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Volumn 6, Issue 9, 2011, Pages

Reversible resistance induced by FLT3 inhibition: A novel resistance mechanism in mutant FLT3-Expressing cells

Author keywords

[No Author keywords available]

Indexed keywords

ADENOSINE TRIPHOSPHATASE INHIBITOR; CD135 ANTIGEN; CYCLOHEXIMIDE; FLT3 LIGAND; HG 78501; MESSENGER RNA; MIDOSTAURIN; UNCLASSIFIED DRUG; DRUG DERIVATIVE; FLT3 PROTEIN, HUMAN; HG 7 85 01 COMPOUND; HG-7-85-01 COMPOUND; PIPERAZINE DERIVATIVE; PROTEIN KINASE INHIBITOR; STAUROSPORINE; THIAZOLE DERIVATIVE; TYROSINE;

EID: 80053280767     PISSN: None     EISSN: 19326203     Source Type: Journal    
DOI: 10.1371/journal.pone.0025351     Document Type: Article
Times cited : (45)

References (44)
  • 1
    • 0141465061 scopus 로고    scopus 로고
    • The role of FLT3 in hematopoeitic malignancies
    • Stirewalt DL, Radich JP, (2003) The role of FLT3 in hematopoeitic malignancies. Nat Rev Cancer 3: 650-665.
    • (2003) Nat Rev Cancer , vol.3 , pp. 650-665
    • Stirewalt, D.L.1    Radich, J.P.2
  • 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, et al. (1996) Internal tandem duplication of the FLT3 gene found in acute myeloid leukemia. Leukemia 10: 1911-1918.
    • (1996) Leukemia , vol.10 , pp. 1911-1918
    • Nakao, M.1    Yokota, S.2    Iwai, T.3    Kaneko, H.4    Horiike, S.5
  • 3
    • 16944366584 scopus 로고    scopus 로고
    • Tandem duplications of the FLT3 receptor gene are associated with leukemic transformation of myelodysplasia
    • Horiike S, Yokota S, Nakao M, Iwai T, Sasai Y, et al. (1997) Tandem duplications of the FLT3 receptor gene are associated with leukemic transformation of myelodysplasia. Leukemia 11: 1442-1446.
    • (1997) Leukemia , vol.11 , pp. 1442-1446
    • Horiike, S.1    Yokota, S.2    Nakao, M.3    Iwai, T.4    Sasai, Y.5
  • 4
    • 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, Hamaguchi M, Ohno R, et al. (1998) Internal tandem duplication of the FLT3 gene is a novel modality of elongation mutation which causes constitutive activation of the product. Leukemia 12: 1333-1337.
    • (1998) Leukemia , vol.12 , pp. 1333-1337
    • Kiyoi, H.1    Towatari, M.2    Yokota, S.3    Hamaguchi, M.4    Ohno, R.5
  • 5
    • 0032757551 scopus 로고    scopus 로고
    • Prognostic value of internal tandem duplication of the FLT3 gene in childhood acute myelogenous leukemia
    • Kondo M, Horibe K, Takahashi Y, Matsumoto K, Fukuda M, et al. (1999) Prognostic value of internal tandem duplication of the FLT3 gene in childhood acute myelogenous leukemia. Med Pediatr Oncol 33: 525-529.
    • (1999) Med Pediatr Oncol , vol.33 , pp. 525-529
    • Kondo, M.1    Horibe, K.2    Takahashi, Y.3    Matsumoto, K.4    Fukuda, M.5
  • 6
    • 0034040255 scopus 로고    scopus 로고
    • Biological characteristics and prognosis of adult acute myeloid leukemia with internal tandem duplications in the FLT3 gene
    • Rombouts WJ, Blokland I, Lowenberg B, Ploemacher RE, (2000) Biological characteristics and prognosis of adult acute myeloid leukemia with internal tandem duplications in the FLT3 gene. Leukemia 14: 675-683.
    • (2000) Leukemia , vol.14 , pp. 675-683
    • Rombouts, W.J.1    Blokland, I.2    Lowenberg, B.3    Ploemacher, R.E.4
  • 7
    • 0035871889 scopus 로고    scopus 로고
    • Activating mutation of D835 within the activation loop of FLT3 in human hematologic malignancies
    • Yamamoto Y, Kiyoi H, Nakano Y, Suzuki R, Kodera Y, et al. (2001) Activating mutation of D835 within the activation loop of FLT3 in human hematologic malignancies. Blood 97: 2434-2439.
    • (2001) Blood , vol.97 , pp. 2434-2439
    • Yamamoto, Y.1    Kiyoi, H.2    Nakano, Y.3    Suzuki, R.4    Kodera, Y.5
  • 8
    • 4444350364 scopus 로고    scopus 로고
    • Identifying and characterizing a novel activating mutation of the FLT3 tyrosine kinase in AML
    • Jiang J, Paez JG, Lee JC, Bo R, Stone RM, et al. (2004) Identifying and characterizing a novel activating mutation of the FLT3 tyrosine kinase in AML. Blood 104: 1855-1858.
    • (2004) Blood , vol.104 , pp. 1855-1858
    • Jiang, J.1    Paez, J.G.2    Lee, J.C.3    Bo, R.4    Stone, R.M.5
  • 9
    • 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, et al. (2005) Identification of a novel activating mutation (Y842C) within the activation loop of FLT3 in patients with acute myeloid leukemia (AML). Blood 105: 335-340.
    • (2005) Blood , vol.105 , pp. 335-340
    • Kindler, T.1    Breitenbuecher, F.2    Kasper, S.3    Estey, E.4    Giles, F.5
  • 10
    • 33645312560 scopus 로고    scopus 로고
    • Point mutations in the juxtamembrane domain of FLT3 define a new class of activating mutations in AML
    • Reindl C, Bagrintseva K, Vempati S, Schnittger S, Ellwart JW, et al. (2006) Point mutations in the juxtamembrane domain of FLT3 define a new class of activating mutations in AML. Blood 107: 3700-3707.
    • (2006) Blood , vol.107 , pp. 3700-3707
    • Reindl, C.1    Bagrintseva, K.2    Vempati, S.3    Schnittger, S.4    Ellwart, J.W.5
  • 11
    • 0036595143 scopus 로고    scopus 로고
    • Inhibition of mutant FLT3 receptors in leukemia cells by the small molecule tyrosine kinase inhibitors PKC412
    • Weisberg E, Boulton C, Kelly LM, Manley P, Fabbro D, et al. (2002) Inhibition of mutant FLT3 receptors in leukemia cells by the small molecule tyrosine kinase inhibitors PKC412. Cancer Cell 1: 433-443.
    • (2002) Cancer Cell , vol.1 , pp. 433-443
    • Weisberg, E.1    Boulton, C.2    Kelly, L.M.3    Manley, P.4    Fabbro, D.5
  • 12
    • 3042581224 scopus 로고    scopus 로고
    • PKC412 FLT3 inhibitor therapy in AML: results of a phase II trial
    • Stone RM, De Angelo J, Galinsky I, Estey E, Klimek V, et al. (2004) PKC412 FLT3 inhibitor therapy in AML: results of a phase II trial. Ann Hematol 83 (Suppl 1): S89-90.
    • (2004) Ann Hematol , vol.83 , Issue.SUPPL. 1 , pp. 89-90
    • Stone, R.M.1    De Angelo, J.2    Galinsky, I.3    Estey, E.4    Klimek, V.5
  • 13
    • 19944427559 scopus 로고    scopus 로고
    • Patients with acute myeloid leukemia and an activating mutation in FLT3 respond to a small-molecule FLT3 tyrosine kinase inhibitor, PKC412
    • Stone RM, DeAngelo DJ, Klimek V, Galinsky I, Estey E, et al. (2005) Patients with acute myeloid leukemia and an activating mutation in FLT3 respond to a small-molecule FLT3 tyrosine kinase inhibitor, PKC412. Blood 105: 54-60.
    • (2005) Blood , vol.105 , pp. 54-60
    • Stone, R.M.1    DeAngelo, D.J.2    Klimek, V.3    Galinsky, I.4    Estey, E.5
  • 14
    • 33751173636 scopus 로고    scopus 로고
    • A phase 2 trial of the FLT3 inhibitor lestaurtinib (CEP701) as first line treatment for older patients with acute myeloid leukemia not considered fit for intenstive chemotherapy
    • Knapper S, Burnett AK, Littlewood T, Kell WJ, Agrawal S, et al. (2006) A phase 2 trial of the FLT3 inhibitor lestaurtinib (CEP701) as first line treatment for older patients with acute myeloid leukemia not considered fit for intenstive chemotherapy. Blood 108: 3262-3270.
    • (2006) Blood , vol.108 , pp. 3262-3270
    • Knapper, S.1    Burnett, A.K.2    Littlewood, T.3    Kell, W.J.4    Agrawal, S.5
  • 15
    • 33846936758 scopus 로고    scopus 로고
    • Prolonged exposure to FLT3 inhibitors leads to resistance via activation of parallel signaling pathways
    • Piloto O, Wright M, Brown P, Kim KT, Levis M, et al. (2007) Prolonged exposure to FLT3 inhibitors leads to resistance via activation of parallel signaling pathways. Blood 109: 1643-1652.
    • (2007) Blood , vol.109 , pp. 1643-1652
    • Piloto, O.1    Wright, M.2    Brown, P.3    Kim, K.T.4    Levis, M.5
  • 16
    • 65449117656 scopus 로고    scopus 로고
    • Enhanced activation of STAT pathways and overexpression of survivin confer resistance to FLT3 inhibitors and could be therapeutic targets in AML
    • Zhou J, Bi C, Janakakumara JV, Liu SC, Chng WJ, et al. (2009) Enhanced activation of STAT pathways and overexpression of survivin confer resistance to FLT3 inhibitors and could be therapeutic targets in AML. Blood 113: 4052-4062.
    • (2009) Blood , vol.113 , pp. 4052-4062
    • Zhou, J.1    Bi, C.2    Janakakumara, J.V.3    Liu, S.C.4    Chng, W.J.5
  • 17
    • 77953070292 scopus 로고    scopus 로고
    • Mechanisms of resistance against PKC412 in resistant FLT3-ITD positive human acute myeloid leukemia cells
    • Stölzel F, Steudel C, Oelschlägel U, Mohr B, Koch S, et al. (2010) Mechanisms of resistance against PKC412 in resistant FLT3-ITD positive human acute myeloid leukemia cells. Ann Hematol 89: 653-662.
    • (2010) Ann Hematol , vol.89 , pp. 653-662
    • Stölzel, F.1    Steudel, C.2    Oelschlägel, U.3    Mohr, B.4    Koch, S.5
  • 18
    • 33646586669 scopus 로고    scopus 로고
    • Preclinical activity of ABT-869: a multitargeted receptor tyrosine kinase inhibitor
    • Albert DH, Tapang P, Magoc TJ, Pease LJ, Reuter DR, et al. (2006) Preclinical activity of ABT-869: a multitargeted receptor tyrosine kinase inhibitor. Mol Cancer Ther 5: 995-1006.
    • (2006) Mol Cancer Ther , vol.5 , pp. 995-1006
    • Albert, D.H.1    Tapang, P.2    Magoc, T.J.3    Pease, L.J.4    Reuter, D.R.5
  • 19
    • 34147102941 scopus 로고    scopus 로고
    • ABT-869, a multitargeted receptor tyrosine kinase inhibitor: inhibition of FLT3 phosphorylation and signaling in acute myeloid leukemia
    • Shankar DB, Li J, Tapang P, Owen J, Pease LJ, et al. (2007) ABT-869, a multitargeted receptor tyrosine kinase inhibitor: inhibition of FLT3 phosphorylation and signaling in acute myeloid leukemia. Blood 109: 3400-3408.
    • (2007) Blood , vol.109 , pp. 3400-3408
    • Shankar, D.B.1    Li, J.2    Tapang, P.3    Owen, J.4    Pease, L.J.5
  • 20
    • 0141842637 scopus 로고    scopus 로고
    • CEP-7055: a novel, orally active pan inhibitor of vascular endothelial growth factor receptor tyrosine kinases with potent antiangiogenic activity and antitumor efficacy in preclinical models
    • Ruggeri B, Singh J, Gingrich D, Angeles T, Albom M, et al. (2003) CEP-7055: a novel, orally active pan inhibitor of vascular endothelial growth factor receptor tyrosine kinases with potent antiangiogenic activity and antitumor efficacy in preclinical models. Cancer Res 63: 5978-5991.
    • (2003) Cancer Res , vol.63 , pp. 5978-5991
    • Ruggeri, B.1    Singh, J.2    Gingrich, D.3    Angeles, T.4    Albom, M.5
  • 21
    • 0036624916 scopus 로고    scopus 로고
    • A FLT3-targeted tyrosine kinase inhibitor is cytotoxic to leukemia cells in vitro and in vivo
    • Levis M, Allebach J, Tse KF, Zheng R, Baldwin BR, et al. (2002) A FLT3-targeted tyrosine kinase inhibitor is cytotoxic to leukemia cells in vitro and in vivo. Blood 99: 3885-91.
    • (2002) Blood , vol.99 , pp. 3885-3891
    • Levis, M.1    Allebach, J.2    Tse, K.F.3    Zheng, R.4    Baldwin, B.R.5
  • 22
    • 77956600334 scopus 로고    scopus 로고
    • Discovery and characterization of novel mutant FLT3 kinase inhibitors
    • Weisberg E, Choi HG, Barrett R, Zhou W, Zhang J, et al. (2010) Discovery and characterization of novel mutant FLT3 kinase inhibitors. Mol Cancer Ther 9: 2468-2477.
    • (2010) Mol Cancer Ther , vol.9 , pp. 2468-2477
    • Weisberg, E.1    Choi, H.G.2    Barrett, R.3    Zhou, W.4    Zhang, J.5
  • 23
    • 0013312329 scopus 로고    scopus 로고
    • Validation of a therapeutic target identified by gene expression based classification
    • Armstrong SA, Kung AL, Mabon ME, Silverman LB, Stam RW, et al. (2003) Validation of a therapeutic target identified by gene expression based classification. Cancer Cell 3: 173-183.
    • (2003) Cancer Cell , vol.3 , pp. 173-183
    • Armstrong, S.A.1    Kung, A.L.2    Mabon, M.E.3    Silverman, L.B.4    Stam, R.W.5
  • 24
    • 0001686739 scopus 로고    scopus 로고
    • Multiple BCR-ABL kinase domain mutations confer polyclonal resistance to the tyrosine kinase inhibitor imatinib (STI571) in chronic phase and blast crisis chronic myeloid leukemia
    • Shah NP, Nicoll JM, Nagar B, Gorre ME, Paquette RL, et al. (2002) Multiple BCR-ABL kinase domain mutations confer polyclonal resistance to the tyrosine kinase inhibitor imatinib (STI571) in chronic phase and blast crisis chronic myeloid leukemia. Cancer Cell 2: 117-125.
    • (2002) Cancer Cell , vol.2 , pp. 117-125
    • Shah, N.P.1    Nicoll, J.M.2    Nagar, B.3    Gorre, M.E.4    Paquette, R.L.5
  • 25
    • 4644240387 scopus 로고    scopus 로고
    • Prediction of resistance to small molecule FLT3 inhibitors: implications for molecularly targeted therapy of acute leukemia
    • Cools J, Mentens N, Furet P, Fabbro D, Clark JJ, et al. (2004) Prediction of resistance to small molecule FLT3 inhibitors: implications for molecularly targeted therapy of acute leukemia. Cancer Res 64: 6385-6389.
    • (2004) Cancer Res , vol.64 , pp. 6385-6389
    • Cools, J.1    Mentens, N.2    Furet, P.3    Fabbro, D.4    Clark, J.J.5
  • 26
    • 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, et al. (2006) Clinical resistance to the kinase inhibitor PKC412 in acute myeloid leukemia by mutation of Asn-676 in the FLT3 tyrosine kinase domain. Blood 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
  • 27
    • 0036093475 scopus 로고    scopus 로고
    • FLT3 internal tandem duplication mutations associated with human acute myeloid leukemias induce myeloproliferative disease in a murine bone marrow transplant model
    • Kelly LM, Liu Q, Kutok JL, Williams IR, Boulton CL, et al. (2002) FLT3 internal tandem duplication mutations associated with human acute myeloid leukemias induce myeloproliferative disease in a murine bone marrow transplant model. Blood 99: 310-318.
    • (2002) Blood , vol.99 , pp. 310-318
    • Kelly, L.M.1    Liu, Q.2    Kutok, J.L.3    Williams, I.R.4    Boulton, C.L.5
  • 28
    • 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, et al. (2009) FMS-like tyrosine kinase 3-internal tandem duplication tyrosine kinase inhibitors display a nonoverlapping profile of resistance mutations in vitro. Cancer Res 69: 3032-3041.
    • (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
  • 29
    • 34247506325 scopus 로고    scopus 로고
    • Identification of BCR-ABL point mutations conferring resistance to the Abl kinase inhibitor AMN107 (nilotinib) by a random mutagenesis study
    • Ray A, Cowan-Jacob SW, Manley PW, Mestan J, Griffin JD, (2007) Identification of BCR-ABL point mutations conferring resistance to the Abl kinase inhibitor AMN107 (nilotinib) by a random mutagenesis study. Blood 109: 5011-5015.
    • (2007) Blood , vol.109 , pp. 5011-5015
    • Ray, A.1    Cowan-Jacob, S.W.2    Manley, P.W.3    Mestan, J.4    Griffin, J.D.5
  • 30
    • 33745069351 scopus 로고    scopus 로고
    • Bcr-Abl resistance screening predicts a limited spectrum of point mutations to be associated with clinical resistance to the Abl kinase inhibitor AMN107
    • Von Bubnoff N, Sanger J, Manley PW, Mestan J, Peschel C, et al. (2006) Bcr-Abl resistance screening predicts a limited spectrum of point mutations to be associated with clinical resistance to the Abl kinase inhibitor AMN107. Blood 108: 1328-1333.
    • (2006) Blood , vol.108 , pp. 1328-1333
    • Von Bubnoff, N.1    Sanger, J.2    Manley, P.W.3    Mestan, J.4    Peschel, C.5
  • 31
    • 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, et al. (2009) A pharmacodynamic study of the FLT3 inhibitor KW-2449 yields insight into the basis for clinical response. Blood 113: 3938-3946.
    • (2009) Blood , vol.113 , pp. 3938-3946
    • Pratz, K.W.1    Cortes, J.2    Roboz, G.J.3    Rao, N.4    Arowojolu, O.5
  • 32
    • 33947547125 scopus 로고    scopus 로고
    • Inhibition of Flt3-activating mutations does not prevent constitutive activation of ERK/Akt/STAT pathways in some AML cells: a possible cause for the limited effectiveness of monotherapy with small-molecule inhibitors
    • Siendones E, Barbarroja N, Torres LA, Buendia P, Velasco F, et al. (2007) Inhibition of Flt3-activating mutations does not prevent constitutive activation of ERK/Akt/STAT pathways in some AML cells: a possible cause for the limited effectiveness of monotherapy with small-molecule inhibitors. Hematol Oncol 25: 30-37.
    • (2007) Hematol Oncol , vol.25 , pp. 30-37
    • Siendones, E.1    Barbarroja, N.2    Torres, L.A.3    Buendia, P.4    Velasco, F.5
  • 33
    • 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, et al. (2010) FLT3-mutant allelic burden and clinical status are predictive of response to FLT3 inhibitors in AML. Blood 115: 1425-1432.
    • (2010) Blood , vol.115 , pp. 1425-1432
    • Pratz, K.W.1    Sato, T.2    Murphy, K.M.3    Stine, A.4    Rajkhowa, T.5
  • 34
    • 77957819681 scopus 로고    scopus 로고
    • The phosphatidylinositol 3-kinase/Akt/mTOR signaling network as a therapeutic target in acute myelogenous leukemia patients
    • Martelli AM, Evangelisti C, Chiarini F, McCubrey JA, (2010) The phosphatidylinositol 3-kinase/Akt/mTOR signaling network as a therapeutic target in acute myelogenous leukemia patients. Oncotarget 1: 89-103.
    • (2010) Oncotarget , vol.1 , pp. 89-103
    • Martelli, A.M.1    Evangelisti, C.2    Chiarini, F.3    McCubrey, J.A.4
  • 35
    • 84862833471 scopus 로고    scopus 로고
    • Over-expression of CKS1B activates both MEK/ERK and JAK/STAT3 signaling pathways and promotes myeloma cell drug-resistance
    • Shi L, Wang S, Zangari M, Xu H, Cao TM, et al. (2010) Over-expression of CKS1B activates both MEK/ERK and JAK/STAT3 signaling pathways and promotes myeloma cell drug-resistance. Oncotarget 1: 22-33.
    • (2010) Oncotarget , vol.1 , pp. 22-33
    • Shi, L.1    Wang, S.2    Zangari, M.3    Xu, H.4    Cao, T.M.5
  • 36
    • 62949093541 scopus 로고    scopus 로고
    • Mechanisms of resistance to FLT3 inhibitors
    • Chu SJ, Small D, (2009) Mechanisms of resistance to FLT3 inhibitors. Drug Resist Updates 12: 8-16.
    • (2009) Drug Resist Updates , vol.12 , pp. 8-16
    • Chu, S.J.1    Small, D.2
  • 37
    • 77950452556 scopus 로고    scopus 로고
    • Increased plasma FLT3 ligand levels following chemotherapy may interfere with the clinical efficacy of FLT3 inhibitors
    • Abstract
    • Sato TKS, Burnett AK, White P, Levis M, (2009) Increased plasma FLT3 ligand levels following chemotherapy may interfere with the clinical efficacy of FLT3 inhibitors. Blood 114 Abstract 937.
    • (2009) Blood , vol.114 , pp. 937
    • Sato, T.K.S.1    Burnett, A.K.2    White, P.3    Levis, M.4
  • 38
    • 78649795419 scopus 로고    scopus 로고
    • Clinical relevance of FLT3 receptor protein expression in Indian patients with acute leukemia
    • Vora HH, Shukla SN, Brahambhatt BV, Mehta SH, Patel NA, et al. (2010) Clinical relevance of FLT3 receptor protein expression in Indian patients with acute leukemia. Asia Pac J Clin Oncol 6: 306-319.
    • (2010) Asia Pac J Clin Oncol , vol.6 , pp. 306-319
    • Vora, H.H.1    Shukla, S.N.2    Brahambhatt, B.V.3    Mehta, S.H.4    Patel, N.A.5
  • 39
    • 29144497917 scopus 로고    scopus 로고
    • Detailed analysis of FLT3 expression levels in acute myeloid leukemia
    • Kuchenbauer F, Kern W, Schoch C, Kohlmann A, Hiddemann W, et al. (2005) Detailed analysis of FLT3 expression levels in acute myeloid leukemia. Haematologica 90: 1617-1625.
    • (2005) Haematologica , vol.90 , pp. 1617-1625
    • Kuchenbauer, F.1    Kern, W.2    Schoch, C.3    Kohlmann, A.4    Hiddemann, W.5
  • 40
    • 77956413528 scopus 로고    scopus 로고
    • High transcript level of FLT3 associated with high risk of relapse in pediatric acute myeloid leukemia
    • Kang HJ, Lee JW, Kho SH, Kim MJ, Seo YJ, et al. (2010) High transcript level of FLT3 associated with high risk of relapse in pediatric acute myeloid leukemia. J Korean Med Sci 25: 841-845.
    • (2010) J Korean Med Sci , vol.25 , pp. 841-845
    • Kang, H.J.1    Lee, J.W.2    Kho, S.H.3    Kim, M.J.4    Seo, Y.J.5
  • 42
    • 70449720501 scopus 로고    scopus 로고
    • FLT3-ITD induces ara-C resistance in myeloid leukemic cells through the repression of the ENT1 expression
    • Jin G, Matsushita H, Asai S, Tsukamoto H, Ono R, et al. (2009) FLT3-ITD induces ara-C resistance in myeloid leukemic cells through the repression of the ENT1 expression. Biochem Biophys Res Commun 390: 1001-1006.
    • (2009) Biochem Biophys Res Commun , vol.390 , pp. 1001-1006
    • Jin, G.1    Matsushita, H.2    Asai, S.3    Tsukamoto, H.4    Ono, R.5
  • 43
    • 3843142735 scopus 로고    scopus 로고
    • In vitro studies of a FLT3 inhibitor combined with chemotherapy: sequence of administration is important to achieve synergistic cytotoxic effects
    • Levis M, Pham R, Smith BD, Small D, (2004) In vitro studies of a FLT3 inhibitor combined with chemotherapy: sequence of administration is important to achieve synergistic cytotoxic effects. Blood 104: 1145-1150.
    • (2004) Blood , vol.104 , pp. 1145-1150
    • Levis, M.1    Pham, R.2    Smith, B.D.3    Small, D.4
  • 44
    • 69249212433 scopus 로고    scopus 로고
    • The FLT3 inhibitor tandutinib (formerly MLN518) has sequence-independent synergistic effects with cytarabine and daunorubicin
    • Schittenhelm MM, Kampa KM, Yee KW, Heinrich MC, (2009) The FLT3 inhibitor tandutinib (formerly MLN518) has sequence-independent synergistic effects with cytarabine and daunorubicin. Cell Cycle 8: 2621-2630.
    • (2009) Cell Cycle , vol.8 , pp. 2621-2630
    • Schittenhelm, M.M.1    Kampa, K.M.2    Yee, K.W.3    Heinrich, M.C.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.