-
1
-
-
0034614637
-
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
-
3
-
-
60749109846
-
Cell cycle, CDKs and cancer: A changing paradigm
-
Malumbres M, Barbacid M. Cell cycle, CDKs and cancer: a changing paradigm. Nat Rev Cancer 2009; 9: 153-166
-
(2009)
Nat Rev Cancer
, vol.9
, pp. 153-166
-
-
Malumbres, M.1
Barbacid, M.2
-
4
-
-
70249090057
-
The rb pathway and cancer therapeutics
-
Du W, Searle JS. The rb pathway and cancer therapeutics. Curr Drug Targets 2009; 10: 581-589
-
(2009)
Curr Drug Targets
, vol.10
, pp. 581-589
-
-
Du, W.1
Searle, J.S.2
-
5
-
-
33645802169
-
Cyclin-dependent kinase pathways as targets for cancer treatment
-
DOI 10.1200/JCO.2005.03.7689
-
Shapiro GI. Cyclin-dependent kinase pathways as targets for cancer treatment. J Clin Oncol 2006; 24: 1770-1783 (Pubitemid 46628473)
-
(2006)
Journal of Clinical Oncology
, vol.24
, Issue.11
, pp. 1770-1783
-
-
Shapiro, G.I.1
-
6
-
-
67650073265
-
Cell cycle kinases as therapeutic targets for cancer
-
Lapenna S, Giordano A. Cell cycle kinases as therapeutic targets for cancer. Nat Rev Drug Discov 2009; 8: 547-566
-
(2009)
Nat Rev Drug Discov
, vol.8
, pp. 547-566
-
-
Lapenna, S.1
Giordano, A.2
-
7
-
-
67650777303
-
Development of cell-cycle inhibitors for cancer therapy
-
Dickson MA, Schwartz GK. Development of cell-cycle inhibitors for cancer therapy. Curr Oncol 2009; 16: 120-127
-
(2009)
Curr Oncol
, vol.16
, pp. 120-127
-
-
Dickson, M.A.1
Schwartz, G.K.2
-
8
-
-
36549040859
-
The selectivity of protein kinase inhibitors: A further update
-
Bain J, Plater L, Elliott M, et al. The selectivity of protein kinase inhibitors: a further update. Biochem J 2007; 408: 297-315.
-
(2007)
Biochem J
, vol.408
, pp. 297-315
-
-
Bain, J.1
Plater, L.2
Elliott, M.3
-
9
-
-
19744365702
-
A small molecule-kinase interaction map for clinical kinase inhibitors
-
Fabian MA, Biggs WH, Treiber DK, et al. A small molecule-kinase interaction map for clinical kinase inhibitors. Nat Biotechnol 2005; 23: 329-336
-
(2005)
Nat Biotechnol
, vol.23
, pp. 329-336
-
-
Fabian, M.A.1
Biggs, W.H.2
Treiber, D.K.3
-
10
-
-
38049018155
-
A quantitative analysis of kinase inhibitor selectivity
-
Karaman MW, Herrgard S, Treiber DK, et al. A quantitative analysis of kinase inhibitor selectivity. Nat Biotechnol 2008; 26: 127-132
-
(2008)
Nat Biotechnol
, vol.26
, pp. 127-132
-
-
Karaman, M.W.1
Herrgard, S.2
Treiber, D.K.3
-
11
-
-
9444228344
-
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
-
12
-
-
33747872306
-
A novel orally active small molecule potently induces G1 arrest in primary myeloma cells and prevents tumor growth by specific inhibition of cyclin-dependent kinase 4/6
-
Baughn LB, Di LM, Wu K, et al. A novel orally active small molecule potently induces G1 arrest in primary myeloma cells and prevents tumor growth by specific inhibition of cyclin-dependent kinase 4/6. Cancer Res 2006; 66: 7661-7667
-
(2006)
Cancer Res
, vol.66
, pp. 7661-7667
-
-
Baughn, L.B.1
Di, L.M.2
Wu, K.3
-
13
-
-
33645471100
-
The cellular phenotype of AZ703, a novel selective imidazo[1,2-a]pyridine cyclin-dependent kinase inhibitor
-
Byth KF, Geh C, Forder CL, Oakes SE, Thomas AP. The cellular phenotype of AZ703, a novel selective imidazo[1,2-a]pyridine cyclin-dependent kinase inhibitor. Mol Cancer Ther 2006; 5: 655-664
-
(2006)
Mol Cancer Ther
, vol.5
, pp. 655-664
-
-
Byth, K.F.1
Geh, C.2
Forder, C.L.3
Oakes, S.E.4
Thomas, A.P.5
-
14
-
-
33749503799
-
Combined depletion of cell cycle and transcriptional cyclin-dependent kinase activities induces apoptosis in cancer cells
-
DOI 10.1158/0008-5472.CAN-06-1758
-
Cai D, Latham VM Jr, Zhang X, Shapiro GI. Combined depletion of cell cycle and transcriptional cyclin-dependent kinase activities induces apoptosis in cancer cells. Cancer Res 2006; 66: 9270-9280 (Pubitemid 44521149)
-
(2006)
Cancer Research
, vol.66
, Issue.18
, pp. 9270-9280
-
-
Cai, D.1
Latham Jr., V.M.2
Zhang, X.3
Shapiro, G.I.4
-
15
-
-
2442678063
-
Flavopiridol induces p53 via initial inhibition of Mdm2 and p21 and, independently of p53, sensitizes apoptosis-reluctant cells to tumor necrosis factor
-
Demidenko ZN, Blagosklonny MV. Flavopiridol induces p53 via initial inhibition of Mdm2 and p21 and, independently of p53, sensitizes apoptosis-reluctant cells to tumor necrosis factor. Cancer Res 2004; 64: 3653-3660
-
(2004)
Cancer Res
, vol.64
, pp. 3653-3660
-
-
Demidenko, Z.N.1
Blagosklonny, M.V.2
-
16
-
-
23044439051
-
Seliciclib (CYC202 or R-roscovitine), a small-molecule cyclin-dependent kinase inhibitor, mediates activity via down-regulation of Mcl-1 in multiple myeloma
-
DOI 10.1182/blood-2005-01-0320
-
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 (Pubitemid 41076452)
-
(2005)
Blood
, vol.106
, Issue.3
, pp. 1042-1047
-
-
Raje, N.1
Kumar, S.2
Hideshima, T.3
Roccaro, A.4
Ishitsuka, K.5
Yasui, H.6
Shiraishi, N.7
Chauhan, D.8
Munshi, N.C.9
Green, S.R.10
Anderson, K.C.11
-
17
-
-
20444477948
-
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
-
DOI 10.1158/0008-5472.CAN-05-0233
-
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 (Pubitemid 40827353)
-
(2005)
Cancer Research
, vol.65
, Issue.12
, pp. 5399-5407
-
-
MacCallum, D.E.1
Melville, J.2
Frame, S.3
Watt, K.4
Anderson, S.5
Gianella-Borradori, A.6
Lane, D.P.7
Green, S.R.8
-
18
-
-
0037058678
-
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
-
19
-
-
12144285797
-
N-(cycloalkylamino)acyl-2-aminothiazole inhibitors of cyclin-dependent kinase 2. N-[5-[[[5-(1,1-dimethylethyl)-2-oxazolyl]methyl]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]methyl]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
-
20
-
-
60849123760
-
Biological characterization of AT7519, a small-molecule inhibitor of cyclin-dependent kinases, in human tumor cell lines
-
Squires MS, Feltell RE, Wallis NG, et al. Biological characterization of AT7519, a small-molecule inhibitor of cyclin-dependent kinases, in human tumor cell lines. Mol Cancer Ther 2009; 8: 324-332
-
(2009)
Mol Cancer Ther
, vol.8
, pp. 324-332
-
-
Squires, M.S.1
Feltell, R.E.2
Wallis, N.G.3
-
21
-
-
24744437350
-
Roscovitine targets, protein kinases and pyridoxal kinase
-
DOI 10.1074/jbc.M500806200
-
Bach S, Knockaert M, Reinhardt J, et al. Roscovitine targets, protein kinases and pyridoxal kinase. J Biol Chem 2005; 280: 31208-31219 (Pubitemid 41291858)
-
(2005)
Journal of Biological Chemistry
, vol.280
, Issue.35
, pp. 31208-31219
-
-
Bach, S.1
Knockaert, M.2
Reinhardt, J.3
Lozach, O.4
Schmitt, S.5
Baratte, B.6
Koken, M.7
Coburn, S.P.8
Tang, L.9
Jiang, T.10
Liang, D.-C.11
Galons, H.12
Dierick, J.-F.13
Pinna, L.A.14
Meggio, F.15
Totzke, F.16
Schachtele, C.17
Lerman, A.S.18
Carnero, A.19
Wan, Y.20
Gray, N.21
Meijer, L.22
more..
-
22
-
-
33747128468
-
Molecular and pharmacodynamic characteristics of the novel multi-target tumor growth inhibitor ZK 304709
-
DOI 10.1016/j.biopha.2006.06.003, PII S0753332206000850
-
Siemeister G, Luecking U, Wagner C, Detjen K, Mc CC, Bosslet K. Molecular and pharmacodynamic characteristics of the novel multi-target tumor growth inhibitor ZK 304709. Biomed Pharmacother 2006; 60: 269-272 (Pubitemid 44223936)
-
(2006)
Biomedicine and Pharmacotherapy
, vol.60
, Issue.6
, pp. 269-272
-
-
Siemeister, G.1
Luecking, U.2
Wagner, C.3
Detjen, K.4
Mc Coy, C.5
Bosslet, K.6
-
23
-
-
0033231301
-
Flavopiridol, a protein kinase inhibitor, down-regulates hypoxic induction of vascular endothelial growth factor expression in human monocytes
-
Melillo G, Sausville EA, Cloud K, Lahusen T, Varesio L, Senderowicz AM. Flavopiridol, a protein kinase inhibitor, down-regulates hypoxic induction of vascular endothelial growth factor expression in human monocytes. Cancer Res 1999; 59: 5433-5437 (Pubitemid 29526451)
-
(1999)
Cancer Research
, vol.59
, Issue.21
, pp. 5433-5437
-
-
Melillo, G.1
Sausville, E.A.2
Cloud, K.3
Lahusen, T.4
Varesio, L.5
Senderowicz, A.M.6
-
24
-
-
34249082749
-
SNS-032 prevents tumor cell-induced angiogenesis by inhibiting vascular endothelial growth factor
-
DOI 10.1593/neo.07136
-
Ali MA, Choy H, Habib AA, Saha D. SNS-032 prevents tumor cell-induced angiogenesis by inhibiting vascular endothelial growth factor. Neoplasia 2007; 9: 370-381 (Pubitemid 46799980)
-
(2007)
Neoplasia
, vol.9
, Issue.5
, pp. 370-381
-
-
Ali, N.A.1
Choy, H.2
Habib, A.A.3
Saha, D.4
-
25
-
-
26944481573
-
A proteome-wide CDK/CRK-specific kinase inhibitor promotes tumor cell death in the absence of cell cycle progression
-
Caligiuri M, Becker F, Murthi K, et al. A proteome-wide CDK/CRK-specific kinase inhibitor promotes tumor cell death in the absence of cell cycle progression. Chem Biol 2005; 12: 1103-1115
-
(2005)
Chem Biol
, vol.12
, pp. 1103-1115
-
-
Caligiuri, M.1
Becker, F.2
Murthi, K.3
-
26
-
-
0034597571
-
Thio- And oxoflavopiridols, cyclin-dependent kinase 1-selective inhibitors: Synthesis and biological effects
-
Kim KS, Sack JS, Tokarski JS, et al. Thio- and oxoflavopiridols, cyclin-dependent kinase 1-selective inhibitors: synthesis and biological effects. J Med Chem 2000; 43: 4126-4134
-
(2000)
J Med Chem
, vol.43
, pp. 4126-4134
-
-
Kim, K.S.1
Sack, J.S.2
Tokarski, J.S.3
-
27
-
-
0037171721
-
Structure-based design and synthesis of 2-benzylidene-benzofuran-3-ones as flavopiridol mimics
-
Schoepfer J, Fretz H, Chaudhuri B, et al. Structure-based design and synthesis of 2-benzylidene-benzofuran-3-ones as flavopiridol mimics. J Med Chem 2002; 45: 1741-1747
-
(2002)
J Med Chem
, vol.45
, pp. 1741-1747
-
-
Schoepfer, J.1
Fretz, H.2
Chaudhuri, B.3
-
28
-
-
70349558526
-
Identification of flavopiridol analogues that selectively inhibit positive transcription elongation factor (P-TEFb) and block HIV-1 replication
-
Ali A, Ghosh A, Nathans RS, et al. 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
-
29
-
-
77950816887
-
-
EJC Supplements
-
Heuer TS. In: EJC Supplements, 20th AACR-NCI-EORTC Symposium on Molecular Targets and Cancer Therapeutics, Discovery, Biology, and Clinical Applications, Geneva, Switzerland, October 21-24, 2008; EJC Supplements 2008; 6 (12): p 94.
-
(2008)
EJC Supplements, 20th AACR-NCI-EORTC Symposium on Molecular Targets and Cancer Therapeutics, Discovery, Biology, and Clinical Applications, Geneva, Switzerland, October 21-24, 2008
, vol.6
, Issue.12
, pp. 94
-
-
Heuer, T.S.1
-
30
-
-
68049125103
-
The development of a selective cyclin-dependent kinase inhibitor that shows antitumor activity
-
Ali S, Heathcote DA, Kroll SH, et al. The development of a selective cyclin-dependent kinase inhibitor that shows antitumor activity. Cancer Res 2009; 69: 6208-6215
-
(2009)
Cancer Res
, vol.69
, pp. 6208-6215
-
-
Ali, S.1
Heathcote, D.A.2
Kroll, S.H.3
-
31
-
-
33750434231
-
Role of the ABCG2 drug transporter in the resistance and oral bioavailability of a potent cyclin-dependent kinase/Aurora kinase inhibitor
-
Seamon JA, Rugg CA, Emanuel S, et al. Role of the ABCG2 drug transporter in the resistance and oral bioavailability of a potent cyclin-dependent kinase/Aurora kinase inhibitor. Mol Cancer Ther 2006; 5: 2459-2467
-
(2006)
Mol Cancer Ther
, vol.5
, pp. 2459-2467
-
-
Seamon, J.A.1
Rugg, C.A.2
Emanuel, S.3
-
32
-
-
0141815505
-
Investigating RNA polymerase II carboxyl-terminal domain (CTD) phosphorylation
-
Palancade B, Bensaude O. Investigating RNA polymerase II carboxyl-terminal domain (CTD) phosphorylation. Eur J Biochem 2003; 270: 3859-3870
-
(2003)
Eur J Biochem
, vol.270
, pp. 3859-3870
-
-
Palancade, B.1
Bensaude, O.2
-
33
-
-
70350442978
-
TFIIH-associated Cdk7 kinase functions in phosphorylation of CTD Ser7 residues, promoter-proximal pausing, and termination by RNA polymerase II
-
Glover-Cutter K, Larochelle S, Erickson B, et al. TFIIH-associated Cdk7 kinase functions in phosphorylation of CTD Ser7 residues, promoter-proximal pausing, and termination by RNA polymerase II. Mol Cell Biol 2009.
-
(2009)
Mol Cell Biol
-
-
Glover-Cutter, K.1
Larochelle, S.2
Erickson, B.3
-
34
-
-
0035943710
-
Flavopiridol inactivates P-TEFb and blocks most RNA polymerase II transcription in vivo
-
Chao SH, Price DH. Flavopiridol inactivates P-TEFb and blocks most RNA polymerase II transcription in vivo. J Biol Chem 2001; 276: 31793-31799
-
(2001)
J Biol Chem
, vol.276
, pp. 31793-31799
-
-
Chao, S.H.1
Price, D.H.2
-
35
-
-
0034812298
-
The cyclin-dependent kinase inhibitor roscovitine inhibits RNA synthesis and triggers nuclear accumulation of p53 that is unmodified at Ser15 and Lys382
-
Ljungman M, Paulsen MT. The cyclin-dependent kinase inhibitor roscovitine inhibits RNA synthesis and triggers nuclear accumulation of p53 that is unmodified at Ser15 and Lys382. Mol Pharmacol 2001; 60: 785-789
-
(2001)
Mol Pharmacol
, vol.60
, pp. 785-789
-
-
Ljungman, M.1
Paulsen, M.T.2
-
36
-
-
0035233239
-
Genomic-scale measurement of mRNA turnover and the mechanisms of action of the anti-cancer drug flavopiridol
-
RESEARCH0041.
-
Lam LT, Pickeral OK, Peng AC, et al. Genomic-scale measurement of mRNA turnover and the mechanisms of action of the anti-cancer drug flavopiridol. Genome Biol 2001; 2: RESEARCH0041.
-
(2001)
Genome Biol
, vol.2
-
-
Lam, L.T.1
Pickeral, O.K.2
Peng, A.C.3
-
37
-
-
0038754616
-
Flavopiridol-induced apoptosis is mediated through up-regulation of E2F1 and repression of Mcl-1
-
Ma Y, Cress WD, Haura EB. 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
-
38
-
-
8844228917
-
Potent antileukemic interactions between flavopiridol and TRAIL/Apo2L involve flavopiridol-mediated XIAP downregulation
-
Rosato RR, Dai Y, Almenara JA, Maggio SC, 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
-
39
-
-
27144434812
-
Transcription inhibition by flavopiridol: Mechanism of chronic lymphocytic leukemia cell death
-
DOI 10.1182/blood-2005-04-1678
-
Chen R, Keating MJ, Gandhi V, Plunkett W. Transcription inhibition by flavopiridol: mechanism of chronic lymphocytic leukemia cell death. Blood 2005; 106: 2513-2519 (Pubitemid 41510827)
-
(2005)
Blood
, vol.106
, Issue.7
, pp. 2513-2519
-
-
Chen, R.1
Keating, M.J.2
Gandhi, V.3
Plunkett, W.4
-
40
-
-
0040932434
-
The novel cyclin-dependent kinase inhibitor flavopiridol downregulates Bcl-2 and induces growth arrest and apoptosis in chronic B-cell leukemia lines
-
Konig A, Schwartz GK, Mohammad RM, Al-Katib A, Gabrilove JL. 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 (Pubitemid 27508436)
-
(1997)
Blood
, vol.90
, Issue.11
, pp. 4307-4312
-
-
Konig, A.1
Schwartz, G.K.2
Mohammad, R.M.3
Al-Katib, A.4
Gabrilove, J.L.5
-
41
-
-
0034661538
-
Protein kinase inhibitors flavopiridol and 7-hydroxy-staurosporine down- Regulate antiapoptosis proteins in B-cell chronic lymphocytic leukemia
-
Kitada S, Zapata JM, Andreeff M, Reed JC. Protein kinase inhibitors flavopiridol and 7-hydroxy-staurosporine down-regulate antiapoptosis proteins in B-cell chronic lymphocytic leukemia. Blood 2000; 96: 393-397 (Pubitemid 30463354)
-
(2000)
Blood
, vol.96
, Issue.2
, pp. 393-397
-
-
Kitada, S.1
Zapata, J.M.2
Andreeff, M.3
Reed, J.C.4
-
42
-
-
11144316653
-
Cyclin-dependent kinase inhibitor Roscovitine induces apoptosis in chronic lymphocytic leukemia cells
-
DOI 10.1038/sj.leu.2403295
-
Hahntow IN, Schneller F, Oelsner M, et al. Cyclin-dependent kinase inhibitor Roscovitine induces apoptosis in chronic lymphocytic leukemia cells. Leukemia 2004; 18: 747-755 (Pubitemid 38500193)
-
(2004)
Leukemia
, vol.18
, Issue.4
, pp. 747-755
-
-
Hahntow, I.N.1
Schneller, F.2
Oelsner, M.3
Weick, K.4
Ringshausen, I.5
Fend, F.6
Peschel, C.7
Decker, T.8
-
43
-
-
21144435503
-
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
-
DOI 10.1182/blood-2004-07-2713
-
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 (Pubitemid 40720798)
-
(2005)
Blood
, vol.105
, Issue.11
, pp. 4484-4491
-
-
Alvi, A.J.1
Austen, B.2
Weston, V.J.3
Fegan, C.4
MacCallum, D.5
Gianella-Borradori, A.6
Lane, D.P.7
Hubank, M.8
Powell, J.E.9
Wei, W.10
Taylor, A.M.R.11
Moss, P.A.H.12
Stankovic, T.13
-
44
-
-
27144512221
-
Roscovitine is an effective inducer of apoptosis of Ewing's sarcoma family tumor cells in vitro and in vivo
-
DOI 10.1158/0008-5472.CAN-05-1276
-
Tirado OM, Mateo-Lozano S, Notario V. Roscovitine is an effective inducer of apoptosis of Ewing's sarcoma family tumor cells In vitro and in vivo. Cancer Res 2005; 65: 9320-9327 (Pubitemid 41507999)
-
(2005)
Cancer Research
, vol.65
, Issue.20
, pp. 9320-9327
-
-
Tirado, O.M.1
Mateo-Lozano, S.2
Notario, V.3
-
45
-
-
25444502962
-
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
-
46
-
-
0036850211
-
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 RG. 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 (Pubitemid 35340731)
-
(2002)
Clinical Cancer Research
, vol.8
, Issue.11
, pp. 3527-3538
-
-
Gojo, I.1
Zhang, B.2
Fenton, R.G.3
-
47
-
-
33947534030
-
Lane DP. p53 in health and disease
-
Vousden KH, Lane DP. p53 in health and disease. Nat Rev Mol Cell Biol 2007; 8: 275-283
-
(2007)
Nat Rev Mol Cell Biol
, vol.8
, pp. 275-283
-
-
Vousden, K.H.1
-
48
-
-
33847271089
-
Coping with stress: Multiple ways to activate p53
-
Horn HF, Vousden KH. Coping with stress: multiple ways to activate p53. Oncogene 2007; 26: 1306-1316
-
(2007)
Oncogene
, vol.26
, pp. 1306-1316
-
-
Horn, H.F.1
Vousden, K.H.2
-
49
-
-
62449278758
-
Targeting p53 for enhanced radio- And chemo-sensitivity
-
Lu C, El-Deiry WS. Targeting p53 for enhanced radio- and chemo-sensitivity. Apoptosis 2009; 14: 597-606.
-
(2009)
Apoptosis
, vol.14
, pp. 597-606
-
-
Lu, C.1
El-Deiry, W.S.2
-
50
-
-
24744434754
-
Accumulation of p53 and reductions in XIAP abundance promote the apoptosis of prostate cancer cells
-
DOI 10.1158/0008-5472.CAN-05-0347
-
Mohapatra S, Chu B, Zhao X, Pledger WJ. Accumulation of p53 and reductions in XIAP abundance promote the apoptosis of prostate cancer cells. Cancer Res 2005; 65: 7717-7723 (Pubitemid 41297246)
-
(2005)
Cancer Research
, vol.65
, Issue.17
, pp. 7717-7723
-
-
Mohapatra, S.1
Chu, B.2
Zhao, X.3
Pledger, W.J.4
-
51
-
-
66749165938
-
Functional p53 in cells contributes to the anticancer effect of the cyclin-dependent kinase inhibitor roscovitine
-
Paprskarova M, Krystof V, Jorda R, et al. Functional p53 in cells contributes to the anticancer effect of the cyclin-dependent kinase inhibitor roscovitine. J Cell Biochem 2009; 107: 428-437
-
(2009)
J Cell Biochem
, vol.107
, pp. 428-437
-
-
Paprskarova, M.1
Krystof, V.2
Jorda, R.3
-
52
-
-
0033539933
-
Potent inhibitors of cyclin-dependent kinase 2 induce nuclear accumulation of wild-type p53 and nucleolar fragmentation in human untransformed and tumor-derived cells
-
David-Pfeuty T. Potent inhibitors of cyclin-dependent kinase 2 induce nuclear accumulation of wild-type p53 and nucleolar fragmentation in human untransformed and tumor-derived cells. Oncogene 1999; 18: 7409-7422 (Pubitemid 30035042)
-
(1999)
Oncogene
, vol.18
, Issue.52
, pp. 7409-7422
-
-
David-Pfeuty, T.1
-
53
-
-
0034848953
-
Potent induction of wild-type p53-dependent transcription in tumour cells by a synthetic inhibitor of cyclin-dependent kinases
-
Kotala V, Uldrijan S, Horky M, Trbusek M, Strnad M, Vojtesek B. Potent induction of wild-type p53-dependent transcription in tumour cells by a synthetic inhibitor of cyclin-dependent kinases. Cell Mol Life Sci 2001; 58: 1333-1339 (Pubitemid 32844102)
-
(2001)
Cellular and Molecular Life Sciences
, vol.58
, Issue.9
, pp. 1333-1339
-
-
Kotala, V.1
Uldrijan, S.2
Horky, M.3
Trbusek, M.4
Strnad, M.5
Vojtesek, B.6
-
54
-
-
0035921573
-
Induction of serl5 and 1ys382 modifications of p53 by blockage of transcription elongation
-
DOI 10.1038/sj.onc.1204734
-
Ljungman M, O'Hagan HM, Paulsen MT. Induction of ser15 and lys382 modifications of p53 by blockage of transcription elongation. Oncogene 2001; 20: 5964-5971 (Pubitemid 32955038)
-
(2001)
Oncogene
, vol.20
, Issue.42
, pp. 5964-5971
-
-
Ljungman, M.1
O'Hagan, H.M.2
Paulsen, M.T.3
-
55
-
-
0033590624
-
Inhibition of RNA polymerase II as a trigger for the p53 response
-
DOI 10.1038/sj.onc.1202356
-
Ljungman M, Zhang F, Chen F, Rainbow AJ, McKay BC. Inhibition of RNA polymerase II as a trigger for the p53 response. Oncogene 1999; 18: 583-592 (Pubitemid 29080315)
-
(1999)
Oncogene
, vol.18
, Issue.3
, pp. 583-592
-
-
Ljungman, M.1
Zhang, F.2
Chen, F.3
Rainbow, A.J.4
McKay, B.C.5
-
56
-
-
0034973788
-
Activation of p53 by roscovitine-mediated suppression of MDM2 expression
-
DOI 10.1038/sj.onc.1204412
-
Lu W, Chen L, Peng Y, Chen J. Activation of p53 by roscovitine-mediated suppression of MDM2 expression. Oncogene 2001; 20: 3206-3216 (Pubitemid 32553673)
-
(2001)
Oncogene
, vol.20
, Issue.25
, pp. 3206-3216
-
-
Lu, W.1
Chen, L.2
Peng, Y.3
Chen, J.4
-
57
-
-
3843086271
-
Nuclear accumulation of p53 following inhibition of transcription is not due to diminished levels of MDM2
-
DOI 10.1038/sj.onc.1207709
-
O'Hagan HM, Ljungman M. Nuclear accumulation of p53 following inhibition of transcription is not due to diminished levels of MDM2. Oncogene 2004; 23: 5505-5512 (Pubitemid 39044061)
-
(2004)
Oncogene
, vol.23
, Issue.32
, pp. 5505-5512
-
-
O'Hagan, H.M.1
Ljungman, M.2
-
58
-
-
0038724615
-
Regulation of HDM2 activity by the ribosomal protein L11
-
DOI 10.1016/S1535-6108(03)00134-X
-
Lohrum MA, Ludwig RL, Kubbutat MH, Hanlon M, Vousden KH. Regulation of HDM2 activity by the ribosomal protein L11. Cancer Cell 2003; 3: 577-587 (Pubitemid 36808652)
-
(2003)
Cancer Cell
, vol.3
, Issue.6
, pp. 577-587
-
-
Lohrum, M.A.E.1
Ludwig, R.L.2
Kubbutat, M.H.G.3
Hanlon, M.4
Vousden, K.H.5
-
59
-
-
0242721592
-
Ribosomal Protein L11 Negatively Regulates Oncoprotein MDM2 and Mediates a p53-Dependent Ribosomal-Stress Checkpoint Pathway
-
DOI 10.1128/MCB.23.23.8902-8912.2003
-
Zhang Y, Wolf GW, Bhat K, et al. Ribosomal protein L11 negatively regulates oncoprotein MDM2 and mediates a p53-dependent ribosomal-stress checkpoint pathway. Mol Cell Biol 2003; 23: 8902-8912 (Pubitemid 37433388)
-
(2003)
Molecular and Cellular Biology
, vol.23
, Issue.23
, pp. 8902-8912
-
-
Zhang, Y.1
Wolf, G.W.2
Bhat, K.3
Jin, A.4
Allio, T.5
Burkhart, W.A.6
Xiong, Y.7
-
60
-
-
7244238177
-
Inhibition of MDM2-mediated p53 ubiquitination and degradation by ribosomal protein L5
-
DOI 10.1074/jbc.M403722200
-
Dai MS, Lu H. Inhibition of MDM2-mediated p53 ubiquitination and degradation by ribosomal protein L5. J Biol Chem 2004; 279: 44475-44482 (Pubitemid 39430853)
-
(2004)
Journal of Biological Chemistry
, vol.279
, Issue.43
, pp. 44475-44482
-
-
Dai, M.-S.1
Lu, H.2
-
61
-
-
4344685939
-
Ribosomal protein L23 activates p53 by inhibiting MDM2 function in response to ribosomal perturbation but not to translation inhibition
-
DOI 10.1128/MCB.24.17.7654-7668.2004
-
Dai MS, Zeng SX, Jin Y, Sun XX, David L, Lu H. Ribosomal protein L23 activates p53 by inhibiting MDM2 function in response to ribosomal perturbation but not to translation inhibition. Mol Cell Biol 2004; 24: 7654-7668 (Pubitemid 39121491)
-
(2004)
Molecular and Cellular Biology
, vol.24
, Issue.17
, pp. 7654-7668
-
-
Dai, M.-S.1
Zeng, S.X.2
Jin, Y.3
Sun, X.-X.4
David, L.5
Lu, H.6
-
62
-
-
4344660471
-
Inhibition of HDM2 and activation of p53 by ribosomal protein L23
-
DOI 10.1128/MCB.24.17.7669-7680.2004
-
Jin A, Itahana K, O'Keefe K, Zhang Y. Inhibition of HDM2 and activation of p53 by ribosomal protein L23. Mol Cell Biol 2004; 24: 7669-7680 (Pubitemid 39121492)
-
(2004)
Molecular and Cellular Biology
, vol.24
, Issue.17
, pp. 7669-7680
-
-
Jin, A.1
Itahana, K.2
O'Keefe, K.3
Zhang, Y.4
-
63
-
-
3242715867
-
Essential role of ribosomal protein L11 in mediating growth inhibition-induced p53 activation
-
DOI 10.1038/sj.emboj.7600247
-
Bhat KP, Itahana K, Jin A, Zhang Y. Essential role of ribosomal protein L11 in mediating growth inhibition-induced p53 activation. EMBO J 2004; 23: 2402-2412 (Pubitemid 38954847)
-
(2004)
EMBO Journal
, vol.23
, Issue.12
, pp. 2402-2412
-
-
Bhat, K.P.1
Itahana, K.2
Jin, A.3
Zhang, Y.4
-
64
-
-
0035921777
-
Common and reversible regulation of wild-type p53 function and of ribosomal biogenesis by protein kinases in human cells
-
DOI 10.1038/sj.onc.1204741
-
David-Pfeuty T, Nouvian-Dooghe Y, Sirri V, Roussel P, Hernandez-Verdun D. Common and reversible regulation of wild-type p53 function and of ribosomal biogenesis by protein kinases in human cells. Oncogene 2001; 20: 5951-5963 (Pubitemid 32955037)
-
(2001)
Oncogene
, vol.20
, Issue.42
, pp. 5951-5963
-
-
David-Pfeuty, T.1
Nouvian-Dooghe, Y.2
Sirri, V.3
Roussel, P.4
Hernandez-Verdun, D.5
-
65
-
-
0041622837
-
Rapid onset of nucleolar disintegration preceding cell cycle arrest in roscovitine-induced apoptosis of human MCF-7 breast cancer cells
-
DOI 10.1002/ijc.11290
-
Wojciechowski J, Horky M, Gueorguieva M, Wesierska-Gadek J. Rapid onset of nucleolar disintegration preceding cell cycle arrest in roscovitine-induced apoptosis of human MCF-7 breast cancer cells. Int J Cancer 2003; 106: 486-495 (Pubitemid 36969788)
-
(2003)
International Journal of Cancer
, vol.106
, Issue.4
, pp. 486-495
-
-
Wojciechowski, J.1
Horky, M.2
Gueorguieva, M.3
Wesierska-Gadek, J.4
-
66
-
-
23844525170
-
Antiproliferative activity of olomoucine II, a novel 2,6,9-trisubstituted purine cyclin-dependent kinase inhibitor
-
Krystof V, McNae IW, Walkinshaw MD, et al. Antiproliferative activity of olomoucine II, a novel 2,6,9-trisubstituted purine cyclin-dependent kinase inhibitor. Cell Mol Life Sci 2005; 62: 1763-1771
-
(2005)
Cell Mol Life Sci
, Issue.62
, pp. 1763-1771
-
-
Krystof, V.1
McNae, I.W.2
Walkinshaw, M.D.3
-
67
-
-
0032549704
-
The Ink4a tumor suppressor gene product, p19Arf, interacts with MDM2 and neutralizes MDM2's inhibition of p53
-
Pomerantz J, Schreiber-Agus N, Liegeois NJ, et al. The Ink4a tumor suppressor gene product, p19Arf, interacts with MDM2 and neutralizes MDM2's inhibition of p53. Cell 1998; 92: 713-723
-
(1998)
Cell
, vol.92
, pp. 713-723
-
-
Pomerantz, J.1
Schreiber-Agus, N.2
Liegeois, N.J.3
-
68
-
-
0032549711
-
ARF promotes MDM2 degradation and stabilizes p53: ARF-INK4a locus deletion impairs both the Rb and p53 tumor suppression pathways
-
Zhang Y, Xiong Y, Yarbrough WG. ARF promotes MDM2 degradation and stabilizes p53: ARF-INK4a locus deletion impairs both the Rb and p53 tumor suppression pathways. Cell 1998; 92: 725-734
-
(1998)
Cell
, vol.92
, pp. 725-734
-
-
Zhang, Y.1
Xiong, Y.2
Yarbrough, W.G.3
-
69
-
-
0032169516
-
The alternative product from the human CDKN2A locus, p14(ARF), participates in a regulatory feedback loop with p53 and MDM2
-
Stott FJ, Bates S, James MC, et al. The alternative product from the human CDKN2A locus, p14(ARF), participates in a regulatory feedback loop with p53 and MDM2. EMBO J 1998; 17: 5001-5014
-
(1998)
EMBO J
, Issue.17
, pp. 5001-5014
-
-
Stott, F.J.1
Bates, S.2
James, M.C.3
-
70
-
-
0032493350
-
Functional and physical interactions of the ARF tumor suppressor with p53 and Mdm2
-
Kamijo T, Weber JD, Zambetti G, Zindy F, Roussel MF, Sherr CJ. Functional and physical interactions of the ARF tumor suppressor with p53 and Mdm2. Proc Natl Acad Sci U S A 1998; 95: 8292-8297
-
Proc Natl Acad Sci U S a 1998
, vol.95
, pp. 8292-8297
-
-
Kamijo, T.1
Weber, J.D.2
Zambetti, G.3
Zindy, F.4
Roussel, M.F.5
Sherr, C.J.6
-
71
-
-
0036302062
-
Nucleophosmin regulates the stability and transcriptional activity of p53
-
Colombo E, Marine JC, Danovi D, Falini B, Pelicci PG. Nucleophosmin regulates the stability and transcriptional activity of p53. Nat Cell Biol 2002; 4: 529-533
-
(2002)
Nat Cell Biol
, vol.4
, pp. 529-533
-
-
Colombo, E.1
Marine, J.C.2
Danovi, D.3
Falini, B.4
Pelicci, P.G.5
-
72
-
-
2342491487
-
Nucleolar protein NPM interacts with HDM2 and protects tumor suppressor protein p53 from HDM2-mediated degradation
-
Kurki S, Peltonen K, Latonen L, et al. Nucleolar protein NPM interacts with HDM2 and protects tumor suppressor protein p53 from HDM2-mediated degradation. Cancer Cell 2004; 5: 465-475
-
(2004)
Cancer Cell
, vol.5
, pp. 465-475
-
-
Kurki, S.1
Peltonen, K.2
Latonen, L.3
-
73
-
-
41449083855
-
Nucleophosmin interacts with HEXIM1 and regulates RNA polymerase II transcription
-
Gurumurthy M, Tan CH, Ng R, et al. Nucleophosmin interacts with HEXIM1 and regulates RNA polymerase II transcription. J Mol Biol 2008; 378: 302-317
-
(2008)
J Mol Biol
, vol.378
, pp. 302-317
-
-
Gurumurthy, M.1
Tan, Ch.2
Ng, R.3
-
74
-
-
68049106187
-
Ubiquitination of HEXIM1 by HDM2
-
Lau J, Lew QJ, Diribarne G, et al. Ubiquitination of HEXIM1 by HDM2. Cell Cycle 2009; 8: 2247-2254
-
(2009)
Cell Cycle
, vol.8
, pp. 2247-2254
-
-
Lau, J.1
Lew, Q.J.2
Diribarne, G.3
-
75
-
-
0034632675
-
Synergistic activation of p53-dependent transcription by two cooperating damage recognition pathways
-
Blaydes JP, Craig AL, Wallace M, et al. Synergistic activation of p53-dependent transcription by two cooperating damage recognition pathways. Oncogene 2000; 19: 3829-3839
-
(2000)
Oncogene
, vol.19
, pp. 3829-3839
-
-
Blaydes, J.P.1
Craig, A.L.2
Wallace, M.3
-
76
-
-
33646757232
-
The complexity of p53 stabilization and activation
-
Lavin MF, Gueven N. The complexity of p53 stabilization and activation. Cell Death Differ 2006; 13: 941-950
-
(2006)
Cell Death Differ
, vol.13
, pp. 941-950
-
-
Lavin, M.F.1
Gueven, N.2
-
77
-
-
33745488640
-
(R)-roscovitine (CYC202, Seliciclib) sensitizes SH-SY5Y neuroblastoma cells to nutlin-3-induced apoptosis
-
Ribas J, Boix J, Meijer L. (R)-roscovitine (CYC202, Seliciclib) sensitizes SH-SY5Y neuroblastoma cells to nutlin-3-induced apoptosis. Exp Cell Res 2006; 312: 2394-2400
-
(2006)
Exp Cell Res
, vol.312
, pp. 2394-2400
-
-
Ribas, J.1
Boix, J.2
Meijer, L.3
-
78
-
-
36249021361
-
Cyclin-dependent kinase inhibitors sensitize tumor cells to nutlin-induced apoptosis: A potent drug combination
-
Cheok CF, Dey A, Lane DP. Cyclin-dependent kinase inhibitors sensitize tumor cells to nutlin-induced apoptosis: a potent drug combination. Mol Cancer Res 2007; 5: 1133-1145
-
(2007)
Mol Cancer Res
, vol.5
, pp. 1133-1145
-
-
Cheok, C.F.1
Dey, A.2
Lane, D.P.3
-
79
-
-
34247470836
-
Second generation inhibitors of BCR-ABL for the treatment of imatinib-resistant chronic myeloid leukaemia
-
Weisberg E, Manley PW, Cowan-Jacob SW, Hochhaus A, Griffin JD. Second generation inhibitors of BCR-ABL for the treatment of imatinib-resistant chronic myeloid leukaemia. Nat Rev Cancer 2007; 7: 345-356
-
(2007)
Nat Rev Cancer
, vol.7
, pp. 345-356
-
-
Weisberg, E.1
Manley, P.W.2
Cowan-Jacob, S.W.3
Hochhaus, A.4
Griffin, J.D.5
-
80
-
-
67649726156
-
Protein kinase inhibitors: Contributions from structure to clinical compounds
-
Johnson LN. Protein kinase inhibitors: contributions from structure to clinical compounds. Q Rev Biophys 2009; 42: 1-40.
-
(2009)
Q Rev Biophys
, vol.42
, pp. 1-40
-
-
Johnson, L.N.1
-
81
-
-
0034721195
-
Identification of novel purine and pyrimidine cyclin-dependent kinase inhibitors with distinct molecular interactions and tumor cell growth inhibition profiles
-
Arris CE, Boyle FT, Calvert AH, et al. Identification of novel purine and pyrimidine cyclin-dependent kinase inhibitors with distinct molecular interactions and tumor cell growth inhibition profiles. J Med Chem 2000; 43: 2797-2804
-
(2000)
J Med Chem
, vol.43
, pp. 2797-2804
-
-
Arris, C.E.1
Boyle, F.T.2
Calvert, A.H.3
-
83
-
-
4644240387
-
Prediction of resistance to small molecule FLT3 inhibitors: Implications for molecularly targeted therapy of acute leukemia
-
Cools J, Mentens N, Furet P, et al. Prediction of resistance to small molecule FLT3 inhibitors: implications for molecularly targeted therapy of acute leukemia. Cancer Res 2004; 64: 6385-6389
-
(2004)
Cancer Res
, vol.64
, pp. 6385-6389
-
-
Cools, J.1
Mentens, N.2
Furet, P.3
-
84
-
-
13844317894
-
EGFR mutation and resistance of non-small-cell lung cancer to gefitinib
-
DOI 10.1056/NEJMoa044238
-
Kobayashi S, Boggon TJ, Dayaram T, et al. EGFR mutation and resistance of non-small-cell lung cancer to gefitinib. N Engl J Med 2005; 352: 786-792 (Pubitemid 40271173)
-
(2005)
New England Journal of Medicine
, vol.352
, Issue.8
, pp. 786-792
-
-
Kobayashi, S.1
Boggon, T.J.2
Dayaram, T.3
Janne, P.A.4
Kocher, O.5
Meyerson, M.6
Johnson, B.E.7
Eck, M.J.8
Tenen, D.G.9
Halmos, B.10
-
85
-
-
44949157910
-
Molecular basis of drug resistance in aurora kinases
-
Girdler F, Sessa F, Patercoli S, Villa F, Musacchio A, Taylor S. Molecular basis of drug resistance in aurora kinases. Chem Biol 2008; 15: 552-562
-
(2008)
Chem Biol
, vol.15
, pp. 552-562
-
-
Girdler, F.1
Sessa, F.2
Patercoli, S.3
Villa, F.4
Musacchio, A.5
Taylor, S.6
-
86
-
-
14744274624
-
Comparative analysis of two clinically active BCR-ABL kinase inhibitors reveals the role of conformation-specific binding in resistance
-
Burgess MR, Skaggs BJ, Shah NP, Lee FY, Sawyers CL. Comparative analysis of two clinically active BCR-ABL kinase inhibitors reveals the role of conformation-specific binding in resistance. Proc Natl Acad Sci U S A 2005; 102: 3395-3400
-
Proc Natl Acad Sci U S a 2005
, vol.102
, pp. 3395-3400
-
-
Burgess, M.R.1
Skaggs, B.J.2
Shah, N.P.3
Lee, F.Y.4
Sawyers, C.L.5
-
87
-
-
33745676300
-
Toward understanding the structural basis of cyclin-dependent kinase 6 specific inhibition
-
DOI 10.1021/jm0600388
-
Lu H, Schulze-Gahmen U. Toward understanding the structural basis of cyclin-dependent kinase 6 specific inhibition. J Med Chem 2006; 49: 3826-3831 (Pubitemid 43967880)
-
(2006)
Journal of Medicinal Chemistry
, vol.49
, Issue.13
, pp. 3826-3831
-
-
Lu, H.1
Schulze-Gahmen, U.2
-
88
-
-
0029029617
-
Mechanism of CDK activation revealed by the structure of a cyclinA-CDK2 complex
-
Jeffrey PD, Russo AA, Polyak K, et al. Mechanism of CDK activation revealed by the structure of a cyclinA-CDK2 complex. Nature 1995; 376: 313-320
-
(1995)
Nature
, vol.376
, pp. 313-320
-
-
Jeffrey, P.D.1
Russo, A.A.2
Polyak, K.3
-
89
-
-
4444247138
-
Mammalian cells cycle without the D-type cyclin-dependent kinases Cdk4 and Cdk6
-
DOI 10.1016/j.cell.2004.08.002, PII S0092867404007500
-
Malumbres M, Sotillo R, Santamaria D, et al. Mammalian cells cycle without the D-type cyclin-dependent kinases Cdk4 and Cdk6. Cell 2004; 118: 493-504. (Pubitemid 39485668)
-
(2004)
Cell
, vol.118
, Issue.4
, pp. 493-504
-
-
Malumbres, M.1
Sotillo, R.2
Santamaria, D.3
Galan, J.4
Cerezo, A.5
Ortega, S.6
Dubus, P.7
Barbacid, M.8
-
90
-
-
34547952048
-
Cdk1 is sufficient to drive the mammalian cell cycle
-
DOI 10.1038/nature06046, PII NATURE06046
-
Santamaria D, Barriere C, Cerqueira A, et al. Cdk1 is sufficient to drive the mammalian cell cycle. Nature 2007; 448: 811-815 (Pubitemid 47266342)
-
(2007)
Nature
, vol.448
, Issue.7155
, pp. 811-815
-
-
Santamaria, D.1
Barriere, C.2
Cerqueira, A.3
Hunt, S.4
Tardy, C.5
Newton, K.6
Caceres, J.F.7
Dubus, P.8
Malumbres, M.9
Barbacid, M.10
-
91
-
-
0033974989
-
Characterization of an ovarian carcinoma cell line resistant to cisplatin and flavopiridol
-
Bible KC, Boerner SA, Kirkland K, et al. Characterization of an ovarian carcinoma cell line resistant to cisplatin and flavopiridol. Clin Cancer Res 2000; 6: 661-670 (Pubitemid 30111492)
-
(2000)
Clinical Cancer Research
, vol.6
, Issue.2
, pp. 661-670
-
-
Bible, K.C.1
Boerner, S.A.2
Kirkland, K.3
Anderl, K.L.4
Bartelt Jr., D.5
Svingen, P.A.6
Kottke, T.J.7
Lee, Y.K.8
Eckdahl, S.9
Stalboerger, P.G.10
Jenkins, R.B.11
Kaufmann, S.H.12
-
92
-
-
0035138482
-
Overexpression of the ATP-binding cassette half-transporter, ABCG2 (MXR/BCRP/ABCP1), in flavopiridol-resistant human breast cancer cells
-
Robey RW, Medina-Perez WY, Nishiyama K, et al. Over-expression of the ATP-binding cassette half-transporter, ABCG2 (MXR/BCRP/ABCP1), in flavopiridol-resistant human breast cancer cells. Clin Cancer Res 2001; 7: 145-152 (Pubitemid 32110217)
-
(2001)
Clinical Cancer Research
, vol.7
, Issue.1
, pp. 145-152
-
-
Robey, R.W.1
Medina-Perez, W.Y.2
Nishiyama, K.3
Lahusen, T.4
Miyake, K.5
Litman, T.6
Senderowicz, A.M.7
Ross, D.D.8
Bates, S.E.9
-
93
-
-
63149115862
-
Identification of genes that confer tumor cell resistance to the aurora B kinase inhibitor, AZD1152
-
Guo J, Anderson MG, Tapang P, et al. Identification of genes that confer tumor cell resistance to the aurora B kinase inhibitor, AZD1152. Pharmacogenom J 2009; 9: 90-102.
-
(2009)
Pharmacogenom J
, vol.9
, pp. 90-102
-
-
Guo, J.1
Anderson, M.G.2
Tapang, P.3
-
94
-
-
0034752936
-
Characterization of a human colorectal carcinoma cell line with acquired resistance to flavopiridol
-
Smith V, Raynaud F, Workman P, Kelland LR. Characterization of a human colorectal carcinoma cell line with acquired resistance to flavopiridol. Mol Pharmacol 2001; 60: 885-893 (Pubitemid 33027422)
-
(2001)
Molecular Pharmacology
, vol.60
, Issue.5
, pp. 885-893
-
-
Smith, V.1
Raynaud, F.2
Workman, P.3
Kelland, L.R.4
-
95
-
-
42049101633
-
The cyclin-dependent kinase inhibitor flavopiridol potentiates the effects of topoisomerase I poisons by suppressing Rad51 expression in a p53-dependent manner
-
DOI 10.1158/0008-5472.CAN-07-2395
-
Ambrosini G, Seelman SL, Qin LX, Schwartz GK. 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 (Pubitemid 351521805)
-
(2008)
Cancer Research
, vol.68
, Issue.7
, pp. 2312-2320
-
-
Ambrosini, G.1
Seelman, S.L.2
Qin, L.-X.3
Schwartz, G.K.4
|