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Volumn 67, Issue 2, 2009, Pages 69-77

Inhibitors of aurora kinases;Les inhibiteurs des kinases Aurora

Author keywords

Aurora kinases; Cell division; Inhibitors of aurora kinases; Tumor

Indexed keywords

2 [[3 [4 [5 [2 (3 FLUOROANILINO) 2 OXOETHYL] 1H PYRAZOL 3 YLAMINO] 7 QUINAZOLINYLOXY]PROPYL](ETHYL)AMINO]ETHYL DIHYDROGEN PHOSPHATE; 2,4 DIMETHYL 5 (2 OXO 1H INDOL 3 YLMETHYLENE) 3 PYRROLEPROPIONIC ACID; 4 [[9 CHLORO 7 (2,6 DIFLUOROPHENYL) 5H PYRIMIDO[5,4 D][2]BENZAZEPIN 2 YL]AMINO]BENZOIC ACID; ANTINEOPLASTIC AGENT; AT 9283; AURORA A KINASE; AURORA B KINASE; AURORA C KINASE; AURORA KINASE INHIBITOR; BIOLOGICAL MARKER; CYCLOPROPANECARBOXYLIC ACID [4 [4 (4 METHYL 1 PIPERAZINYL) 6 (5 METHYL 2H PYRAZOL 3 YLAMINO) 2 PYRIMIDINYLTHIO]PHENYL]AMIDE; DEXAMETHASONE; DOCETAXEL; ENDOSTATIN; FLUOROURACIL; GEMCITABINE; GRANULOCYTE COLONY STIMULATING FACTOR; IMATINIB; IRINOTECAN; N [4 [6 METHOXY 7 (3 MORPHOLINOPROPOXY) 4 QUINAZOLINYLAMINO]PHENYL]BENZAMIDE; NAVELBINE; OXALIPLATIN; PHA 680632; PHA 739358; RECOMBINANT GRANULOCYTE COLONY STIMULATING FACTOR; TAMOXIFEN CITRATE; UNCLASSIFIED DRUG; VINCRISTINE SULFATE;

EID: 68949171956     PISSN: 00034509     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.pharma.2008.12.005     Document Type: Short Survey
Times cited : (8)

References (56)
  • 2
    • 68949194034 scopus 로고    scopus 로고
    • L'inhibiteur de kinases Aurora VX680, chef de file d'une nouvelle famille d'agents antitumoraux
    • Lavelle F. L'inhibiteur de kinases Aurora VX680, chef de file d'une nouvelle famille d'agents antitumoraux. Bull cancer 91 (2004) 330-331
    • (2004) Bull cancer , vol.91 , pp. 330-331
    • Lavelle, F.1
  • 4
    • 0242551545 scopus 로고    scopus 로고
    • The cellular geography of kinases Aurora
    • Carmena M., and Earnshaw W.C. The cellular geography of kinases Aurora. Nat Rev Mol Cell Biol 4 (2003) 842-854
    • (2003) Nat Rev Mol Cell Biol , vol.4 , pp. 842-854
    • Carmena, M.1    Earnshaw, W.C.2
  • 6
    • 33846391959 scopus 로고    scopus 로고
    • Structural basis for the inhibition of Aurora A kinase by a novel class of high affinity disubstituted pyrimidine inhibitors
    • Tari L.W., Hoffman I.D., Bensen D.C., Hunter M.J., Nix J., Nelson K.J., et al. Structural basis for the inhibition of Aurora A kinase by a novel class of high affinity disubstituted pyrimidine inhibitors. Bioorg Med Chem Lett 17 (2007) 688-691
    • (2007) Bioorg Med Chem Lett , vol.17 , pp. 688-691
    • Tari, L.W.1    Hoffman, I.D.2    Bensen, D.C.3    Hunter, M.J.4    Nix, J.5    Nelson, K.J.6
  • 7
    • 33745444343 scopus 로고    scopus 로고
    • Le cycle de division cellulaire et sa régulation.
    • hors série
    • Meijer L. Le cycle de division cellulaire et sa régulation. Bull Cancer 2006;41-53 [hors série]
    • (2006) Bull Cancer , pp. 41-53
    • Meijer, L.1
  • 11
    • 20844436307 scopus 로고    scopus 로고
    • Mechanism of Aurora B activation by INCENP and inhibition by hesperadin
    • Sessa F., Mapelli M., Ciferri C., Tarricone C., and Areces L.B. Mechanism of Aurora B activation by INCENP and inhibition by hesperadin. Mol Cell 18 (2005) 379-391
    • (2005) Mol Cell , vol.18 , pp. 379-391
    • Sessa, F.1    Mapelli, M.2    Ciferri, C.3    Tarricone, C.4    Areces, L.B.5
  • 13
    • 0032408639 scopus 로고    scopus 로고
    • Identification and characterization of STK12/Aik2: a human gene related to Aurora of Drosphila and yeast IPL1
    • Kimura M., Matsuda Y., Yoshioka T., Sumi N., and Okano Y. Identification and characterization of STK12/Aik2: a human gene related to Aurora of Drosphila and yeast IPL1. Cytogenet Cell Genet 82 (1998) 147-152
    • (1998) Cytogenet Cell Genet , vol.82 , pp. 147-152
    • Kimura, M.1    Matsuda, Y.2    Yoshioka, T.3    Sumi, N.4    Okano, Y.5
  • 14
    • 84859561032 scopus 로고    scopus 로고
    • Kinases Aurora as an anticancer target
    • Ikezoe T. Kinases Aurora as an anticancer target. Cancer Lett 262 (2008) 1-9
    • (2008) Cancer Lett , vol.262 , pp. 1-9
    • Ikezoe, T.1
  • 15
    • 0031764068 scopus 로고    scopus 로고
    • Protein kinase profile of sperm and eggs: cloning and characterization of two novels testis specific protein kinases (AIE1, AEI2) related to yeast and fly chromosome segregation regulators
    • Tseng T.C., Chen S.H., Hsu Y., and Tang T.K. Protein kinase profile of sperm and eggs: cloning and characterization of two novels testis specific protein kinases (AIE1, AEI2) related to yeast and fly chromosome segregation regulators. DNA Cell Biol 17 (1998) 823-833
    • (1998) DNA Cell Biol , vol.17 , pp. 823-833
    • Tseng, T.C.1    Chen, S.H.2    Hsu, Y.3    Tang, T.K.4
  • 16
    • 68949165641 scopus 로고    scopus 로고
    • Montembault E, Prigent C. Kinases Aurora: therapeutic potential. Drugs of the future. 2005:30. http://mandrake.med.univ-rennes1.fr/Intranet/projet_labo/publi_pdf/AUROR A %20 KINASES:%20THERAPEUTIC %20POTENTIAL.pdf consulté le 16 avril 2008.
    • Montembault E, Prigent C. Kinases Aurora: therapeutic potential. Drugs of the future. 2005:30. http://mandrake.med.univ-rennes1.fr/Intranet/projet_labo/publi_pdf/AUROR A %20 KINASES:%20THERAPEUTIC %20POTENTIAL.pdf consulté le 16 avril 2008.
  • 17
    • 33751426181 scopus 로고    scopus 로고
    • Aurora kinase inhibition downregulates NFKB and sensitises tumour cells to chemotherapeutic agents
    • Sun C., Chan F., Briassouli P., and Linardopoulos S. Aurora kinase inhibition downregulates NFKB and sensitises tumour cells to chemotherapeutic agents. Biochem Bioph Res Co 352 (2007) 220-225
    • (2007) Biochem Bioph Res Co , vol.352 , pp. 220-225
    • Sun, C.1    Chan, F.2    Briassouli, P.3    Linardopoulos, S.4
  • 18
    • 0030962953 scopus 로고    scopus 로고
    • A putative serine/threonine kinase encoding gene BTAK on chromosome 20q13 is amplified and overexpressed in human breast cancer cell lines
    • Sen S., Zhou H., and White R.A. A putative serine/threonine kinase encoding gene BTAK on chromosome 20q13 is amplified and overexpressed in human breast cancer cell lines. Oncogene 14 (1997) 2195-2200
    • (1997) Oncogene , vol.14 , pp. 2195-2200
    • Sen, S.1    Zhou, H.2    White, R.A.3
  • 19
    • 0038341158 scopus 로고    scopus 로고
    • The kinases Aurora: role in cell transformation and tumorigenesis
    • Katayama H., Brinkley W.R., and Sen S. The kinases Aurora: role in cell transformation and tumorigenesis. Cancer Metastasis Rev 22 (2003) 451-464
    • (2003) Cancer Metastasis Rev , vol.22 , pp. 451-464
    • Katayama, H.1    Brinkley, W.R.2    Sen, S.3
  • 20
    • 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 (2004) 55-62
    • (2004) Nat Genet , vol.36 , pp. 55-62
    • Katayama, H.1    Sasai, K.2    Kawai, H.3    Yuan, Z.M.4    Bondaruk, J.5    Suzuki, F.6
  • 21
    • 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 (2004) 52175-52182
    • (2004) J Biol Chem , vol.279 , pp. 52175-52182
    • Liu, Q.1    Kaneko, S.2    Yang, L.3    Feldman, R.I.4    Nicosia, S.V.5    Chen, J.6
  • 22
    • 1642361744 scopus 로고    scopus 로고
    • Overexpression and amplification of Aurora-A in hepatocellular carcinoma
    • Jeng M.Y., Peng S.Y., Lin C.Y., and Hsu H.C. Overexpression and amplification of Aurora-A in hepatocellular carcinoma. Clin Cancer Res 10 (2004) 2065-2071
    • (2004) Clin Cancer Res , vol.10 , pp. 2065-2071
    • Jeng, M.Y.1    Peng, S.Y.2    Lin, C.Y.3    Hsu, H.C.4
  • 23
    • 0037586498 scopus 로고    scopus 로고
    • AURORA-A amplification overrides the mitotic spindle assembly checkpoint, inducing resistance to Taxol
    • Anand S., Penrhyn-Lowe S., and Venkitaraman A.R. AURORA-A amplification overrides the mitotic spindle assembly checkpoint, inducing resistance to Taxol. Cancer Cell 3 (2003) 51-62
    • (2003) Cancer Cell , vol.3 , pp. 51-62
    • Anand, S.1    Penrhyn-Lowe, S.2    Venkitaraman, A.R.3
  • 24
    • 0037105758 scopus 로고    scopus 로고
    • Increased mitotic phosphorylation of histone H3 attributable to AIM-1/Aurora-B overexpression contributes to chromosome number instability
    • Ota T., Suto S., Katayama H., Han Z.B., Suzuki F., Maeda M., et al. Increased mitotic phosphorylation of histone H3 attributable to AIM-1/Aurora-B overexpression contributes to chromosome number instability. Cancer Res 62 (2002) 5168-5177
    • (2002) Cancer Res , vol.62 , pp. 5168-5177
    • Ota, T.1    Suto, S.2    Katayama, H.3    Han, Z.B.4    Suzuki, F.5    Maeda, M.6
  • 25
    • 0032213515 scopus 로고    scopus 로고
    • Multinuclearity and increased ploidy caused by overexpression of the Aurora and Ipl1-like midbody-associated protein mitotic kinase in human cancer cells
    • Tatsuka M., Katayama H., Ota T., Taraka T., Odashima S., Suzuki F., et al. Multinuclearity and increased ploidy caused by overexpression of the Aurora and Ipl1-like midbody-associated protein mitotic kinase in human cancer cells. Cancer Res 58 (1998) 4811-4816
    • (1998) Cancer Res , vol.58 , pp. 4811-4816
    • Tatsuka, M.1    Katayama, H.2    Ota, T.3    Taraka, T.4    Odashima, S.5    Suzuki, F.6
  • 26
    • 68949184298 scopus 로고    scopus 로고
    • 16 avril
    • http://www.crimsoncanary.com/Documents/Aurora_Kinase.pdf Consulté le 16 avril 2008.
    • (2008)
    • Consulté le1
  • 27
    • 68949187426 scopus 로고    scopus 로고
    • 12 novembre
    • http://www.pnas.org/content/104/10/4106/suppl/DC1 Consulté le 12 novembre 2008.
    • (2008)
    • Consulté le1
  • 28
    • 42749087793 scopus 로고    scopus 로고
    • Molecular docking/dynamics studies of Aurora A kinase inhibitors
    • Talele T., and McLaughlin M. Molecular docking/dynamics studies of Aurora A kinase inhibitors. J Mol Graph Model 26 (2008) 1213-1222
    • (2008) J Mol Graph Model , vol.26 , pp. 1213-1222
    • Talele, T.1    McLaughlin, M.2
  • 29
    • 2342639645 scopus 로고    scopus 로고
    • VX-680, a potent and selective small-molecule inhibitor of the Kinases Aurora suppresses tumor growth in vivo
    • Harrington E.A., Bebbington D., Moore J., Rasmussen R.K., Ajose-Adeogun A.Q., Nakayama T., et al. VX-680, a potent and selective small-molecule inhibitor of the Kinases Aurora suppresses tumor growth in vivo. Nat Med 10 (2004) 262-267
    • (2004) Nat Med , vol.10 , pp. 262-267
    • Harrington, E.A.1    Bebbington, D.2    Moore, J.3    Rasmussen, R.K.4    Ajose-Adeogun, A.Q.5    Nakayama, T.6
  • 30
    • 33750374052 scopus 로고    scopus 로고
    • A phase I clinical and pharmacokinetic trial of the Aurora kinase inhibitor MK-0457 in cancer patients
    • abstract 3008 18S
    • Rubin E.H., Shapiro G.I., and Stein MN. A phase I clinical and pharmacokinetic trial of the Aurora kinase inhibitor MK-0457 in cancer patients. J Clin Oncol 24 (2006) abstract 3008 18S
    • (2006) J Clin Oncol , vol.24
    • Rubin, E.H.1    Shapiro, G.I.2    Stein MN3
  • 32
    • 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 (2007) 500-502
    • (2007) Blood , vol.109 , pp. 500-502
    • Giles, F.J.1    Cortes, J.2    Jones, D.3    Bergstrom, D.4    Kantarjian, H.5    Freedman, S.J.6
  • 33
    • 34247615972 scopus 로고    scopus 로고
    • Structural basis for potent inhibition of the kinases Aurora and a T315I multi-drug resistant mutant form of Abl kinase by VX-680
    • Cheetman G.M.T., Charlton P.A., Golec J.M.C., and Pollard J.R. Structural basis for potent inhibition of the kinases Aurora and a T315I multi-drug resistant mutant form of Abl kinase by VX-680. Cancer Lett 251 (2007) 323-329
    • (2007) Cancer Lett , vol.251 , pp. 323-329
    • Cheetman, G.M.T.1    Charlton, P.A.2    Golec, J.M.C.3    Pollard, J.R.4
  • 35
    • 0347324949 scopus 로고    scopus 로고
    • Aurora -a kinase maintains the fidelity of early and late mitotic events in Hela cells
    • Marumoto T., Honda S., Hara T., Nitta M., Hirota T., Kohmura E., et al. Aurora -a kinase maintains the fidelity of early and late mitotic events in Hela cells. J Biol. Chem. 278 (2003) 51786-51795
    • (2003) J Biol. Chem. , vol.278 , pp. 51786-51795
    • Marumoto, T.1    Honda, S.2    Hara, T.3    Nitta, M.4    Hirota, T.5    Kohmura, E.6
  • 36
    • 34250201840 scopus 로고    scopus 로고
    • MLN8054, a small-molecule inhibitor of Aurora-A, causes spindle pole and chromosome congression defects leading to aneuploidy
    • Hoar K., Chakravarty A., Rabino C., Wysong D., Bowman D., Roy N., et al. MLN8054, a small-molecule inhibitor of Aurora-A, causes spindle pole and chromosome congression defects leading to aneuploidy. Mol Cell Biol 12 (2007) 4513-4525
    • (2007) Mol Cell Biol , vol.12 , pp. 4513-4525
    • Hoar, K.1    Chakravarty, A.2    Rabino, C.3    Wysong, D.4    Bowman, D.5    Roy, N.6
  • 37
    • 34347218996 scopus 로고    scopus 로고
    • Localization of human TACC3 to mitotic spindles is mediated by phosphorylation on Ser558 by Aurora A: a novel pharmacodynamic method for measuring Aurora A activity
    • LeRoy P.J., Hunter J.J., Hoar K.M., Burke K.E., Shinde V., Ruan J., et al. Localization of human TACC3 to mitotic spindles is mediated by phosphorylation on Ser558 by Aurora A: a novel pharmacodynamic method for measuring Aurora A activity. Cancer Res 67 (2007) 5362-5370
    • (2007) Cancer Res , vol.67 , pp. 5362-5370
    • LeRoy, P.J.1    Hunter, J.J.2    Hoar, K.M.3    Burke, K.E.4    Shinde, V.5    Ruan, J.6
  • 39
    • 34247603906 scopus 로고    scopus 로고
    • Discovery, synthesis, and in vivo activity of a new class of pyrazoloquinazolines as selective inhibitors of Aurora B kinase
    • Mortlock A.A., Foote K.M., Heron N.M., Jung F.H., Pasquet G., Lohmann, et al. Discovery, synthesis, and in vivo activity of a new class of pyrazoloquinazolines as selective inhibitors of Aurora B kinase. J Med Chem 50 (2007) 2213-2224
    • (2007) J Med Chem , vol.50 , pp. 2213-2224
    • Mortlock, A.A.1    Foote, K.M.2    Heron, N.M.3    Jung, F.H.4    Pasquet, G.5    Lohmann6
  • 40
    • 43449138516 scopus 로고    scopus 로고
    • Effects of the Aurora kinase inhibitors AZD1152-HQPA and ZM447439 on growth arrest and polyploidy in acute myeloid leukaemia cell lines and primary blasts
    • Walsby E., Walsh V., Pepper C., Burnett A., and Mills K. Effects of the Aurora kinase inhibitors AZD1152-HQPA and ZM447439 on growth arrest and polyploidy in acute myeloid leukaemia cell lines and primary blasts. Haematologica 93 (2008) 662-669
    • (2008) Haematologica , vol.93 , pp. 662-669
    • Walsby, E.1    Walsh, V.2    Pepper, C.3    Burnett, A.4    Mills, K.5
  • 41
    • 44349168457 scopus 로고    scopus 로고
    • Enhancement of radiation response in p-53-deficient cancer cells by the Aurora-B kinase inhibitor AZD1152
    • Tao Y., Zhang P., Girdler F., Frascogna V., Castedo M., Bourhis J., et al. Enhancement of radiation response in p-53-deficient cancer cells by the Aurora-B kinase inhibitor AZD1152. Oncogene 27 (2008) 3244-3255
    • (2008) Oncogene , vol.27 , pp. 3244-3255
    • Tao, Y.1    Zhang, P.2    Girdler, F.3    Frascogna, V.4    Castedo, M.5    Bourhis, J.6
  • 42
    • 38349108184 scopus 로고    scopus 로고
    • The selective Aurora B kinase inhibitor AZD1152 is a potential new treatment for multiple myeloma
    • Evans R.P., Naber C., Steffler T., Checkland T., Maxwell C.A., Keats J.J., et al. The selective Aurora B kinase inhibitor AZD1152 is a potential new treatment for multiple myeloma. Br J Haemotol 140 (2008) 295-302
    • (2008) Br J Haemotol , vol.140 , pp. 295-302
    • Evans, R.P.1    Naber, C.2    Steffler, T.3    Checkland, T.4    Maxwell, C.A.5    Keats, J.J.6
  • 43
    • 34548822673 scopus 로고    scopus 로고
    • AZD1152, a novel and selective Aurora B kinase inhibitor, induces growh arrest, apoptosis, and sensibilization for tubulin depolymerising agent or topoisomerase II inhibitor in human acute leukemia cells in vitro and in vivo
    • Yang J., Ikezoe T., Nishioka C., Tasaka T., Taniguchi A., Kuwayama Y., et al. AZD1152, a novel and selective Aurora B kinase inhibitor, induces growh arrest, apoptosis, and sensibilization for tubulin depolymerising agent or topoisomerase II inhibitor in human acute leukemia cells in vitro and in vivo. Blood 110 (2007) 2034-2040
    • (2007) Blood , vol.110 , pp. 2034-2040
    • Yang, J.1    Ikezoe, T.2    Nishioka, C.3    Tasaka, T.4    Taniguchi, A.5    Kuwayama, Y.6
  • 45
    • 34548548332 scopus 로고    scopus 로고
    • Crystal structure of the T315I Abl mutant in complex with the kinases Aurora inhibitor PHA-739358
    • Modugno M., Casale E., Soncini C., Rosettani P., Colombo R., Lupi R., et al. Crystal structure of the T315I Abl mutant in complex with the kinases Aurora inhibitor PHA-739358. Cancer Res 67 (2007) 7987-7990
    • (2007) Cancer Res , vol.67 , pp. 7987-7990
    • Modugno, M.1    Casale, E.2    Soncini, C.3    Rosettani, P.4    Colombo, R.5    Lupi, R.6
  • 46
    • 43249111278 scopus 로고    scopus 로고
    • Simultaneous targeting of kinases Aurora and Bcr-Abl kinase by the small molecule inhibitor PHA-739358 is effective against imatinib-resistant BCR-ABL mutations including T315I
    • Gontarewicz A., Balabano S., Keller G., Colombo R., Graziano A., Pesenti D., et al. Simultaneous targeting of kinases Aurora and Bcr-Abl kinase by the small molecule inhibitor PHA-739358 is effective against imatinib-resistant BCR-ABL mutations including T315I. Blood 111 (2008) 4355-4364
    • (2008) Blood , vol.111 , pp. 4355-4364
    • Gontarewicz, A.1    Balabano, S.2    Keller, G.3    Colombo, R.4    Graziano, A.5    Pesenti, D.6
  • 47
    • 42249115712 scopus 로고    scopus 로고
    • Combination of vascular endothelial growth factor receptor: platelet-derived growth factor receptor inhibition markedly improves radiation tumor therapy
    • Timke C., Zieher H., Roth A., Hauser K., Lipson K.E., Weber K.J., et al. Combination of vascular endothelial growth factor receptor: platelet-derived growth factor receptor inhibition markedly improves radiation tumor therapy. Clin Cancer Res 14 (2008) 2210-2219
    • (2008) Clin Cancer Res , vol.14 , pp. 2210-2219
    • Timke, C.1    Zieher, H.2    Roth, A.3    Hauser, K.4    Lipson, K.E.5    Weber, K.J.6
  • 48
    • 68949179718 scopus 로고    scopus 로고
    • 12 novembre
    • http://www.nci.nih.gov/Templates/drugdictionary.aspx?CdrID=489092 Consulté le 12 novembre 2008.
    • (2008)
    • Consulté le1
  • 49
    • 33947612000 scopus 로고    scopus 로고
    • Tyrosine kinase inhibitor SU6668 represses chondrosarcoma growth via antiangiogenesis in vivo
    • Klenke F.M., Abdollahi A., Bertl E., Gebhard M.M., Ewerbeck V., Huber P.E., et al. Tyrosine kinase inhibitor SU6668 represses chondrosarcoma growth via antiangiogenesis in vivo. BMC Cancer 7 (2007) 49
    • (2007) BMC Cancer , vol.7 , pp. 49
    • Klenke, F.M.1    Abdollahi, A.2    Bertl, E.3    Gebhard, M.M.4    Ewerbeck, V.5    Huber, P.E.6
  • 50
    • 23044510618 scopus 로고    scopus 로고
    • Proteomic characterization of the angiogenesis inhibitor SU6668 reveals multiple impacts on cellular kinase signalling
    • Godl K., Gruss O.J., Eickhoff J., Wissing J., Blencke S., Weber M., et al. Proteomic characterization of the angiogenesis inhibitor SU6668 reveals multiple impacts on cellular kinase signalling. Cancer Res 65 (2005) 6919-6926
    • (2005) Cancer Res , vol.65 , pp. 6919-6926
    • Godl, K.1    Gruss, O.J.2    Eickhoff, J.3    Wissing, J.4    Blencke, S.5    Weber, M.6
  • 51
    • 34548506467 scopus 로고    scopus 로고
    • Tumor-host interaction in the optimization of paclitaxel-based combination therapies with vascular targeting compounds
    • Giavazzi R., Bani M.R., and Taraboletti G. Tumor-host interaction in the optimization of paclitaxel-based combination therapies with vascular targeting compounds. Cancer Metastasis Rev 26 (2007) 481-488
    • (2007) Cancer Metastasis Rev , vol.26 , pp. 481-488
    • Giavazzi, R.1    Bani, M.R.2    Taraboletti, G.3
  • 52
    • 34247490648 scopus 로고    scopus 로고
    • Pathological animal models in the experimental evaluation of tumour microvasculature with magnetic resonance imaging
    • Faccioli N., Marzola P., Boschi F., D'Onofrio M., and Pozzi Mucelli R. Pathological animal models in the experimental evaluation of tumour microvasculature with magnetic resonance imaging. Radiol Med 112 (2007) 319-328
    • (2007) Radiol Med , vol.112 , pp. 319-328
    • Faccioli, N.1    Marzola, P.2    Boschi, F.3    D'Onofrio, M.4    Pozzi Mucelli, R.5
  • 53
    • 68949174931 scopus 로고    scopus 로고
    • Effect of endostatine and SU6668 combined with 5-FU on human colon cancer xenograft in nude mice
    • Zeng Q.L., Chu Z.H., Zhou K., and Luo X.J. Effect of endostatine and SU6668 combined with 5-FU on human colon cancer xenograft in nude mice. Zonghua Wei Chang Wai Ke Za Zhi 11 (2008) 376-378
    • (2008) Zonghua Wei Chang Wai Ke Za Zhi , vol.11 , pp. 376-378
    • Zeng, Q.L.1    Chu, Z.H.2    Zhou, K.3    Luo, X.J.4
  • 54
    • 70249100515 scopus 로고    scopus 로고
    • Phase I and pharmacodynamic trial of AT9283, an aurora kinase inhibitor refractory leukaemia
    • Foran J.M., Ravandi F., O'Brien S.M., Borthakur G., Rios M., et al. Phase I and pharmacodynamic trial of AT9283, an aurora kinase inhibitor refractory leukaemia. Journal of clinical oncology 26 (2008) 2008-2518
    • (2008) Journal of clinical oncology , vol.26 , pp. 2008-2518
    • Foran, J.M.1    Ravandi, F.2    O'Brien, S.M.3    Borthakur, G.4    Rios, M.5
  • 55
    • 34250771649 scopus 로고    scopus 로고
    • À novel treatment strategy targeting kinases Aurora in acute myelogenous leukemia
    • Ikezoe T., Yang J., Nishioka C., Tasaka T., Tanigucchi A., Kuwayama Y., et al. À novel treatment strategy targeting kinases Aurora in acute myelogenous leukemia. Mol Cancer Ther 6 (2007) 1851-1857
    • (2007) Mol Cancer Ther , vol.6 , pp. 1851-1857
    • Ikezoe, T.1    Yang, J.2    Nishioka, C.3    Tasaka, T.4    Tanigucchi, A.5    Kuwayama, Y.6
  • 56
    • 68949165639 scopus 로고    scopus 로고
    • Aurora kinase inhibitor ZM447439 blocks chromosome-induced spindle assembly, the completion of chromosome condensation, and the etablishment of the spindle integrity checkpoint in xenopus egg extracts
    • Gadea B.B., and Ruderman J.V. Aurora kinase inhibitor ZM447439 blocks chromosome-induced spindle assembly, the completion of chromosome condensation, and the etablishment of the spindle integrity checkpoint in xenopus egg extracts. Mol Cell Biomech 10 (2004) 1091
    • (2004) Mol Cell Biomech , vol.10 , pp. 1091
    • Gadea, B.B.1    Ruderman, J.V.2


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