Overexpression of the MDM2 Oncogene in Leukemia and Lymphoma
Abstract
A cellular phosphoprotein that binds to and inactivates p53 has recently been identified as a product of the oncogene MDM2. Amplification of the MDM2 gene was found in more than a third of sarcomas and in a subset of malignant gliomas. Despite the absence of amplification, the MDM2 gene was overexpressed in some types of leukemias and lymphomas. Overexpression was significantly more frequent in the low-grade type of B-cell non-Hodgkin's lymphoma (B-NHL) than in the intermediate/high grade types of lymphoma and the overexpression was also significantly more frequent in the advanced rather than the earlier stages of B-cell chronic lymphocytic leukemia (B-CLL) and B-NHL. This suggests that MDM2 could play a role, via the p53 pathway, in tumorigenicity and/or in disease progression in some hematological malignancies. However, in the light of our findings that, in a few cases, both the overexpression of MDM2 and mutant-type p53 was seen, it is possible that MDM2 overexpression may also promote neoplastic growth by mechanisms other than inactivation of the p53 protein.
Integrity signals
Registry
Cites
Statistics
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?
Mdm2 overexpression due to amplification or other mechanisms has been detected in patients with a variety of human cancers that also harbor mutant p53 or lack p53.
“Mdm2 overexpression due to amplification or other mechanisms has been detected in patients with a variety of human cancers that also harbor mutant p53 or lack p53 (12, 51).”
From Mdm2 Promotes Genetic Instability and Transformation Independent of p53 (2008) · cites this paper as [51]
Cites
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 · see citing works
Association of Human Papillomavirus Types 16 and 18 E6 Proteins with p53
Werness, B. A., Levine, A. J., & Howley, P. M. (1990) · Science · doi:10.1126/science.2157286 · Cited by 2,562 · see citing works
T antigen is bound to a host protein in SY40-transformed cells
Lane, D. P., & Crawford, L. V. (1979) · Nature · doi:10.1038/278261a0 · Cited by 2,443 · see citing works
Chromosome 17 Deletions and p53 Gene Mutations in Colorectal Carcinomas
Baker, S. J., Fearon, E. R., Nigro, J. M., Hamilton, S. R., Preisinger, A. C., Jessup, J. M., vanTuinen, P., Ledbetter, D. H., Barker, D. F., Nakamura, Y., et al. (1989) · Science · doi:10.1126/science.2649981 · Cited by 2,067 · see citing works
Amplification of a gene encoding a p53-associated protein in human sarcomas
Oliner, J. D., Kinzler, K. W., Meltzer, P. S., George, D. L., & Vogelstein, B. (1992) · Nature · doi:10.1038/358080a0 · Cited by 1,949 · see citing works
Vogelstein, B. (1992) · Cell · doi:10.1016/0092-8674(92)90421-8 · Cited by 1,862 · see citing works
The p53-mdm-2 autoregulatory feedback loop.
Wu, X., Bayle, J. H., Olson, D., & Levine, A. J. (1993) · Genes & Development · doi:10.1101/gad.7.7a.1126 · Cited by 1,801 · see citing works
Oncoprotein MDM2 conceals the activation domain of tumour suppressor p53
Oliner, J. D., Pietenpol, J. A., Thiagalingam, S., Gyuris, J., Kinzler, K. W., & Vogelstein, B. (1993) · Nature · doi:10.1038/362857a0 · Cited by 1,447 · see citing works
mdm2 expression is induced by wild type p53 activity.
Barak, Y., Juven, T., Haffner, R., & Oren, M. (1993) · The EMBO Journal · doi:10.1002/j.1460-2075.1993.tb05678.x · Cited by 1,290 · see citing works
p53: A Frequent Target for Genetic Abnormalities in Lung Cancer
Takahashi, T., Nau, M. M., Chiba, I., Birrer, M. J., Rosenberg, R. K., Vinocour, M., Levitt, M. L., Pass, H. I., Gazdar, A. F., & Minna, J. D. (1989) · Science · doi:10.1126/science.2554494 · Cited by 1,196 · see citing works
Gaïdano, G., Ballerini, P. F., Gong, J. Z., Inghirami, G., Neri, A., Newcomb, E. W., MAGRATH, I. T., Knowles, D., & Dalla‐Favera, R. (1991) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.88.12.5413 · Cited by 884 · see citing works
Sarnow, P., Ho, Y.-S., Williams, J., & Levine, A. J. (1982) · Cell · doi:10.1016/0092-8674(82)90356-7 · Cited by 836 · see citing works
Induction of nuclear accumulation of the tumor-suppressor protein p53 by DNA-damaging agents.
Fritsche, M., Haessler, C., & Brandner, G. (1993) · PubMed · Cited by 763 · see citing works
Fakharzadeh, S. S., Trusko, S. P., & George, D. L. (1991) · The EMBO Journal · doi:10.1002/j.1460-2075.1991.tb07676.x · Cited by 704 · see citing works
Mapping of the p53 and mdm-2 Interaction Domains
Chen, J., Maréchal, V., & Levine, A. J. (1993) · Molecular and Cellular Biology · doi:10.1128/mcb.13.7.4107 · Cited by 689 · see citing works
Milner, J., & Medcalf, E. (1991) · Cell · doi:10.1016/0092-8674(91)90384-b · Cited by 612 · see citing works
Reifenberger, G., Liu, L., Ichimura, K., Schmidt, E., & Collins, V. P. (1993) · PubMed · Cited by 562 · see citing works
A comparison of the biological activities of wild‐type and mutant p53
Zambetti, G. P., & Levine, A. J. (1993) · The FASEB Journal · doi:10.1096/fasebj.7.10.8344485 · Cited by 413 · see citing works
Hinds, P. W., Finlay, C. A., Quartin, R. S., Baker, S. J., Fearon, E. R., Vogelstein, B., & Levine, A. J. (1990) · PubMed · Cited by 408 · see citing works
Frequent mutation of the p53 gene in human esophageal cancer.
Hollstein, M. C., Metcalf, R. A., Welsh, J. A., Montesano, R., & Harris, C. C. (1990) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.87.24.9958 · Cited by 383 · see citing works
CAHILLY, L. A., Yang‐Feng, T. L., Francke, U., & George, D. L. (1987) · Somatic Cell and Molecular Genetics · doi:10.1007/bf01535205 · Cited by 355 · see citing works
MDM2 gene amplification in metastatic osteosarcoma.
Ladanyi, M., Cha, C. H., Lewis, R., Jhanwar, S. C., Huvos, A. G., & Healey, J. H. (1993) · PubMed · Cited by 342 · see citing works
Identification and preliminary characterization of a protein motif related to the zinc finger.
Lovering, R. C., Hanson, I. M., Borden, K. L. B., Martin, S. R., O’Reilly, N., Evan, G. I., Rahman, D., Pappin, D., Trowsdale, J., & Freemont, P. S. (1993) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.90.6.2112 · Cited by 338 · see citing works
Juven‐Gershon, T., Barak, Y., Zauberman, A., George, D. L., & Oren, M. (1993) · PubMed · Cited by 332 · see citing works
The Ribosomal L5 Protein Is Associated with mdm-2 and mdm-2-p53 Complexes
Maréchal, V., Elenbaas, B., Piette, J., Nicolas, J. C., & Levine, A. J. (1994) · Molecular and Cellular Biology · doi:10.1128/mcb.14.11.7414 · Cited by 318 · see citing works
The mdm-2 oncogene can overcome wild-type p53 suppression of transformed cell growth.
Finlay, C. A. (1993) · Molecular and Cellular Biology · doi:10.1128/mcb.13.1.301 · Cited by 311 · see citing works
The human MDM-2 oncogene is overexpressed in leukemias
Bueso-Ramos, C., Yang, Y. S., deLeon, E., McCown, P., Stass, S. A., & Albitar, M. X. (1993) · Blood · doi:10.1182/blood.v82.9.2617.bloodjournal8292617 · Cited by 294 · see citing works
Interactions between p53 and MDM2 in a mammalian cell cycle checkpoint pathway.
Chen, C. Y., Oliner, J., Zhan, Q., Fornace, A. J., Vogelstein, B., & Kastan, M. B. (1994) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.91.7.2684 · Cited by 271 · see citing works
The mdm-2 gene is induced in response to UV light in a p53-dependent manner.
Perry, M. E., Piette, J., Zawadzki, J., Harvey, D., & Levine, A. J. (1993) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.90.24.11623 · Cited by 247 · see citing works
Altered Patterns of MDM2 and TP53 Expression in Human Bladder Cancer
LIANES, P., Orlow, I., Zhang, Z., Oliva, M. R., Sarkis, A. S., Reuter, V. E., & Cordon‐Cardo, C. (1994) · JNCI Journal of the National Cancer Institute · doi:10.1093/jnci/86.17.1325 · Cited by 194 · see citing works
Identification and characterization of multiple mdm-2 proteins and mdm-2-p53 protein complexes.
Olson, D. C., Maréchal, V., Momand, J. A., Chen, J., Romocki, C., & Levine, A. J. (1993) · PubMed · Cited by 188 · see citing works
MDM2 Gene Amplification and Transcript Levels in Human Sarcomas: Relationship to TP53 Gene Status
Flørenes, V. A., Mælandsmo, G. M., Forus, A., Andreassen, Å. K., Myklebost, O., & Fodstad, Ø. (1994) · JNCI Journal of the National Cancer Institute · doi:10.1093/jnci/86.17.1297 · Cited by 188 · see citing works
Watanabe, T., Hotta, T., Ichikawa, A., Kinoshita, T., Nagai, H., Uchida, T., Murate, T., & Saito, H. (1994) · Blood · doi:10.1182/blood.v84.9.3158.3158 · Cited by 170 · see citing works
Self-citationMutations of p53 gene and their relation to disease progression in B- cell lymphoma
Ichikawa, A., Hotta, T., Takagi, N., Tsushita, K., Kinoshita, T., Nagai, H., Murakami, Y., Hayashi, K., & Saito, H. (1992) · Blood · doi:10.1182/blood.v79.10.2701.2701 · Cited by 163 · see citing works
Self-citationZauberman, A., Barak, Y., Ragimov, N., Levy, N., & Oren, M. (1993) · The EMBO Journal · doi:10.1002/j.1460-2075.1993.tb05941.x · Cited by 151 · see citing works
Landers, J. E., Haines, D. S., STRAUSS, J. F., & George, D. L. (1994) · PubMed · Cited by 143 · see citing works
Mashal, R. D., Shtalrid, M., Talpaz, M., Kantarjian, H., Smith, L., Beran, M., Cork, A., Trujillo, J., Gutterman, J. U., & Deisseroth, A. (1990) · Blood · doi:10.1182/blood.v75.1.180.180 · Cited by 141 · see citing works
The p53-binding protein MDM2 gene is differentially expressed in human breast carcinoma.
Sheikh, M. S., Shao, Z. M., Hussain, A., & Fontana, J. A. (1993) · PubMed · Cited by 127 · see citing works
Mutations of the p53 gene in myelodysplastic syndrome (MDS) and MDS- derived leukemia
Sugimoto, K., Hirano, N., Toyoshima, H., Chiba, S., Mano, H., Takaku, F., Yazaki, Y., & Hirai, H. (1993) · Blood · doi:10.1182/blood.v81.11.3022.3022 · Cited by 123 · see citing works
Mutations of p53 gene and their relation to disease progression in B- cell lymphoma
Ichikawa, A., Hotta, T., Takagi, N., et al. (1992) · Blood · doi:10.1182/blood.v79.10.2701.bloodjournal79102701 · Cited by 123 · see citing works
Self-citationMashal, R. D., Shtalrid, M., Talpaz, M., et al. (1990) · Blood · doi:10.1182/blood.v75.1.180.bloodjournal751180 · Cited by 109 · see citing works
Mutations of the p53 gene in lymphoid leukemia
Sugimoto, K., Toyoshima, H., Sakai, R., Miyagawa, K., Hagiwara, K., Hirai, H., Ishikawa, F., & Takaku, F. (1991) · Blood · doi:10.1182/blood.v77.6.1153.1153 · Cited by 97 · see citing works
Oncogene Amplification in Urothelial Cancers With p53 Gene Mutation or MDM2 Amplification
Habuchi, T., Kinoshita, H., Yamada, H., Kakehi, Y., Ogawa, O., Wu, W., Takahashi, R., Sugiyama, T., & Yoshida, O. (1994) · JNCI Journal of the National Cancer Institute · doi:10.1093/jnci/86.17.1331 · Cited by 96 · see citing works
Boddy, M. N., Freemont, P. S., & Borden, K. L. B. (1994) · Trends in Biochemical Sciences · doi:10.1016/0968-0004(94)90020-5 · Cited by 91 · see citing works
Over‐expression of the MDM2 gene is found in some cases of haematological malignancies
Quesnel, B., Preudhomme, C., Oscier, D. G., Lepelley, P., Hooghe, M. C., Facon, T. T. F., Zandecki, M., & Fenaux, P. (1994) · British Journal of Haematology · doi:10.1111/j.1365-2141.1994.tb05044.x · Cited by 64 · see citing works
Abnormal expression of the p53-binding protein MDM2 in Hodgkin's disease
Chilosi, M., Doglioni, C., Menestrina, F., Montagna, L., Rigo, A., Lestani, M., Barbareschi, M., Scarpa, A., Mariuzzi, G., & Pizzolo, G. (1994) · Blood · doi:10.1182/blood.v84.12.4295.bloodjournal84124295 · Cited by 45 · see citing works
Inactive p53 mutants may enhance the transcriptional activity of wild-type p53.
Zhang, W., Shay, J. W., & Deisseroth, A. (1993) · PubMed · Cited by 30 · see citing works
p53 and mdm2 are expressed independently during cellular proliferation.
Mosner, J., & Deppert, W. (1994) · PubMed · Cited by 29 · see citing works
Absence of amplification of MDM2 gene, a regulator of p53 function, in myelodysplastic syndromes.
Preudhomme, C., Quesnel, B., Vachée, A., Lepelley, P., Collyn-d'Hooghe, M., Wattel, E., & Fenaux, P. (1993) · PubMed · Cited by 23 · see citing works
Lack of MDM2 amplification in human leukaemia
Ridge, S. A., Dyer, M. J. S., Greaves, M. F., & Wiedemann, L. M. (1994) · British Journal of Haematology · doi:10.1111/j.1365-2141.1994.tb04754.x · Cited by 21 · see citing works
Rearrangement and expression of MDM2 oncogene in chronic lymphocytic leukemia
Huang, Y. Q., Raphael, B. G., Buchbinder, A., Li, J. J., Zhang, W. G., & Friedman‐Kien, A. E. (1994) · American Journal of Hematology · doi:10.1002/ajh.2830470215 · Cited by 14 · see citing works
Flagged first, then by citations
Cited by
Sorted by citations
The MDM2 gene amplification database
Momand, J. (1998) · Nucleic Acids Research · doi:10.1093/nar/26.15.3453 · Cited by 982 · see citing works
The MDM2-p53 pathway revisited
Nag, S. A., Jiangjiang, Q., Kalkunte, S. S., Ming-hai, W., & Zhang, R. (2013) · Journal of Biomedical Research · doi:10.7555/jbr.27.20130030 · Cited by 414 · see citing works
ΔNp73, A Dominant-Negative Inhibitor of Wild-type p53 and TAp73, Is Up-regulated in Human Tumors
Zaika, A., Slade, N., Erster, S. H., Sansome, C., Joseph, T. W., Pearl, M. L., Chalas, E., & Moll, U. M. (2002) · The Journal of Experimental Medicine · doi:10.1084/jem.20020179 · Cited by 316 · see citing works
Barrans, S., Carter, I. W. J., Owen, R. G., Davies, F. E., Patmore, R. D., Haynes, A., Morgan, G. J., & Jack, A. (2002) · Blood · doi:10.1182/blood.v99.4.1136 · Cited by 276 · see citing works
Negative regulation of bcl-2 expression by p53 in hematopoietic cells
Wu, Y.-L., Mehew, J. W., Heckman, C. A., Arcinas, M., & Boxer, L. M. (2001) · Oncogene · doi:10.1038/sj.onc.1204067 · Cited by 221 · see citing works
p53-Independent Role of MDM2 in TGF-β1 Resistance
Sun, P., Dong, P., Dai, K., Hannon, G. J., & Beach, D. (1998) · Science · doi:10.1126/science.282.5397.2270 · Cited by 194 · see citing works
Frequent Methylation Silencing of p15INK4b(MTS2) and p16INK4a (MTS1) in B-Cell and T-Cell Lymphomas
Baur, A. S., Shaw, P., Hirt‐Burri, N., Delacrétaz, F., Bosman, F. T., & Chaubert, P. (1999) · Blood · doi:10.1182/blood.v94.5.1773 · Cited by 168 · see citing works
Suppression of p53 by Notch in lymphomagenesis: implications for initiation and regression
Beverly, L. J., Felsher, D. W., & Capobianco, A. J. (2005) · Cancer Research · doi:10.1158/0008-5472.can-05-1664 · Cited by 157 · see citing works
Targeting MDM2-p53 Interaction for Cancer Therapy: Are We There Yet?
Nag, S. A., Zhang, X., Srivenugopal, K. S., Wang, M.-H., Wang, W., & Zhang, R. (2014) · Current Medicinal Chemistry · doi:10.2174/09298673113206660325 · Cited by 151 · see citing works
Proteomic analysis of mantle-cell lymphoma by protein microarray
Ghobrial, I. M., McCormick, D., Kaufmann, S. H., Leontovich, A. A., Loegering, D. A., Dai, N. T., Krajnik, K. L., Stenson, M. J., Melhem, M. F., Novak, A. J., et al. (2005) · Blood · doi:10.1182/blood-2004-10-3999 · Cited by 136 · see citing works
Mdm2 Binds to Nbs1 at Sites of DNA Damage and Regulates Double Strand Break Repair
Alt, J. R., Bouska, A., Fernandez, M. R., Cerny, R. L., Xiao, H., & Eischen, C. M. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m413387200 · Cited by 131 · see citing works
Mdm2 haplo‐insufficiency profoundly inhibits Myc‐induced lymphomagenesis
Alt, J. R., Greiner, T. C., Cleveland, J. L., & Eischen, C. M. (2003) · The EMBO Journal · doi:10.1093/emboj/cdg133 · Cited by 129 · see citing works
Regulation of the MDM2-p53 Pathway by Ribosomal Protein L11 Involves a Post-ubiquitination Mechanism
Dai, M., Shi, D., Jin, Y., Sun, X., Zhang, Y., Grossman, S. R., & Lu, H. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.m602596200 · Cited by 122 · see citing works
Mdm2 Promotes Genetic Instability and Transformation Independent of p53
Bouska, A., Lushnikova, T., Plaza, S., & Eischen, C. M. (2008) · Molecular and Cellular Biology · doi:10.1128/mcb.01584-07 · Cited by 105 · see citing works
Anil, B., Riedinger, C., Endicott, J., & Noble, M. E. M. (2013) · Acta Crystallographica Section D Biological Crystallography · doi:10.1107/s0907444913004459 · Cited by 95 · see citing works
Saddler, C. M., Ouillette, P. D., Kujawski, L. A., Shangary, S. K., Talpaz, M., Kaminski, M. S., Erba, H. P., Shedden, K., Wang, S., & Malek, S. N. (2007) · Blood · doi:10.1182/blood-2007-09-112698 · Cited by 96 · see citing works
Nuclear degradation of p53 occurs during down‐regulation of the p53 response after DNA damage
Shirangi, T. R., Zaika, A., & Moll, U. M. (2002) · The FASEB Journal · doi:10.1096/fj.01-0617fje · Cited by 96 · see citing works
Wang, P., Lushnikova, T., Odvody, J., Greiner, T. C., Jones, S. N., & Eischen, C. M. (2008) · Oncogene · doi:10.1038/sj.onc.1210788 · Cited by 86 · see citing works
Balance of Yin and Yang: Ubiquitylation-Mediated Regulation of p53 and c-Myc
Dai, M., Jin, Y., Gallegos, J. R., & Lu, H. (2006) · Neoplasia · doi:10.1593/neo.06334 · Cited by 83 · see citing works
The expression of iASPP in acute leukemias
Zhang, X., Wang, M., Zhou, C., Chen, S., & Wang, J. (2004) · Leukemia Research · doi:10.1016/j.leukres.2004.07.001 · Cited by 82 · see citing works
Quijano, S., López, A., Rasillo, A., Sayagués, J. M., Bárrena, S., Sánchez, M. L., Teodósio, C., Giraldo, P., Giralt, M., Pérez-Caro, M., et al. (2007) · Cytometry Part B Clinical Cytometry · doi:10.1002/cyto.b.20390 · Cited by 73 · see citing works
Mdm2 affects genome stability independent of p53
Bouska, A., & Eischen, C. M. (2009) · Cancer Research · doi:10.1158/0008-5472.can-08-3732 · Cited by 71 · see citing works
Regulation of the p53 Family Proteins by the Ubiquitin Proteasomal Pathway
Bang, S., Kaur, S., & Kurokawa, M. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms21010261 · Cited by 69 · see citing works
Davies, A. J., Lee, A. M., Taylor, C., Clear, A. J., Goff, L. K., Iqbal, S., Heavens, D., Calaminici, M., Norton, A. J., Lister, T. A., et al. (2005) · Leukemia · doi:10.1038/sj.leu.2403802 · Cited by 68 · see citing works
The Many Faces of MDM2 Binding Partners
Riley, M. F., & Lozano, G. (2012) · Genes & Cancer · doi:10.1177/1947601912455322 · Cited by 64 · see citing works
Murine Double Minute-2 Prevents p53-Overactivation-Related Cell Death (Podoptosis) of Podocytes
Thomasová, D., Bruns, H., Kretschmer, V., Ebrahim, M., Romoli, S., Liapis, H., Kotb, A. M., Endlich, N., & Anders, H. (2014) · Journal of the American Society of Nephrology · doi:10.1681/asn.2014040345 · Cited by 63 · see citing works
Suppression of Ras/Mapk pathway signaling inhibits Myc-induced lymphomagenesis
Gramling, M., & Eischen, C. M. (2012) · Cell Death and Differentiation · doi:10.1038/cdd.2012.1 · Cited by 45 · see citing works
Reproducibility of MDM2 and CDK4 Staining in Soft Tissue Tumors
Binh, M. B. N., Sastre‐Garau, X., Guillou, L., Aurias, A., & Coindre, J. (2006) · American Journal of Clinical Pathology · doi:10.1309/vmbp-67qu-nn6q-3j0e · Cited by 44 · see citing works
MDM2 promotes genome instability by ubiquitinating the transcription factor HBP1
Cao, Z., Xue, J., Cheng, Y., Wang, J., Liu, Y., Li, H., Jiang, W., Li, G., Gui, Y., & Zhang, X. (2019) · Oncogene · doi:10.1038/s41388-019-0761-2 · Cited by 38 · see citing works
MdmX regulates transformation and chromosomal stability in p53-deficient cells
Matijasevic, Z., Krzywicka-Racka, A., Sluder, G., & Jones, S. N. (2008) · Cell Cycle · doi:10.4161/cc.7.19.6797 · Cited by 34 · see citing works
Eischen, C. M., Alt, J. R., & Wang, P. (2004) · Oncogene · doi:10.1038/sj.onc.1208052 · Cited by 32 · see citing works
Direct transcriptional regulation of MDM2 by Fli-1
Truong, A. H. L., Cervi, D. N., Lee, J., & Ben‐David, Y. (2004) · Oncogene · doi:10.1038/sj.onc.1208323 · Cited by 32 · see citing works
Phang, B. H., Linn, Y. C., Li, H., & Sabapathy, K. (2008) · European Journal of Cancer · doi:10.1016/j.ejca.2008.02.007 · Cited by 32 · see citing works
B-cell chronic lymphocytic leukemia: Recent progress in biology, diagnosis, and therapy
Montserrat, E., Bosch, F., & Rozmán, C. (1997) · Annals of Oncology · doi:10.1093/annonc/8.suppl_1.s93 · Cited by 29 · see citing works
MDM2’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 27 · see citing works
Cressey, R., Pimpa, S., Tontrong, W., Wattananupong, O., & Leartprasertsuke, N. (2005) · Cancer Letters · doi:10.1016/j.canlet.2005.03.023 · Cited by 25 · see citing works
p53 pathway gene single nucleotide polymorphisms and chronic lymphocytic leukemia
Lahiri, O., Harris, S., Packham, G., & Howell, M. (2007) · Cancer Genetics and Cytogenetics · doi:10.1016/j.cancergencyto.2007.07.013 · Cited by 20 · see citing works
Stromal-MDM2 Promotes Lung Cancer Cell Invasion through Tumor–Host Feedback Signaling
Kamer, I., Daniel‐Meshulam, I., Zadok, O., Bab-Dinitz, E., Perry, G., Feniger-Barish, R., Perelman, M., Barshack, I., Ben‐Nun, A., Onn, A., et al. (2020) · Molecular Cancer Research · doi:10.1158/1541-7786.mcr-19-0395 · Cited by 19 · see citing works
Riley, M. F., You, M. J., Multani, A. S., & Lozano, G. (2015) · Oncogene · doi:10.1038/onc.2015.88 · Cited by 19 · see citing works
Targeting cell membrane HDM2: A novel therapeutic approach for acute myeloid leukemia
Wang, H., Zhao, D., Nguyen, L. X. T., Wu, H., Li, L., Dong, D. F., Troadec, E., Zhu, Y., Hoang, D. H., Stein, A. S., et al. (2019) · Leukemia · doi:10.1038/s41375-019-0522-9 · Cited by 19 · see citing works
Plasmacytomagenesis in Eμ-v-abl transgenic mice is accelerated when apoptosis is restrained
Vandenberg, C. J., Waring, P., Strasser, A., & Cory, S. (2014) · Blood · doi:10.1182/blood-2014-04-570770 · Cited by 15 · see citing works
Lin, J., Jin, X., Page, C., Sondak, V. K., Jiang, G., & Reynolds, R. K. (2000) · PubMed · Cited by 15 · see citing works
Analysis of Nuclear and Cytoplasmic Degradation of p53 in Cells after Stress
Joseph, T. W., & Moll, U. M. (2003) · Humana Press eBooks · doi:10.1385/1-59259-408-5:211 · Cited by 13 · see citing works
MDM2 Implications for Potential Molecular Pathogenic Therapies of Soft-Tissue Tumors
Sun, S. Y. (2023) · Journal of Clinical Medicine · doi:10.3390/jcm12113638 · Cited by 12 · see citing works
Sugimoto, K., Kawamata, N., Sakajiri, S., & Oshimi, K. (2002) · Japanese Journal of Cancer Research · doi:10.1111/j.1349-7006.2002.tb01234.x · Cited by 12 · see citing works
Microbial influences on hormesis, oncogenesis, and therapy: A review of the literature
Clanton, R., Saucier, D., Ford, J. R., & Akabani, G. (2015) · Environmental Research · doi:10.1016/j.envres.2015.06.026 · Cited by 11 · see citing works
Phang, B. H., Chua, H. W., Li, H., Linn, Y. C., & Sabapathy, K. (2011) · PLoS ONE · doi:10.1371/journal.pone.0015320 · Cited by 11 · see citing works
A functional wild-type p53 gene is expressed in human acute myeloid leukemia cell lines.
Sutcliffe, T. L., Fu, L., Abraham, J., Vaziri, H., & Benchimol, S. (1998) · PubMed · doi:10.1182/blood.v92.8.2977.spll5_2977_2979 · Cited by 11 · see citing works
A Functional Wild-Type p53 Gene Is Expressed in Human Acute Myeloid Leukemia Cell Lines
Sutcliffe, T. L., Fu, L., Abraham, J., Vaziri, H., & Benchimol, S. (1998) · Blood · doi:10.1182/blood.v92.8.2977 · Cited by 10 · see citing works
Adoptive Immunotherapy With Antigen‐Specific T Cells
Riddell, S. R., & Greenberg, P. D. (2003) · doi:10.1002/9780470987070.ch29 · Cited by 10 · see citing works
Enhanced Apoptotic Activity of a p53 Variant in Tumors Resistant to Wild-Type p53 Treatment
Atencio, I. A., Avanzini, J. B., Johnson, D. E., Neuteboom, S., Vaillancourt, M.-T., Nielsen, L. L., Hajian, G., Sutjipto, S., Sugarman, B. J., Philopena, J. M., et al. (2001) · Molecular Therapy · doi:10.1006/mthe.2001.0416 · Cited by 9 · see citing works
Reed, S. M., Hagen, J., Muniz, V. P., Rosean, T. R., Borcherding, N. C., Sciegienka, S. J., Goeken, J. A., Naumann, P. W., Zhang, W., Tompkins, V. S., et al. (2014) · PLoS ONE · doi:10.1371/journal.pone.0112126 · Cited by 8 · see citing works
Combination therapy with the type II anti-CD20 antibody obinutuzumab
Klein, C., Bacac, M., Umaña, P., & Fingerle‐Rowson, G. (2017) · Expert Opinion on Investigational Drugs · doi:10.1080/13543784.2017.1373087 · Cited by 7 · see citing works
Herok, M., Wawrzynów, B., Maluszek, M. J., Olszewski, M. B., Żylicz, M., & Żylicz, M. (2021) · Cancers · doi:10.3390/cancers13184501 · Cited by 5 · see citing works
Ribrag, V., & Bosq, J. (2002) · Encyclopédie médico-chirurgicale. Hématologie · doi:10.1016/s1155-1984(02)00044-4 · Cited by 4 · see citing works
Tripathi, R. S., Anifowose, A., Lu, W., Yang, X., & Wang, B. (2022) · Journal of Enzyme Inhibition and Medicinal Chemistry · doi:10.1080/14756366.2022.2116699 · Cited by 4 · see citing works
Targeting the MDM2–p53 interaction as a therapeutic strategy for the treatment of cancer
Peirce, S. K. (2010) · Cell Health and Cytoskeleton · doi:10.2147/chc.s4952 · Cited by 3 · see citing works
Activation of wild-type p53 by MDM2 inhibitors: a new strategy for lymphoma treatment
Pujals, A., Favre, L., Gaulard, P., & Wiels, J. (2015) · Blood and Lymphatic Cancer Targets and Therapy · doi:10.2147/blctt.s60486 · Cited by 3 · see citing works
Ribrag, V., Camara‐Clayette, V., Bosq, J., & Vasstezky, Y. (2012) · Encyclopédie médico-chirurgicale. Hématologie · doi:10.1016/s1155-1984(12)55448-8 · Cited by 3 · see citing works
Implications of ubiquitination and the maintenance of replication fork stability in cancer therapy
Xia, D., Zhu, X., Wang, Y., Gong, P., Su, H.-S., & Xu, X. (2023) · Bioscience Reports · doi:10.1042/bsr20222591 · Cited by 3 · see citing works
Murphy, M. E., & Levine, A. J. (1998) · Springer eBooks · doi:10.1007/978-1-4615-5287-1_2 · Cited by 3 · see citing works
Mansour, M. A., Hassan, G. S., Jaballah, M. Y., Serya, R. A. T., Dege, N., Şahın, O., Sharaky, M. M., Zhang, X., Su, R., De, K., et al. (2025) · Archiv der Pharmazie · doi:10.1002/ardp.70085 · Cited by 2 · see citing works
Salomao, N., Maslah, N., Giulianelli, A., Drevon, L., Aguinaga, L., Gu, X., Cassinat, B., Giraudier, S., Fenaux, P., & Fåhræus, R. (2022) · British Journal of Haematology · doi:10.1111/bjh.18608 · Cited by 2 · see citing works
Genetics of Chronic Lymphocytic Leukemia: Practical Aspects and Prognostic Significance
Put, N., Włodarska, I., Vandenberghe, P., & Michaux, L. (2012) · InTech eBooks · doi:10.5772/29336 · Cited by 2 · see citing works
Kim, D., Choi, S.-H., Yeom, Y. I., Min, S., & Kim, I. (2016) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2016.08.063 · Cited by 2 · see citing works
Wang, C., Liu, W.-T., Guo, H., Lan, T., Wang, T., & Wang, B. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26115286 · Cited by 1 · see citing works
Ubiquitin E3 Ligases and p53 in Doxorubicin-Induced Cardiotoxicity
Tachibana, S., Otaki, Y., Goto, J., Watanabe, T., & Watanabe, M. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms262110252 · Cited by 1 · see citing works
Self-citationNutraceuticals in Preventive Oncology: Chemical Biology and Translational Pharmaceutical Science
Zhang, R., & Nag, S. A. (2014) · AAPS advances in the pharmaceutical sciences series · doi:10.1007/978-3-319-06151-1_16 · Cited by 1 · see citing works
MDM2 (transformed mouse 3T3 cell double minute 2, p53 binding protein)
Villalona-Calero, M., & Duan, W. (2011) · Atlas of Genetics and Cytogenetics in Oncology and Haematology · doi:10.4267/2042/38406 · Cited by 1 · see citing works
Maclean, K. H., & Cleveland, J. L. (2006) · Cambridge University Press eBooks · doi:10.1017/cbo9780511471001.013 · Cited by 1 · see citing works
MDM2 Oncogene Copy Number Alterations in Chronic Lymphocytic Leukemia
Sookaromdee, P., & Wiwanitkit, V. (2019) · Turkish Journal of Hematology · doi:10.4274/tjh.galenos.2019.2019.0179 · Cited by 1 · see citing works
Mouse models in the recognition of tumor antigens
DeLeo, A. B., Beckebaum, S., & Cicinnati, V. R. (2003) · CRC Press eBooks · doi:10.1201/9780203217658.pt1
p53 Tumor Suppressor Opens Gateways for Cancer Therapy
Dai, M., Gallegos, J. R., & Lu, H. (2008) · CRC Press eBooks · doi:10.1201/9780849387999.ch48
Bang, S., Bhatt, H. C., Chen, Y. Y., & Kurokawa, M. (2017) · Springer eBooks · doi:10.1007/978-3-319-67199-4_101574
Bang, S., Bhatt, H. C., Chen, Y. Y., & Kurokawa, M. (2016) · Springer eBooks · doi:10.1007/978-1-4614-6438-9_101574-1
Targeting the p53/MDM2 Pathway for Cancer Therapy
Klein, C., & Vassilev, L. T. (2008) · Humana Press eBooks · doi:10.1007/978-1-59745-274-8_2
Navigating the p53‐MDM2 Landscape: Molecular Insights and Therapeutic Strategies
Mansour, M. A., Hassan, G. S., & Abouzid, K. A. M. (2026) · Archiv der Pharmazie · doi:10.1002/ardp.70264
GARTE, S. J. (1998) · Springer eBooks · doi:10.1007/978-1-4615-4989-5_3
- Authors
- Watanabe, T., Ichikawa, A., Saito, H., & Hotta, T.
- Affiliations
- Nagoya University Hospital (JP)
- Venue
- Leukemia & Lymphoma
- Publisher
- Informa UK Limited
- Published
- 1996-01
- Volume
- 21
- Issue
- 5-6
- Pages
- 391-397
- ISSN
- 1026-8022 (ISSN-L)
- 1042-8194
- 1029-2403
- OpenAlex
- W2037076884
- Cited by
- 80
- References
- 49
- Citations by year
- 2026: 1 · 2025: 3 · 2023: 2 · 2022: 2 · 2021: 1 · 2020: 3 · 2019: 4 · 2017: 2 · 2016: 2 · 2015: 3 · 2014: 5 · 2013: 2 · 2012: 5
- FWCI
- 1.20
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Leukemia & lymphoma/Leukemia and lymphoma (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Oncology › Cancer-related Molecular Pathways
- Health Sciences › Medicine › Pathology and Forensic Medicine › Lymphoma Diagnosis and Treatment
- Health Sciences › Medicine › Genetics › Chronic Lymphocytic Leukemia Research
- Keywords
- gene overexpression, p53 inactivation, B-cell non-Hodgkin lymphoma, chronic lymphocytic leukemia, hematologic malignancies, lymphoma progression, mutant p53, tumor suppressor pathways
- MeSH terms
- Animals, Gene Amplification, Humans, Leukemia, Lymphoma, Neoplasm Proteins, Neoplasms, Nuclear Proteins, Oncogenes, Proto-Oncogene Proteins, Gene Expression Regulation, Neoplastic, Gene Expression Regulation, Leukemic, Genes, p53, Tumor Suppressor Protein p53, Mice, Proto-Oncogene Proteins c-mdm2
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