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Volumn 17, Issue 2, 2012, Pages 199-209

FLT3 signaling and the development of inhibitors that target FLT3 kinase activity

Author keywords

Acute myeloid leukemia; FLT3 ITD; Hematopoietic progenitors; Receptor tyrosine kinases

Indexed keywords

ADENOSINE TRIPHOSPHATE; ANTILEUKEMIC AGENT; BIM PROTEIN; CD135 ANTIGEN; FI 700; KW 2449; LESTAURTINIB; MIDOSTAURIN; PONATINIB; PROTEIN BCL 2; PROTEIN MCL 1; PROTEIN TYROSINE KINASE INHIBITOR; QUIZARTINIB; SORAFENIB; STAT5A PROTEIN; STAT5B PROTEIN; SUNITINIB; TANDUTINIB; UNCLASSIFIED DRUG; ANTINEOPLASTIC AGENT; FLT3 PROTEIN, HUMAN; PROTEIN KINASE INHIBITOR;

EID: 84861516763     PISSN: 08939675     EISSN: 21626448     Source Type: Journal    
DOI: 10.1615/CritRevOncog.v17.i2.50     Document Type: Review
Times cited : (8)

References (50)
  • 1
    • 0141465061 scopus 로고    scopus 로고
    • The role of FLT3 in haemopoietic malignancies
    • Stirewalt DG, Radich JP. The role of FLT3 in haemopoietic malignancies. Nat Rev Cancer. 2003;3:650-665.
    • (2003) Nat Rev Cancer , vol.3 , pp. 650-665
    • Stirewalt, D.G.1    Radich, J.P.2
  • 3
    • 0029998037 scopus 로고    scopus 로고
    • FLT3 receptor expression on the surface of normal and malignant human hematopoietic cells
    • Turner AM, Lin NL, Issarachai S, Lyman SD, Broudy VC. FLT3 receptor expression on the surface of normal and malignant human hematopoietic cells. Blood. 1996;88:3383-90.
    • (1996) Blood , vol.88 , pp. 3383-3390
    • Turner, A.M.1    Lin, N.L.2    Issarachai, S.3    Lyman, S.D.4    Broudy, V.C.5
  • 6
    • 16944365287 scopus 로고    scopus 로고
    • Internal tandem duplication of the FLT3 gene is preferentially seen in acute myeloid leukemia and myelodysplastic syndrome among various hematological malignancies. A study on a large series of patients and cell lines
    • Yokota S, Kiyoi H, Nakao M, Iwai T, Misawa S, Okuda T, Sonoda Y, Abe T, Kahsima K, Matsuo Y, Naoe T. Internal tandem duplication of the FLT3 gene is preferentially seen in acute myeloid leukemia and myelodysplastic syndrome among various hematological malignancies. A study on a large series of patients and cell lines. Leukemia. 1997;11(10):1605-1609.
    • (1997) Leukemia , vol.11 , Issue.10 , pp. 1605-1609
    • Yokota, S.1    Kiyoi, H.2    Nakao, M.3    Iwai, T.4    Misawa, S.5    Okuda, T.6    Sonoda, Y.7    Abe, T.8    Kahsima, K.9    Matsuo, Y.10    Naoe, T.11
  • 9
    • 34147147730 scopus 로고    scopus 로고
    • FLT3 Mutations: Biology and Treatment
    • Small D. FLT3 Mutations: Biology and Treatment. Hematology. 2006:178-84.
    • (2006) Hematology , pp. 178-184
    • Small, D.1
  • 10
    • 15244348388 scopus 로고    scopus 로고
    • Src family tyrosine kinases are activated by Flt3 and are involved in the proliferative effects of leukemia-associated Flt3 mutations
    • Robinson LJ, Xue J, Corey SJ. Src family tyrosine kinases are activated by Flt3 and are involved in the proliferative effects of leukemia-associated Flt3 mutations. Exp Hematol. 2005;33:469-479.
    • (2005) Exp Hematol , vol.33 , pp. 469-479
    • Robinson, L.J.1    Xue, J.2    Corey, S.J.3
  • 13
    • 0034598830 scopus 로고    scopus 로고
    • Tandem-duplicated Flt3 constitutively activates STAT5 and MAP kinase and introduces autonomous cell growth in IL-3-dependent cell lines
    • Hayakawa F, Towatari M, Kiyoi H, Tanimoto M, Kitamura T, Saito H, Naoe T. Tandem-duplicated Flt3 constitutively activates STAT5 and MAP kinase and introduces autonomous cell growth in IL-3-dependent cell lines. Oncogene. 2000;19(5):624-631.
    • (2000) Oncogene , vol.19 , Issue.5 , pp. 624-631
    • Hayakawa, F.1    Towatari, M.2    Kiyoi, H.3    Tanimoto, M.4    Kitamura, T.5    Saito, H.6    Naoe, T.7
  • 17
    • 77955709330 scopus 로고    scopus 로고
    • Ubiquitin conjugase UBCH8 targets active FMS-like tyrosine kinase 3 for proteasomal degradation
    • Buchwald M, Pietschmann K, Muller JP, Bohmer FD, Heinzel T, Kramer OH. Ubiquitin conjugase UBCH8 targets active FMS-like tyrosine kinase 3 for proteasomal degradation. Leukemia. 2010;24(8):1412-1421.
    • (2010) Leukemia , vol.24 , Issue.8 , pp. 1412-1421
    • Buchwald, M.1    Pietschmann, K.2    Muller, J.P.3    Bohmer, F.D.4    Heinzel, T.5    Kramer, O.H.6
  • 18
    • 80052221156 scopus 로고    scopus 로고
    • c-Cbl and Cbl-b mediate 17-AAG-induced degradation of autophosphorylated Flt3-ITD through the ubiquitin proteasome pathway
    • Oshikawa G, Nagao T, Wu N, Kurosu T, Miura O. c-Cbl and Cbl-b mediate 17-AAG-induced degradation of autophosphorylated Flt3-ITD through the ubiquitin proteasome pathway. J Biol Chem. 2011;286:30263-30273.
    • (2011) J Biol Chem , vol.286 , pp. 30263-30273
    • Oshikawa, G.1    Nagao, T.2    Wu, N.3    Kurosu, T.4    Miura, O.5
  • 23
    • 15944363056 scopus 로고    scopus 로고
    • Identification of Lin-Sca1+kit+CD34+Flt3- short-term hematopoietic stem cells capable of rapidly reconstituting and rescuing myeloablated transplant recipients
    • Yang L, Bryder D, Adolfsson J, Nygren J, Mansson R, Sigvardsson M, Jacobsen SEW. Identification of Lin-Sca1+kit+CD34+Flt3- short-term hematopoietic stem cells capable of rapidly reconstituting and rescuing myeloablated transplant recipients. Blood. 2005;105:2717-2723.
    • (2005) Blood , vol.105 , pp. 2717-2723
    • Yang, L.1    Bryder, D.2    Adolfsson, J.3    Nygren, J.4    Mansson, R.5    Sigvardsson, M.6    Jacobsen, S.E.W.7
  • 26
    • 43549123118 scopus 로고    scopus 로고
    • Knock-in of an internal tandem duplication mutation into murine FLT3 confers myeloproliferative disease in a mouse model
    • Li L, Piloto O, Nguyen HB, Greenberg K, Takamiya K, Racke F, Huso D, Small D. Knock-in of an internal tandem duplication mutation into murine FLT3 confers myeloproliferative disease in a mouse model. Blood. 2008;111(7):3849-3858.
    • (2008) Blood , vol.111 , Issue.7 , pp. 3849-3858
    • Li, L.1    Piloto, O.2    Nguyen, H.B.3    Greenberg, K.4    Takamiya, K.5    Racke, F.6    Huso, D.7    Small, D.8
  • 28
    • 77957965853 scopus 로고    scopus 로고
    • Myeloid leukemia development in c-Cbl RING finger mutant mice is dependent on FLT3 signaling
    • Rathinam C, Thien CBF, Flavell RA, Langdon WY. Myeloid leukemia development in c-Cbl RING finger mutant mice is dependent on FLT3 signaling. Cancer Cell. 2010;18:341-352.
    • (2010) Cancer Cell , vol.18 , pp. 341-352
    • Rathinam, C.1    Thien, C.B.F.2    Flavell, R.A.3    Langdon, W.Y.4
  • 29
    • 33745298429 scopus 로고    scopus 로고
    • Rational design of inhibitors that bind to inactive kinase conformations
    • Liu Y, Gray NS. Rational design of inhibitors that bind to inactive kinase conformations. Nat Chem Biol. 2006;2(7):358-364.
    • (2006) Nat Chem Biol , vol.2 , Issue.7 , pp. 358-364
    • Liu, Y.1    Gray, N.S.2
  • 30
    • 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; 16:1162-1174.
    • (2011) Oncologist , vol.16 , pp. 1162-1174
    • Fathi, A.T.1    Chabner, B.A.2
  • 31
    • 79952043438 scopus 로고    scopus 로고
    • FLT3 inhibitors: A story of the old and the new
    • Fathi A, Levis M. FLT3 inhibitors: a story of the old and the new. Curr Opin Hematol. 2011;18(2):71-76.
    • (2011) Curr Opin Hematol , vol.18 , Issue.2 , pp. 71-76
    • Fathi, A.1    Levis, M.2
  • 32
    • 80052015797 scopus 로고    scopus 로고
    • Emerging FMS-like tyrosine kinase 3 inhibitors for the treatment of acute myelogenous leukemia
    • Prescott H, Kantarjian H, Cortes J, Ravandi F. Emerging FMS-like tyrosine kinase 3 inhibitors for the treatment of acute myelogenous leukemia. Expert Opin Emerg Drugs. 2011;16: 407-423.
    • (2011) Expert Opin Emerg Drugs , vol.16 , pp. 407-423
    • Prescott, H.1    Kantarjian, H.2    Cortes, J.3    Ravandi, F.4
  • 33
    • 77954494236 scopus 로고    scopus 로고
    • FLT3 inhibitors for the treatment of acute myeloid leukemia
    • Wiernik PH. FLT3 inhibitors for the treatment of acute myeloid leukemia. Clin Adv Hematol Oncol. 2010;8(6):429-436, 444.
    • (2010) Clin Adv Hematol Oncol , vol.8 , Issue.6
    • Wiernik, P.H.1
  • 34
    • 78649931161 scopus 로고    scopus 로고
    • Will newer tyrosine kinase inhibitors have an impact in AML?
    • Levis MJ. Will newer tyrosine kinase inhibitors have an impact in AML? Best Pract Res Clin Haematol. 2010;23(4):489-494.
    • (2010) Best Pract Res Clin Haematol , vol.23 , Issue.4 , pp. 489-494
    • Levis, M.J.1
  • 36
    • 79959813961 scopus 로고    scopus 로고
    • FLT3/ITD AML and the law of unintended consequences
    • Levis M. FLT3/ITD AML and the law of unintended consequences. Blood. 2011;117(26):6987-6990.
    • (2011) Blood , vol.117 , Issue.26 , pp. 6987-6990
    • Levis, M.1
  • 41
    • 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(7):1425-1432.
    • (2010) Blood , vol.115 , Issue.7 , pp. 1425-1432
    • Pratz, K.W.1    Sato, T.2    Murphy, K.M.3    Stine, A.4    Rajkhowa, T.5    Levis, M.6
  • 42
    • 74249116380 scopus 로고    scopus 로고
    • Selective FLT3 inhibitor FI-700 neutralizes Mcl-1 and enhances p53-mediated apoptosis in AML cells with activating mutations of FLT3 through Mcl-1/ Noxa axis
    • Kojima K, Konopleva M, Tsao T, Andreeff M, Ishida H, Shiotsu Y, Jin L, Tabe Y, Nakakuma H. Selective FLT3 inhibitor FI-700 neutralizes Mcl-1 and enhances p53-mediated apoptosis in AML cells with activating mutations of FLT3 through Mcl-1/ Noxa axis. Leukemia. 2010;24(1):33-43.
    • (2010) Leukemia , vol.24 , Issue.1 , pp. 33-43
    • Kojima, K.1    Konopleva, M.2    Tsao, T.3    Andreeff, M.4    Ishida, H.5    Shiotsu, Y.6    Jin, L.7    Tabe, Y.8    Nakakuma, H.9
  • 47
    • 72249087752 scopus 로고    scopus 로고
    • Identification of N-(5-tert-butylisoxazol- 3-yl)-N'-{4-[7-(2-morpholin-4-yl-ethoxy) imidazo[2,1-b][1,3]benzothiazol-2-yl]phenyl}urea dihydrochloride (AC220), a uniquely potent, selective, and efficacious FMS-like tyrosine kinase-3 (FLT3) inhibitor
    • Chao Q, Sprankle KG, Grotzfeld RM, Lai AG, Carter TA, Velasco AM, Gunawardane RN, Cramer MD, Gardner MF, James J, Zarrinkar PP, Patel HK, Bhagwat SS. Identification of N-(5-tert-butylisoxazol- 3-yl)-N'-{4-[7-(2-morpholin-4-yl-ethoxy) imidazo[2,1-b][1,3]benzothiazol-2-yl]phenyl}urea dihydrochloride (AC220), a uniquely potent, selective, and efficacious FMS-like tyrosine kinase-3 (FLT3) inhibitor. J Med Chem. 2009;52(23): 7808-7816.
    • (2009) J Med Chem , vol.52 , Issue.23 , pp. 7808-7816
    • Chao, Q.1    Sprankle, K.G.2    Grotzfeld, R.M.3    Lai, A.G.4    Carter, T.A.5    Velasco, A.M.6    Gunawardane, R.N.7    Cramer, M.D.8    Gardner, M.F.9    James, J.10    Zarrinkar, P.P.11    Patel, H.K.12    Bhagwat, S.S.13


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.