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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
Cited by
Sorted by citations
Items 901–1,000 of 1,001
Chambon, V., Vacher, M., Jullien, M., May, E., & Bourdon, J. (2000) · Oncogene · doi:10.1038/sj.onc.1203960 · Cited by 28
Genetic dissection of melanoma pathways in the mouse
Yang, F. C., Merlino, G. T., & Chin, L. (2001) · Seminars in Cancer Biology · doi:10.1006/scbi.2000.0376 · Cited by 28
Self-citationMDM2’s dual mRNA binding domains co-ordinate its oncogenic and tumour suppressor activities
Gnanasundram, S. V., Malbert-Colas, L., Chen, S., Fusée, L. T. S., Daskalogianni, C., Müller, P., Salomao, N., & Fåhræus, R. (2020) · Nucleic Acids Research · doi:10.1093/nar/gkaa431 · Cited by 28
Pan, M., & Blattner, C. (2021) · Cancers · doi:10.3390/cancers13040745 · Cited by 27
Cyclin‐dependent kinases as therapeutic targets in melanoma
Miller, D. M., & Flaherty, K. T. (2014) · Pigment Cell & Melanoma Research · doi:10.1111/pcmr.12211 · Cited by 28
Koehn, J., Krapfenbauer, K., Huber, S., Stein, E., Sutter, W., Watzinger, F., Erović, B. M., Thurnher, D., Schindler, T. H., Fountoulakis, M., et al. (2008) · Journal of Proteome Research · doi:10.1021/pr800077a · Cited by 27
Alternative product of the p16/CKDN2A locus connects the Rb and p53 tumor suppressors
James, M. C., & Peters, G. G. (2000) · Springer eBooks · doi:10.1007/978-1-4615-4253-7_7 · Cited by 27
Deregulation of cell growth and malignant transformation.
Šulić, S., Panić, L., Đikić, I., & Volarević, S. (2005) · PubMed · Cited by 27
Riemenschneider, M. J., & Reifenberger, G. (2009) · Recent results in cancer research/Recent Results in Cancer Research · doi:10.1007/978-3-540-31206-2_1 · Cited by 27
Deregulation of the Cell Cycle by the Epstein–Barr Virus
O’Nions, J., & Allday, M. J. (2004) · Advances in cancer research · doi:10.1016/s0065-230x(04)92006-4 · Cited by 28
Differential apoptosis by gallotannin in human colon cancer cells with distinct p53 status
Al‐Ayyoubi, S., & Gali‐Muhtasib, H. U. (2006) · Molecular Carcinogenesis · doi:10.1002/mc.20252 · Cited by 29
Abnormal Expression of Cell Cycle Regulatory Proteins in Ductal and Lobular Carcinomas of the Breast
Geradts, J., & Ingram, C. D. (2000) · Modern Pathology · doi:10.1038/modpathol.3880172 · Cited by 27
Monoclonal Antibodies to the Mouse p19 Arf Tumor Suppressor Protein
Bertwistle, D., Zindy, F., Sherr, C. J., & Roussel, M. F. (2004) · Hybridoma and Hybridomics · doi:10.1089/hyb.2004.23.293 · Cited by 27
The Tumor Suppressor ARF Regulates Innate Immune Responses in Mice
Través, P. G., López-Fontal, R., Luque, A., & Hortelano, S. (2011) · The Journal of Immunology · doi:10.4049/jimmunol.1004070 · Cited by 27
MYL6B, a myosin light chain, promotes MDM2-mediated p53 degradation and drives HCC development
Xie, X., Wang, X., Liao, W., Fei, R., Wu, N., Xu, C., Chen, Q., Wei, L., Wang, Y., & Chen, H. (2018) · Journal of Experimental & Clinical Cancer Research · doi:10.1186/s13046-018-0693-7 · Cited by 26
Timmerman, D. M., Remmers, T. L., Hillenius, S., & Looijenga, L. H. J. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22105377 · Cited by 26
Chinnasri, P., Pairojkul, C., Jearanaikoon, P., Sripa, B., Bhudhisawasdi, V., Tantimavanich, S., & Limpaiboon, T. (2009) · Human Pathology · doi:10.1016/j.humpath.2008.11.002 · Cited by 26
Szklarczyk, R., Heringa, J., Pond, S. L. K., & Nekrutenko, A. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0703238104 · Cited by 26
ARF antagonizes the ability of Miz-1 to inhibit p53-mediated transactivation
Miao, L., Song, Z., Jin, L., Zhu, Y., Wen, L., & Wu, M. (2009) · Oncogene · doi:10.1038/onc.2009.372 · Cited by 26
p53 status dictates responses of B lymphomas to monotherapy with proteasome inhibitors
Yu, D., Carroll, M. P., & Thomas‐Tikhonenko, A. (2007) · Blood · doi:10.1182/blood-2006-10-050294 · Cited by 26
The promiscuity of ARF interactions with the proteasome
Pollice, A., Vivo, M., & Mantia, G. L. (2008) · FEBS Letters · doi:10.1016/j.febslet.2008.09.026 · Cited by 28
Integration of the PRB and P53 Cell Cycle Control Pathways
Stewart, C. L., Soria, A. M., & Hamel, P. A. (2001) · Journal of Neuro-Oncology · doi:10.1023/a:1010615822317 · Cited by 27
D’Orazi, G., Marchetti, A., Crescenzi, M., Coen, S., Sacchi, A., & Soddu, S. (2000) · The Journal of Gene Medicine · doi:10.1002/(sici)1521-2254(200001/02)2:1 · Cited by 26
Phillips, D. C., Hunt, J. T., Moneypenny, C. G., MacLean, K. H., McKenzie, P., Harris, L. C., & Houghton, J. A. (2007) · Cell Death and Differentiation · doi:10.1038/sj.cdd.4402198 · Cited by 26
Reconstitution of the NF1 GAP-related domain in NF1-deficient human Schwann cells
Thomas, S. L., Deadwyler, G., Tang, J. M., Stubbs, E. B., Muir, D., Hiatt, K. K., Clapp, D. W., & Vries, G. H. D. (2006) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2006.07.159 · Cited by 29
The role of Ink4a/Arf in ErbB2 mammary gland tumorigenesis.
D’Amico, M., Wu, K., Vizio, D. D., Reutens, A. T., Stahl, M. C., Fu, M., Albanese, C., Russell, R. G., Muller, W. J., White, M. A., et al. (2003) · PubMed · Cited by 26
Self-citationDavid-Pfeuty, T., & Nouvian-Dooghe, Y. (2002) · Oncogene · doi:10.1038/sj.onc.1205871 · Cited by 26
Calabrò, V., Mansueto, G., Santoro, R., Gentilella, A., Pollice, A., Ghioni, P., Guerrini, L., & Mantia, G. L. (2004) · Molecular and Cellular Biology · doi:10.1128/mcb.24.19.8529-8540.2004 · Cited by 26
Tokunaga, H., Shariat, S. F., Green, A. E., Brown, R. M., Zhou, J.-H., Benedict, W. F., & Lerner, S. P. (2001) · International Journal of Radiation Oncology*Biology*Physics · doi:10.1016/s0360-3016(01)01586-3 · Cited by 26
Herzog, C. R., Noh, S. J., Lantry, L. E., Guan, K.-L., & You, M. (1999) · Molecular Carcinogenesis · doi:10.1002/(sici)1098-2744(199906)25:2 · Cited by 26
Zeng, X., Keller, D., Wu, L., & Lu, H. (2000) · PubMed · Cited by 26
The DNA Damage Checkpoint and Human CancerPreprint
Schultz, L. B., Chehab, N. H., Malikzay, A., DiTullio, R. A., Stavridi, E. S., & Halazonetis, T. D. (2000) · Cold Spring Harbor Symposia on Quantitative Biology · doi:10.1101/sqb.2000.65.489 · Cited by 26
A Review of the Regulatory Mechanisms of N-Myc on Cell Cycle
Li, H., Dong, L., Jin, M.-J., Li, Q.-Y., Wang, X. Q., Jia, M., Song, J., Zhang, S., & Yuan, S. (2023) · Molecules · doi:10.3390/molecules28031141 · Cited by 25
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Chang, Z., Guo, C., Ahronowitz, I. Z., Stemmer-Rachamimov, A. O., MacCollin, M., & Nunes, F. P. (2008) · Journal of Neuro-Oncology · doi:10.1007/s11060-008-9721-3 · Cited by 25
P14ARF: The Absence that Makes the Difference
Cilluffo, D., Barra, V., & Leonardo, A. D. (2020) · Genes · doi:10.3390/genes11070824 · Cited by 25
Tomicic, M. T., Krämer, F., Nguyen, A., Schwarzenbach, C., & Christmann, M. (2021) · Cancers · doi:10.3390/cancers13092019 · Cited by 28
Histopathology, pathogenesis and molecular genetics in primary central nervous system lymphomas.
Nakamura, M., Shimada, K., Ishida, E., & Konishi, N. (2004) · PubMed · doi:10.14670/hh-19.211 · Cited by 25
PLAGL2 controls the stability of Pirh2, an E3 ubiquitin ligase for p53
Zheng, G., Ning, J., & Yang, Y. (2007) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2007.10.003 · Cited by 25
Requirement for HDM2 Activity in the Rapid Degradation of p53 in Neuroblastoma
Isaacs, J. S., Saito, S., & Neckers, L. Μ. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m100638200 · Cited by 25
Lin, J. (1992) · International Journal of Oncology · doi:10.3892/ijo_00000023 · Cited by 25
Overproduction of MDM2 in vivo disrupts S phase independent of E2F1.
Reinke, V., Bortner, D. M., Amelse, L. L., Lundgren, K., Rosenberg, M. P., Finlay, C. A., & Lozano, G. (1999) · PubMed · Cited by 25
Restoration of p53 tumor suppressor pathway in human cervical carcinoma cells by sodium arsenite
Chou, R., & Huang, H. (2002) · Biochemical and Biophysical Research Communications · doi:10.1016/s0006-291x(02)00212-7 · Cited by 25
Pathogenetic and biologic significance of TP14ARF alterations in nonsmall cell lung carcinoma
Park, M.-J., Shimizu, K., 中野, 哲., Park, Y. B., Kohno, T., Tani, M., & Yokota, J. (2003) · Cancer Genetics and Cytogenetics · doi:10.1016/s0165-4608(02)00645-3 · Cited by 25
Grüttgen, A., Reichenzeller, M., Jünger, M., Schlien, S., Affolter, A., & Bosch, F. X. (2001) · The Journal of Pathology · doi:10.1002/path.906 · Cited by 25
Aberrations of the p14ARF and p16INK4a Genes in Renal Cell Carcinomas
Kawada, Y., Nakamura, M., Ishida, E., Shimada, K., Oosterwijk, E., Uemura, H., Hirao, Y., Chul, K. S., & Konishi, N. (2001) · Japanese Journal of Cancer Research · doi:10.1111/j.1349-7006.2001.tb02152.x · Cited by 25
Hiebert, S. W., Reed-Inderbitzin, E. F., Amann, J. M., Irvin, B. J., Durst, K. L., & Linggi, B. E. (2003) · Blood Cells Molecules and Diseases · doi:10.1016/s1079-9796(03)00021-4 · Cited by 26
Growth Factors in Lens Development
Lang, R. A., & McAvoy, J. W. (2004) · Cambridge University Press eBooks · doi:10.1017/cbo9780511529825.012 · Cited by 25
Kaji, T., Kaieda, I., Hisatsune, T., & Kaminogawa, S. (2002) · Nitric Oxide · doi:10.1006/niox.2001.0389 · Cited by 25
Molecular Basis of BRAF Inhibitor Resistance in Melanoma: A Systematic Review
Cosci, I., Salizzato, V., Fiore, P. D., Pigozzo, J., Guarneri, V., D, S. M. M., Ferlin, A., Mathlouthi, S., Piccin, L., & Garofalo, M. (2025) · Pharmaceuticals · doi:10.3390/ph18081235 · Cited by 26
Post-Translational Regulation of ARF: Perspective in Cancer
Seo, J., Seong, D., Lee, S. R., Oh, D., & Song, J. (2020) · Biomolecules · doi:10.3390/biom10081143 · Cited by 25
Boldrin, E., Gaffo, E., Niedermayer, A., Boer, J. M., Zimmermann, M., Weichenhan, D., Claus, R., Münch, V., Sun, Q., Enzenmüller, S., et al. (2021) · Blood · doi:10.1182/blood.2020007591 · Cited by 24
Sato, S., Ishikawa, H., Yoshikawa, H., Izumikawa, K., Simpson, R. J., & Takahashi, N. (2015) · Nucleic Acids Research · doi:10.1093/nar/gkv1069 · Cited by 24
Geng, J., Goh, W. L., Zhang, C., Lane, D. P., Liu, B., Ghadessy, F. J., & Tan, Y. N. (2015) · Journal of Materials Chemistry B · doi:10.1039/c5tb00819k · Cited by 24
Lessard, F., Stefanovsky, V. Y., Tremblay, M. G., & Moss, T. (2012) · Nucleic Acids Research · doi:10.1093/nar/gks198 · Cited by 27
NMI mediates transcription-independent ARF regulation in response to cellular stresses
Li, Z., Hou, J., Sun, L., Wen, T., Wang, L., Zhao, X., Xie, Q., & Zhang, S. Q. (2012) · Molecular Biology of the Cell · doi:10.1091/mbc.e12-04-0304 · Cited by 25
Zhu, M., Zhang, J., Zhan, D., Zhang, Y., Wang, R., Karaplis, A. C., Goltzman, D., & Miao, D. (2015) · Journal of Bone and Mineral Research · doi:10.1002/jbmr.2544 · Cited by 24
Genetic Alterations of the p14ARF-hdm2-p53 Regulatory Pathway in Breast Carcinoma
Ho, G. H., Calvano, J. E., Bisogna, M., Abouezzi, Z. E., Borgen, P. I., Cordon‐Cardo, C., & Zee, K. J. V. (2001) · Breast Cancer Research and Treatment · doi:10.1023/a:1010686518990 · Cited by 24
Self-citationMolecular markers in bladder cancer
Hussain, S. A., & James, N. D. (2005) · Seminars in Radiation Oncology · doi:10.1016/j.semradonc.2004.07.007 · Cited by 24
A strong candidate gene for the Papg1 locus on mouse chromosome 4 affecting lung tumor progression
Zhang, Z., Wang, Y., Herzog, C. R., Liu, G., Lee, H., DePinho, R. A., & You, M. (2002) · Oncogene · doi:10.1038/sj.onc.1205725 · Cited by 24
Self-citationp53 in breast cancer: mutation and countermeasures
Kumar, S. R. (2007) · Frontiers in bioscience · doi:10.2741/2378 · Cited by 24
Xu, L., Flynn, B. J., Ungar, S., Pass, H. I., Linnainmaa, K., Mattson, K. V., & Gerwin, B. I. (1999) · Carcinogenesis · doi:10.1093/carcin/20.5.773 · Cited by 24
Chao, H. H., Buchmann, A. M., & DeCaprio, J. A. (2000) · Molecular and Cellular Biology · doi:10.1128/mcb.20.20.7624-7633.2000 · Cited by 25
Yamato, K., Hashimoto, S., Okahashi, N., Ishisaki, A., Nonaka, K., Koseki, T., Kizaki, M., Ikeda, Y., & Nishihara, T. (2000) · Experimental Cell Research · doi:10.1006/excr.2000.4876 · Cited by 24
Ota, K., Dohi, Y., Brydun, A., Nakanome, A., Ito, S., & Igarashi, K. (2010) · Antioxidants and Redox Signaling · doi:10.1089/ars.2010.3574 · Cited by 23
Tursiella, M. L., Bowman, E., Wanzeck, K. C., Throm, R. E., Liao, J., Zhu, J., & Sample, C. E. (2014) · PLoS Pathogens · doi:10.1371/journal.ppat.1004415 · Cited by 23
Jaworski, M., Hailfinger, S., Buchmann, A., Hergenhahn, M., Hollstein, M., Ittrich, C., & Schwarz, M. (2005) · Carcinogenesis · doi:10.1093/carcin/bgi142 · Cited by 23
Catani, J. P. P., Medrano, R. F. V., Hunger, A., Valle, P. R. D., Adjemian, S., Zanatta, D. B., Kroemer, G., Costanzi-Strauss, E., & Strauss, B. E. (2016) · Translational Oncology · doi:10.1016/j.tranon.2016.09.011 · Cited by 24
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Aleotti, V., Catoni, C., Poggiana, C., Rosato, A., Facchinetti, A., & Scaini, M. C. (2021) · Cancers · doi:10.3390/cancers13246217 · Cited by 23
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Yang, M., Wu, S., Su, X., & May, W. S. (2006) · Blood · doi:10.1182/blood-2006-06-029645 · Cited by 23
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Rizos, H., McKenzie, H. A., Ayub, A. L. P., Woodruff, S., Becker, T. M., Scurr, L. L., Stahl, J., & Kefford, R. F. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.m609405200 · Cited by 23
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Lemaire, C., Godefroy, N., Ferecatu, I., Rincheval, V., Renaud, F., Trotot, P. K., Bouleau, S., Mignotte, B., & Vayssière, J. (2005) · Oncogene · doi:10.1038/sj.onc.1208493 · Cited by 23
Savarese, T. M., Jang, T., Low, H. P., Salmonsen, R. A., Litofsky, N. S., Matijašević, Z., Ross, A. H., & Recht, L. D. (2005) · Journal of neurosurgery · doi:10.3171/jns.2005.102.1.0098 · Cited by 23
The MDM2 Oncoprotein Promotes Apoptosis in p53-Deficient Human Medullary Thyroid Carcinoma Cells
Dilla, T., Velasco, J. A., Medina, D. L., Jf, G.-P., & Santisteban, P. (2000) · Endocrinology · doi:10.1210/endo.141.1.7265 · Cited by 23
p16INK4A(CDKN2A) Gene Deletion Is a Frequent Genetic Event in Synovial Sarcomas
Subramaniam, M. M., Noguera, R., Piqueras, M., Navarro, S., López‐Guerrero, J. A., & Llombart‐Bosch, A. (2006) · American Journal of Clinical Pathology · doi:10.1309/e2aay2xxn431wl81 · Cited by 23
Duncan, M. K., Cvekl, A., Kantorow, M., & Piatigorsky, J. (2004) · Cambridge University Press eBooks · doi:10.1017/cbo9780511529825.006 · Cited by 23
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Gump, J. M., McGavran, L., Wei, Q., & Hunger, S. P. (2001) · The American journal of pediatric hematology/oncology · doi:10.1097/00043426-200110000-00005 · Cited by 23
Zheng, X., Wang, Y.-F., Liu, B., Liu, C., Liu, D., Zhu, J., Yang, C., Yan, J., Liao, X., Meng, X., et al. (2014) · Nucleic Acid Therapeutics · doi:10.1089/nat.2013.0459 · Cited by 22
Aberrant expression of pRb, p16, p14ARF, MDM2, p21 and p53 in stage I adenocarcinomas of the lung
Xue, Q., Sano, T., Kashiwabara, K., Saitō, M., Oyama, T., & Nakajima, T. (2002) · Pathology International · doi:10.1046/j.1440-1827.2002.01321.x · Cited by 22
Bailey, K. A., Xia, Y., Ward, W. O., Knapp, G. W., Mo, J., Mumford, J. L., Owen, R. D., & Thai, S. (2009) · Toxicologic Pathology · doi:10.1177/0192623309351725 · Cited by 22
Harajly, M., Zalzali, H., Nawaz, Z., Ghayad, S. E., Ghamloush, F., Basma, H., Zainedin, S., Rabeh, W., Jabbour, M. N., Tawil, A. N., et al. (2015) · Molecular and Cellular Biology · doi:10.1128/mcb.00747-15 · Cited by 24
Divan, A., Lawry, J., DUNSMORE, I. R., Parsons, M. A., & Royds, J. A. (2001) · PubMed · Cited by 22
Subash‐Babu, P., Alshammari, G. M., Savarimuthu Ignacimuthu, S. J., & Alshatwi, A. A. (2017) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2016.12.091 · Cited by 22
Yeom, S., Kim, S. S., Jeong, H., & Jang, K. L. (2017) · Journal of General Virology · doi:10.1099/jgv.0.000856 · Cited by 22
Dobrzycka, K. M., Kang, K., Jiang, S., Meyer, R., Rao, P. H., Lee, A. V., & Oesterreich, S. (2006) · Cancer Research · doi:10.1158/0008-5472.can-06-1381 · Cited by 23
Liver-directed viral therapy for cancer
Warren, R. S., & Kirn, D. H. (2002) · Surgical Oncology Clinics of North America · doi:10.1016/s1055-3207(02)00043-1 · Cited by 22
Lens Induction and Determination
Fisher, M. A., & Grainger, R. M. (2004) · Cambridge University Press eBooks · doi:10.1017/cbo9780511529825.003 · Cited by 22
Cell Cycle Checkpoint Genes and Cancer
Funk, J. O. (2006) · Encyclopedia of Life Sciences · doi:10.1038/npg.els.0006046 · Cited by 22
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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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