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Volumn 123, Issue 10, 2014, Pages 1525-1534

TTT-3002 is a novel FLT3 tyrosine kinase inhibitor with activity against FLT3-associated leukemias in vitro and in vivo

Author keywords

[No Author keywords available]

Indexed keywords

ANTINEOPLASTIC AGENT; CD135 ANTIGEN; PROTEIN TYROSINE KINASE INHIBITOR; SORAFENIB; STAT5 PROTEIN; TTT 3002; UNCLASSIFIED DRUG;

EID: 84897557274     PISSN: 00064971     EISSN: 15280020     Source Type: Journal    
DOI: 10.1182/blood-2013-08-523035     Document Type: Article
Times cited : (19)

References (39)
  • 1
    • 15544389069 scopus 로고    scopus 로고
    • Advances in understanding the biology and genetics of acute myelocytic leukemia
    • McKenzie SB. Advances in understanding the biology and genetics of acute myelocytic leukemia. Clin Lab Sci. 2005;18(1):28-37.
    • (2005) Clin Lab Sci , vol.18 , Issue.1 , pp. 28-37
    • McKenzie, S.B.1
  • 3
    • 80052965501 scopus 로고    scopus 로고
    • Further activation of FLT3 mutants by FLT3 ligand
    • Zheng R, Bailey E, Nguyen B, et al. Further activation of FLT3 mutants by FLT3 ligand. Oncogene. 2011;30(38):4004-4014.
    • (2011) Oncogene , vol.30 , Issue.38 , pp. 4004-4014
    • Zheng, R.1    Bailey, E.2    Nguyen, B.3
  • 4
    • 0034605042 scopus 로고    scopus 로고
    • Essential role of signal transducer and activator of transcription (Stat)5a but not Stat5b for Flt3-dependent signaling
    • Zhang S, Fukuda S, Lee Y, et al. Essential role of signal transducer and activator of transcription (Stat)5a but not Stat5b for Flt3-dependent signaling. J Exp Med. 2000;192(5):719-728.
    • (2000) J Exp Med , vol.192 , Issue.5 , pp. 719-728
    • Zhang, S.1    Fukuda, S.2    Lee, Y.3
  • 5
    • 0035383768 scopus 로고    scopus 로고
    • FLT3, RAS, and TP53 mutations in elderly patients with acute myeloid leukemia
    • Stirewalt DL, Kopecky KJ, Meshinchi S, et al. FLT3, RAS, and TP53 mutations in elderly patients with acute myeloid leukemia. Blood. 2001;97(11):3589-3595.
    • (2001) Blood , vol.97 , Issue.11 , pp. 3589-3595
    • Stirewalt, D.L.1    Kopecky, K.J.2    Meshinchi, S.3
  • 6
    • 0031686409 scopus 로고    scopus 로고
    • Internal tandem duplication of the FLT3 gene is a novel modality of elongation mutation which causes constitutive activation of the product
    • Kiyoi H, Towatari M, Yokota S, et al. Internal tandem duplication of the FLT3 gene is a novel modality of elongation mutation which causes constitutive activation of the product. Leukemia. 1998;12(9):1333-1337. (Pubitemid 28442377)
    • (1998) Leukemia , vol.12 , Issue.9 , pp. 1333-1337
    • Kiyoi, H.1    Towatari, M.2    Yokota, S.3    Hamaguchi, M.4    Ohno, R.5    Saito, H.6    Naoe, T.7
  • 9
    • 0033820091 scopus 로고    scopus 로고
    • Constitutive activation of FLT3 stimulates multiple intracellular signal transducers and results in transformation
    • Tse KF, Mukherjee G, Small D. Constitutive activation of FLT3 stimulates multiple intracellular signal transducers and results in transformation. Leukemia. 2000;14(10):1766-1776.
    • (2000) Leukemia , vol.14 , Issue.10 , pp. 1766-1776
    • Tse, K.F.1    Mukherjee, G.2    Small, D.3
  • 10
    • 0141836914 scopus 로고    scopus 로고
    • FLT3: ITDoes matter in leukemia
    • DOI 10.1038/sj.leu.2403099
    • Levis M, Small D. FLT3: ITDoes matter in leukemia. Leukemia. 2003;17(9):1738-1752. (Pubitemid 37185249)
    • (2003) Leukemia , vol.17 , Issue.9 , pp. 1738-1752
    • Levis, M.1    Small, D.2
  • 11
    • 0036720398 scopus 로고    scopus 로고
    • The roles of FLT3 in hematopoiesis and leukemia
    • DOI 10.1182/blood-2002-02-0492
    • Gilliland DG, Griffin JD. The roles of FLT3 in hematopoiesis and leukemia. Blood. 2002;100(5):1532-1542. (Pubitemid 34925124)
    • (2002) Blood , vol.100 , Issue.5 , pp. 1532-1542
    • Gary, G.D.1    Griffin, J.D.2
  • 12
    • 24144454630 scopus 로고    scopus 로고
    • FLT3 tyrosine kinase inhibitors
    • DOI 10.1532/IJH97.05079
    • Levis M, Small D. FLT3 tyrosine kinase inhibitors. Int J Hematol. 2005;82(2):100-107. (Pubitemid 41233167)
    • (2005) International Journal of Hematology , vol.82 , Issue.2 , pp. 100-107
    • Levis, M.1    Small, D.2
  • 13
    • 33847195060 scopus 로고    scopus 로고
    • Antitumor activity of sorafenib in FLT3-driven leukemic cells
    • Auclair D, Miller D, Yatsula V, et al. Antitumor activity of sorafenib in FLT3-driven leukemic cells. Leukemia. 2007;21(3):439-445.
    • (2007) Leukemia , vol.21 , Issue.3 , pp. 439-445
    • Auclair, D.1    Miller, D.2    Yatsula, V.3
  • 14
    • 78650972911 scopus 로고    scopus 로고
    • Phase I study of sorafenib in patients with refractory or relapsed acute leukemias
    • Borthakur G, Kantarjian H, Ravandi F, et al. Phase I study of sorafenib in patients with refractory or relapsed acute leukemias. Haematologica. 2011;96(1):62-68.
    • (2011) Haematologica , vol.96 , Issue.1 , pp. 62-68
    • Borthakur, G.1    Kantarjian, H.2    Ravandi, F.3
  • 16
    • 77951645227 scopus 로고    scopus 로고
    • Phase I/II study of combination therapy with sorafenib, idarubicin, and cytarabine in younger patients with acute myeloid leukemia
    • Ravandi F, Cortes JE, Jones D, et al. Phase I/II study of combination therapy with sorafenib, idarubicin, and cytarabine in younger patients with acute myeloid leukemia. J Clin Oncol. 2010;28(11):1856-1862.
    • (2010) J Clin Oncol , vol.28 , Issue.11 , pp. 1856-1862
    • Ravandi, F.1    Cortes, J.E.2    Jones, D.3
  • 17
    • 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, 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(12):3294-3301.
    • (2011) Blood , vol.117 , Issue.12 , pp. 3294-3301
    • Levis, M.1    Ravandi, F.2    Wang, E.S.3
  • 18
    • 1842420032 scopus 로고    scopus 로고
    • Single-agent CEP-701, a novel FLT3 inhibitor, shows biologic and clinical activity in patients with relapsed or refractory acute myeloid leukemia
    • DOI 10.1182/blood-2003-11-3775
    • Smith BD, Levis M, Beran M, et al. Single-agent CEP-701, a novel FLT3 inhibitor, shows biologic and clinical activity in patients with relapsed or refractory acute myeloid leukemia. Blood. 2004;103(10):3669-3676. (Pubitemid 38596280)
    • (2004) Blood , vol.103 , Issue.10 , pp. 3669-3676
    • Smith, B.D.1    Levis, M.2    Beran, M.3    Giles, F.4    Kantarjian, H.5    Berg, K.6    Murphy, K.M.7    Dauses, T.8    Allebach, J.9    Small, D.10
  • 19
    • 80052231301 scopus 로고    scopus 로고
    • FLT3 inhibition as therapy in acute myeloid leukemia: A record of trials and tribulations
    • Fathi AT, Chabner BA. FLT3 inhibition as therapy in acute myeloid leukemia: a record of trials and tribulations. Oncologist. 2011;16(8):1162-1174.
    • (2011) Oncologist , vol.16 , Issue.8 , pp. 1162-1174
    • Fathi, A.T.1    Chabner, B.A.2
  • 20
    • 78049426367 scopus 로고    scopus 로고
    • Phase IIB trial of oral Midostaurin (PKC412), the FMS-like tyrosine kinase 3 receptor (FLT3) and multitargeted 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, et al. Phase IIB trial of oral Midostaurin (PKC412), the FMS-like tyrosine kinase 3 receptor (FLT3) and multitargeted 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(28):4339-4345.
    • (2010) J Clin Oncol , vol.28 , Issue.28 , pp. 4339-4345
    • Fischer, T.1    Stone, R.M.2    Deangelo, D.J.3
  • 21
    • 33751170444 scopus 로고    scopus 로고
    • Plasma inhibitory activity (PIA): A pharmacodynamic assay reveals insights into the basis for cytotoxic response to FLT3 inhibitors
    • Levis M, Brown P, Smith BD, et al. Plasma inhibitory activity (PIA): a pharmacodynamic assay reveals insights into the basis for cytotoxic response to FLT3 inhibitors. Blood. 2006;108(10):3477-3483.
    • (2006) Blood , vol.108 , Issue.10 , pp. 3477-3483
    • Levis, M.1    Brown, P.2    Smith, B.D.3
  • 22
    • 33751177110 scopus 로고    scopus 로고
    • The effects of lestaurtinib (CEP701) and PKC412 on primary AML blasts: The induction of cytotoxicity varies with dependence on FLT3 signaling in both FLT3-mutated and wild-type cases
    • Knapper S, Mills KI, Gilkes AF, Austin SJ, Walsh V, Burnett AK. The effects of lestaurtinib (CEP701) and PKC412 on primary AML blasts: the induction of cytotoxicity varies with dependence on FLT3 signaling in both FLT3-mutated and wild-type cases. Blood. 2006;108(10):3494-3503.
    • (2006) Blood , vol.108 , Issue.10 , pp. 3494-3503
    • Knapper, S.1    Mills, K.I.2    Gilkes, A.F.3    Austin, S.J.4    Walsh, V.5    Burnett, A.K.6
  • 23
    • 77956943977 scopus 로고    scopus 로고
    • Drug resistance in mutant FLT3-positive AML
    • Weisberg E, Sattler M, Ray A, Griffin JD. Drug resistance in mutant FLT3-positive AML. Oncogene. 2010;29(37):5120-5134.
    • (2010) Oncogene , vol.29 , Issue.37 , pp. 5120-5134
    • Weisberg, E.1    Sattler, M.2    Ray, A.3    Griffin, J.D.4
  • 24
    • 84863785488 scopus 로고    scopus 로고
    • Selective FLT3 inhibition of FLT3-ITD+ acute myeloid leukaemia resulting in secondary D835Y mutation: A model for emerging clinical resistance patterns
    • Moore AS, Faisal A, Gonzalez de Castro D, et al. Selective FLT3 inhibition of FLT3-ITD+ acute myeloid leukaemia resulting in secondary D835Y mutation: a model for emerging clinical resistance patterns. Leukemia. 2012;26(7):1462-1470.
    • (2012) Leukemia , vol.26 , Issue.7 , pp. 1462-1470
    • Moore, A.S.1    Faisal, A.2    Gonzalez De Castro, D.3
  • 25
    • 4644240387 scopus 로고    scopus 로고
    • Prediction of resistance to small molecule FLT3 inhibitors: Implications for molecularly targeted therapy of acute leukemia
    • DOI 10.1158/0008-5472.CAN-04-2148
    • Cools J, Mentens N, Furet P, et al. Prediction of resistance to small molecule FLT3 inhibitors: implications for molecularly targeted therapy of acute leukemia. Cancer Res. 2004;64(18):6385-6389. (Pubitemid 39297890)
    • (2004) Cancer Research , vol.64 , Issue.18 , pp. 6385-6389
    • Cools, J.1    Mentens, N.2    Furet, P.3    Fabbro, D.4    Clark, J.J.5    Griffin, J.D.6    Marynen, P.7    Gilliland, D.G.8
  • 26
    • 84873567125 scopus 로고    scopus 로고
    • Mutations of FLT3/ITD confer resistance to multiple tyrosine kinase inhibitors
    • Williams AB, Nguyen B, Li L, et al. Mutations of FLT3/ITD confer resistance to multiple tyrosine kinase inhibitors. Leukemia. 2013;27(1):48-55.
    • (2013) Leukemia , vol.27 , Issue.1 , pp. 48-55
    • Williams, A.B.1    Nguyen, B.2    Li, L.3
  • 27
    • 84863376366 scopus 로고    scopus 로고
    • Knock-in of a FLT3/ITD mutation cooperates with a NUP98-HOXD13 fusion to generate acute myeloid leukemia in a mouse model
    • Greenblatt S, Li L, Slape C, et al. Knock-in of a FLT3/ITD mutation cooperates with a NUP98-HOXD13 fusion to generate acute myeloid leukemia in a mouse model. Blood. 2012;119(12):2883-2894.
    • (2012) Blood , vol.119 , Issue.12 , pp. 2883-2894
    • Greenblatt, S.1    Li, L.2    Slape, C.3
  • 28
    • 79953115783 scopus 로고    scopus 로고
    • Defective nonhomologous end joining blocks B-cell development in FLT3/ITD mice
    • Li L, Zhang L, Fan J, et al. Defective nonhomologous end joining blocks B-cell development in FLT3/ITD mice. Blood. 2011;117(11):3131-3139.
    • (2011) Blood , vol.117 , Issue.11 , pp. 3131-3139
    • Li, L.1    Zhang, L.2    Fan, J.3
  • 29
    • 84871581831 scopus 로고    scopus 로고
    • Kinase inhibitors arrest neurodegeneration in cell and C. Elegans models of LRRK2 toxicity
    • Yao C, Johnson WM, Gao Y, et al. Kinase inhibitors arrest neurodegeneration in cell and C. elegans models of LRRK2 toxicity. Hum Mol Genet. 2013;22(2):328-344.
    • (2013) Hum Mol Genet , vol.22 , Issue.2 , pp. 328-344
    • Yao, C.1    Johnson, W.M.2    Gao, Y.3
  • 30
    • 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, et al. AC220 is a uniquely potent and selective inhibitor of FLT3 for the treatment of acute myeloid leukemia (AML). Blood. 2009;114(14):2984-2992.
    • (2009) Blood , vol.114 , Issue.14 , pp. 2984-2992
    • Zarrinkar, P.P.1    Gunawardane, R.N.2    Cramer, M.D.3
  • 31
    • 84876491866 scopus 로고    scopus 로고
    • Transient exposure to quizartinib mediates sustained inhibition of FLT3 signaling while specifically inducing apoptosis in FLT3-activated leukemia cells
    • Gunawardane RN, Nepomuceno RR, Rooks AM, et al. Transient exposure to quizartinib mediates sustained inhibition of FLT3 signaling while specifically inducing apoptosis in FLT3-activated leukemia cells. Mol Cancer Ther. 2013;12(4):438-447.
    • (2013) Mol Cancer Ther , vol.12 , Issue.4 , pp. 438-447
    • Gunawardane, R.N.1    Nepomuceno, R.R.2    Rooks, A.M.3
  • 32
    • 0029097145 scopus 로고
    • Targeted disruption of the flk2/flt3 gene leads to deficiencies in primitive hematopoietic progenitors
    • Mackarehtschian K, Hardin JD, Moore KA, Boast S, Goff SP, Lemischka IR. Targeted disruption of the flk2/flt3 gene leads to deficiencies in primitive hematopoietic progenitors. Immunity. 1995;3(1):147-161.
    • (1995) Immunity , vol.3 , Issue.1 , pp. 147-161
    • Mackarehtschian, K.1    Hardin, J.D.2    Moore, K.A.3    Boast, S.4    Goff, S.P.5    Lemischka, I.R.6
  • 35
    • 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
    • DOI 10.1182/blood-2002-05-1440
    • Fröhling S, Schlenk RF, Breitruck J, et al AML Study Group Ulm. Acute myeloid leukemia. 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(13):4372-4380. (Pubitemid 35434129)
    • (2002) Blood , vol.100 , Issue.13 , pp. 4372-4380
    • Frohling, S.1    Schlenk, R.F.2    Breitruck, J.3    Benner, A.4    Kreitmeier, S.5    Tobis, K.6    Dohner, H.7    Dohner, K.8
  • 37
    • 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, 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(22):5133-5143.
    • (2012) Blood , vol.119 , Issue.22 , pp. 5133-5143
    • Man, C.H.1    Fung, T.K.2    Ho, C.3
  • 38
    • 84873083526 scopus 로고    scopus 로고
    • FLT3 inhibitor treatment in FLT3-mutated AML is associated with development of secondary FLT3-TKD mutations
    • [abstract]
    • Alvarado T, Kantarjian H, Ravandi F, et al. FLT3 inhibitor treatment in FLT3-mutated AML is associated with development of secondary FLT3-TKD mutations. [abstract] Blood. 2008;118:1493.
    • (2008) Blood , vol.118 , pp. 1493
    • Alvarado, T.1    Kantarjian, H.2    Ravandi, F.3
  • 39
    • 84873078929 scopus 로고    scopus 로고
    • Acquired point mutations of TKD are responsible for sorafenib resistance in FLT3-ITD mutant AML
    • [abstract]
    • Zhang W, Konopleva M, Jacamo RO, et al. Acquired point mutations of TKD are responsible for sorafenib resistance in FLT3-ITD mutant AML [abstract]. Blood. 2011;118(21):3505.
    • (2011) Blood , vol.118 , Issue.21 , pp. 3505
    • Zhang, W.1    Konopleva, M.2    Jacamo, R.O.3


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