97650, P01CA047179)
- Topics
- Health Sciences › Medicine › Oncology › Cancer-related Molecular Pathways
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Heat shock proteins research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › PI3K/AKT/mTOR signaling in cancer
- Keywords
- p19ARF, INK4A, MDM2, p53, tumor suppression, protein-protein interaction, p53 degradation, p53 transactivation, oncogenic transformation, Rb pathway, viral oncoproteins, dominant-negative mutant
- MeSH terms
- Animals, Biotin, Cell Line, Deoxyuracil Nucleotides, Lens, Crystalline, Neoplasm Proteins, Nuclear Proteins, Osteoblasts, Proteins, Proto-Oncogene Proteins, Staining and Labeling, Transformation, Genetic, Tumor Suppressor Protein p53, Retinoblastoma Protein, Apoptosis, Genes, p16, Tumor Suppressor Protein p14ARF, Mice, Proto-Oncogene Proteins c-mdm2, DNA Fragmentation
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