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Volumn 2, Issue 4, 2007, Pages 539-560

Targeting cell cycle kinases and kinesins in anticancer drug development

Author keywords

Aurora kinase; Cell cycle; Checkpoint inhibitors; Cyclin dependent kinase; Mitotic kinesins; Polo like kinase

Indexed keywords

7 HYDROXYSTAUROSPORINE; ANTINEOPLASTIC AGENT; BUTYROLACTONE; CARBOPLATIN; CELL CYCLE PROTEIN; CHECKPOINT KINASE 1; CISPLATIN; CYCLIN DEPENDENT KINASE; CYCLIN DEPENDENT KINASE INHIBITOR; CYCLINE; DOCETAXEL; FLAVOPIRIDOL; FLUOROURACIL; GAMMA GLUTAMYLTRANSFERASE; GEMCITABINE; INDIRUBIN; INDISULAM; IRINOTECAN; KINESIN; MITOXANTRONE; N [5 (5 TERT BUTYL 2 OXAZOLYLMETHYLTHIO) 2 THIAZOLYL]ISONIPECOTAMIDE; PACLITAXEL; PAULLONE DERIVATIVE; PD 0332991; PHOSPHOTRANSFERASE; ROSCOVITINE; STAUROSPORINE; TOPOTECAN; UNCLASSIFIED DRUG; UNINDEXED DRUG; ZK 304709;

EID: 34447503273     PISSN: 17460441     EISSN: None     Source Type: Journal    
DOI: 10.1517/17460441.2.4.539     Document Type: Review
Times cited : (12)

References (217)
  • 1
    • 0034614637 scopus 로고    scopus 로고
    • The hallmarks of cancer
    • HANAHAN D, WEINBERG RA: The hallmarks of cancer. Cell (2000) 100:57-70.
    • (2000) Cell , vol.100 , pp. 57-70
    • HANAHAN, D.1    WEINBERG, R.A.2
  • 2
    • 0036220822 scopus 로고    scopus 로고
    • Complexities in the development of cyclin-dependent kinase inhibitor drugs
    • SAUSVILLE EA: Complexities in the development of cyclin-dependent kinase inhibitor drugs. Trends Mol. Med. (2002) 8:S32-37.
    • (2002) Trends Mol. Med , vol.8
    • SAUSVILLE, E.A.1
  • 3
    • 18744377748 scopus 로고    scopus 로고
    • Drugging cell cycle kinases in cancer therapy
    • BLAGDEN S, DE BONO J: Drugging cell cycle kinases in cancer therapy. Curr. Drug Targets (2005) 6:325-335.
    • (2005) Curr. Drug Targets , vol.6 , pp. 325-335
    • BLAGDEN, S.1    DE BONO, J.2
  • 5
    • 0034654378 scopus 로고    scopus 로고
    • Cyclin F regulates the nuclear localization of cyclin B1 through a cyclin-cyclin interaction
    • KONG M, BARNES EA, OLLENDORFF V, DONOGHUE DJ: Cyclin F regulates the nuclear localization of cyclin B1 through a cyclin-cyclin interaction. Embo. J. (2000) 19:1378-1388.
    • (2000) Embo. J , vol.19 , pp. 1378-1388
    • KONG, M.1    BARNES, E.A.2    OLLENDORFF, V.3    DONOGHUE, D.J.4
  • 6
    • 0016793098 scopus 로고
    • Genetic control of cell size at cell division in yeast
    • NURSE P: Genetic control of cell size at cell division in yeast. Nature (1975) 256:547-551.
    • (1975) Nature , vol.256 , pp. 547-551
    • NURSE, P.1
  • 7
    • 0015076873 scopus 로고
    • Cytoplasmic control of nuclear behavior during meiotic maturation of frog oocytes
    • MASUI Y, MARKERT CL: Cytoplasmic control of nuclear behavior during meiotic maturation of frog oocytes. J. Exp. Zool. (1971) 177:129-145.
    • (1971) J. Exp. Zool , vol.177 , pp. 129-145
    • MASUI, Y.1    MARKERT, C.L.2
  • 8
    • 0015080763 scopus 로고
    • The interaction of steroids with rana pipiens oocytes in the induction of maturation
    • SMITH LD, ECKER RE: The interaction of steroids with rana pipiens oocytes in the induction of maturation. Dev. Biol. (1971) 25:232-247.
    • (1971) Dev. Biol , vol.25 , pp. 232-247
    • SMITH, L.D.1    ECKER, R.E.2
  • 9
    • 0020622592 scopus 로고
    • Formation in vitro of sperm pronuclei and mitotic chromosomes induced by amphibian ooplasmic components
    • LOHKA MJ, MASUI Y: Formation in vitro of sperm pronuclei and mitotic chromosomes induced by amphibian ooplasmic components. Science (1983) 220:719-721.
    • (1983) Science , vol.220 , pp. 719-721
    • LOHKA, M.J.1    MASUI, Y.2
  • 10
    • 0031951182 scopus 로고    scopus 로고
    • Functional inactivation of the retinoblastoma protein requires sequential modification by at least two distinct cyclin-cdk complexes
    • LUNDBERG AS, WEINBERG RA: Functional inactivation of the retinoblastoma protein requires sequential modification by at least two distinct cyclin-cdk complexes. Mol. Cell Biol. (1998) 18:753-761.
    • (1998) Mol. Cell Biol , vol.18 , pp. 753-761
    • LUNDBERG, A.S.1    WEINBERG, R.A.2
  • 11
    • 0033578816 scopus 로고    scopus 로고
    • CDK phosphorylation triggers sequential intramolecular interactions that progressively block Rb functions as cells move through G1
    • HARBOUR JW, LUO RX, DEI SANTI A et al.: CDK phosphorylation triggers sequential intramolecular interactions that progressively block Rb functions as cells move through G1. Cell (1999) 98:859-869.
    • (1999) Cell , vol.98 , pp. 859-869
    • HARBOUR, J.W.1    LUO, R.X.2    DEI SANTI, A.3
  • 12
    • 0028171292 scopus 로고
    • G1 phase progression: Cycling on cue
    • SHERR CJ: G1 phase progression: cycling on cue. Cell (1994) 79:551-555.
    • (1994) Cell , vol.79 , pp. 551-555
    • SHERR, C.J.1
  • 13
    • 0026176336 scopus 로고
    • Cyclins: Wheels within wheels
    • PINES J: Cyclins: wheels within wheels. Cell Growth Differ. (1991) 2:305-310.
    • (1991) Cell Growth Differ , vol.2 , pp. 305-310
    • PINES, J.1
  • 14
    • 0028988585 scopus 로고
    • Inhibitors of mammalian G1 cyclin-dependent kinases
    • SHERR CJ, ROBERTS JM: Inhibitors of mammalian G1 cyclin-dependent kinases. Genes Dev. (1995) 9:1149-1163.
    • (1995) Genes Dev , vol.9 , pp. 1149-1163
    • SHERR, C.J.1    ROBERTS, J.M.2
  • 15
    • 0032004973 scopus 로고    scopus 로고
    • The role of Cdk7 in CAK function, a retro-retrospective
    • HARPER JW, ELLEDGE SJ: The role of Cdk7 in CAK function, a retro-retrospective. Genes Dev. (1998) 12:285-289.
    • (1998) Genes Dev , vol.12 , pp. 285-289
    • HARPER, J.W.1    ELLEDGE, S.J.2
  • 16
    • 0033919678 scopus 로고    scopus 로고
    • Analysis of CAK activities from human cells
    • KALDIS P, SOLOMON MJ: Analysis of CAK activities from human cells. Eur. J. Biochem. (2000) 267:4213-4221.
    • (2000) Eur. J. Biochem , vol.267 , pp. 4213-4221
    • KALDIS, P.1    SOLOMON, M.J.2
  • 18
    • 22344456265 scopus 로고    scopus 로고
    • A structural perspective of CTD function
    • MEINHART A, KAMENSKI T, HOEPPNER S et al.: A structural perspective of CTD function. Genes Dev. (2005) 19:1401-1415.
    • (2005) Genes Dev , vol.19 , pp. 1401-1415
    • MEINHART, A.1    KAMENSKI, T.2    HOEPPNER, S.3
  • 19
    • 0036545816 scopus 로고    scopus 로고
    • RNA polymerase II carboxy-terminal domain kinases: Emerging clues to their function
    • PRELICH G: RNA polymerase II carboxy-terminal domain kinases: emerging clues to their function. Eukaryot. Cell (2002) 1:153-162.
    • (2002) Eukaryot. Cell , vol.1 , pp. 153-162
    • PRELICH, G.1
  • 20
    • 0031847296 scopus 로고    scopus 로고
    • Cdk2/cdc2 expression in colon carcinogenesis and effects of cdk2/cdc2 inhibitor in colon cancer cells
    • YAMAMOTO H, MONDEN T, MIYOSHI H et al.: Cdk2/cdc2 expression in colon carcinogenesis and effects of cdk2/cdc2 inhibitor in colon cancer cells. Int. J. Oncol. (1998) 13:233-239.
    • (1998) Int. J. Oncol , vol.13 , pp. 233-239
    • YAMAMOTO, H.1    MONDEN, T.2    MIYOSHI, H.3
  • 21
    • 0031686141 scopus 로고    scopus 로고
    • Active cyclin A-Cdk2 complex, a possible critical factor for cell proliferation in human primary lung carcinomas
    • DOBASHI Y, SHOJI M, JIANG SX et al.: Active cyclin A-Cdk2 complex, a possible critical factor for cell proliferation in human primary lung carcinomas. Am. J. Pathol. (1998) 153:963-972.
    • (1998) Am. J. Pathol , vol.153 , pp. 963-972
    • DOBASHI, Y.1    SHOJI, M.2    JIANG, S.X.3
  • 22
    • 0041854279 scopus 로고    scopus 로고
    • Cyclin-dependent kinase 2 is essential for meiosis but not for mitotic cell division in mice
    • ORTEGA S, PRIETO I, ODAJIMA J et al.: Cyclin-dependent kinase 2 is essential for meiosis but not for mitotic cell division in mice. Nat. Genet. (2003) 35:25-31.
    • (2003) Nat. Genet , vol.35 , pp. 25-31
    • ORTEGA, S.1    PRIETO, I.2    ODAJIMA, J.3
  • 23
    • 0041327168 scopus 로고    scopus 로고
    • Proliferation of cancer cells despite Cdk2 inhibition
    • TETSU O, MCCORMICK F: Proliferation of cancer cells despite Cdk2 inhibition. Cancer Cell (2003) 3:233-245.
    • (2003) Cancer Cell , vol.3 , pp. 233-245
    • TETSU, O.1    MCCORMICK, F.2
  • 24
    • 0029398189 scopus 로고
    • Gene amplification in human gliomas
    • COLLINS VP: Gene amplification in human gliomas. Glia. (1995) 15:289-296.
    • (1995) Glia , vol.15 , pp. 289-296
    • COLLINS, V.P.1
  • 25
    • 0027978368 scopus 로고
    • Amplification of multiple genes from chromosomal region 12q13-14 in human malignant gliomas: Preliminary mapping of the amplicons shows preferential involvement of Cdk4, SAS, and MDM2
    • REIFENBERGER G, REIFENBERGER J, ICHIMURA K et al.: Amplification of multiple genes from chromosomal region 12q13-14 in human malignant gliomas: preliminary mapping of the amplicons shows preferential involvement of Cdk4, SAS, and MDM2. Cancer Res (1994) 54:4299-4303.
    • (1994) Cancer Res , vol.54 , pp. 4299-4303
    • REIFENBERGER, G.1    REIFENBERGER, J.2    ICHIMURA, K.3
  • 26
    • 0032919173 scopus 로고    scopus 로고
    • Gene amplification and overexpression of Cdk4 in sporadic breast carcinomas is associated with high tumor cell proliferation
    • AN HX, BECKMANN MW, REIFENBERGER G et al.: Gene amplification and overexpression of Cdk4 in sporadic breast carcinomas is associated with high tumor cell proliferation. Am. J. Pathol. (1999) 154:113-118.
    • (1999) Am. J. Pathol , vol.154 , pp. 113-118
    • AN, H.X.1    BECKMANN, M.W.2    REIFENBERGER, G.3
  • 27
    • 19944429304 scopus 로고    scopus 로고
    • Cdk4 is a probable target gene in a novel amplicon at 12q13.3-q14.1 in lung cancer
    • WIKMAN H, NYMARK P, VAYRYNEN A et al.: Cdk4 is a probable target gene in a novel amplicon at 12q13.3-q14.1 in lung cancer. Genes Chrom. Can. (2005) 42:193-199.
    • (2005) Genes Chrom. Can , vol.42 , pp. 193-199
    • WIKMAN, H.1    NYMARK, P.2    VAYRYNEN, A.3
  • 28
    • 0035032709 scopus 로고    scopus 로고
    • Dedifferentiation of a well-differentiated liposarcoma to a highly malignant metastatic osteosarcoma: Amplification of 12q14 at all stages and gain of 1q22-q24 associated with metastases
    • FORUS A, LARRAMENDY ML, MEZA-ZEPEDA LA et al.: Dedifferentiation of a well-differentiated liposarcoma to a highly malignant metastatic osteosarcoma: amplification of 12q14 at all stages and gain of 1q22-q24 associated with metastases. Cancer Genet. Cytogenet. (2001) 125:100-111.
    • (2001) Cancer Genet. Cytogenet , vol.125 , pp. 100-111
    • FORUS, A.1    LARRAMENDY, M.L.2    MEZA-ZEPEDA, L.A.3
  • 29
    • 0027454445 scopus 로고
    • Coamplification of the Cdk4 gene with MDM2 and GLI in human sarcomas
    • KHATIB ZA, MATSUSHIME H, VALENTINE M et al.: Coamplification of the Cdk4 gene with MDM2 and GLI in human sarcomas. Cancer Res. (1993) 53:5535-5541.
    • (1993) Cancer Res , vol.53 , pp. 5535-5541
    • KHATIB, Z.A.1    MATSUSHIME, H.2    VALENTINE, M.3
  • 30
    • 0035963435 scopus 로고    scopus 로고
    • Specific protection against breast cancers by cyclin D1 ablation
    • YU Q, GENG Y, SICINSKI P: Specific protection against breast cancers by cyclin D1 ablation. Nature (2001) 411:1017-1021.
    • (2001) Nature , vol.411 , pp. 1017-1021
    • YU, Q.1    GENG, Y.2    SICINSKI, P.3
  • 31
    • 1242293761 scopus 로고    scopus 로고
    • The role of the cyclin D1-dependent kinases in ErbB2-mediated breast cancer
    • YANG C, IONESCU-TIBA V, BURNS K et al.: The role of the cyclin D1-dependent kinases in ErbB2-mediated breast cancer. Am. J. Pathol. (2004) 164:1031-1038.
    • (2004) Am. J. Pathol , vol.164 , pp. 1031-1038
    • YANG, C.1    IONESCU-TIBA, V.2    BURNS, K.3
  • 32
    • 30344479175 scopus 로고    scopus 로고
    • Cyclin D1-dependent kinase activity in murine development and mammary tumorigenesis
    • LANDIS MW, PAWLYK BS, LI T et al.: Cyclin D1-dependent kinase activity in murine development and mammary tumorigenesis. Cancer Cell (2006) 9:13-22.
    • (2006) Cancer Cell , vol.9 , pp. 13-22
    • LANDIS, M.W.1    PAWLYK, B.S.2    LI, T.3
  • 33
    • 30344470210 scopus 로고    scopus 로고
    • Requirement for Cdk4 kinase function in breast cancer
    • YU Q, SICINSKA E, GENG Y et al.: Requirement for Cdk4 kinase function in breast cancer. Cancer Cell (2006) 9:23-32.
    • (2006) Cancer Cell , vol.9 , pp. 23-32
    • YU, Q.1    SICINSKA, E.2    GENG, Y.3
  • 34
    • 0242708738 scopus 로고    scopus 로고
    • Small-molecule cyclin-dependent kinase modulators
    • SENDEROWICZ AM: Small-molecule cyclin-dependent kinase modulators. Oncogene (2003) 22:6609-6620.
    • (2003) Oncogene , vol.22 , pp. 6609-6620
    • SENDEROWICZ, A.M.1
  • 35
    • 0034162636 scopus 로고    scopus 로고
    • Preclinical and clinical development of cyclin-dependent kinase modulators
    • SENDEROWICZ AM, SAUSVILLE EA: Preclinical and clinical development of cyclin-dependent kinase modulators. J. Natl. Cancer Inst. (2000) 92:376-387.
    • (2000) J. Natl. Cancer Inst , vol.92 , pp. 376-387
    • SENDEROWICZ, A.M.1    SAUSVILLE, E.A.2
  • 36
    • 0033568521 scopus 로고    scopus 로고
    • Down-regulation of cyclin D1 by transcriptional repression in MCF-7 human breast carcinoma cells induced by flavopiridol
    • CARLSON B, LAHUSEN T, SINGH S et al.: Down-regulation of cyclin D1 by transcriptional repression in MCF-7 human breast carcinoma cells induced by flavopiridol. Cancer Res. (1999) 59:4634-4641.
    • (1999) Cancer Res , vol.59 , pp. 4634-4641
    • CARLSON, B.1    LAHUSEN, T.2    SINGH, S.3
  • 37
    • 0032212885 scopus 로고    scopus 로고
    • Flavopiridol, a novel cyclin-dependent kinase inhibitor, suppresses the growth of head and neck squamous cell carcinomas by inducing apoptosis
    • PATEL V, SENDEROWICZ AM, PINTO D Jr: et al.: Flavopiridol, a novel cyclin-dependent kinase inhibitor, suppresses the growth of head and neck squamous cell carcinomas by inducing apoptosis. J. Clin. Invest. (1998) 102:1674-1681.
    • (1998) J. Clin. Invest , vol.102 , pp. 1674-1681
    • PATEL, V.1    SENDEROWICZ, A.M.2    PINTO Jr, D.3
  • 38
    • 2942582482 scopus 로고    scopus 로고
    • Flavopiridol: Pleiotropic biological effects enhance its anti-cancer activity
    • NEWCOMB EW: Flavopiridol: pleiotropic biological effects enhance its anti-cancer activity. Anticancer Drugs (2004) 15:411-419.
    • (2004) Anticancer Drugs , vol.15 , pp. 411-419
    • NEWCOMB, E.W.1
  • 39
    • 0029895439 scopus 로고    scopus 로고
    • UCN-01: A potent abrogator of G2 checkpoint function in cancer cells with disrupted p53
    • WANG Q, FAN S, EASTMAN A et al.: UCN-01: a potent abrogator of G2 checkpoint function in cancer cells with disrupted p53. J. Natl. Cancer Inst. (1996) 88:956-965.
    • (1996) J. Natl. Cancer Inst , vol.88 , pp. 956-965
    • WANG, Q.1    FAN, S.2    EASTMAN, A.3
  • 40
    • 0034655281 scopus 로고    scopus 로고
    • The radiosensitizing agent 7-hydroxystaurosporine (UCN-01) inhibits the DNA damage checkpoint kinase hChk1
    • BUSBY EC, LEISTRITZ DF, ABRAHAM RT et al.: The radiosensitizing agent 7-hydroxystaurosporine (UCN-01) inhibits the DNA damage checkpoint kinase hChk1. Cancer Res. (2000) 60:2108-2112.
    • (2000) Cancer Res , vol.60 , pp. 2108-2112
    • BUSBY, E.C.1    LEISTRITZ, D.F.2    ABRAHAM, R.T.3
  • 41
    • 0037108873 scopus 로고    scopus 로고
    • UCN-01 inhibits p53 up-regulation and abrogates gamma-radiation-induced G(2)-M checkpoint independently of p53 by targeting both of the checkpoint kinases, Chk2 and Chk1
    • YU Q, LA ROSE J, ZHANG H et al.: UCN-01 inhibits p53 up-regulation and abrogates gamma-radiation-induced G(2)-M checkpoint independently of p53 by targeting both of the checkpoint kinases, Chk2 and Chk1. Cancer Res (2002) 62:5743-5748.
    • (2002) Cancer Res , vol.62 , pp. 5743-5748
    • YU, Q.1    LA ROSE, J.2    ZHANG, H.3
  • 42
    • 0037034928 scopus 로고    scopus 로고
    • Interference with PDK1-Akt survival signaling pathway by UCN-01 (7-hydroxystaurosporine)
    • SATO S, FUJITA N, TSURUO T: Interference with PDK1-Akt survival signaling pathway by UCN-01 (7-hydroxystaurosporine). Oncogene (2002) 21:1727-1738.
    • (2002) Oncogene , vol.21 , pp. 1727-1738
    • SATO, S.1    FUJITA, N.2    TSURUO, T.3
  • 43
    • 31544452150 scopus 로고    scopus 로고
    • Phase I trial of UCN-01 in combination with topotecan in patients with advanced solid cancers: A Princess Margaret Hospital Phase II Consortium study
    • HOTTE SJ, OZA A, WINQUIST EW et al.: Phase I trial of UCN-01 in combination with topotecan in patients with advanced solid cancers: a Princess Margaret Hospital Phase II Consortium study. Ann. Oncol. (2006) 17:334-340.
    • (2006) Ann. Oncol , vol.17 , pp. 334-340
    • HOTTE, S.J.1    OZA, A.2    WINQUIST, E.W.3
  • 44
    • 0034773165 scopus 로고    scopus 로고
    • E7070, a novel sulphonamide agent with potent antitumour activity in vitro and in vivo
    • OZAWA Y, SUGI NH, NAGASU T et al.: E7070, a novel sulphonamide agent with potent antitumour activity in vitro and in vivo. Eur. J. Cancer (2001) 37:2275-2282.
    • (2001) Eur. J. Cancer , vol.37 , pp. 2275-2282
    • OZAWA, Y.1    SUGI, N.H.2    NAGASU, T.3
  • 45
    • 1642494839 scopus 로고    scopus 로고
    • The cyclin-dependent kinase inhibitor CYC202 (R-roscovitine) inhibits retinoblastoma protein phosphorylation, causes loss of cyclin D1, and activates the mitogen-activated protein kinase pathway
    • WHITTAKER SR, WALTON MI, GARRETT MD, WORKMAN P: The cyclin-dependent kinase inhibitor CYC202 (R-roscovitine) inhibits retinoblastoma protein phosphorylation, causes loss of cyclin D1, and activates the mitogen-activated protein kinase pathway. Cancer Res. (2004) 64:262-272.
    • (2004) Cancer Res , vol.64 , pp. 262-272
    • WHITTAKER, S.R.1    WALTON, M.I.2    GARRETT, M.D.3    WORKMAN, P.4
  • 46
    • 0037058678 scopus 로고    scopus 로고
    • In vitro and in vivo antitumor properties of the cyclin dependent kinase inhibitor CYC202 (R-roscovitine)
    • MCCLUE SJ, BLAKE D, CLARKE R et al.: In vitro and in vivo antitumor properties of the cyclin dependent kinase inhibitor CYC202 (R-roscovitine). Int. J. Cancer (2002) 102:463-468.
    • (2002) Int. J. Cancer , vol.102 , pp. 463-468
    • MCCLUE, S.J.1    BLAKE, D.2    CLARKE, R.3
  • 47
    • 33845915536 scopus 로고    scopus 로고
    • Roscovitine regulates invasive breast cancer cell (MDA-MB231) proliferation and survival through cell cycle regulatory protein Cdk5
    • GOODYEAR S, SHARMA MC: Roscovitine regulates invasive breast cancer cell (MDA-MB231) proliferation and survival through cell cycle regulatory protein Cdk5. Exp. Mol. Pathol. (2006) 82(1):25-32.
    • (2006) Exp. Mol. Pathol , vol.82 , Issue.1 , pp. 25-32
    • GOODYEAR, S.1    SHARMA, M.C.2
  • 48
    • 27644591251 scopus 로고    scopus 로고
    • In vitro and in vivo pharmacokinetic-pharmacodynamic relationships for the trisubstituted aminopurine cyclin-dependent kinase inhibitors olomoucine, bohemine and CYC202
    • RAYNAUD FI, WHITTAKER SR, FISCHER PM et al.: In vitro and in vivo pharmacokinetic-pharmacodynamic relationships for the trisubstituted aminopurine cyclin-dependent kinase inhibitors olomoucine, bohemine and CYC202. Clin. Cancer Res. (2005) 11:4875-4887.
    • (2005) Clin. Cancer Res , vol.11 , pp. 4875-4887
    • RAYNAUD, F.I.1    WHITTAKER, S.R.2    FISCHER, P.M.3
  • 49
    • 14044257773 scopus 로고    scopus 로고
    • Roscovitine-induced up-regulation of p53AIP1 protein precedes the onset of apoptosis in human MCF-7 breast cancer cells
    • WESIERSKA-GADEK J, GUEORGUIEVA M, HORKY M: Roscovitine-induced up-regulation of p53AIP1 protein precedes the onset of apoptosis in human MCF-7 breast cancer cells. Mol. Cancer Ther. (2005) 4:113-124.
    • (2005) Mol. Cancer Ther , vol.4 , pp. 113-124
    • WESIERSKA-GADEK, J.1    GUEORGUIEVA, M.2    HORKY, M.3
  • 50
    • 33847045212 scopus 로고    scopus 로고
    • Roscovitine-activated HIP2 kinase induces phosphorylation of wt p53 at Ser-46 in human MCF-7 breast cancer cells
    • WESIERSKA-GADEK J, SCHMITZ ML, RANFTLER C: Roscovitine-activated HIP2 kinase induces phosphorylation of wt p53 at Ser-46 in human MCF-7 breast cancer cells. J. Cell Biochem. (2007) 100:865-874.
    • (2007) J. Cell Biochem , vol.100 , pp. 865-874
    • WESIERSKA-GADEK, J.1    SCHMITZ, M.L.2    RANFTLER, C.3
  • 51
    • 12144285797 scopus 로고    scopus 로고
    • N-(cycloalkylamino)acyl-2-aminothiazole inhibitors of cyclin-dependent kinase 2. N-[5- [5-(1,1-dimethylethyl)-2-oxazolyl]m ethyl]thio]-2-thiazolyl]-4-piperidinecarboxamide (BMS-387032), a highly efficacious and selective antitumor agent
    • MISRA RN, XIAO HY, KIM KS et al.: N-(cycloalkylamino)acyl-2-aminothiazole inhibitors of cyclin-dependent kinase 2. N-[5- [5-(1,1-dimethylethyl)-2-oxazolyl]m ethyl]thio]-2-thiazolyl]-4-piperidinecarboxamide (BMS-387032), a highly efficacious and selective antitumor agent. J. Med. Chem. (2004) 47:1719-1728.
    • (2004) J. Med. Chem , vol.47 , pp. 1719-1728
    • MISRA, R.N.1    XIAO, H.Y.2    KIM, K.S.3
  • 52
    • 33747128468 scopus 로고    scopus 로고
    • Molecular and pharmacodynamic characteristics of the novel multi-target tumor growth Inhibitor ZK-304709
    • SIEMEISTER G, LUECKING U, WAGNER C et al.: Molecular and pharmacodynamic characteristics of the novel multi-target tumor growth Inhibitor ZK-304709. Biomed. Pharmacother. (2006) 60:269-272.
    • (2006) Biomed. Pharmacother , vol.60 , pp. 269-272
    • SIEMEISTER, G.1    LUECKING, U.2    WAGNER, C.3
  • 53
    • 20244365948 scopus 로고    scopus 로고
    • Discovery of a potent and selective inhibitor of cyclin-dependent kinase 4/6
    • TOOGOOD PL, HARVEY PJ, REPINE JT et al.: Discovery of a potent and selective inhibitor of cyclin-dependent kinase 4/6. J. Med. Chem. (2005) 48:2388-2406.
    • (2005) J. Med. Chem , vol.48 , pp. 2388-2406
    • TOOGOOD, P.L.1    HARVEY, P.J.2    REPINE, J.T.3
  • 54
    • 33645802169 scopus 로고    scopus 로고
    • CYCLIN-dependent kinase pathways as targets for cancer treatment
    • SHAPIRO GI: CYCLIN-dependent kinase pathways as targets for cancer treatment. J. Clin. Oncol. (2006) 24:1770-1783.
    • (2006) J. Clin. Oncol , vol.24 , pp. 1770-1783
    • SHAPIRO, G.I.1
  • 55
    • 9444228344 scopus 로고    scopus 로고
    • Specific inhibition of cyclin-dependent kinase 4/6 by PD 0332991 and associated antitumor activity in human tumor xenografts
    • FRY DW, HARVEY PJ, KELLER PR et al.: Specific inhibition of cyclin-dependent kinase 4/6 by PD 0332991 and associated antitumor activity in human tumor xenografts. Mol. Cancer Ther. (2004) 3:1427-1438.
    • (2004) Mol. Cancer Ther , vol.3 , pp. 1427-1438
    • FRY, D.W.1    HARVEY, P.J.2    KELLER, P.R.3
  • 56
    • 0031670668 scopus 로고    scopus 로고
    • Phase I trial of continuous infusion flavopiridol, a novel cyclin-dependent kinase inhibitor, in patients with refractory neoplasms
    • SENDEROWICZ AM, HEADLEE D, STINSON SF et al.: Phase I trial of continuous infusion flavopiridol, a novel cyclin-dependent kinase inhibitor, in patients with refractory neoplasms. J. Clin. Oncol. (1998) 16:2986-2999.
    • (1998) J. Clin. Oncol , vol.16 , pp. 2986-2999
    • SENDEROWICZ, A.M.1    HEADLEE, D.2    STINSON, S.F.3
  • 57
    • 0036450831 scopus 로고    scopus 로고
    • Phase I clinical and pharmacokinetic trial of the cyclin-dependent kinase inhibitor flavopiridol
    • THOMAS JP, TUTSCH KD, CLEARY JF et al.: Phase I clinical and pharmacokinetic trial of the cyclin-dependent kinase inhibitor flavopiridol. Cancer Chemother. Pharmacol. (2002) 50:465-472.
    • (2002) Cancer Chemother. Pharmacol , vol.50 , pp. 465-472
    • THOMAS, J.P.1    TUTSCH, K.D.2    CLEARY, J.F.3
  • 58
    • 0033955395 scopus 로고    scopus 로고
    • Flavopiridol, a novel cyclin-dependent kinase inhibitor, in metastatic renal cancer: A University of Chicago Phase II Consortium study
    • STADLER WM, VOGELZANG NJ, AMATO R et al.: Flavopiridol, a novel cyclin-dependent kinase inhibitor, in metastatic renal cancer: a University of Chicago Phase II Consortium study. J. Clin. Oncol. (2000) 18:371-375.
    • (2000) J. Clin. Oncol , vol.18 , pp. 371-375
    • STADLER, W.M.1    VOGELZANG, N.J.2    AMATO, R.3
  • 59
    • 0035300684 scopus 로고    scopus 로고
    • Phase II study of the cyclin-dependent kinase inhibitor flavopiridol administered to patients with advanced gastric carcinoma
    • SCHWARTZ GK, ILSON D, SALTZ L et al.: Phase II study of the cyclin-dependent kinase inhibitor flavopiridol administered to patients with advanced gastric carcinoma. J. Clin. Oncol. (2001) 19:1985-1992.
    • (2001) J. Clin. Oncol , vol.19 , pp. 1985-1992
    • SCHWARTZ, G.K.1    ILSON, D.2    SALTZ, L.3
  • 60
    • 0034900178 scopus 로고    scopus 로고
    • A Phase II trial of the cyclin-dependent kinase inhibitor flavopiridol in patients with previously untreated stage i.v. non-small cell lung cancer
    • SHAPIRO GI, SUPKO JG, PATTERSON A et al.: A Phase II trial of the cyclin-dependent kinase inhibitor flavopiridol in patients with previously untreated stage i.v. non-small cell lung cancer. Clin Cancer Res (2001) 7:1590-1599.
    • (2001) Clin Cancer Res , vol.7 , pp. 1590-1599
    • SHAPIRO, G.I.1    SUPKO, J.G.2    PATTERSON, A.3
  • 61
    • 0036240601 scopus 로고    scopus 로고
    • Seventy-two hour continuous infusion flavopiridol in relapsed and refractory mantle cell lymphoma
    • LIN TS, HOWARD OM, NEUBERG DS et al.: Seventy-two hour continuous infusion flavopiridol in relapsed and refractory mantle cell lymphoma. Leuk. Lymphoma (2002) 43:793-797.
    • (2002) Leuk. Lymphoma , vol.43 , pp. 793-797
    • LIN, T.S.1    HOWARD, O.M.2    NEUBERG, D.S.3
  • 62
    • 0043011497 scopus 로고    scopus 로고
    • Phase II study of flavopiridol in patients with advanced colorectal cancer
    • AKLILU M, KINDLER HL, DONEHOWER RC et al.: Phase II study of flavopiridol in patients with advanced colorectal cancer. Ann. Oncol. (2003) 14:1270-1273.
    • (2003) Ann. Oncol , vol.14 , pp. 1270-1273
    • AKLILU, M.1    KINDLER, H.L.2    DONEHOWER, R.C.3
  • 63
    • 10744230675 scopus 로고    scopus 로고
    • A Phase II trial of flavopiridol (NSC 649890) in patients with previously untreated metastatic androgen-independent prostate cancer
    • LIU G, GANDARA DR, LARA PN Jr et al.: A Phase II trial of flavopiridol (NSC 649890) in patients with previously untreated metastatic androgen-independent prostate cancer. Clin. Cancer Res. (2004) 10:924-928.
    • (2004) Clin. Cancer Res , vol.10 , pp. 924-928
    • LIU, G.1    GANDARA, D.R.2    LARA Jr, P.N.3
  • 64
    • 20344382459 scopus 로고    scopus 로고
    • Flavopiridol administered as a 24-hour continuous infusion in chronic lymphocytic leukemia lacks clinical activity
    • FLINN IW, BYRD JC, BARTLETT N et al.: Flavopiridol administered as a 24-hour continuous infusion in chronic lymphocytic leukemia lacks clinical activity. Leuk. Res. (2005) 29:1253-1257.
    • (2005) Leuk. Res , vol.29 , pp. 1253-1257
    • FLINN, I.W.1    BYRD, J.C.2    BARTLETT, N.3
  • 65
    • 20344368831 scopus 로고    scopus 로고
    • Treatment of relapsed chronic lymphocytic leukemia by 72-hour continuous infusion or 1-hour bolus infusion of flavopiridol: Results from Cancer and Leukemia Group B study 19805
    • BYRD JC, PETERSON BL, GABRILOVE J et al.: Treatment of relapsed chronic lymphocytic leukemia by 72-hour continuous infusion or 1-hour bolus infusion of flavopiridol: results from Cancer and Leukemia Group B study 19805. Clin. Cancer Res. (2005) 11:4176-4181.
    • (2005) Clin. Cancer Res , vol.11 , pp. 4176-4181
    • BYRD, J.C.1    PETERSON, B.L.2    GABRILOVE, J.3
  • 66
    • 0036789539 scopus 로고    scopus 로고
    • Phase I clinical and pharmacokinetic study of flavopiridol administered as a daily 1-hour infusion in patients with advanced neoplasms
    • TAN AR, HEADLEE D, MESSMANN R et al.: Phase I clinical and pharmacokinetic study of flavopiridol administered as a daily 1-hour infusion in patients with advanced neoplasms. J. Clin. Oncol. (2002) 20:4074-4082.
    • (2002) J. Clin. Oncol , vol.20 , pp. 4074-4082
    • TAN, A.R.1    HEADLEE, D.2    MESSMANN, R.3
  • 67
    • 0032055497 scopus 로고    scopus 로고
    • Flavopiridol induces apoptosis of normal lymphoid cells, causes immunosuppression, and has potent antitumor activity in vivo against human leukemia and lymphoma xenografts
    • ARGUELLO F, ALEXANDER M, STERRY JA et al.: Flavopiridol induces apoptosis of normal lymphoid cells, causes immunosuppression, and has potent antitumor activity in vivo against human leukemia and lymphoma xenografts. Blood (1998) 91:2482-2490.
    • (1998) Blood , vol.91 , pp. 2482-2490
    • ARGUELLO, F.1    ALEXANDER, M.2    STERRY, J.A.3
  • 68
    • 4243385594 scopus 로고    scopus 로고
    • A Phase I pharmacokinetic (PK)-pharmacodynamic (PD) study of flavopiridol by 24 hours continuous infusion (CI) repeating every week
    • abstr 371
    • SASAKI Y, SASAKI T, MINAMI H et al.: A Phase I pharmacokinetic (PK)-pharmacodynamic (PD) study of flavopiridol by 24 hours continuous infusion (CI) repeating every week. Proc. Am. Soc. Clin. Oncol. 21:(2002) (abstr 371).
    • (2002) Proc. Am. Soc. Clin. Oncol , vol.21
    • SASAKI, Y.1    SASAKI, T.2    MINAMI, H.3
  • 69
    • 0038473927 scopus 로고    scopus 로고
    • Flavopiridol in untreated or relapsed mantle-cell lymphoma: Results of a Phase II study of the National Cancer Institute of Canada Clinical Trials Group
    • KOUROUKIS CT, BELCH A, CRUMP M et al.: Flavopiridol in untreated or relapsed mantle-cell lymphoma: results of a Phase II study of the National Cancer Institute of Canada Clinical Trials Group. J. Clin. Oncol. (2003) 21:1740-1745.
    • (2003) J. Clin. Oncol , vol.21 , pp. 1740-1745
    • KOUROUKIS, C.T.1    BELCH, A.2    CRUMP, M.3
  • 70
    • 3542996265 scopus 로고    scopus 로고
    • Phase II trial of flavopiridol, a cyclin dependent kinase inhibitor, in untreated metastatic malignant melanoma
    • BURDETTE-RADOUX S, TOZER RG, LOHMANN RC et al.: Phase II trial of flavopiridol, a cyclin dependent kinase inhibitor, in untreated metastatic malignant melanoma. Invest. New Drugs (2004) 22:315-322.
    • (2004) Invest. New Drugs , vol.22 , pp. 315-322
    • BURDETTE-RADOUX, S.1    TOZER, R.G.2    LOHMANN, R.C.3
  • 71
    • 22544456878 scopus 로고    scopus 로고
    • A Phase II evaluation of flavopiridol as second-line chemotherapy of endometrial carcinoma: A Gynecologic Oncology Group study
    • GRENDYS EC Jr, BLESSING JA, BURGER R, HOFFMAN J: A Phase II evaluation of flavopiridol as second-line chemotherapy of endometrial carcinoma: a Gynecologic Oncology Group study. Gynecol. Oncol. (2005) 98:249-253.
    • (2005) Gynecol. Oncol , vol.98 , pp. 249-253
    • GRENDYS Jr, E.C.1    BLESSING, J.A.2    BURGER, R.3    HOFFMAN, J.4
  • 72
    • 21244469349 scopus 로고    scopus 로고
    • A Phase II study of flavopridol in patients with advanced renal cell carcinoma: Results of Southwest oncology group trial 0109
    • Van VELDHUIZEN PJ, FAULKENER JR, LARA P Jr et al.: A Phase II study of flavopridol in patients with advanced renal cell carcinoma: results of Southwest oncology group trial 0109. Can. Chemother. Pharmacol. (2005)56:39-45.
    • (2005) Can. Chemother. Pharmacol , vol.56 , pp. 39-45
    • Van VELDHUIZEN, P.J.1    FAULKENER, J.R.2    LARA Jr, P.3
  • 73
    • 33645393211 scopus 로고    scopus 로고
    • Flavopiridol in patients with relapsed or refractory multiple myeloma: A Phase 2 trial with clinical and pharmacodynamic end-points
    • DISPENZIERI A, GERTZ MA, LACY MQ et al.: Flavopiridol in patients with relapsed or refractory multiple myeloma: a Phase 2 trial with clinical and pharmacodynamic end-points. Haematol. (2006) 91:390-393.
    • (2006) Haematol , vol.91 , pp. 390-393
    • DISPENZIERI, A.1    GERTZ, M.A.2    LACY, M.Q.3
  • 74
    • 0037086282 scopus 로고    scopus 로고
    • Selective sensitization of transformed cells to flavopiridol-induced apoptosis following recruitment to S-phase
    • MATRANGA CB, SHAPIRO GI: Selective sensitization of transformed cells to flavopiridol-induced apoptosis following recruitment to S-phase. Cancer Res. (2002) 62:1707-1717.
    • (2002) Cancer Res , vol.62 , pp. 1707-1717
    • MATRANGA, C.B.1    SHAPIRO, G.I.2
  • 75
    • 0032804733 scopus 로고    scopus 로고
    • Sequential dependent enhancement of caspase activation and apoptosis by flavopiridol on paclitaxel-treated human gastric and breast cancer cells
    • MOTWANI M, DELOHERY TM, SCHWARTZ GK: Sequential dependent enhancement of caspase activation and apoptosis by flavopiridol on paclitaxel-treated human gastric and breast cancer cells. Clin. Cancer Res. (1999) 5:1876-1883.
    • (1999) Clin. Cancer Res , vol.5 , pp. 1876-1883
    • MOTWANI, M.1    DELOHERY, T.M.2    SCHWARTZ, G.K.3
  • 76
    • 0348075994 scopus 로고    scopus 로고
    • Flavopiridol enhances the effect of docetaxel in vitro and in vivo in human gastric cancer cells
    • MOTWANI M, RIZZO C, SIROTNAK F et al.: Flavopiridol enhances the effect of docetaxel in vitro and in vivo in human gastric cancer cells. Mol. Cancer Ther. (2003) 2:549-555.
    • (2003) Mol. Cancer Ther , vol.2 , pp. 549-555
    • MOTWANI, M.1    RIZZO, C.2    SIROTNAK, F.3
  • 77
    • 0034887130 scopus 로고    scopus 로고
    • Flavopiridol increases sensitization to gemcitabine in human gastrointestinal cancer cell lines and correlates with down-regulation of ribonucleotide reductase M2 subunit
    • JUNG CP, MOTWANI MV, SCHWARTZ GK: Flavopiridol increases sensitization to gemcitabine in human gastrointestinal cancer cell lines and correlates with down-regulation of ribonucleotide reductase M2 subunit. Clin. Cancer Res. (2001) 7:2527-2536.
    • (2001) Clin. Cancer Res , vol.7 , pp. 2527-2536
    • JUNG, C.P.1    MOTWANI, M.V.2    SCHWARTZ, G.K.3
  • 78
    • 0037089691 scopus 로고    scopus 로고
    • Phase I study of the cyclin-dependent kinase inhibitor flavopiridol in combination with paclitaxel in patients with advanced solid tumors
    • SCHWARTZ GK, O'REILLY E, ILSON D et al.: Phase I study of the cyclin-dependent kinase inhibitor flavopiridol in combination with paclitaxel in patients with advanced solid tumors. J. Clin. Oncol. (2002) 20:2157-2170.
    • (2002) J. Clin. Oncol , vol.20 , pp. 2157-2170
    • SCHWARTZ, G.K.1    O'REILLY, E.2    ILSON, D.3
  • 79
    • 4143122204 scopus 로고    scopus 로고
    • Phase I trial of the cyclin-dependent kinase inhibitor flavopiridol in combination with docetaxel in patients with metastatic breast cancer
    • TAN AR, YANG X, BERMAN A et al.: Phase I trial of the cyclin-dependent kinase inhibitor flavopiridol in combination with docetaxel in patients with metastatic breast cancer. Clin. Cancer Res. (2004) 10:5038-5047.
    • (2004) Clin. Cancer Res , vol.10 , pp. 5038-5047
    • TAN, A.R.1    YANG, X.2    BERMAN, A.3
  • 80
    • 21044432331 scopus 로고    scopus 로고
    • A Phase I clinical trial of the sequential combination of irinotecan followed by flavopiridol
    • SHAH MA, KORTMANSKY J, MOTWANI M et al.: A Phase I clinical trial of the sequential combination of irinotecan followed by flavopiridol. Clin. Cancer Res. (2005) 11:3836-3845.
    • (2005) Clin. Cancer Res , vol.11 , pp. 3836-3845
    • SHAH, M.A.1    KORTMANSKY, J.2    MOTWANI, M.3
  • 81
    • 23844536143 scopus 로고    scopus 로고
    • Phase 1 trial of flavopiridol combined with cisplatin or carboplatin in patients with advanced malignancies with the assessment of pharmacokinetic and pharmacodynamic end points
    • BIBLE KC, LENSING JL, NELSON SA et al.: Phase 1 trial of flavopiridol combined with cisplatin or carboplatin in patients with advanced malignancies with the assessment of pharmacokinetic and pharmacodynamic end points. Clin. Cancer Res. (2005) 11:5935-5941.
    • (2005) Clin. Cancer Res , vol.11 , pp. 5935-5941
    • BIBLE, K.C.1    LENSING, J.L.2    NELSON, S.A.3
  • 82
    • 28544443503 scopus 로고    scopus 로고
    • Phase I and pharmacokinetic study of flavopiridol followed by 1-β-D-arabinofuranosylcytosine and mitoxantrone in relapsed and refractory adult acute leukemias
    • KARP JE, PASSANITI A, GOJO I et al.: Phase I and pharmacokinetic study of flavopiridol followed by 1-β-D-arabinofuranosylcytosine and mitoxantrone in relapsed and refractory adult acute leukemias. Clin. Cancer Res. (2005) 11:8403-8412.
    • (2005) Clin. Cancer Res , vol.11 , pp. 8403-8412
    • KARP, J.E.1    PASSANITI, A.2    GOJO, I.3
  • 83
    • 0035871444 scopus 로고    scopus 로고
    • Phase I trial of 72-hour continuous infusion UCN-01 in patients with refractory neoplasms
    • SAUSVILLE EA, ARBUCK SG, MESSMANN R et al.: Phase I trial of 72-hour continuous infusion UCN-01 in patients with refractory neoplasms. J. Clin. Oncol. (2001) 19:2319-2333.
    • (2001) J. Clin. Oncol , vol.19 , pp. 2319-2333
    • SAUSVILLE, E.A.1    ARBUCK, S.G.2    MESSMANN, R.3
  • 84
    • 34447570041 scopus 로고    scopus 로고
    • Phase I study of UCN-01 by 3-hour infusion (Meeting abstract 611)
    • TAMURA T, SASAKI Y, MINAMI H et al.: Phase I study of UCN-01 by 3-hour infusion (Meeting abstract 611). In: ASCO Annual Meeting. (1999).
    • (1999) ASCO Annual Meeting
    • TAMURA, T.1    SASAKI, Y.2    MINAMI, H.3
  • 85
    • 12244307462 scopus 로고    scopus 로고
    • A Phase I and pharmacokinetic study of short infusions of UCN-01 in patients with refractory solid tumors
    • DEES EC, BAKER SD, O'REILLY S et al.: A Phase I and pharmacokinetic study of short infusions of UCN-01 in patients with refractory solid tumors. Clin. Cancer Res. (2005) 11:664-671.
    • (2005) Clin. Cancer Res , vol.11 , pp. 664-671
    • DEES, E.C.1    BAKER, S.D.2    O'REILLY, S.3
  • 86
    • 0029938768 scopus 로고    scopus 로고
    • Blocking of glioma proliferation in vitro and in vivo and potentiating the effects of BCNU and cisplatin: UCN-01, a selective protein kinase C inhibitor
    • POLLACK IF, KAWECKI S, LAZO JS: Blocking of glioma proliferation in vitro and in vivo and potentiating the effects of BCNU and cisplatin: UCN-01, a selective protein kinase C inhibitor. J. Neurosurg. (1996) 84:1024-1032.
    • (1996) J. Neurosurg , vol.84 , pp. 1024-1032
    • POLLACK, I.F.1    KAWECKI, S.2    LAZO, J.S.3
  • 87
    • 0031670310 scopus 로고    scopus 로고
    • UCN-01 suppresses thymidylate synthase gene expression and enhances 5-fluorouracil-induced apoptosis in a sequence-dependent manner
    • HSUEH CT, KELSEN D, SCHWARTZ GK: UCN-01 suppresses thymidylate synthase gene expression and enhances 5-fluorouracil-induced apoptosis in a sequence-dependent manner. Clin. Cancer Res. (1998) 4:2201-2206.
    • (1998) Clin. Cancer Res , vol.4 , pp. 2201-2206
    • HSUEH, C.T.1    KELSEN, D.2    SCHWARTZ, G.K.3
  • 88
    • 20144373035 scopus 로고    scopus 로고
    • Phase I trial of the cyclin-dependent kinase inhibitor and protein kinase C inhibitor 7-hydroxystaurosporine in combination with fluorouracil in patients with advanced solid tumors
    • KORTMANSKY J, SHAH MA, KAUBISCH A et al.: Phase I trial of the cyclin-dependent kinase inhibitor and protein kinase C inhibitor 7-hydroxystaurosporine in combination with fluorouracil in patients with advanced solid tumors. J. Clin. Oncol. (2005) 23:1875-1884.
    • (2005) J. Clin. Oncol , vol.23 , pp. 1875-1884
    • KORTMANSKY, J.1    SHAH, M.A.2    KAUBISCH, A.3
  • 89
    • 20444506407 scopus 로고    scopus 로고
    • The cyclin-dependent kinase inhibitor UCN-01 plus cisplatin in advanced solid tumors: A California cancer consortium Phase I pharmacokinetic and molecular correlative trial
    • LARA PN, Jr:, MACK PC, SYNOLD T et al.: The cyclin-dependent kinase inhibitor UCN-01 plus cisplatin in advanced solid tumors: a California cancer consortium Phase I pharmacokinetic and molecular correlative trial. Clin. Cancer Res. (2005) 11:4444-4450.
    • (2005) Clin. Cancer Res , vol.11 , pp. 4444-4450
    • LARA Jr, P.N.1    MACK, P.C.2    SYNOLD, T.3
  • 90
    • 3042582607 scopus 로고    scopus 로고
    • Time to disease progression to evaluate a novel protein kinase C inhibitor, UCN-01, in renal cell carcinoma
    • RINI BI, WEINBERG V, SHAW V et al.: Time to disease progression to evaluate a novel protein kinase C inhibitor, UCN-01, in renal cell carcinoma. Cancer (2004) 101:90-95.
    • (2004) Cancer , vol.101 , pp. 90-95
    • RINI, B.I.1    WEINBERG, V.2    SHAW, V.3
  • 91
    • 0034772246 scopus 로고    scopus 로고
    • Phase I and pharmacokinetic study of E7070, a novel sulfonamide, given at a daily times five schedule in patients with solid tumors. A study by the EORTC-early clinical studies group (ECSG)
    • PUNT CJ, FUMOLEAU P, VAN DE WALLE B et al.: Phase I and pharmacokinetic study of E7070, a novel sulfonamide, given at a daily times five schedule in patients with solid tumors. A study by the EORTC-early clinical studies group (ECSG). Ann. Oncol. (2001) 12:1289-1293.
    • (2001) Ann. Oncol , vol.12 , pp. 1289-1293
    • PUNT, C.J.1    FUMOLEAU, P.2    VAN DE WALLE, B.3
  • 92
    • 0037102283 scopus 로고    scopus 로고
    • Phase I and pharmacokinetic study of E7070, a novel chloroindolyl sulfonamide cell-cycle inhibitor, administered as a one-hour infusion every three weeks in patients with advanced cancer
    • RAYMOND E, TEN BOKKEL HUININK WW, TAIEB J et al.: Phase I and pharmacokinetic study of E7070, a novel chloroindolyl sulfonamide cell-cycle inhibitor, administered as a one-hour infusion every three weeks in patients with advanced cancer. J. Clin. Oncol. (2002) 20:3508-3521.
    • (2002) J. Clin. Oncol , vol.20 , pp. 3508-3521
    • RAYMOND, E.1    TEN BOKKEL HUININK, W.W.2    TAIEB, J.3
  • 93
    • 0038402755 scopus 로고    scopus 로고
    • Phase I clinical and pharmacokinetic study of E7070, a novel sulfonamide given as a 5-day continuous infusion repeated every 3 weeks in patients with solid tumours. A study by the EORTC Early Clinical Study Group (ECSG)
    • TERRET C, ZANETTA S, ROCHE H et al.: Phase I clinical and pharmacokinetic study of E7070, a novel sulfonamide given as a 5-day continuous infusion repeated every 3 weeks in patients with solid tumours. A study by the EORTC Early Clinical Study Group (ECSG). Eur. J. Cancer (2003) 39:1097-1104.
    • (2003) Eur. J. Cancer , vol.39 , pp. 1097-1104
    • TERRET, C.1    ZANETTA, S.2    ROCHE, H.3
  • 94
    • 0242525657 scopus 로고    scopus 로고
    • Phase I and pharmacokinetic study of E7070, a chloroindolyl-sulfonamide anticancer agent, administered on a weekly schedule to patients with solid tumors
    • DITTRICH C, DUMEZ H, CALVERT H et al.: Phase I and pharmacokinetic study of E7070, a chloroindolyl-sulfonamide anticancer agent, administered on a weekly schedule to patients with solid tumors. Clin. Cancer Res. (2003) 9:5195-5204.
    • (2003) Clin. Cancer Res , vol.9 , pp. 5195-5204
    • DITTRICH, C.1    DUMEZ, H.2    CALVERT, H.3
  • 95
    • 0000287733 scopus 로고    scopus 로고
    • Phase I trial of five-days continuous infusion E7070 N-(3-chloro-7-indolyl)-1,4-benzenedisulfo namide] in patients with solid tumors
    • DROZ JP: Phase I trial of five-days continuous infusion E7070 N-(3-chloro-7-indolyl)-1,4-benzenedisulfo namide] in patients with solid tumors. Proc. American Association of Cancer Res. (2000) 41:609.
    • (2000) Proc. American Association of Cancer Res , vol.41 , pp. 609
    • DROZ, J.P.1
  • 96
    • 3242712108 scopus 로고    scopus 로고
    • A Phase II clinical and pharmacodynamic study of E7070 in patients with metastatic, recurrent, or refractory squamous cell carcinoma of the head and neck: Modulation of retinoblasmma protein phosphorylation by a novel chloroindolyl sulfonamide cell cycle inhibitor
    • HADDAD RI, WEINSTEIN LJ, WIECZOREK TJ et al.: A Phase II clinical and pharmacodynamic study of E7070 in patients with metastatic, recurrent, or refractory squamous cell carcinoma of the head and neck: modulation of retinoblasmma protein phosphorylation by a novel chloroindolyl sulfonamide cell cycle inhibitor. Clin. Cancer Res. (2004) 10:4680-4687.
    • (2004) Clin. Cancer Res , vol.10 , pp. 4680-4687
    • HADDAD, R.I.1    WEINSTEIN, L.J.2    WIECZOREK, T.J.3
  • 97
    • 19944427395 scopus 로고    scopus 로고
    • Phase II study of E7070 in patients with metastatic melanoma
    • SMYTH JF, AAMDAL S, AWADA A et al.: Phase II study of E7070 in patients with metastatic melanoma. Ann. Oncol. (2005) 16:158-161.
    • (2005) Ann. Oncol , vol.16 , pp. 158-161
    • SMYTH, J.F.1    AAMDAL, S.2    AWADA, A.3
  • 98
    • 34447555105 scopus 로고    scopus 로고
    • A multicentre randomised Phase II study of E7070 in patients with colorectal cancer who have failed 5-fluorouracil-based chemotherapy
    • Edition
    • MAINWARING PN, VAN CUTSEM E, VAN LAETHEM J et al.: A multicentre randomised Phase II study of E7070 in patients with colorectal cancer who have failed 5-fluorouracil-based chemotherapy. In ASCO Annual Meeting (Abstract 611), Edition (2002).
    • (2002) ASCO Annual Meeting (Abstract 611)
    • MAINWARING, P.N.1    VAN CUTSEM, E.2    VAN LAETHEM, J.3
  • 99
    • 34447574115 scopus 로고    scopus 로고
    • A Phase II and pharmacodynamic study of E7070 in patients with non-small cell lung cancer (NSCLC) who have failed platinum-based chemotherapy
    • Abstract 1306, Edition
    • TALBOT D, NORBURY C, SLADE M et al.: A Phase II and pharmacodynamic study of E7070 in patients with non-small cell lung cancer (NSCLC) who have failed platinum-based chemotherapy. In: ASCO Annual Meeting (Abstract 1306), Edition (2002).
    • (2002) ASCO Annual Meeting
    • TALBOT, D.1    NORBURY, C.2    SLADE, M.3
  • 100
    • 34447547018 scopus 로고    scopus 로고
    • PIERGA J, FAIVRE S, VERA K et al.: A Phase I and pharmacokinetic (PK) trial of CYC202, a novel oral cyclin-dependent kinase (CDK) inhibitor, in patients (pts) with advanced solid tumors. Proc. Am. Soc. Clin. Oncol. (2003) 22:abstr 840
    • PIERGA J, FAIVRE S, VERA K et al.: A Phase I and pharmacokinetic (PK) trial of CYC202, a novel oral cyclin-dependent kinase (CDK) inhibitor, in patients (pts) with advanced solid tumors. Proc. Am. Soc. Clin. Oncol. (2003) 22:abstr 840
  • 101
    • 34447546020 scopus 로고    scopus 로고
    • A Phase I trial of the oral cyclin dependent kinase inhibitor CYC202 patients with advanced malignancy, abstr 838
    • BENSON C, WHITE J, TWELVES C et al.: A Phase I trial of the oral cyclin dependent kinase inhibitor CYC202 in patients with advanced malignancy. Proc. Am. Soc. Clin. Oncol. (2003) 22: abstr 838.
    • (2003) Proc. Am. Soc. Clin. Oncol , vol.22
    • BENSON, C.1    WHITE, J.2    TWELVES, C.3
  • 102
    • 34447580352 scopus 로고    scopus 로고
    • WHITE JD, CASSIDY J, TWELVES C et al.: A Phase I trial of the oral cyclin dependent kinase inhibitor CYC202 in patients with advanced malignancy. Journal of Clinical Oncology, (2004 ASCO Annual Meeting Proceedings (Post-Meeting Edition). 22, No 14S (July 15 Supplement), (2004) 3042.
    • WHITE JD, CASSIDY J, TWELVES C et al.: A Phase I trial of the oral cyclin dependent kinase inhibitor CYC202 in patients with advanced malignancy. Journal of Clinical Oncology, (2004 ASCO Annual Meeting Proceedings (Post-Meeting Edition). Vol. 22, No 14S (July 15 Supplement), (2004) 3042.
  • 103
    • 20444477948 scopus 로고    scopus 로고
    • Seliciclib (CYC202, R-roscovitine) induces cell death in multiple myeloma cells by inhibition of RNA polymerase II-dependent transcription and down-regulation of Mcl-1
    • MACCALLUM DE, MELVILLE J, FRAME S et al.: Seliciclib (CYC202, R-roscovitine) induces cell death in multiple myeloma cells by inhibition of RNA polymerase II-dependent transcription and down-regulation of Mcl-1. Cancer Res. (2005) 65:5399-5407.
    • (2005) Cancer Res , vol.65 , pp. 5399-5407
    • MACCALLUM, D.E.1    MELVILLE, J.2    FRAME, S.3
  • 104
    • 23044439051 scopus 로고    scopus 로고
    • Seliciclib (CYC202 or R-roscovitine), a small-molecule cyclin-dependent kinase inhibitor, mediates activity via down-regulation of Mcl-1 in multiple myeloma
    • RAJE N, KUMAR S, HIDESHIMA T et al.: Seliciclib (CYC202 or R-roscovitine), a small-molecule cyclin-dependent kinase inhibitor, mediates activity via down-regulation of Mcl-1 in multiple myeloma. Blood (2005) 106:1042-1047.
    • (2005) Blood , vol.106 , pp. 1042-1047
    • RAJE, N.1    KUMAR, S.2    HIDESHIMA, T.3
  • 105
    • 21144435503 scopus 로고    scopus 로고
    • A novel CDK inhibitor, CYC202 (R-roscovitine), overcomes the defect in p53-dependent apoptosis in B-CLL by down-regulation of genes involved in transcription regulation and survival
    • ALVI AJ, AUSTEN B, WESTON VJ et al.: A novel CDK inhibitor, CYC202 (R-roscovitine), overcomes the defect in p53-dependent apoptosis in B-CLL by down-regulation of genes involved in transcription regulation and survival. Blood (2005) 105:4484-4491.
    • (2005) Blood , vol.105 , pp. 4484-4491
    • ALVI, A.J.1    AUSTEN, B.2    WESTON, V.J.3
  • 106
    • 25444502962 scopus 로고    scopus 로고
    • In vitro activity of cyclin-dependent kinase inhibitor CYC202 (seliciclib, R-roscovitine) in mantle cell lymphomas
    • LACRIMA K, VALENTINI A, LAMBERTINI C et al.: In vitro activity of cyclin-dependent kinase inhibitor CYC202 (seliciclib, R-roscovitine) in mantle cell lymphomas. Ann. Oncol. (2005) 16 :1169-1176.
    • (2005) Ann. Oncol , vol.16 , pp. 1169-1176
    • LACRIMA, K.1    VALENTINI, A.2    LAMBERTINI, C.3
  • 107
    • 34447575908 scopus 로고    scopus 로고
    • SIEGEL-LAKHAI WS, RODENSTEIN DO, BEIJNEN JH et al.: Phase I study of seliciclib (CYC202 or R-roscovitine) in combination with gemcitabine (gem)/cisplatin (cis) in patients with advanced non-small-cell lung cancer (NSCLC). J. Clin. Oncol. ASCO Annual Meeting Proceedings. (2005) 23(16 Suppl.):2060.
    • SIEGEL-LAKHAI WS, RODENSTEIN DO, BEIJNEN JH et al.: Phase I study of seliciclib (CYC202 or R-roscovitine) in combination with gemcitabine (gem)/cisplatin (cis) in patients with advanced non-small-cell lung cancer (NSCLC). J. Clin. Oncol. ASCO Annual Meeting Proceedings. (2005) 23(16 Suppl.):2060.
  • 108
    • 1642405155 scopus 로고    scopus 로고
    • A Phase I study to determine the safety and pharmacokinetics (PK) of BMS-387032 given intravenously every three weeks in patients with metastatic refractory solid tumors
    • Abstract 798
    • JONES SF, BURRIS HA, KIES M et al.: A Phase I study to determine the safety and pharmacokinetics (PK) of BMS-387032 given intravenously every three weeks in patients with metastatic refractory solid tumors. Proc. Am. Soc. Clin. Oncol. (2003) 22:Abstract 798.
    • (2003) Proc. Am. Soc. Clin. Oncol , vol.22
    • JONES, S.F.1    BURRIS, H.A.2    KIES, M.3
  • 109
    • 9744261178 scopus 로고    scopus 로고
    • Phase I study of BMS-387032, a cyclin dependent kinase (CDK) 2 inhibitor
    • Abstract 835
    • MCCORMICk J, GADGEEL SM, HELMKE W et al.: Phase I study of BMS-387032, a cyclin dependent kinase (CDK) 2 inhibitor. Proc. Am. Soc. Clin. Oncol. (2003) 22:Abstract 835.
    • (2003) Proc. Am. Soc. Clin. Oncol , vol.22
    • MCCORMICk, J.1    GADGEEL, S.M.2    HELMKE, W.3
  • 110
    • 1642405155 scopus 로고    scopus 로고
    • A Phase I study to determine the safety and pharmacokinetics (PK) of BMS-387032 with a 24-hr infusion given every three weeks in patients with metastatic refractory solid tumors
    • Abstract 799
    • SHAPIRO G, LEWIS N, BAI S et al.: A Phase I study to determine the safety and pharmacokinetics (PK) of BMS-387032 with a 24-hr infusion given every three weeks in patients with metastatic refractory solid tumors. Proc. Am. Soc. Clin. Oncol. (2003) 22:Abstract 799.
    • (2003) Proc. Am. Soc. Clin. Oncol , vol.22
    • SHAPIRO, G.1    LEWIS, N.2    BAI, S.3
  • 111
    • 34447573133 scopus 로고    scopus 로고
    • GRAHAM J, WAGNER K, PLUMMER R et al.: Phase I dose-escalation study of novel oral multi-target tumor growth inhibitor (MTGI) ZK 304709 administered daily for 7 days of a 21-day cycle to patients with advanced solid tumors. J. Clin. Oncol. ASCO Annual Meeting Proceedings Part I. (2006) 24(18 Suppl.):2073.
    • GRAHAM J, WAGNER K, PLUMMER R et al.: Phase I dose-escalation study of novel oral multi-target tumor growth inhibitor (MTGI) ZK 304709 administered daily for 7 days of a 21-day cycle to patients with advanced solid tumors. J. Clin. Oncol. ASCO Annual Meeting Proceedings Part I. (2006) 24(18 Suppl.):2073.
  • 112
    • 34447541529 scopus 로고    scopus 로고
    • AHMED S, MOLIFE R, SHAW H et al.: Phase I dose-escalation study of ZK 304709, an oral multi-target tumor growth inhibitor (MTGI), administered for 14 days of a 28-day cycle. J. Clin. Oncol. ASCO Annual Meeting Proceedings Part I. (2006) 24(18 Suppl.):2076.
    • AHMED S, MOLIFE R, SHAW H et al.: Phase I dose-escalation study of ZK 304709, an oral multi-target tumor growth inhibitor (MTGI), administered for 14 days of a 28-day cycle. J. Clin. Oncol. ASCO Annual Meeting Proceedings Part I. (2006) 24(18 Suppl.):2076.
  • 113
    • 2342593974 scopus 로고    scopus 로고
    • Aurora kinases dawn as cancer drug targets
    • SAUSVILLE EA: Aurora kinases dawn as cancer drug targets. Nat. Med. (2004) 10:234-235.
    • (2004) Nat. Med , vol.10 , pp. 234-235
    • SAUSVILLE, E.A.1
  • 115
    • 0347985493 scopus 로고    scopus 로고
    • Regulation of aurora-A kinase on the mitotic spindle
    • KUFER TA, NIGG EA, SILLJE HH: Regulation of aurora-A kinase on the mitotic spindle. Chromosoma (2003) 112:159-163.
    • (2003) Chromosoma , vol.112 , pp. 159-163
    • KUFER, T.A.1    NIGG, E.A.2    SILLJE, H.H.3
  • 116
    • 0034609753 scopus 로고    scopus 로고
    • The mitotic serine/ threonine kinase Aurora2/AIK is regulated by phosphorylation and degradation
    • WALTER AO, SEGHEZZI W, KORVER W et al.: The mitotic serine/ threonine kinase Aurora2/AIK is regulated by phosphorylation and degradation. Oncogene (2000) 19:4906-4916.
    • (2000) Oncogene , vol.19 , pp. 4906-4916
    • WALTER, A.O.1    SEGHEZZI, W.2    KORVER, W.3
  • 117
    • 85047694628 scopus 로고    scopus 로고
    • Aurora A and B kinases as targets for cancer: Will they be selective for tumors?
    • MATTHEWS N, VISINTIN C, HARTZOULAKIS B et al.: Aurora A and B kinases as targets for cancer: will they be selective for tumors? Expt. Rev. Anticancer Ther. (2006) 6:109-120.
    • (2006) Expt. Rev. Anticancer Ther , vol.6 , pp. 109-120
    • MATTHEWS, N.1    VISINTIN, C.2    HARTZOULAKIS, B.3
  • 118
    • 10344236486 scopus 로고    scopus 로고
    • Aurora-kinase inhibitors as anticancer agents
    • KEEN N, TAYLOR S: Aurora-kinase inhibitors as anticancer agents. Nat. Rev. Cancer (2004) 4:927-936.
    • (2004) Nat. Rev. Cancer , vol.4 , pp. 927-936
    • KEEN, N.1    TAYLOR, S.2
  • 119
    • 7744222944 scopus 로고    scopus 로고
    • Chromosomal passengers: The four-dimensional regulation of mitotic events
    • VAGNARELLI P, EARNSHAW WC: Chromosomal passengers: the four-dimensional regulation of mitotic events. Chromosoma (2004) 113:211-222.
    • (2004) Chromosoma , vol.113 , pp. 211-222
    • VAGNARELLI, P.1    EARNSHAW, W.C.2
  • 120
    • 3342887700 scopus 로고    scopus 로고
    • Borealin: A novel chromosomal passenger required for stability of the bipolar mitotic spindle
    • GASSMANN R, CARVALHO A, HENZING AJ et al.: Borealin: a novel chromosomal passenger required for stability of the bipolar mitotic spindle. J. Cell Biol. (2004) 166:179-191.
    • (2004) J. Cell Biol , vol.166 , pp. 179-191
    • GASSMANN, R.1    CARVALHO, A.2    HENZING, A.J.3
  • 121
    • 19944394833 scopus 로고    scopus 로고
    • Aurora-C kinase is a novel chromosomal passenger protein that can complement aurora-B kinase function in mitotic cells
    • SASAI K, KATAYAMA H, STENOIEN DL et al.: Aurora-C kinase is a novel chromosomal passenger protein that can complement aurora-B kinase function in mitotic cells. Cell Motil. Cytoskeleton (2004) 59:249-263.
    • (2004) Cell Motil. Cytoskeleton , vol.59 , pp. 249-263
    • SASAI, K.1    KATAYAMA, H.2    STENOIEN, D.L.3
  • 122
    • 8744313990 scopus 로고    scopus 로고
    • Direct association with inner centromere protein (INCENP) activates the novel chromosomal passenger protein, aurora-C
    • LI X, SAKASHITA G, MATSUZAKI H et al.: Direct association with inner centromere protein (INCENP) activates the novel chromosomal passenger protein, aurora-C. J. Biol. Chem. (2004) 279:47201-47211.
    • (2004) J. Biol. Chem , vol.279 , pp. 47201-47211
    • LI, X.1    SAKASHITA, G.2    MATSUZAKI, H.3
  • 123
    • 34447580351 scopus 로고    scopus 로고
    • LANDEN CN, IMMANENI A, DEAVERS MT et al.: Overexpression of the centrosomal protein aurora-A kinase is associated with poor prognosis in epithelial ovarian cancer patients. J. Clin. Oncol. ASCO Annual Meeting Proceedings Part I. (2006) 23(16 Suppl.):5039.
    • LANDEN CN, IMMANENI A, DEAVERS MT et al.: Overexpression of the centrosomal protein aurora-A kinase is associated with poor prognosis in epithelial ovarian cancer patients. J. Clin. Oncol. ASCO Annual Meeting Proceedings Part I. (2006) 23(16 Suppl.):5039.
  • 124
    • 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, WHITE RA: A putative serine/threonine kinase encoding gene BTAK on chromosome 20q13 is amplified and overexpressed in human breast cancer cell lines. Oncogene (1997) 14:2195-2200.
    • (1997) Oncogene , vol.14 , pp. 2195-2200
    • SEN, S.1    ZHOU, H.2    WHITE, R.A.3
  • 125
    • 17744384260 scopus 로고    scopus 로고
    • Tumour-amplified kinase BTAK is amplified and overexpressed in gastric cancers with possible involvement in aneuploid formation
    • SAKAKURA C, HAGIWARA A, YASUOKA R et al.: Tumour-amplified kinase BTAK is amplified and overexpressed in gastric cancers with possible involvement in aneuploid formation. Br. J. Cancer (2001) 84:824-831.
    • (2001) Br. J. Cancer , vol.84 , pp. 824-831
    • SAKAKURA, C.1    HAGIWARA, A.2    YASUOKA, R.3
  • 126
    • 0037019736 scopus 로고    scopus 로고
    • Amplification/overexpression of a mitotic kinase gene in human bladder cancer
    • SEN S, ZHOU H, ZHANG RD et al.: Amplification/overexpression of a mitotic kinase gene in human bladder cancer. J. Natl. Cancer Inst. (2002) 94:1320-1329.
    • (2002) J. Natl. Cancer Inst , vol.94 , pp. 1320-1329
    • SEN, S.1    ZHOU, H.2    ZHANG, R.D.3
  • 127
    • 0032100685 scopus 로고    scopus 로고
    • A homologue of Drosophila aurora kinase is oncogenic and amplified in human colorectal cancers
    • BISCHOFF JR, ANDERSON L, ZHU Y et al.: A homologue of Drosophila aurora kinase is oncogenic and amplified in human colorectal cancers. EMBO J. (1998) 17:3052-3065.
    • (1998) EMBO J , vol.17 , pp. 3052-3065
    • BISCHOFF, J.R.1    ANDERSON, L.2    ZHU, Y.3
  • 128
    • 0031714080 scopus 로고    scopus 로고
    • Tumour amplified kinase STK15/ BTAK induces centrosome amplification, aneuploidy and transformation
    • ZHOU H, KUANG J, ZHONG L et al.: Tumour amplified kinase STK15/ BTAK induces centrosome amplification, aneuploidy and transformation. Nat. Genet. (1998) 20:189-193.
    • (1998) Nat. Genet , vol.20 , pp. 189-193
    • ZHOU, H.1    KUANG, J.2    ZHONG, L.3
  • 129
    • 13944254035 scopus 로고    scopus 로고
    • Overexpression of aurora-A potentiates HRAS-mediated oncogenic transformation and is implicated in oral carcinogenesis
    • TATSUKA M, SATO S, KITAJIMA S et al.: Overexpression of aurora-A potentiates HRAS-mediated oncogenic transformation and is implicated in oral carcinogenesis. Oncogene (2005) 24:1122-1127.
    • (2005) Oncogene , vol.24 , pp. 1122-1127
    • TATSUKA, M.1    SATO, S.2    KITAJIMA, S.3
  • 130
    • 1842589396 scopus 로고    scopus 로고
    • High expression of aurora-B/ aurora and Ipll-like midbody-associated protein (AIM-1) in astrocytomas
    • ARAKI K, NOZAKI K, UEBA T et al.: High expression of aurora-B/ aurora and Ipll-like midbody-associated protein (AIM-1) in astrocytomas. J. Neurooncol. (2004) 67:53-64.
    • (2004) J. Neurooncol , vol.67 , pp. 53-64
    • ARAKI, K.1    NOZAKI, K.2    UEBA, T.3
  • 131
    • 2942567904 scopus 로고    scopus 로고
    • Aurora B expression in normal testis and seminomas
    • CHIEFFI P, TRONCONE G, CALEO A et al.: Aurora B expression in normal testis and seminomas. J. Endocrinol. (2004) 181:263-270.
    • (2004) J. Endocrinol , vol.181 , pp. 263-270
    • CHIEFFI, P.1    TRONCONE, G.2    CALEO, A.3
  • 132
    • 20044390030 scopus 로고    scopus 로고
    • Aurora B overexpression associates with the thyroid carcinoma undifferentiated phenotype and is required for thyroid carcinoma cell proliferation
    • SORRENTINO R, LIBERTINI S, PALLANTE PL et al.: Aurora B overexpression associates with the thyroid carcinoma undifferentiated phenotype and is required for thyroid carcinoma cell proliferation. J. Clin. Endocrinol. Metab. (2005) 90:928-935.
    • (2005) J. Clin. Endocrinol. Metab , vol.90 , pp. 928-935
    • SORRENTINO, R.1    LIBERTINI, S.2    PALLANTE, P.L.3
  • 133
    • 0033532869 scopus 로고    scopus 로고
    • Mitotic kinase expression and colorectal cancer progression
    • KATAYAMA H, OTA T, JISAKI F et al.: Mitotic kinase expression and colorectal cancer progression. J. Natl. Cancer Inst. (1999) 91:1160-1162.
    • (1999) J. Natl. Cancer Inst , vol.91 , pp. 1160-1162
    • KATAYAMA, H.1    OTA, T.2    JISAKI, F.3
  • 134
    • 34447580350 scopus 로고    scopus 로고
    • NAIR JS, TSE A, KEEN N, GK S: A novel aurora B kinase inhibitor with potent anticancer activity either as a single agent or in combination with chemotherapy. J. Clin. Oncol. ASCO Annual Meeting Proceedings Part I. (2006) 22(14 Suppl.):9568.
    • NAIR JS, TSE A, KEEN N, GK S: A novel aurora B kinase inhibitor with potent anticancer activity either as a single agent or in combination with chemotherapy. J. Clin. Oncol. ASCO Annual Meeting Proceedings Part I. (2006) 22(14 Suppl.):9568.
  • 135
    • 0032212717 scopus 로고    scopus 로고
    • Cloning of STK13, a third human protein kinase related to Drosophila aurora and budding yeast Ipll that maps on chromosome 19q13.3-ter
    • BERNARD M, SANSEAU P, HENRY C et al.: Cloning of STK13, a third human protein kinase related to Drosophila aurora and budding yeast Ipll that maps on chromosome 19q13.3-ter. Genomics (1998) 53:406-409.
    • (1998) Genomics , vol.53 , pp. 406-409
    • BERNARD, M.1    SANSEAU, P.2    HENRY, C.3
  • 136
    • 0031764068 scopus 로고    scopus 로고
    • Protein kinase profile of sperm and eggs: Cloning and characterization of two novel testis-specific protein kinases (AIE1, AIE2) related to yeast and fly chromosome segregation regulators
    • TSENG TC, CHEN SH, HSU YP, TANG TK: Protein kinase profile of sperm and eggs: cloning and characterization of two novel testis-specific protein kinases (AIE1, AIE2) related to yeast and fly chromosome segregation regulators. DNA Cell Biol. (1998) 17:823-833.
    • (1998) DNA Cell Biol , vol.17 , pp. 823-833
    • TSENG, T.C.1    CHEN, S.H.2    HSU, Y.P.3    TANG, T.K.4
  • 137
    • 0033548619 scopus 로고    scopus 로고
    • Cell cycle-dependent expression and centrosome localization of a third human aurora/ Ipll-related protein kinase, AIK3
    • KIMURA M, MATSUDA Y, YOSHIOKA T, OKANO Y: Cell cycle-dependent expression and centrosome localization of a third human aurora/ Ipll-related protein kinase, AIK3. J. Biol. Chem. (1999) 274:7334-7340.
    • (1999) J. Biol. Chem , vol.274 , pp. 7334-7340
    • KIMURA, M.1    MATSUDA, Y.2    YOSHIOKA, T.3    OKANO, Y.4
  • 138
    • 0033756439 scopus 로고    scopus 로고
    • Centrosomal kinases, HsAIRK1 and HsAIRK3, are overexpressed in primary colorectal cancers
    • TAKAHASHI T, FUTAMURA M, YOSHIMI N et al.: Centrosomal kinases, HsAIRK1 and HsAIRK3, are overexpressed in primary colorectal cancers. Jpn. J. Cancer Res. (2000) 91:1007-1014.
    • (2000) Jpn. J. Cancer Res , vol.91 , pp. 1007-1014
    • TAKAHASHI, T.1    FUTAMURA, M.2    YOSHIMI, N.3
  • 139
    • 34447553837 scopus 로고    scopus 로고
    • RUBIN EH, SHAPIRO GI, STEIN MN et al.: A Phase I clinical and pharmacokinetic (PK) trial of the aurora kinase (AK) inhibitor MK-0457 in cancer patients. J. Clin. Oncol. ASCO Annual Meeting Proceedings Part I. (2006) 24(18 Suppl.):3009.
    • RUBIN EH, SHAPIRO GI, STEIN MN et al.: A Phase I clinical and pharmacokinetic (PK) trial of the aurora kinase (AK) inhibitor MK-0457 in cancer patients. J. Clin. Oncol. ASCO Annual Meeting Proceedings Part I. (2006) 24(18 Suppl.):3009.
  • 140
    • 34447574114 scopus 로고    scopus 로고
    • SCHELLENS JH, BOSS D, WITTEVEEN PO et al.: Phase I and pharmacological study of the novel aurora kinase inhibitor AZD1152. J. Clin. Oncol. ASCO Annual Meeting Proceedings Part I. (2006) 24(18 Suppl.):3008.
    • SCHELLENS JH, BOSS D, WITTEVEEN PO et al.: Phase I and pharmacological study of the novel aurora kinase inhibitor AZD1152. J. Clin. Oncol. ASCO Annual Meeting Proceedings Part I. (2006) 24(18 Suppl.):3008.
  • 141
    • 0023804548 scopus 로고
    • Polo, a mitotic mutant of Drosophila displaying abnormal spindle poles
    • SUNKEL CE, GLOVER DM: Polo, a mitotic mutant of Drosophila displaying abnormal spindle poles. J. Cell Sci. (1988) 89(Pt 1):25-38.
    • (1988) J. Cell Sci , vol.89 , Issue.PART 1 , pp. 25-38
    • SUNKEL, C.E.1    GLOVER, D.M.2
  • 142
    • 0027280212 scopus 로고
    • A conserved mitotic kinase active at late anaphase-telophase in syncytial Drosophila embryos
    • FENTON B, GLOVER DM: A conserved mitotic kinase active at late anaphase-telophase in syncytial Drosophila embryos. Nature (1993) 363:637-640.
    • (1993) Nature , vol.363 , pp. 637-640
    • FENTON, B.1    GLOVER, D.M.2
  • 143
    • 0032535244 scopus 로고    scopus 로고
    • Polo-like kinases: A team that plays throughout mitosis
    • GLOVER DM, HAGAN IM, TAVARES AA: Polo-like kinases: a team that plays throughout mitosis. Genes Dev. (1998) 12:3777-3787.
    • (1998) Genes Dev , vol.12 , pp. 3777-3787
    • GLOVER, D.M.1    HAGAN, I.M.2    TAVARES, A.A.3
  • 144
    • 33645316142 scopus 로고    scopus 로고
    • Targeting polo-like kinase 1 for cancer therapy
    • STREBHARDT K, ULLRICH A: Targeting polo-like kinase 1 for cancer therapy. Nat. Rev. Cancer (2006) 6:321-330.
    • (2006) Nat. Rev. Cancer , vol.6 , pp. 321-330
    • STREBHARDT, K.1    ULLRICH, A.2
  • 145
    • 3142638869 scopus 로고    scopus 로고
    • Polo-like kinase-2 is required for centriole duplication in mammalian cells
    • WARNKE S, KEMMLER S, HAMES RS et al.: Polo-like kinase-2 is required for centriole duplication in mammalian cells. Curr. Biol. (2004)14:1200-1207.
    • (2004) Curr. Biol , vol.14 , pp. 1200-1207
    • WARNKE, S.1    KEMMLER, S.2    HAMES, R.S.3
  • 146
    • 0034671732 scopus 로고    scopus 로고
    • Incomplete cytokinesis and induction of apoptosis by overexpression of the mammalian polo-like kinase, Plk3
    • CONN CW, HENNIGAN RF, DAI W et al.: Incomplete cytokinesis and induction of apoptosis by overexpression of the mammalian polo-like kinase, Plk3. Cancer Res. (2000) 60:6826-6831.
    • (2000) Cancer Res , vol.60 , pp. 6826-6831
    • CONN, C.W.1    HENNIGAN, R.F.2    DAI, W.3
  • 147
    • 23044488055 scopus 로고    scopus 로고
    • Plk4 haploinsufficiency causes mitotic infidelity and carcinogenesis
    • KO MA, ROSARIO CO, HUDSON JW et al.: Plk4 haploinsufficiency causes mitotic infidelity and carcinogenesis. Nat. Genet. (2005) 37:883-888.
    • (2005) Nat. Genet , vol.37 , pp. 883-888
    • KO, M.A.1    ROSARIO, C.O.2    HUDSON, J.W.3
  • 148
    • 29044431521 scopus 로고    scopus 로고
    • SAK/ PLK4 is required for centriole duplication and flagella development
    • BETTENCOURT-DIAS M, RODRIGUES-MARTINS A, CARPENTER L et al.: SAK/ PLK4 is required for centriole duplication and flagella development. Curr. Biol. (2005) 15:2199-2207.
    • (2005) Curr. Biol , vol.15 , pp. 2199-2207
    • BETTENCOURT-DIAS, M.1    RODRIGUES-MARTINS, A.2    CARPENTER, L.3
  • 149
    • 13244269808 scopus 로고    scopus 로고
    • Polo-like kinases and oncogenesis
    • ECKERDT F, YUAN J, STREBHARDT K: Polo-like kinases and oncogenesis. Oncogene (2005) 24:267-276.
    • (2005) Oncogene , vol.24 , pp. 267-276
    • ECKERDT, F.1    YUAN, J.2    STREBHARDT, K.3
  • 150
    • 0035836079 scopus 로고    scopus 로고
    • Expression of polo-like kinase in ovarian cancer is associated with histological grade and clinical stage
    • TAKAI N, MIYAZAKI T, FUJISAWA K et al.: Expression of polo-like kinase in ovarian cancer is associated with histological grade and clinical stage. Cancer Lett. (2001) 164:41-49.
    • (2001) Cancer Lett , vol.164 , pp. 41-49
    • TAKAI, N.1    MIYAZAKI, T.2    FUJISAWA, K.3
  • 151
    • 0035839314 scopus 로고    scopus 로고
    • Polo-like kinase (PLK) expression in endometrial carcinoma
    • TAKAI N, MIYAZAKI T, FUJISAWA K et al.: Polo-like kinase (PLK) expression in endometrial carcinoma. Cancer Lett (2001) 169:41-49.
    • (2001) Cancer Lett , vol.169 , pp. 41-49
    • TAKAI, N.1    MIYAZAKI, T.2    FUJISAWA, K.3
  • 152
    • 0031051218 scopus 로고    scopus 로고
    • Prognostic significance of polo-like kinase (PLK) expression in non-small cell lung cancer
    • WOLF G, ELEZ R, DOERMER A et al.: Prognostic significance of polo-like kinase (PLK) expression in non-small cell lung cancer. Oncogene (1997) 14:543-549.
    • (1997) Oncogene , vol.14 , pp. 543-549
    • WOLF, G.1    ELEZ, R.2    DOERMER, A.3
  • 153
    • 0033564832 scopus 로고    scopus 로고
    • Prognostic significance of polo-like kinase (PLK) expression in squamous cell carcinomas of the head and neck
    • KNECHT R, ELEZ R, OECHLER M et al.: Prognostic significance of polo-like kinase (PLK) expression in squamous cell carcinomas of the head and neck. Cancer Res. (1999) 59:2794-2797.
    • (1999) Cancer Res , vol.59 , pp. 2794-2797
    • KNECHT, R.1    ELEZ, R.2    OECHLER, M.3
  • 154
    • 4444354564 scopus 로고    scopus 로고
    • Identification of human polo-like kinase 1 as a potential therapeutic target in pancreatic cancer
    • GRAY PJ Jr, BEARSS DJ, HAN H et al.: Identification of human polo-like kinase 1 as a potential therapeutic target in pancreatic cancer. Mol. Cancer Ther. (2004) 3:641-646.
    • (2004) Mol. Cancer Ther , vol.3 , pp. 641-646
    • GRAY Jr, P.J.1    BEARSS, D.J.2    HAN, H.3
  • 155
    • 0031581099 scopus 로고    scopus 로고
    • On the regulation and function of human polo-like kinase 1 (PLK1): Effects of overexpression on cell cycle progression
    • MUNDT KE, GOLSTEYN RM, LANE HA, NIGG EA: On the regulation and function of human polo-like kinase 1 (PLK1): effects of overexpression on cell cycle progression. Biochem. Biophys. Res. Commun. (1997) 239:377-385.
    • (1997) Biochem. Biophys. Res. Commun , vol.239 , pp. 377-385
    • MUNDT, K.E.1    GOLSTEYN, R.M.2    LANE, H.A.3    NIGG, E.A.4
  • 156
    • 0037133203 scopus 로고    scopus 로고
    • Functional studies on the role of the C-terminal domain of mammalian polo-like kinase
    • JANG YJ, LIN CY, MA S, ERIKSON RL: Functional studies on the role of the C-terminal domain of mammalian polo-like kinase. Proc. Natl. Acad. Sci. USA (2002) 99:1984-1989.
    • (2002) Proc. Natl. Acad. Sci. USA , vol.99 , pp. 1984-1989
    • JANG, Y.J.1    LIN, C.Y.2    MA, S.3    ERIKSON, R.L.4
  • 157
    • 0034282252 scopus 로고    scopus 로고
    • Polo-like kinase-1 is a target of the DNA damage checkpoint
    • SMITS VA, KLOMPMAKER R, ARNAUD L et al.: Polo-like kinase-1 is a target of the DNA damage checkpoint. Nat. Cell Biol. (2000) 2:672-676.
    • (2000) Nat. Cell Biol , vol.2 , pp. 672-676
    • SMITS, V.A.1    KLOMPMAKER, R.2    ARNAUD, L.3
  • 158
    • 4444321565 scopus 로고    scopus 로고
    • Polo-like kinase-1 controls recovery from a G2 DNA damage-induced arrest in mammalian cells
    • VAN VUGT MA, BRAS A, MEDEMA RH: Polo-like kinase-1 controls recovery from a G2 DNA damage-induced arrest in mammalian cells. Mol. Cell. (2004) 15:799-811.
    • (2004) Mol. Cell , vol.15 , pp. 799-811
    • VAN VUGT MA, B.A.1    MEDEMA, R.H.2
  • 159
    • 23844494690 scopus 로고    scopus 로고
    • Restarting the cell cycle when the checkpoint comes to a halt
    • VAN VUGT MA, BRAS A, MEDEMA RH: Restarting the cell cycle when the checkpoint comes to a halt. Cancer Res. (2005) 65:7037-7040.
    • (2005) Cancer Res , vol.65 , pp. 7037-7040
    • VAN VUGT MA, B.A.1    MEDEMA, R.H.2
  • 160
    • 2942623616 scopus 로고    scopus 로고
    • Polo-like kinase 1 (Plk1) inhibits p53 function by physical interaction and phosphorylation
    • ANDO K, OZAKI T, YAMAMOTO H et al.: Polo-like kinase 1 (Plk1) inhibits p53 function by physical interaction and phosphorylation. J. Biol. Chem. (2004) 279:25549-25561.
    • (2004) J. Biol. Chem , vol.279 , pp. 25549-25561
    • ANDO, K.1    OZAKI, T.2    YAMAMOTO, H.3
  • 161
    • 0029770725 scopus 로고    scopus 로고
    • Prk, a cytokine-inducible human protein serine/threonine kinase whose expression appears to be down-regulated in lung carcinomas
    • LI B, OUYANG B, PAN H et al.: Prk, a cytokine-inducible human protein serine/threonine kinase whose expression appears to be down-regulated in lung carcinomas. J. Biol. Chem. (1996) 271:19402-19408.
    • (1996) J. Biol. Chem , vol.271 , pp. 19402-19408
    • LI, B.1    OUYANG, B.2    PAN, H.3
  • 162
    • 17144458001 scopus 로고    scopus 로고
    • PRK, a cell cycle gene localized to 8p21, is downregulated in head and neck cancer
    • DAI W, LI Y, OUYANG B et al.: PRK, a cell cycle gene localized to 8p21, is downregulated in head and neck cancer. Genes Chrom. Can. (2000) 27:332-336.
    • (2000) Genes Chrom. Can , vol.27 , pp. 332-336
    • DAI, W.1    LI, Y.2    OUYANG, B.3
  • 163
    • 0036134506 scopus 로고    scopus 로고
    • Down-regulation of PLK3 gene expression by types and amount of dietary fat in rat colon tumors
    • DAI W, LIU T, WANG Q et al.: Down-regulation of PLK3 gene expression by types and amount of dietary fat in rat colon tumors. Int. J. Oncol. (2002) 20:121-126.
    • (2002) Int. J. Oncol , vol.20 , pp. 121-126
    • DAI, W.1    LIU, T.2    WANG, Q.3
  • 164
    • 34447577132 scopus 로고    scopus 로고
    • MUNZERT G, STEINBILD S, FROST A et al.: A Phase I study of two administration schedules of the polo-like kinase 1 inhibitor BI 2536 in patients with advanced solid tumors. J. Clin. Oncol. ASCO Annual Meeting Proceedings Part I. (2006) 24(18 Suppl.):3069.
    • MUNZERT G, STEINBILD S, FROST A et al.: A Phase I study of two administration schedules of the polo-like kinase 1 inhibitor BI 2536 in patients with advanced solid tumors. J. Clin. Oncol. ASCO Annual Meeting Proceedings Part I. (2006) 24(18 Suppl.):3069.
  • 165
    • 34447579387 scopus 로고    scopus 로고
    • HOFHEINZ R, HOCHHAUS A, AL-BATRAN S et al.: A Phase I repeated dose escalation study of the polo-like kinase 1 inhibitor BI 2536 in patients with advanced solid tumours. J. Clin. Oncol. ASCO Annual Meeting Proceedings Part I. (2006) 24(18 Suppl.):2038.
    • HOFHEINZ R, HOCHHAUS A, AL-BATRAN S et al.: A Phase I repeated dose escalation study of the polo-like kinase 1 inhibitor BI 2536 in patients with advanced solid tumours. J. Clin. Oncol. ASCO Annual Meeting Proceedings Part I. (2006) 24(18 Suppl.):2038.
  • 166
    • 20044394975 scopus 로고    scopus 로고
    • HMN-214, a novel oral antimicrotubular agent and inhibitor of polo-like- and cyclin-dependent kinases: Clinical, pharmacokinetic (PK) and pharmacodynamic (PD) relationships observed in a Phase I trial of a daily x 5 schedule every 28 days
    • Abstract 514
    • PATNAIK A, FORERO L, GOETZ A et al.: HMN-214, a novel oral antimicrotubular agent and inhibitor of polo-like- and cyclin-dependent kinases: clinical, pharmacokinetic (PK) and pharmacodynamic (PD) relationships observed in a Phase I trial of a daily x 5 schedule every 28 days. Proc. Am. Soc. Clin. Oncol. (2003) 22:Abstract 514.
    • (2003) Proc. Am. Soc. Clin. Oncol , vol.22
    • PATNAIK, A.1    FORERO, L.2    GOETZ, A.3
  • 167
    • 33749010621 scopus 로고    scopus 로고
    • A Phase I pharmacokinetic study of HMN-214, a novel oral stilbene derivative with polo-like kinase-1-interacting properties, in patients with advanced solid tumors
    • GARLAND LL, TAYLOR C, PILKINGTON DL et al.: A Phase I pharmacokinetic study of HMN-214, a novel oral stilbene derivative with polo-like kinase-1-interacting properties, in patients with advanced solid tumors. Clin. Cancer Res. (2006) 12:5182-5189.
    • (2006) Clin. Cancer Res , vol.12 , pp. 5182-5189
    • GARLAND, L.L.1    TAYLOR, C.2    PILKINGTON, D.L.3
  • 168
    • 34447547016 scopus 로고    scopus 로고
    • OHNUMA T, CHO SY, ROBOZ J et al.: Phase I study of ON 01910.Na by 3-day continuous infusion (CI) in patients (pts) with advanced cancer. J. Clin. Oncol. ASCO Annual Meeting Proceedings Part I. (2006) 24(18 Suppl.):13137.
    • OHNUMA T, CHO SY, ROBOZ J et al.: Phase I study of ON 01910.Na by 3-day continuous infusion (CI) in patients (pts) with advanced cancer. J. Clin. Oncol. ASCO Annual Meeting Proceedings Part I. (2006) 24(18 Suppl.):13137.
  • 169
    • 34447568653 scopus 로고    scopus 로고
    • DONEHOWER RC, JIMENO A, LI J et al.: Phase I study of ON-01910.Na, a novel cell cycle inhibitor in adult patients with solid tumors. J. Clin. Oncol. ASCO Annual Meeting Proceedings Part I. (2006) 24(18 Suppl.):13026.
    • DONEHOWER RC, JIMENO A, LI J et al.: Phase I study of ON-01910.Na, a novel cell cycle inhibitor in adult patients with solid tumors. J. Clin. Oncol. ASCO Annual Meeting Proceedings Part I. (2006) 24(18 Suppl.):13026.
  • 170
    • 11244309692 scopus 로고    scopus 로고
    • New microtubule/tubulin-targeted anticancer drugs and novel chemotherapeutic strategies
    • WILSON L, JORDAN MA: New microtubule/tubulin-targeted anticancer drugs and novel chemotherapeutic strategies. J. Chemother. (2004) 16(Suppl. 4):83-85.
    • (2004) J. Chemother , vol.16 , Issue.SUPPL. 4 , pp. 83-85
    • WILSON, L.1    JORDAN, M.A.2
  • 171
    • 1542379866 scopus 로고    scopus 로고
    • Mechanism of taxane neurotoxicity
    • HAGIWARA H, SUNADA Y: Mechanism of taxane neurotoxicity. Breast Cancer (2004) 11:82-85.
    • (2004) Breast Cancer , vol.11 , pp. 82-85
    • HAGIWARA, H.1    SUNADA, Y.2
  • 172
    • 0035433029 scopus 로고    scopus 로고
    • Past and future of the mitotic spindle as an oncology target
    • WOOD KW, CORNWELL WD, JACKSON JR: Past and future of the mitotic spindle as an oncology target. Curr. Opin. Pharmacol. (2001) 1:370-377.
    • (2001) Curr. Opin. Pharmacol , vol.1 , pp. 370-377
    • WOOD, K.W.1    CORNWELL, W.D.2    JACKSON, J.R.3
  • 173
    • 2342563857 scopus 로고    scopus 로고
    • Antitumor activity of a kinesin inhibitor
    • SAKOWICZ R, FINER JT, BERAUD C et al.: Antitumor activity of a kinesin inhibitor. Cancer Res. (2004) 64:3276-3280.
    • (2004) Cancer Res , vol.64 , pp. 3276-3280
    • SAKOWICZ, R.1    FINER, J.T.2    BERAUD, C.3
  • 174
    • 0029417238 scopus 로고
    • Phosphorylation by p34cdc2 regulates spindle association of human Eg5, a kinesin-related motor essential for bipolar spindle formation in vivo
    • BLANGY A, LANE HA, D'HERIN P et al.: Phosphorylation by p34cdc2 regulates spindle association of human Eg5, a kinesin-related motor essential for bipolar spindle formation in vivo. Cell (1995) 83:1159-1169.
    • (1995) Cell , vol.83 , pp. 1159-1169
    • BLANGY, A.1    LANE, H.A.2    D'HERIN, P.3
  • 176
    • 15744404844 scopus 로고    scopus 로고
    • Mitotic kinesin inhibitors induce mitotic arrest and cell death in Taxol-resistant and -sensitive cancer cells
    • MARCUS AI, PETERS U, THOMAS SL et al.: Mitotic kinesin inhibitors induce mitotic arrest and cell death in Taxol-resistant and -sensitive cancer cells. J. Biol. Chem. (2005) 280:11569-11577.
    • (2005) J. Biol. Chem , vol.280 , pp. 11569-11577
    • MARCUS, A.I.1    PETERS, U.2    THOMAS, S.L.3
  • 177
    • 0030665077 scopus 로고    scopus 로고
    • CENP-E is a plus end-directed kinetochore motor required for metaphase chromosome alignment
    • WOOD KW, SAKOWICZ R, GOLDSTEIN LS, CLEVELAND DW: CENP-E is a plus end-directed kinetochore motor required for metaphase chromosome alignment. Cell (1997) 91:357-366.
    • (1997) Cell , vol.91 , pp. 357-366
    • WOOD, K.W.1    SAKOWICZ, R.2    GOLDSTEIN, L.S.3    CLEVELAND, D.W.4
  • 178
    • 0038446875 scopus 로고    scopus 로고
    • Activating and silencing the mitotic checkpoint through CENP-E-dependent activation/inactivation of BubR1
    • MAO Y, ABRIEU A, CLEVELAND DW: Activating and silencing the mitotic checkpoint through CENP-E-dependent activation/inactivation of BubR1. Cell (2003) 114:87-98.
    • (2003) Cell , vol.114 , pp. 87-98
    • MAO, Y.1    ABRIEU, A.2    CLEVELAND, D.W.3
  • 179
    • 0035172929 scopus 로고    scopus 로고
    • CENP-E is essential for reliable bioriented spindle attachment, but chromosome alignment can be achieved via redundant mechanisms in mammalian cells
    • MCEWEN BF, CHAN GK, ZUBROWSKI B et al.: CENP-E is essential for reliable bioriented spindle attachment, but chromosome alignment can be achieved via redundant mechanisms in mammalian cells. Mol. Biol. Cell (2001) 12:2776-2789.
    • (2001) Mol. Biol. Cell , vol.12 , pp. 2776-2789
    • MCEWEN, B.F.1    CHAN, G.K.2    ZUBROWSKI, B.3
  • 180
    • 0001665802 scopus 로고    scopus 로고
    • CENP-E forms a link between attachment of spindle microtubules to kinetochores and the mitotic checkpoint
    • YAO X, ABRIEU A, ZHENG Y et al.: CENP-E forms a link between attachment of spindle microtubules to kinetochores and the mitotic checkpoint. Nat. Cell Biol. (2000) 2:484-491.
    • (2000) Nat. Cell Biol , vol.2 , pp. 484-491
    • YAO, X.1    ABRIEU, A.2    ZHENG, Y.3
  • 181
    • 0036744787 scopus 로고    scopus 로고
    • Unstable kinetochore-microtubule capture and chromosomal instability following deletion of CENP-E
    • PUTKEY FR, CRAMER T, MORPHEW MK et al.: Unstable kinetochore-microtubule capture and chromosomal instability following deletion of CENP-E. Dev. Cell. (2002) 3:351-365.
    • (2002) Dev. Cell , vol.3 , pp. 351-365
    • PUTKEY, F.R.1    CRAMER, T.2    MORPHEW, M.K.3
  • 182
    • 0242552464 scopus 로고    scopus 로고
    • Farnesyltransferase inhibitors and their potential in the treatment of breast carcinoma
    • DE BONO JS, TA EK: Farnesyltransferase inhibitors and their potential in the treatment of breast carcinoma. Seminars in oncology (2003) 30:79-92.
    • (2003) Seminars in oncology , vol.30 , pp. 79-92
    • DE BONO, J.S.1    TA, E.K.2
  • 183
    • 22244459880 scopus 로고    scopus 로고
    • Induction of apoptosis by an inhibitor of the mitotic kinesin KSP requires both activation of the spindle assembly checkpoint and mitotic slippage
    • TAO W, SOUTH VJ, ZHANG Y et al.: Induction of apoptosis by an inhibitor of the mitotic kinesin KSP requires both activation of the spindle assembly checkpoint and mitotic slippage. Cancer Cell (2005) 8:49-59.
    • (2005) Cancer Cell , vol.8 , pp. 49-59
    • TAO, W.1    SOUTH, V.J.2    ZHANG, Y.3
  • 184
    • 34447555103 scopus 로고    scopus 로고
    • Clinical investigator's brochure for SB-715992 (GlaxoSmithKline Group Company): In Edition.
    • Clinical investigator's brochure for SB-715992 (GlaxoSmithKline Group Company): In Edition.
  • 185
    • 33645023929 scopus 로고    scopus 로고
    • Increased therapeutic potential of an experimental anti-mitotic inhibitor SB715992 by genistein in PC-3 human prostate cancer cell line
    • DAVIS DA, SARKAR SH, HUSSAIN M et al.: Increased therapeutic potential of an experimental anti-mitotic inhibitor SB715992 by genistein in PC-3 human prostate cancer cell line. BMC Cancer (2006) 6:22.
    • (2006) BMC Cancer , vol.6 , pp. 22
    • DAVIS, D.A.1    SARKAR, S.H.2    HUSSAIN, M.3
  • 186
    • 34447563078 scopus 로고    scopus 로고
    • JONES SF, PLUMMER ER, BURRIS HA et al.: Phase I study of ispinesib in combination with carboplatin in patients with advanced solid tumors. J. Clin. Oncol. ASCO Annual Meeting Proceedings Part I. (2006) 24(18 Suppl.):2027.
    • JONES SF, PLUMMER ER, BURRIS HA et al.: Phase I study of ispinesib in combination with carboplatin in patients with advanced solid tumors. J. Clin. Oncol. ASCO Annual Meeting Proceedings Part I. (2006) 24(18 Suppl.):2027.
  • 187
    • 34447579386 scopus 로고    scopus 로고
    • BURRIS HA, LORUSSO P, JONES S et al.: Phase I trial of novel kinesin spindle protein (KSP) inhibitor SB-715992 i.v days 1, 8, 15 q 28 days. J. Clin. Oncol. ASCO Annual Meeting Proceedings Part I. (2006) 24(18 Suppl.):2004.
    • BURRIS HA, LORUSSO P, JONES S et al.: Phase I trial of novel kinesin spindle protein (KSP) inhibitor SB-715992 i.v days 1, 8, 15 q 28 days. J. Clin. Oncol. ASCO Annual Meeting Proceedings Part I. (2006) 24(18 Suppl.):2004.
  • 188
    • 34447546019 scopus 로고    scopus 로고
    • CHU QS, HOLEN KD, ROWINSKY EK et al.: Phase I trial of novel kinesin spindle protein (KSP) inhibitor SB-715992 i.v Q 21 days. J. Clin. Oncol. ASCO Annual Meeting Proceedings Part I. (2006) 24(18 Suppl.):2078.
    • CHU QS, HOLEN KD, ROWINSKY EK et al.: Phase I trial of novel kinesin spindle protein (KSP) inhibitor SB-715992 i.v Q 21 days. J. Clin. Oncol. ASCO Annual Meeting Proceedings Part I. (2006) 24(18 Suppl.):2078.
  • 189
    • 34447534646 scopus 로고    scopus 로고
    • HEATH EI, ALOUSI A, EDER JP et al.: A Phase I dose escalation trial of ispinesib (SB-715992) administered days 1-3 of a 21-day cycle in patients with advanced solid tumors. J. Clin. Oncol. ASCO Annual Meeting Proceedings Part I. (2006) 24(18 Suppl.):2026.
    • HEATH EI, ALOUSI A, EDER JP et al.: A Phase I dose escalation trial of ispinesib (SB-715992) administered days 1-3 of a 21-day cycle in patients with advanced solid tumors. J. Clin. Oncol. ASCO Annual Meeting Proceedings Part I. (2006) 24(18 Suppl.):2026.
  • 191
    • 34447557137 scopus 로고    scopus 로고
    • JONES SF, PLUMMER ER, BURRIS HA et al.: Phase I study of ispinesib in combination with carboplatin in patients with advanced solid tumors. J. Clin. Oncol. ASCO Annual Meeting Proceedings Part I. (2006) 24(18 Suppl.):2027.
    • JONES SF, PLUMMER ER, BURRIS HA et al.: Phase I study of ispinesib in combination with carboplatin in patients with advanced solid tumors. J. Clin. Oncol. ASCO Annual Meeting Proceedings Part I. (2006) 24(18 Suppl.):2027.
  • 192
    • 34447541527 scopus 로고    scopus 로고
    • EI-KHOUEIRY AB, IQBAL DA, SINGH DA et al.: A randomized Phase II non-comparative study of Ispinesib given weekly or every three weeks in metastatic colorectal cancer. A California Cancer Consortium Study (CCC-P). J. Clin. Oncol. ASCO Annual Meeting Proceedings Part I. (2006) 24(18 Suppl.):3595.
    • EI-KHOUEIRY AB, IQBAL DA, SINGH DA et al.: A randomized Phase II non-comparative study of Ispinesib given weekly or every three weeks in metastatic colorectal cancer. A California Cancer Consortium Study (CCC-P). J. Clin. Oncol. ASCO Annual Meeting Proceedings Part I. (2006) 24(18 Suppl.):3595.
  • 193
    • 42549153290 scopus 로고    scopus 로고
    • Phase II, open label study of SB-715992 (ispinesib) in subjects with advanced or metastatic breast cancer
    • Abstract 1089
    • MILLER K, NG C, ANG P et al.: Phase II, open label study of SB-715992 (ispinesib) in subjects with advanced or metastatic breast cancer. San Antonio Breast Cancer Symposium (2005) Abstract 1089.
    • (2005) San Antonio Breast Cancer Symposium
    • MILLER, K.N.C.1    ANG, P.2
  • 194
    • 34447575125 scopus 로고    scopus 로고
    • HOLEN KD, BELANI CP, WILDING G et al.: Phase I study to determine tolerability and pharmacokinetics (PK) of SB-743921, a novel kinesin spindle protein (KSP) inhibitor. J. Clin. Oncol. ASCO Annual Meeting Proceedings Part I. (2006) 24(18 Suppl.):2000.
    • HOLEN KD, BELANI CP, WILDING G et al.: Phase I study to determine tolerability and pharmacokinetics (PK) of SB-743921, a novel kinesin spindle protein (KSP) inhibitor. J. Clin. Oncol. ASCO Annual Meeting Proceedings Part I. (2006) 24(18 Suppl.):2000.
  • 195
    • 34447565334 scopus 로고    scopus 로고
    • STEIN MN, RUBIN EH, SCOTT PD et al.: Phase I clinical and pharmacokinetic (PK) trial of the kinesin spindle protein (KSP) inhibitor MK-0731 in cancer patients. J. Clin. Oncol. ASCO Annual Meeting Proceedings Part I. (2006) 24(18 Suppl.):2001.
    • STEIN MN, RUBIN EH, SCOTT PD et al.: Phase I clinical and pharmacokinetic (PK) trial of the kinesin spindle protein (KSP) inhibitor MK-0731 in cancer patients. J. Clin. Oncol. ASCO Annual Meeting Proceedings Part I. (2006) 24(18 Suppl.):2001.
  • 196
    • 33344476097 scopus 로고    scopus 로고
    • DNA damage checkpoints in mammals
    • NIIDA H, NAKANISHI M: DNA damage checkpoints in mammals. Mutagenesis (2006) 21:3-9.
    • (2006) Mutagenesis , vol.21 , pp. 3-9
    • NIIDA, H.1    NAKANISHI, M.2
  • 197
    • 3242879828 scopus 로고    scopus 로고
    • Chk1 in the DNA damage response: Conserved roles from yeasts to mammals
    • CHEN Y, SANCHEZ Y: Chk1 in the DNA damage response: conserved roles from yeasts to mammals. DNA Repair (Amsterdam) (2004) 3:1025-1032.
    • (2004) DNA Repair (Amsterdam) , vol.3 , pp. 1025-1032
    • CHEN, Y.1    SANCHEZ, Y.2
  • 198
    • 33748073782 scopus 로고    scopus 로고
    • Targeting the double-strand DNA break repair pathway as a therapeutic strategy
    • LORD CJ, GARRETT MD, ASHWORTH A: Targeting the double-strand DNA break repair pathway as a therapeutic strategy. Clin. Cancer Res. (2006) 12:4463-4468.
    • (2006) Clin. Cancer Res , vol.12 , pp. 4463-4468
    • LORD, C.J.1    GARRETT, M.D.2    ASHWORTH, A.3
  • 199
    • 1542725073 scopus 로고    scopus 로고
    • Targeting the checkpoint kinases: Chemosensitization versus chemoprotection
    • ZHOU BB, BARTEK J: Targeting the checkpoint kinases: chemosensitization versus chemoprotection. Nat. Rev. Cancer (2004) 4:216-225.
    • (2004) Nat. Rev. Cancer , vol.4 , pp. 216-225
    • ZHOU, B.B.1    BARTEK, J.2
  • 200
    • 18544384850 scopus 로고    scopus 로고
    • Novel indication for cancer therapy: Chk1 inhibition sensitizes tumor cells to antimitotics
    • XIAO Z, XUE J, SEMIZAROV D et al.: Novel indication for cancer therapy: Chk1 inhibition sensitizes tumor cells to antimitotics. Int. J. Cancer (2005) 115:528-538.
    • (2005) Int. J. Cancer , vol.115 , pp. 528-538
    • XIAO, Z.1    XUE, J.2    SEMIZAROV, D.3
  • 201
    • 14844315930 scopus 로고    scopus 로고
    • A novel mechanism of checkpoint abrogation conferred by Chk1 downregulation
    • XIAO Z, XUE J, SOWIN TJ et al.: A novel mechanism of checkpoint abrogation conferred by Chk1 downregulation. Oncogene (2005) 24:1403-1411.
    • (2005) Oncogene , vol.24 , pp. 1403-1411
    • XIAO, Z.1    XUE, J.2    SOWIN, T.J.3
  • 202
    • 21644456228 scopus 로고    scopus 로고
    • Targeting the cell division cycle in cancer: CDK and cell cycle checkpoint kinase inhibitors
    • COLLINS I, GARRETT MD: Targeting the cell division cycle in cancer: CDK and cell cycle checkpoint kinase inhibitors. Curr. Opin. Pharmacol. (2005) 5:366-373.
    • (2005) Curr. Opin. Pharmacol , vol.5 , pp. 366-373
    • COLLINS, I.1    GARRETT, M.D.2
  • 203
    • 34447534645 scopus 로고    scopus 로고
    • MCARTHUR GA, RALEIGH J, BLASINA A et al.: Imaging with FLT-PET demonstrates that PF-477736, an inhibitor of Chk1 kinase, overcomes a cell cycle checkpoint induced by gemcitabine in PC-3 xenografts. Journal of Clinical Oncology, (2006) ASCO Annual Meeting Proceedings Part I. 24, No. 18S (June 20 Supplement), (2006) 3045.
    • MCARTHUR GA, RALEIGH J, BLASINA A et al.: Imaging with FLT-PET demonstrates that PF-477736, an inhibitor of Chk1 kinase, overcomes a cell cycle checkpoint induced by gemcitabine in PC-3 xenografts. Journal of Clinical Oncology, (2006) ASCO Annual Meeting Proceedings Part I. Vol. 24, No. 18S (June 20 Supplement), (2006) 3045.
  • 204
    • 23244443806 scopus 로고    scopus 로고
    • New checkpoint blockers begin human trials
    • July 20
    • GARBER K: New checkpoint blockers begin human trials. Journal of the National Cancer Institute, Vol. 97, No. 14, July 20, (2005) 1026-1028.
    • (2005) Journal of the National Cancer Institute , vol.97 , Issue.14 , pp. 1026-1028
    • GARBER, K.1
  • 205
    • 0038739131 scopus 로고    scopus 로고
    • Never say never. The NIMA-related protein kinases in mitotic control
    • O'CONNELL MJ, KRIEN MJ, HUNTER T: Never say never. The NIMA-related protein kinases in mitotic control. Trends Cell Biol. (2003) 13:221-228.
    • (2003) Trends Cell Biol , vol.13 , pp. 221-228
    • O'CONNELL, M.J.1    KRIEN, M.J.2    HUNTER, T.3
  • 206
    • 0026048594 scopus 로고
    • Parallel activation of the NIMA and p34cdc2 cell cycle-regulated protein kinases is required to initiate mitosis in A. nidulans
    • OSMANI AH, MCGUIRE SL, OSMANI SA: Parallel activation of the NIMA and p34cdc2 cell cycle-regulated protein kinases is required to initiate mitosis in A. nidulans. Cell (1991) 67:283-291.
    • (1991) Cell , vol.67 , pp. 283-291
    • OSMANI, A.H.1    MCGUIRE, S.L.2    OSMANI, S.A.3
  • 207
    • 1542395668 scopus 로고    scopus 로고
    • Nek8, a NIMA family kinase member, is overexpressed in primary human breast tumors
    • BOWERS AJ, BOYLAN JF: Nek8, a NIMA family kinase member, is overexpressed in primary human breast tumors. Gene (2004) 328:135-142.
    • (2004) Gene , vol.328 , pp. 135-142
    • BOWERS, A.J.1    BOYLAN, J.F.2
  • 208
    • 33644830944 scopus 로고    scopus 로고
    • Targeting the cell cycle: A new approach to cancer therapy
    • SCHWARTZ GK, SHAH MA: Targeting the cell cycle: a new approach to cancer therapy. J. Clin. Oncol. (2005) 23:9408-9421.
    • (2005) J. Clin. Oncol , vol.23 , pp. 9408-9421
    • SCHWARTZ, G.K.1    SHAH, M.A.2
  • 209
    • 0142116249 scopus 로고    scopus 로고
    • Cdk2 knockout mice are viable
    • BERTHET C, ALEEM E, COPPOLA V et al.: Cdk2 knockout mice are viable. Curr. Biol. (2003) 13:1775-1785.
    • (2003) Curr. Biol , vol.13 , pp. 1775-1785
    • BERTHET, C.1    ALEEM, E.2    COPPOLA, V.3
  • 210
    • 20444410393 scopus 로고    scopus 로고
    • Cdk2 is dispensable for cell cycle inhibition and tumor suppression mediated by p27(Kip1) and p21(Cip1)
    • MARTIN A, ODAJIMA J, HUNT SL et al.: Cdk2 is dispensable for cell cycle inhibition and tumor suppression mediated by p27(Kip1) and p21(Cip1). Cancer Cell. (2005) 7:591-598.
    • (2005) Cancer Cell , vol.7 , pp. 591-598
    • MARTIN, A.1    ODAJIMA, J.2    HUNT, S.L.3
  • 211
    • 0037311226 scopus 로고    scopus 로고
    • Rapid induction of apoptosis by combination of flavopiridol and tumor necrosis factor (TNF)-α or TNF-related apoptosis-inducing ligand in human cancer cell lines
    • KIM DM, KOO SY, JEON K et al.: Rapid induction of apoptosis by combination of flavopiridol and tumor necrosis factor (TNF)-α or TNF-related apoptosis-inducing ligand in human cancer cell lines. Cancer Res. (2003) 63:621-626.
    • (2003) Cancer Res , vol.63 , pp. 621-626
    • KIM, D.M.1    KOO, S.Y.2    JEON, K.3
  • 212
    • 0242468166 scopus 로고    scopus 로고
    • Proteasome inhibitors potentiate leukemic cell apoptosis induced by the cyclin-dependent kinase inhibitor flavopiridol through a SAPK/JNK- and NF-kappaB-dependent process
    • DAI Y, RAHMANI M, GRANT S: Proteasome inhibitors potentiate leukemic cell apoptosis induced by the cyclin-dependent kinase inhibitor flavopiridol through a SAPK/JNK- and NF-kappaB-dependent process. Oncogene (2003) 22:7108-7122.
    • (2003) Oncogene , vol.22 , pp. 7108-7122
    • DAI, Y.1    RAHMANI, M.2    GRANT, S.3
  • 213
    • 7744235176 scopus 로고    scopus 로고
    • Targeting cell cycle and apoptosis for the treatment of human malignancies
    • SENDEROWICZ AM: Targeting cell cycle and apoptosis for the treatment of human malignancies. Curr. Opin. Cell Biol. (2004) 16:670-678.
    • (2004) Curr. Opin. Cell Biol , vol.16 , pp. 670-678
    • SENDEROWICZ, A.M.1
  • 214
    • 0034730127 scopus 로고    scopus 로고
    • Histone deacetylase inhibitor selectively induces p21WAF1 expression and gene-associated histone acetylation
    • RICHON VM, SANDHOFF TW, RIFKIND RA, MARKS PA: Histone deacetylase inhibitor selectively induces p21WAF1 expression and gene-associated histone acetylation. Proc. Natl. Acad. Sci USA (2000) 97:10014-10019.
    • (2000) Proc. Natl. Acad. Sci USA , vol.97 , pp. 10014-10019
    • RICHON, V.M.1    SANDHOFF, T.W.2    RIFKIND, R.A.3    MARKS, P.A.4
  • 215
    • 0347993069 scopus 로고    scopus 로고
    • Hsp90 inhibition depletes Chk1 and sensitizes tumor cells to replication stress
    • ARLANDER SJ, EAPEN AK, VROMAN BT et al.: Hsp90 inhibition depletes Chk1 and sensitizes tumor cells to replication stress. J. Biol. Chem. (2003) 278:52572-52577.
    • (2003) J. Biol. Chem , vol.278 , pp. 52572-52577
    • ARLANDER, S.J.1    EAPEN, A.K.2    VROMAN, B.T.3
  • 216
    • 10744221485 scopus 로고    scopus 로고
    • In vivo activation of the p53 pathway by small-molecule antagonists of MDM2
    • VASSILEV LT, VU BT, GRAVES B et al.: In vivo activation of the p53 pathway by small-molecule antagonists of MDM2. Science (2004) 303:844-848.
    • (2004) Science , vol.303 , pp. 844-848
    • VASSILEV, L.T.1    VU, B.T.2    GRAVES, B.3
  • 217
    • 20044390359 scopus 로고    scopus 로고
    • Patterns of resistance and incomplete response to docetaxel by gene expression profiling in breast cancer patients
    • CHANG JC, WOOTEN EC, TSIMELZON A et al.: Patterns of resistance and incomplete response to docetaxel by gene expression profiling in breast cancer patients. J. Clin. Oncol. (2005) 23:1169-1177.
    • (2005) J. Clin. Oncol , vol.23 , pp. 1169-1177
    • CHANG, J.C.1    WOOTEN, E.C.2    TSIMELZON, A.3


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