메뉴 건너뛰기




Volumn 10, Issue 11, 2010, Pages 1058-1070

Flavopiridol, the first cyclin-dependent kinase inhibitor: Recent advances in combination chemotherapy

Author keywords

Anticancer; Cancer; CDKIs; Combination therapy; Flavonoid; Flavopiridol

Indexed keywords

2 FLUOROPHENYL; 5 METHYLISOXAZOLE; 7 HYDROXYSTAUROSPORINE; BENZYLOXYCARBONYLLEUCYLLEUCYLLEUCINAL; BORTEZOMIB; BRYOSTATIN; BUTYRIC ACID; CYCLIN DEPENDENT KINASE INHIBITOR; DEPSIPEPTIDE; DESCHLOROFLAVOPIRIDOL; DOCETAXEL; DOXORUBICIN; ETOPOSIDE; FLAVOPIRIDOL; GEMCITABINE; GENISTEIN; HISTONE DEACETYLASE INHIBITOR; IMATINIB; ISOCOUMARIN DERIVATIVE; LACTACYSTIN; MINOCYCLINE; OXOFLAVOPIRIDOL; PACLITAXEL; PROTEASOME INHIBITOR; QUERCETIN; QUINOLONE DERIVATIVE; THIOFLAVOPIRIDOL; TRASTUZUMAB; UNCLASSIFIED DRUG; UNINDEXED DRUG; VORINOSTAT;

EID: 77956637674     PISSN: 13895575     EISSN: None     Source Type: Journal    
DOI: 10.2174/1389557511009011058     Document Type: Article
Times cited : (57)

References (112)
  • 1
    • 0036401813 scopus 로고    scopus 로고
    • Flavonoids as anticancer agents: Structure-activity relationship study
    • López-Lázaro, M. Flavonoids as anticancer agents: structure-activity relationship study. Curr. Med. Chem. Anticancer Agents., 2002, 2, 691-714.
    • (2002) Curr. Med. Chem. Anticancer Agents , vol.2 , pp. 691-714
    • López-Lázaro, M.1
  • 2
    • 1042278138 scopus 로고    scopus 로고
    • Flavopiridol inhibits NF-κB activation induced by various carcinogens and inflammatory agents through inhibition of I B kinase and p65 phosphorylation: Abrogation of cyclin D1, cyclooxygenase-2, and matrix metalloprotease-9
    • Takada, Y.; Aggarwal, B.B. Flavopiridol inhibits NF-κB activation induced by various carcinogens and inflammatory agents through inhibition of I B kinase and p65 phosphorylation: abrogation of cyclin D1, cyclooxygenase-2, and matrix metalloprotease-9. J. Biol. Chem., 2004, 279, 4750-4759.
    • (2004) J. Biol. Chem , vol.279 , pp. 4750-4759
    • Takada, Y.1    Aggarwal, B.B.2
  • 3
    • 0033646291 scopus 로고    scopus 로고
    • Flavopiridol, the first cyclin-dependent kinase inhibitor to enter the clinic: Current status
    • Kelland, L.R. Flavopiridol, the first cyclin-dependent kinase inhibitor to enter the clinic: current status. Expert. Opin. Investig. Drugs., 2000, 9, 2903-2911.
    • (2000) Expert. Opin. Investig. Drugs , vol.9 , pp. 2903-2911
    • Kelland, L.R.1
  • 4
    • 3042536038 scopus 로고    scopus 로고
    • Preclinical and clinical development of the cyclin-dependent kinase inhibitor flavopiridol
    • Shapiro, G.I. Preclinical and clinical development of the cyclin-dependent kinase inhibitor flavopiridol. Clin. Cancer Res., 2004, 10, 4270s-4275s.
    • (2004) Clin. Cancer Res , vol.10
    • Shapiro, G.I.1
  • 5
    • 0040932434 scopus 로고    scopus 로고
    • The novel cyclin-dependent kinase inhibitor flavopiridol downregulates Bcl-2 and induces growth arrest and apoptosis in chronic B-cell leukemia lines
    • König, A.; Schwartz, G.K.; Mohammad, R.M.; Al-Katib, A.; Gabrilove, J.L. The novel cyclin-dependent kinase inhibitor flavopiridol downregulates Bcl-2 and induces growth arrest and apoptosis in chronic B-cell leukemia lines. Blood, 1997, 90, 4307-4312.
    • (1997) Blood , vol.90 , pp. 4307-4312
    • König, A.1    Schwartz, G.K.2    Mohammad, R.M.3    Al-Katib, A.4    Gabrilove, J.L.5
  • 6
    • 0036850211 scopus 로고    scopus 로고
    • The cyclin-dependent kinase inhibitor flavopiridol induces apoptosis in multiple myeloma cells through transcriptional repression and down-regulation of Mcl-1
    • Gojo, I.; Zhang, B.; Fenton, R.G. The cyclin-dependent kinase inhibitor flavopiridol induces apoptosis in multiple myeloma cells through transcriptional repression and down-regulation of Mcl-1. Clin. Cancer Res., 2002, 8, 3527-3538.
    • (2002) Clin. Cancer Res , vol.8 , pp. 3527-3538
    • Gojo, I.1    Zhang, B.2    Fenton, R.G.3
  • 7
    • 0034661538 scopus 로고    scopus 로고
    • Protein kinase inhibitors flavopiridol and 7-hydroxy-staurosporine down-regulate antiapoptosis proteins in B-cell chronic lymphocytic leukemia
    • Kitada, S.; Zapata, J.M.; Andreeff, M.; Reed, J.C. Protein kinase inhibitors flavopiridol and 7-hydroxy-staurosporine down-regulate antiapoptosis proteins in B-cell chronic lymphocytic leukemia. Blood, 2000, 96, 393-397.
    • (2000) Blood , vol.96 , pp. 393-397
    • Kitada, S.1    Zapata, J.M.2    Andreeff, M.3    Reed, J.C.4
  • 9
    • 0036632965 scopus 로고    scopus 로고
    • Flavopiridol and trastuzumab synergistically inhibit proliferation of breast cancer cells: Association with selective cooperative inhibition of cyclin D1-dependent kinase and Akt signaling pathways
    • Wu, K.; Wang, C.; D'Amico, M.; Lee, R.J.; Albanese, C.; Pestell, R.G.; Mani, S. Flavopiridol and trastuzumab synergistically inhibit proliferation of breast cancer cells: association with selective cooperative inhibition of cyclin D1-dependent kinase and Akt signaling pathways. Mol. Cancer Ther., 2002, 1, 695-706.
    • (2002) Mol. Cancer Ther , vol.1 , pp. 695-706
    • Wu, K.1    Wang, C.2    D'Amico, M.3    Lee, R.J.4    Albanese, C.5    Pestell, R.G.6    Mani, S.7
  • 11
    • 0033231301 scopus 로고    scopus 로고
    • Flavopiridol, a protein kinase inhibitor, downregulates hypoxic induction of vascular endothelial growth factor expression in human monocytes
    • Melillo, G.; Sausville, E.A.; Cloud, K.; Lahusen, T.; Varesio, L.; Senderowicz, A.M. Flavopiridol, a protein kinase inhibitor, downregulates hypoxic induction of vascular endothelial growth factor expression in human monocytes. Cancer Res., 1999, 59, 5433-5437.
    • (1999) Cancer Res , vol.59 , pp. 5433-5437
    • Melillo, G.1    Sausville, E.A.2    Cloud, K.3    Lahusen, T.4    Varesio, L.5    Senderowicz, A.M.6
  • 12
    • 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, T.M.; Schwartz, G.K. 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
  • 13
    • 0030812207 scopus 로고    scopus 로고
    • Cytotoxic synergy between flavopiridol (NSC 649890, L86-8275) and various antineoplastic agents: The importance of sequence of administration
    • Bible, K.C.; Kaufmann, S.H. Cytotoxic synergy between flavopiridol (NSC 649890, L86-8275) and various antineoplastic agents: the importance of sequence of administration. Cancer Res., 1997, 57, 3375-3380.
    • (1997) Cancer Res , vol.57 , pp. 3375-3380
    • Bible, K.C.1    Kaufmann, S.H.2
  • 15
    • 0346734278 scopus 로고    scopus 로고
    • The cyclindependent kinase inhibitor flavopiridol potentiates γ-irradiation-induced apoptosis in colon and gastric cancer cells
    • Jung, C.; Motwani, M.; Kortmansky, J.; Sirotnak, F.M.; She, Y.; Gonen, M.; Haimovitz-Friedman, A.; Schwartz, G.K. The cyclindependent kinase inhibitor flavopiridol potentiates γ-irradiation-induced apoptosis in colon and gastric cancer cells. Clin. Cancer Res., 2003, 9, 6052-6061.
    • (2003) Clin. Cancer Res , vol.9 , pp. 6052-6061
    • Jung, C.1    Motwani, M.2    Kortmansky, J.3    Sirotnak, F.M.4    She, Y.5    Gonen, M.6    Haimovitz-Friedman, A.7    Schwartz, G.K.8
  • 16
    • 12344294326 scopus 로고    scopus 로고
    • Flavopiridol as a radio-sensitizer for esophageal cancer cell lines
    • Sato, S.; Kajiyama, Y.; Sugano, M.; Iwanuma, Y.; Tsurumaru, M. Flavopiridol as a radio-sensitizer for esophageal cancer cell lines. Dis. Esophagus., 2004, 17, 338-344.
    • (2004) Dis. Esophagus , vol.17 , pp. 338-344
    • Sato, S.1    Kajiyama, Y.2    Sugano, M.3    Iwanuma, Y.4    Tsurumaru, M.5
  • 17
    • 0037086282 scopus 로고    scopus 로고
    • Selective sensitization of trans-formed cells to flavopiridol-induced apoptosis following recruitment to S-phase
    • Matranga, C.B.; Shapiro, G.I. Selective sensitization of trans-formed 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
  • 18
    • 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.; She, Y.; Schwartz, G.K. 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    She, Y.4    Schwartz, G.K.5
  • 21
    • 37549040614 scopus 로고    scopus 로고
    • Extrinsic pathway-and cathepsin-dependent induction of mitochondrial dysfunction are essential for synergistic flavopiridol and vorinostat lethality in breast cancer cells
    • Mitchell, C.; Park, M.A.; Zhang, G.; Yacoub, A.; Curiel, D.T.; Fisher, P.B.; Roberts, J.D.; Grant, S.; Dent, P. Extrinsic pathway-and cathepsin-dependent induction of mitochondrial dysfunction are essential for synergistic flavopiridol and vorinostat lethality in breast cancer cells. Mol. Cancer Ther., 2007, 6, 3101-3112.
    • (2007) Mol. Cancer Ther , vol.6 , pp. 3101-3112
    • Mitchell, C.1    Park, M.A.2    Zhang, G.3    Yacoub, A.4    Curiel, D.T.5    Fisher, P.B.6    Roberts, J.D.7    Grant, S.8    Dent, P.9
  • 22
    • 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, D.M.; Koo, S.Y.; Jeon, K.; Kim, M.H.; Lee, J.; Hong, C.Y.; Jeong, S. 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    Kim, M.H.4    Lee, J.5    Hong, C.Y.6    Jeong, S.7
  • 23
    • 12344252927 scopus 로고    scopus 로고
    • The small-molecule Bcl-2 inhibitor HA14-1 interacts synergistically with flavopiridol to induce mitochondrial injury and apoptosis in human myeloma cells through a free radical-dependent and Jun NH2-terminal kinase-dependent mechanism
    • Pei, X.Y.; Dai, Y.; Grant, S. The small-molecule Bcl-2 inhibitor HA14-1 interacts synergistically with flavopiridol to induce mitochondrial injury and apoptosis in human myeloma cells through a free radical-dependent and Jun NH2-terminal kinase-dependent mechanism. Mol. Cancer Ther., 2004, 3, 1513-1524.
    • (2004) Mol. Cancer Ther , vol.3 , pp. 1513-1524
    • Pei, X.Y.1    Dai, Y.2    Grant, S.3
  • 27
    • 0035951928 scopus 로고    scopus 로고
    • A stereo-controlled approach to substituted piperidones and piperidines: Flavopiridol D-ring analogs
    • Gross, A.; Borcherding, D.R.; Friedrich, D.; Sabol, J.S. A stereo-controlled approach to substituted piperidones and piperidines: flavopiridol D-ring analogs. Tetrahedron. Lett., 2001, 42, 1631-1633.
    • (2001) Tetrahedron. Lett , vol.42 , pp. 1631-1633
    • Gross, A.1    Borcherding, D.R.2    Friedrich, D.3    Sabol, J.S.4
  • 28
    • 70349558526 scopus 로고    scopus 로고
    • Identification of flavopiridol analogues that selectively inhibit positive transcription elongation factor (P-TEFb) and block HIV-1 replication
    • Ali, A.; Ghosh, A.; Nathans, R.S.; Sharova, N.; O'Brien, S.; Cao, H.; Stevenson, M.; Rana, T.M. Identification of flavopiridol analogues that selectively inhibit positive transcription elongation factor (P-TEFb) and block HIV-1 replication. ChemBioChem., 2009, 10, 2072-2080.
    • (2009) ChemBioChem , vol.10 , pp. 2072-2080
    • Ali, A.1    Ghosh, A.2    Nathans, R.S.3    Sharova, N.4    O'Brien, S.5    Cao, H.6    Stevenson, M.7    Rana, T.M.8
  • 30
    • 44649155314 scopus 로고    scopus 로고
    • New combination therapies with cell-cycle agents
    • Deep, G.; Agarwal, R. New combination therapies with cell-cycle agents. Curr. Opin. Investig. Drugs., 2008, 9, 591-604.
    • (2008) Curr. Opin. Investig. Drugs , vol.9 , pp. 591-604
    • Deep, G.1    Agarwal, R.2
  • 31
    • 0038052805 scopus 로고    scopus 로고
    • The cell cycle: A review of regulation, deregulation and therapeutic targets in cancer
    • Vermeulen, K.; Van Bockstaele, D.R.; Berneman, Z.N. The cell cycle: a review of regulation, deregulation and therapeutic targets in cancer. Cell. Prolif., 2003, 36, 131-149.
    • (2003) Cell. Prolif , vol.36 , pp. 131-149
    • Vermeulen, K.1    van Bockstaele, D.R.2    Berneman, Z.N.3
  • 32
    • 0037210732 scopus 로고    scopus 로고
    • Flavopiridol, a cyclin dependent kinase (CDK) inhibitor, induces apoptosis by regulating Bcl-x in oral cancer cells
    • Mihara, M.; Shintani, S.; Nakashiro, K.; Hamakawa, H. Flavopiridol, a cyclin dependent kinase (CDK) inhibitor, induces apoptosis by regulating Bcl-x in oral cancer cells. Oral. Oncol., 2003, 39, 49-55.
    • (2003) Oral. Oncol , vol.39 , pp. 49-55
    • Mihara, M.1    Shintani, S.2    Nakashiro, K.3    Hamakawa, H.4
  • 33
    • 0028828204 scopus 로고
    • Cyclins and cyclin-dependent kinases: Theme and variations
    • Pines, J. Cyclins and cyclin-dependent kinases: theme and variations. Adv. Cancer Res., 1995, 66, 181-212.
    • (1995) Adv. Cancer Res , vol.66 , pp. 181-212
    • Pines, J.1
  • 35
    • 13244268318 scopus 로고    scopus 로고
    • Clinical anticancer drug development: Targeting the cyclin-dependent kinases
    • Benson, C.; Kaye, S.; Workman, P.; Garrett, M.; Walton, M.; de Bono, J. Clinical anticancer drug development: targeting the cyclin-dependent kinases. Br. J. Cancer, 2005, 92, 7-12.
    • (2005) Br. J. Cancer , vol.92 , pp. 7-12
    • Benson, C.1    Kaye, S.2    Workman, P.3    Garrett, M.4    Walton, M.5    de Bono, J.6
  • 36
    • 0042303844 scopus 로고    scopus 로고
    • Cyclin-dependent kinase inhibitors
    • Dai, Y.; Grant, S. Cyclin-dependent kinase inhibitors. Curr. Opin. Pharmacol., 2003, 3, 362-370.
    • (2003) Curr. Opin. Pharmacol , vol.3 , pp. 362-370
    • Dai, Y.1    Grant, S.2
  • 37
    • 0034162636 scopus 로고    scopus 로고
    • Preclinical and Clinical Development of Cyclin-Dependent Kinase Modulators
    • Senderowicz, A.M.; Sausville, E.A. 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
  • 38
    • 0033375469 scopus 로고    scopus 로고
    • Flavopiridol: The first cyclin-dependent kinase inhibitor in human clinical trials
    • Senderowicz, A.M. Flavopiridol: the first cyclin-dependent kinase inhibitor in human clinical trials. Invest. New. Drugs, 1999, 17, 313-320.
    • (1999) Invest. New. Drugs , vol.17 , pp. 313-320
    • Senderowicz, A.M.1
  • 41
    • 0029665778 scopus 로고    scopus 로고
    • Flavopiridol induces G1 arrest with inhibition of cyclin-dependent kinase (CDK) 2 and CDK4 in human breast carcinoma cells
    • Carlson, B.A.; Dubay, M.M.; Sausville, E.A.; Brizuela, L.; Worland, P.J. Flavopiridol induces G1 arrest with inhibition of cyclin-dependent kinase (CDK) 2 and CDK4 in human breast carcinoma cells. Cancer Res., 1996, 56, 2973-2978.
    • (1996) Cancer Res , vol.56 , pp. 2973-2978
    • Carlson, B.A.1    Dubay, M.M.2    Sausville, E.A.3    Brizuela, L.4    Worland, P.J.5
  • 43
    • 0001842945 scopus 로고    scopus 로고
    • Cyclin D1 and CDK6 are the targets for flavopiridol-mediated G1 block in MCF10A breast epithelial cell line [abstract]
    • Singh, S.S.; Sausville, E.A.; Senderowicz, A.M. Cyclin D1 and CDK6 are the targets for flavopiridol-mediated G1 block in MCF10A breast epithelial cell line [abstract]. Proc. Am. Assoc. Cancer Res., 1999, 40, 28.
    • (1999) Proc. Am. Assoc. Cancer Res , vol.40 , pp. 28
    • Singh, S.S.1    Sausville, E.A.2    Senderowicz, A.M.3
  • 44
    • 0027433237 scopus 로고
    • Alteration of the phosphorylation state of p34cdc2 kinase by the flavone L86-8275 in breast carcinoma cells. Correlation with decreased H1 kinase activity
    • Worland, P.J.; Kaur, G.; Stetler-Stevenson, M.; Sebers, S.; Sartor, O.; Sausville, E.A. Alteration of the phosphorylation state of p34cdc2 kinase by the flavone L86-8275 in breast carcinoma cells. Correlation with decreased H1 kinase activity. Biochem. Pharmacol., 1993, 46, 1831-1840.
    • (1993) Biochem. Pharmacol , vol.46 , pp. 1831-1840
    • Worland, P.J.1    Kaur, G.2    Stetler-Stevenson, M.3    Sebers, S.4    Sartor, O.5    Sausville, E.A.6
  • 45
    • 0035055595 scopus 로고    scopus 로고
    • Mechanisms of action of flavopiridol. Crit
    • Sedlacek, H.H. Mechanisms of action of flavopiridol. Crit. Rev. Oncol. Hematol., 2001, 38, 139-170.
    • (2001) Rev. Oncol. Hematol , vol.38 , pp. 139-170
    • Sedlacek, H.H.1
  • 46
    • 0036057475 scopus 로고    scopus 로고
    • The cell cycle as a target for cancer therapy: Basic and clinical findings with the small molecule inhibitors flavopiridol and UCN-01
    • Senderowicz, A.M. The cell cycle as a target for cancer therapy: basic and clinical findings with the small molecule inhibitors flavopiridol and UCN-01. Oncologist, 2002, 7(Suppl 3), 12-19.
    • (2002) Oncologist , vol.7 , Issue.SUPPL. 3 , pp. 12-19
    • Senderowicz, A.M.1
  • 48
    • 0034111019 scopus 로고    scopus 로고
    • P-TEFb, a cyclin-dependent kinase controlling elongation by RNA polymerase II
    • Price, D.H. P-TEFb, a cyclin-dependent kinase controlling elongation by RNA polymerase II. Mol. Cell. Biol., 2000, 20, 2629-2634.
    • (2000) Mol. Cell. Biol , vol.20 , pp. 2629-2634
    • Price, D.H.1
  • 49
    • 0036233675 scopus 로고    scopus 로고
    • Developmental therapeutics program at the NCI: Molecular target and drug discovery process
    • Monga, M.; Sausville, E.A. Developmental therapeutics program at the NCI: molecular target and drug discovery process. Leukemia, 2002, 16, 520-526.
    • (2002) Leukemia , vol.16 , pp. 520-526
    • Monga, M.1    Sausville, E.A.2
  • 50
    • 0040379168 scopus 로고    scopus 로고
    • Cell cycle-independent induction of apoptosis by the anti-tumor drug Flavopiridol in endothelial cells
    • Brüsselbach, S.; Nettelbeck, D.M.; Sedlacek, H.H.; Müller, R. Cell cycle-independent induction of apoptosis by the anti-tumor drug Flavopiridol in endothelial cells. Int. J. Cancer, 1998, 77, 146-152.
    • (1998) Int. J. Cancer , vol.77 , pp. 146-152
    • Brüsselbach, S.1    Nettelbeck, D.M.2    Sedlacek, H.H.3    Müller, R.4
  • 52
    • 0032533599 scopus 로고    scopus 로고
    • Flavopiridol induces apoptosis in chronic lymphocytic leukemia cells via activation of caspase-3 without evidence of bcl-2 modulation or dependence on functional p53
    • Byrd, J.C.; Shinn, C.; Waselenko, J.K.; Fuchs, E.J.; Lehman, T.A.; Nguyen, P.L.; Flinn, I.W.; Diehl, L.F.; Sausville, E.; Grever, M.R. Flavopiridol induces apoptosis in chronic lymphocytic leukemia cells via activation of caspase-3 without evidence of bcl-2 modulation or dependence on functional p53. Blood, 1998, 92, 3804-3816.
    • (1998) Blood , vol.92 , pp. 3804-3816
    • Byrd, J.C.1    Shinn, C.2    Waselenko, J.K.3    Fuchs, E.J.4    Lehman, T.A.5    Nguyen, P.L.6    Flinn, I.W.7    Diehl, L.F.8    Sausville, E.9    Grever, M.R.10
  • 53
    • 0034935026 scopus 로고    scopus 로고
    • Flavopiridol circumvents Bcl-2 family mediated inhibition of apoptosis and drug resistance in B-cell chronic lymphocytic leukaemia
    • Pepper, C.; Thomas, A.; Hoy, T.; Fegan, C.; Bentley, P. Flavopiridol circumvents Bcl-2 family mediated inhibition of apoptosis and drug resistance in B-cell chronic lymphocytic leukaemia. Br. J. Haematol., 2001, 114, 70-77.
    • (2001) Br. J. Haematol , vol.114 , pp. 70-77
    • Pepper, C.1    Thomas, A.2    Hoy, T.3    Fegan, C.4    Bentley, P.5
  • 54
    • 0038754616 scopus 로고    scopus 로고
    • Flavopiridol-induced apoptosis is mediated through up-regulation of E2F1 and repression of Mcl-1
    • Ma, Y.; Cress, W.D.; Haura, E.B. Flavopiridol-induced apoptosis is mediated through up-regulation of E2F1 and repression of Mcl-1. Mol. Cancer Ther., 2003, 2, 73-81.
    • (2003) Mol. Cancer Ther , vol.2 , pp. 73-81
    • Ma, Y.1    Cress, W.D.2    Haura, E.B.3
  • 55
    • 0033159624 scopus 로고    scopus 로고
    • Induction of Differentiation Accompanies Inhibition of CDK2 In a Non-small Cell Lung Cancer Cell Line
    • Lee, H.R.; Chang, T.H.; Tebalt, M.J. 3rd.; Senderowicz, A.M.; Szabo, E. Induction of differentiation accompanies inhibition of CDK2 in a non-small cell lung cancer cell line. Int. J. Oncol., 1999, 15, 161-166.
    • (1999) Int. J. Oncol , vol.15 , pp. 161-166
    • Lee, H.R.1    Chang, T.H.2    Tebalt 3rd, M.J.3    Senderowicz, A.M.4    Szabo, E.5
  • 56
    • 33745083046 scopus 로고    scopus 로고
    • Sequential combination of flavopiridol and docetaxel reduces the levels of X-linked inhibitor of apoptosis and AKT proteins and stimulates apoptosis in human LNCaP prostate cancer cells
    • Gomez, L.A.; de Las Pozas, A.; Perez-Stable, C. Sequential combination of flavopiridol and docetaxel reduces the levels of X-linked inhibitor of apoptosis and AKT proteins and stimulates apoptosis in human LNCaP prostate cancer cells. Mol. Cancer Ther., 2006, 5, 1216-1226.
    • (2006) Mol. Cancer Ther , vol.5 , pp. 1216-1226
    • Gomez, L.A.1    de Las Pozas, A.2    Perez-Stable, C.3
  • 57
    • 33749076241 scopus 로고    scopus 로고
    • Sequential combinations of flavopiridol and docetaxel inhibit prostate tumors, induce apoptosis, and decrease angiogenesis in the G /T-15 transgenic mouse model of prostate cancer
    • Reiner, T.; de las Pozas, A.; Perez-Stable, C. Sequential combinations of flavopiridol and docetaxel inhibit prostate tumors, induce apoptosis, and decrease angiogenesis in the G /T-15 transgenic mouse model of prostate cancer. Prostate, 2006, 66, 1487-1497.
    • (2006) Prostate , vol.66 , pp. 1487-1497
    • Reiner, T.1    de Las Pozas, A.2    Perez-Stable, C.3
  • 58
    • 1942510415 scopus 로고    scopus 로고
    • Enhancement of radiation effects by combined docetaxel and flavopiridol treatment in lung cancer cells
    • Kim, J.C.; Saha, D.; Cao, Q.; Choy, H. Enhancement of radiation effects by combined docetaxel and flavopiridol treatment in lung cancer cells. Radiother. Oncol., 2004, 71, 213-221.
    • (2004) Radiother. Oncol , vol.71 , pp. 213-221
    • Kim, J.C.1    Saha, D.2    Cao, Q.3    Choy, H.4
  • 59
    • 0038204415 scopus 로고    scopus 로고
    • The diverse functions of histone acetyltransferase complexes
    • Carrozza, M.J.; Utley, R.T.; Workman, J.L.; Côté, J. The diverse functions of histone acetyltransferase complexes. Trends Genet., 2003, 19, 321-329.
    • (2003) Trends Genet , vol.19 , pp. 321-329
    • Carrozza, M.J.1    Utley, R.T.2    Workman, J.L.3    Côté, J.4
  • 60
    • 0036279185 scopus 로고    scopus 로고
    • HDAC's at work: Everyone doing their part
    • Peterson, C.L. HDAC's at work: everyone doing their part. Mol. Cell., 2002, 9, 921-922.
    • (2002) Mol. Cell , vol.9 , pp. 921-922
    • Peterson, C.L.1
  • 61
    • 0035467951 scopus 로고    scopus 로고
    • Histone acetylation/deacetylation and cancer: An open and shut case?
    • Gray, S.G.; Teh, B.T. Histone acetylation/deacetylation and cancer: an open and shut case? Curr. Mol. Med., 2001, 1, 401-429.
    • (2001) Curr. Mol. Med , vol.1 , pp. 401-429
    • Gray, S.G.1    Teh, B.T.2
  • 62
    • 0032581341 scopus 로고    scopus 로고
    • Sodium butyrate stimulates PKC activation and induces differential expression of certain PKC isoforms during erythroid differentiation
    • Rivero, J.A.; Adunyah, S.E. Sodium butyrate stimulates PKC activation and induces differential expression of certain PKC isoforms during erythroid differentiation. Biochem. Biophys. Res. Commun., 1998, 248, 664-648.
    • (1998) Biochem. Biophys. Res. Commun , vol.248 , pp. 664-648
    • Rivero, J.A.1    Adunyah, S.E.2
  • 64
    • 0037674946 scopus 로고    scopus 로고
    • Enhancement of depsipeptide-mediated apoptosis of lung or esophageal cancer cells by flavopiridol: Activation of the mitochondria-dependent death-signaling pathway
    • Nguyen, D.M.; Schrump, W.D.; Tsai, W.S.; Chen, A.; Stewart, J.H. 4th; Steiner, F.; Schrump, D.S. Enhancement of depsipeptide-mediated apoptosis of lung or esophageal cancer cells by flavopiridol: activation of the mitochondria-dependent death-signaling pathway. J. Thorac. Cardiovasc. Surg., 2003, 125, 1132-1142.
    • (2003) J. Thorac. Cardiovasc. Surg , vol.125 , pp. 1132-1142
    • Nguyen, D.M.1    Schrump, W.D.2    Tsai, W.S.3    Chen, A.4    Stewart 4th, J.H.5    Steiner, F.6    Schrump, D.S.7
  • 65
    • 0036050151 scopus 로고    scopus 로고
    • Synergistic induction of mitochondrial damage and apoptosis in human leukemia cells by flavopiridol and the histone deacetylase inhibitor suberoylanilide hydroxamic acid (SAHA)
    • Almenara, J.; Rosato, R.; Grant, S. Synergistic induction of mitochondrial damage and apoptosis in human leukemia cells by flavopiridol and the histone deacetylase inhibitor suberoylanilide hydroxamic acid (SAHA). Leukemia, 2002, 16, 1331-1343.
    • (2002) Leukemia , vol.16 , pp. 1331-1343
    • Almenara, J.1    Rosato, R.2    Grant, S.3
  • 67
    • 1842481018 scopus 로고    scopus 로고
    • Abrogation of p21 expression by flavopiridol enhances depsipeptide-mediated apoptosis in malignant pleural mesothelioma cells
    • Nguyen, D.M.; Schrump, W.D.; Chen, G.A.; Tsai, W.; Nguyen, P.; Trepel, J.B.; Schrump, D.S. Abrogation of p21 expression by flavopiridol enhances depsipeptide-mediated apoptosis in malignant pleural mesothelioma cells. Clin. Cancer Res., 2004, 10, 1813-1825.
    • (2004) Clin. Cancer Res , vol.10 , pp. 1813-1825
    • Nguyen, D.M.1    Schrump, W.D.2    Chen, G.A.3    Tsai, W.4    Nguyen, P.5    Trepel, J.B.6    Schrump, D.S.7
  • 68
    • 4844224868 scopus 로고    scopus 로고
    • Contribution of disruption of the nuclear factor-κ;B pathway to induction of apoptosis in human leukemia cells by histone deacetylase inhibitors and flavopiridol
    • Gao, N.; Dai, Y.; Rahmani, M.; Dent, P.; Grant, S. Contribution of disruption of the nuclear factor-κ;B pathway to induction of apoptosis in human leukemia cells by histone deacetylase inhibitors and flavopiridol. Mol. Pharmacol., 2004, 66, 956-963.
    • (2004) Mol. Pharmacol , vol.66 , pp. 956-963
    • Gao, N.1    Dai, Y.2    Rahmani, M.3    Dent, P.4    Grant, S.5
  • 70
    • 77953163130 scopus 로고    scopus 로고
    • Enhancement of radiation effects by flavopiridol in uterine cervix cancer cells
    • Kim, S.; Wu, H.G.; Shin, J.H.; Park, H.J.; Kim, I.A.; Kim, I.H. Enhancement of radiation effects by flavopiridol in uterine cervix cancer cells. Cancer Res. Treat., 2005, 37, 191-195.
    • (2005) Cancer Res. Treat , vol.37 , pp. 191-195
    • Kim, S.1    Wu, H.G.2    Shin, J.H.3    Park, H.J.4    Kim, I.A.5    Kim, I.H.6
  • 72
    • 0038745560 scopus 로고    scopus 로고
    • Flavopiridol, a cyclin-dependent kinase inhibitor, enhances radiosensitivity of ovarian carcinoma cells
    • Raju, U.; Nakata, E.; Mason, K.A.; Ang, K.K.; Milas, L. Flavopiridol, a cyclin-dependent kinase inhibitor, enhances radiosensitivity of ovarian carcinoma cells. Cancer Res., 2003, 63, 3263-3267.
    • (2003) Cancer Res , vol.63 , pp. 3263-3267
    • Raju, U.1    Nakata, E.2    Mason, K.A.3    Ang, K.K.4    Milas, L.5
  • 75
    • 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-κB-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-κB-dependent process. Oncogene, 2003, 22, 7108-7122.
    • (2003) Oncogene , vol.22 , pp. 7108-7122
    • Dai, Y.1    Rahmani, M.2    Grant, S.3
  • 76
    • 0036715327 scopus 로고    scopus 로고
    • Flavopiridol potentiates STI571-induced mitochondrial damage and apoptosis in BCR-ABL-positive human leukemia cells
    • Yu, C.; Krystal, G.; Dent, P.; Grant, S. Flavopiridol potentiates STI571-induced mitochondrial damage and apoptosis in BCR-ABL-positive human leukemia cells. Clin. Cancer Res., 2002, 8, 2976-2984.
    • (2002) Clin. Cancer Res , vol.8 , pp. 2976-2984
    • Yu, C.1    Krystal, G.2    Dent, P.3    Grant, S.4
  • 77
    • 3142554015 scopus 로고    scopus 로고
    • Bortezomib and flavopiridol interact synergistically to induce apoptosis in chronic myeloid leukemia cells resistant to imatinib mesylate through both Bcr/Abl-dependent and -independent mechanisms
    • Dai, Y.; Rahmani, M.; Pei, X.Y.; Dent, P.; Grant, S. Bortezomib and flavopiridol interact synergistically to induce apoptosis in chronic myeloid leukemia cells resistant to imatinib mesylate through both Bcr/Abl-dependent and -independent mechanisms. Blood, 2004, 104, 509-518.
    • (2004) Blood , vol.104 , pp. 509-518
    • Dai, Y.1    Rahmani, M.2    Pei, X.Y.3    Dent, P.4    Grant, S.5
  • 78
    • 0037089564 scopus 로고    scopus 로고
    • Rate-limiting effects of Cyclin D1 in transformation by ErbB2 predicts synergy between herceptin and flavopiridol
    • Nahta, R.; Iglehart, J.D.; Kempkes, B.; Schmidt, E.V. Rate-limiting effects of Cyclin D1 in transformation by ErbB2 predicts synergy between herceptin and flavopiridol. Cancer Res., 2002, 62, 2267-2271.
    • (2002) Cancer Res , vol.62 , pp. 2267-2271
    • Nahta, R.1    Iglehart, J.D.2    Kempkes, B.3    Schmidt, E.V.4
  • 79
    • 0037742257 scopus 로고    scopus 로고
    • Epidermal growth factor receptor expression is a candidate target of the synergistic combination of trastuzumab and flavopiridol in breast cancer
    • Nahta, R.; Trent, S.; Yang, C.; Schmidt, E.V. Epidermal growth factor receptor expression is a candidate target of the synergistic combination of trastuzumab and flavopiridol in breast cancer. Cancer Res., 2003, 63, 3626-3631.
    • (2003) Cancer Res , vol.63 , pp. 3626-3631
    • Nahta, R.1    Trent, S.2    Yang, C.3    Schmidt, E.V.4
  • 80
    • 12844277942 scopus 로고    scopus 로고
    • Combination therapy for adult T-cell leukemia-xenografted mice: Flavopiridol and anti-CD25 monoclonal antibody
    • Zhang, M.; Zhang, Z.; Goldman, C.K.; Janik, J.; Waldmann, T.A. Combination therapy for adult T-cell leukemia-xenografted mice: flavopiridol and anti-CD25 monoclonal antibody. Blood, 2005, 105, 1231-1236.
    • (2005) Blood , vol.105 , pp. 1231-1236
    • Zhang, M.1    Zhang, Z.2    Goldman, C.K.3    Janik, J.4    Waldmann, T.A.5
  • 81
    • 16844372227 scopus 로고    scopus 로고
    • Sequence dependent potentiation of gemcitabine by flavopiridol in human breast cancer cells
    • Ali, S.; El-Rayes, B.F.; Aranha, O.; Sarkar, F.H.; Philip, P.A. Sequence dependent potentiation of gemcitabine by flavopiridol in human breast cancer cells. Breast Cancer Res. Treat., 2005, 90, 25-31.
    • (2005) Breast Cancer Res. Treat , vol.90 , pp. 25-31
    • Ali, S.1    El-Rayes, B.F.2    Aranha, O.3    Sarkar, F.H.4    Philip, P.A.5
  • 82
    • 33748954290 scopus 로고    scopus 로고
    • Efficacy of sequential treatment of HCT116 colon cancer monolayers and xenografts with docetaxel, flavopiridol, and 5-fluorouracil
    • Guo, J.; Zhou, A.W.; Fu, Y.C.; Verma, U.N.; Tripathy, D.; Frenkel, E.P.; Becerra, C.R. Efficacy of sequential treatment of HCT116 colon cancer monolayers and xenografts with docetaxel, flavopiridol, and 5-fluorouracil. Acta Pharmacol. Sin., 2006, 27, 1375-1381.
    • (2006) Acta Pharmacol. Sin , vol.27 , pp. 1375-1381
    • Guo, J.1    Zhou, A.W.2    Fu, Y.C.3    Verma, U.N.4    Tripathy, D.5    Frenkel, E.P.6    Becerra, C.R.7
  • 83
    • 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, C.P.; Motwani, M.V.; Schwartz, G.K. 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
  • 84
    • 0035679234 scopus 로고    scopus 로고
    • Augmentation of apoptosis and tumor regression by flavopiridol in the presence of CPT-11 in Hct116 colon cancer monolayers and xenografts
    • Motwani, M.; Jung, C.; Sirotnak, F.M.; She, Y.; Shah, M.A.; Gonen, M.; Schwartz, G.K. Augmentation of apoptosis and tumor regression by flavopiridol in the presence of CPT-11 in Hct116 colon cancer monolayers and xenografts. Clin. Cancer Res., 2001, 7, 4209-4219.
    • (2001) Clin. Cancer Res , vol.7 , pp. 4209-4219
    • Motwani, M.1    Jung, C.2    Sirotnak, F.M.3    She, Y.4    Shah, M.A.5    Gonen, M.6    Schwartz, G.K.7
  • 85
    • 0004592963 scopus 로고    scopus 로고
    • Flavopiridol (Flavo) potentiates the SN-38-induced apopotosis in association with down regulation of cyclin dependent kinase inhibitor p21waf1/cip1 in HCT-116 cells
    • Motwani, M.; Schwartz, G.K. Flavopiridol (Flavo) potentiates the SN-38-induced apopotosis in association with down regulation of cyclin dependent kinase inhibitor p21waf1/cip1 in HCT-116 cells. Proc. Am. Assoc. Cancer Res., 2000, 40, 209.
    • (2000) Proc. Am. Assoc. Cancer Res , vol.40 , pp. 209
    • Motwani, M.1    Schwartz, G.K.2
  • 86
    • 42049101633 scopus 로고    scopus 로고
    • The cyclin-dependent kinase inhibitor flavopiridol potentiates the effects of topoisomerase I poisons by suppressing Rad51 expression in a p53-dependent manner
    • Ambrosini, G.; Seelman, S.L.; Qin, L.X.; Schwartz, G.K. The cyclin-dependent kinase inhibitor flavopiridol potentiates the effects of topoisomerase I poisons by suppressing Rad51 expression in a p53-dependent manner. Cancer Res., 2008, 68, 2312-2320.
    • (2008) Cancer Res , vol.68 , pp. 2312-2320
    • Ambrosini, G.1    Seelman, S.L.2    Qin, L.X.3    Schwartz, G.K.4
  • 87
    • 22144460455 scopus 로고    scopus 로고
    • A study of cytotoxic synergy of UCN-01 and flavopiridol in syngeneic pair of cell lines
    • Wu, K.; D'Amico, M.; Wang, C.; Albanese, C.; Pestell, R.G.; Mani, S. A study of cytotoxic synergy of UCN-01 and flavopiridol in syngeneic pair of cell lines. Invest. New. Drugs., 2005, 23, 299-309.
    • (2005) Invest. New. Drugs , vol.23 , pp. 299-309
    • Wu, K.1    D'amico, M.2    Wang, C.3    Albanese, C.4    Pestell, R.G.5    Mani, S.6
  • 88
    • 0035866789 scopus 로고    scopus 로고
    • Selective sensitization of retinoblastoma protein-deficient sarcoma cells to doxorubicin by flavopiridol-mediated inhibition of cyclin-dependent kinase 2 kinase activity
    • Li, W.; Fan, J.; Bertino, J.R. Selective sensitization of retinoblastoma protein-deficient sarcoma cells to doxorubicin by flavopiridol-mediated inhibition of cyclin-dependent kinase 2 kinase activity. Cancer Res., 2001, 61, 2579-2582.
    • (2001) Cancer Res , vol.61 , pp. 2579-2582
    • Li, W.1    Fan, J.2    Bertino, J.R.3
  • 89
    • 63149183822 scopus 로고    scopus 로고
    • Retinoblastoma tumor suppressor gene expression determines the response to sequential flavopiridol and doxorubicin treatment in small-cell lung carcinoma
    • Budak-Alpdogan, T.; Chen, B.; Warrier, A.; Medina, D.J.; Moore, D.; Bertino, J.R. Retinoblastoma tumor suppressor gene expression determines the response to sequential flavopiridol and doxorubicin treatment in small-cell lung carcinoma. Clin. Cancer Res., 2009, 15, 1232-1240.
    • (2009) Clin. Cancer Res , vol.15 , pp. 1232-1240
    • Budak-Alpdogan, T.1    Chen, B.2    Warrier, A.3    Medina, D.J.4    Moore, D.5    Bertino, J.R.6
  • 90
    • 33749004024 scopus 로고    scopus 로고
    • Flavopiridol induces cellular FLICE-inhibitory protein degradation by the proteasome and promotes TRAIL-induced early signaling and apoptosis in breast tumor cells
    • Palacios, C.; Yerbes, R.; López-Rivas, A. Flavopiridol induces cellular FLICE-inhibitory protein degradation by the proteasome and promotes TRAIL-induced early signaling and apoptosis in breast tumor cells. Cancer Res., 2006, 66, 8858-8869.
    • (2006) Cancer Res , vol.66 , pp. 8858-8869
    • Palacios, C.1    Yerbes, R.2    López-Rivas, A.3
  • 91
    • 8844228917 scopus 로고    scopus 로고
    • Potent antileukemic interactions between flavopiridol and TRAIL/Apo2L involve flavopiridol-mediated XIAP downregulation
    • Rosato, R.R.; Dai, Y.; Almenara, J.A.; Maggio, S.C.; Grant, S. Potent antileukemic interactions between flavopiridol and TRAIL/Apo2L involve flavopiridol-mediated XIAP downregulation. Leukemia, 2004, 18, 1780-1788.
    • (2004) Leukemia , vol.18 , pp. 1780-1788
    • Rosato, R.R.1    Dai, Y.2    Almenara, J.A.3    Maggio, S.C.4    Grant, S.5
  • 92
    • 42449146711 scopus 로고    scopus 로고
    • Delayed combinatorial treatment with flavopiridol and minocycline provides longer term protection for neuronal soma but not dendrites following global ischemia
    • Iyirhiaro, G.O.; Brust, T.B.; Rashidian, J.; Galehdar, Z.; Osman, A.; Phillips, M.; Slack, R.S.; Macvicar, B.A.; Park, D.S. Delayed combinatorial treatment with flavopiridol and minocycline provides longer term protection for neuronal soma but not dendrites following global ischemia. J. Neurochem., 2008, 105, 703-713.
    • (2008) J. Neurochem , vol.105 , pp. 703-713
    • Iyirhiaro, G.O.1    Brust, T.B.2    Rashidian, J.3    Galehdar, Z.4    Osman, A.5    Phillips, M.6    Slack, R.S.7    Macvicar, B.A.8    Park, D.S.9
  • 94
    • 0037609180 scopus 로고    scopus 로고
    • Protein kinase C-dependent activation of the tumor necrosis factor receptor-mediated extrinsic cell death pathway underlies enhanced apoptosis in human myeloid leukemia cells exposed to bryostatin 1 and flavopiridol
    • Cartee, L.; Maggio, S.C.; Smith, R.; Sankala, H.M.; Dent, P.; Grant, S. Protein kinase C-dependent activation of the tumor necrosis factor receptor-mediated extrinsic cell death pathway underlies enhanced apoptosis in human myeloid leukemia cells exposed to bryostatin 1 and flavopiridol. Mol. Cancer Ther., 2003, 2, 83-93.
    • (2003) Mol. Cancer Ther , vol.2 , pp. 83-93
    • Cartee, L.1    Maggio, S.C.2    Smith, R.3    Sankala, H.M.4    Dent, P.5    Grant, S.6
  • 95
    • 33644857142 scopus 로고    scopus 로고
    • Flavopiridol disrupts STAT3/DNA interactions, attenuates STAT3-directed transcription, and combines with the Jak kinase inhibitor AG490 to achieve cytotoxic synergy
    • Lee, Y.K.; Isham, C.R.; Kaufman, S.H.; Bible, K.C. Flavopiridol disrupts STAT3/DNA interactions, attenuates STAT3-directed transcription, and combines with the Jak kinase inhibitor AG490 to achieve cytotoxic synergy. Mol. Cancer Ther., 2006, 5, 138-148.
    • (2006) Mol. Cancer Ther , vol.5 , pp. 138-148
    • Lee, Y.K.1    Isham, C.R.2    Kaufman, S.H.3    Bible, K.C.4
  • 96
    • 50449108847 scopus 로고    scopus 로고
    • Combinatorial antileukemic disruption of oxidative homeostasis and mitochondrial stability by the redox reactive thalidomide 2-(2,4-difluoro-phenyl)-4,5,6,7-tetrafluoro-1Hisoindole-1,3(2H)-dione (CPS49) and flavopiridol
    • Ge, Y.; Byun, J.S.; De Luca, P.; Gueron, G.; Yabe, I.M.; Sadiq-Ali, S.G.; Figg, W.D.; Quintero, J.; Haggerty, C.M.; Li, Q.Q.; De Siervi, A.; Gardner, K. Combinatorial antileukemic disruption of oxidative homeostasis and mitochondrial stability by the redox reactive thalidomide 2-(2,4-difluoro-phenyl)-4,5,6,7-tetrafluoro-1Hisoindole-1,3(2H)-dione (CPS49) and flavopiridol. Mol. Pharmacol., 2008, 74, 872-883.
    • (2008) Mol. Pharmacol , vol.74 , pp. 872-883
    • Ge, Y.1    Byun, J.S.2    de Luca, P.3    Gueron, G.4    Yabe, I.M.5    Sadiq-Ali, S.G.6    Figg, W.D.7    Quintero, J.8    Haggerty, C.M.9    Li, Q.Q.10    de Siervi, A.11    Gardner, K.12
  • 98
    • 0142148097 scopus 로고    scopus 로고
    • Acquired cellular resistance to flavopiridol in a human colon carcinoma cell line involves up-regulation of the telomerase catalytic subunit and telomere elongation. Sensitivity of resistant cells to combination treatment with a telomerase inhibitor
    • Incles, C.M.; Schultes, C.M.; Kelland, L.R.; Neidle, S. Acquired cellular resistance to flavopiridol in a human colon carcinoma cell line involves up-regulation of the telomerase catalytic subunit and telomere elongation. Sensitivity of resistant cells to combination treatment with a telomerase inhibitor. Mol. Pharmacol., 2003, 64, 1101-1108.
    • (2003) Mol. Pharmacol , vol.64 , pp. 1101-1108
    • Incles, C.M.1    Schultes, C.M.2    Kelland, L.R.3    Neidle, S.4
  • 99
    • 0030824869 scopus 로고    scopus 로고
    • Potentiation of apoptosis by flavopiridol in mitomycin-C-treated gastric and breast cancer cells
    • Schwartz, G.K.; Farsi, K.; Maslak, P.; Kelsen, D.P.; Spriggs, D. Potentiation of apoptosis by flavopiridol in mitomycin-C-treated gastric and breast cancer cells. Clin. Cancer Res., 1997, 3, 1467-1472.
    • (1997) Clin. Cancer Res , vol.3 , pp. 1467-1472
    • Schwartz, G.K.1    Farsi, K.2    Maslak, P.3    Kelsen, D.P.4    Spriggs, D.5
  • 100
    • 77951551332 scopus 로고    scopus 로고
    • A combination of cisplatin-eluting gelatin microspheres and flavopiridol enhances antitumour effects in a rabbit VX2 liver tumour model
    • Nitta, N.; Sonoda, A.; Seko, A.; Ohta, S.; Nagatani, Y.; Tsuchiya, K.; Otani, H.; Tanaka, T.; Kanasaki, S.; Takahashi, M.; Murata, K. A combination of cisplatin-eluting gelatin microspheres and flavopiridol enhances antitumour effects in a rabbit VX2 liver tumour model. Br. J. Radiol., 2010, 83(989), 428-432.
    • (2010) Br. J. Radiol , vol.83 , Issue.989 , pp. 428-432
    • Nitta, N.1    Sonoda, A.2    Seko, A.3    Ohta, S.4    Nagatani, Y.5    Tsuchiya, K.6    Otani, H.7    Tanaka, T.8    Kanasaki, S.9    Takahashi, M.10    Murata, K.11
  • 103


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.