메뉴 건너뛰기




Volumn 8, Issue 8, 2013, Pages

The Conformational Control Inhibitor of Tyrosine Kinases DCC-2036 Is Effective for Imatinib-Resistant Cells Expressing T674I FIP1L1-PDGFRα

Author keywords

[No Author keywords available]

Indexed keywords

1,4 DIAMINO 1,4 BIS(2 AMINOPHENYLTHIO) 2,3 DICYANOBUTADIENE; 2 MORPHOLINO 8 PHENYLCHROMONE; ALLOGRAFT INFLAMMATORY FACTOR 1; BIM PROTEIN; CASPASE 3; CYTOCHROME C; IMATINIB; MITOGEN ACTIVATED PROTEIN KINASE 1; MITOGEN ACTIVATED PROTEIN KINASE 3; NICOTINAMIDE ADENINE DINUCLEOTIDE ADENOSINE DIPHOSPHATE RIBOSYLTRANSFERASE; PLATELET DERIVED GROWTH FACTOR ALPHA RECEPTOR; PROTEIN BAX; PROTEIN KINASE B; PROTEIN MCL 1; REBASTINIB; STAT3 PROTEIN; SURVIVIN; X LINKED INHIBITOR OF APOPTOSIS;

EID: 84883248427     PISSN: None     EISSN: 19326203     Source Type: Journal    
DOI: 10.1371/journal.pone.0073059     Document Type: Article
Times cited : (10)

References (38)
  • 1
    • 0016430025 scopus 로고
    • The hypereosinophilic syndrome: analysis of fourteen cases with review of the literature
    • Chusid MJ, Dale DC, West BC, Wolff SM, (1975) The hypereosinophilic syndrome: analysis of fourteen cases with review of the literature. Medicine (Baltimore) 54: 1-27.
    • (1975) Medicine (Baltimore) , vol.54 , pp. 1-27
    • Chusid, M.J.1    Dale, D.C.2    West, B.C.3    Wolff, S.M.4
  • 2
    • 58949090059 scopus 로고    scopus 로고
    • Alemtuzumab therapy for hypereosinophilic syndrome and chronic eosinophilic leukemia
    • Verstovsek S, Tefferi A, Kantarjian H, Manshouri T, Luthra R, et al. (2009) Alemtuzumab therapy for hypereosinophilic syndrome and chronic eosinophilic leukemia. Clin Cancer Res 15: 368-373.
    • (2009) Clin Cancer Res , vol.15 , pp. 368-373
    • Verstovsek, S.1    Tefferi, A.2    Kantarjian, H.3    Manshouri, T.4    Luthra, R.5
  • 3
    • 70349256226 scopus 로고    scopus 로고
    • The 2008 revision of the World Health Organization (WHO) classification of myeloid neoplasms and acute leukemia: rationale and important changes
    • Vardiman JW, Thiele J, Arber DA, Brunning RD, Borowitz MJ, et al. (2009) The 2008 revision of the World Health Organization (WHO) classification of myeloid neoplasms and acute leukemia: rationale and important changes. Blood 114: 937-951.
    • (2009) Blood , vol.114 , pp. 937-951
    • Vardiman, J.W.1    Thiele, J.2    Arber, D.A.3    Brunning, R.D.4    Borowitz, M.J.5
  • 4
    • 77952314695 scopus 로고    scopus 로고
    • Screening for diverse PDGFRA or PDGFRB fusion genes is facilitated by generic quantitative reverse transcriptase polymerase chain reaction analysis
    • Erben P, Gosenca D, Muller MC, Reinhard J, Score J, et al. (2010) Screening for diverse PDGFRA or PDGFRB fusion genes is facilitated by generic quantitative reverse transcriptase polymerase chain reaction analysis. Haematologica 95: 738-744.
    • (2010) Haematologica , vol.95 , pp. 738-744
    • Erben, P.1    Gosenca, D.2    Muller, M.C.3    Reinhard, J.4    Score, J.5
  • 5
    • 34248569784 scopus 로고    scopus 로고
    • Molecular mechanisms underlying FIP1L1-PDGFRA-mediated myeloproliferation
    • Buitenhuis M, Verhagen LP, Cools J, Coffer PJ, (2007) Molecular mechanisms underlying FIP1L1-PDGFRA-mediated myeloproliferation. Cancer Res 67: 3759-3766.
    • (2007) Cancer Res , vol.67 , pp. 3759-3766
    • Buitenhuis, M.1    Verhagen, L.P.2    Cools, J.3    Coffer, P.J.4
  • 6
    • 65549103881 scopus 로고    scopus 로고
    • FIP1L1-PDGFRalpha imposes eosinophil lineage commitment on hematopoietic stem/progenitor cells
    • Fukushima K, Matsumura I, Ezoe S, Tokunaga M, Yasumi M, et al. (2009) FIP1L1-PDGFRalpha imposes eosinophil lineage commitment on hematopoietic stem/progenitor cells. J Biol Chem 284: 7719-7732.
    • (2009) J Biol Chem , vol.284 , pp. 7719-7732
    • Fukushima, K.1    Matsumura, I.2    Ezoe, S.3    Tokunaga, M.4    Yasumi, M.5
  • 7
    • 77749288978 scopus 로고    scopus 로고
    • Mechanisms of resistance to tyrosine kinase inhibitors in chronic myeloid leukemia and recent therapeutic strategies to overcome resistance
    • Bixby D, Talpaz M (2009) Mechanisms of resistance to tyrosine kinase inhibitors in chronic myeloid leukemia and recent therapeutic strategies to overcome resistance. Hematology Am Soc Hematol Educ Program: 461-476.
    • (2009) Hematology Am Soc Hematol Educ Program , pp. 461-476
    • Bixby, D.1    Talpaz, M.2
  • 8
    • 84856759425 scopus 로고    scopus 로고
    • Limited clinical activity of nilotinib and sorafenib in FIP1L1-PDGFRA positive chronic eosinophilic leukemia with imatinib-resistant T674I mutation
    • Metzgeroth G, Erben P, Martin H, Mousset S, Teichmann M, et al. (2012) Limited clinical activity of nilotinib and sorafenib in FIP1L1-PDGFRA positive chronic eosinophilic leukemia with imatinib-resistant T674I mutation. Leukemia 26: 162-164.
    • (2012) Leukemia , vol.26 , pp. 162-164
    • Metzgeroth, G.1    Erben, P.2    Martin, H.3    Mousset, S.4    Teichmann, M.5
  • 9
    • 79955485779 scopus 로고    scopus 로고
    • The ABL switch control inhibitor DCC-2036 is active against the chronic myeloid leukemia mutant BCR-ABLT315I and exhibits a narrow resistance profile
    • Eide CA, Adrian LT, Tyner JW, Mac Partlin M, Anderson DJ, et al. (2011) The ABL switch control inhibitor DCC-2036 is active against the chronic myeloid leukemia mutant BCR-ABLT315I and exhibits a narrow resistance profile. Cancer Res 71: 3189-3195.
    • (2011) Cancer Res , vol.71 , pp. 3189-3195
    • Eide, C.A.1    Adrian, L.T.2    Tyner, J.W.3    Mac Partlin, M.4    Anderson, D.J.5
  • 10
    • 79953765304 scopus 로고    scopus 로고
    • Conformational control inhibition of the BCR-ABL1 tyrosine kinase, including the gatekeeper T315I mutant, by the switch-control inhibitor DCC-2036
    • Chan WW, Wise SC, Kaufman MD, Ahn YM, Ensinger CL, et al. (2011) Conformational control inhibition of the BCR-ABL1 tyrosine kinase, including the gatekeeper T315I mutant, by the switch-control inhibitor DCC-2036. Cancer Cell 19: 556-568.
    • (2011) Cancer Cell , vol.19 , pp. 556-568
    • Chan, W.W.1    Wise, S.C.2    Kaufman, M.D.3    Ahn, Y.M.4    Ensinger, C.L.5
  • 11
    • 73949151915 scopus 로고    scopus 로고
    • The antitumor activity of homoharringtonine against human mast cells harboring the KIT D816V mutation
    • Jin Y, Lu Z, Cao K, Zhu Y, Chen Q, et al. (2010) The antitumor activity of homoharringtonine against human mast cells harboring the KIT D816V mutation. Mol Cancer Ther 9: 211-223.
    • (2010) Mol Cancer Ther , vol.9 , pp. 211-223
    • Jin, Y.1    Lu, Z.2    Cao, K.3    Zhu, Y.4    Chen, Q.5
  • 12
    • 63549123206 scopus 로고    scopus 로고
    • Triptolide inhibits Bcr-Abl transcription and induces apoptosis in STI571-resistant chronic myelogenous leukemia cells harboring T315I mutation
    • Shi X, Jin Y, Cheng C, Zhang H, Zou W, et al. (2009) Triptolide inhibits Bcr-Abl transcription and induces apoptosis in STI571-resistant chronic myelogenous leukemia cells harboring T315I mutation. Clin Cancer Res 15: 1686-1697.
    • (2009) Clin Cancer Res , vol.15 , pp. 1686-1697
    • Shi, X.1    Jin, Y.2    Cheng, C.3    Zhang, H.4    Zou, W.5
  • 13
    • 0344987881 scopus 로고    scopus 로고
    • A tyrosine kinase created by fusion of the PDGFRA and FIP1L1 genes as a therapeutic target of imatinib in idiopathic hypereosinophilic syndrome
    • Cools J, DeAngelo DJ, Gotlib J, Stover EH, Legare RD, et al. (2003) A tyrosine kinase created by fusion of the PDGFRA and FIP1L1 genes as a therapeutic target of imatinib in idiopathic hypereosinophilic syndrome. N Engl J Med 348: 1201-1214.
    • (2003) N Engl J Med , vol.348 , pp. 1201-1214
    • Cools, J.1    DeAngelo, D.J.2    Gotlib, J.3    Stover, E.H.4    Legare, R.D.5
  • 14
    • 1642324059 scopus 로고    scopus 로고
    • The EOL-1 cell line as an in vitro model for the study of FIP1L1-PDGFRA-positive chronic eosinophilic leukemia
    • Cools J, Quentmeier H, Huntly BJ, Marynen P, Griffin JD, et al. (2004) The EOL-1 cell line as an in vitro model for the study of FIP1L1-PDGFRA-positive chronic eosinophilic leukemia. Blood 103: 2802-2805.
    • (2004) Blood , vol.103 , pp. 2802-2805
    • Cools, J.1    Quentmeier, H.2    Huntly, B.J.3    Marynen, P.4    Griffin, J.D.5
  • 15
    • 84859393317 scopus 로고    scopus 로고
    • Cyclin-dependent kinase 7/9 inhibitor SNS-032 abrogates FIP1-like-1 platelet-derived growth factor receptor alpha and bcr-abl oncogene addiction in malignant hematologic cells
    • Wu Y, Chen C, Sun X, Shi X, Jin B, et al. (2012) Cyclin-dependent kinase 7/9 inhibitor SNS-032 abrogates FIP1-like-1 platelet-derived growth factor receptor alpha and bcr-abl oncogene addiction in malignant hematologic cells. Clin Cancer Res 18: 1966-1978.
    • (2012) Clin Cancer Res , vol.18 , pp. 1966-1978
    • Wu, Y.1    Chen, C.2    Sun, X.3    Shi, X.4    Jin, B.5
  • 16
    • 0034750172 scopus 로고    scopus 로고
    • Cytochrome c release is upstream to activation of caspase-9, caspase-8, and caspase-3 in the enhanced apoptosis of anaplastic thyroid cancer cells induced by manumycin and paclitaxel
    • Pan J, Xu G, Yeung SC, (2001) Cytochrome c release is upstream to activation of caspase-9, caspase-8, and caspase-3 in the enhanced apoptosis of anaplastic thyroid cancer cells induced by manumycin and paclitaxel. J Clin Endocrinol Metab 86: 4731-4740.
    • (2001) J Clin Endocrinol Metab , vol.86 , pp. 4731-4740
    • Pan, J.1    Xu, G.2    Yeung, S.C.3
  • 17
    • 18144363210 scopus 로고    scopus 로고
    • Farnesyltransferase inhibitors induce DNA damage via reactive oxygen species in human cancer cells
    • Pan J, She M, Xu ZX, Sun L, Yeung SC, (2005) Farnesyltransferase inhibitors induce DNA damage via reactive oxygen species in human cancer cells. Cancer Res 65: 3671-3681.
    • (2005) Cancer Res , vol.65 , pp. 3671-3681
    • Pan, J.1    She, M.2    Xu, Z.X.3    Sun, L.4    Yeung, S.C.5
  • 18
    • 71049169262 scopus 로고    scopus 로고
    • Triptolide abrogates oncogene FIP1L1-PDGFRalpha addiction and induces apoptosis in hypereosinophilic syndrome
    • Jin Y, Chen Q, Lu Z, Chen B, Pan J, (2009) Triptolide abrogates oncogene FIP1L1-PDGFRalpha addiction and induces apoptosis in hypereosinophilic syndrome. Cancer Sci 100: 2210-2217.
    • (2009) Cancer Sci , vol.100 , pp. 2210-2217
    • Jin, Y.1    Chen, Q.2    Lu, Z.3    Chen, B.4    Pan, J.5
  • 19
    • 84861552793 scopus 로고    scopus 로고
    • The Skp2-SCF E3 ligase regulates Akt ubiquitination, glycolysis, herceptin sensitivity, and tumorigenesis
    • Chan CH, Li CF, Yang WL, Gao Y, Lee SW, et al. (2012) The Skp2-SCF E3 ligase regulates Akt ubiquitination, glycolysis, herceptin sensitivity, and tumorigenesis. Cell 149: 1098-1111.
    • (2012) Cell , vol.149 , pp. 1098-1111
    • Chan, C.H.1    Li, C.F.2    Yang, W.L.3    Gao, Y.4    Lee, S.W.5
  • 20
    • 69549116880 scopus 로고    scopus 로고
    • The E3 ligase TRAF6 regulates Akt ubiquitination and activation
    • Yang WL, Wang J, Chan CH, Lee SW, Campos AD, et al. (2009) The E3 ligase TRAF6 regulates Akt ubiquitination and activation. Science 325: 1134-1138.
    • (2009) Science , vol.325 , pp. 1134-1138
    • Yang, W.L.1    Wang, J.2    Chan, C.H.3    Lee, S.W.4    Campos, A.D.5
  • 21
    • 77649178833 scopus 로고    scopus 로고
    • Celastrol, a novel HSP90 inhibitor, depletes Bcr-Abl and induces apoptosis in imatinib-resistant chronic myelogenous leukemia cells harboring T315I mutation
    • Lu Z, Jin Y, Qiu L, Lai Y, Pan J, (2010) Celastrol, a novel HSP90 inhibitor, depletes Bcr-Abl and induces apoptosis in imatinib-resistant chronic myelogenous leukemia cells harboring T315I mutation. Cancer Lett 290: 182-191.
    • (2010) Cancer Lett , vol.290 , pp. 182-191
    • Lu, Z.1    Jin, Y.2    Qiu, L.3    Lai, Y.4    Pan, J.5
  • 22
    • 24644523246 scopus 로고    scopus 로고
    • Resistance to tyrosine kinase inhibitors: calling on extra forces
    • Cools J, Maertens C, Marynen P, (2005) Resistance to tyrosine kinase inhibitors: calling on extra forces. Drug Resist Updat 8: 119-129.
    • (2005) Drug Resist Updat , vol.8 , pp. 119-129
    • Cools, J.1    Maertens, C.2    Marynen, P.3
  • 23
    • 33747203008 scopus 로고    scopus 로고
    • Sorafenib is a potent inhibitor of FIP1L1-PDGFRalpha and the imatinib-resistant FIP1L1-PDGFRalpha T674I mutant
    • Lierman E, Folens C, Stover EH, Mentens N, Van Miegroet H, et al. (2006) Sorafenib is a potent inhibitor of FIP1L1-PDGFRalpha and the imatinib-resistant FIP1L1-PDGFRalpha T674I mutant. Blood 108: 1374-1376.
    • (2006) Blood , vol.108 , pp. 1374-1376
    • Lierman, E.1    Folens, C.2    Stover, E.H.3    Mentens, N.4    Van Miegroet, H.5
  • 25
    • 84873043988 scopus 로고    scopus 로고
    • Activation of apoptosis by cytoplasmic microinjection of cytochrome c
    • Kole AJ, Knight ER, Deshmukh M (2011) Activation of apoptosis by cytoplasmic microinjection of cytochrome c. J Vis Exp.
    • (2011) J Vis Exp
    • Kole, A.J.1    Knight, E.R.2    Deshmukh, M.3
  • 26
    • 35648965243 scopus 로고    scopus 로고
    • Induction of BIM is essential for apoptosis triggered by EGFR kinase inhibitors in mutant EGFR-dependent lung adenocarcinomas
    • Gong Y, Somwar R, Politi K, Balak M, Chmielecki J, et al. (2007) Induction of BIM is essential for apoptosis triggered by EGFR kinase inhibitors in mutant EGFR-dependent lung adenocarcinomas. PLoS Med 4: e294.
    • (2007) PLoS Med , vol.4
    • Gong, Y.1    Somwar, R.2    Politi, K.3    Balak, M.4    Chmielecki, J.5
  • 27
    • 77952004119 scopus 로고    scopus 로고
    • Role for the proapoptotic factor BIM in mediating imatinib-induced apoptosis in a c-KIT-dependent gastrointestinal stromal tumor cell line
    • Gordon PM, Fisher DE, (2010) Role for the proapoptotic factor BIM in mediating imatinib-induced apoptosis in a c-KIT-dependent gastrointestinal stromal tumor cell line. J Biol Chem 285: 14109-14114.
    • (2010) J Biol Chem , vol.285 , pp. 14109-14114
    • Gordon, P.M.1    Fisher, D.E.2
  • 28
  • 29
    • 17444405985 scopus 로고    scopus 로고
    • Direct transcriptional regulation of Bim by FoxO3a mediates STI571-induced apoptosis in Bcr-Abl-expressing cells
    • Essafi A, Fernandez de Mattos S, Hassen YA, Soeiro I, Mufti GJ, et al. (2005) Direct transcriptional regulation of Bim by FoxO3a mediates STI571-induced apoptosis in Bcr-Abl-expressing cells. Oncogene 24: 2317-2329.
    • (2005) Oncogene , vol.24 , pp. 2317-2329
    • Essafi, A.1    Fernandez de Mattos, S.2    Hassen, Y.A.3    Soeiro, I.4    Mufti, G.J.5
  • 30
    • 43449132366 scopus 로고    scopus 로고
    • Multisite phosphorylation regulates Bim stability and apoptotic activity
    • Hubner A, Barrett T, Flavell RA, Davis RJ, (2008) Multisite phosphorylation regulates Bim stability and apoptotic activity. Mol Cell 30: 415-425.
    • (2008) Mol Cell , vol.30 , pp. 415-425
    • Hubner, A.1    Barrett, T.2    Flavell, R.A.3    Davis, R.J.4
  • 31
    • 0242521470 scopus 로고    scopus 로고
    • Phosphorylation of Bim-EL by Erk1/2 on serine 69 promotes its degradation via the proteasome pathway and regulates its proapoptotic function
    • Luciano F, Jacquel A, Colosetti P, Herrant M, Cagnol S, et al. (2003) Phosphorylation of Bim-EL by Erk1/2 on serine 69 promotes its degradation via the proteasome pathway and regulates its proapoptotic function. Oncogene 22: 6785-6793.
    • (2003) Oncogene , vol.22 , pp. 6785-6793
    • Luciano, F.1    Jacquel, A.2    Colosetti, P.3    Herrant, M.4    Cagnol, S.5
  • 32
    • 66849087150 scopus 로고    scopus 로고
    • FIP1L1-PDGFRalpha D842V, a novel panresistant mutant, emerging after treatment of FIP1L1-PDGFRalpha T674I eosinophilic leukemia with single agent sorafenib
    • Lierman E, Michaux L, Beullens E, Pierre P, Marynen P, et al. (2009) FIP1L1-PDGFRalpha D842V, a novel panresistant mutant, emerging after treatment of FIP1L1-PDGFRalpha T674I eosinophilic leukemia with single agent sorafenib. Leukemia 23: 845-851.
    • (2009) Leukemia , vol.23 , pp. 845-851
    • Lierman, E.1    Michaux, L.2    Beullens, E.3    Pierre, P.4    Marynen, P.5
  • 33
    • 13544267772 scopus 로고    scopus 로고
    • Myeloid blast crisis evolving during imatinib treatment of an FIP1L1-PDGFR alpha-positive chronic myeloproliferative disease with prominent eosinophilia
    • von Bubnoff N, Sandherr M, Schlimok G, Andreesen R, Peschel C, et al. (2005) Myeloid blast crisis evolving during imatinib treatment of an FIP1L1-PDGFR alpha-positive chronic myeloproliferative disease with prominent eosinophilia. Leukemia 19: 286-287.
    • (2005) Leukemia , vol.19 , pp. 286-287
    • von Bubnoff, N.1    Sandherr, M.2    Schlimok, G.3    Andreesen, R.4    Peschel, C.5
  • 34
    • 65549100146 scopus 로고    scopus 로고
    • A novel FIP1L1-PDGFRA mutant destabilizing the inactive conformation of the kinase domain in chronic eosinophilic leukemia/hypereosinophilic syndrome
    • Salemi S, Yousefi S, Simon D, Schmid I, Moretti L, et al. (2009) A novel FIP1L1-PDGFRA mutant destabilizing the inactive conformation of the kinase domain in chronic eosinophilic leukemia/hypereosinophilic syndrome. Allergy 64: 913-918.
    • (2009) Allergy , vol.64 , pp. 913-918
    • Salemi, S.1    Yousefi, S.2    Simon, D.3    Schmid, I.4    Moretti, L.5
  • 35
    • 56349117935 scopus 로고    scopus 로고
    • Combination of imatinib and vinorelbine enhances cell growth inhibition in breast cancer cells via PDGFR beta signalling
    • Weigel MT, Meinhold-Heerlein I, Bauerschlag DO, Schem C, Bauer M, et al. (2009) Combination of imatinib and vinorelbine enhances cell growth inhibition in breast cancer cells via PDGFR beta signalling. Cancer Lett 273: 70-79.
    • (2009) Cancer Lett , vol.273 , pp. 70-79
    • Weigel, M.T.1    Meinhold-Heerlein, I.2    Bauerschlag, D.O.3    Schem, C.4    Bauer, M.5
  • 36
    • 33745632099 scopus 로고    scopus 로고
    • Combination treatment of imatinib-sensitive and -resistant BCR-ABL-positive CML cells with imatinib and farnesyltransferase inhibitors
    • Radujkovic A, Topaly J, Fruehauf S, Zeller WJ, (2006) Combination treatment of imatinib-sensitive and-resistant BCR-ABL-positive CML cells with imatinib and farnesyltransferase inhibitors. Anticancer Res 26: 2169-2177.
    • (2006) Anticancer Res , vol.26 , pp. 2169-2177
    • Radujkovic, A.1    Topaly, J.2    Fruehauf, S.3    Zeller, W.J.4
  • 37
    • 79251506692 scopus 로고    scopus 로고
    • Targeting the BCR-ABL signaling pathway in therapy-resistant Philadelphia chromosome-positive leukemia
    • O'Hare T, Deininger MW, Eide CA, Clackson T, Druker BJ, (2011) Targeting the BCR-ABL signaling pathway in therapy-resistant Philadelphia chromosome-positive leukemia. Clin Cancer Res 17: 212-221.
    • (2011) Clin Cancer Res , vol.17 , pp. 212-221
    • O'Hare, T.1    Deininger, M.W.2    Eide, C.A.3    Clackson, T.4    Druker, B.J.5
  • 38
    • 77953636478 scopus 로고    scopus 로고
    • Discovery of a small-molecule type II inhibitor of wild-type and gatekeeper mutants of BCR-ABL, PDGFRalpha, Kit, and Src kinases: novel type II inhibitor of gatekeeper mutants
    • Weisberg E, Choi HG, Ray A, Barrett R, Zhang J, et al. (2010) Discovery of a small-molecule type II inhibitor of wild-type and gatekeeper mutants of BCR-ABL, PDGFRalpha, Kit, and Src kinases: novel type II inhibitor of gatekeeper mutants. Blood 115: 4206-4216.
    • (2010) Blood , vol.115 , pp. 4206-4216
    • Weisberg, E.1    Choi, H.G.2    Ray, A.3    Barrett, R.4    Zhang, J.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.