메뉴 건너뛰기




Volumn 50, Issue 3, 2009, Pages 437-446

Activity of FB2, a novel dual Abl/Src tyrosine kinase inhibitor, against imatinib-resistant chronic myeloid leukemia in vivo and in vitro

Author keywords

Bcr Abl; Chronic myelogenous leukemia; Imatinib; Inhibitor; Resistance; Src

Indexed keywords

ABELSON KINASE; BCR ABL PROTEIN; CYCLOPHOSPHAMIDE; DASATINIB; IMATINIB; N (THIAZOL 2 YL)PYRIMIDIN 4 AMINE DERIVATIVE; PROTEIN KINASE LYN; PROTEIN KINASE P60; PROTEIN TYROSINE KINASE INHIBITOR; UNCLASSIFIED DRUG;

EID: 67650928403     PISSN: 10428194     EISSN: 10292403     Source Type: Journal    
DOI: 10.1080/10428190802709438     Document Type: Article
Times cited : (4)

References (43)
  • 1
    • 0015694748 scopus 로고
    • Letter: A new consistent chromosomal abnormality in chronic myelogenous leukaemia identified by quinacrine fluorescence and Giemsa staining
    • Rowley, J. D. (1973) Letter: A new consistent chromosomal abnormality in chronic myelogenous leukaemia identified by quinacrine fluorescence and Giemsa staining. Nature, 243, pp. 290-293.
    • (1973) Nature , vol.243 , pp. 290-293
    • Rowley, J.D.1
  • 2
    • 0020333906 scopus 로고
    • A cellular oncogene is translocated to the Philadelphia chromosome in chronic myelocytic leukaemia
    • de Klein, A., van Kessel, A. G., Grosveld, G., Bartram, C. R., Hagemeijer, A. Bootsma, D. et al. (1982) A cellular oncogene is translocated to the Philadelphia chromosome in chronic myelocytic leukaemia. Nature, 300, pp. 765-767.
    • (1982) Nature , vol.300 , pp. 765-767
    • de Klein, A.1    van Kessel, A.G.2    Grosveld, G.3    Bartram, C.R.4    Hagemeijer, A.5    Bootsma, D.6
  • 3
    • 0035979656 scopus 로고    scopus 로고
    • Bcr-Abl inhibition as a modality of CML therapeutics
    • Buchdunger, E., Matter, A. and Druker, B. J. (2001) Bcr-Abl inhibition as a modality of CML therapeutics. Biochim Biophys Acta, 1551, pp. M11-M18.
    • (2001) Biochim Biophys Acta , vol.1551
    • Buchdunger, E.1    Matter, A.2    Druker, B.J.3
  • 4
    • 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., Varadi, A., Sarkadi, B. and Keri, G. (2002) Interaction of tyrosine kinase inhibitors with the human multidrug transporter proteins, MDR1 and MRP1. Biochim Biophys Acta, 1587, pp. 318-325.
    • (2002) Biochim Biophys Acta , vol.1587 , pp. 318-325
    • Hegedus, T.1    Orfi, L.2    Seprodi, A.3    Varadi, A.4    Sarkadi, B.5    Keri, G.6
  • 5
    • 0035800507 scopus 로고    scopus 로고
    • Clinical resistance to STI-571 cancer therapy caused by BCR-ABL gene mutation or amplification
    • Gorre, M. E., Mohammed, M., Ellwood, K., Hsu, N., Paquette, R. Rao, P. N. et al. (2001) Clinical resistance to STI-571 cancer therapy caused by BCR-ABL gene mutation or amplification. Science, 293, pp. 876-880.
    • (2001) Science , vol.293 , pp. 876-880
    • Gorre, M.E.1    Mohammed, M.2    Ellwood, K.3    Hsu, N.4    Paquette, R.5    Rao, P.N.6
  • 6
    • 0036493544 scopus 로고    scopus 로고
    • Ph(+) acute lymphoblastic leukemia resistant to the tyrosine kinase inhibitor STI571 has a unique BCR-ABL gene mutation
    • Hofmann, W. K., Jones, L. C., Lemp, N. A., de Vos, S., Gschaidmeier, H. Hoelzer, D. et al. (2002) Ph(+) acute lymphoblastic leukemia resistant to the tyrosine kinase inhibitor STI571 has a unique BCR-ABL gene mutation. Blood, 99, pp. 1860-1862.
    • (2002) Blood , vol.99 , pp. 1860-1862
    • Hofmann, W.K.1    Jones, L.C.2    Lemp, N.A.3    de Vos, S.4    Gschaidmeier, H.5    Hoelzer, D.6
  • 7
    • 0348140591 scopus 로고    scopus 로고
    • Mechanisms and implications of imatinib resistance mutations in BCR-ABL
    • Nardi, V., Azam, M. and Daley, G. Q. (2004) Mechanisms and implications of imatinib resistance mutations in BCR-ABL. Curr Opin Hematol, 11, pp. 35-43.
    • (2004) Curr Opin Hematol , vol.11 , pp. 35-43
    • Nardi, V.1    Azam, M.2    Daley, G.Q.3
  • 8
    • 14944361257 scopus 로고    scopus 로고
    • Can we afford to let sleeping dogs lie?
    • Deininger, M. W. and Holyoake, T. L. (2005) Can we afford to let sleeping dogs lie?. Blood, 105, pp. 1840-1841.
    • (2005) Blood , vol.105 , pp. 1840-1841
    • Deininger, M.W.1    Holyoake, T.L.2
  • 9
    • 0037438640 scopus 로고    scopus 로고
    • BCR-ABL independence and LYN kinase over expression 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. (2003) BCR-ABL independence and LYN kinase over expression in chronic myelogenous leukemia cells selected for resistance to STI571. Blood, 101, pp. 690-698.
    • (2003) Blood , vol.101 , pp. 690-698
    • Donato, N.J.1    Wu, J.Y.2    Stapley, J.3    Gallick, G.4    Lin, H.5    Arlinghaus, R.6
  • 10
    • 4544343214 scopus 로고    scopus 로고
    • A Bcr/Abl-independent, Lyn-dependent form of imatinib mesylate (STI-571) resistance is associated with altered expression of Bcl-2
    • Dai, Y., Rahmani, M., Corey, S. J., Dent, P. and Grant, S. (2004) A Bcr/ Abl-independent, Lyn-dependent form of imatinib mesylate (STI-571) resistance is associated with altered expression of Bcl-2. J Biol Chem, 279, pp. 34227-34239.
    • (2004) J Biol Chem , vol.279 , pp. 34227-34239
    • Dai, Y.1    Rahmani, M.2    Corey, S.J.3    Dent, P.4    Grant, S.5
  • 11
    • 2342629325 scopus 로고    scopus 로고
    • Imatinib (STI571) resistance in chronic myelogenous leukemia: Molecular basis of the underlying mechanisms and potential strategies for treatment
    • Cowan-Jacob, S. W., Guez, V., Fendrich, G., Griffin, J. D., Fabbro, D. Furet, P. et al. (2004) Imatinib (STI571) resistance in chronic myelogenous leukemia: Molecular basis of the underlying mechanisms and potential strategies for treatment. Mini Rev Med Chem, 4, pp. 285-299.
    • (2004) Mini Rev Med Chem , vol.4 , pp. 285-299
    • Cowan-Jacob, S.W.1    Guez, V.2    Fendrich, G.3    Griffin, J.D.4    Fabbro, D.5    Furet, P.6
  • 12
    • 33745283618 scopus 로고    scopus 로고
    • The structure of Dasatinib (BMS-354825) bound to activated ABL kinase domain elucidates its inhibitory activity against imatinib-resistant ABL mutants
    • Tokarski, J. S., Newitt, J. A., Chang, C. Y., Cheng, J. D., Wittekind, M. Kiefer, S. E. et al. (2006) The structure of Dasatinib (BMS-354825) bound to activated ABL kinase domain elucidates its inhibitory activity against imatinib-resistant ABL mutants. Cancer Res, 66, pp. 5790-5797.
    • (2006) Cancer Res , vol.66 , pp. 5790-5797
    • Tokarski, J.S.1    Newitt, J.A.2    Chang, C.Y.3    Cheng, J.D.4    Wittekind, M.5    Kiefer, S.E.6
  • 13
    • 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., Assouline, S. and Scapozza, L. (2005) Abl inhibitor BMS354825 binding mode in Abelson kinase revealed by molecular docking studies. Leukemia, 19, pp. 1267-1269.
    • (2005) Leukemia , vol.19 , pp. 1267-1269
    • Gambacorti-Passerini, C.1    Gasser, M.2    Ahmed, S.3    Assouline, S.4    Scapozza, L.5
  • 14
    • 27144547509 scopus 로고    scopus 로고
    • Action of the Src family kinase inhibitor, dasatinib (BMS-354825), on human prostate cancer cells
    • Nam, S., Kim, D., Cheng, J. Q., Zhang, S., Lee, J. H. Buettner, R. et al. (2005) Action of the Src family kinase inhibitor, dasatinib (BMS-354825), on human prostate cancer cells. Cancer Res, 65, pp. 9185-9189.
    • (2005) Cancer Res , vol.65 , pp. 9185-9189
    • Nam, S.1    Kim, D.2    Cheng, J.Q.3    Zhang, S.4    Lee, J.H.5    Buettner, R.6
  • 15
    • 33645821453 scopus 로고    scopus 로고
    • Potent inhibition of platelet-derived growth factor-induced responses in vascular smooth muscle cells by BMS-354825 (dasatinib)
    • Chen, Z., Lee, F. Y., Bhalla, K. N. and Wu, J. (2006) Potent inhibition of platelet-derived growth factor-induced responses in vascular smooth muscle cells by BMS-354825 (dasatinib). Mol Pharmacol, 69, pp. 1527-1533.
    • (2006) Mol Pharmacol , vol.69 , pp. 1527-1533
    • Chen, Z.1    Lee, F.Y.2    Bhalla, K.N.3    Wu, J.4
  • 16
    • 38349178550 scopus 로고    scopus 로고
    • Establishment of an imatinib resistant cell line K562/G01 and its characterization
    • Qi, J., Peng, H., Gu, Z. L., Liang, Z. Q. and Yang, C. Z. (2004) Establishment of an imatinib resistant cell line K562/G01 and its characterization. Zhonghua Xue Ye Xue Za Zhi, 25, pp. 337-341.
    • (2004) Zhonghua Xue Ye Xue Za Zhi , vol.25 , pp. 337-341
    • Qi, J.1    Peng, H.2    Gu, Z.L.3    Liang, Z.Q.4    Yang, C.Z.5
  • 17
    • 34347207593 scopus 로고    scopus 로고
    • Expression of sialidase Neu2 in leukemic K562 cells induces apoptosis by impairing Bcr-Abl/Src kinases signaling
    • Tringali, C., Lupo, B., Anastasia, L., Papini, N., Monti, E. Bresciani, R. et al. (2007) Expression of sialidase Neu2 in leukemic K562 cells induces apoptosis by impairing Bcr-Abl/Src kinases signaling. J Biol Chem, 282, pp. 14364-14372.
    • (2007) J Biol Chem , vol.282 , pp. 14364-14372
    • Tringali, C.1    Lupo, B.2    Anastasia, L.3    Papini, N.4    Monti, E.5    Bresciani, R.6
  • 18
    • 2042458747 scopus 로고    scopus 로고
    • Relationships between drug activity in NCI preclinical in vitro and in vivo models and early clinical trials
    • Johnson, J. I., Decker, S., Zaharevitz, D., Rubinstein, L. V., Venditti, J. M. Schepartz, S. et al. (2001) Relationships between drug activity in NCI preclinical in vitro and in vivo models and early clinical trials. Br J Cancer, 84, pp. 1424-1431.
    • (2001) Br J Cancer , vol.84 , pp. 1424-1431
    • Johnson, J.I.1    Decker, S.2    Zaharevitz, D.3    Rubinstein, L.V.4    Venditti, J.M.5    Schepartz, S.6
  • 19
    • 27644545666 scopus 로고    scopus 로고
    • Strategies for overcoming ABC-transporters-mediated multidrug resistance (MDR) of tumor cells
    • Borowski, E., Bontemps-Gracz, M. M. and Piwkowska, A. (2005) Strategies for overcoming ABC-transporters-mediated multidrug resistance (MDR) of tumor cells. Acta Biochim Pol, 52, pp. 609-627.
    • (2005) Acta Biochim Pol , vol.52 , pp. 609-627
    • Borowski, E.1    Bontemps-Gracz, M.M.2    Piwkowska, A.3
  • 20
    • 0036176510 scopus 로고    scopus 로고
    • Mechanisms of cancer drug resistance
    • Gottesman, M. M. (2002) Mechanisms of cancer drug resistance. Annu Rev Med, 53, pp. 615-627.
    • (2002) Annu Rev Med , vol.53 , pp. 615-627
    • Gottesman, M.M.1
  • 21
    • 0024329881 scopus 로고
    • The biochemistry of P-glycoprotein-mediated multidrug resistance
    • Endicott, J. A. and Ling, V. (1989) The biochemistry of P-glycoprotein-mediated multidrug resistance. Annu Rev Biochem, 58, pp. 137-171.
    • (1989) Annu Rev Biochem , vol.58 , pp. 137-171
    • Endicott, J.A.1    Ling, V.2
  • 22
    • 0027305734 scopus 로고
    • Daunorubicin uptake by leukemic cells: Correlations with treatment outcome and mdr1 expression
    • Marie, J. P., Faussat-Suberville, A. M., Zhou, D. and Zittoun, R. (1993) Daunorubicin uptake by leukemic cells: Correlations with treatment outcome and mdr1 expression. Leukemia, 7, pp. 825-831.
    • (1993) Leukemia , vol.7 , pp. 825-831
    • Marie, J.P.1    Faussat-Suberville, A.M.2    Zhou, D.3    Zittoun, R.4
  • 23
    • 0001686739 scopus 로고    scopus 로고
    • Multiple BCR-ABL kinase domain mutations confer polyclonal resistance to the tyrosine kinase inhibitor imatinib (STI571) in chronic phase and blast crisis chronic myeloid leukemia
    • Shah, N. P., Nicoll, J. M., Nagar, B., Gorre, M. E., Paquette, R. L. Kuriyan, J. et al. (2002) Multiple BCR-ABL kinase domain mutations confer polyclonal resistance to the tyrosine kinase inhibitor imatinib (STI571) in chronic phase and blast crisis chronic myeloid leukemia. Cancer Cell, 2, pp. 117-125.
    • (2002) Cancer Cell , vol.2 , pp. 117-125
    • Shah, N.P.1    Nicoll, J.M.2    Nagar, B.3    Gorre, M.E.4    Paquette, R.L.5    Kuriyan, J.6
  • 24
    • 0034161460 scopus 로고    scopus 로고
    • Induction of resistance to the Abelson inhibitor STI571 in human leukemic cells through gene amplification
    • le Coutre, P, Tassi, E., Varella-Garcia, M., Barni, R., Mologni, L. Cabrita, G. et al. (2000) Induction of resistance to the Abelson inhibitor STI571 in human leukemic cells through gene amplification. Blood, 95, pp. 1758-1766.
    • (2000) Blood , vol.95 , pp. 1758-1766
    • le Coutre, P.1    Tassi, E.2    Varella-Garcia, M.3    Barni, R.4    Mologni, L.5    Cabrita, G.6
  • 25
    • 0037108879 scopus 로고    scopus 로고
    • Molecular characterization and sensitivity of STI-571 (imatinib mesylate, Gleevec)-resistant, Bcr-Abl-positive, human acute leukemia cells to SRC kinase inhibitor PD180970 and 17-allylamino-17-demethoxygeldanamycin
    • Nimmanapalli, R., O'Bryan, E., Huang, M., Bali, P., Burnette, P. K. Loughran, T. et al. (2002) Molecular characterization and sensitivity of STI-571 (imatinib mesylate, Gleevec)-resistant, Bcr-Abl-positive, human acute leukemia cells to SRC kinase inhibitor PD180970 and 17-allylamino-17-demethoxygeldanamycin. Cancer Res, 62, pp. 5761-5769.
    • (2002) Cancer Res , vol.62 , pp. 5761-5769
    • Nimmanapalli, R.1    O'Bryan, E.2    Huang, M.3    Bali, P.4    Burnette, P.K.5    Loughran, T.6
  • 26
    • 0030031766 scopus 로고    scopus 로고
    • Inhibition of the Abl protein-tyrosine kinase in vitro and in vivo by a 2-phenylaminopyrimidine derivative
    • Buchdunger, E., Zimmermann, J., Mett, H., Meyer, T., Muller, M. Druker, B. J. et al. (1996) Inhibition of the Abl protein-tyrosine kinase in vitro and in vivo by a 2-phenylaminopyrimidine derivative. Cancer Res, 56, pp. 100-104.
    • (1996) Cancer Res , vol.56 , pp. 100-104
    • Buchdunger, E.1    Zimmermann, J.2    Mett, H.3    Meyer, T.4    Muller, M.5    Druker, B.J.6
  • 27
    • 0033816156 scopus 로고    scopus 로고
    • Abl protein-tyrosine kinase inhibitor STI571 inhibits in vitro signal transduction mediated by c-kit and platelet-derived growth factor receptors
    • Buchdunger, E., Cioffi, C. L., Law, N., Stover, D., Ohno-Jones, S. Druker, B. J. et al. (2000) Abl protein-tyrosine kinase inhibitor STI571 inhibits in vitro signal transduction mediated by c-kit and platelet-derived growth factor receptors. J Pharmacol Exp Ther, 295, pp. 139-145.
    • (2000) J Pharmacol Exp Ther , vol.295 , pp. 139-145
    • Buchdunger, E.1    Cioffi, C.L.2    Law, N.3    Stover, D.4    Ohno-Jones, S.5    Druker, B.J.6
  • 28
    • 0029947186 scopus 로고    scopus 로고
    • Effects of a selective inhibitor of the Abl tyrosine kinase on the growth of Bcr-Abl positive cells
    • Druker, B. J., Tamura, S., Buchdunger, E., Ohno, S., Segal, G. M. Fanning, S. et al. (1996) Effects of a selective inhibitor of the Abl tyrosine kinase on the growth of Bcr-Abl positive cells. Nat Med, 2, pp. 561-566.
    • (1996) Nat Med , vol.2 , pp. 561-566
    • Druker, B.J.1    Tamura, S.2    Buchdunger, E.3    Ohno, S.4    Segal, G.M.5    Fanning, S.6
  • 29
    • 0036770178 scopus 로고    scopus 로고
    • Identification and treatment of chemoresistant inoperable or metastatic GIST: Experience with the selective tyrosine kinase inhibitor imatinib mesylate (STI571)
    • Demetri, G. D. (2002) Identification and treatment of chemoresistant inoperable or metastatic GIST: Experience with the selective tyrosine kinase inhibitor imatinib mesylate (STI571). Eur J Cancer, 38, pp. S52-S59.
    • (2002) Eur J Cancer , vol.38
    • Demetri, G.D.1
  • 30
    • 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. (2004) Imatinib mesylate resistance through BCR-ABL independence in chronic myelogenous leukemia. Cancer Res, 64, pp. 672-677.
    • (2004) Cancer Res , vol.64 , pp. 672-677
    • Donato, N.J.1    Wu, J.Y.2    Stapley, J.3    Lin, H.4    Arlinghaus, R.5    Aggarwal, B.B.6
  • 31
    • 0029683347 scopus 로고    scopus 로고
    • Activation of Src kinases p53/56lyn and p59hck by p210bcr/abl in myeloid cells
    • Danhauser-Riedl, S., Warmuth, M., Druker, B. J., Emmerich, B. and Hallek, M. (1996) Activation of Src kinases p53/56lyn and p59hck by p210bcr/abl in myeloid cells. Cancer Res, 56, pp. 3589-3596.
    • (1996) Cancer Res , vol.56 , pp. 3589-3596
    • Danhauser-Riedl, S.1    Warmuth, M.2    Druker, B.J.3    Emmerich, B.4    Hallek, M.5
  • 32
    • 19944428353 scopus 로고    scopus 로고
    • Discovery of N-(2-chloro-6-methyl-phenyl)-2-(6-(4-(2-hydroxyethyl)- piperazin-1-yl)-2-methylpyrimidin-4-ylamino)thiazole-5-carboxamide (BMS-354825), a dual Src/Abl kinase inhibitor with potent antitumor activity in preclinical assays
    • Lombardo, L. J., Lee, F. Y., Chen, P., Norris, D., Barrish, J. C. Behnia, K. et al. (2004) Discovery of N-(2-chloro-6-methyl-phenyl)-2-(6-(4-(2-hydroxyethyl)- piperazin-1-yl)-2-methylpyrimidin-4-ylamino)thiazole-5-carboxamide (BMS-354825), a dual Src/Abl kinase inhibitor with potent antitumor activity in preclinical assays. J Med Chem, 47, pp. 6658-6661.
    • (2004) J Med Chem , vol.47 , pp. 6658-6661
    • Lombardo, L.J.1    Lee, F.Y.2    Chen, P.3    Norris, D.4    Barrish, J.C.5    Behnia, K.6
  • 33
    • 0031455168 scopus 로고    scopus 로고
    • The Src family kinase Hck interacts with Bcr-Abl by a kinase-independent mechanism and phosphorylates the Grb2-binding site of Bcr
    • Warmuth, M., Bergmann, M., Priess, A., Hauslmann, K., Emmerich, B. and Hallek, M. (1997) The Src family kinase Hck interacts with Bcr-Abl by a kinase-independent mechanism and phosphorylates the Grb2-binding site of Bcr. J Biol Chem, 272, pp. 33260-33270.
    • (1997) J Biol Chem , vol.272 , pp. 33260-33270
    • Warmuth, M.1    Bergmann, M.2    Priess, A.3    Hauslmann, K.4    Emmerich, B.5    Hallek, M.6
  • 35
    • 0037328534 scopus 로고    scopus 로고
    • The interaction of the Bcr-Abl tyrosine kinase with the Src kinase Hck is mediated by multiple binding domains
    • Stanglmaier, M., Warmuth, M., Kleinlein, I., Reis, S. and Hallek, M. (2003) The interaction of the Bcr-Abl tyrosine kinase with the Src kinase Hck is mediated by multiple binding domains. Leukemia, 17, pp. 283-289.
    • (2003) Leukemia , vol.17 , pp. 283-289
    • Stanglmaier, M.1    Warmuth, M.2    Kleinlein, I.3    Reis, S.4    Hallek, M.5
  • 36
    • 0034674707 scopus 로고    scopus 로고
    • Transformation of myeloid leukemia cells to cytokine independence by Bcr-Abl is suppressed by kinase-defective Hck
    • Lionberger, J. M., Wilson, M. B. and Smithgall, T. E. (2000) Transformation of myeloid leukemia cells to cytokine independence by Bcr-Abl is suppressed by kinase-defective Hck. J Biol Chem, 275, pp. 18581-18585.
    • (2000) J Biol Chem , vol.275 , pp. 18581-18585
    • Lionberger, J.M.1    Wilson, M.B.2    Smithgall, T.E.3
  • 37
    • 0037153476 scopus 로고    scopus 로고
    • Selective pyrrolo-pyrimidine inhibitors reveal a necessary role for Src family kinases in Bcr-Abl signal transduction and oncogenesis
    • Wilson, M. B., Schreiner, S. J., Choi, H. J., Kamens, J. and Smithgall, T. E. (2002) Selective pyrrolo-pyrimidine inhibitors reveal a necessary role for Src family kinases in Bcr-Abl signal transduction and oncogenesis. Oncogene, 21, pp. 8075-8088.
    • (2002) Oncogene , vol.21 , pp. 8075-8088
    • Wilson, M.B.1    Schreiner, S.J.2    Choi, H.J.3    Kamens, J.4    Smithgall, T.E.5
  • 38
    • 0037438513 scopus 로고    scopus 로고
    • Dual-specific Src and Abl kinase inhibitors, PP1 and CGP76030, inhibit growth and survival of cells expressing imatinib mesylate-resistant Bcr-Abl kinases
    • Warmuth, M., Simon, N., Mitina, O., Mathes, R., Fabbro, D. Manley, P. W. et al. (2003) Dual-specific Src and Abl kinase inhibitors, PP1 and CGP76030, inhibit growth and survival of cells expressing imatinib mesylate-resistant Bcr-Abl kinases. Blood, 101, pp. 664-672.
    • (2003) Blood , vol.101 , pp. 664-672
    • Warmuth, M.1    Simon, N.2    Mitina, O.3    Mathes, R.4    Fabbro, D.5    Manley, P.W.6
  • 39
    • 33847306882 scopus 로고    scopus 로고
    • Nonreceptor tyrosine kinases in prostate cancer
    • Chang, Y. M., Kung, H. J. and Evans, C. P. (2007) Nonreceptor tyrosine kinases in prostate cancer. Neoplasia, 9, pp. 90-100.
    • (2007) Neoplasia , vol.9 , pp. 90-100
    • Chang, Y.M.1    Kung, H.J.2    Evans, C.P.3
  • 40
    • 36248973171 scopus 로고    scopus 로고
    • The role of Src in prostate cancer
    • Fizazi, K. (2007) The role of Src in prostate cancer. Ann Oncol, 18, pp. 1765-1773.
    • (2007) Ann Oncol , vol.18 , pp. 1765-1773
    • Fizazi, K.1
  • 41
    • 33846870586 scopus 로고    scopus 로고
    • Src as a therapeutic target in anti-hormone/anti-growth factor-resistant breast cancer
    • Hiscox, S., Morgan, L., Green, T. and Nicholson, R. I. (2006) Src as a therapeutic target in anti-hormone/anti-growth factor-resistant breast cancer. Endocr Relat Cancer, 13, pp. S53-S59.
    • (2006) Endocr Relat Cancer , vol.13
    • Hiscox, S.1    Morgan, L.2    Green, T.3    Nicholson, R.I.4
  • 42
    • 0034099236 scopus 로고    scopus 로고
    • Elevated levels of p66 Shc are found in breast cancer cell lines and primary tumors with high metastatic potential
    • Jackson, J. G., Yoneda, T., Clark, G. M. and Yee, D. (2000) Elevated levels of p66 Shc are found in breast cancer cell lines and primary tumors with high metastatic potential. Clin Cancer Res, 6, pp. 1135-1139.
    • (2000) Clin Cancer Res , vol.6 , pp. 1135-1139
    • Jackson, J.G.1    Yoneda, T.2    Clark, G.M.3    Yee, D.4
  • 43
    • 0035826165 scopus 로고    scopus 로고
    • Alterations in the focal adhesion kinase/Src signal transduction pathway correlate with increased migratory capacity of prostate carcinoma cells
    • Slack, J. K., Adams, R. B., Rovin, J. D., Bissonette, E. A., Stoker, C. E. and Parsons, J. T. (2001) Alterations in the focal adhesion kinase/ Src signal transduction pathway correlate with increased migratory capacity of prostate carcinoma cells. Oncogene, 20, pp. 1152-1163.
    • (2001) Oncogene , vol.20 , pp. 1152-1163
    • Slack, J.K.1    Adams, R.B.2    Rovin, J.D.3    Bissonette, E.A.4    Stoker, C.E.5    Parsons, J.T.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.