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Volumn 14, Issue 2, 2015, Pages 375-383

AMG 925 is a dual FLT3/CDK4 inhibitor with the potential to overcome FLT3 inhibitor resistance in acute myeloid leukemia

Author keywords

[No Author keywords available]

Indexed keywords

AMG 925; ANTILEUKEMIC AGENT; BETA ACTIN; CD135 ANTIGEN; CYCLIN DEPENDENT KINASE 4; CYCLIN DEPENDENT KINASE INHIBITOR; D 835; FURODAZOLE; MESSENGER RNA; MITOGEN ACTIVATED PROTEIN KINASE; PALBOCICLIB; PROTEIN KINASE B; PROTEIN TYROSINE KINASE INHIBITOR; QUIZARTINIB; RETINOBLASTOMA PROTEIN; SORAFENIB; STAT5 PROTEIN; UNCLASSIFIED DRUG; 2-HYDROXY-1-(2-((9-(4-METHYLCYCLOHEXYL)-9H-PYRIDO(4',3'-4,5)PYRROLO(2,3-D)PYRIMIDIN-2-YL)AMINO)-7,8-DIHYDRO-1,6-NAPHTHYRIDIN-6(5H)-YL)ETHANONE; BENZOTHIAZOLE DERIVATIVE; CARBANILAMIDE DERIVATIVE; FUSED HETEROCYCLIC RINGS; NAPHTHYRIDINE DERIVATIVE; PIPERAZINE DERIVATIVE; PROTEIN KINASE INHIBITOR; PYRIDINE DERIVATIVE;

EID: 84923366197     PISSN: 15357163     EISSN: 15388514     Source Type: Journal    
DOI: 10.1158/1535-7163.MCT-14-0388     Document Type: Article
Times cited : (27)

References (45)
  • 1
    • 0037114829 scopus 로고    scopus 로고
    • Prognostic significance of activating FLT3 mutations in younger adults (16 to 60 years) with acute myeloid leukemia and normal cytogenetics: A study of the AML Study Group Ulm
    • Frohling S, Schlenk RF, Breitruck J, Benner A, Kreitmeier S, Tobis K, et al. Prognostic significance of activating FLT3 mutations in younger adults (16 to 60 years) with acute myeloid leukemia and normal cytogenetics: a study of the AML Study Group Ulm. Blood 2002;100:4372-80.
    • (2002) Blood , vol.100 , pp. 4372-4380
    • Frohling, S.1    Schlenk, R.F.2    Breitruck, J.3    Benner, A.4    Kreitmeier, S.5    Tobis, K.6
  • 2
    • 0030451722 scopus 로고    scopus 로고
    • Internal tandem duplication of the flt3 gene found in acute myeloid leukemia
    • Nakao M, Yokota S, Iwai T, Kaneko H, Horiike S, Kashima K, et al. Internal tandem duplication of the flt3 gene found in acute myeloid leukemia. Leukemia 1996;10:1911-8.
    • (1996) Leukemia , vol.10 , pp. 1911-1918
    • Nakao, M.1    Yokota, S.2    Iwai, T.3    Kaneko, H.4    Horiike, S.5    Kashima, K.6
  • 3
    • 0035885955 scopus 로고    scopus 로고
    • The presence of a FLT3 internal tandem duplication in patients with acute myeloid leukemia (AML) adds important prognostic information to cytogenetic risk group and response to the first cycle of chemotherapy: Analysis of 854 patients from the United Kingdom Medical Research Council AML 10 and 12 trials
    • Kottaridis PD, Gale RE, Frew ME, Harrison G, Langabeer SE, Belton AA, et al. The presence of a FLT3 internal tandem duplication in patients with acute myeloid leukemia (AML) adds important prognostic information to cytogenetic risk group and response to the first cycle of chemotherapy: analysis of 854 patients from the United Kingdom Medical Research Council AML 10 and 12 trials. Blood 2001;98:1752-9.
    • (2001) Blood , vol.98 , pp. 1752-1759
    • Kottaridis, P.D.1    Gale, R.E.2    Frew, M.E.3    Harrison, G.4    Langabeer, S.E.5    Belton, A.A.6
  • 4
    • 84897511335 scopus 로고    scopus 로고
    • Activating FLT3 mutants show distinct gain-of-function phenotypes in vitro and a characteristic signaling pathway profile associated with prognosis in acute myeloid leukemia
    • Janke H, Pastore F, Schumacher D, Herold T, Hopfner KP, Schneider S, et al. Activating FLT3 mutants show distinct gain-of-function phenotypes in vitro and a characteristic signaling pathway profile associated with prognosis in acute myeloid leukemia. PLoS ONE 2014;9:e89560.
    • (2014) PLoS ONE , vol.9 , pp. e89560
    • Janke, H.1    Pastore, F.2    Schumacher, D.3    Herold, T.4    Hopfner, K.P.5    Schneider, S.6
  • 5
    • 78650073854 scopus 로고    scopus 로고
    • FLT3 as a therapeutic target in AML: Still challenging after all these years
    • Kindler T, Lipka DB, Fischer T. FLT3 as a therapeutic target in AML: still challenging after all these years. Blood 2010;116:5089-102.
    • (2010) Blood , vol.116 , pp. 5089-5102
    • Kindler, T.1    Lipka, D.B.2    Fischer, T.3
  • 6
    • 84879132548 scopus 로고    scopus 로고
    • FLT3 inhibitors for acute myeloid leukemia: A review of their efficacy and mechanisms of resistance
    • Grunwald MR, Levis MJ. FLT3 inhibitors for acute myeloid leukemia: a review of their efficacy and mechanisms of resistance. Int J Hematol 2013;97:683-94.
    • (2013) Int J Hematol , vol.97 , pp. 683-694
    • Grunwald, M.R.1    Levis, M.J.2
  • 7
    • 78049426367 scopus 로고    scopus 로고
    • Phase IIB trial of oral Midostaurin (PKC412), the FMS-like tyrosine kinase 3 receptor (FLT3) and multi-targeted kinase inhibitor, in patients with acute myeloid leukemia and high-risk myelodysplastic syndrome with either wild-type or mutated FLT3
    • Fischer T, Stone RM, Deangelo DJ, Galinsky I, Estey E, Lanza C, et al. Phase IIB trial of oral Midostaurin (PKC412), the FMS-like tyrosine kinase 3 receptor (FLT3) and multi-targeted kinase inhibitor, in patients with acute myeloid leukemia and high-risk myelodysplastic syndrome with either wild-type or mutated FLT3. J Clin Oncol 2010;28:4339-45.
    • (2010) J Clin Oncol , vol.28 , pp. 4339-4345
    • Fischer, T.1    Stone, R.M.2    Deangelo, D.J.3    Galinsky, I.4    Estey, E.5    Lanza, C.6
  • 8
    • 79953124734 scopus 로고    scopus 로고
    • Results from a randomized trial of salvage chemotherapy followed by lestaurtinib for patients with FLT3 mutant AML in first relapse
    • Levis M, Ravandi F, Wang ES, Baer MR, Perl A, Coutre S, et al. Results from a randomized trial of salvage chemotherapy followed by lestaurtinib for patients with FLT3 mutant AML in first relapse. Blood 2011;117:3294-301.
    • (2011) Blood , vol.117 , pp. 3294-3301
    • Levis, M.1    Ravandi, F.2    Wang, E.S.3    Baer, M.R.4    Perl, A.5    Coutre, S.6
  • 9
    • 62949087552 scopus 로고    scopus 로고
    • A pharmacodynamic study of the FLT3 inhibitor KW-2449 yields insight into the basis for clinical response
    • Pratz KW, Cortes J, Roboz GJ, Rao N, Arowojolu O, Stine A, et al. A pharmacodynamic study of the FLT3 inhibitor KW-2449 yields insight into the basis for clinical response. Blood 2009;113:3938-46.
    • (2009) Blood , vol.113 , pp. 3938-3946
    • Pratz, K.W.1    Cortes, J.2    Roboz, G.J.3    Rao, N.4    Arowojolu, O.5    Stine, A.6
  • 10
    • 77949887020 scopus 로고    scopus 로고
    • FLT3-mutant allelic burden and clinical status are predictive of response to FLT3 inhibitors in AML
    • Pratz KW, Sato T, Murphy KM, Stine A, Rajkhowa T, Levis M. FLT3-mutant allelic burden and clinical status are predictive of response to FLT3 inhibitors in AML. Blood 2010;115:1425-32.
    • (2010) Blood , vol.115 , pp. 1425-1432
    • Pratz, K.W.1    Sato, T.2    Murphy, K.M.3    Stine, A.4    Rajkhowa, T.5    Levis, M.6
  • 11
    • 84869090342 scopus 로고    scopus 로고
    • High activity of sorafenib in FLT3-ITD-positive acute myeloid leukemia synergizes with allo-immune effects to induce sustained responses
    • Metzelder SK, Schroeder T, Finck A, Scholl S, Fey M, Gotze K, et al. High activity of sorafenib in FLT3-ITD-positive acute myeloid leukemia synergizes with allo-immune effects to induce sustained responses. Leukemia 2012;26:2353-9.
    • (2012) Leukemia , vol.26 , pp. 2353-2359
    • Metzelder, S.K.1    Schroeder, T.2    Finck, A.3    Scholl, S.4    Fey, M.5    Gotze, K.6
  • 12
    • 70449475105 scopus 로고    scopus 로고
    • AC220 is a uniquely potent and selective inhibitor of FLT3 for the treatment of acute myeloid leukemia (AML)
    • Zarrinkar PP, Gunawardane RN, Cramer MD, Gardner MF, Brigham D, Belli B, et al. AC220 is a uniquely potent and selective inhibitor of FLT3 for the treatment of acute myeloid leukemia (AML). Blood 2009;114:2984-92.
    • (2009) Blood , vol.114 , pp. 2984-2992
    • Zarrinkar, P.P.1    Gunawardane, R.N.2    Cramer, M.D.3    Gardner, M.F.4    Brigham, D.5    Belli, B.6
  • 13
    • 84874598006 scopus 로고    scopus 로고
    • Quizartinib (AC220) is a potent second generation class III tyrosine kinase inhibitor that displays a distinct inhibition profile against mutant-FLT3, -PDGFRA and -KIT isoforms
    • Kampa-Schittenhelm KM, Heinrich MC, Akmut F, Dohner H, Dohner K, Schittenhelm MM. Quizartinib (AC220) is a potent second generation class III tyrosine kinase inhibitor that displays a distinct inhibition profile against mutant-FLT3, -PDGFRA and -KIT isoforms. Mol Cancer 2013;12:19.
    • (2013) Mol Cancer , vol.12 , pp. 19
    • Kampa-Schittenhelm, K.M.1    Heinrich, M.C.2    Akmut, F.3    Dohner, H.4    Dohner, K.5    Schittenhelm, M.M.6
  • 14
    • 84887793880 scopus 로고    scopus 로고
    • The role of quizartinib in the treatment of acute myeloid leukemia
    • Ostronoff F, Estey E. The role of quizartinib in the treatment of acute myeloid leukemia. Expert Opin Investig Drugs 2013;22:1659-69.
    • (2013) Expert Opin Investig Drugs , vol.22 , pp. 1659-1669
    • Ostronoff, F.1    Estey, E.2
  • 15
    • 84860747223 scopus 로고    scopus 로고
    • Validation of ITD mutations in FLT3 as a therapeutic target in human acute myeloid leukaemia
    • Smith CC, Wang Q, Chin CS, Salerno S, Damon LE, Levis MJ, et al. Validation of ITD mutations in FLT3 as a therapeutic target in human acute myeloid leukaemia. Nature 2012;485:260-3.
    • (2012) Nature , vol.485 , pp. 260-263
    • Smith, C.C.1    Wang, Q.2    Chin, C.S.3    Salerno, S.4    Damon, L.E.5    Levis, M.J.6
  • 17
    • 34249733270 scopus 로고    scopus 로고
    • DNA profiling analysis of 100 consecutive de novo acute myeloid leukemia cases reveals patterns of genomic instability that affect all cytogenetic risk groups
    • Suela J, Alvarez S, Cifuentes F, Largo C, Ferreira BI, Blesa D, et al. DNA profiling analysis of 100 consecutive de novo acute myeloid leukemia cases reveals patterns of genomic instability that affect all cytogenetic risk groups. Leukemia 2007;21:1224-31.
    • (2007) Leukemia , vol.21 , pp. 1224-1231
    • Suela, J.1    Alvarez, S.2    Cifuentes, F.3    Largo, C.4    Ferreira, B.I.5    Blesa, D.6
  • 18
    • 84912056282 scopus 로고    scopus 로고
    • Preclinical evaluation of AMG 925, a FLT3/CDK4 dual kinase inhibitor for treating acute myeloid leukemia
    • Keegan K, Li C, Li Z, Ma J, Ragains M, Coberly S, et al. Preclinical evaluation of AMG 925, a FLT3/CDK4 dual kinase inhibitor for treating acute myeloid leukemia. Mol Cancer Ther 2014;13:880-9.
    • (2014) Mol Cancer Ther , vol.13 , pp. 880-889
    • Keegan, K.1    Li, C.2    Li, Z.3    Ma, J.4    Ragains, M.5    Coberly, S.6
  • 19
    • 84899573074 scopus 로고    scopus 로고
    • Discovery of AMG 925, a FLT3 and CDK4 dual kinase inhibitor with preferential affinity for the activated state of FLT3
    • Li Z, Wang X, Eksterowicz J, Gribble MW, Alba GQ, Ayres M, et al. Discovery of AMG 925, a FLT3 and CDK4 dual kinase inhibitor with preferential affinity for the activated state of FLT3. J Med Chem 2014;57:3430-49.
    • (2014) J Med Chem , vol.57 , pp. 3430-3449
    • Li, Z.1    Wang, X.2    Eksterowicz, J.3    Gribble, M.W.4    Alba, G.Q.5    Ayres, M.6
  • 21
    • 84880481139 scopus 로고    scopus 로고
    • CDK4: A key player in the cell cycle, development, and cancer
    • Baker SJ, Reddy EP. CDK4: a key player in the cell cycle, development, and cancer. Genes Cancer 2012;3:658-69.
    • (2012) Genes Cancer , vol.3 , pp. 658-669
    • Baker, S.J.1    Reddy, E.P.2
  • 22
    • 0034306996 scopus 로고    scopus 로고
    • The Rb/E2F pathway: Expanding roles and emerging paradigms
    • Harbour JW, Dean DC. The Rb/E2F pathway: expanding roles and emerging paradigms. Genes Dev 2000;14:2393-409.
    • (2000) Genes Dev , vol.14 , pp. 2393-2409
    • Harbour, J.W.1    Dean, D.C.2
  • 23
    • 0035063183 scopus 로고    scopus 로고
    • The Rb/E2F pathway and cancer
    • Nevins JR. The Rb/E2F pathway and cancer. Hum Mol Genet 2001;10:699-703.
    • (2001) Hum Mol Genet , vol.10 , pp. 699-703
    • Nevins, J.R.1
  • 24
    • 0037075887 scopus 로고    scopus 로고
    • Cyclin D-dependent kinases, INK4 inhibitors and cancer
    • Ortega S, Malumbres M, Barbacid M. Cyclin D-dependent kinases, INK4 inhibitors and cancer. Biochim Biophys Acta 2002;1602:73-87.
    • (2002) Biochim Biophys Acta , vol.1602 , pp. 73-87
    • Ortega, S.1    Malumbres, M.2    Barbacid, M.3
  • 26
    • 27144458683 scopus 로고    scopus 로고
    • Cyclins and CDKS in development and cancer: Lessons from genetically modified mice
    • Santamaria D, Ortega S. Cyclins and CDKS in development and cancer: lessons from genetically modified mice. Front Biosci 2006;11:1164-88.
    • (2006) Front Biosci , vol.11 , pp. 1164-1188
    • Santamaria, D.1    Ortega, S.2
  • 27
    • 84875697676 scopus 로고    scopus 로고
    • Results of a randomized phase 2 study of PD 0332991, a cyclin-dependent kinase (CDK) 4/6 inhibitor, in combination with letrozole vs letrozole alone for first-line treatment of ER+/HER2- advanced breast cancer (BC)
    • Finn RSCJ, Lang I, Boer K, Bondarenko IM, Kulyk SO, Ettl J, et al. Results of a randomized phase 2 study of PD 0332991, a cyclin-dependent kinase (CDK) 4/6 inhibitor, in combination with letrozole vs letrozole alone for first-line treatment of ER+/HER2- advanced breast cancer (BC). Cancer Res 2012;72.
    • (2012) Cancer Res , pp. 72
    • Finn, R.S.C.J.1    Lang, I.2    Boer, K.3    Bondarenko, I.M.4    Kulyk, S.O.5    Ettl, J.6
  • 28
    • 0021332973 scopus 로고
    • Retinoblastoma: Clues to human oncogenesis
    • Murphree AL, Benedict WF. Retinoblastoma: clues to human oncogenesis. Science 1984;223:1028-33.
    • (1984) Science , vol.223 , pp. 1028-1033
    • Murphree, A.L.1    Benedict, W.F.2
  • 29
    • 0028275733 scopus 로고
    • Deletions of the cyclin-dependent kinase-4 inhibitor gene in multiple human cancers
    • Nobori T, Miura K, Wu DJ, Lois A, Takabayashi K, Carson DA. Deletions of the cyclin-dependent kinase-4 inhibitor gene in multiple human cancers. Nature 1994;368:753-6.
    • (1994) Nature , vol.368 , pp. 753-756
    • Nobori, T.1    Miura, K.2    Wu, D.J.3    Lois, A.4    Takabayashi, K.5    Carson, D.A.6
  • 30
    • 0348149013 scopus 로고    scopus 로고
    • Epigenetic inactivation of INK4/CDK/RB cell cycle pathway in acute leukemias
    • Chim CS, Wong AS, Kwong YL. Epigenetic inactivation of INK4/CDK/RB cell cycle pathway in acute leukemias. Ann Hematol 2003;82:738-42.
    • (2003) Ann Hematol , vol.82 , pp. 738-742
    • Chim, C.S.1    Wong, A.S.2    Kwong, Y.L.3
  • 31
    • 77951045228 scopus 로고    scopus 로고
    • Signatures of polycomb repression and reduced H3K4 trimethylation are associated with p15INK4b DNA methylation in AML
    • Paul TA, Bies J, Small D, Wolff L. Signatures of polycomb repression and reduced H3K4 trimethylation are associated with p15INK4b DNA methylation in AML. Blood 2010;115:3098-108.
    • (2010) Blood , vol.115 , pp. 3098-3108
    • Paul, T.A.1    Bies, J.2    Small, D.3    Wolff, L.4
  • 32
    • 34548838818 scopus 로고    scopus 로고
    • Pharmacologic inhibition of CDK4/6: Mechanistic evidence for selective activity or acquired resistance in acute myeloid leukemia
    • Wang L, Wang J, Blaser BW, Duchemin AM, Kusewitt DF, Liu T, et al. Pharmacologic inhibition of CDK4/6: mechanistic evidence for selective activity or acquired resistance in acute myeloid leukemia. Blood 2007;110:2075-83.
    • (2007) Blood , vol.110 , pp. 2075-2083
    • Wang, L.1    Wang, J.2    Blaser, B.W.3    Duchemin, A.M.4    Kusewitt, D.F.5    Liu, T.6
  • 34
    • 30144432781 scopus 로고    scopus 로고
    • Clinical resistance to the kinase inhibitor PKC412 in acute myeloid leukemia by mutation of Asn-676 in the FLT3 tyrosine kinase domain
    • Heidel F, Solem FK, Breitenbuecher F, Lipka DB, Kasper S, Thiede MH, et al. Clinical resistance to the kinase inhibitor PKC412 in acute myeloid leukemia by mutation of Asn-676 in the FLT3 tyrosine kinase domain. Blood 2006;107:293-300.
    • (2006) Blood , vol.107 , pp. 293-300
    • Heidel, F.1    Solem, F.K.2    Breitenbuecher, F.3    Lipka, D.B.4    Kasper, S.5    Thiede, M.H.6
  • 35
    • 19944427369 scopus 로고    scopus 로고
    • Identification of a novel activating mutation (Y842C) within the activation loop of FLT3 in patients with acute myeloid leukemia (AML)
    • Kindler T, Breitenbuecher F, Kasper S, Estey E, Giles F, Feldman E, et al. Identification of a novel activating mutation (Y842C) within the activation loop of FLT3 in patients with acute myeloid leukemia (AML). Blood 2005;105:335-40.
    • (2005) Blood , vol.105 , pp. 335-340
    • Kindler, T.1    Breitenbuecher, F.2    Kasper, S.3    Estey, E.4    Giles, F.5    Feldman, E.6
  • 36
    • 66149152278 scopus 로고    scopus 로고
    • FMS-like tyrosine kinase 3-internal tandem duplication tyrosine kinase inhibitors display a nonoverlapping profile of resistance mutations in vitro
    • von Bubnoff N, Engh RA, Aberg E, Sanger J, Peschel C, Duyster J. FMS-like tyrosine kinase 3-internal tandem duplication tyrosine kinase inhibitors display a nonoverlapping profile of resistance mutations in vitro. Cancer Res 2009;69:3032-41.
    • (2009) Cancer Res , vol.69 , pp. 3032-3041
    • Von Bubnoff, N.1    Engh, R.A.2    Aberg, E.3    Sanger, J.4    Peschel, C.5    Duyster, J.6
  • 37
    • 4444247138 scopus 로고    scopus 로고
    • Mammalian cells cycle without the D-type cyclin-dependent kinases Cdk4 and Cdk6
    • Malumbres M, Sotillo R, Santamaria D, Galan J, Cerezo A, Ortega S, et al. Mammalian cells cycle without the D-type cyclin-dependent kinases Cdk4 and Cdk6. Cell 2004;118:493-504.
    • (2004) Cell , vol.118 , pp. 493-504
    • Malumbres, M.1    Sotillo, R.2    Santamaria, D.3    Galan, J.4    Cerezo, A.5    Ortega, S.6
  • 38
    • 69249230769 scopus 로고    scopus 로고
    • Mammalian cell-cycle regulation: Several Cdks, numerous cyclins and diverse compensatory mechanisms
    • Satyanarayana A, Kaldis P. Mammalian cell-cycle regulation: several Cdks, numerous cyclins and diverse compensatory mechanisms. Oncogene 2009;28:2925-39.
    • (2009) Oncogene , vol.28 , pp. 2925-2939
    • Satyanarayana, A.1    Kaldis, P.2
  • 40
    • 81155153252 scopus 로고    scopus 로고
    • Patterns of molecular response to and relapse after combination of sorafenib, idarubicin, and cytarabine in patients with FLT3 mutant acute myeloid leukemia
    • Al-Kali A, Cortes J, Faderl S, Jones D, Abril C, Pierce S, et al. Patterns of molecular response to and relapse after combination of sorafenib, idarubicin, and cytarabine in patients with FLT3 mutant acute myeloid leukemia. Clin Lymphoma Myeloma Leuk 2011;11:361-6.
    • (2011) Clin Lymphoma Myeloma Leuk , vol.11 , pp. 361-366
    • Al-Kali, A.1    Cortes, J.2    Faderl, S.3    Jones, D.4    Abril, C.5    Pierce, S.6
  • 41
    • 84865865542 scopus 로고    scopus 로고
    • Phase IB study of the FLT3 kinase inhibitor midostaurin with chemotherapy in younger newly diagnosed adult patients with acute myeloid leukemia
    • Stone RM, Fischer T, Paquette R, Schiller G, Schiffer CA, Ehninger G, et al. Phase IB study of the FLT3 kinase inhibitor midostaurin with chemotherapy in younger newly diagnosed adult patients with acute myeloid leukemia. Leukemia 2012;26:2061-8.
    • (2012) Leukemia , vol.26 , pp. 2061-2068
    • Stone, R.M.1    Fischer, T.2    Paquette, R.3    Schiller, G.4    Schiffer, C.A.5    Ehninger, G.6
  • 42
    • 84861906112 scopus 로고    scopus 로고
    • Sorafenib treatment of FLT3-ITD+ acute myeloid leukemia: Favorable initial outcome and mechanisms of subsequent nonresponsiveness associated with the emergence of a D835 mutation
    • Man CH, Fung TK, Ho C, Han HHC, Chow HCH, Ma ACH, et al. Sorafenib treatment of FLT3-ITD+ acute myeloid leukemia: favorable initial outcome and mechanisms of subsequent nonresponsiveness associated with the emergence of a D835 mutation. Blood 2012;119:5133-43.
    • (2012) Blood , vol.119 , pp. 5133-5143
    • Man, C.H.1    Fung, T.K.2    Ho, C.3    Han, H.H.C.4    Chow, H.C.H.5    Ma, A.C.H.6
  • 44
    • 34250372017 scopus 로고    scopus 로고
    • Expression of p16Ink4a compensates for p18Ink4c loss in cyclin-dependent kinase 4/6-dependent tumors and tissues
    • Ramsey MR, Krishnamurthy J, Pei XH, Torrice C, Lin W, Carrasco DR, et al. Expression of p16Ink4a compensates for p18Ink4c loss in cyclin-dependent kinase 4/6-dependent tumors and tissues. Cancer Res 2007;67:4732-41.
    • (2007) Cancer Res , vol.67 , pp. 4732-4741
    • Ramsey, M.R.1    Krishnamurthy, J.2    Pei, X.H.3    Torrice, C.4    Lin, W.5    Carrasco, D.R.6
  • 45
    • 84874322664 scopus 로고    scopus 로고
    • Selective Akt inhibitors synergizewith tyrosine kinase inhibitors and effectively override stroma-associated cytoprotection of mutant FLT3-positive AML cells
    • Weisberg E, Liu Q, Zhang X, Nelson E, Sattler M, Liu F, et al. Selective Akt inhibitors synergizewith tyrosine kinase inhibitors and effectively override stroma-associated cytoprotection of mutant FLT3-positive AML cells. PLoS ONE 2013;8:e56473.
    • (2013) PLoS ONE , vol.8 , pp. e56473
    • Weisberg, E.1    Liu, Q.2    Zhang, X.3    Nelson, E.4    Sattler, M.5    Liu, F.6


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