-
1
-
-
77954187741
-
DNA topoisomerases and their poisoning by anticancer and antibacterial drugs
-
Pommier Y, Leo E, Zhang H, Marchand C. DNA topoisomerases and their poisoning by anticancer and antibacterial drugs. Chem Biol 2010;17:421-33.
-
(2010)
Chem Biol
, vol.17
, pp. 421-433
-
-
Pommier, Y.1
Leo, E.2
Zhang, H.3
Marchand, C.4
-
2
-
-
67650682519
-
DNA topoisomerase I inhibitors: Chemistry, biology, and interfacial inhibition
-
Pommier Y. DNA topoisomerase I inhibitors: chemistry, biology, and interfacial inhibition. Chem Rev 2009;109:2894-902.
-
(2009)
Chem Rev
, vol.109
, pp. 2894-2902
-
-
Pommier, Y.1
-
3
-
-
0034923502
-
DNA topoisomerases: Structure, function, and mechanism
-
DOI 10.1146/annurev.biochem.70.1.369
-
Champoux JJ. DNA topoisomerases: structure, function, and mechanism. Annu Rev Biochem 2001;70:369-413. (Pubitemid 32662215)
-
(2001)
Annual Review of Biochemistry
, vol.70
, pp. 369-413
-
-
Champoux, J.J.1
-
4
-
-
39749119942
-
Next generation topoisomerase I inhibitors: Rationale and biomarker strategies
-
DOI 10.1016/j.bcp.2007.10.016, PII S0006295207006946
-
Teicher BA. Next generation topoisomerase I inhibitors: rationale and biomarker strategies. Biochem Pharmacol 2008;75:1262-71. (Pubitemid 351305209)
-
(2008)
Biochemical Pharmacology
, vol.75
, Issue.6
, pp. 1262-1271
-
-
Teicher, B.A.1
-
5
-
-
66849113688
-
The indenoisoquinoline noncamptothecin topoisomerase I inhibitors: Update and perspectives
-
Pommier Y, Cushman M. The indenoisoquinoline noncamptothecin topoisomerase I inhibitors: update and perspectives. Mol Cancer Ther 2009;8:1008-14.
-
(2009)
Mol Cancer Ther
, vol.8
, pp. 1008-1014
-
-
Pommier, Y.1
Cushman, M.2
-
6
-
-
33745278845
-
Repair of Topoisomerase I-Mediated DNA Damage
-
DOI 10.1016/S0079-6603(06)81005-6, PII S0079660306810056, Progress in Nuclei Acid Research and Molecular Biology
-
Pommier Y, Barcelo JM, Rao VA, Sordet O, Jobson AG, Thibaut L, et al. Repair of topoisomerase I-mediated DNA damage. Prog Nucleic Acid Res Mol Biol 2006;81:179-229. (Pubitemid 44767505)
-
(2006)
Progress in Nucleic Acid Research and Molecular Biology
, vol.81
, pp. 179-229
-
-
Pommier, Y.1
Barcelo, J.M.2
Rao, V.A.3
Sordet, O.4
Jobson, A.G.5
Thibaut, L.6
Miao, Z.7
Seiler, J.A.8
Zhang, H.9
Marchand, C.10
Agama, K.11
Nitiss, J.L.12
Redon, C.13
-
7
-
-
0031815336
-
Protein-linked DNA strand breaks induced by NSC 314622, a novel noncamptothecin topoisomerase I poison
-
Kohlhagen G, Paull K, Cushman M, Nagafufuji P, Pommier Y. Protein-linked DNA strand breaks induced by NSC 314622, a non-camptothecin topoisomerase I poison. Mol Pharmacol 1998;54:50-8. (Pubitemid 28337586)
-
(1998)
Molecular Pharmacology
, vol.54
, Issue.1
, pp. 50-58
-
-
Kohlhagen, G.1
Paull, K.D.2
Cushman, M.3
Nagafuji, P.4
Pommier, Y.5
-
8
-
-
35948968756
-
Novel indenoisoquinolines NSC 725776 and NSC 724998 produce persistent topoisomerase I cleavage complexes and overcome multidrug resistance
-
DOI 10.1158/0008-5472.CAN-07-0938
-
Antony S, Agama KK, Miao ZH, Takagi K, Wright MH, Robles AI, et al. Novel indenoisoquinolines NSC 725776 and NSC 724998 produce persistent topoisomerase I cleavage complexes and overcome multidrug resistance. Cancer Res 2007;67:10397-405. (Pubitemid 350070815)
-
(2007)
Cancer Research
, vol.67
, Issue.21
, pp. 10397-10405
-
-
Antony, S.1
Agama, K.K.2
Miao, Z.-H.3
Takagi, K.4
Wright, M.H.5
Robles, A.I.6
Varticovski, L.7
Nagarajan, M.8
Morrell, A.9
Cushman, M.10
Pommier, Y.11
-
9
-
-
22744438407
-
Synthesis and mechanism of action studies of a series of norindenoisoquinoline topoisomerase I poisons reveal an inhibitor with a flipped orientation in the ternary DNA-enzyme-inhibitor complex as determined by X-ray crystallographic analysis
-
DOI 10.1021/jm050076b
-
Ioanoviciu A, Antony S, Pommier Y, Staker BL, Stewart L, Cushman M. Synthesis and mechanism of action studies of a series of norindenoisoquinoline topoisomerase I poisons reveal an inhibitor with a flipped orientation in the ternary DNA-Enzyme-Inhibitor complex as determined by X-ray crystallographic analysis. J Med Chem 2005;48: 4803-14. (Pubitemid 41033123)
-
(2005)
Journal of Medicinal Chemistry
, vol.48
, Issue.15
, pp. 4803-4814
-
-
Ioanoviciu, A.1
Antony, S.2
Pommier, Y.3
Staker, B.L.4
Stewart, L.5
Cushman, M.6
-
10
-
-
77955443849
-
Proteomic analysis of nuclei isolated from cancer cell lines treated with indenoisoquinoline NSC 724998, a novel topoisomerase I inhibitor
-
Han B, Stockwin LH, Hancock C, Yu SX, Hollingshead MG, Newton DL. Proteomic analysis of nuclei isolated from cancer cell lines treated with indenoisoquinoline NSC 724998, a novel topoisomerase I inhibitor. J Proteome Res 2010;9:4016-27.
-
(2010)
J Proteome Res
, vol.9
, pp. 4016-4027
-
-
Han, B.1
Stockwin, L.H.2
Hancock, C.3
Yu, S.X.4
Hollingshead, M.G.5
Newton, D.L.6
-
11
-
-
78349238215
-
Development of a validated immunofluorescence assay for gH2AX as a pharmacodynamic marker of topoisomerase I inhibitor activity
-
Kinders R, Hollingshead MG, Lawrence S, Ji J, Tabb B, Bonner WM, et al. Development of a validated immunofluorescence assay for gH2AX as a pharmacodynamic marker of topoisomerase I inhibitor activity. Clin Cancer Res 2010;16:5447-57.
-
(2010)
Clin Cancer Res
, vol.16
, pp. 5447-5457
-
-
Kinders, R.1
Hollingshead, M.G.2
Lawrence, S.3
Ji, J.4
Tabb, B.5
Bonner, W.M.6
-
12
-
-
0030870632
-
Abrogation of an S-phase checkpoint and potentiation of camptothecin cytotoxicity by 7-hydroxystaurosporine (UCN-01) in human cancer cell lines, possibly influenced by p53 function
-
Shao R-G, Cao C-X, Shimizu T, O'Connor P, Kohn KW, Pommier Y. Abrogation of an S-phase checkpoint and potentiation of camptothecin cytotoxicity by 7-hydroxystaurosporine (UCN-01) in human cancer cell lines, possibly influenced by p53. Cancer Res 1997;57:4029-35. (Pubitemid 27427693)
-
(1997)
Cancer Research
, vol.57
, Issue.18
, pp. 4029-4035
-
-
Shao, R.-G.1
Cao, C.-X.2
Shimizu, T.3
O'Connor, P.M.4
Kohn, K.W.5
Pommier, Y.6
-
13
-
-
2942599254
-
Abrogation of Chk1-mediated S/G2 checkpoint by UCN-01 enhances ara-C-induced cytotoxicity in human colon cancer cells
-
Shao RG, Cao CX, Pommier Y. Abrogation of Chk1-mediated S/G2 checkpoint by UCN-01 enhances ara-C-induced cytotoxicity in human colon cancer cells. Acta Pharmacol Sin 2004;25:756-62. (Pubitemid 38736101)
-
(2004)
Acta Pharmacologica Sinica
, vol.25
, Issue.6
, pp. 756-762
-
-
Shao, R.-G.1
Cao, C.-X.2
Pommier, Y.3
-
14
-
-
79959604565
-
A phase 1 study of UCN-01 in combination with irinotecan in patients with resistant solid tumor malignancies
-
Fracasso PM, Williams KJ, Chen RC, Picus J, Ma CX, Ellis MJ, et al. A phase 1 study of UCN-01 in combination with irinotecan in patients with resistant solid tumor malignancies. Cancer Chemother Pharmacol 2011;67:1225-37.
-
(2011)
Cancer Chemother Pharmacol
, vol.67
, pp. 1225-1237
-
-
Fracasso, P.M.1
Williams, K.J.2
Chen, R.C.3
Picus, J.4
Ma, C.X.5
Ellis, M.J.6
-
15
-
-
34547902426
-
The intra-S-phase checkpoint affects both DNA replication initiation and elongation: Single-cell and -DNA fiber analyses
-
DOI 10.1128/MCB.02278-06
-
Seiler JA, Conti C, Syed A, Aladjem MI, Pommier Y. The intra-S-phase checkpoint affects both DNA replication initiation and elongation: single-cell and -DNA fiber analyses. Mol Cell Biol 2007;27:5806-18. (Pubitemid 47257835)
-
(2007)
Molecular and Cellular Biology
, vol.27
, Issue.16
, pp. 5806-5818
-
-
Seiler, J.A.1
Conti, C.2
Syed, A.3
Aladjem, M.I.4
Pommier, Y.5
-
16
-
-
22944462043
-
Targeting Chk2 kinase: Molecular interaction maps and therapeutic rationale
-
DOI 10.2174/1381612054546716
-
Pommier Y, Sordet O, Rao A, Zhang H, Kohn KW. Targeting Chk2 kinase: molecular interaction maps and therapeutic rationale. Curr Pharm Des 2005;11:2855-72. (Pubitemid 41051871)
-
(2005)
Current Pharmaceutical Design
, vol.11
, Issue.22
, pp. 2855-2872
-
-
Pommier, Y.1
Sordet, O.2
Rao, V.A.3
Zhang, H.4
Kohn, K.W.5
-
18
-
-
36448973875
-
CHK2 kinase: Cancer susceptibility and cancer therapy - Two sides of the same coin?
-
DOI 10.1038/nrc2251, PII NRC2251
-
Antoni L, Sodha N, Collins I, Garrett MD. CHK2 kinase: cancer susceptibility and cancer therapy - two sides of the same coin?Nat Rev Cancer 2007;7:925-36. (Pubitemid 350165855)
-
(2007)
Nature Reviews Cancer
, vol.7
, Issue.12
, pp. 925-936
-
-
Antoni, L.1
Sodha, N.2
Collins, I.3
Garrett, M.D.4
-
19
-
-
79955720082
-
Anticancer therapy with checkpoint inhibitors: What, where and when?
-
Garrett MD, Collins I. Anticancer therapy with checkpoint inhibitors: what, where and when?Trends Pharmacol Sci 2011;32:308-16.
-
(2011)
Trends Pharmacol Sci
, vol.32
, pp. 308-316
-
-
Garrett, M.D.1
Collins, I.2
-
20
-
-
79955686677
-
CHK1 inhibitors in combination chemotherapy: Thinking beyond the cell cycle
-
Dent P, Tang Y, Yacoub A, Dai Y, Fisher PB, Grant S. CHK1 inhibitors in combination chemotherapy: thinking beyond the cell cycle. Mol Interv 2011;11:133-40.
-
(2011)
Mol Interv
, vol.11
, pp. 133-140
-
-
Dent, P.1
Tang, Y.2
Yacoub, A.3
Dai, Y.4
Fisher, P.B.5
Grant, S.6
-
21
-
-
0037032835
-
The protein kinase complement of the human genome
-
DOI 10.1126/science.1075762
-
Manning G, Whyte DB, Martinez R, Hunter T, Sudarsanam S. The protein kinase complement of the human genome. Science 2002;298: 1912-34. (Pubitemid 35425239)
-
(2002)
Science
, vol.298
, Issue.5600
, pp. 1912-1934
-
-
Manning, G.1
Whyte, D.B.2
Martinez, R.3
Hunter, T.4
Sudarsanam, S.5
-
22
-
-
0037108873
-
2-M checkpoint independently of p53 by targeting both of the checkpoint kinases, Chk2 and Chk1
-
Yu Q, La Rose J, Zhang H, Takemura H, Kohn KW, Pommier Y. 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;62:5743-8. (Pubitemid 35204730)
-
(2002)
Cancer Research
, vol.62
, Issue.20
, pp. 5743-5748
-
-
Yu, Q.1
La, R.J.2
Zhang, H.3
Takemura, H.4
Kohn, K.W.5
Pommier, Y.6
-
23
-
-
34748854847
-
Identification of a bis-guanylhydrazone [4,40-diacetyldiphenylurea- bis(guanylhydrazone); NSC 109555] as a novel chemotype for inhibition of Chk2 kinase
-
DOI 10.1124/mol.107.035832
-
Jobson AG, Cardellina JH 2nd, Scudiero D, Kondapaka S, Zhang H, Kim H, et al. Identification of a bis-guanylhydrazone [4,40-diacetyldiphenylurea- bis(guanylhydrazone); NSC 109555] as a novel chemotype for inhibition of chk2 kinase. Mol Pharmacol 2007;72:876-84. (Pubitemid 47481411)
-
(2007)
Molecular Pharmacology
, vol.72
, Issue.4
, pp. 876-884
-
-
Jobson, A.G.1
Cardellina II, J.H.2
Scudiero, D.3
Kondapaka, S.4
Zhang, H.5
Kim, H.6
Shoemaker, R.7
Pommier, Y.8
-
24
-
-
77958498222
-
The ATM-Chk2 and ATR-Chk1 pathways in DNA damage signaling and cancer
-
Smith J, Tho LM, Xu N, Gillespie DA. The ATM-Chk2 and ATR-Chk1 pathways in DNA damage signaling and cancer. Adv Cancer Res 2010;108:73-112.
-
(2010)
Adv Cancer Res
, vol.108
, pp. 73-112
-
-
Smith, J.1
Tho, L.M.2
Xu, N.3
Gillespie, D.A.4
-
25
-
-
17644432403
-
2/M DNA damage checkpoint
-
Liu Q, Guntuku S, Cui XS, Matsuoka S, Cortez D, Tamai K, et al. Chk1 is an essential kinase that is regulated by Atr and required for the G(2)/M DNA damage checkpoint. Genes Dev 2000;14:1448-59. (Pubitemid 30421838)
-
(2000)
Genes and Development
, vol.14
, Issue.12
, pp. 1448-1459
-
-
Liu, Q.1
Guntuku, S.2
Cui, X.-S.3
Matsuoka, S.4
Cortez, D.5
Tamai, K.6
Luo, G.7
Carattini-Rivera, S.8
DeMayo, F.9
Bradley, A.10
Donehower, L.A.11
Elledge, S.J.12
-
26
-
-
65249182632
-
The DNA-damage effector checkpoint kinase 1 is essential for chromosome segregation and cytokinesis
-
Peddibhotla S, Lam MH, Gonzalez-Rimbau M, Rosen JM. The DNA-damage effector checkpoint kinase 1 is essential for chromosome segregation and cytokinesis. Proc Natl Acad Sci U S A 2009;106:5159-64.
-
(2009)
Proc Natl Acad Sci U S A
, vol.106
, pp. 5159-5164
-
-
Peddibhotla, S.1
Lam, M.H.2
Gonzalez-Rimbau, M.3
Rosen, J.M.4
-
27
-
-
78649336706
-
The DNA damage response: Making it safe to play with knives
-
Ciccia A, Elledge SJ. The DNA damage response: making it safe to play with knives. Mol Cell 2010;40:179-204.
-
(2010)
Mol Cell
, vol.40
, pp. 179-204
-
-
Ciccia, A.1
Elledge, S.J.2
-
28
-
-
52949139387
-
AZD7762, a novel checkpoint kinase inhibitor, drives checkpoint abrogation and potentiates DNA-targeted therapies
-
Zabludoff SD, Deng C, Grondine MR, Sheehy AM, Ashwell S, Caleb BL, et al. AZD7762, a novel checkpoint kinase inhibitor, drives checkpoint abrogation and potentiates DNA-targeted therapies. Mol Cancer Ther 2008;7:2955-66.
-
(2008)
Mol Cancer Ther
, vol.7
, pp. 2955-2966
-
-
Zabludoff, S.D.1
Deng, C.2
Grondine, M.R.3
Sheehy, A.M.4
Ashwell, S.5
Caleb, B.L.6
-
29
-
-
77953506262
-
Chk1 inhibition after replicative stress activates a double strand break response mediated by ATM and DNA-dependent protein kinase
-
McNeely S, Conti C, Sheikh T, Patel H, Zabludoff S, Pommier Y, et al. Chk1 inhibition after replicative stress activates a double strand break response mediated by ATM and DNA-dependent protein kinase. Cell Cycle 2010;9:995-1004.
-
(2010)
Cell Cycle
, vol.9
, pp. 995-1004
-
-
McNeely, S.1
Conti, C.2
Sheikh, T.3
Patel, H.4
Zabludoff, S.5
Pommier, Y.6
-
30
-
-
77950650401
-
In vitro and in vivo radiation sensitization of human tumor cells by a novel checkpoint kinase inhibitor, AZD7762
-
Mitchell JB, Choudhuri R, Fabre K, Sowers AL, Citrin D, Zabludoff SD, et al. In vitro and in vivo radiation sensitization of human tumor cells by a novel checkpoint kinase inhibitor, AZD7762. Clin Cancer Res 2010;16:2076-84.
-
(2010)
Clin Cancer Res
, vol.16
, pp. 2076-2084
-
-
Mitchell, J.B.1
Choudhuri, R.2
Fabre, K.3
Sowers, A.L.4
Citrin, D.5
Zabludoff, S.D.6
-
31
-
-
77953770987
-
Mechanism of radiosensitization by the Chk1/2 inhibitor AZD7762 involves abrogation of the G2 checkpoint and inhibition of homologous recombinational DNA repair
-
Morgan MA, Parsels LA, Zhao L, Parsels JD, Davis MA, Hassan MC, et al. Mechanism of radiosensitization by the Chk1/2 inhibitor AZD7762 involves abrogation of the G2 checkpoint and inhibition of homologous recombinational DNA repair. Cancer Res 2010;70:4972-81.
-
(2010)
Cancer Res
, vol.70
, pp. 4972-4981
-
-
Morgan, M.A.1
Parsels, L.A.2
Zhao, L.3
Parsels, J.D.4
Davis, M.A.5
Hassan, M.C.6
-
32
-
-
80051957430
-
Checkpoint kinase inhibitor synergizes with DNA-damaging agents in G(1) checkpoint- Defective neuroblastoma
-
Xu H, Cheung IY, Wei XX, Tran H, Gao X, Cheung NK. Checkpoint kinase inhibitor synergizes with DNA-damaging agents in G(1) checkpoint- defective neuroblastoma. Int J Cancer 2011;129:1953-62.
-
(2011)
Int J Cancer
, vol.129
, pp. 1953-1962
-
-
Xu, H.1
Cheung, I.Y.2
Wei, X.X.3
Tran, H.4
Gao, X.5
Cheung, N.K.6
-
33
-
-
33749028012
-
Defective Mre11-dependent activation of Chk2 by ataxia telangiectasia mutated in colorectal carcinoma cells in response to replication-dependent DNA double strand breaks
-
DOI 10.1074/jbc.M603747200
-
Takemura H, Rao VA, Sordet O, Furuta T, Miao ZH, Meng L, et al. Defective Mre11-dependent activation of Chk2 by ataxia telangiectasia Mutated in Colorectal carcinoma cells in response to replication- dependent DNA double strand breaks. J Biol Chem 2006;281:30814-23. (Pubitemid 44582136)
-
(2006)
Journal of Biological Chemistry
, vol.281
, Issue.41
, pp. 30814-30823
-
-
Takemura, H.1
Rao, V.A.2
Sordet, O.3
Furuta, T.4
Miao, Z.-H.5
Meng, L.6
Zhang, H.7
Pommier, Y.8
-
34
-
-
33846856967
-
CHIR-124, a novel potent inhibitor of Chk1, potentiates the cytotoxicity of topoisomerase I poisons in vitro and in vivo
-
DOI 10.1158/1078-0432.CCR-06-1424
-
Tse AN, Rendahl KG, Sheikh T, Cheema H, Aardalen K, Embry M, et al. CHIR-124, a novel potent inhibitor of Chk1, potentiates the cytotoxicity of topoisomerase I poisons in vitro and in vivo. Clin Cancer Res 2007;13:591-602. (Pubitemid 46225366)
-
(2007)
Clinical Cancer Research
, vol.13
, Issue.2 I
, pp. 591-602
-
-
Tse, A.N.1
Rendahl, K.G.2
Sheikh, T.3
Cheema, H.4
Aardalen, K.5
Embry, M.6
Ma, S.7
Moler, E.J.8
Zhi, J.N.9
De Menezes, D.E.L.10
Hibner, B.11
Gesner, T.G.12
Schwartz, G.K.13
-
35
-
-
0035425354
-
Targeting the molecular mechanism of DNA replication
-
DOI 10.1016/S1359-6446(01)01854-2, PII S1359644601018542
-
Conti C, Caburet S, Bensimon A. Targeting the molecular mechanism of DNA replication. Drug Discov Today 2001;6:786-92. (Pubitemid 32722221)
-
(2001)
Drug Discovery Today
, vol.6
, Issue.15
, pp. 786-792
-
-
Conti, C.1
Caburet, S.2
Bensimon, A.3
-
36
-
-
37249004667
-
The mammalian DNA replication elongation checkpoint: Implication of Chk1 and relationship with origin firing as determined by single DNA molecule and single cell analyses
-
Conti C, Seiler J, Pommier Y. The mammalian dna replication elongation checkpoint: implication of Chk1 and relationship with origin firing as determined by single dna molecule and single cell analyses. Cell Cycle 2007;6:2760-7. (Pubitemid 350277167)
-
(2007)
Cell Cycle
, vol.6
, Issue.22
, pp. 2760-2767
-
-
Conti, C.1
Seiler, J.A.2
Pommier, Y.3
-
37
-
-
52949092763
-
Replication fork movement sets chromatin loop size and origin choice in mammalian cells
-
Courbet S, Gay S, Arnoult N, Wronka G, Anglana M, Brison O, et al. Replication fork movement sets chromatin loop size and origin choice in mammalian cells. Nature 2008;455:557-60.
-
(2008)
Nature
, vol.455
, pp. 557-560
-
-
Courbet, S.1
Gay, S.2
Arnoult, N.3
Wronka, G.4
Anglana, M.5
Brison, O.6
-
38
-
-
0035890407
-
Destabilization of CHK2 by a missense mutation associated with Li-Fraumeni syndrome
-
Lee SB, Kim SH, Bell DW, Wahrer DC, Schiripo TA, Jorczak MM, et al. Destabilization of CHK2 by a missense mutation associated with Li- Fraumeni syndrome. Cancer Res 2001;61:8062-7. (Pubitemid 33091590)
-
(2001)
Cancer Research
, vol.61
, Issue.22
, pp. 8062-8067
-
-
Sean, B.L.1
Sang, H.K.2
Bell, D.W.3
Wahrer, D.C.R.4
Schiripo, T.A.5
Jorczak, M.M.6
Sgroi, D.C.7
Garber, J.E.8
Li, F.P.9
Nichols, K.E.10
Varley, J.M.11
Godwin, A.K.12
Shannon, K.M.13
Harlow, E.14
Haber, D.A.15
-
39
-
-
10644270921
-
p73 induction after DNA damage is regulated by checkpoint kinases Chk1 and Chk2
-
DOI 10.1101/gad.1221004
-
Urist M, Tanaka T, Poyurovsky MV, Prives C. p73 induction after DNA damage is regulated by checkpoint kinases Chk1 and Chk2. Genes Dev 2004;18:3041-54. (Pubitemid 39658173)
-
(2004)
Genes and Development
, vol.18
, Issue.24
, pp. 3041-3054
-
-
Urist, M.1
Tanaka, T.2
Poyurovsky, M.V.3
Prives, C.4
-
40
-
-
0038054343
-
The Chk2 tumor suppressor is not required for p53 responses in human cancer cells
-
DOI 10.1074/jbc.M213159200
-
Jallepalli PV, Lengauer C, Vogelstein B, Bunz F. The Chk2 tumor suppressor is not required for p53 responses in human cancer cells. J Biol Chem 2003;278:20475-9. (Pubitemid 36806343)
-
(2003)
Journal of Biological Chemistry
, vol.278
, Issue.23
, pp. 20475-20479
-
-
Jallepalli, P.V.1
Lengauer, C.2
Vogelsteint, B.3
Bunz, F.4
-
41
-
-
0024460479
-
Protein-linked DNA strand breaks induced in mammalian cells by camptothecin, an inhibitor of topoisomerase I
-
Covey JM, Jaxel C, Kohn KW, Pommier Y. Protein-linked DNA strand breaks induced in mammalian cells by camptothecin, an inhibitor of topoisomerase I. Cancer Res 1989;49:5016-22. (Pubitemid 19239335)
-
(1989)
Cancer Research
, vol.49
, Issue.18
, pp. 5016-5022
-
-
Covey, J.M.1
Jaxel, C.2
Kohn, K.W.3
Pommier, Y.4
-
42
-
-
0028012774
-
The structural basis of camptothecin interactions with human serum albumin: Impact on drug stability
-
Burke TG, Mi Z. The structural basis of camptothecin interactions with human serum albumin: impact on drug stability. J Med Chem 1994;37:40-6. (Pubitemid 24058811)
-
(1994)
Journal of Medicinal Chemistry
, vol.37
, Issue.1
, pp. 40-46
-
-
Burke, T.G.1
Mi, Z.2
-
43
-
-
0037180432
-
The mechanism of topoisomerase I poisoning by a camptothecin analog
-
DOI 10.1073/pnas.242259599
-
Staker BL, Hjerrild K, Feese MD, Behnke CA, Burgin AB Jr, Stewart L. The mechanism of topoisomerase I poisoning by a camptothecin analog. Proc Natl Acad Sci U S A 2002;99:15387-92. (Pubitemid 35403944)
-
(2002)
Proceedings of the National Academy of Sciences of the United States of America
, vol.99
, Issue.24
, pp. 15387-15392
-
-
Staker, B.L.1
Hjerrild, K.2
Feese, M.D.3
Behnke, C.A.4
Burgin Jr., A.B.5
Stewart, L.6
-
44
-
-
33749034730
-
Topoisomerase I inhibitors: Camptothecins and beyond
-
DOI 10.1038/nrc1977, PII NRC1977
-
Pommier Y. Topoisomerase I inhibitors: camptothecins and beyond. Nat Rev Cancer 2006;6:789-802. (Pubitemid 44450467)
-
(2006)
Nature Reviews Cancer
, vol.6
, Issue.10
, pp. 789-802
-
-
Pommier, Y.1
-
45
-
-
0035802112
-
Activation of mammalian Chk1 during DNA replication arrest: A role for Chk1 in the intra-S phase checkpoint monitoring replication origin firing
-
DOI 10.1083/jcb.200104099
-
Feijoo C, Hall-Jackson C, Wu R, Jenkins D, Leitch J, Gilbert DM, et al. Activation of mammalian Chk1 during DNA replication arrest: a role for Chk1 in the intra-S phase checkpoint monitoring replication origin firing. J Cell Biol 2001;154:913-23. (Pubitemid 34286172)
-
(2001)
Journal of Cell Biology
, vol.154
, Issue.5
, pp. 913-923
-
-
Feijoo, C.1
Hall-Jackson, C.2
Wu, R.3
Jenkins, D.4
Leitch, J.5
Gilbert, D.M.6
Smythe, C.7
-
46
-
-
0036510055
-
The DNA damage-dependent intra-S phase checkpoint is regulated by parallel pathways
-
Falck J, Petrini JH, Williams BR, Lukas J, Bartek J. The DNA damage-dependent intra-S phase checkpoint is regulated by parallel pathways. Nat Genet 2002;30:290-4.
-
(2002)
Nat Genet
, vol.30
, pp. 290-294
-
-
Falck, J.1
Petrini, J.H.2
Williams, B.R.3
Lukas, J.4
Bartek, J.5
-
47
-
-
79954567265
-
Replication-fork stalling and processing at a single psoralen interstrand crosslink in Xenopus egg extracts
-
Le Breton C, Hennion M, Arimondo PB, Hyrien O. Replication-fork stalling and processing at a single psoralen interstrand crosslink in Xenopus egg extracts. PLoS One 2011;6:e18554.
-
(2011)
PLoS One
, vol.6
-
-
Le Breton, C.1
Hennion, M.2
Arimondo, P.B.3
Hyrien, O.4
-
48
-
-
0023552288
-
UCN-01, a selective inhibitor of protein kinase C from Streptomyces
-
Takahashi I, Kobayashi E, Asano K, Yoshida M, Nakano H. UCN-01, a selective inhibitor of protein kinase C from Streptomyces. J Antibiot (Tokyo) 1987;40:1782-4. (Pubitemid 18023359)
-
(1987)
Journal of Antibiotics
, vol.40
, Issue.12
, pp. 1782-1784
-
-
Takahashi, I.1
Kobayashi, E.2
Asano, K.3
Yoshida, M.4
Nakano, H.5
-
49
-
-
0037034928
-
Interference with PDK1-Akt survival signaling pathway by UCN-01 (7-hydroxystaurosporine)
-
DOI 10.1038/sj/onc/1205225
-
Sato S, Fujita N, Tsuruo T. Interference with PDK1-Akt survival signaling pathway by UCN-01 (7-hydroxystaurosporine). Oncogene 2002;21:1727-38. (Pubitemid 34259036)
-
(2002)
Oncogene
, vol.21
, Issue.11
, pp. 1727-1738
-
-
Sato, S.1
Fujita, N.2
Tsuruo, T.3
-
50
-
-
77958480403
-
Cooperative functions of Chk1 and Chk2 reduce tumour susceptibility in vivo
-
Niida H, Murata K, Shimada M, Ogawa K, Ohta K, Suzuki K, et al. Cooperative functions of Chk1 and Chk2 reduce tumour susceptibility in vivo. EMBO J 2010;29:3558-70.
-
(2010)
EMBO J
, vol.29
, pp. 3558-3570
-
-
Niida, H.1
Murata, K.2
Shimada, M.3
Ogawa, K.4
Ohta, K.5
Suzuki, K.6
|