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Volumn 8, Issue 9, 2008, Pages 1387-1398

Abl tyrosine kinase inhibitors for overriding Bcr-Abl/T315I: From the second to third generation

Author keywords

Aurora kinase; Bosutinib; Chronic myeloid leukemia; Dasatinib; Farnesyl transferase; HDAC; Heat shock protein; Imatinib; INNO 406; Nilotinib; T3151

Indexed keywords

3 BENZYL 7 CYANO 2,3,4,5 TETRAHYDRO 1 (1H IMIDAZOL 4 YLMETHYL) 4 (2 THIENYLSULFONYL) 1H 1,4 BENZODIAZEPINE; 4 (3 DIMETHYLAMINO 1 PYRROLIDINYLMETHYL) 3 TRIFLUOROMETHYL N [4 METHYL 3 [[4 (5 PYRIMIDINYL) 2 PYRIMIDINYL]AMINO]PHENYL]BENZAMIDE; 4 [N (2 HYDROXYETHYL) N [2 (3 INDOLYL)ETHYL]AMINOMETHYL]CINNAMOHYDROXAMIC ACID; ABELSON KINASE; ADAPHOSTIN; ANTILEUKEMIC AGENT; AT 9283; AURORA KINASE INHIBITOR; BOSUTINIB; CGX 653; CYCLOPROPANECARBOXYLIC ACID [4 [4 (4 METHYL 1 PIPERAZINYL) 6 (5 METHYL 2H PYRAZOL 3 YLAMINO) 2 PYRIMIDINYLTHIO]PHENYL]AMIDE; DASATINIB; DORAMAPIMOD; GELDANAMYCIN; HEAT SHOCK PROTEIN 90 INHIBITOR; HISTONE DEACETYLASE INHIBITOR; HOMOHARRINGTONINE; IMATINIB; MYELOSTAT; NILOTINIB; OMACETAXINE MEPESUCCINATE; ONO 12380; PANOBINOSTAT; PHA 739358; PROTEIN FARNESYLTRANSFERASE INHIBITOR; PROTEIN TYROSINE KINASE INHIBITOR; PROTOPORPHYRIN ZINC; SGX 393; TANESPIMYCIN; TANESPIMYCIN HYDROQUINONE; UNCLASSIFIED DRUG; UNINDEXED DRUG; VORINOSTAT;

EID: 55349096495     PISSN: 14737140     EISSN: 17448328     Source Type: Journal    
DOI: 10.1586/14737140.8.9.1387     Document Type: Review
Times cited : (48)

References (105)
  • 1
    • 0141528828 scopus 로고    scopus 로고
    • Chronic myeloid leukemia-advances in biology and new approaches to treatment
    • Goldman JM, Melo JV. Chronic myeloid leukemia-advances in biology and new approaches to treatment. N. Engl. J. Med. 349, 1451-1464 (2003).
    • (2003) N. Engl. J. Med , vol.349 , pp. 1451-1464
    • Goldman, J.M.1    Melo, J.V.2
  • 2
    • 0035810142 scopus 로고    scopus 로고
    • Activity of a specific inhibitor of the BCR-ABL tyrosine kinase in the blast crisis of chronic myeloid leukemia and acute lymphoblastic leukemia with the Philadelphia chromosome
    • Druker BJ, Sawyers CL, Kantarjian H et al. Activity of a specific inhibitor of the BCR-ABL tyrosine kinase in the blast crisis of chronic myeloid leukemia and acute lymphoblastic leukemia with the Philadelphia chromosome. N. Engl. J. Med. 344, 1038-1042 (2001).
    • (2001) N. Engl. J. Med , vol.344 , pp. 1038-1042
    • Druker, B.J.1    Sawyers, C.L.2    Kantarjian, H.3
  • 3
    • 0037105560 scopus 로고    scopus 로고
    • A Phase 2 study of imatinib in patients with relapsed or refractory Philadelphia chromosome-positive acute lymphoid leukemias
    • Ottmann OG, Druker BJ, Sawyers CL et al. A Phase 2 study of imatinib in patients with relapsed or refractory Philadelphia chromosome-positive acute lymphoid leukemias. Blood 100, 1965-1971 (2002).
    • (2002) Blood , vol.100 , pp. 1965-1971
    • Ottmann, O.G.1    Druker, B.J.2    Sawyers, C.L.3
  • 4
    • 0035800507 scopus 로고    scopus 로고
    • Clinical resistance to STI-571 cancer therapy caused by BCR-ABL gene mutation or amplification
    • Gorre ME, Mohammed M, Ellwood K et al. Clinical resistance to STI-571 cancer therapy caused by BCR-ABL gene mutation or amplification. Science 293, 876-880 (2001).
    • (2001) Science , vol.293 , pp. 876-880
    • Gorre, M.E.1    Mohammed, M.2    Ellwood, K.3
  • 5
    • 0036493544 scopus 로고    scopus 로고
    • + acute lymphoblastic leukemia resistant to the tyrosine kinase inhibitor ST1571 has a unique BCR-ABL gene mutation
    • + acute lymphoblastic leukemia resistant to the tyrosine kinase inhibitor ST1571 has a unique BCR-ABL gene mutation. Blood 99, 1860-1862 (2002).
    • (2002) Blood , vol.99 , pp. 1860-1862
    • Hofmann, W.K.1    Jones, L.C.2    Lemp, N.A.3
  • 6
    • 0348140591 scopus 로고    scopus 로고
    • Mechanisms and implications of imatinib resistance mutations in BCR-ABL
    • Nardi V, Azam M, Daley GQ. Mechanisms and implications of imatinib resistance mutations in BCR-ABL. Curr. Opin. Hematol. 11, 35-43 (2004).
    • (2004) Curr. Opin. Hematol , vol.11 , pp. 35-43
    • Nardi, V.1    Azam, M.2    Daley, G.Q.3
  • 7
    • 15944404601 scopus 로고    scopus 로고
    • The development of imatinib as a therapeutic agent for chronic myeloid leukemia
    • Deininger M, Buchdunger E, Druker BJ. The development of imatinib as a therapeutic agent for chronic myeloid leukemia. Blood 105, 2640-2653 (2005).
    • (2005) Blood , vol.105 , pp. 2640-2653
    • Deininger, M.1    Buchdunger, E.2    Druker, B.J.3
  • 8
    • 33947386190 scopus 로고    scopus 로고
    • Resistance to imatinib mesylate in chronic myeloid leukaemia
    • Melo JV, Chuah C. Resistance to imatinib mesylate in chronic myeloid leukaemia. Cancer Lett. 249, 121-132 (2007).
    • (2007) Cancer Lett , vol.249 , pp. 121-132
    • Melo, J.V.1    Chuah, C.2
  • 9
    • 55349096650 scopus 로고    scopus 로고
    • Chronic myeloid leukemia: Molecular monitoring in clinical practice
    • Branford S. Chronic myeloid leukemia: molecular monitoring in clinical practice. Hematology Am. Soc. hematol. Educ. Program 376-383 (2007).
    • (2007) Hematology Am. Soc. hematol. Educ. Program , pp. 376-383
    • Branford, S.1
  • 10
    • 3142676436 scopus 로고    scopus 로고
    • Overriding imatinib resistance with a novel ABL kinase inhibitor
    • Shah NP, Tran C, Lee FY et al. Overriding imatinib resistance with a novel ABL kinase inhibitor. Science 305, 399-401 (2004).
    • (2004) Science , vol.305 , pp. 399-401
    • Shah, N.P.1    Tran, C.2    Lee, F.Y.3
  • 11
    • 13844251975 scopus 로고    scopus 로고
    • Characterization of AMN 107, a selective inhibitor of native and mutant Bcr-Abl
    • Weisberg D, Manley PW, Breitenstein W et al. Characterization of AMN 107, a selective inhibitor of native and mutant Bcr-Abl. Cancer Cell 7, 129-141 (2005).
    • (2005) Cancer Cell , vol.7 , pp. 129-141
    • Weisberg, D.1    Manley, P.W.2    Breitenstein, W.3
  • 12
    • 0037439689 scopus 로고    scopus 로고
    • SKI-606, a 4-anilino-3-quinolinecarbonitrile dual inhibitor of Src and Abl kinases, is a potent antiproliferative agent against chronic myelogenous leukemia cells in culture and causes regression of K562 xenografts in nude mice
    • Golas JM, Arndt K, Etienne D et al. SKI-606, a 4-anilino-3-quinolinecarbonitrile dual inhibitor of Src and Abl kinases, is a potent antiproliferative agent against chronic myelogenous leukemia cells in culture and causes regression of K562 xenografts in nude mice. Cancer Res. 3, 375-381 (2003).
    • (2003) Cancer Res , vol.3 , pp. 375-381
    • Golas, J.M.1    Arndt, K.2    Etienne, D.3
  • 13
    • 28444479480 scopus 로고    scopus 로고
    • NS-187, a potent and selective dual Bcr-Abl/Lyn tyrosine kinase inhibitor, is a novel agent for imatinib-resistant leukemia
    • Kimura S, Naito H, Segawa H et al. NS-187, a potent and selective dual Bcr-Abl/Lyn tyrosine kinase inhibitor, is a novel agent for imatinib-resistant leukemia. Blood 106, 3948-3954 (2005).
    • (2005) Blood , vol.106 , pp. 3948-3954
    • Kimura, S.1    Naito, H.2    Segawa, H.3
  • 14
    • 33747154547 scopus 로고    scopus 로고
    • Evolving concepts in the management of chronic myeloid leukemia: Recommendations from an expert panel on behalf of the European LeukemiaNet
    • Baccarani M, Saglio G, Goldman J et al. Evolving concepts in the management of chronic myeloid leukemia: recommendations from an expert panel on behalf of the European LeukemiaNet. Blood 108, 1809-1820 (2006).
    • (2006) Blood , vol.108 , pp. 1809-1820
    • Baccarani, M.1    Saglio, G.2    Goldman, J.3
  • 15
    • 34548021652 scopus 로고    scopus 로고
    • + leukemias in the imatinib and post-imatinib eras
    • Davidson DF Ed, Nova Publisher, NY, USA
    • + leukemias in the imatinib and post-imatinib eras. In: Bone Marrow Transplantation: New Research. Davidson DF (Ed.). Nova Publisher, NY, USA 1-38 (2006).
    • (2006) Bone Marrow Transplantation: New Research , pp. 1-38
    • Kimura, S.1    Maekawa, T.2
  • 16
    • 0003405565 scopus 로고
    • Ries LAG, Miller BA, Hankey BF et al, Eds, National Cancer Institute, MD, USA 234
    • SEER Cancer Statistics Review, 1973-1991: Tables and Graphs. Ries LAG, Miller BA, Hankey BF et al. (Eds). National Cancer Institute, MD, USA 234 (1994).
    • (1994) SEER Cancer Statistics Review, 1973-1991: Tables and Graphs
  • 17
    • 0027204137 scopus 로고
    • Chronic myeloid leukemia: A concise update
    • Kantarjian HM, Deisseroth A, Kurzrock R et al. Chronic myeloid leukemia: a concise update. Blood 82, 691-703 (1993).
    • (1993) Blood , vol.82 , pp. 691-703
    • Kantarjian, H.M.1    Deisseroth, A.2    Kurzrock, R.3
  • 18
    • 0023673351 scopus 로고
    • Cytogenetics of chronic myelogenous leukemia
    • Bernstein R. Cytogenetics of chronic myelogenous leukemia. Semin. Hematol. 25, 20-34 (1988).
    • (1988) Semin. Hematol , vol.25 , pp. 20-34
    • Bernstein, R.1
  • 19
    • 0025209916 scopus 로고
    • Acute leukaemia in bcr/abl transgenic mice
    • Heisterkamp N, Jenster G, ten Hoeve J et al. Acute leukaemia in bcr/abl transgenic mice. Nature 344, 251-253 (1990).
    • (1990) Nature , vol.344 , pp. 251-253
    • Heisterkamp, N.1    Jenster, G.2    ten Hoeve, J.3
  • 20
    • 0025117392 scopus 로고
    • Induction of chronic myelogenous leukemia in mice by the P210bcr/abl gene of the Philadelphia chromosome
    • Daley GQ, Van Etten RA, Baltimore D. Induction of chronic myelogenous leukemia in mice by the P210bcr/abl gene of the Philadelphia chromosome. Science 247, 824-830 (1990).
    • (1990) Science , vol.247 , pp. 824-830
    • Daley, G.Q.1    Van Etten, R.A.2    Baltimore, D.3
  • 21
    • 0025271543 scopus 로고
    • Bcr-abl, The hallmark of chronic myeloid leukaemia in man, induces multiple haematopoietic neoplasms in mice
    • Elefanty AG, Hariharan IK, Cory S. Bcr-abl, The hallmark of chronic myeloid leukaemia in man, induces multiple haematopoietic neoplasms in mice. EMBO J. 9, 1069-1078 (1990).
    • (1990) EMBO J , vol.9 , pp. 1069-1078
    • Elefanty, A.G.1    Hariharan, I.K.2    Cory, S.3
  • 22
    • 10744233716 scopus 로고    scopus 로고
    • Imatinib compared with interferon and low-dose cytarabine for newly diagnosed chronic-phase chronic myeloid leukemia
    • O'Brien SG, Guilhot F, Larson RA et al. Imatinib compared with interferon and low-dose cytarabine for newly diagnosed chronic-phase chronic myeloid leukemia. N. Engl. J. Med. 348, 994-1004 (2003).
    • (2003) N. Engl. J. Med , vol.348 , pp. 994-1004
    • O'Brien, S.G.1    Guilhot, F.2    Larson, R.A.3
  • 23
    • 33845444046 scopus 로고    scopus 로고
    • Five-year follow-up of patients receiving imatinib for chronic myeloid leukemia
    • Druker BJ, Guilhot F, O'Brien SG et al. Five-year follow-up of patients receiving imatinib for chronic myeloid leukemia. N. Engl. J. Med. 355, 2408-2417 (2006).
    • (2006) N. Engl. J. Med , vol.355 , pp. 2408-2417
    • Druker, B.J.1    Guilhot, F.2    O'Brien, S.G.3
  • 24
    • 4344672552 scopus 로고    scopus 로고
    • Imatinib therapy in chronic myelogenous leukemia: Strategies to avoid and overcome resistance
    • Hochhaus A, La Rosee P. Imatinib therapy in chronic myelogenous leukemia: strategies to avoid and overcome resistance. Leukemia 18, 132-1331 (2004).
    • (2004) Leukemia , vol.18 , pp. 132-1331
    • Hochhaus, A.1    La Rosee, P.2
  • 26
    • 0037130294 scopus 로고    scopus 로고
    • Interaction of tyrosine kinase inhibitors with the human multidrug transporter proteins, MDR1 and MRP1
    • Hegedus T, Orfi L, Seprodi A et al. Interaction of tyrosine kinase inhibitors with the human multidrug transporter proteins, MDR1 and MRP1. Biochim. Biophys. Acta. 1587, 318-325 (2002).
    • (2002) Biochim. Biophys. Acta , vol.1587 , pp. 318-325
    • Hegedus, T.1    Orfi, L.2    Seprodi, A.3
  • 27
    • 0037438640 scopus 로고    scopus 로고
    • BCR-ABL independence and LYN kinase overexpression in chronic myelogenous leukemia cells selected for resistance to STI571
    • Donato NJ, Wu JY, Stapley J et al. BCR-ABL independence and LYN kinase overexpression in chronic myelogenous leukemia cells selected for resistance to STI571. Blood 101, 690-698 (2003).
    • (2003) Blood , vol.101 , pp. 690-698
    • Donato, N.J.1    Wu, J.Y.2    Stapley, J.3
  • 28
    • 37049028176 scopus 로고    scopus 로고
    • Most CML patients who have a suboptimal response to imatinib have low OCT-1 activity: Higher doses of imatinib may overcome the negative impact of low OCT-1 activity
    • White DL, Saunders VA, Dang P et al. Most CML patients who have a suboptimal response to imatinib have low OCT-1 activity: higher doses of imatinib may overcome the negative impact of low OCT-1 activity. Blood 110, 4064-4072 (2007).
    • (2007) Blood , vol.110 , pp. 4064-4072
    • White, D.L.1    Saunders, V.A.2    Dang, P.3
  • 29
    • 11144354274 scopus 로고    scopus 로고
    • High-dose imatinib mesylate therapy in newly diagnosed Philadelphia chromosome-positive chronic phase chronic myeloid leukemia
    • Kantarjian H, Talpaz M, O'Brien S et al. High-dose imatinib mesylate therapy in newly diagnosed Philadelphia chromosome-positive chronic phase chronic myeloid leukemia. Blood 103, 2873-2878 (2004).
    • (2004) Blood , vol.103 , pp. 2873-2878
    • Kantarjian, H.1    Talpaz, M.2    O'Brien, S.3
  • 30
    • 0141790853 scopus 로고    scopus 로고
    • + leukemia activity of imatinib mesylate
    • + leukemia activity of imatinib mesylate. Blood 102, 2229-2235 (2003).
    • (2003) Blood , vol.102 , pp. 2229-2235
    • Kuroda, J.1    Kimura, S.2    Segawa, H.3
  • 31
    • 0347569568 scopus 로고    scopus 로고
    • Chronic myeloid leukemia - still a few questions
    • Goldman JM. Chronic myeloid leukemia - still a few questions. Exp. Hematol. 32, 2-10 (2004).
    • (2004) Exp. Hematol , vol.32 , pp. 2-10
    • Goldman, J.M.1
  • 32
    • 33745102555 scopus 로고    scopus 로고
    • Dasatinib in imatinib-resistant Philadelphia chromosome-positive leukemias
    • Talpaz M, Shah NP, Kantarjian H et al. Dasatinib in imatinib-resistant Philadelphia chromosome-positive leukemias. N. Engl. J. Med. 354, 2531-2541 (2006).
    • (2006) N. Engl. J. Med , vol.354 , pp. 2531-2541
    • Talpaz, M.1    Shah, N.P.2    Kantarjian, H.3
  • 33
    • 40849135781 scopus 로고    scopus 로고
    • Comparison of imatinib, dasatinib, nilotinib and INNO-406 in imatinib-resistant cell lines
    • Deguchi Y, Kimura S, Ashihara E et al. Comparison of imatinib, dasatinib, nilotinib and INNO-406 in imatinib-resistant cell lines. Leuk. Res. 32, 980-983 (2008).
    • (2008) Leuk. Res , vol.32 , pp. 980-983
    • Deguchi, Y.1    Kimura, S.2    Ashihara, E.3
  • 35
    • 21744450304 scopus 로고    scopus 로고
    • Abl inhibitor BMS354825 binding mode in Abelson kinase revealed by molecular docking studies
    • Gambacorti-Passerini C, Gasser M, Ahmed S et al. Abl inhibitor BMS354825 binding mode in Abelson kinase revealed by molecular docking studies. Leukemia 19, 1267-1269 (2005).
    • (2005) Leukemia , vol.19 , pp. 1267-1269
    • Gambacorti-Passerini, C.1    Gasser, M.2    Ahmed, S.3
  • 36
    • 37049014938 scopus 로고    scopus 로고
    • Chemical proteomic profiles of the BCR-ABL inhibitors imatinib, nilotinib, and dasatinib reveal novel kinase and nonkinase targets
    • Rix U, Hantschel O, Dümberger G et al. Chemical proteomic profiles of the BCR-ABL inhibitors imatinib, nilotinib, and dasatinib reveal novel kinase and nonkinase targets. Blood 110, 4055-4063 (2007).
    • (2007) Blood , vol.110 , pp. 4055-4063
    • Rix, U.1    Hantschel, O.2    Dümberger, G.3
  • 37
    • 34249074686 scopus 로고    scopus 로고
    • Dasatinib or high-dose imatinib for chronic-phase chronic myeloid leukemia after failure of first-line imatinib: A randomized Phase 2 trial
    • Kantarjian H, Pasquini R, Hamerschlak N et al. Dasatinib or high-dose imatinib for chronic-phase chronic myeloid leukemia after failure of first-line imatinib: a randomized Phase 2 trial. Blood 109, 5143-5150 (2007)
    • (2007) Blood , vol.109 , pp. 5143-5150
    • Kantarjian, H.1    Pasquini, R.2    Hamerschlak, N.3
  • 38
    • 21144451094 scopus 로고    scopus 로고
    • In vitro activity of Bcr-Abl inhibitors AMN107 and BMS-354825 against clinically relevant imatinib-resistant Abl kinase domain mutants
    • O'Hare T, Walters DK, Stoffregen EP et al. In vitro activity of Bcr-Abl inhibitors AMN107 and BMS-354825 against clinically relevant imatinib-resistant Abl kinase domain mutants. Cancer Res. 65, 4500-4555 (2005).
    • (2005) Cancer Res , vol.65 , pp. 4500-4555
    • O'Hare, T.1    Walters, D.K.2    Stoffregen, E.P.3
  • 39
    • 36348968931 scopus 로고    scopus 로고
    • Nilotinib (formerly AMN107), a highly selective BCR-ABL tyrosine kinase inhibitor, is effective in patients with Philadelphia chromosome-positive chronic myelogenous leukemia in chronic phase following imatinib resistance and intolerance
    • Kantarjian HM, Giles F, Gattermann N et al. Nilotinib (formerly AMN107), a highly selective BCR-ABL tyrosine kinase inhibitor, is effective in patients with Philadelphia chromosome-positive chronic myelogenous leukemia in chronic phase following imatinib resistance and intolerance. Blood 110, 3540-3546 (2007).
    • (2007) Blood , vol.110 , pp. 3540-3546
    • Kantarjian, H.M.1    Giles, F.2    Gattermann, N.3
  • 40
    • 41349083969 scopus 로고    scopus 로고
    • Nilotinib (formerly AMN107), a highly selective BCR-ABL tyrosine kinase inhibitor, is active in patients with imatinib-resistant or -intolerant accelerated-phase chronic myelogenous leukemia
    • le Coutre P, Ottmann OG, Giles F et al. Nilotinib (formerly AMN107), a highly selective BCR-ABL tyrosine kinase inhibitor, is active in patients with imatinib-resistant or -intolerant accelerated-phase chronic myelogenous leukemia. Blood 111, 1834-1839 (2008)
    • (2008) Blood , vol.111 , pp. 1834-1839
    • le Coutre, P.1    Ottmann, O.G.2    Giles, F.3
  • 41
    • 35548957866 scopus 로고    scopus 로고
    • Goldman JM. How I treat chronic myeloid leukemia in the imatinib era. Blood 110, 2828-2837 (2007)
    • Goldman JM. How I treat chronic myeloid leukemia in the imatinib era. Blood 110, 2828-2837 (2007)
  • 42
    • 47649093491 scopus 로고    scopus 로고
    • Bosutinib (SKI-606) demonstrates clinical activity and is well tolerated among patients with AP and BPCML and Ph plus ALL
    • Gambacorti-Passerini C, Kantarjian H, Bruemmendorf T et al. Bosutinib (SKI-606) demonstrates clinical activity and is well tolerated among patients with AP and BPCML and Ph plus ALL. Blood 110, 146A-146A (2007).
    • (2007) Blood , vol.110
    • Gambacorti-Passerini, C.1    Kantarjian, H.2    Bruemmendorf, T.3
  • 43
    • 33749538244 scopus 로고    scopus 로고
    • New tyrosine kinase inhibitors in the treatment of chronic myeloid leukemia
    • Kimura S, Ashihara E, Maekawa T. New tyrosine kinase inhibitors in the treatment of chronic myeloid leukemia. Curr. Pharm. Biotechnol. 7, 371-379 (2006).
    • (2006) Curr. Pharm. Biotechnol , vol.7 , pp. 371-379
    • Kimura, S.1    Ashihara, E.2    Maekawa, T.3
  • 44
    • 34247381158 scopus 로고    scopus 로고
    • Structural factors contributing to the Abl/Lyn dual inhibitory activity of 3-substituted benzamide derivatives
    • Horio T, Hamasaki T, Inoue T et al. Structural factors contributing to the Abl/Lyn dual inhibitory activity of 3-substituted benzamide derivatives. Bioorg. Med. Chem. Lett. 17, 2712-2717 (2007)
    • (2007) Bioorg. Med. Chem. Lett , vol.17 , pp. 2712-2717
    • Horio, T.1    Hamasaki, T.2    Inoue, T.3
  • 45
    • 33748094100 scopus 로고    scopus 로고
    • In vivo antiproliferative effect of NS-187, a dual Bcr-Abl/Lyn tyrosine kinase inhibitor, on leukemic cells harbouring Abl kinase domain mutations
    • Naito H, Kimura S, Nakaya Y et al. In vivo antiproliferative effect of NS-187, a dual Bcr-Abl/Lyn tyrosine kinase inhibitor, on leukemic cells harbouring Abl kinase domain mutations. Leuk. Res. 30, 1443-1446 (2006).
    • (2006) Leuk. Res , vol.30 , pp. 1443-1446
    • Naito, H.1    Kimura, S.2    Nakaya, Y.3
  • 46
    • 33846018356 scopus 로고    scopus 로고
    • + leukemia cells in the central nervous system and cyclosporine A augments its in vivo activity
    • + leukemia cells in the central nervous system and cyclosporine A augments its in vivo activity. Blood 109, 306-314 (2007).
    • (2007) Blood , vol.109 , pp. 306-314
    • Yokota, A.1    Kimura, S.2    Masuda, S.3
  • 47
    • 45749104554 scopus 로고    scopus 로고
    • A Phase I study of INNO-406 in patients with advanced Philadelphia (Ph plus) chromosome-positive leukemias who are resistant or intolerant to imatinib and second generation tyrosine kinase inhibitors
    • Kantarjian HM, Cortes J, Le Coutre P et al. A Phase I study of INNO-406 in patients with advanced Philadelphia (Ph plus) chromosome-positive leukemias who are resistant or intolerant to imatinib and second generation tyrosine kinase inhibitors. Blood 110, 144A-144A (2007).
    • (2007) Blood , vol.110
    • Kantarjian, H.M.1    Cortes, J.2    Le Coutre, P.3
  • 48
    • 34548721201 scopus 로고    scopus 로고
    • Clinical outcome of 27 imatinib mesylate-resistant chronic myelogenous leukemia patients harboring a 73151 BCR-ABL mutation
    • Nicolini FE, Hayette S, Corm S et al. Clinical outcome of 27 imatinib mesylate-resistant chronic myelogenous leukemia patients harboring a 73151 BCR-ABL mutation. Haematologica 92, 1238-1241 (2007).
    • (2007) Haematologica , vol.92 , pp. 1238-1241
    • Nicolini, F.E.1    Hayette, S.2    Corm, S.3
  • 49
    • 33846228789 scopus 로고    scopus 로고
    • Contribution of ABL kinase domain mutations to imatinib resistance in different subsets of Philadelphia-positive patients: By the GIMEMA Working Party on Chronic Myeloid Leukemia
    • Soverini S, Colarossi S, Gnani A et al. Contribution of ABL kinase domain mutations to imatinib resistance in different subsets of Philadelphia-positive patients: by the GIMEMA Working Party on Chronic Myeloid Leukemia. Clin. Cancer Res. 12, 7374-7379 (2006).
    • (2006) Clin. Cancer Res , vol.12 , pp. 7374-7379
    • Soverini, S.1    Colarossi, S.2    Gnani, A.3
  • 50
    • 33750077276 scopus 로고    scopus 로고
    • Frequency and clinical significance of BCR-ABL mutations in patients with chronic myeloid leukemia treated with imatinib mesylate
    • Jabbour E, Kantarjian H, Jones D et al. Frequency and clinical significance of BCR-ABL mutations in patients with chronic myeloid leukemia treated with imatinib mesylate. Leukemia 20, 1767-1773 (2006).
    • (2006) Leukemia , vol.20 , pp. 1767-1773
    • Jabbour, E.1    Kantarjian, H.2    Jones, D.3
  • 51
    • 47249123747 scopus 로고    scopus 로고
    • Characteristics and outcome of patients with chronic myeloid leukemia and T315I mutation following failure of imatinib mesylate therapy
    • Jabbour E, Kantarjian H, Jones D et al. Characteristics and outcome of patients with chronic myeloid leukemia and T315I mutation following failure of imatinib mesylate therapy. Blood 112(1), 53-55 (2008).
    • (2008) Blood , vol.112 , Issue.1 , pp. 53-55
    • Jabbour, E.1    Kantarjian, H.2    Jones, D.3
  • 52
    • 0034665713 scopus 로고    scopus 로고
    • Structural mechanism for STI-571 inhibition of Abelson tyrosine kinase
    • Schindler T Bornmann W, Pellicena P et al. Structural mechanism for STI-571 inhibition of Abelson tyrosine kinase. Science 289, 938-942 (2000).
    • (2000) Science , vol.289 , pp. 938-942
    • Schindler, T.1    Bornmann, W.2    Pellicena, P.3
  • 53
    • 0037199996 scopus 로고    scopus 로고
    • Analysis of the structural basis of specificity of the Abl kinase by STI571
    • Corbin AS, Buchdunger E, Furet P, Druker BJ. Analysis of the structural basis of specificity of the Abl kinase by STI571. J. Biol. Chem. 277, 32214-32219 (2001).
    • (2001) J. Biol. Chem , vol.277 , pp. 32214-32219
    • Corbin, A.S.1    Buchdunger, E.2    Furet, P.3    Druker, B.J.4
  • 54
    • 23844553757 scopus 로고    scopus 로고
    • T3151-mutated Bcr-Abl in chronic myeloid leukemia and imatinib: Insights from a computational study
    • Pricl S, Fermeglia M, Ferrone M, Tamborini E. T3151-mutated Bcr-Abl in chronic myeloid leukemia and imatinib: insights from a computational study. Mol. Cancer Ther. 4, 1167-1174 (2005)
    • (2005) Mol. Cancer Ther , vol.4 , pp. 1167-1174
    • Pricl, S.1    Fermeglia, M.2    Ferrone, M.3    Tamborini, E.4
  • 55
    • 42149097162 scopus 로고    scopus 로고
    • Molecular basis explanation for imatinib resistance of BCR-ABL due to T315I and P-loop mutations from molecular dynamics simulations
    • Lee TS, Potts SJ, Kantarjian H et al. Molecular basis explanation for imatinib resistance of BCR-ABL due to T315I and P-loop mutations from molecular dynamics simulations. Cancer 112, 1744-1753 (2008).
    • (2008) Cancer , vol.112 , pp. 1744-1753
    • Lee, T.S.1    Potts, S.J.2    Kantarjian, H.3
  • 56
    • 33745114173 scopus 로고    scopus 로고
    • AMN107 (nilotinib): A novel and selective inhibitor of BCR-ABL
    • Weisberg E, Manley P, Mestan J et al. AMN107 (nilotinib): a novel and selective inhibitor of BCR-ABL. Brit. J. Cancer 94, 1765-1769 (2006).
    • (2006) Brit. J. Cancer , vol.94 , pp. 1765-1769
    • Weisberg, E.1    Manley, P.2    Mestan, J.3
  • 57
    • 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 nilotinib (AMN107)
    • von Bubnoff N, Manley PW, Mestan J et al. BCR-ABL resistance screening predicts a limited spectrum of point mutations to be associated with clinical resistance to the ABL kinase inhibitor nilotinib (AMN107). Blood 108, 1328-1333 (2006).
    • (2006) Blood , vol.108 , pp. 1328-1333
    • von Bubnoff, N.1    Manley, P.W.2    Mestan, J.3
  • 58
    • 33646755174 scopus 로고    scopus 로고
    • A Src-like inactive conformation in the ABL Tyrosine Kinase Domain
    • Levinson NM, Kuchment O, Shen K et al. A Src-like inactive conformation in the ABL Tyrosine Kinase Domain. PLoS Biol. 4, e144 (2006).
    • (2006) PLoS Biol , vol.4
    • Levinson, N.M.1    Kuchment, O.2    Shen, K.3
  • 59
    • 13844261144 scopus 로고    scopus 로고
    • A non-ATP-competitive inhibitor of BCR-ABL overrides imatinib resistance
    • Gumireddy K, Baker SJ, Cosenza SC et al. A non-ATP-competitive inhibitor of BCR-ABL overrides imatinib resistance. Proc. Natl Acad. Sci. USA 102, 1992-1997 (2005).
    • (2005) Proc. Natl Acad. Sci. USA , vol.102 , pp. 1992-1997
    • Gumireddy, K.1    Baker, S.J.2    Cosenza, S.C.3
  • 60
    • 23344440655 scopus 로고    scopus 로고
    • Inhibition of drug-resistant mutants of ABL, KIT, and EGF receptor kinases
    • Carter TA, Wodicka LM, Shah NP et al. Inhibition of drug-resistant mutants of ABL, KIT, and EGF receptor kinases. Proc. Natl Acad. Sci. USA 102, 11011-11016 (2005)
    • (2005) Proc. Natl Acad. Sci. USA , vol.102 , pp. 11011-11016
    • Carter, T.A.1    Wodicka, L.M.2    Shah, N.P.3
  • 61
    • 21244476768 scopus 로고    scopus 로고
    • BIRB796 inhibits all p38 MAPK isoforms in vitro and in vivo
    • Kuma Y, Sabic, G, Bain J et al. BIRB796 inhibits all p38 MAPK isoforms in vitro and in vivo. J. Biol. Chem. 280, 19472-19479 (2005)
    • (2005) J. Biol. Chem , vol.280 , pp. 19472-19479
    • Kuma, Y.1    Sabic, G.2    Bain, J.3
  • 62
    • 27144549921 scopus 로고    scopus 로고
    • BIRB-796 is not an effective ABL(T315I) inhibitor
    • O'Hare T, Druker BJ. BIRB-796 is not an effective ABL(T315I) inhibitor. Nat. Biotechnol. 23, 1209-1210 (2005).
    • (2005) Nat. Biotechnol , vol.23 , pp. 1209-1210
    • O'Hare, T.1    Druker, B.J.2
  • 65
    • 0038341158 scopus 로고    scopus 로고
    • The Aurora kinases: Role in cell transformation and tumorigenesis
    • Katayama H, Brinkley WR, Sen S. The Aurora kinases: role in cell transformation and tumorigenesis. Cancer Metastasis Rev. 22, 451-464 (2003).
    • (2003) Cancer Metastasis Rev , vol.22 , pp. 451-464
    • Katayama, H.1    Brinkley, W.R.2    Sen, S.3
  • 66
    • 10344236486 scopus 로고    scopus 로고
    • Aurora-kinase inhibitors as anticancer agents
    • Keen N, Taylor S. Aurora-kinase inhibitors as anticancer agents. Nat. Rev. Cancer 4, 927-936 (2004).
    • (2004) Nat. Rev. Cancer , vol.4 , pp. 927-936
    • Keen, N.1    Taylor, S.2
  • 67
    • 2342639645 scopus 로고    scopus 로고
    • VX-680, a potent and selective small-molecule inhibitor of the Aurora kinases, suppresses tumor growth in vivo
    • Harrington EA, Bebbington D, Moore J. et al. VX-680, a potent and selective small-molecule inhibitor of the Aurora kinases, suppresses tumor growth in vivo. Nat. Med. 10, 262-267 (2004).
    • (2004) Nat. Med , vol.10 , pp. 262-267
    • Harrington, E.A.1    Bebbington, D.2    Moore, J.3
  • 68
    • 31644438945 scopus 로고    scopus 로고
    • Structure of the kinase domain of an imatinib-resistant Abl mutant in complex with the Aurora kinase inhibitor VX-680
    • Young MA, Shah NP, Chao LH et al. Structure of the kinase domain of an imatinib-resistant Abl mutant in complex with the Aurora kinase inhibitor VX-680. Cancer Res. 66, 1007-1014 (2006).
    • (2006) Cancer Res , vol.66 , pp. 1007-1014
    • Young, M.A.1    Shah, N.P.2    Chao, L.H.3
  • 69
    • 34247615972 scopus 로고    scopus 로고
    • Structural basis for potent inhibition of the Aurora kinases and a T315I multi-drug resistant mutant form of Abl kinase by VX-680
    • Cheetham GM, Chariton PA, Golec JM, Pollard JR. Structural basis for potent inhibition of the Aurora kinases and a T315I multi-drug resistant mutant form of Abl kinase by VX-680. Cancer Lett., 251, 323-329 (2007)
    • (2007) Cancer Lett , vol.251 , pp. 323-329
    • Cheetham, G.M.1    Chariton, P.A.2    Golec, J.M.3    Pollard, J.R.4
  • 70
    • 34848911943 scopus 로고    scopus 로고
    • Sequential ABL kinase inhibitor therapy selects for compound drug-resistant BCR-ABL mutations with altered oncogenic potency
    • Shah NP, Skaggs BJ, Branford S et al. Sequential ABL kinase inhibitor therapy selects for compound drug-resistant BCR-ABL mutations with altered oncogenic potency. J. Clin. Invest. 117, 2562-2569 (2007).
    • (2007) J. Clin. Invest , vol.117 , pp. 2562-2569
    • Shah, N.P.1    Skaggs, B.J.2    Branford, S.3
  • 71
    • 33846240316 scopus 로고    scopus 로고
    • MK-0457, a novel kinase inhibitor, is active in patients with chronic myeloid leukemia or acute lymphocytic leukemia with the T315I BCR-ABL mutation
    • Giles FJ, Cortes J, Jones D et al. MK-0457, a novel kinase inhibitor, is active in patients with chronic myeloid leukemia or acute lymphocytic leukemia with the T315I BCR-ABL mutation. Blood 109, 500-502 (2007).
    • (2007) Blood , vol.109 , pp. 500-502
    • Giles, F.J.1    Cortes, J.2    Jones, D.3
  • 72
    • 33845367377 scopus 로고    scopus 로고
    • Fancelli D, Moll J, Varasi M et al. 1,4,5,6-tetrahydropyrrolo [3,4-c]pyrazoles: identification of a potent Aurora kinase inhibitor with a favorable antitumor kinase inhibition profile. J. Med. Chem. 49, 7247-7251 (2006).
    • Fancelli D, Moll J, Varasi M et al. 1,4,5,6-tetrahydropyrrolo [3,4-c]pyrazoles: identification of a potent Aurora kinase inhibitor with a favorable antitumor kinase inhibition profile. J. Med. Chem. 49, 7247-7251 (2006).
  • 73
    • 34548548332 scopus 로고    scopus 로고
    • Crystal structure of the T315I Abl mutant in complex with the aurora kinases inhibitor PHA-739358
    • Modugno M, Casale E, Soncini C et al. Crystal structure of the T315I Abl mutant in complex with the aurora kinases inhibitor PHA-739358. Cancer Res. 67, 7987-7990 (2007).
    • (2007) Cancer Res , vol.67 , pp. 7987-7990
    • Modugno, M.1    Casale, E.2    Soncini, C.3
  • 74
    • 43249111278 scopus 로고    scopus 로고
    • Simultaneous targeting of Aurora kinases and Bcr-Abl kinase by the small molecule inhibitor PHA-739358 is effective against imatinib-resistant BCR-ABL mutations including T315I
    • Gontarewicz A, Balabanov S, Keller G et al. Simultaneous targeting of Aurora kinases and Bcr-Abl kinase by the small molecule inhibitor PHA-739358 is effective against imatinib-resistant BCR-ABL mutations including T315I. Blood 111, 4355-4364 (2008).
    • (2008) Blood , vol.111 , pp. 4355-4364
    • Gontarewicz, A.1    Balabanov, S.2    Keller, G.3
  • 76
    • 0033564350 scopus 로고    scopus 로고
    • Sequential homoharringtonine and interferon-α in the treatment of early chronic phase chronic myelogenous leukemia
    • O'Brien S, Kantarjian H, Koller C et al. Sequential homoharringtonine and interferon-α in the treatment of early chronic phase chronic myelogenous leukemia. Blood 93, 4149-4153 (1999)
    • (1999) Blood , vol.93 , pp. 4149-4153
    • O'Brien, S.1    Kantarjian, H.2    Koller, C.3
  • 77
    • 34548745204 scopus 로고    scopus 로고
    • BCR-ABL (T315I) transcript disappearance in an imatinib-resistant CML patient treated with homoharringtonine: A new therapeutic challenge?
    • Legros L, Hayette S, Nicolini FE et al. BCR-ABL (T315I) transcript disappearance in an imatinib-resistant CML patient treated with homoharringtonine: a new therapeutic challenge? Leukemia 21, 2204-2206 (2007).
    • (2007) Leukemia , vol.21 , pp. 2204-2206
    • Legros, L.1    Hayette, S.2    Nicolini, F.E.3
  • 78
    • 34948830170 scopus 로고    scopus 로고
    • Interferon-α or homoharringtonine as salvage treatment for chronic myeloid leukemia patients who acquire the T315I BCR-ABL mutation
    • de Lavallade H, Khorashad JS, Davis HP et al. Interferon-α or homoharringtonine as salvage treatment for chronic myeloid leukemia patients who acquire the T315I BCR-ABL mutation. Blood 110, 2779-2780 (2007).
    • (2007) Blood , vol.110 , pp. 2779-2780
    • de Lavallade, H.1    Khorashad, J.S.2    Davis, H.P.3
  • 79
    • 42649143835 scopus 로고    scopus 로고
    • Homoharringtonine for the treatment of chronic myelogenous leukemia
    • Quintás-Cardama A, Cortes J. Homoharringtonine for the treatment of chronic myelogenous leukemia. Expert. Opin. Pharmacother. 9, 1029-1037 (2008).
    • (2008) Expert. Opin. Pharmacother , vol.9 , pp. 1029-1037
    • Quintás-Cardama, A.1    Cortes, J.2
  • 80
    • 43749086323 scopus 로고    scopus 로고
    • SGX393 inhibits the CML mutant Bcr-Abl T315I and preempts in vitro resistance when combined with nilotinib or dasatinib
    • O'Hare T, Eide CA, Tyner JW et al. SGX393 inhibits the CML mutant Bcr-Abl T315I and preempts in vitro resistance when combined with nilotinib or dasatinib. Proc. Natl Acad. Sci. USA 105, 5507-5512 (2008).
    • (2008) Proc. Natl Acad. Sci. USA , vol.105 , pp. 5507-5512
    • O'Hare, T.1    Eide, C.A.2    Tyner, J.W.3
  • 81
    • 0037108448 scopus 로고    scopus 로고
    • BCR-ABL point mutants isolated from patients with imatinib mesylate-resistant chronic myeloid leukemia remain sensitive to inhibitors of the BCR-ABL chaperone heat shock protein 90
    • Gorre ME, Enwood-Yen K, Chiosis G, Rosen N, Sawyers CL. BCR-ABL point mutants isolated from patients with imatinib mesylate-resistant chronic myeloid leukemia remain sensitive to inhibitors of the BCR-ABL chaperone heat shock protein 90. Blood 100, 3041-3044 (2002)
    • (2002) Blood , vol.100 , pp. 3041-3044
    • Gorre, M.E.1    Enwood-Yen, K.2    Chiosis, G.3    Rosen, N.4    Sawyers, C.L.5
  • 82
    • 34547137932 scopus 로고    scopus 로고
    • Inhibition of heat shock protein 90 prolongs survival of mice with BCR-ABL-T315I-induced leukemia and suppresses leukemic stem cells
    • Peng C, Brain J, Hu Y et al. Inhibition of heat shock protein 90 prolongs survival of mice with BCR-ABL-T315I-induced leukemia and suppresses leukemic stem cells. Blood 110, 678-685 (2007).
    • (2007) Blood , vol.110 , pp. 678-685
    • Peng, C.1    Brain, J.2    Hu, Y.3
  • 83
    • 2342642883 scopus 로고    scopus 로고
    • Identification of heme oxygenase-1 as a novel BCR/ABL-dependent survival factor in chronic myeloid leukemia
    • Mayerhofer M, Florian S, Krauth MT et al. Identification of heme oxygenase-1 as a novel BCR/ABL-dependent survival factor in chronic myeloid leukemia. Cancer Res. 64, 3148-3154 (2004).
    • (2004) Cancer Res , vol.64 , pp. 3148-3154
    • Mayerhofer, M.1    Florian, S.2    Krauth, M.T.3
  • 84
    • 41349085365 scopus 로고    scopus 로고
    • Targeting of heat shock protein 32 (Hsp32)/heme oxygenase-1 (HO-1) in leukemic cells in chronic myeloid leukemia: A novel approach to overcome resistance against imatinib
    • Mayerhofer M, Gleixner KV, Mayerhofer J et al. Targeting of heat shock protein 32 (Hsp32)/heme oxygenase-1 (HO-1) in leukemic cells in chronic myeloid leukemia: a novel approach to overcome resistance against imatinib. Blood 111, 2200-2210 (2008).
    • (2008) Blood , vol.111 , pp. 2200-2210
    • Mayerhofer, M.1    Gleixner, K.V.2    Mayerhofer, J.3
  • 85
    • 0043016178 scopus 로고    scopus 로고
    • Histone deacetylase inhibitor LAQ824 both lowers expression and promotes proteasomal degradation of Bcr-Abl and induces apoptosis of imatinib mesylate-sensitive or -refractory chronic myelogenous leukemia-blast crisis cells
    • Nimmanapalli R, Fuino L, Bali P et al. Histone deacetylase inhibitor LAQ824 both lowers expression and promotes proteasomal degradation of Bcr-Abl and induces apoptosis of imatinib mesylate-sensitive or -refractory chronic myelogenous leukemia-blast crisis cells. Cancer Res. 63, 5126-5135 (2003).
    • (2003) Cancer Res , vol.63 , pp. 5126-5135
    • Nimmanapalli, R.1    Fuino, L.2    Bali, P.3
  • 86
    • 20844444898 scopus 로고    scopus 로고
    • Combination of the histone deacetylase inhibitor LBH589 and the hsp90 inhibitor 17-AAG is highly active against human CML-BC cells and AML cells with activating mutation of FLT-3
    • George P, Bali P, Annavarapu S et al. Combination of the histone deacetylase inhibitor LBH589 and the hsp90 inhibitor 17-AAG is highly active against human CML-BC cells and AML cells with activating mutation of FLT-3. Blood 105, 1768-1776 (2005).
    • (2005) Blood , vol.105 , pp. 1768-1776
    • George, P.1    Bali, P.2    Annavarapu, S.3
  • 87
    • 33745888156 scopus 로고    scopus 로고
    • Combined effects of novel tyrosine kinase inhibitor AMN107 and histone deacetylase inhibitor LBH589 against Bcr-Abl- expressing human leukemia cells
    • Fiskus W, Pranpat M, Bali P et al. Combined effects of novel tyrosine kinase inhibitor AMN107 and histone deacetylase inhibitor LBH589 against Bcr-Abl- expressing human leukemia cells. Blood 108, 645-652 (2006).
    • (2006) Blood , vol.108 , pp. 645-652
    • Fiskus, W.1    Pranpat, M.2    Bali, P.3
  • 88
    • 33750303818 scopus 로고    scopus 로고
    • Cotreatment with vorinostat (suberoylanilide hydroxamic acid) enhances activity of dasatinib (BMS-354825) against imatinib mesylate-sensitive or imatinib mesylate-resistant chronic myelogenous leukemia cells
    • Fiskus W, Pranpat M, Balasis M et al. Cotreatment with vorinostat (suberoylanilide hydroxamic acid) enhances activity of dasatinib (BMS-354825) against imatinib mesylate-sensitive or imatinib mesylate-resistant chronic myelogenous leukemia cells. Clin. Cancer Res. 12, 5869-5878 (2006).
    • (2006) Clin. Cancer Res , vol.12 , pp. 5869-5878
    • Fiskus, W.1    Pranpat, M.2    Balasis, M.3
  • 89
    • 34347394714 scopus 로고    scopus 로고
    • Targeting autophagy augments the anticancer activity of the histone deacetylase inhibitor SAHA to overcome Bcr-Abl-mediated drug resistance
    • Carew JS, Nawrocki ST, Kahue CN et al. Targeting autophagy augments the anticancer activity of the histone deacetylase inhibitor SAHA to overcome Bcr-Abl-mediated drug resistance. Blood 110, 313-322 (2007)
    • (2007) Blood , vol.110 , pp. 313-322
    • Carew, J.S.1    Nawrocki, S.T.2    Kahue, C.N.3
  • 90
    • 41949088658 scopus 로고    scopus 로고
    • BMS-214662 potently induces apoptosis of chronic myeloid leukemia stem and progenitor cells and synergizes with tyrosine kinase inhibitors
    • Copland M, Pellicano F, Richmond L et al. BMS-214662 potently induces apoptosis of chronic myeloid leukemia stem and progenitor cells and synergizes with tyrosine kinase inhibitors. Blood 111, 2843-2853 (2008).
    • (2008) Blood , vol.111 , pp. 2843-2853
    • Copland, M.1    Pellicano, F.2    Richmond, L.3
  • 91
    • 33746638536 scopus 로고    scopus 로고
    • Adaphostin and bortezomib induce oxidative injury and apoptosis in imatinib mesylate-resistant hematopoietic cells expressing mutant forms of Bcr/Abl
    • Dasmahapatra G, Nguyen TK, Dent P, Grant S. Adaphostin and bortezomib induce oxidative injury and apoptosis in imatinib mesylate-resistant hematopoietic cells expressing mutant forms of Bcr/Abl. Leuk. Res. 30, 1263-1272 (2006).
    • (2006) Leuk. Res , vol.30 , pp. 1263-1272
    • Dasmahapatra, G.1    Nguyen, T.K.2    Dent, P.3    Grant, S.4
  • 92
    • 33746139407 scopus 로고    scopus 로고
    • Janus kinase 2: A critical target in chronic myelogenous leukemia
    • Samanta AK, Lin H, Sun T, Kantarjian H, Arlinghaus RB. Janus kinase 2: a critical target in chronic myelogenous leukemia. Cancer Res. 66, 6468-6472 (2006).
    • (2006) Cancer Res , vol.66 , pp. 6468-6472
    • Samanta, A.K.1    Lin, H.2    Sun, T.3    Kantarjian, H.4    Arlinghaus, R.B.5
  • 93
    • 33749626306 scopus 로고    scopus 로고
    • Regulation and targeting of Eg5, a mitotic motor protein in blast crisis CML: Overcoming imatinib resistance
    • Carter BZ, Mak DH, Shi Y et al. Regulation and targeting of Eg5, a mitotic motor protein in blast crisis CML: overcoming imatinib resistance. Cell Cycle 5, 2223-2229 (2006).
    • (2006) Cell Cycle , vol.5 , pp. 2223-2229
    • Carter, B.Z.1    Mak, D.H.2    Shi, Y.3
  • 94
    • 34147155353 scopus 로고    scopus 로고
    • Activation of a novel Bcr/Abl destruction pathway by WP1130 induces apoptosis of chronic myelogenous leukemia cells
    • Bartholomeusz GA, Talpaz M, Kapuria V et al. Activation of a novel Bcr/Abl destruction pathway by WP1130 induces apoptosis of chronic myelogenous leukemia cells. Blood 109, 3470-3478 (2007).
    • (2007) Blood , vol.109 , pp. 3470-3478
    • Bartholomeusz, G.A.1    Talpaz, M.2    Kapuria, V.3
  • 95
    • 45149100643 scopus 로고    scopus 로고
    • Effective killing of Gleevec-resistant CML cells with T315I mutation by a natural compound PEITC through redox-mediated mechanism
    • Zhang H, Trachootham D, Lu W et al. Effective killing of Gleevec-resistant CML cells with T315I mutation by a natural compound PEITC through redox-mediated mechanism. Leukemia 22, 1191-1199 (2008).
    • (2008) Leukemia , vol.22 , pp. 1191-1199
    • Zhang, H.1    Trachootham, D.2    Lu, W.3
  • 96
    • 20844434173 scopus 로고    scopus 로고
    • Synergistic interactions between imatinib mesylate and the novel phosphoinositide-dependent kinase-1 inhibitor OSU-03012 in overcoming imatinib mesylate resistance
    • Tseng PH, Lin HP, Zhu J et al. Synergistic interactions between imatinib mesylate and the novel phosphoinositide-dependent kinase-1 inhibitor OSU-03012 in overcoming imatinib mesylate resistance. Blood 105, 4021-4027 (2005).
    • (2005) Blood , vol.105 , pp. 4021-4027
    • Tseng, P.H.1    Lin, H.P.2    Zhu, J.3
  • 97
    • 40749121701 scopus 로고    scopus 로고
    • Targeting 14-3-3 sensitizes native and mutant BCR-ABL to inhibition with U0126, rapamycin and Bcl-2 inhibitor GX15-070
    • Dong S, Kang S, Lonial S et al. Targeting 14-3-3 sensitizes native and mutant BCR-ABL to inhibition with U0126, rapamycin and Bcl-2 inhibitor GX15-070. Leukemia 22, 572-577 (2008).
    • (2008) Leukemia , vol.22 , pp. 572-577
    • Dong, S.1    Kang, S.2    Lonial, S.3
  • 98
    • 34548169642 scopus 로고    scopus 로고
    • Crystal structure of the T315I mutant of AbI kinase
    • Zhou T, Parillon L, Li F et al. Crystal structure of the T315I mutant of AbI kinase. Chem. Biol. Drug Des. 70, 171-181 (2007)
    • (2007) Chem. Biol. Drug Des , vol.70 , pp. 171-181
    • Zhou, T.1    Parillon, L.2    Li, F.3
  • 99
    • 34548412863 scopus 로고    scopus 로고
    • + human leukemia cells in association with signal transducer and activator of transcription 5 inhibition and myeloid cell leukemia-1 down-regulation
    • + human leukemia cells in association with signal transducer and activator of transcription 5 inhibition and myeloid cell leukemia-1 down-regulation. Mol. Pharmacol. 72, 788-795 (2007).
    • (2007) Mol. Pharmacol , vol.72 , pp. 788-795
    • Rahmani, M.1    Nguyen, T.K.2    Dent, P.3    Grant, S.4
  • 100
    • 34648832173 scopus 로고    scopus 로고
    • FTY720, a new alternative for treating blast crisis chronic myelogenous leukemia and Philadelphia chromosome-positive acute lymphocytic leukemia
    • Neviani P, Santhanam R, Oaks JJ et al. FTY720, a new alternative for treating blast crisis chronic myelogenous leukemia and Philadelphia chromosome-positive acute lymphocytic leukemia. J. Clin. Invest. 117, 2408-2421 (2007)
    • (2007) J. Clin. Invest , vol.117 , pp. 2408-2421
    • Neviani, P.1    Santhanam, R.2    Oaks, J.J.3
  • 101
    • 44949253057 scopus 로고    scopus 로고
    • Imatinib mesylate-resistant human chronic myelogenous leukemia cell lines exhibit high sensitivity to the phytoalexin resveratrol
    • Puissant A, Grosso S, Jacquel A et al. Imatinib mesylate-resistant human chronic myelogenous leukemia cell lines exhibit high sensitivity to the phytoalexin resveratrol. FASEB J. 22(6), 1894-1904 (2008).
    • (2008) FASEB J , vol.22 , Issue.6 , pp. 1894-1904
    • Puissant, A.1    Grosso, S.2    Jacquel, A.3
  • 102
    • 37349090416 scopus 로고    scopus 로고
    • Evaluation of antileukaemic effects of rapamycin in patients with imatinib-resistant chronic myeloid leukaemia
    • Sillaber C, Mayerhofer M, Böhm A et al. Evaluation of antileukaemic effects of rapamycin in patients with imatinib-resistant chronic myeloid leukaemia. Eur. J. Clin. Invest. 38, 43-52 (2008)
    • (2008) Eur. J. Clin. Invest , vol.38 , pp. 43-52
    • Sillaber, C.1    Mayerhofer, M.2    Böhm, A.3
  • 103
    • 43749121647 scopus 로고    scopus 로고
    • DCC-2036: A novel switch pocket inhibitor of ABL tyrosine kinase with therapeutic efficacy against BCR-ABL T3151 in vivo and in a CML mouse model
    • Van Etten RA, Chan WW, Zaleskas VM et al. DCC-2036: a novel switch pocket inhibitor of ABL tyrosine kinase with therapeutic efficacy against BCR-ABL T3151 in vivo and in a CML mouse model. Blood 110, 142A-143A (2007)
    • (2007) Blood , vol.110
    • Van Etten, R.A.1    Chan, W.W.2    Zaleskas, V.M.3
  • 104
    • 22144443475 scopus 로고    scopus 로고
    • Drug resistance in cancer: Principles of emergence and prevention
    • Komarova NL, Wodarz D. Drug resistance in cancer: principles of emergence and prevention. Proc. Natl Acad. Sci. USA 102, 9714-9719 (2005).
    • (2005) Proc. Natl Acad. Sci. USA , vol.102 , pp. 9714-9719
    • Komarova, N.L.1    Wodarz, D.2
  • 105
    • 47049127238 scopus 로고    scopus 로고
    • Emerging stem cell concepts for imatinib-resistant chronic myeloid leukaemia: Implications for the biology, management, and therapy of the disease
    • Epub ahead of print
    • Valent P. Emerging stem cell concepts for imatinib-resistant chronic myeloid leukaemia: implications for the biology, management, and therapy of the disease. Br. J. Haematol. (2008) (Epub ahead of print).
    • (2008) Br. J. Haematol
    • Valent, P.1


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