메뉴 건너뛰기




Volumn 79, Issue 5, 2010, Pages 688-697

Targets and effectors of the cellular response to aurora kinase inhibitor MK-0457 (VX-680) in imatinib sensitive and resistant chronic myelogenous leukemia

Author keywords

Inhibitor; Kinase; Leukemia; Resistance; Signal transduction

Indexed keywords

AURORA KINASE; AURORA KINASE INHIBITOR; BCR ABL PROTEIN; CYCLOPROPANECARBOXYLIC ACID [4 [4 (4 METHYL 1 PIPERAZINYL) 6 (5 METHYL 2H PYRAZOL 3 YLAMINO) 2 PYRIMIDINYLTHIO]PHENYL]AMIDE; DASATINIB; IMATINIB; PROTEIN KINASE LYN; PROTEIN MDM2; PROTEIN P53; PROTEIN SERINE THREONINE KINASE; UNCLASSIFIED DRUG;

EID: 71849102704     PISSN: 00062952     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bcp.2009.10.009     Document Type: Article
Times cited : (28)

References (39)
  • 1
    • 58149398623 scopus 로고    scopus 로고
    • Translation of the Philadelphia chromosome into therapy for CML
    • Druker B.J. Translation of the Philadelphia chromosome into therapy for CML. Blood 112 December 15(13) (2008) 4808-4817
    • (2008) Blood , vol.112 , Issue.December 1513 , pp. 4808-4817
    • Druker, B.J.1
  • 2
    • 61849163272 scopus 로고    scopus 로고
    • Molecular biology of bcr-abl1-positive chronic myeloid leukemia
    • Epub 2008 Sep 30
    • Quintás-Cardama A., and Cortes J. Molecular biology of bcr-abl1-positive chronic myeloid leukemia. Blood 113 February 19(8) (2009) 1619-1630 Epub 2008 Sep 30
    • (2009) Blood , vol.113 , Issue.February 198 , pp. 1619-1630
    • Quintás-Cardama, A.1    Cortes, J.2
  • 3
    • 45749083360 scopus 로고    scopus 로고
    • First-line management of CML: a state of the art review
    • Hochhaus A. First-line management of CML: a state of the art review. J Natl Compr Canc Netw 6 March (Suppl. 2) (2008) S1-S10
    • (2008) J Natl Compr Canc Netw , vol.6 , Issue.March SUPPL. 2
    • Hochhaus, A.1
  • 4
    • 45749084492 scopus 로고    scopus 로고
    • New Bcr-Abl inhibitors in chronic myeloid leukemia: keeping resistance in check
    • O'Hare T., Eide C.A., and Deininger M.W. New Bcr-Abl inhibitors in chronic myeloid leukemia: keeping resistance in check. Expert Opin Investig Drugs 17 June (6) (2008) 865-878
    • (2008) Expert Opin Investig Drugs , vol.17 , Issue.June 6 , pp. 865-878
    • O'Hare, T.1    Eide, C.A.2    Deininger, M.W.3
  • 5
    • 34848929062 scopus 로고    scopus 로고
    • Flying under the radar: the new wave of BCR-ABL inhibitors
    • Quintás-Cardama A., Kantarjian H., and Cortes J. Flying under the radar: the new wave of BCR-ABL inhibitors. Nat Rev Drug Discov 6 October (10) (2007) 834-848
    • (2007) Nat Rev Drug Discov , vol.6 , Issue.October 10 , pp. 834-848
    • Quintás-Cardama, A.1    Kantarjian, H.2    Cortes, J.3
  • 6
    • 51649120694 scopus 로고    scopus 로고
    • Therapeutic options against BCR-ABL1 T315I-positive chronic myelogenous leukemia
    • Quintás-Cardama A., and Cortes J. Therapeutic options against BCR-ABL1 T315I-positive chronic myelogenous leukemia. Clin Cancer Res 14 July 15 (14) (2008) 4392-4399
    • (2008) Clin Cancer Res , vol.14 , Issue.July 15 14 , pp. 4392-4399
    • Quintás-Cardama, A.1    Cortes, J.2
  • 7
    • 34848911943 scopus 로고    scopus 로고
    • Sequential ABL kinase inhibitor therapy selects for compound drug-resistant BCR-ABL mutations with altered oncogenic potency
    • Sep
    • Shah N.P., Skaggs B.J., Branford S., Hughes T.P., Nicoll J.M., Paquette R.L., et al. Sequential ABL kinase inhibitor therapy selects for compound drug-resistant BCR-ABL mutations with altered oncogenic potency. J Clin Invest 117 9 (2007) 2562-2569 Sep
    • (2007) J Clin Invest , vol.117 , Issue.9 , pp. 2562-2569
    • Shah, N.P.1    Skaggs, B.J.2    Branford, S.3    Hughes, T.P.4    Nicoll, J.M.5    Paquette, R.L.6
  • 8
    • 3142676436 scopus 로고    scopus 로고
    • Overriding imatinib resistance with a novel ABL kinase inhibitor
    • Shah N.P., Tran C., Lee F.Y., Chen P., Norris D., and Sawyers C.L. Overriding imatinib resistance with a novel ABL kinase inhibitor. Science 305 July 16 (5682) (2004) 399-401
    • (2004) Science , vol.305 , Issue.July 16 5682 , pp. 399-401
    • Shah, N.P.1    Tran, C.2    Lee, F.Y.3    Chen, P.4    Norris, D.5    Sawyers, C.L.6
  • 9
    • 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 M.A., Shah N.P., Chao L.H., Seeliger M., Milanov Z.V., Biggs III W.H., 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 January 15 (2) (2006) 1007-10014
    • (2006) Cancer Res , vol.66 , Issue.January 15 2 , pp. 1007-10014
    • Young, M.A.1    Shah, N.P.2    Chao, L.H.3    Seeliger, M.4    Milanov, Z.V.5    Biggs III, W.H.6
  • 10
    • 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 F.J., Cortes J., Jones D., Bergstrom D., Kantarjian H., and Freedman S.J. 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 January 15 (2) (2007) 500-502
    • (2007) Blood , vol.109 , Issue.January 15 2 , pp. 500-502
    • Giles, F.J.1    Cortes, J.2    Jones, D.3    Bergstrom, D.4    Kantarjian, H.5    Freedman, S.J.6
  • 11
    • 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 G.M., Charlton P.A., Golec J.M., and Pollard J.R. 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 June 28 (2) (2007) 323-329
    • (2007) Cancer Lett , vol.251 , Issue.June 28 2 , pp. 323-329
    • Cheetham, G.M.1    Charlton, P.A.2    Golec, J.M.3    Pollard, J.R.4
  • 12
    • 43549114588 scopus 로고    scopus 로고
    • Activity of a novel aurora kinase inhibitor against the T315I mutant form of BCR-ABL: in vitro and in vivo studies
    • Akahane D., Tauchi T., Okabe S., Nunoda K., and Ohyashiki K. Activity of a novel aurora kinase inhibitor against the T315I mutant form of BCR-ABL: in vitro and in vivo studies. Cancer Sci 99 June (6) (2008) 1251-1257
    • (2008) Cancer Sci , vol.99 , Issue.June 6 , pp. 1251-1257
    • Akahane, D.1    Tauchi, T.2    Okabe, S.3    Nunoda, K.4    Ohyashiki, K.5
  • 13
    • 60849121700 scopus 로고    scopus 로고
    • Mechanism of MK-0457 efficacy against BCR-ABL positive leukemia cells
    • Okabe S., Tauchi T., Ohyashiki J.H., and Ohyashiki K. Mechanism of MK-0457 efficacy against BCR-ABL positive leukemia cells. Biochem Biophys Res Commun 380 March 20 (4) (2009) 775-779
    • (2009) Biochem Biophys Res Commun , vol.380 , Issue.March 20 4 , pp. 775-779
    • Okabe, S.1    Tauchi, T.2    Ohyashiki, J.H.3    Ohyashiki, K.4
  • 14
    • 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 C.A., Pei X.Y., Nguyen T.K., Dent P., et al. Vorinostat synergistically potentiates MK-0457 lethality in chronic myelogenous leukemia cells sensitive and resistant to imatinib mesylate. Blood 112 August 1 (3) (2008) 793-804
    • (2008) Blood , vol.112 , Issue.August 1 3 , pp. 793-804
    • Dai, Y.1    Chen, S.2    Venditti, C.A.3    Pei, X.Y.4    Nguyen, T.K.5    Dent, P.6
  • 16
    • 2342639645 scopus 로고    scopus 로고
    • VX-680, a potent and selective small-molecule inhibitor of the aurora kinases, suppresses tumor growth in vivo
    • Harrington E.A., Bebbington D., Moore J., Rasmussen R.K., Ajose-Adeogun A.O., Nakayama T., et al. VX-680, a potent and selective small-molecule inhibitor of the aurora kinases, suppresses tumor growth in vivo. Nat Med 10 March (3) (2004) 262-267
    • (2004) Nat Med , vol.10 , Issue.March 3 , pp. 262-267
    • Harrington, E.A.1    Bebbington, D.2    Moore, J.3    Rasmussen, R.K.4    Ajose-Adeogun, A.O.5    Nakayama, T.6
  • 17
    • 0037438640 scopus 로고    scopus 로고
    • BCR-ABL independence and LYN kinase overexpression in chronic myelogenous leukemia cells selected for resistance to STI571
    • Donato N.J., Wu J.Y., Stapley J., Gallick G., Lin H., Arlinghaus R., et al. BCR-ABL independence and LYN kinase overexpression in chronic myelogenous leukemia cells selected for resistance to STI571. Blood 101 January 15 (2) (2003) 690-698
    • (2003) Blood , vol.101 , Issue.January 15 2 , pp. 690-698
    • Donato, N.J.1    Wu, J.Y.2    Stapley, J.3    Gallick, G.4    Lin, H.5    Arlinghaus, R.6
  • 18
    • 34147155353 scopus 로고    scopus 로고
    • Activation of a novel Bcr/Abl destruction pathway by WP1130 induces apoptosis of chronic myelogenous leukemia cells
    • Bartholomeusz G.A., Talpaz M., Kapuria V., Kong L.Y., Wang S., Estrov Z., et al. Activation of a novel Bcr/Abl destruction pathway by WP1130 induces apoptosis of chronic myelogenous leukemia cells. Blood 109 April 15 (8) (2007) 3470-3478
    • (2007) Blood , vol.109 , Issue.April 15 8 , pp. 3470-3478
    • Bartholomeusz, G.A.1    Talpaz, M.2    Kapuria, V.3    Kong, L.Y.4    Wang, S.5    Estrov, Z.6
  • 19
    • 9144234689 scopus 로고    scopus 로고
    • Imatinib mesylate resistance through BCR-ABL independence in chronic myelogenous leukemia
    • Donato N.J., Wu J.Y., Stapley J., Lin H., Arlinghaus R., Aggarwal B.B., et al. Imatinib mesylate resistance through BCR-ABL independence in chronic myelogenous leukemia. Cancer Res 64 January 15 (2) (2004) 672-677
    • (2004) Cancer Res , vol.64 , Issue.January 15 2 , pp. 672-677
    • Donato, N.J.1    Wu, J.Y.2    Stapley, J.3    Lin, H.4    Arlinghaus, R.5    Aggarwal, B.B.6
  • 20
    • 0030008056 scopus 로고    scopus 로고
    • Role of granulocyte-macrophage colony-stimulating factor in Philadelphia (Ph1)-positive acute lymphoblastic leukemia: studies on two newly established Ph1-positive acute lymphoblastic leukemia cell lines (Z-119 and Z-181)
    • Estrov Z., Talpaz M., Zipf T.F., Kantarjian H.M., Ku S., Ouspenskaia M.V., et al. Role of granulocyte-macrophage colony-stimulating factor in Philadelphia (Ph1)-positive acute lymphoblastic leukemia: studies on two newly established Ph1-positive acute lymphoblastic leukemia cell lines (Z-119 and Z-181). J Cell Physiol 166 March (3) (1996) 618-630
    • (1996) J Cell Physiol , vol.166 , Issue.March 3 , pp. 618-630
    • Estrov, Z.1    Talpaz, M.2    Zipf, T.F.3    Kantarjian, H.M.4    Ku, S.5    Ouspenskaia, M.V.6
  • 21
    • 46849114097 scopus 로고    scopus 로고
    • Association between imatinib-resistant BCR-ABL mutation-negative leukemia and persistent activation of LYN kinase
    • Wu J., Meng F., Kong L.Y., Peng Z., Ying Y., Bornmann W.G., et al. Association between imatinib-resistant BCR-ABL mutation-negative leukemia and persistent activation of LYN kinase. J Natl Cancer Inst 100 July 2 (13) (2008) 926-939
    • (2008) J Natl Cancer Inst , vol.100 , Issue.July 2 13 , pp. 926-939
    • Wu, J.1    Meng, F.2    Kong, L.Y.3    Peng, Z.4    Ying, Y.5    Bornmann, W.G.6
  • 22
    • 13244259472 scopus 로고    scopus 로고
    • Regulation of ultraviolet B-induced phosphorylation of histone H3 at serine 10 by Fyn kinase
    • He Z., Cho Y.Y., Ma W.Y., Choi H.S., Bode A.M., and Dong Z. Regulation of ultraviolet B-induced phosphorylation of histone H3 at serine 10 by Fyn kinase. J Biol Chem 280 January 28 (4) (2005) 2446-2454
    • (2005) J Biol Chem , vol.280 , Issue.January 28 4 , pp. 2446-2454
    • He, Z.1    Cho, Y.Y.2    Ma, W.Y.3    Choi, H.S.4    Bode, A.M.5    Dong, Z.6
  • 23
    • 53449095193 scopus 로고    scopus 로고
    • Concomitant inhibition of Mdm2-p53 interaction and aurora kinases activates the p53-dependent postmitotic checkpoints and synergistically induces p53-mediated mitochondrial apoptosis along with reduced endoreduplication in acute myelogenous leukemia
    • Kojima K., Konopleva M., Tsao T., Nakakuma H., and Andreeff M. Concomitant inhibition of Mdm2-p53 interaction and aurora kinases activates the p53-dependent postmitotic checkpoints and synergistically induces p53-mediated mitochondrial apoptosis along with reduced endoreduplication in acute myelogenous leukemia. Blood 112 October 1 (7) (2008) 2886-2895
    • (2008) Blood , vol.112 , Issue.October 1 7 , pp. 2886-2895
    • Kojima, K.1    Konopleva, M.2    Tsao, T.3    Nakakuma, H.4    Andreeff, M.5
  • 24
    • 33747877023 scopus 로고    scopus 로고
    • The aurora kinase inhibitor VX-680 induces endoreduplication and apoptosis preferentially in cells with compromised p53-dependent postmitotic checkpoint function
    • Gizatullin F., Yao Y., Kung V., Harding M.W., Loda M., and Shapiro G.I. The aurora kinase inhibitor VX-680 induces endoreduplication and apoptosis preferentially in cells with compromised p53-dependent postmitotic checkpoint function. Cancer Res 66 August 1 (15) (2006) 7668-7677
    • (2006) Cancer Res , vol.66 , Issue.August 1 15 , pp. 7668-7677
    • Gizatullin, F.1    Yao, Y.2    Kung, V.3    Harding, M.W.4    Loda, M.5    Shapiro, G.I.6
  • 25
    • 63049135651 scopus 로고    scopus 로고
    • Short and long-term tumor cell responses to aurora kinase inhibitors
    • Dreier M.R., Grabovich A.Z., Katusin J.D., and Taylor W.R. Short and long-term tumor cell responses to aurora kinase inhibitors. Exp Cell Res 315 April 15 (7) (2009) 1085-1099
    • (2009) Exp Cell Res , vol.315 , Issue.April 15 7 , pp. 1085-1099
    • Dreier, M.R.1    Grabovich, A.Z.2    Katusin, J.D.3    Taylor, W.R.4
  • 26
    • 65249100143 scopus 로고    scopus 로고
    • Small-molecule inhibitors of the MDM2-p53 protein-protein interaction to reactivate p53 function: a novel approach for cancer therapy
    • Shangary S., and Wang S. Small-molecule inhibitors of the MDM2-p53 protein-protein interaction to reactivate p53 function: a novel approach for cancer therapy. Annu Rev Pharmacol Toxicol 49 (2009) 223-241
    • (2009) Annu Rev Pharmacol Toxicol , vol.49 , pp. 223-241
    • Shangary, S.1    Wang, S.2
  • 27
    • 46449088111 scopus 로고    scopus 로고
    • Metabolism and disposition of dasatinib after oral administration to humans
    • Christopher L.J., Cui D., Wu C., Luo R., Manning J.A., Bonacorsi S.J., et al. Metabolism and disposition of dasatinib after oral administration to humans. Drug Metab Dispos 36 July (7) (2008) 1357-1364
    • (2008) Drug Metab Dispos , vol.36 , Issue.July 7 , pp. 1357-1364
    • Christopher, L.J.1    Cui, D.2    Wu, C.3    Luo, R.4    Manning, J.A.5    Bonacorsi, S.J.6
  • 28
    • 48749099909 scopus 로고    scopus 로고
    • Centrosome aberrations and G1 phase arrest after in vitro and in vivo treatment with the SRC/ABL inhibitor dasatinib
    • Fabarius A., Giehl M., Rebacz B., Krämer A., Frank O., Haferlach C., et al. Centrosome aberrations and G1 phase arrest after in vitro and in vivo treatment with the SRC/ABL inhibitor dasatinib. Haematologica 93 August (8) (2008) 1145-1154
    • (2008) Haematologica , vol.93 , Issue.August 8 , pp. 1145-1154
    • Fabarius, A.1    Giehl, M.2    Rebacz, B.3    Krämer, A.4    Frank, O.5    Haferlach, C.6
  • 29
    • 33646250535 scopus 로고    scopus 로고
    • Pathobiology of lymphoid and myeloid blast crisis and management issues
    • Ilaria Jr. R.L. Pathobiology of lymphoid and myeloid blast crisis and management issues. Hematol Am Soc Hematol Educ Program (2005) 188-194
    • (2005) Hematol Am Soc Hematol Educ Program , pp. 188-194
    • Ilaria Jr., R.L.1
  • 31
    • 55349124289 scopus 로고    scopus 로고
    • Aurora kinase A inhibition leads to p73-dependent apoptosis in p53-deficient cancer cells
    • Dar A.A., Belkhiri A., Ecsedy J., Zaika A., and El-Rifai W. Aurora kinase A inhibition leads to p73-dependent apoptosis in p53-deficient cancer cells. Cancer Res 68 November 1 (21) (2008) 8998-9004
    • (2008) Cancer Res , vol.68 , Issue.November 1 21 , pp. 8998-9004
    • Dar, A.A.1    Belkhiri, A.2    Ecsedy, J.3    Zaika, A.4    El-Rifai, W.5
  • 32
    • 47549118837 scopus 로고    scopus 로고
    • Aurora-A overexpression induces cellular senescence in mammary gland hyperplastic tumors developed in p53-deficient mice
    • Zhang D., Shimizu T., Araki N., Hirota T., Yoshie M., Ogawa K., et al. Aurora-A overexpression induces cellular senescence in mammary gland hyperplastic tumors developed in p53-deficient mice. Oncogene 27 July 17 (31) (2008) 4305-4314
    • (2008) Oncogene , vol.27 , Issue.July 17 31 , pp. 4305-4314
    • Zhang, D.1    Shimizu, T.2    Araki, N.3    Hirota, T.4    Yoshie, M.5    Ogawa, K.6
  • 33
    • 10644227569 scopus 로고    scopus 로고
    • Aurora-A abrogation of p53 DNA binding and transactivation activity by phosphorylation of serine 215
    • Liu Q., Kaneko S., Yang L., Feldman R.I., Nicosia S.V., Chen J., et al. Aurora-A abrogation of p53 DNA binding and transactivation activity by phosphorylation of serine 215. J Biol Chem 279 December 10 (50) (2004) 52175-52182
    • (2004) J Biol Chem , vol.279 , Issue.December 10 50 , pp. 52175-52182
    • Liu, Q.1    Kaneko, S.2    Yang, L.3    Feldman, R.I.4    Nicosia, S.V.5    Chen, J.6
  • 34
    • 9144251019 scopus 로고    scopus 로고
    • Phosphorylation by aurora kinase A induces Mdm2-mediated destabilization and inhibition of p53
    • Katayama H., Sasai K., Kawai H., Yuan Z.M., Bondaruk J., Suzuki F., et al. Phosphorylation by aurora kinase A induces Mdm2-mediated destabilization and inhibition of p53. Nat Genet 36 January (1) (2004) 55-62
    • (2004) Nat Genet , vol.36 , Issue.January 1 , pp. 55-62
    • Katayama, H.1    Sasai, K.2    Kawai, H.3    Yuan, Z.M.4    Bondaruk, J.5    Suzuki, F.6
  • 35
    • 0027207728 scopus 로고
    • Genetic alterations in the p53 gene in the blast crisis of chronic myelogenous leukemia: analysis by polymerase chain reaction based techniques
    • Neubauer A., He M., Schmidt C.A., Huhn D., and Liu E.T. Genetic alterations in the p53 gene in the blast crisis of chronic myelogenous leukemia: analysis by polymerase chain reaction based techniques. Leukemia 7 April (4) (1993) 593-600
    • (1993) Leukemia , vol.7 , Issue.April 4 , pp. 593-600
    • Neubauer, A.1    He, M.2    Schmidt, C.A.3    Huhn, D.4    Liu, E.T.5
  • 36
    • 2542500611 scopus 로고    scopus 로고
    • The biology of CML blast crisis
    • Calabretta B., and Perrotti D. The biology of CML blast crisis. Blood 103 June 1 (11) (2004) 4010-4022
    • (2004) Blood , vol.103 , Issue.June 1 11 , pp. 4010-4022
    • Calabretta, B.1    Perrotti, D.2
  • 37
    • 57149098598 scopus 로고    scopus 로고
    • Evidence that resistance to nilotinib may be due to BCR-ABL, Pgp, or Src kinase overexpression
    • Mahon F.X., Hayette S., Lagarde V., Belloc F., Turcq B., Nicolini F., et al. Evidence that resistance to nilotinib may be due to BCR-ABL, Pgp, or Src kinase overexpression. Cancer Res 68 December 1 (23) (2008) 9809-9816
    • (2008) Cancer Res , vol.68 , Issue.December 1 23 , pp. 9809-9816
    • Mahon, F.X.1    Hayette, S.2    Lagarde, V.3    Belloc, F.4    Turcq, B.5    Nicolini, F.6
  • 38
    • 19944433530 scopus 로고    scopus 로고
    • Chemical proteomic analysis reveals alternative modes of action for pyrido[2,3-d]pyrimidine kinase inhibitors
    • Wissing J., Godl K., Brehmer D., Blencke S., Weber M., Habenberger P., et al. Chemical proteomic analysis reveals alternative modes of action for pyrido[2,3-d]pyrimidine kinase inhibitors. Mol Cell Proteomics 3 December (12) (2004) 1181-1193
    • (2004) Mol Cell Proteomics , vol.3 , Issue.December 12 , pp. 1181-1193
    • Wissing, J.1    Godl, K.2    Brehmer, D.3    Blencke, S.4    Weber, M.5    Habenberger, P.6
  • 39
    • 0034095603 scopus 로고    scopus 로고
    • The pyrido[2,3-d]pyrimidine derivative PD180970 inhibits p210Bcr-Abl tyrosine kinase and induces apoptosis of K562 leukemic cells
    • Dorsey J.F., Jove R., Kraker A.J., and Wu J. The pyrido[2,3-d]pyrimidine derivative PD180970 inhibits p210Bcr-Abl tyrosine kinase and induces apoptosis of K562 leukemic cells. Cancer Res 60 June 15 (12) (2000) 3127-3131
    • (2000) Cancer Res , vol.60 , Issue.June 15 12 , pp. 3127-3131
    • Dorsey, J.F.1    Jove, R.2    Kraker, A.J.3    Wu, J.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.