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Volumn 17, Issue 10, 2011, Pages 3219-3232

HDAC inhibitors potentiate the activity of the BCR/ABL kinase inhibitor KW-2449 in imatinib-sensitive or -resistant BCR/ABL+ leukemia cells in vitro and in vivo

Author keywords

[No Author keywords available]

Indexed keywords

APICIDIN; AURORA KINASE INHIBITOR; BCR ABL PROTEIN; CD19 ANTIGEN; CD34 ANTIGEN; CD45 ANTIGEN; CRK LIKE PROTEIN; DASATINIB; ENTINOSTAT; GAMMA HISTONE H2AX; HISTONE DEACETYLASE INHIBITOR; HISTONE H2AX; IMATINIB; KW 2449; NICOTINAMIDE ADENINE DINUCLEOTIDE ADENOSINE DIPHOSPHATE RIBOSYLTRANSFERASE; PROCASPASE 3; PROTEIN BCL 2; PROTEIN KINASE LYN; REACTIVE OXYGEN METABOLITE; SCAVENGER; STAT5 PROTEIN; SUBERIC BISHYDROXAMATE; UNCLASSIFIED DRUG; VORINOSTAT;

EID: 79956056274     PISSN: 10780432     EISSN: 15573265     Source Type: Journal    
DOI: 10.1158/1078-0432.CCR-11-0234     Document Type: Article
Times cited : (73)

References (41)
  • 1
    • 58149398623 scopus 로고    scopus 로고
    • Translation of the Philadelphia chromosome into therapy for CML
    • Druker BJ. Translation of the Philadelphia chromosome into therapy for CML. Blood 2008;112:4808-17.
    • (2008) Blood , vol.112 , pp. 4808-4817
    • Druker, B.J.1
  • 2
    • 36049016022 scopus 로고    scopus 로고
    • A review of the clinical and economic outcomes of imatinib in Philadelphia chromosome-positive acute lymphoblastic leukemia
    • DOI 10.1517/14656566.8.16.2775
    • Carpiuc KT, Stephens JM, Botteman MF, Feng W, Hay JW. A review of the clinical and economic outcomes of imatinib in Philadelphia chromosome- positive acute lymphoblastic leukemia. Expert Opin Pharmacother 2007;8:2775-87. (Pubitemid 350193716)
    • (2007) Expert Opinion on Pharmacotherapy , vol.8 , Issue.16 , pp. 2775-2787
    • Carpiuc, K.T.1    Stephens, J.M.2    Botteman, M.F.3    Feng, W.4    Hay, J.W.5
  • 3
    • 70450193142 scopus 로고    scopus 로고
    • Imatinib and beyond- exploring the full potential of targeted therapy for CML
    • Quintas-Cardama A, Kantarjian H, Cortes J. Imatinib and beyond- exploring the full potential of targeted therapy for CML. Nat Rev Clin Oncol 2009;6:535-43.
    • (2009) Nat Rev Clin Oncol , vol.6 , pp. 535-543
    • Quintas-Cardama, A.1    Kantarjian, H.2    Cortes, J.3
  • 4
    • 34848929062 scopus 로고    scopus 로고
    • Flying under the radar: The new wave of BCR-ABL inhibitors
    • DOI 10.1038/nrd2324, PII NRD2324
    • Quintas-Cardama A, Kantarjian H, Cortes J. Flying under the radar: the new wave of BCR-ABL inhibitors. Nat Rev Drug Discov 2007;6:834-48. (Pubitemid 47500507)
    • (2007) Nature Reviews Drug Discovery , vol.6 , Issue.10 , pp. 834-848
    • Quintas-Cardama, A.1    Kantarjian, H.2    Cortes, J.3
  • 5
    • 77957041354 scopus 로고    scopus 로고
    • Resistance to imatinib: Mutations and beyond
    • La RP, Deininger MW. Resistance to imatinib: mutations and beyond. Semin Hematol 2010;47:335-43.
    • (2010) Semin Hematol , vol.47 , pp. 335-343
    • La, R.P.1    Deininger, M.W.2
  • 6
    • 34548825795 scopus 로고    scopus 로고
    • Bcr-Abl kinase domain mutations, drug resistance and the road to a cure of chronic myeloid leukemia
    • O'Hare T, Eide CA, Deininger MW. Bcr-Abl kinase domain mutations, drug resistance and the road to a cure of chronic myeloid leukemia. Blood 2007;110:2242-7.
    • (2007) Blood , vol.110 , pp. 2242-2247
    • O'Hare, T.1    Eide, C.A.2    Deininger, M.W.3
  • 9
    • 70349566478 scopus 로고    scopus 로고
    • KW-2449, a novel multikinase inhibitor, suppresses the growth of leukemia cells with FLT3 mutations or T315I-mutated BCR/ABL translocation
    • Shiotsu Y, Kiyoi H, Ishikawa Y, Tanizaki R, Shimizu M, Umehara H, et al. KW-2449, a novel multikinase inhibitor, suppresses the growth of leukemia cells with FLT3 mutations or T315I-mutated BCR/ABL translocation. Blood 2009;114:1607-17.
    • (2009) Blood , vol.114 , pp. 1607-1617
    • Shiotsu, Y.1    Kiyoi, H.2    Ishikawa, Y.3    Tanizaki, R.4    Shimizu, M.5    Umehara, H.6
  • 10
    • 62949087552 scopus 로고    scopus 로고
    • A pharmacodynamic study of the FLT3 inhibitor KW-2449 yields insight into the basis for clinical response
    • Pratz KW, Cortes J, Roboz GJ, Rao N, Arowojolu O, Stine A, et al. A pharmacodynamic study of the FLT3 inhibitor KW-2449 yields insight into the basis for clinical response. Blood 2008;113:3839-46.
    • (2008) Blood , vol.113 , pp. 3839-3846
    • Pratz, K.W.1    Cortes, J.2    Roboz, G.J.3    Rao, N.4    Arowojolu, O.5    Stine, A.6
  • 11
    • 33748451151 scopus 로고    scopus 로고
    • Anticancer activities of histone deacetylase inhibitors
    • DOI 10.1038/nrd2133, PII NRD2133
    • Bolden JE, Peart MJ, Johnstone RW. Anticancer activities of histone deacetylase inhibitors. Nat Rev Drug Discov 2006;5:769-84. (Pubitemid 44348499)
    • (2006) Nature Reviews Drug Discovery , vol.5 , Issue.9 , pp. 769-784
    • Bolden, J.E.1    Peart, M.J.2    Johnstone, R.W.3
  • 13
    • 21244467166 scopus 로고    scopus 로고
    • Epigenetic and chromatin modifiers as targeted therapy of hematologic malignancies
    • DOI 10.1200/JCO.2005.16.600
    • Bhalla KN. Epigenetic and chromatin modifiers as targeted therapy of hematologic malignancies. J Clin Oncol 2005;23:3971-93. (Pubitemid 46218700)
    • (2005) Journal of Clinical Oncology , vol.23 , Issue.17 , pp. 3971-3993
    • Bhalla, K.N.1
  • 15
    • 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
    • DOI 10.1158/1078-0432.CCR-06-0980
    • Fiskus W, Pranpat M, Balasis M, Bali P, Estrella V, Kumaraswamy S, 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 2006;12:5869-78. (Pubitemid 44629620)
    • (2006) Clinical Cancer Research , vol.12 , Issue.19 , pp. 5869-5878
    • Fiskus, W.1    Pranpat, M.2    Balasis, M.3    Bali, P.4    Estrella, V.5    Kumaraswamy, S.6    Rao, R.7    Rocha, K.8    Herger, B.9    Lee, F.10    Richon, V.11    Bhalla, K.12
  • 16
    • 50949133899 scopus 로고    scopus 로고
    • Vorinostat synergistically potentiates MK-0457 lethality in chronic myelogenous leukemia cells sensitive and resistant to imatinib mesylate
    • Dai Y, Chen S, Venditti CA, Pei XY, Nguyen TK, Dent P, et al. Vorinostat synergistically potentiates MK-0457 lethality in chronic myelogenous leukemia cells sensitive and resistant to imatinib mesylate. Blood 2008;112:793-804.
    • (2008) Blood , vol.112 , pp. 793-804
    • Dai, Y.1    Chen, S.2    Venditti, C.A.3    Pei, X.Y.4    Nguyen, T.K.5    Dent, P.6
  • 17
    • 58149144779 scopus 로고    scopus 로고
    • Cotreatment with vorinostat enhances activity of MK-0457 (VX-680) against acute and chronic myelogenous leukemia cells
    • Fiskus W, Wang Y, Joshi R, Rao R, Yang Y, Chen J, et al. Cotreatment with vorinostat enhances activity of MK-0457 (VX-680) against acute and chronic myelogenous leukemia cells. Clin Cancer Res 2008;14: 6106-15.
    • (2008) Clin Cancer Res , vol.14 , pp. 6106-6115
    • Fiskus, W.1    Wang, Y.2    Joshi, R.3    Rao, R.4    Yang, Y.5    Chen, J.6
  • 18
    • 77956956848 scopus 로고    scopus 로고
    • Efficacy of MK-0457 and in combination with vorinostat against Philadelphia chromosome positive acute lymphoblastic leukemia cells
    • Okabe S, Tauchi T, Ohyashiki K. Efficacy of MK-0457 and in combination with vorinostat against Philadelphia chromosome positive acute lymphoblastic leukemia cells. Ann Hematol 2010;89:1081-7.
    • (2010) Ann Hematol , vol.89 , pp. 1081-1087
    • Okabe, S.1    Tauchi, T.2    Ohyashiki, K.3
  • 19
    • 33646227904 scopus 로고    scopus 로고
    • Synergistic interactions between DMAG and mitogen-activated protein kinase kinase 1/2 inhibitors in Bcr/abl +leukemia cells sensitive and resistant to imatinib mesylate
    • Nguyen TK, Rahmani M, Gao N, Kramer L, Corbin AS, Druker BJ, et al. Synergistic interactions between DMAG and mitogen-activated protein kinase kinase 1/2 inhibitors in Bcr/abl +leukemia cells sensitive and resistant to imatinib mesylate. Clin Cancer Res 2006;12:2239-47.
    • (2006) Clin Cancer Res , vol.12 , pp. 2239-2247
    • Nguyen, T.K.1    Rahmani, M.2    Gao, N.3    Kramer, L.4    Corbin, A.S.5    Druker, B.J.6
  • 20
    • 34247372619 scopus 로고    scopus 로고
    • + human leukemia cells to the dual Abl/Src inhibitor BMS-354/825
    • DOI 10.1182/blood-2006-09-045039
    • Nguyen TK, Rahmani M, Harada H, Dent P, Grant S. MEK1/2 inhibitors sensitize Bcr/Abl+ human leukemia cells to the dual Abl/Src inhibitor BMS-354/825. Blood 2007;109:4006-15. (Pubitemid 46641754)
    • (2007) Blood , vol.109 , Issue.9 , pp. 4006-4015
    • Nguyen, T.K.1    Rahmani, M.2    Harada, H.3    Dent, P.4    Grant, S.5
  • 21
    • 33746238104 scopus 로고    scopus 로고
    • The three-substituted indolinone cyclin-dependent kinase 2 inhibitor 3-[1-(3H-imidazol-4- yl)-meth-(Z)-ylidene]-5-methoxy-1,3-dihydro-indol-2-on e (SU9516) kills human leukemia cells via down-regulation of Mcl-1 through a transcriptional mechanism
    • Gao N, Kramer L, Rahmani M, Dent P, Grant S. The three-substituted indolinone cyclin-dependent kinase 2 inhibitor 3-[1-(3H-imidazol-4- yl)-meth-(Z)-ylidene]-5-methoxy-1,3-dihydro-indol-2-on e (SU9516) kills human leukemia cells via down-regulation of Mcl-1 through a transcriptional mechanism. Mol Pharmacol 2006;70:645-55.
    • (2006) Mol Pharmacol , vol.70 , pp. 645-655
    • Gao, N.1    Kramer, L.2    Rahmani, M.3    Dent, P.4    Grant, S.5
  • 22
    • 34247372619 scopus 로고    scopus 로고
    • + human leukemia cells to the dual Abl/Src inhibitor BMS-354/825
    • DOI 10.1182/blood-2006-09-045039
    • Nguyen TK, Rahmani M, Harada H, Dent P, Grant S. MEK1/2 inhibitors sensitize Bcr/Abl+ human leukemia cells to the dual Abl/Src inhibitor BMS-354/825. Blood 2007;109:4006-15. (Pubitemid 46641754)
    • (2007) Blood , vol.109 , Issue.9 , pp. 4006-4015
    • Nguyen, T.K.1    Rahmani, M.2    Harada, H.3    Dent, P.4    Grant, S.5
  • 24
    • 0038079767 scopus 로고    scopus 로고
    • The histone deacetylase inhibitor MS-275 promotes differentiation or apoptosis in human leukemia cells through a process regulated by generation of reactive oxygen species and induction of p21CIP1/WAF1 1
    • Rosato RR, Almenara JA, Grant S. The histone deacetylase inhibitor MS-275 promotes differentiation or apoptosis in human leukemia cells through a process regulated by generation of reactive oxygen species and induction of p21CIP1/WAF1 1. Cancer Res 2003;63:3637-45.
    • (2003) Cancer Res , vol.63 , pp. 3637-3645
    • Rosato, R.R.1    Almenara, J.A.2    Grant, S.3
  • 26
    • 79955992229 scopus 로고    scopus 로고
    • Philadelphia chromosome- positive acute lymphoblastic leukemia: Current treatment and future perspectives
    • Lee HJ, Thompson JE, Wang ES, Wetzler M. Philadelphia chromosome- positive acute lymphoblastic leukemia: current treatment and future perspectives. Cancer 2010.
    • (2010) Cancer
    • Lee, H.J.1    Thompson, J.E.2    Wang, E.S.3    Wetzler, M.4
  • 27
    • 34247470836 scopus 로고    scopus 로고
    • Second generation inhibitors of BCR-ABL for the treatment of imatinib-resistant chronic myeloid leukaemia
    • DOI 10.1038/nrc2126, PII NRC2126
    • Weisberg E, Manley PW, Cowan-Jacob SW, Hochhaus A, Griffin JD. Second generation inhibitors of BCR-ABL for the treatment of imatinib- resistant chronic myeloid leukaemia. Nat Rev Cancer 2007;7: 345-56. (Pubitemid 46652483)
    • (2007) Nature Reviews Cancer , vol.7 , Issue.5 , pp. 345-356
    • Weisberg, E.1    Manley, P.W.2    Cowan-Jacob, S.W.3    Hochhaus, A.4    Griffin, J.D.5
  • 28
    • 77952105211 scopus 로고    scopus 로고
    • Effective targeting of quiescent chronic myelogenous leukemia stem cells by histone deacetylase inhibitors in combination with imatinib mesylate
    • Zhang B, Strauss AC, Chu S, Li M, Ho Y, Shiang KD, et al. Effective targeting of quiescent chronic myelogenous leukemia stem cells by histone deacetylase inhibitors in combination with imatinib mesylate. Cancer Cell 2010;17:427-42.
    • (2010) Cancer Cell , vol.17 , pp. 427-442
    • Zhang, B.1    Strauss, A.C.2    Chu, S.3    Li, M.4    Ho, Y.5    Shiang, K.D.6
  • 30
    • 22844432021 scopus 로고    scopus 로고
    • Inhibiition of histone deacetylase 6 acetylates and disrupts the chaperone function of heat shock protein 90: A novel basis of antileukemia activity of histone deacetylase inhibitors
    • Bali P, Pranpat M, Bradner J, Balasis M, Fiskus W, Guo F, et al. Inhibiition of histone deacetylase 6 acetylates and disrupts the chaperone function of heat shock protein 90: a novel basis of antileukemia activity of histone deacetylase inhibitors. J Biol Chem 2005.
    • (2005) J Biol Chem
    • Bali, P.1    Pranpat, M.2    Bradner, J.3    Balasis, M.4    Fiskus, W.5    Guo, F.6
  • 31
    • 77956930519 scopus 로고    scopus 로고
    • A specific need for CRKL in p210BCR-ABL-induced transformation of mouse hematopoietic progenitors
    • Seo JH, Wood LJ, Agarwal A, O'Hare T, Elsea CR, Griswold IJ, et al. A specific need for CRKL in p210BCR-ABL-induced transformation of mouse hematopoietic progenitors. Cancer Res 2010;70:7325-35.
    • (2010) Cancer Res , vol.70 , pp. 7325-7335
    • Seo, J.H.1    Wood, L.J.2    Agarwal, A.3    O'Hare, T.4    Elsea, C.R.5    Griswold, I.J.6
  • 32
    • 0029810923 scopus 로고    scopus 로고
    • Constitutive activation of STAT5 by the BCR-ABL oncogene in chronic myelogenous leukemia
    • Shuai K, Halpern J, ten HJ, Rao X, Sawyers CL. Constitutive activation of STAT5 by the BCR-ABL oncogene in chronic myelogenous leukemia. Oncogene 1996;13:247-54.
    • (1996) Oncogene , vol.13 , pp. 247-254
    • Shuai, K.1    Halpern, J.2    Ten, H.J.3    Rao, X.4    Sawyers, C.L.5
  • 35
    • 47549107231 scopus 로고    scopus 로고
    • Pharmacological inhibition of c-Abl compromises genetic stability and DNA repair in Bcr-Abl-negative cells
    • DOI 10.1038/onc.2008.68, PII ONC200868
    • Fanta S, Sonnenberg M, Skorta I, Duyster J, Miething C, Aulitzky WE, et al. Pharmacological inhibition of c-Abl compromises genetic stability and DNA repair in Bcr-Abl-negative cells. Oncogene 2008; 27:4380-4. (Pubitemid 352009999)
    • (2008) Oncogene , vol.27 , Issue.31 , pp. 4380-4384
    • Fanta, S.1    Sonnenberg, M.2    Skorta, I.3    Duyster, J.4    Miething, C.5    Aulitzky, W.E.6    Van Der, K.H.7
  • 37
    • 55749113687 scopus 로고    scopus 로고
    • Role of histone deacetylase inhibitor-induced reactive oxygen species and DNA damage in LAQ-824/fludarabine antileukemic interactions
    • Rosato RR, Almenara JA, Maggio SC, Coe S, Atadja P, Dent P, et al. Role of histone deacetylase inhibitor-induced reactive oxygen species and DNA damage in LAQ-824/fludarabine antileukemic interactions. Mol Cancer Ther 2008;7:3285-97.
    • (2008) Mol Cancer Ther , vol.7 , pp. 3285-3297
    • Rosato, R.R.1    Almenara, J.A.2    Maggio, S.C.3    Coe, S.4    Atadja, P.5    Dent, P.6
  • 38
    • 77957091318 scopus 로고    scopus 로고
    • Histone deacetylase inhibitor induces DNA damage, which normal but not transformed cells can repair
    • Lee JH, Choy ML, Ngo L, Foster SS, Marks PA. Histone deacetylase inhibitor induces DNA damage, which normal but not transformed cells can repair. Proc Natl Acad Sci U S A 2010;107: 14639-44.
    • (2010) Proc Natl Acad Sci U S A , vol.107 , pp. 14639-14644
    • Lee, J.H.1    Choy, M.L.2    Ngo, L.3    Foster, S.S.4    Marks, P.A.5
  • 39
    • 66249093516 scopus 로고    scopus 로고
    • AZD1152 rapidly and negatively affects the growth and survival of human acute myeloid leukemia cells in vitro and in vivo
    • Oke A, Pearce D, Wilkinson RW, Crafter C, Odedra R, Cavenagh J, et al. AZD1152 rapidly and negatively affects the growth and survival of human acute myeloid leukemia cells in vitro and in vivo. Cancer Res 2009;69:4150-8.
    • (2009) Cancer Res , vol.69 , pp. 4150-4158
    • Oke, A.1    Pearce, D.2    Wilkinson, R.W.3    Crafter, C.4    Odedra, R.5    Cavenagh, J.6
  • 40
    • 77950949478 scopus 로고    scopus 로고
    • Aurora kinase inhibitors: Novel small molecules with promising activity in acute myeloid and Philadelphia-positive leukemias
    • Moore AS, Blagg J, Linardopoulos S, Pearson AD. Aurora kinase inhibitors: novel small molecules with promising activity in acute myeloid and Philadelphia-positive leukemias. Leukemia 2010;24: 671-8.
    • (2010) Leukemia , vol.24 , pp. 671-678
    • Moore, A.S.1    Blagg, J.2    Linardopoulos, S.3    Pearson, A.D.4
  • 41
    • 33744486584 scopus 로고    scopus 로고
    • Dasatinib (BMS-354825) targets an earlier progenitor population than imatinib in primary CML but does not eliminate the quiescent fraction
    • DOI 10.1182/blood-2005-07-2947
    • Copland M, Hamilton A, Elrick LJ, Baird JW, Allan EK, Jordanides N, et al. Dasatinib (BMS-354825) targets an earlier progenitor population than imatinib in primary CML but does not eliminate the quiescent fraction. Blood 2006;107:4532-9. (Pubitemid 43801382)
    • (2006) Blood , vol.107 , Issue.11 , pp. 4532-4539
    • Copland, M.1    Hamilton, A.2    Elrick, L.J.3    Baird, J.W.4    Allan, E.K.5    Jordanides, N.6    Barow, M.7    Mountford, J.C.8    Holyoake, T.L.9


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