메뉴 건너뛰기




Volumn 13, Issue 3, 2014, Pages 217-236

Drugging the p53 pathway: Understanding the route to clinical efficacy

Author keywords

[No Author keywords available]

Indexed keywords

ANTINEOPLASTIC AGENT; APR 246; CYTARABINE; DASATINIB; DOXORUBICIN; DS 3032B; MI 773; NAVITOCLAX; PRIMA 1; PROTEIN MDM2; PROTEIN P53; RG 7112; RO 5503781; SORAFENIB; UNCLASSIFIED DRUG; ZINC;

EID: 84895779578     PISSN: 14741776     EISSN: 14741784     Source Type: Journal    
DOI: 10.1038/nrd4236     Document Type: Review
Times cited : (648)

References (240)
  • 1
    • 84875519528 scopus 로고    scopus 로고
    • Mdm2 in evolution
    • Lane, D. P. & Verma, C. Mdm2 in evolution. Genes Cancer 3, 320-324 (2012
    • (2012) Genes Cancer , vol.3 , pp. 320-324
    • Lane, D.P.1    Verma, C.2
  • 2
    • 77956188419 scopus 로고    scopus 로고
    • Regulation of the p53 pathway by ubiquitin and related proteins
    • Hock, A. & Vousden, K. H. Regulation of the p53 pathway by ubiquitin and related proteins. Int. J. Biochem. Cell Biol. 42, 1618-1621 (2010
    • (2010) Int. J. Biochem. Cell Biol , vol.42 , pp. 1618-1621
    • Hock, A.1    Vousden, K.H.2
  • 3
    • 79961076734 scopus 로고    scopus 로고
    • The p53 inhibitors MDM2/MDMX complex is required for control of p53 activity in vivo
    • Huang, L. et al. The p53 inhibitors MDM2/MDMX complex is required for control of p53 activity in vivo. Proc. Natl Acad. Sci. USA 108, 12001-12006 (2011
    • (2011) Proc. Natl Acad. Sci. USA , vol.108 , pp. 12001-12006
    • Huang, L.1
  • 5
    • 10744221485 scopus 로고    scopus 로고
    • In vivo activation of the p53 pathway by small-molecule antagonists of MDM2
    • Vassilev, L. T. et al. In vivo activation of the p53 pathway by small-molecule antagonists of MDM2. Science 303, 844-848 (2004
    • (2004) Science , vol.303 , pp. 844-848
    • Vassilev, L.T.1
  • 6
    • 0030460978 scopus 로고    scopus 로고
    • The p53 response to ionising radiation in adult and developing murine tissues
    • MacCallum, D. E. et al. The p53 response to ionising radiation in adult and developing murine tissues. Oncogene 13, 2575-2587 (1996
    • (1996) Oncogene , vol.13 , pp. 2575-2587
    • MacCallum, D.E.1
  • 7
    • 0031003552 scopus 로고    scopus 로고
    • Transgenic mice with p53 responsive lacZ: 53 activity varies dramatically during normal development and determines radiation and drug sensitivity in vivo
    • Komarova, E. A. et al. Transgenic mice with p53 responsive lacZ: 53 activity varies dramatically during normal development and determines radiation and drug sensitivity in vivo. EMBO J. 16, 1391-1400 (1997
    • (1997) EMBO J. , vol.16 , pp. 1391-1400
    • Komarova, E.A.1
  • 8
    • 33748670457 scopus 로고    scopus 로고
    • The pathological response to DNA damage does not contribute to p53 mediated tumour suppression
    • Christophorou, MOA., Ringshausen, I., Finch, A. J., Swigart, L. B. & Evan, G. I. The pathological response to DNA damage does not contribute to p53 mediated tumour suppression. Nature 443, 214-217 (2006
    • (2006) Nature , vol.443 , pp. 214-217
    • Christophorou, M.O.A.1    Ringshausen, I.2    Finch, A.J.3    Swigart, L.B.4    Evan, G.I.5
  • 9
    • 33845185824 scopus 로고    scopus 로고
    • Mdm2 is critically and continuously required to suppress lethal p53 activity in vivo
    • Ringshausen, I., O'Shea, C. C., Finch, A. J., Swigart, L. B. & Evan, G. I. Mdm2 is critically and continuously required to suppress lethal p53 activity in vivo. Cancer Cell 10, 501-514 (2006
    • (2006) Cancer Cell , vol.10 , pp. 501-514
    • Ringshausen, I.1    O'Shea, C.C.2    Finch, A.J.3    Swigart, L.B.4    Evan, G.I.5
  • 10
    • 33645711615 scopus 로고    scopus 로고
    • Tumor suppression by p53 without accelerated aging: Just enough of a good thing
    • Mendrysa, S. M. & Perry, M. E. Tumor suppression by p53 without accelerated aging: Just enough of a good thing? Cell Cycle 5, 714-717 (2006
    • (2006) Cell Cycle , vol.5 , pp. 714-717
    • Mendrysa, S.M.1    Perry, M.E.2
  • 11
    • 0037220737 scopus 로고    scopus 로고
    • Mdm2 is critical for inhibition of p53 during lymphopoiesis and the response to ionizing irradiation
    • Mendrysa, S. M. et al. Mdm2 is critical for inhibition of p53 during lymphopoiesis and the response to ionizing irradiation. Mol. Cell. Biol. 23, 462-472 (2003
    • (2003) Mol. Cell. Biol , vol.23 , pp. 462-472
    • Mendrysa, S.M.1
  • 12
    • 8844278362 scopus 로고    scopus 로고
    • A single nucleotide polymorphism in the MDM2 promoter attenuates the p53 tumor suppressor pathway and accelerates tumor formation in humans
    • Bond, G. L. et al. A single nucleotide polymorphism in the MDM2 promoter attenuates the p53 tumor suppressor pathway and accelerates tumor formation in humans. Cell 119, 591-602 (2004
    • (2004) Cell , vol.119 , pp. 591-602
    • Bond, G.L.1
  • 13
    • 0037112844 scopus 로고    scopus 로고
    • Super p53 mice exhibit enhanced DNA damage response, are tumor resistant and age normally
    • Garcia-Cao, I. et al. Super p53 mice exhibit enhanced DNA damage response, are tumor resistant and age normally. EMBO J. 21, 6225-6235 (2002
    • (2002) EMBO J. , vol.21 , pp. 6225-6235
    • Garcia-Cao, I.1
  • 15
    • 33845611951 scopus 로고    scopus 로고
    • Modeling the therapeutic efficacy of p53 restoration in tumors
    • Martins, C. P., Brown-Swigart, L. & Evan, G. I. Modeling the therapeutic efficacy of p53 restoration in tumors. Cell 127, 1323-1334 (2006
    • (2006) Cell , vol.127 , pp. 1323-1334
    • Martins, C.P.1    Brown-Swigart, L.2    Evan, G.I.3
  • 16
    • 33846899456 scopus 로고    scopus 로고
    • Restoration of p53 function leads to tumour regression in vivo
    • Ventura, A. et al. Restoration of p53 function leads to tumour regression in vivo. Nature 445, 661-665 (2007
    • (2007) Nature , vol.445 , pp. 661-665
    • Ventura, A.1
  • 17
    • 33846937033 scopus 로고    scopus 로고
    • Senescence and tumour clearance is triggered by p53 restoration in murine liver carcinomas
    • Xue, W. et al. Senescence and tumour clearance is triggered by p53 restoration in murine liver carcinomas. Nature 445, 656-660 (2007
    • (2007) Nature , vol.445 , pp. 656-660
    • Xue, W.1
  • 18
    • 84861973567 scopus 로고    scopus 로고
    • Tumor suppression in the absence of p53 mediated cell-cycle arrest, apoptosis, and senescence
    • Li, T. et al. Tumor suppression in the absence of p53 mediated cell-cycle arrest, apoptosis, and senescence. Cell 149, 1269-1283 (2012
    • (2012) Cell , vol.149 , pp. 1269-1283
    • Li, T.1
  • 19
    • 79955795151 scopus 로고    scopus 로고
    • Distinct p53 transcriptional programs dictate acute DNA-damage responses and tumor suppression
    • Brady, C. A. et al. Distinct p53 transcriptional programs dictate acute DNA-damage responses and tumor suppression. Cell 145, 571-583 (2011
    • (2011) Cell , vol.145 , pp. 571-583
    • Brady, C.A.1
  • 20
    • 80054736586 scopus 로고    scopus 로고
    • Full p53 transcriptional activation potential is dispensable for tumor suppression in diverse lineages
    • Jiang, D. et al. Full p53 transcriptional activation potential is dispensable for tumor suppression in diverse lineages. Proc. Natl Acad. Sci. USA 108, 17123-17128 (2011
    • (2011) Proc. Natl Acad. Sci. USA , vol.108 , pp. 17123-17128
    • Jiang, D.1
  • 21
    • 0028978183 scopus 로고
    • Mice lacking p21CIP1/WAF1 undergo normal development, but are defective in G1 checkpoint control
    • Deng, C., Zhang, P., Harper, J. W., Elledge, S. J. & Leder, P. Mice lacking p21CIP1/WAF1 undergo normal development, but are defective in G1 checkpoint control. Cell 82, 675-684 (1995
    • (1995) Cell , vol.82 , pp. 675-684
    • Deng, C.1    Zhang, P.2    Harper, J.W.3    Elledge, S.J.4    Leder, P.5
  • 22
    • 0242410719 scopus 로고    scopus 로고
    • P53-And drug-induced apoptotic responses mediated by bh3 only proteins puma and noxa
    • Villunger, A. et al. p53-And drug-induced apoptotic responses mediated by BH3 only proteins Puma and Noxa. Science 302, 1036-1038 (2003
    • (2003) Science , vol.302 , pp. 1036-1038
    • Villunger, A.1
  • 23
    • 84878546043 scopus 로고    scopus 로고
    • P53 efficiently suppresses tumor development in the complete absence of its cell-cycle inhibitory and proapoptotic effectors p21 puma and noxa
    • Valente, L. J. et al. p53 efficiently suppresses tumor development in the complete absence of its cell-cycle inhibitory and proapoptotic effectors p21, Puma, and Noxa. Cell Rep. 3, 1339-1345 (2013
    • (2013) Cell Rep , vol.3 , pp. 1339-1345
    • Valente, L.J.1
  • 24
    • 28644447272 scopus 로고    scopus 로고
    • The antioxidant function of the p53 tumor suppressor
    • Sablina, A. A. et al. The antioxidant function of the p53 tumor suppressor. Nature Med. 11, 1306-1313 (2005
    • (2005) Nature Med , vol.11 , pp. 1306-1313
    • Sablina, A.A.1
  • 25
    • 0031771497 scopus 로고    scopus 로고
    • The human arf cell cycle regulatory gene promoter is a cpg island which can be silenced by dna methylation and down-regulated by wild-Type p53
    • Robertson, K. D. & Jones, P. A. The human ARF cell cycle regulatory gene promoter is a CpG island which can be silenced by DNA methylation and down-regulated by wild-Type p53. Mol. Cell. Biol. 18, 6457-6473 (1998
    • (1998) Mol. Cell. Biol , vol.18 , pp. 6457-6473
    • Robertson, K.D.1    Jones, P.A.2
  • 26
    • 84859564524 scopus 로고    scopus 로고
    • Small molecules that bind the Mdm2 RING stabilize and activate p53
    • Roxburgh, P. et al. Small molecules that bind the Mdm2 RING stabilize and activate p53. Carcinogenesis 33, 791-798 (2012
    • (2012) Carcinogenesis , vol.33 , pp. 791-798
    • Roxburgh, P.1
  • 27
    • 84875179160 scopus 로고    scopus 로고
    • Liberation of functional p53 by proteasome inhibition in human papilloma virus-positive head and neck squamous cell carcinoma cells promotes apoptosis and cell cycle arrest
    • Li, C. & Johnson, D. E. Liberation of functional p53 by proteasome inhibition in human papilloma virus-positive head and neck squamous cell carcinoma cells promotes apoptosis and cell cycle arrest. Cell Cycle 12, 923-934 (2013
    • (2013) Cell Cycle , vol.12 , pp. 923-934
    • Li, C.1    Johnson, D.E.2
  • 28
    • 53349153446 scopus 로고    scopus 로고
    • Targeting tumor cells expressing p53 with a water-soluble inhibitor of Hdm2
    • Kitagaki, J., Agama, K. K., Pommier, Y., Yang, Y. & Weissman, A. M. Targeting tumor cells expressing p53 with a water-soluble inhibitor of Hdm2. Mol. Cancer Ther. 7, 2445-2454 (2008
    • (2008) Mol. Cancer Ther , vol.7 , pp. 2445-2454
    • Kitagaki, J.1    Agama, K.K.2    Pommier, Y.3    Yang, Y.4    Weissman, A.M.5
  • 29
    • 42949114938 scopus 로고    scopus 로고
    • Discovery, in vivo activity, and mechanism of action of a small-molecule p53 activator
    • Lain, S. et al. Discovery, in vivo activity, and mechanism of action of a small-molecule p53 activator. Cancer Cell 13, 454-463 (2008
    • (2008) Cancer Cell , vol.13 , pp. 454-463
    • Lain, S.1
  • 30
    • 0032055501 scopus 로고    scopus 로고
    • Genetic selection of intragenic suppressor mutations that reverse the effect of common p53 cancer mutations
    • Brachmann, R. K., Yu, K., Eby, Y., Pavletich, N. P. & Boeke, J. D. Genetic selection of intragenic suppressor mutations that reverse the effect of common p53 cancer mutations. EMBO J. 17, 1847-1859 (1998
    • (1998) EMBO J. , vol.17 , pp. 1847-1859
    • Brachmann, R.K.1    Yu, K.2    Eby, Y.3    Pavletich, N.P.4    Boeke, J.D.5
  • 31
    • 0034141471 scopus 로고    scopus 로고
    • Mechanism of rescue of common p53 cancer mutations by second-site suppressor mutations
    • Nikolova, P. V., Wong, K. B., DeDecker, B., Henckel, J. & Fersht, A. R. Mechanism of rescue of common p53 cancer mutations by second-site suppressor mutations. EMBO J. 19, 370-378 (2000
    • (2000) EMBO J. , vol.19 , pp. 370-378
    • Nikolova, P.V.1    Wong, K.B.2    Dedecker, B.3    Henckel, J.4    Fersht, A.R.5
  • 32
    • 34248379012 scopus 로고    scopus 로고
    • Impact of mutant p53 functional properties on TP53 mutation patterns and tumor phenotype: Lessons from recent developments in the IARC TP53 database
    • Petitjean, A. et al. Impact of mutant p53 functional properties on TP53 mutation patterns and tumor phenotype: Lessons from recent developments in the IARC TP53 database. Hum. Mutat. 28, 622-629 (2007
    • (2007) Hum. Mutat , vol.28 , pp. 622-629
    • Petitjean, A.1
  • 35
    • 0027964904 scopus 로고
    • Immunochemical analysis of the interaction of p53 with mdm2; Fine mapping of the mdm2 binding site on p53 using synthetic peptides
    • Picksley, S. M., Vojtesek, B., Sparks, A. & Lane, D. P. Immunochemical analysis of the interaction of p53 with MDM2; fine mapping of the MDM2 binding site on p53 using synthetic peptides. Oncogene 9, 2523-2529 (1994
    • (1994) Oncogene , vol.9 , pp. 2523-2529
    • Picksley, S.M.1    Vojtesek, B.2    Sparks, A.3    Lane, D.P.4
  • 36
    • 0030575937 scopus 로고    scopus 로고
    • Structure of the MDM2 oncoprotein bound to the p53 tumor suppressor transactivation domain
    • Kussie, P. H. et al. Structure of the MDM2 oncoprotein bound to the p53 tumor suppressor transactivation domain. Science 274, 948-953 (1996
    • (1996) Science , vol.274 , pp. 948-953
    • Kussie, P.H.1
  • 37
    • 0031282325 scopus 로고    scopus 로고
    • Design of a synthetic mdm2 binding mini protein that activates the p53 response in vivo
    • Bottger, A. et al. Design of a synthetic Mdm2 binding mini protein that activates the p53 response in vivo. Curr. Biol. 7, 860-869 (1997
    • (1997) Curr. Biol , vol.7 , pp. 860-869
    • Bottger, A.1
  • 38
    • 0034716943 scopus 로고    scopus 로고
    • A small synthetic peptide, which inhibits the p53 hdm2 interaction, stimulates the p53 pathway in tumour cell lines
    • Chene, P. et al. A small synthetic peptide, which inhibits the p53 hdm2 interaction, stimulates the p53 pathway in tumour cell lines. J. Mol. Biol. 299, 245-253 (2000
    • (2000) J. Mol. Biol , vol.299 , pp. 245-253
    • Chene, P.1
  • 40
    • 13944274061 scopus 로고    scopus 로고
    • Discovery and cocrystal structure of benzodiazepinedione HDM2 antagonists that activate p53 in cells
    • Grasberger, B. L. et al. Discovery and cocrystal structure of benzodiazepinedione HDM2 antagonists that activate p53 in cells. J. Med. Chem. 48, 909-912 (2005
    • (2005) J. Med. Chem , vol.48 , pp. 909-912
    • Grasberger, B.L.1
  • 41
    • 70949084205 scopus 로고    scopus 로고
    • Discovery and optimization of chromenotriazolopyrimidines as potent inhibitors of the mouse double minute 2-Tumor protein 53 protein-protein interaction
    • Allen, J. G. et al. Discovery and optimization of chromenotriazolopyrimidines as potent inhibitors of the mouse double minute 2-Tumor protein 53 protein-protein interaction. J. Med. Chem. 52, 7044-7053 (2009
    • (2009) J. Med. Chem , vol.52 , pp. 7044-7053
    • Allen, J.G.1
  • 42
    • 0034801374 scopus 로고    scopus 로고
    • Toward proteomimetics: Terphenyl derivatives as structural and functional mimics of extended regions of an α helix
    • Orner, B. P., Ernst, J. T. & Hamilton, A. D. Toward proteomimetics: Terphenyl derivatives as structural and functional mimics of extended regions of an α helix. J. Am. Chem. Soc. 123, 5382-5383 (2001
    • (2001) J. Am. Chem. Soc , vol.123 , pp. 5382-5383
    • Orner, B.P.1    Ernst, J.T.2    Hamilton, A.D.3
  • 43
    • 18844423053 scopus 로고    scopus 로고
    • Terphenyl-based helical mimetics that disrupt the p53/HDM2 interaction
    • Yin, H. et al. Terphenyl-based helical mimetics that disrupt the p53/HDM2 interaction. Angew. Chem. Int. Ed. Engl. 44, 2704-2707 (2005
    • (2005) Angew. Chem. Int. Ed. Engl , vol.44 , pp. 2704-2707
    • Yin, H.1
  • 44
    • 20144367578 scopus 로고    scopus 로고
    • Chalcones: An update on cytotoxic and chemoprotective properties
    • Go, M. L., Wu, X. & Liu, X. L. Chalcones: An update on cytotoxic and chemoprotective properties. Curr. Med. Chem. 12, 483-499 (2005
    • (2005) Curr. Med. Chem , vol.12 , pp. 483-499
    • Go, M.L.1    Wu, X.2    Liu, X.L.3
  • 45
    • 0035895350 scopus 로고    scopus 로고
    • Chalcone derivatives antagonize interactions between the human oncoprotein mdm2 and p53
    • Stoll, R. et al. Chalcone derivatives antagonize interactions between the human oncoprotein MDM2 and p53. Biochemistry 40, 336-344 (2001
    • (2001) Biochemistry , vol.40 , pp. 336-344
    • Stoll, R.1
  • 46
    • 41649102468 scopus 로고    scopus 로고
    • Temporal activation of p53 by a specific MDM2 inhibitor is selectively toxic to tumors and leads to complete tumor growth inhibition
    • Shangary, S. et al. Temporal activation of p53 by a specific MDM2 inhibitor is selectively toxic to tumors and leads to complete tumor growth inhibition. Proc. Natl Acad. Sci. USA 105, 3933-3938 (2008
    • (2008) Proc. Natl Acad. Sci. USA , vol.105 , pp. 3933-3938
    • Shangary, S.1
  • 47
    • 84880169797 scopus 로고    scopus 로고
    • A potent small-molecule inhibitor of the MDM2-p53 interaction (MI 888) achieved complete and durable tumor regression in mice
    • Zhao, Y. et al. A potent small-molecule inhibitor of the MDM2-p53 interaction (MI 888) achieved complete and durable tumor regression in mice. J. Med. Chem. 56, 5553-5561 (2013
    • (2013) J. Med. Chem , vol.56 , pp. 5553-5561
    • Zhao, Y.1
  • 48
    • 77954850783 scopus 로고    scopus 로고
    • Robust generation of lead compounds for protein-protein interactions by computational and MCR chemistry: 53/Hdm2 antagonists
    • Czarna, A. et al. Robust generation of lead compounds for protein-protein interactions by computational and MCR chemistry: 53/Hdm2 antagonists. Angew. Chem. Int. Ed. 49, 5352-5356 (2010
    • (2010) Angew. Chem. Int. Ed. , vol.49 , pp. 5352-5356
    • Czarna, A.1
  • 49
    • 84895801307 scopus 로고    scopus 로고
    • 3 imidazolyl-indoles for the treatment of proliferative diseases
    • Boettcher, A. et al. 3 imidazolyl-indoles for the treatment of proliferative diseases. WO Patent 2008119741 (2008
    • (2008) WO Patent 2008119741
    • Boettcher, A.1
  • 50
    • 79952260443 scopus 로고    scopus 로고
    • Isoindolinone inhibitors of the murine double minute 2 (MDM2)-p53 protein-protein interaction: Structure-Activity studies leading to improved potency
    • Hardcastle, I. R. et al. Isoindolinone inhibitors of the murine double minute 2 (MDM2)-p53 protein-protein interaction: Structure-Activity studies leading to improved potency. J. Med. Chem. 54, 1233-1243 (2011
    • (2011) J. Med. Chem , vol.54 , pp. 1233-1243
    • Hardcastle, I.R.1
  • 52
    • 83755220071 scopus 로고    scopus 로고
    • Translational approaches targeting the p53 pathway for anti-cancer therapy
    • Essmann, F. & Schulze-Osthoff, K. Translational approaches targeting the p53 pathway for anti-cancer therapy. Br. J. Pharmacol. 165, 328-344 (2012
    • (2012) Br. J. Pharmacol , vol.165 , pp. 328-344
    • Essmann, F.1    Schulze-Osthoff, K.2
  • 53
    • 84895809830 scopus 로고    scopus 로고
    • Substituted piperidines that increase P53 activity and the uses thereof
    • Bogen, S. L. et al. Substituted piperidines that increase P53 activity and the uses thereof. WO Patent 2011046771A1 (2011
    • (2011) WO Patent 2011046771A1
    • Bogen, S.L.1
  • 54
    • 84880165688 scopus 로고    scopus 로고
    • Syn thesis in vitro, and in cell studies of a new series of [indoline 3,2Ŷ thiazolidine] based p53 modulators
    • Bertamino, A. et al. Synthesis, in vitro, and in cell studies of a new series of [indoline 3,2Ŷ thiazolidine]-based p53 modulators. J. Med. Chem. 56, 5407-5421 (2013
    • (2013) J. Med. Chem , vol.56 , pp. 5407-5421
    • Bertamino, A.1
  • 55
    • 3843055877 scopus 로고    scopus 로고
    • A nonpeptidic sulfonamide inhibits the p53 mdm2 interaction and activates p53 dependent transcription in mdm2 overexpressing cells
    • Galatin, P. S. & Abraham, D. J. A nonpeptidic sulfonamide inhibits the p53 mdm2 interaction and activates p53 dependent transcription in mdm2 overexpressing cells. J. Med. Chem. 47, 4163-4165 (2004
    • (2004) J. Med. Chem , vol.47 , pp. 4163-4165
    • Galatin, P.S.1    Abraham, D.J.2
  • 56
    • 84862296171 scopus 로고    scopus 로고
    • Structure-based design of novel inhibitors of the MDM2-p53 interaction
    • Rew, Y. et al. Structure-based design of novel inhibitors of the MDM2-p53 interaction. J. Med. Chem. 55, 4936-4954 (2012
    • (2012) J. Med. Chem , vol.55 , pp. 4936-4954
    • Rew, Y.1
  • 57
    • 84878096164 scopus 로고    scopus 로고
    • Rational design and binding mode duality of MDM2-p53 inhibitors
    • Gonzalez-Lopez de Turiso, F. et al. Rational design and binding mode duality of MDM2-p53 inhibitors. J. Med. Chem. 56, 4053-4070 (2013
    • (2013) J. Med. Chem , vol.56 , pp. 4053-4070
    • Gonzalez-Lopez De Turiso, F.1
  • 58
    • 84864478361 scopus 로고    scopus 로고
    • An expeditious synthesis of the MDM2-p53 inhibitor AM 8553
    • Lucas, B. S. et al. An expeditious synthesis of the MDM2-p53 inhibitor AM 8553. J. Am. Chem. Soc. 134, 12855-12860 (2012
    • (2012) J. Am. Chem. Soc , vol.134 , pp. 12855-12860
    • Lucas, B.S.1
  • 59
    • 79954591069 scopus 로고    scopus 로고
    • Understanding small-molecule binding to MDM2: Insights into structural effects of isoindolinone inhibitors from NMR spectroscopy
    • Riedinger, C. et al. Understanding small-molecule binding to MDM2: Insights into structural effects of isoindolinone inhibitors from NMR spectroscopy. Chem. Biol. Drug Design 77, 301-308 (2011
    • (2011) Chem. Biol. Drug Design , vol.77 , pp. 301-308
    • Riedinger, C.1
  • 60
    • 84867488138 scopus 로고    scopus 로고
    • Ordering of the N terminus of human MDM2 by small molecule inhibitors
    • Michelsen, K. et al. Ordering of the N terminus of human MDM2 by small molecule inhibitors. J. Am. Chem. Soc. 134, 17059-17067 (2012
    • (2012) J. Am. Chem. Soc , vol.134 , pp. 17059-17067
    • Michelsen, K.1
  • 61
    • 84876999513 scopus 로고    scopus 로고
    • In vitro selection of mutant hdm2 resistant to nutlin inhibition
    • Wei, S. J. et al. In vitro selection of mutant HDM2 resistant to Nutlin inhibition. PLoS ONE 8, e62564 (2013
    • (2013) PLoS ONE , vol.8
    • Wei, S.J.1
  • 62
    • 84877690432 scopus 로고    scopus 로고
    • Discovery of rg7112: A small-molecule mdm2 inhibitor in clinical development
    • Vu, B. et al. Discovery of RG7112: A small-molecule MDM2 inhibitor in clinical development. ACS Med. Chem. Lett. 4, 466-469 (2013
    • (2013) ACS Med. Chem. Lett , vol.4 , pp. 466-469
    • Vu, B.1
  • 63
    • 84880896065 scopus 로고    scopus 로고
    • Discovery of RG7388, a potent and selective p53 MDM2 inhibitor in clinical development
    • Ding, Q. et al. Discovery of RG7388, a potent and selective p53 MDM2 inhibitor in clinical development. J. Med. Chem. 56, 5979-5983 (2013
    • (2013) J. Med. Chem , vol.56 , pp. 5979-5983
    • Ding, Q.1
  • 64
    • 58749094954 scopus 로고    scopus 로고
    • Targeting mdm2 and mdmx in cancer therapy: Better living through medicinal chemistry
    • Wade, M. & Wahl, G. M. Targeting Mdm2 and Mdmx in cancer therapy: Better living through medicinal chemistry? Mol. Cancer Res. 7, 1-11 (2009
    • (2009) Mol. Cancer Res , vol.7 , pp. 1-11
    • Wade, M.1    Wahl, G.M.2
  • 65
    • 84864677524 scopus 로고    scopus 로고
    • Mdm4 is a key therapeutic target in cutaneous melanoma
    • Gembarska, A. et al. MDM4 is a key therapeutic target in cutaneous melanoma. Nature Med. 18, 1239-1247 (2012
    • (2012) Nature Med , vol.18 , pp. 1239-1247
    • Gembarska, A.1
  • 66
    • 84877826693 scopus 로고    scopus 로고
    • Restoring p53 function in human melanoma cells by inhibiting mdm2 and cyclin b1/cdk1 phosphorylated nuclear iaspp
    • Lu, M. et al. Restoring p53 function in human melanoma cells by inhibiting MDM2 and cyclin B1/CDK1 phosphorylated nuclear iASPP. Cancer Cell 23, 618-633 (2013
    • (2013) Cancer Cell , vol.23 , pp. 618-633
    • Lu, M.1
  • 67
    • 79955991034 scopus 로고    scopus 로고
    • Mechanism-specific signatures for small-molecule p53 activators
    • van Leeuwen, I. M. et al. Mechanism-specific signatures for small-molecule p53 activators. Cell Cycle 10, 1590-1598 (2011
    • (2011) Cell Cycle , vol.10 , pp. 1590-1598
    • Van Leeuwen, I.M.1
  • 68
    • 84875712215 scopus 로고    scopus 로고
    • Discovery of a new small-molecule inhibitor of p53-MDM2 interaction using a yeast-based approach
    • Leo, M. et al. Discovery of a new small-molecule inhibitor of p53-MDM2 interaction using a yeast-based approach. Biochem. Pharmacol. 85, 1234-1245 (2013
    • (2013) Biochem. Pharmacol , vol.85 , pp. 1234-1245
    • Leo, M.1
  • 69
    • 84872577314 scopus 로고    scopus 로고
    • Siladenoserinols A-L: New sulfonated serinol derivatives from a tunicate as inhibitors of p53-Hdm2 interaction
    • Nakamura, Y. et al. Siladenoserinols A-L: New sulfonated serinol derivatives from a tunicate as inhibitors of p53-Hdm2 interaction. Org. Lett. 15, 322-325 (2012
    • (2012) Org. Lett , vol.15 , pp. 322-325
    • Nakamura, Y.1
  • 70
    • 77951224332 scopus 로고    scopus 로고
    • Identification and characterization of the first small molecule inhibitor of mdmx
    • Reed, D. et al. Identification and characterization of the first small molecule inhibitor of MDMX. J. Biol. Chem. 285, 10786-10796 (2010
    • (2010) J. Biol. Chem , vol.285 , pp. 10786-10796
    • Reed, D.1
  • 71
    • 84878819607 scopus 로고    scopus 로고
    • Affinity-based screening of MDM2/MDMX-p53 interaction inhibitors by chemical array: Identification of novel peptidic inhibitors
    • Noguchi, T. et al. Affinity-based screening of MDM2/MDMX-p53 interaction inhibitors by chemical array: Identification of novel peptidic inhibitors. Bioorg. Med. Chem. Lett. 23, 3802-3805 (2013
    • (2013) Bioorg. Med. Chem. Lett , vol.23 , pp. 3802-3805
    • Noguchi, T.1
  • 72
    • 84863966819 scopus 로고    scopus 로고
    • Activation of the p53 pathway by small-molecule-induced MDM2 and MDMX dimerization
    • Graves, B. et al. Activation of the p53 pathway by small-molecule-induced MDM2 and MDMX dimerization. Proc. Natl Acad. Sci. USA 109, 11788-11793 (2012
    • (2012) Proc. Natl Acad. Sci. USA , vol.109 , pp. 11788-11793
    • Graves, B.1
  • 73
    • 84875492142 scopus 로고    scopus 로고
    • On the interaction mechanisms of a p53 peptide and nutlin with the mdm2 and mdmx proteins: A brownian dynamics study
    • ElSawy, K. M. et al. On the interaction mechanisms of a p53 peptide and nutlin with the MDM2 and MDMX proteins: A Brownian dynamics study. Cell Cycle 12, 394-404 (2013
    • (2013) Cell Cycle , vol.12 , pp. 394-404
    • Elsawy, K.M.1
  • 74
    • 84881508478 scopus 로고    scopus 로고
    • Identification of a second nutlin 3 responsive interaction site in the n terminal domain of mdm2 using hydrogen/deuterium exchange mass spectrometry
    • Hernychova, L. et al. Identification of a second Nutlin 3 responsive interaction site in the N terminal domain of MDM2 using hydrogen/deuterium exchange mass spectrometry. Proteomics 13, 2512-2525 (2013
    • (2013) Proteomics , vol.13 , pp. 2512-2525
    • Hernychova, L.1
  • 75
    • 63849271797 scopus 로고    scopus 로고
    • Structural basis for high-Affinity peptide inhibition of p53 interactions with mdm2 and mdmx
    • Pazgier, M. et al. Structural basis for high-Affinity peptide inhibition of p53 interactions with MDM2 and MDMX. Proc. Natl Acad. Sci. USA 106, 4665-4670 (2009
    • (2009) Proc. Natl Acad. Sci. USA , vol.106 , pp. 4665-4670
    • Pazgier, M.1
  • 76
    • 76249126943 scopus 로고    scopus 로고
    • Structure-based design of high affinity peptides inhibiting the interaction of p53 with mdm2 and mdmx
    • Phan, J. et al. Structure-based design of high affinity peptides inhibiting the interaction of p53 with MDM2 and MDMX. J. Biol. Chem. 285, 2174-2183 (2010
    • (2010) J. Biol. Chem , vol.285 , pp. 2174-2183
    • Phan, J.1
  • 77
    • 77951766329 scopus 로고    scopus 로고
    • Systematic mutational analysis of peptide inhibition of the p53 mdm2/mdmx interactions
    • Li, C. et al. Systematic mutational analysis of peptide inhibition of the p53 MDM2/MDMX interactions. J. Mol. Biol. 398, 200-213 (2010
    • (2010) J. Mol. Biol , vol.398 , pp. 200-213
    • Li, C.1
  • 78
    • 77956280014 scopus 로고    scopus 로고
    • D peptide inhibitors of the p53 mdm2 interaction for targeted molecular therapy of malignant neoplasms
    • Liu, M. et al. D peptide inhibitors of the p53 MDM2 interaction for targeted molecular therapy of malignant neoplasms. Proc. Natl Acad. Sci. USA 107, 14321-14326 (2010
    • (2010) Proc. Natl Acad. Sci. USA , vol.107 , pp. 14321-14326
    • Liu, M.1
  • 79
    • 53849128197 scopus 로고    scopus 로고
    • Multiple peptide conformations give rise to similar binding affinities: Molecular simulations of p53 mdm2
    • Dastidar, S. G., Lane, D. P. & Verma, C. S. Multiple peptide conformations give rise to similar binding affinities: Molecular simulations of p53 MDM2. J. Am. Chem. Soc. 130, 13514-13515 (2008
    • (2008) J. Am. Chem. Soc , vol.130 , pp. 13514-13515
    • Dastidar, S.G.1    Lane, D.P.2    Verma, C.S.3
  • 80
    • 80052319750 scopus 로고    scopus 로고
    • C terminal substitution of MDM2 interacting peptides modulates binding affinity by distinctive mechanisms
    • Brown, C. J. et al. C terminal substitution of MDM2 interacting peptides modulates binding affinity by distinctive mechanisms. PLoS ONE 6, e24122 (2011
    • (2011) PLoS ONE , vol.6
    • Brown, C.J.1
  • 81
    • 84867669239 scopus 로고    scopus 로고
    • Improved eIF4E binding peptides by phage display guided design: Plasticity of interacting surfaces yield collective effects
    • Zhou, W. et al. Improved eIF4E binding peptides by phage display guided design: Plasticity of interacting surfaces yield collective effects. PLoS ONE 7, e47235 (2012
    • (2012) PLoS ONE , vol.7
    • Zhou, W.1
  • 82
    • 0034697649 scopus 로고    scopus 로고
    • An all-hydrocarbon cross-linking system for enhancing the helicity and metabolic stability of peptides
    • Schafmeister, C. E., Po, J. & Verdine, G. L. An all-hydrocarbon cross-linking system for enhancing the helicity and metabolic stability of peptides. J. Am. Chem. Soc. 122, 5891-5892 (2000
    • (2000) J. Am. Chem. Soc , vol.122 , pp. 5891-5892
    • Schafmeister, C.E.1    Po, J.2    Verdine, G.L.3
  • 83
  • 84
    • 78249268240 scopus 로고    scopus 로고
    • A stapled p53 helix overcomes HDMX-mediated suppression of p53
    • Bernal, F. et al. A stapled p53 helix overcomes HDMX-mediated suppression of p53. Cancer Cell 18, 411-422 (2010
    • (2010) Cancer Cell , vol.18 , pp. 411-422
    • Bernal, F.1
  • 85
    • 84875207784 scopus 로고    scopus 로고
    • Stapled peptides with improved potency and specificity that activate p53
    • Brown, C. J. et al. Stapled peptides with improved potency and specificity that activate p53. ACS Chem. Biol. 8, 506-512 (2013
    • (2013) ACS Chem. Biol , vol.8 , pp. 506-512
    • Brown, C.J.1
  • 86
    • 84883432191 scopus 로고    scopus 로고
    • Stapled α-helical peptide drug development: A potent dual inhibitor of MDM2 and MDMX for p53 dependent cancer therapy
    • Chang, Y. S. et al. Stapled α-helical peptide drug development: A potent dual inhibitor of MDM2 and MDMX for p53 dependent cancer therapy. Proc. Natl Acad. Sci. USA 110, E3445-E3454 (2013
    • (2013) Proc. Natl Acad. Sci. USA , vol.110
    • Chang, Y.S.1
  • 87
    • 84867630243 scopus 로고    scopus 로고
    • A spiroligomer alpha-helix mimic that binds HDM2, penetrates human cells and stabilizes HDM2 in cell culture
    • Brown, Z. Z. et al. A spiroligomer alpha-helix mimic that binds HDM2, penetrates human cells and stabilizes HDM2 in cell culture. PLoS ONE 7, e45948 (2012
    • (2012) PLoS ONE , vol.7
    • Brown, Z.Z.1
  • 88
    • 84881250938 scopus 로고    scopus 로고
    • In vivo activation of the p53 tumor suppressor pathway by an engineered cyclotide
    • Ji, Y. et al. In vivo activation of the p53 tumor suppressor pathway by an engineered cyclotide. J. Am. Chem. Soc. 135, 11623-11633 (2013
    • (2013) J. Am. Chem. Soc , vol.135 , pp. 11623-11633
    • Ji, Y.1
  • 89
    • 4444291734 scopus 로고    scopus 로고
    • Activation of apoptosis in vivo by a hydrocarbon-stapled BH3 helix
    • Walensky, L. D. et al. Activation of apoptosis in vivo by a hydrocarbon-stapled BH3 helix. Science 305, 1466-1470 (2004
    • (2004) Science , vol.305 , pp. 1466-1470
    • Walensky, L.D.1
  • 90
    • 33749660845 scopus 로고    scopus 로고
    • A stapled bid bh3 helix directly binds and activates bax
    • Walensky, L. D. et al. A stapled BID BH3 helix directly binds and activates BAX. Mol. Cell 24, 199-210 (2006
    • (2006) Mol. Cell , vol.24 , pp. 199-210
    • Walensky, L.D.1
  • 91
    • 84874027448 scopus 로고    scopus 로고
    • Stabilizing the pro-Apoptotic BimBH3 helix (BimSAHB) does not necessarily enhance affinity or biological activity
    • Okamoto, T. et al. Stabilizing the pro-Apoptotic BimBH3 helix (BimSAHB) does not necessarily enhance affinity or biological activity. ACS Chem. Biol. 8, 297-302 (2013
    • (2013) ACS Chem. Biol , vol.8 , pp. 297-302
    • Okamoto, T.1
  • 92
    • 70349240216 scopus 로고    scopus 로고
    • Adaptive evolution of p53 thermodynamic stability
    • Khoo, K. H., Andreeva, A. & Fersht, A. R. Adaptive evolution of p53 thermodynamic stability. J. Mol. Biol. 393, 161-175 (2009
    • (2009) J. Mol. Biol , vol.393 , pp. 161-175
    • Khoo, K.H.1    Andreeva, A.2    Fersht, A.R.3
  • 93
    • 47649096991 scopus 로고    scopus 로고
    • Structural biology of the tumor suppressor p53
    • Joerger, A. C. & Fersht, A. R. Structural biology of the tumor suppressor p53. Annu. Rev. Biochem. 77, 557-582 (2008
    • (2008) Annu. Rev. Biochem , vol.77 , pp. 557-582
    • Joerger, A.C.1    Fersht, A.R.2
  • 94
    • 0037180511 scopus 로고    scopus 로고
    • Chemical chaperones increase the cellular activity of n370s beta-glucosidase: A therapeutic strategy for gaucher disease
    • Sawkar, A. R. et al. Chemical chaperones increase the cellular activity of N370S beta-glucosidase: A therapeutic strategy for Gaucher disease. Proc. Natl Acad. Sci. USA 99, 15428-15433 (2002
    • (2002) Proc. Natl Acad. Sci. USA , vol.99 , pp. 15428-15433
    • Sawkar, A.R.1
  • 95
    • 27744459735 scopus 로고    scopus 로고
    • Gaucher disease-Associated glucocerebrosidases show mutation-dependent chemical chaperoning profiles
    • Sawkar, A. R. et al. Gaucher disease-Associated glucocerebrosidases show mutation-dependent chemical chaperoning profiles. Chem. Biol. 12, 1235-1244 (2005
    • (2005) Chem. Biol , vol.12 , pp. 1235-1244
    • Sawkar, A.R.1
  • 96
    • 84879748358 scopus 로고    scopus 로고
    • Monitoring drug target engagement in cells and tissues using the cellular thermal shift assay
    • Martinez Molina, D. et al. Monitoring drug target engagement in cells and tissues using the cellular thermal shift assay. Science 341, 84-87 (2013
    • (2013) Science , vol.341 , pp. 84-87
    • Martinez Molina, D.1
  • 97
    • 48749103325 scopus 로고    scopus 로고
    • Targeted rescue of a destabilized mutant of p53 by an in silico screened drug
    • Boeckler, F. M. et al. Targeted rescue of a destabilized mutant of p53 by an in silico screened drug. Proc. Natl Acad. Sci. USA 105, 10360-10365 (2008
    • (2008) Proc. Natl Acad. Sci. USA , vol.105 , pp. 10360-10365
    • Boeckler, F.M.1
  • 98
    • 84859993146 scopus 로고    scopus 로고
    • Halogen-enriched fragment libraries as leads for drug rescue of mutant p53
    • Wilcken, R. et al. Halogen-enriched fragment libraries as leads for drug rescue of mutant p53. J. Am. Chem. Soc. 134, 6810-6818 (2012
    • (2012) J. Am. Chem. Soc , vol.134 , pp. 6810-6818
    • Wilcken, R.1
  • 99
    • 84880234835 scopus 로고    scopus 로고
    • Small molecule induced reactivation of mutant p53 in cancer cells
    • Liu, X. et al. Small molecule induced reactivation of mutant p53 in cancer cells. Nucleic Acids Res. 41, 6034-6044 (2013
    • (2013) Nucleic Acids Res , vol.41 , pp. 6034-6044
    • Liu, X.1
  • 100
    • 75149134332 scopus 로고    scopus 로고
    • Toward the rational design of p53 stabilizing drugs: Probing the surface of the oncogenic Y220C mutant
    • Basse, N. et al. Toward the rational design of p53 stabilizing drugs: Probing the surface of the oncogenic Y220C mutant. Chem. Biol. 17, 46-56 (2010
    • (2010) Chem. Biol , vol.17 , pp. 46-56
    • Basse, N.1
  • 101
    • 0036128899 scopus 로고    scopus 로고
    • Restoration of the tumor suppressor function to mutant p53 by a low-molecular-weight compound
    • Bykov, V. J. et al. Restoration of the tumor suppressor function to mutant p53 by a low-molecular-weight compound. Nature Med. 8, 282-288 (2002
    • (2002) Nature Med , vol.8 , pp. 282-288
    • Bykov, V.J.1
  • 102
    • 52449087539 scopus 로고    scopus 로고
    • Prima 1met inhibits growth of mouse tumors carrying mutant p53
    • Zache, N., Lambert, J. M., Wiman, K. G. & Bykov, V. J. PRIMA 1MET inhibits growth of mouse tumors carrying mutant p53. Cell Oncol. 30, 411-418 (2008
    • (2008) Cell Oncol , vol.30 , pp. 411-418
    • Zache, N.1    Lambert, J.M.2    Wiman, K.G.3    Bykov, V.J.4
  • 103
    • 79955495593 scopus 로고    scopus 로고
    • Prima 1met/apr 246 induces apoptosis and tumor growth delay in small cell lung cancer expressing mutant p53
    • Zandi, R. et al. PRIMA 1Met/APR 246 induces apoptosis and tumor growth delay in small cell lung cancer expressing mutant p53. Clin. Cancer Res. 17, 2830-2841 (2011
    • (2011) Clin. Cancer Res , vol.17 , pp. 2830-2841
    • Zandi, R.1
  • 104
    • 84867615093 scopus 로고    scopus 로고
    • Targeting p53 in vivo: A first in human study with p53 targeting compound APR 246 in refractory hematologic malignancies and prostate cancer
    • Lehmann, S. et al. Targeting p53 in vivo: A first in human study with p53 targeting compound APR 246 in refractory hematologic malignancies and prostate cancer. J. Clin. Oncol. 30, 3633-3639 (2012
    • (2012) J. Clin. Oncol , vol.30 , pp. 3633-3639
    • Lehmann, S.1
  • 105
    • 65449144050 scopus 로고    scopus 로고
    • Prima 1 reactivates mutant p53 by covalent binding to the core domain
    • Lambert, J. M. et al. PRIMA 1 reactivates mutant p53 by covalent binding to the core domain. Cancer Cell 15, 376-388 (2009
    • (2009) Cancer Cell , vol.15 , pp. 376-388
    • Lambert, J.M.1
  • 106
    • 78649658937 scopus 로고    scopus 로고
    • Stabilization of mutant p53 via alkylation of cysteines and effects on dna binding
    • Kaar, J. L. et al. Stabilization of mutant p53 via alkylation of cysteines and effects on DNA binding. Protein Sci. 19, 2267-2278 (2010
    • (2010) Protein Sci , vol.19 , pp. 2267-2278
    • Kaar, J.L.1
  • 107
    • 84879147794 scopus 로고    scopus 로고
    • Computational identification of a transiently open L1/S3 pocket for reactivation of mutant p53
    • Wassman, C. D. et al. Computational identification of a transiently open L1/S3 pocket for reactivation of mutant p53. Nature Commun. 4, 1407 (2013
    • (2013) Nature Commun , vol.4 , Issue.1407
    • Wassman, C.D.1
  • 108
    • 79955780678 scopus 로고    scopus 로고
    • Identification of two reactive cysteine residues in the tumor suppressor protein p53 using top-down FTICR mass spectrometry
    • Scotcher, J. et al. Identification of two reactive cysteine residues in the tumor suppressor protein p53 using top-down FTICR mass spectrometry. J. Am. Soc. Mass Spectrom. 22, 888-897 (2011
    • (2011) J. Am. Soc. Mass Spectrom , vol.22 , pp. 888-897
    • Scotcher, J.1
  • 109
    • 77954754565 scopus 로고    scopus 로고
    • Targeted quantitation of site-specific cysteine oxidation in endogenous proteins using a differential alkylation and multiple reaction monitoring mass spectrometry approach
    • Held, J. M. et al. Targeted quantitation of site-specific cysteine oxidation in endogenous proteins using a differential alkylation and multiple reaction monitoring mass spectrometry approach. Mol. Cell Proteom. 9, 1400-1410 (2010
    • (2010) Mol. Cell Proteom , vol.9 , pp. 1400-1410
    • Held, J.M.1
  • 110
    • 84873434176 scopus 로고    scopus 로고
    • Impaired epithelial differentiation of induced pluripotent stem cells from ectodermal dysplasia-related patients is rescued by the small compound APR 246/PRIMA 1MET
    • Shalom-Feuerstein, R. et al. Impaired epithelial differentiation of induced pluripotent stem cells from ectodermal dysplasia-related patients is rescued by the small compound APR 246/PRIMA 1MET. Proc. Natl Acad. Sci. USA 110, 2152-2156 (2013
    • (2013) Proc. Natl Acad. Sci. USA , vol.110 , pp. 2152-2156
    • Shalom-Feuerstein, R.1
  • 111
    • 84873426374 scopus 로고    scopus 로고
    • APR 246/PRIMA 1(MET) rescues epidermal differentiation in skin keratinocytes derived from EEC syndrome patients with p63 mutations
    • Shen, J. et al. APR 246/PRIMA 1(MET) rescues epidermal differentiation in skin keratinocytes derived from EEC syndrome patients with p63 mutations. Proc. Natl Acad. Sci. USA 110, 2157-2162 (2013
    • (2013) Proc. Natl Acad. Sci. USA , vol.110 , pp. 2157-2162
    • Shen, J.1
  • 112
    • 78650027467 scopus 로고    scopus 로고
    • Prima 1(met)/apr 246 targets mutant forms of p53 family members p63 and p73
    • Rokaeus, N. et al. PRIMA 1(MET)/APR 246 targets mutant forms of p53 family members p63 and p73. Oncogene 29, 6442-6451 (2010
    • (2010) Oncogene , vol.29 , pp. 6442-6451
    • Rokaeus, N.1
  • 113
    • 84855903282 scopus 로고    scopus 로고
    • Targeting the p53 signaling pathway in cancer therapy - the promises, challenges and perils
    • Stegh, A. H. Targeting the p53 signaling pathway in cancer therapy-The promises, challenges and perils. Expert Opin. Ther. Targets 16, 67-83 (2012
    • (2012) Expert Opin. Ther. Targets , vol.16 , pp. 67-83
    • Stegh, A.H.1
  • 114
    • 0027983669 scopus 로고
    • Crystal structure of a p53 tumor suppressor-DNA complex: Understanding tumorigenic mutations
    • Cho, Y., Gorina, S., Jeffrey, P. D. & Pavletich, N. P. Crystal structure of a p53 tumor suppressor-DNA complex: Understanding tumorigenic mutations. Science 265, 346-355 (1994
    • (1994) Science , vol.265 , pp. 346-355
    • Cho, Y.1    Gorina, S.2    Jeffrey, P.D.3    Pavletich, N.P.4
  • 115
    • 77954681706 scopus 로고    scopus 로고
    • The missing zinc: P53 misfolding and cancer
    • Loh, S. N. The missing zinc: P53 misfolding and cancer. Metallomics 2, 442-449 (2010
    • (2010) Metallomics , vol.2 , pp. 442-449
    • Loh, S.N.1
  • 116
    • 34047224955 scopus 로고    scopus 로고
    • Structure-function-rescue: The diverse nature of common p53 cancer mutants
    • Joerger, A. C. & Fersht, A. R. Structure-function-rescue: The diverse nature of common p53 cancer mutants. Oncogene 26, 2226-2242 (2007
    • (2007) Oncogene , vol.26 , pp. 2226-2242
    • Joerger, A.C.1    Fersht, A.R.2
  • 117
    • 77955470408 scopus 로고    scopus 로고
    • Regulation of p53 activity by hipk2: Molecular mechanisms and therapeutical implications in human cancer cells
    • Puca, R., Nardinocchi, L., Givol, D. & D'Orazi, G. Regulation of p53 activity by HIPK2: Molecular mechanisms and therapeutical implications in human cancer cells. Oncogene 29, 4378-4387 (2010
    • (2010) Oncogene , vol.29 , pp. 4378-4387
    • Puca, R.1    Nardinocchi, L.2    Givol, D.3    D'Orazi, G.4
  • 118
    • 79956022145 scopus 로고    scopus 로고
    • Restoring p53 active conformation by zinc increases the response of mutant p53 tumor cells to anticancer drugs
    • Puca, R. et al. Restoring p53 active conformation by zinc increases the response of mutant p53 tumor cells to anticancer drugs. Cell Cycle 10, 1679-1689 (2011
    • (2011) Cell Cycle , vol.10 , pp. 1679-1689
    • Puca, R.1
  • 119
    • 11144315535 scopus 로고    scopus 로고
    • Small molecule rita binds to p53, blocks p53 hdm 2 interaction and activates p53 function in tumors
    • Issaeva, N. et al. Small molecule RITA binds to p53, blocks p53 HDM 2 interaction and activates p53 function in tumors. Nature Med. 10, 1321-1328 (2004
    • (2004) Nature Med , vol.10 , pp. 1321-1328
    • Issaeva, N.1
  • 120
    • 78650978663 scopus 로고    scopus 로고
    • MI 219 zinc combination: A new paradigm in MDM2 inhibitor-based therapy
    • Azmi, A. S. et al. MI 219 zinc combination: A new paradigm in MDM2 inhibitor-based therapy. Oncogene 30, 117-126 (2011
    • (2011) Oncogene , vol.30 , pp. 117-126
    • Azmi, A.S.1
  • 122
    • 54849413018 scopus 로고    scopus 로고
    • Introducing sense into nonsense in treatments of human genetic diseases
    • Linde, L. & Kerem, B. Introducing sense into nonsense in treatments of human genetic diseases. Trends Genet. 24, 552-563 (2008
    • (2008) Trends Genet , vol.24 , pp. 552-563
    • Linde, L.1    Kerem, B.2
  • 123
    • 68649089108 scopus 로고    scopus 로고
    • Pharmaceuticals targeting nonsense mutations in genetic diseases: Progress in development
    • Rowe, S. M. & Clancy, J. P. Pharmaceuticals targeting nonsense mutations in genetic diseases: Progress in development. BioDrugs 23, 165-174 (2009
    • (2009) BioDrugs , vol.23 , pp. 165-174
    • Rowe, S.M.1    Clancy, J.P.2
  • 124
    • 79955588050 scopus 로고    scopus 로고
    • Rescue of non-sense mutated p53 tumor suppressor gene by aminoglycosides
    • Floquet, C., Deforges, J., Rousset, J. P. & Bidou, L. Rescue of non-sense mutated p53 tumor suppressor gene by aminoglycosides. Nucleic Acids Res. 39, 3350-3362 (2011
    • (2011) Nucleic Acids Res , vol.39 , pp. 3350-3362
    • Floquet, C.1    Deforges, J.2    Rousset, J.P.3    Bidou, L.4
  • 125
    • 78349290383 scopus 로고    scopus 로고
    • Ataluren (PTC124) induces cystic fibrosis transmembrane conductance regulator protein expression and activity in children with nonsense mutation cystic fibrosis
    • Sermet-Gaudelus, I. et al. Ataluren (PTC124) induces cystic fibrosis transmembrane conductance regulator protein expression and activity in children with nonsense mutation cystic fibrosis. Am. J. Respir. Crit. Care Med. 182, 1262-1272 (2010
    • (2010) Am. J. Respir. Crit. Care Med , vol.182 , pp. 1262-1272
    • Sermet-Gaudelus, I.1
  • 126
    • 50149098401 scopus 로고    scopus 로고
    • Effectiveness of PTC124 treatment of cystic fibrosis caused by nonsense mutations: A prospective phase II trial
    • Kerem, E. et al. Effectiveness of PTC124 treatment of cystic fibrosis caused by nonsense mutations: A prospective phase II trial. Lancet 372, 719-727 (2008
    • (2008) Lancet , vol.372 , pp. 719-727
    • Kerem, E.1
  • 127
    • 77950430317 scopus 로고    scopus 로고
    • Molecular basis for the high-Affinity binding and stabilization of firefly luciferase by PTC124
    • Auld, D. S. et al. Molecular basis for the high-Affinity binding and stabilization of firefly luciferase by PTC124. Proc. Natl Acad. Sci. USA 107, 4878-4883 (2010
    • (2010) Proc. Natl Acad. Sci. USA , vol.107 , pp. 4878-4883
    • Auld, D.S.1
  • 128
    • 62549134976 scopus 로고    scopus 로고
    • Mechanism of PTC124 activity in cell-based luciferase assays of nonsense codon suppression
    • Auld, D. S., Thorne, N., Maguire, W. F. & Inglese, J. Mechanism of PTC124 activity in cell-based luciferase assays of nonsense codon suppression. Proc. Natl Acad. Sci. USA 106, 3585-3590 (2009
    • (2009) Proc. Natl Acad. Sci. USA , vol.106 , pp. 3585-3590
    • Auld, D.S.1    Thorne, N.2    Maguire, W.F.3    Inglese, J.4
  • 129
    • 84865794295 scopus 로고    scopus 로고
    • Read-Through compound 13 restores dystrophin expression and improves muscle function in the mdx mouse model for Duchenne muscular dystrophy
    • Kayali, R. et al. Read-Through compound 13 restores dystrophin expression and improves muscle function in the mdx mouse model for Duchenne muscular dystrophy. Hum. Mol. Genet. 21, 4007-4020 (2012
    • (2012) Hum. Mol. Genet , vol.21 , pp. 4007-4020
    • Kayali, R.1
  • 130
    • 69749128490 scopus 로고    scopus 로고
    • Specific activation of the p53 pathway by low dose actinomycin d: A new route to p53 based cyclotherapy
    • Choong, M. L., Yang, H., Lee, M. A. & Lane, D. P. Specific activation of the p53 pathway by low dose actinomycin D: A new route to p53 based cyclotherapy. Cell Cycle 8, 2810-2818 (2009
    • (2009) Cell Cycle , vol.8 , pp. 2810-2818
    • Choong, M.L.1    Yang, H.2    Lee, M.A.3    Lane, D.P.4
  • 131
    • 20444477948 scopus 로고    scopus 로고
    • Seliciclib (cyc202, r roscovitine) induces cell death in multiple myeloma cells by inhibition of rna polymerase ii dependent transcription and down-regulation of mcl 1
    • MacCallum, D. E. et al. Seliciclib (CYC202, R roscovitine) induces cell death in multiple myeloma cells by inhibition of RNA polymerase II dependent transcription and down-regulation of Mcl 1. Cancer Res. 65, 5399-5407 (2005
    • (2005) Cancer Res , vol.65 , pp. 5399-5407
    • MacCallum, D.E.1
  • 132
    • 0343044332 scopus 로고    scopus 로고
    • Effects on normal fibroblasts and neuroblastoma cells of the activation of the p53 response by the nuclear export inhibitor leptomycin b
    • Smart, P. et al. Effects on normal fibroblasts and neuroblastoma cells of the activation of the p53 response by the nuclear export inhibitor leptomycin B. Oncogene 18, 7378-7386 (1999
    • (1999) Oncogene , vol.18 , pp. 7378-7386
    • Smart, P.1
  • 133
    • 84871962551 scopus 로고    scopus 로고
    • Novel dna damage checkpoints mediating cell death induced by the nedd8 activating enzyme inhibitor mln4924
    • Blank, J. L. et al. Novel DNA damage checkpoints mediating cell death induced by the NEDD8 activating enzyme inhibitor MLN4924. Cancer Res. 73, 225-234 (2013
    • (2013) Cancer Res , vol.73 , pp. 225-234
    • Blank, J.L.1
  • 134
    • 84863011183 scopus 로고    scopus 로고
    • Activation of p53 by sirt1 inhibition enhances elimination of cml leukemia stem cells in combination with imatinib
    • Li, L. et al. Activation of p53 by SIRT1 inhibition enhances elimination of CML leukemia stem cells in combination with imatinib. Cancer Cell 21, 266-281 (2012
    • (2012) Cancer Cell , vol.21 , pp. 266-281
    • Li, L.1
  • 135
    • 84859766621 scopus 로고    scopus 로고
    • Pharmacological inhibition of Mdm2 triggers growth arrest and promotes DNA breakage in mouse colon tumors and human colon cancer cells
    • Rigatti, M. J., Verma, R., Belinsky, G. S., Rosenberg, D. W. & Giardina, C. Pharmacological inhibition of Mdm2 triggers growth arrest and promotes DNA breakage in mouse colon tumors and human colon cancer cells. Mol. Carcinog. 51, 363-378 (2012
    • (2012) Mol. Carcinog , vol.51 , pp. 363-378
    • Rigatti, M.J.1    Verma, R.2    Belinsky, G.S.3    Rosenberg, D.W.4    Giardina, C.5
  • 137
    • 35448932303 scopus 로고    scopus 로고
    • The MDM 2 antagonist nutlin 3 promotes the maturation of acute myeloid leukemic blasts
    • Secchiero, P. et al. The MDM 2 antagonist nutlin 3 promotes the maturation of acute myeloid leukemic blasts. Neoplasia 9, 853-861 (2007
    • (2007) Neoplasia , vol.9 , pp. 853-861
    • Secchiero, P.1
  • 138
    • 84862832557 scopus 로고    scopus 로고
    • Structural insights into the dual-Targeting mechanism of nutlin 3
    • Shin, J. S. et al. Structural insights into the dual-Targeting mechanism of Nutlin 3. Biochem. Biophys. Res. Commun. 420, 48-53 (2012
    • (2012) Biochem. Biophys. Res. Commun , vol.420 , pp. 48-53
    • Shin, J.S.1
  • 139
    • 77955907917 scopus 로고    scopus 로고
    • Multiple distinct molecular mechanisms influence sensitivity and resistance to mdm2 inhibitors in adult acute myelogenous leukemia
    • Long, J. et al. Multiple distinct molecular mechanisms influence sensitivity and resistance to MDM2 inhibitors in adult acute myelogenous leukemia. Blood 116, 71-80 (2010
    • (2010) Blood , vol.116 , pp. 71-80
    • Long, J.1
  • 140
    • 33646574651 scopus 로고    scopus 로고
    • Functional integrity of the p53 mediated apoptotic pathway induced by the nongenotoxic agent nutlin 3 in b cell chronic lymphocytic leukemia (b cll
    • Secchiero, P. et al. Functional integrity of the p53 mediated apoptotic pathway induced by the nongenotoxic agent nutlin 3 in B cell chronic lymphocytic leukemia (B CLL). Blood 107, 4122-4129 (2006
    • (2006) Blood , vol.107 , pp. 4122-4129
    • Secchiero, P.1
  • 141
    • 77957174185 scopus 로고    scopus 로고
    • Molecular mechanisms of nutlin-induced apoptosis in multiple myeloma: Evidence for p53 transcription-dependent and-independent pathways
    • Saha, M. N., Jiang, H. & Chang, H. Molecular mechanisms of nutlin-induced apoptosis in multiple myeloma: Evidence for p53 transcription-dependent and-independent pathways. Cancer Biol. Ther. 10, 567-578 (2010
    • (2010) Cancer Biol. Ther , vol.10 , pp. 567-578
    • Saha, M.N.1    Jiang, H.2    Chang, H.3
  • 142
    • 70449727603 scopus 로고    scopus 로고
    • Antitumor activity of the selective MDM2 antagonist nutlin 3 against chemoresistant neuroblastoma with wild-Type p53
    • Van Maerken, T. et al. Antitumor activity of the selective MDM2 antagonist nutlin 3 against chemoresistant neuroblastoma with wild-Type p53. J. Natl Cancer Inst. 101, 1562-1574 (2009
    • (2009) J. Natl Cancer Inst , vol.101 , pp. 1562-1574
    • Van Maerken, T.1
  • 143
    • 61349120257 scopus 로고    scopus 로고
    • MDM2 antagonist nutlin 3 displays antiproliferative and proapoptotic activity in mantle cell lymphoma
    • Tabe, Y. et al. MDM2 antagonist nutlin 3 displays antiproliferative and proapoptotic activity in mantle cell lymphoma. Clin. Cancer Res. 15, 933-942 (2009
    • (2009) Clin. Cancer Res , vol.15 , pp. 933-942
    • Tabe, Y.1
  • 145
    • 84874259421 scopus 로고    scopus 로고
    • Correlation of tp53 and mdm2 genotypes with response to therapy in sarcoma
    • Ohnstad, H. O. et al. Correlation of TP53 and MDM2 genotypes with response to therapy in sarcoma. Cancer 119, 1013-1022 (2013
    • (2013) Cancer , vol.119 , pp. 1013-1022
    • Ohnstad, H.O.1
  • 146
    • 32444449180 scopus 로고    scopus 로고
    • Small-molecule MDM2 antagonists reveal aberrant p53 signaling in cancer: Implications for therapy
    • Tovar, C. et al. Small-molecule MDM2 antagonists reveal aberrant p53 signaling in cancer: Implications for therapy. Proc. Natl Acad. Sci. USA 103, 1888-1893 (2006
    • (2006) Proc. Natl Acad. Sci. USA , vol.103 , pp. 1888-1893
    • Tovar, C.1
  • 147
    • 48849109488 scopus 로고    scopus 로고
    • Multiple p53 independent gene silencing mechanisms define the cellular response to p53 activation
    • Paris, R., Henry, R. E., Stephens, S. J., McBryde, M. & Espinosa, J. M. Multiple p53 independent gene silencing mechanisms define the cellular response to p53 activation. Cell Cycle 7, 2427-2433 (2008
    • (2008) Cell Cycle , vol.7 , pp. 2427-2433
    • Paris, R.1    Henry, R.E.2    Stephens, S.J.3    McBryde, M.4    Espinosa, J.M.5
  • 148
    • 79955447216 scopus 로고    scopus 로고
    • P53 hypersensitivity is the predominant mechanism of the unique responsiveness of testicular germ cell tumor (TGCT) cells to cisplatin
    • Gutekunst, M. et al. p53 hypersensitivity is the predominant mechanism of the unique responsiveness of testicular germ cell tumor (TGCT) cells to cisplatin. PLoS ONE 6, e19198 (2011
    • (2011) PLoS ONE , vol.6
    • Gutekunst, M.1
  • 149
    • 84874856381 scopus 로고    scopus 로고
    • Cisplatin hypersensitivity of testicular germ cell tumors is determined by high constitutive Noxa levels mediated by Oct 4
    • Gutekunst, M. et al. Cisplatin hypersensitivity of testicular germ cell tumors is determined by high constitutive Noxa levels mediated by Oct 4. Cancer Res. 73, 1460-1469 (2013
    • (2013) Cancer Res , vol.73 , pp. 1460-1469
    • Gutekunst, M.1
  • 150
    • 70649113052 scopus 로고    scopus 로고
    • Genetic variants in TPMT and COMT are associated with hearing loss in children receiving cisplatin chemotherapy
    • Ross, C. J. et al. Genetic variants in TPMT and COMT are associated with hearing loss in children receiving cisplatin chemotherapy. Nature Genet. 41, 1345-1349 (2009
    • (2009) Nature Genet , vol.41 , pp. 1345-1349
    • Ross, C.J.1
  • 151
    • 84874948475 scopus 로고    scopus 로고
    • A threshold mechanism mediates p53 cell fate decision between growth arrest and apoptosis
    • Kracikova, M., Akiri, G., George, A., Sachidanandam, R. & Aaronson, S. A. A threshold mechanism mediates p53 cell fate decision between growth arrest and apoptosis. Cell Death Differ. 20, 576-588 (2013
    • (2013) Cell Death Differ , vol.20 , pp. 576-588
    • Kracikova, M.1    Akiri, G.2    George, A.3    Sachidanandam, R.4    Aaronson, S.A.5
  • 152
    • 84876914265 scopus 로고    scopus 로고
    • Mdm2 small-molecule antagonist rg7112 activates p53 signaling and regresses human tumors in preclinical cancer models
    • Tovar, C. et al. MDM2 small-molecule antagonist RG7112 activates p53 signaling and regresses human tumors in preclinical cancer models. Cancer Res. 73, 2587-2597 (2013
    • (2013) Cancer Res , vol.73 , pp. 2587-2597
    • Tovar, C.1
  • 153
    • 84868203735 scopus 로고    scopus 로고
    • Effect of the mdm2 antagonist rg7112 on the p53 pathway in patients with mdm2 amplified, well-differentiated or dedifferentiated liposarcoma: An exploratory proof of mechanism study
    • Ray-Coquard, I. et al. Effect of the MDM2 antagonist RG7112 on the p53 pathway in patients with MDM2 amplified, well-differentiated or dedifferentiated liposarcoma: An exploratory proof of mechanism study. Lancet Oncol. 13, 1133-1140 (2012
    • (2012) Lancet Oncol , vol.13 , pp. 1133-1140
    • Ray-Coquard, I.1
  • 154
    • 53349103292 scopus 로고    scopus 로고
    • Modelling myc inhibition as a cancer therapy
    • Soucek, L. et al. Modelling Myc inhibition as a cancer therapy. Nature 455, 679-683 (2008
    • (2008) Nature , vol.455 , pp. 679-683
    • Soucek, L.1
  • 155
    • 75649131205 scopus 로고    scopus 로고
    • Simultaneous activation of p53 and inhibition of XIAP enhance the activation of apoptosis signaling pathways in AML
    • Carter, B. Z. et al. Simultaneous activation of p53 and inhibition of XIAP enhance the activation of apoptosis signaling pathways in AML. Blood 115, 306-314 (2010
    • (2010) Blood , vol.115 , pp. 306-314
    • Carter, B.Z.1
  • 156
    • 79951696692 scopus 로고    scopus 로고
    • A p53 independent role for the mdm2 antagonist nutlin 3 in dna damage response initiation
    • Valentine, J. M., Kumar, S. & Moumen, A. A p53 independent role for the MDM2 antagonist Nutlin 3 in DNA damage response initiation. BMC Cancer 11, 79 (2011
    • (2011) BMC Cancer , vol.11 , Issue.79
    • Valentine, J.M.1    Kumar, S.2    Moumen, A.3
  • 157
    • 84896702778 scopus 로고    scopus 로고
    • Activation of p53 by the MDM2 inhibitor RG7112 impairs thrombopoiesis
    • Iancu-Rubin, C. et al. Activation of p53 by the MDM2 inhibitor RG7112 impairs thrombopoiesis. Exp. Hematol. http://dx.doi.org/10.1016/j.exphem.2013. 11.012 (2013
    • (2013) Exp. Hematol
    • Iancu-Rubin, C.1
  • 158
    • 84875490185 scopus 로고    scopus 로고
    • Cancer genome landscapes
    • Vogelstein, B. et al. Cancer genome landscapes. Science 339, 1546-1558 (2013
    • (2013) Science , vol.339 , pp. 1546-1558
    • Vogelstein, B.1
  • 159
    • 84856098041 scopus 로고    scopus 로고
    • Adaptation of cancer cells from different entities to the MDM2 inhibitor nutlin 3 results in the emergence of p53 mutated multi-drug-resistant cancer cells
    • Michaelis, M. et al. Adaptation of cancer cells from different entities to the MDM2 inhibitor nutlin 3 results in the emergence of p53 mutated multi-drug-resistant cancer cells. Cell Death Dis. 2, e243 (2011
    • (2011) Cell Death Dis , vol.2
    • Michaelis, M.1
  • 160
    • 81255185485 scopus 로고    scopus 로고
    • Acquisition of p53 mutations in response to the non-genotoxic p53 activator Nutlin 3
    • Aziz, M. H., Shen, H. & Maki, C. G. Acquisition of p53 mutations in response to the non-genotoxic p53 activator Nutlin 3. Oncogene 30, 4678-4686 (2011
    • (2011) Oncogene , vol.30 , pp. 4678-4686
    • Aziz, M.H.1    Shen, H.2    Maki, C.G.3
  • 161
    • 84867417876 scopus 로고    scopus 로고
    • Drug resistance to inhibitors of the human double minute 2 e3 ligase is mediated by point mutations of p53, but can be overcome with the p53 targeting agent rita
    • Jones, R. J., Bjorklund, C. C., Baladandayuthapani, V., Kuhn, D. J. & Orlowski, R. Z. Drug resistance to inhibitors of the human double minute 2 E3 ligase is mediated by point mutations of p53, but can be overcome with the p53 targeting agent RITA. Mol. Cancer Ther. 11, 2243-2253 (2012
    • (2012) Mol. Cancer Ther , vol.11 , pp. 2243-2253
    • Jones, R.J.1    Bjorklund, C.C.2    Baladandayuthapani, V.3    Kuhn, D.J.4    Orlowski, R.Z.5
  • 162
    • 33646343474 scopus 로고    scopus 로고
    • An shrna barcode screen provides insight into cancer cell vulnerability to mdm2 inhibitors
    • Brummelkamp, T. R. et al. An shRNA barcode screen provides insight into cancer cell vulnerability to MDM2 inhibitors. Nature Chem. Biol. 2, 202-206 (2006
    • (2006) Nature Chem. Biol , vol.2 , pp. 202-206
    • Brummelkamp, T.R.1
  • 163
    • 84876245628 scopus 로고    scopus 로고
    • Using a preclinical mouse model of high-grade astrocytoma to optimize p53 restoration therapy
    • Shchors, K. et al. Using a preclinical mouse model of high-grade astrocytoma to optimize p53 restoration therapy. Proc. Natl Acad. Sci. USA 110, E1480-E1489 (2013
    • (2013) Proc. Natl Acad. Sci. USA , vol.110
    • Shchors, K.1
  • 164
    • 84861482216 scopus 로고    scopus 로고
    • Phase II study of single-Agent navitoclax (ABT 263) and biomarker correlates in patients with relapsed small cell lung cancer
    • Rudin, C. M. et al. Phase II study of single-Agent navitoclax (ABT 263) and biomarker correlates in patients with relapsed small cell lung cancer. Clin. Cancer Res. 18, 3163-3169 (2012
    • (2012) Clin. Cancer Res , vol.18 , pp. 3163-3169
    • Rudin, C.M.1
  • 165
    • 84863116430 scopus 로고    scopus 로고
    • Substantial susceptibility of chronic lymphocytic leukemia to BCL2 inhibition: Results of a phase i study of navitoclax in patients with relapsed or refractory disease
    • Roberts, A. W. et al. Substantial susceptibility of chronic lymphocytic leukemia to BCL2 inhibition: Results of a phase I study of navitoclax in patients with relapsed or refractory disease. J. Clin. Oncol. 30, 488-496 (2012
    • (2012) J. Clin. Oncol , vol.30 , pp. 488-496
    • Roberts, A.W.1
  • 166
    • 33750834023 scopus 로고    scopus 로고
    • The BH3 mimetic ABT 737 targets selective Bcl 2 proteins and efficiently induces apoptosis via Bak/Bax if Mcl 1 is neutralized
    • van Delft, M. F. et al. The BH3 mimetic ABT 737 targets selective Bcl 2 proteins and efficiently induces apoptosis via Bak/Bax if Mcl 1 is neutralized. Cancer Cell 10, 389-399 (2006
    • (2006) Cancer Cell , vol.10 , pp. 389-399
    • Van Delft, M.F.1
  • 167
    • 33750628289 scopus 로고    scopus 로고
    • Mechanisms of apoptosis sensitivity and resistance to the BH3 mimetic ABT 737 in acute myeloid leukemia
    • Konopleva, M. et al. Mechanisms of apoptosis sensitivity and resistance to the BH3 mimetic ABT 737 in acute myeloid leukemia. Cancer Cell 10, 375-388 (2006
    • (2006) Cancer Cell , vol.10 , pp. 375-388
    • Konopleva, M.1
  • 168
    • 77951442337 scopus 로고    scopus 로고
    • Acquired resistance to ABT 737 in lymphoma cells that up regulate MCL 1 and BFL 1
    • Yecies, D., Carlson, N. E., Deng, J. & Letai, A. Acquired resistance to ABT 737 in lymphoma cells that up regulate MCL 1 and BFL 1. Blood 115, 3304-3313 (2010
    • (2010) Blood , vol.115 , pp. 3304-3313
    • Yecies, D.1    Carlson, N.E.2    Deng, J.3    Letai, A.4
  • 169
    • 84865733257 scopus 로고    scopus 로고
    • Bcl 2 is a better abt 737 target than bcl xl or bcl w and only noxa overcomes resistance mediated by mcl 1, bfl 1, or bcl b
    • Rooswinkel, R. W., van de Kooij, B., Verheij, M. & Borst, J. Bcl 2 is a better ABT 737 target than Bcl xL or Bcl w and only Noxa overcomes resistance mediated by Mcl 1, Bfl 1, or Bcl B. Cell Death Dis. 3, e366 (2012
    • (2012) Cell Death Dis , vol.3
    • Rooswinkel, R.W.1    Van De Kooij, B.2    Verheij, M.3    Borst, J.4
  • 170
    • 79959223906 scopus 로고    scopus 로고
    • Npmc+ aml cell line shows differential protein expression and lower sensitivity to dna-damaging and p53 inducing anticancer compounds
    • Lew, Q. J. et al. NPMc+ AML cell line shows differential protein expression and lower sensitivity to DNA-damaging and p53 inducing anticancer compounds. Cell Cycle 10, 1978-1987 (2011
    • (2011) Cell Cycle , vol.10 , pp. 1978-1987
    • Lew, Q.J.1
  • 171
    • 34248177222 scopus 로고    scopus 로고
    • Mitogen-Activated protein kinase kinase inhibition enhances nuclear proapoptotic function of p53 in acute myelogenous leukemia cells
    • Kojima, K., Konopleva, M., Samudio, I. J., Ruvolo, V. & Andreeff, M. Mitogen-Activated protein kinase kinase inhibition enhances nuclear proapoptotic function of p53 in acute myelogenous leukemia cells. Cancer Res. 67, 3210-3219 (2007
    • (2007) Cancer Res , vol.67 , pp. 3210-3219
    • Kojima, K.1    Konopleva, M.2    Samudio, I.J.3    Ruvolo, V.4    Andreeff, M.5
  • 172
    • 84859627981 scopus 로고    scopus 로고
    • Mek inhibition enhances abt 737 induced leukemia cell apoptosis via prevention of erk-Activated mcl 1 induction and modulation of mcl 1/bim complex
    • Konopleva, M. et al. MEK inhibition enhances ABT 737 induced leukemia cell apoptosis via prevention of ERK-Activated MCL 1 induction and modulation of MCL 1/BIM complex. Leukemia 26, 778-787 (2012
    • (2012) Leukemia , vol.26 , pp. 778-787
    • Konopleva, M.1
  • 173
    • 84856270102 scopus 로고    scopus 로고
    • Anti-Apoptotic Mcl 1 is essential for the development and sustained growth of acute myeloid leukemia
    • Glaser, S. P. et al. Anti-Apoptotic Mcl 1 is essential for the development and sustained growth of acute myeloid leukemia. Genes Dev. 26, 120-125 (2012
    • (2012) Genes Dev , vol.26 , pp. 120-125
    • Glaser, S.P.1
  • 174
    • 84867490138 scopus 로고    scopus 로고
    • Relative mitochondrial priming of myeloblasts and normal HSCs determines chemotherapeutic success in AML
    • Vo, T. T. et al. Relative mitochondrial priming of myeloblasts and normal HSCs determines chemotherapeutic success in AML. Cell 151, 344-355 (2012
    • (2012) Cell , vol.151 , pp. 344-355
    • Vo, T.T.1
  • 175
    • 82255192310 scopus 로고    scopus 로고
    • Pretreatment mitochondrial priming correlates with clinical response to cytotoxic chemotherapy
    • Ni Chonghaile, T. et al. Pretreatment mitochondrial priming correlates with clinical response to cytotoxic chemotherapy. Science 334, 1129-1133 (2011
    • (2011) Science , vol.334 , pp. 1129-1133
    • Ni Chonghaile, T.1
  • 176
    • 33645511223 scopus 로고    scopus 로고
    • Levels of hdmx expression dictate the sensitivity of normal and transformed cells to nutlin 3
    • Patton, J. T. et al. Levels of HdmX expression dictate the sensitivity of normal and transformed cells to Nutlin 3. Cancer Res. 66, 3169-3176 (2006
    • (2006) Cancer Res , vol.66 , pp. 3169-3176
    • Patton, J.T.1
  • 177
    • 33845251005 scopus 로고    scopus 로고
    • Hdmx modulates the outcome of p53 activation in human tumor cells
    • Wade, M., Wong, E. T., Tang, M., Stommel, J. M. & Wahl, G. M. Hdmx modulates the outcome of p53 activation in human tumor cells. J. Biol. Chem. 281, 33036-33044 (2006
    • (2006) J. Biol. Chem , vol.281 , pp. 33036-33044
    • Wade, M.1    Wong, E.T.2    Tang, M.3    Stommel, J.M.4    Wahl, G.M.5
  • 178
    • 84860389276 scopus 로고    scopus 로고
    • Validation of MdmX as a therapeutic target for reactivating p53 in tumors
    • Garcia, D. et al. Validation of MdmX as a therapeutic target for reactivating p53 in tumors. Genes Dev. 25, 1746-1757 (2011
    • (2011) Genes Dev , vol.25 , pp. 1746-1757
    • Garcia, D.1
  • 179
    • 84894239668 scopus 로고    scopus 로고
    • Inhibition of Nutlin-resistant HDM2 mutants by stapled peptides
    • Wei, S. J. Inhibition of Nutlin-resistant HDM2 mutants by stapled peptides. PLoS ONE 8, e81068 (2013
    • (2013) PLoS ONE , vol.8
    • Wei, S.J.1
  • 180
    • 58349112761 scopus 로고    scopus 로고
    • Reversal of P glycoprotein-mediated multidrug resistance by the murine double minute 2 antagonist nutlin 3
    • Michaelis, M. et al. Reversal of P glycoprotein-mediated multidrug resistance by the murine double minute 2 antagonist nutlin 3. Cancer Res. 69, 416-421 (2009
    • (2009) Cancer Res , vol.69 , pp. 416-421
    • Michaelis, M.1
  • 181
    • 33745488640 scopus 로고    scopus 로고
    • R roscovitine (cyc202, seliciclib) sensitizes sh sy5y neuroblastoma cells to nutlin 3 induced apoptosis
    • Ribas, J., Boix, J. & Meijer, L. (R)-roscovitine (CYC202, seliciclib) sensitizes SH SY5Y neuroblastoma cells to nutlin 3 induced apoptosis. Exp. Cell Res. 312, 2394-2400 (2006
    • (2006) Exp. Cell Res , vol.312 , pp. 2394-2400
    • Ribas, J.1    Boix, J.2    Meijer, L.3
  • 182
    • 36249021361 scopus 로고    scopus 로고
    • Cyclin-dependent kinase inhibitors sensitize tumor cells to nutlin-induced apoptosis: A potent drug combination
    • Cheok, C. F., Dey, A. & Lane, D. P. Cyclin-dependent kinase inhibitors sensitize tumor cells to nutlin-induced apoptosis: A potent drug combination. Mol. Cancer Res. 5, 1133-1145 (2007
    • (2007) Mol. Cancer Res , vol.5 , pp. 1133-1145
    • Cheok, C.F.1    Dey, A.2    Lane, D.P.3
  • 183
    • 53449095193 scopus 로고    scopus 로고
    • Concomitant inhibition of Mdm2 p53 interaction and Aurora kinases activates the p53 dependent postmitotic checkpoints and synergistically induces p53 mediated mitochondrial apoptosis along with reduced endoreduplication in acute myelogenous leukemia
    • Kojima, K., Konopleva, M., Tsao, T., Nakakuma, H. & Andreeff, M. Concomitant inhibition of Mdm2 p53 interaction and Aurora kinases activates the p53 dependent postmitotic checkpoints and synergistically induces p53 mediated mitochondrial apoptosis along with reduced endoreduplication in acute myelogenous leukemia. Blood 112, 2886-2895 (2008
    • (2008) Blood , vol.112 , pp. 2886-2895
    • Kojima, K.1    Konopleva, M.2    Tsao, T.3    Nakakuma, H.4    Andreeff, M.5
  • 184
    • 77955709042 scopus 로고    scopus 로고
    • Combination of nutlin 3 and VX 680 selectively targets p53 mutant cells with reversible effects on cells expressing wild-Type p53
    • Cheok, C. F., Kua, N., Kaldis, P. & Lane, D. P. Combination of nutlin 3 and VX 680 selectively targets p53 mutant cells with reversible effects on cells expressing wild-Type p53. Cell Death Differ. 17, 1486-1500 (2010
    • (2010) Cell Death Differ , vol.17 , pp. 1486-1500
    • Cheok, C.F.1    Kua, N.2    Kaldis, P.3    Lane, D.P.4
  • 185
    • 33646550549 scopus 로고    scopus 로고
    • MDM2 antagonists activate p53 and synergize with genotoxic drugs in B cell chronic lymphocytic leukemia cells
    • Coll-Mulet, L. et al. MDM2 antagonists activate p53 and synergize with genotoxic drugs in B cell chronic lymphocytic leukemia cells. Blood 107, 4109-4114 (2006
    • (2006) Blood , vol.107 , pp. 4109-4114
    • Coll-Mulet, L.1
  • 186
    • 33644979375 scopus 로고    scopus 로고
    • Radiosensitization of lung cancer by nutlin, an inhibitor of murine double minute 2
    • Cao, C. et al. Radiosensitization of lung cancer by nutlin, an inhibitor of murine double minute 2. Mol. Cancer Ther. 5, 411-417 (2006
    • (2006) Mol. Cancer Ther , vol.5 , pp. 411-417
    • Cao, C.1
  • 187
    • 42249102761 scopus 로고    scopus 로고
    • Nutlin 3 radiosensitizes hypoxic prostate cancer cells independent of p53
    • Supiot, S., Hill, R. P. & Bristow, R. G. Nutlin 3 radiosensitizes hypoxic prostate cancer cells independent of p53. Mol. Cancer Ther. 7, 993-999 (2008
    • (2008) Mol. Cancer Ther , vol.7 , pp. 993-999
    • Supiot, S.1    Hill, R.P.2    Bristow, R.G.3
  • 188
    • 77950212489 scopus 로고    scopus 로고
    • Blockade of mitogen-Activated protein kinase/extracellular signal-regulated kinase kinase and murine double minute synergistically induces apoptosis in acute myeloid leukemia via BH3 only proteins Puma and Bim
    • Zhang, W. et al. Blockade of mitogen-Activated protein kinase/extracellular signal-regulated kinase kinase and murine double minute synergistically induces apoptosis in acute myeloid leukemia via BH3 only proteins Puma and Bim. Cancer Res. 70, 2424-2434 (2010
    • (2010) Cancer Res , vol.70 , pp. 2424-2434
    • Zhang, W.1
  • 189
    • 77952122464 scopus 로고    scopus 로고
    • 1,25 dihydroxyvitamin D3 enhances the apoptotic activity of MDM2 antagonist nutlin 3a in acute myeloid leukemia cells expressing wild-Type p53
    • Thompson, T., Andreeff, M., Studzinski, G. P. & Vassilev, L. T. 1,25 dihydroxyvitamin D3 enhances the apoptotic activity of MDM2 antagonist nutlin 3a in acute myeloid leukemia cells expressing wild-Type p53. Mol. Cancer Ther. 9, 1158-1168 (2010
    • (2010) Mol. Cancer Ther , vol.9 , pp. 1158-1168
    • Thompson, T.1    Andreeff, M.2    Studzinski, G.P.3    Vassilev, L.T.4
  • 190
    • 84860750821 scopus 로고    scopus 로고
    • Synergistic induction of p53 mediated apoptosis by valproic acid and nutlin 3 in acute myeloid leukemia
    • McCormack, E. et al. Synergistic induction of p53 mediated apoptosis by valproic acid and nutlin 3 in acute myeloid leukemia. Leukemia 26, 910-917 (2012
    • (2012) Leukemia , vol.26 , pp. 910-917
    • McCormack, E.1
  • 191
    • 0037184969 scopus 로고    scopus 로고
    • Acetylation of p53 inhibits its ubiquitination by Mdm2
    • Li, M., Luo, J., Brooks, C. L. & Gu, W. Acetylation of p53 inhibits its ubiquitination by Mdm2. J. Biol. Chem. 277, 50607-50611 (2002
    • (2002) J. Biol. Chem , vol.277 , pp. 50607-50611
    • Li, M.1    Luo, J.2    Brooks, C.L.3    Gu, W.4
  • 192
    • 47749096347 scopus 로고    scopus 로고
    • BH3 activation blocks Hdmx suppression of apoptosis and cooperates with Nutlin to induce cell death
    • Wade, M., Rodewald, L. W., Espinosa, J. M. & Wahl, G. M. BH3 activation blocks Hdmx suppression of apoptosis and cooperates with Nutlin to induce cell death. Cell Cycle 7, 1973-1982 (2008
    • (2008) Cell Cycle , vol.7 , pp. 1973-1982
    • Wade, M.1    Rodewald, L.W.2    Espinosa, J.M.3    Wahl, G.M.4
  • 193
    • 33845421171 scopus 로고    scopus 로고
    • Concomitant inhibition of MDM2 and Bcl 2 protein function synergistically induce mitochondrial apoptosis in AML
    • Kojima, K. et al. Concomitant inhibition of MDM2 and Bcl 2 protein function synergistically induce mitochondrial apoptosis in AML. Cell Cycle 5, 2778-2786 (2006
    • (2006) Cell Cycle , vol.5 , pp. 2778-2786
    • Kojima, K.1
  • 194
    • 84873079604 scopus 로고    scopus 로고
    • Mdm2 antagonists induce apoptosis and synergize with cisplatin overcoming chemoresistance in TP53 wild-Type ovarian cancer cells
    • Mir, R. et al. Mdm2 antagonists induce apoptosis and synergize with cisplatin overcoming chemoresistance in TP53 wild-Type ovarian cancer cells. Int. J. Cancer 132, 1525-1536 (2013
    • (2013) Int. J. Cancer , vol.132 , pp. 1525-1536
    • Mir, R.1
  • 195
    • 79955518716 scopus 로고    scopus 로고
    • MDM2 antagonists boost antitumor effect of androgen withdrawal: Implications for therapy of prostate cancer
    • Tovar, C. et al. MDM2 antagonists boost antitumor effect of androgen withdrawal: Implications for therapy of prostate cancer. Mol. Cancer 10, 49 (2011
    • (2011) Mol. Cancer , vol.10 , Issue.49
    • Tovar, C.1
  • 196
    • 0036738149 scopus 로고    scopus 로고
    • Stromal cells prevent apoptosis of AML cells by up regulation of anti-Apoptotic proteins
    • Konopleva, M. et al. Stromal cells prevent apoptosis of AML cells by up regulation of anti-Apoptotic proteins. Leukemia 16, 1713-1724 (2002
    • (2002) Leukemia , vol.16 , pp. 1713-1724
    • Konopleva, M.1
  • 197
    • 84868013848 scopus 로고    scopus 로고
    • Decreased mitochondrial apoptotic priming underlies stroma-mediated treatment resistance in chronic lymphocytic leukemia
    • Davids, M. S. et al. Decreased mitochondrial apoptotic priming underlies stroma-mediated treatment resistance in chronic lymphocytic leukemia. Blood 120, 3501-3509 (2012
    • (2012) Blood , vol.120 , pp. 3501-3509
    • Davids, M.S.1
  • 198
    • 84862905519 scopus 로고    scopus 로고
    • ATM and MET kinases are synthetic lethal with nongenotoxic activation of p53
    • Sullivan, K. D. et al. ATM and MET kinases are synthetic lethal with nongenotoxic activation of p53. Nature Chem. Biol. 8, 646-654 (2012
    • (2012) Nature Chem. Biol , vol.8 , pp. 646-654
    • Sullivan, K.D.1
  • 199
    • 79951831707 scopus 로고    scopus 로고
    • Dasatinib plus Nutlin 3 shows synergistic antileukemic activity in both p53 wild-Type and p53 mutated B chronic lymphocytic leukemias by inhibiting the Akt pathway
    • Zauli, G. et al. Dasatinib plus Nutlin 3 shows synergistic antileukemic
    • (2011) Clin. Cancer Res , vol.17 , pp. 762-770
    • Zauli, G.1
  • 200
    • 84868598894 scopus 로고    scopus 로고
    • The sorafenib plus nutlin 3 combination promotes synergistic cytotoxicity in acute myeloid leukemic cells irrespectively of FLT3 and p53 status
    • Zauli, G. et al. The sorafenib plus nutlin 3 combination promotes synergistic cytotoxicity in acute myeloid leukemic cells irrespectively of FLT3 and p53 status. Haematologica 97, 1722-1730 (2012
    • (2012) Haematologica , vol.97 , pp. 1722-1730
    • Zauli, G.1
  • 201
    • 33947324969 scopus 로고    scopus 로고
    • A dominant role for p53 dependent cellular senescence in radiosensitization of human prostate cancer cells
    • Lehmann, B. D. et al. A dominant role for p53 dependent cellular senescence in radiosensitization of human prostate cancer cells. Cell Cycle 6, 595-605 (2007
    • (2007) Cell Cycle , vol.6 , pp. 595-605
    • Lehmann, B.D.1
  • 202
    • 0035359505 scopus 로고    scopus 로고
    • Exploiting cancer cell cycling for selective protection of normal cells
    • Blagosklonny, M. V. & Pardee, A. B. Exploiting cancer cell cycling for selective protection of normal cells. Cancer Res. 61, 4301-4305 (2001
    • (2001) Cancer Res , vol.61 , pp. 4301-4305
    • Blagosklonny, M.V.1    Pardee, A.B.2
  • 203
    • 0036491845 scopus 로고    scopus 로고
    • The restriction point of the cell cycle
    • Blagosklonny, M. V. & Pardee, A. B. The restriction point of the cell cycle. Cell Cycle 1, 103-110 (2002
    • (2002) Cell Cycle , vol.1 , pp. 103-110
    • Blagosklonny, M.V.1    Pardee, A.B.2
  • 204
    • 16444380911 scopus 로고    scopus 로고
    • Activation of p53 by MDM2 antagonists can protect proliferating cells from mitotic inhibitors
    • Carvajal, D. et al. Activation of p53 by MDM2 antagonists can protect proliferating cells from mitotic inhibitors. Cancer Res. 65, 1918-1924 (2005
    • (2005) Cancer Res , vol.65 , pp. 1918-1924
    • Carvajal, D.1
  • 205
    • 33751291771 scopus 로고    scopus 로고
    • Nongenotoxic p53 activation protects cells against S phase-specific chemotherapy
    • Kranz, D. & Dobbelstein, M. Nongenotoxic p53 activation protects cells against S phase-specific chemotherapy. Cancer Res. 66, 10274-10280 (2006
    • (2006) Cancer Res , vol.66 , pp. 10274-10280
    • Kranz, D.1    Dobbelstein, M.2
  • 206
    • 0027109075 scopus 로고
    • Cancer. P53, guardian of the genome
    • Lane, D. P. Cancer. p53, guardian of the genome. Nature 358, 15-16 (1992
    • (1992) Nature , vol.358 , pp. 15-16
    • Lane, D.P.1
  • 207
    • 84860780032 scopus 로고    scopus 로고
    • An evaluation of small-molecule p53 activators as chemoprotectants ameliorating adverse effects of anticancer drugs in normal cells
    • van Leeuwen, I. M., Rao, B., Sachweh, M. C. & Lain, S. An evaluation of small-molecule p53 activators as chemoprotectants ameliorating adverse effects of anticancer drugs in normal cells. Cell Cycle 11, 1851-1861 (2012
    • (2012) Cell Cycle , vol.11 , pp. 1851-1861
    • Van Leeuwen, I.M.1    Rao, B.2    Sachweh, M.C.3    Lain, S.4
  • 208
    • 84868615579 scopus 로고    scopus 로고
    • Cyclotherapy: Opening a therapeutic window in cancer treatment
    • van Leeuwen, I. M. Cyclotherapy: Opening a therapeutic window in cancer treatment. Oncotarget 3, 596-600 (2012
    • (2012) Oncotarget , vol.3 , pp. 596-600
    • Van Leeuwen, I.M.1
  • 209
    • 62649112876 scopus 로고    scopus 로고
    • A panel of isogenic human cancer cells suggests a therapeutic approach for cancers with inactivated p53
    • Sur, S. et al. A panel of isogenic human cancer cells suggests a therapeutic approach for cancers with inactivated p53. Proc. Natl Acad. Sci. USA 106, 3964-3969 (2009
    • (2009) Proc. Natl Acad. Sci. USA , vol.106 , pp. 3964-3969
    • Sur, S.1
  • 210
    • 0034664733 scopus 로고    scopus 로고
    • P53AIP1, a potential mediator of p53 dependent apoptosis, and its regulation by ser 46 phosphorylated p53
    • Oda, K. et al. p53AIP1, a potential mediator of p53 dependent apoptosis, and its regulation by Ser 46 phosphorylated p53. Cell 102, 849-862 (2000
    • (2000) Cell , vol.102 , pp. 849-862
    • Oda, K.1
  • 211
    • 0029802591 scopus 로고    scopus 로고
    • P53 levels functional domains and dna damage determine the extent of the apoptotic response of tumor cells
    • Chen, X. & Ko, L. J., Jayaraman, L. & Prives, C. p53 levels, functional domains, and DNA damage determine the extent of the apoptotic response of tumor cells. Genes Dev. 10, 2438-2451 (1996
    • (1996) Genes Dev , vol.10 , pp. 2438-2451
    • Chen, X.1    Ko, L.J.2    Jayaraman, L.3    Prives, C.4
  • 212
    • 41149090794 scopus 로고    scopus 로고
    • Algorithm for prediction of tumour suppressor p53 affinity for binding sites in DNA
    • Veprintsev, D. B. & Fersht, A. R. Algorithm for prediction of tumour suppressor p53 affinity for binding sites in DNA. Nucleic Acids Res. 36, 1589-1598 (2008
    • (2008) Nucleic Acids Res , vol.36 , pp. 1589-1598
    • Veprintsev, D.B.1    Fersht, A.R.2
  • 213
    • 77951942433 scopus 로고    scopus 로고
    • DNA binding cooperativity of p53 modulates the decision between cell-cycle arrest and apoptosis
    • Schlereth, K. et al. DNA binding cooperativity of p53 modulates the decision between cell-cycle arrest and apoptosis. Mol. Cell 38, 356-368 (2010
    • (2010) Mol. Cell , vol.38 , pp. 356-368
    • Schlereth, K.1
  • 214
    • 77958515009 scopus 로고    scopus 로고
    • Life or death: 53 induced apoptosis requires DNA binding cooperativity
    • Schlereth, K., Charles, J. P., Bretz, A. C. & Stiewe, T. Life or death: 53 induced apoptosis requires DNA binding cooperativity. Cell Cycle 9, 4068-4076 (2010
    • (2010) Cell Cycle , vol.9 , pp. 4068-4076
    • Schlereth, K.1    Charles, J.P.2    Bretz, A.C.3    Stiewe, T.4
  • 215
    • 84878582588 scopus 로고    scopus 로고
    • P53 DNA binding cooperativity is essential for apoptosis and tumor suppression in vivo
    • Timofeev, O. et al. p53 DNA binding cooperativity is essential for apoptosis and tumor suppression in vivo. Cell Rep. 3, 1512-1525 (2013
    • (2013) Cell Rep , vol.3 , pp. 1512-1525
    • Timofeev, O.1
  • 216
    • 17944379798 scopus 로고    scopus 로고
    • ASPP proteins specifically stimulate the apoptotic function of p53
    • Samuels-Lev, Y. et al. ASPP proteins specifically stimulate the apoptotic function of p53. Mol. Cell 8, 781-794 (2001
    • (2001) Mol. Cell , vol.8 , pp. 781-794
    • Samuels-Lev, Y.1
  • 217
    • 33749118677 scopus 로고    scopus 로고
    • Iaspp preferentially binds p53 proline-rich region and modulates apoptotic function of codon 72 polymorphic p53
    • Bergamaschi, D. et al. iASPP preferentially binds p53 proline-rich region and modulates apoptotic function of codon 72 polymorphic p53. Nature Genet. 38, 1133-1141 (2006
    • (2006) Nature Genet , vol.38 , pp. 1133-1141
    • Bergamaschi, D.1
  • 218
    • 10644278820 scopus 로고    scopus 로고
    • The expression of iASPP in acute leukemias
    • Zhang, X., Wang, M., Zhou, C., Chen, S. & Wang, J. The expression of iASPP in acute leukemias. Leuk. Res. 29, 179-183 (2005
    • (2005) Leuk. Res , vol.29 , pp. 179-183
    • Zhang, X.1    Wang, M.2    Zhou, C.3    Chen, S.4    Wang, J.5
  • 219
    • 80455129998 scopus 로고    scopus 로고
    • Iaspp and chemoresistance in ovarian cancers: Effects on paclitaxel-mediated mitotic catastrophe
    • Jiang, L. et al. iASPP and chemoresistance in ovarian cancers: Effects on paclitaxel-mediated mitotic catastrophe. Clin. Cancer Res. 17, 6924-6933 (2011
    • (2011) Clin. Cancer Res , vol.17 , pp. 6924-6933
    • Jiang, L.1
  • 220
    • 65549120715 scopus 로고    scopus 로고
    • Modes of p53 regulation
    • Kruse, J. P. & Gu, W. Modes of p53 regulation. Cell 137, 609-622 (2009
    • (2009) Cell , vol.137 , pp. 609-622
    • Kruse, J.P.1    Gu, W.2
  • 222
    • 84861355836 scopus 로고    scopus 로고
    • Atm phosphorylation of mdm2 ser394 regulates the amplitude and duration of the dna damage response in mice
    • Gannon, H. S., Woda, B. A. & Jones, S. N. ATM phosphorylation of Mdm2 Ser394 regulates the amplitude and duration of the DNA damage response in mice. Cancer Cell 21, 668-679 (2012
    • (2012) Cancer Cell , vol.21 , pp. 668-679
    • Gannon, H.S.1    Woda, B.A.2    Jones, S.N.3
  • 223
    • 0034737438 scopus 로고    scopus 로고
    • Damage-mediated phosphorylation of human p53 threonine 18 through a cascade mediated by a casein 1 like kinase effect on mdm2 binding
    • Sakaguchi, K. et al. Damage-mediated phosphorylation of human p53 threonine 18 through a cascade mediated by a casein 1 like kinase. Effect on Mdm2 binding. J. Biol. Chem. 275, 9278-9283 (2000
    • (2000) J. Biol. Chem , vol.275 , pp. 9278-9283
    • Sakaguchi, K.1
  • 224
    • 18244379872 scopus 로고    scopus 로고
    • Homeodomain-interacting protein kinase 2 phosphorylates p53 at ser 46 and mediates apoptosis
    • D'Orazi, G. et al. Homeodomain-interacting protein kinase 2 phosphorylates p53 at Ser 46 and mediates apoptosis. Nature Cell Biol. 4, 11-19 (2002
    • (2002) Nature Cell Biol , vol.4 , pp. 11-19
    • D'Orazi, G.1
  • 225
    • 0036141392 scopus 로고    scopus 로고
    • Regulation of p53 activity by its interaction with homeodomain- interacting protein kinase 2
    • Hofmann, T. G. et al. Regulation of p53 activity by its interaction with homeodomain-interacting protein kinase 2. Nature Cell Biol. 4, 1-10 (2002
    • (2002) Nature Cell Biol , vol.4 , pp. 1-10
    • Hofmann, T.G.1
  • 226
    • 84856019043 scopus 로고    scopus 로고
    • Inability of p53 reactivating compounds Nutlin 3 and RITA to overcome p53 resistance in tumor cells deficient in p53Ser46 phosphorylation
    • Ma, T. et al. Inability of p53 reactivating compounds Nutlin 3 and RITA to overcome p53 resistance in tumor cells deficient in p53Ser46 phosphorylation. Biochem. Biophys. Res. Commun. 417, 931-937 (2012
    • (2012) Biochem. Biophys. Res. Commun , vol.417 , pp. 931-937
    • Ma, T.1
  • 227
    • 84857997208 scopus 로고    scopus 로고
    • Dr4:tbid axis drives the p53 apoptotic response by promoting oligomerization of poised bax
    • Henry, R. E., Andrysik, Z., Paris, R., Galbraith, M. D. & Espinosa, J. M. A. DR4:tBID axis drives the p53 apoptotic response by promoting oligomerization of poised BAX. EMBO J. 31, 1266-1278 (2012
    • (2012) EMBO J. , vol.31 , pp. 1266-1278
    • Henry, R.E.1    Andrysik, Z.2    Paris, R.3    Galbraith, M.D.4    Espinosa, J.M.A.5
  • 228
    • 44049095767 scopus 로고    scopus 로고
    • In several cell types tumour suppressor p53 induces apoptosis largely via Puma but Noxa can contribute
    • Michalak, E. M., Villunger, A., Adams, J. M. & Strasser, A. In several cell types tumour suppressor p53 induces apoptosis largely via Puma but Noxa can contribute. Cell Death Differ. 15, 1019-1029 (2008
    • (2008) Cell Death Differ , vol.15 , pp. 1019-1029
    • Michalak, E.M.1    Villunger, A.2    Adams, J.M.3    Strasser, A.4
  • 229
    • 78650047484 scopus 로고    scopus 로고
    • Maximal killing of lymphoma cells by dna damage-inducing therapy requires not only the p53 targets puma and noxa, but also bim
    • Happo, L. et al. Maximal killing of lymphoma cells by DNA damage-inducing therapy requires not only the p53 targets Puma and Noxa, but also Bim. Blood 116, 5256-5267 (2010
    • (2010) Blood , vol.116 , pp. 5256-5267
    • Happo, L.1
  • 230
    • 19944432123 scopus 로고    scopus 로고
    • Differential targeting of prosurvival Bcl 2 proteins by their BH3 only ligands allows complementary apoptotic function
    • Chen, L. et al. Differential targeting of prosurvival Bcl 2 proteins by their BH3 only ligands allows complementary apoptotic function. Mol. Cell 17, 393-403 (2005
    • (2005) Mol. Cell , vol.17 , pp. 393-403
    • Chen, L.1
  • 231
    • 0037349289 scopus 로고    scopus 로고
    • P53 has a direct apoptogenic role at the mitochondria
    • Mihara, M. et al. p53 has a direct apoptogenic role at the mitochondria. Mol. Cell 11, 577-590 (2003
    • (2003) Mol. Cell , vol.11 , pp. 577-590
    • Mihara, M.1
  • 232
    • 0842278331 scopus 로고    scopus 로고
    • Direct activation of Bax by p53 mediates mitochondrial membrane permeabilization and apoptosis
    • Chipuk, J. E. et al. Direct activation of Bax by p53 mediates mitochondrial membrane permeabilization and apoptosis. Science 303, 1010-1014 (2004
    • (2004) Science , vol.303 , pp. 1010-1014
    • Chipuk, J.E.1
  • 233
    • 84876291823 scopus 로고    scopus 로고
    • Non-cell-Autonomous tumor suppression by p53
    • Lujambio, A. et al. Non-cell-Autonomous tumor suppression by p53. Cell 153, 449-460 (2013
    • (2013) Cell , vol.153 , pp. 449-460
    • Lujambio, A.1
  • 234
    • 84862124987 scopus 로고    scopus 로고
    • P53 mediated senescence impairs the apoptotic response to chemotherapy and clinical outcome in breast cancer
    • Jackson, J. G. et al. p53 mediated senescence impairs the apoptotic response to chemotherapy and clinical outcome in breast cancer. Cancer Cell 21, 793-806 (2012
    • (2012) Cancer Cell , vol.21 , pp. 793-806
    • Jackson, J.G.1
  • 235
    • 4344610526 scopus 로고    scopus 로고
    • Small-molecule antagonists of p53 MDM2 binding: Research tools and potential therapeutics
    • Vassilev, L. T. Small-molecule antagonists of p53 MDM2 binding: Research tools and potential therapeutics. Cell Cycle 3, 419-421 (2004
    • (2004) Cell Cycle , vol.3 , pp. 419-421
    • Vassilev, L.T.1
  • 237
    • 33644873086 scopus 로고    scopus 로고
    • Benzodiazepinedione inhibitors of the Hdm2:p53 complex suppress human tumor cell proliferation in vitro and sensitize tumors to doxorubicin in vivo
    • Koblish, H. K. et al. Benzodiazepinedione inhibitors of the Hdm2:p53 complex suppress human tumor cell proliferation in vitro and sensitize tumors to doxorubicin in vivo. Mol. Cancer Ther. 5, 160-169 (2006
    • (2006) Mol. Cancer Ther , vol.5 , pp. 160-169
    • Koblish, H.K.1
  • 238
    • 6344246456 scopus 로고    scopus 로고
    • Tnf-related apoptosis-inducing ligand (trail): A potential candidate for combined treatment of hematological malignancies
    • Secchiero, P., Vaccarezza, M., Gonelli, A. & Zauli, G. TNF-related apoptosis-inducing ligand (TRAIL): A potential candidate for combined treatment of hematological malignancies. Curr. Pharm. Des. 10, 3673-3681 (2004
    • (2004) Curr. Pharm. des , vol.10 , pp. 3673-3681
    • Secchiero, P.1    Vaccarezza, M.2    Gonelli, A.3    Zauli, G.4
  • 240
    • 84881006591 scopus 로고    scopus 로고
    • Prognostic impact and targeting of CRM1 in acute myeloid leukemia
    • Kojima, K. et al. Prognostic impact and targeting of CRM1 in acute myeloid leukemia. Blood 121, 4166-4174 (2013
    • (2013) Blood , vol.121 , pp. 4166-4174
    • Kojima, K.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.