-
1
-
-
0030615323
-
G1 phase accumulation induced by UCN-01 is associated with dephosphorylation of Rb and CDK2 proteins as well as induction of CDK inhibitor p21/Cip1/WAF1/Sdi1 in p53-mutated human epidermoid carcinoma A431 cells
-
T. Akiyama, T. Yoshida, T. Tsujita, M. Shimizu, T. Mizukami, and M. Okabe et al. G1 phase accumulation induced by UCN-01 is associated with dephosphorylation of Rb and CDK2 proteins as well as induction of CDK inhibitor p21/Cip1/WAF1/Sdi1 in p53-mutated human epidermoid carcinoma A431 cells Cancer Res 57 1997 1495 1501
-
(1997)
Cancer Res
, vol.57
, pp. 1495-1501
-
-
Akiyama, T.1
Yoshida, T.2
Tsujita, T.3
Shimizu, M.4
Mizukami, T.5
Okabe, M.6
-
2
-
-
52949145309
-
Keeping checkpoint kinases in line: New selective inhibitors in clinical trials
-
S. Ashwell, J.W. Janetka, and S. Zabludoff Keeping checkpoint kinases in line: New selective inhibitors in clinical trials Expert Opin Investig Drugs 17 2008 1331 1340
-
(2008)
Expert Opin Investig Drugs
, vol.17
, pp. 1331-1340
-
-
Ashwell, S.1
Janetka, J.W.2
Zabludoff, S.3
-
3
-
-
0032817385
-
Differential gene expression in colon carcinoma cells and tissues detected with a cDNA array
-
S. Backert, M. Gelos, U. Kobalz, M.L. Hanski, C. Bohm, and B. Mann et al. Differential gene expression in colon carcinoma cells and tissues detected with a cDNA array Int J Cancer 82 1999 868 874
-
(1999)
Int J Cancer
, vol.82
, pp. 868-874
-
-
Backert, S.1
Gelos, M.2
Kobalz, U.3
Hanski, M.L.4
Bohm, C.5
Mann, B.6
-
4
-
-
46249091563
-
The checkpoint kinases Chk1 and Chk2 regulate the functional associations between hBRCA2 and Rad51 in response to DNA damage
-
E.M. Bahassi, J.L. Ovesen, A.L. Riesenberg, W.Z. Bernstein, P.E. Hasty, and P.J. Stambrook The checkpoint kinases Chk1 and Chk2 regulate the functional associations between hBRCA2 and Rad51 in response to DNA damage Oncogene 27 2008 3977 3985
-
(2008)
Oncogene
, vol.27
, pp. 3977-3985
-
-
Bahassi, E.M.1
Ovesen, J.L.2
Riesenberg, A.L.3
Bernstein, W.Z.4
Hasty, P.E.5
Stambrook, P.J.6
-
5
-
-
84859611140
-
Therapeutic targeting of Chk1 in NSCLC stem cells during chemotherapy
-
M. Bartucci, S. Svensson, P. Romania, R. Dattilo, M. Patrizii, and M. Signore et al. Therapeutic targeting of Chk1 in NSCLC stem cells during chemotherapy Cell Death Differ 19 2012 768 778
-
(2012)
Cell Death Differ
, vol.19
, pp. 768-778
-
-
Bartucci, M.1
Svensson, S.2
Romania, P.3
Dattilo, R.4
Patrizii, M.5
Signore, M.6
-
6
-
-
77949410508
-
Regulators of cyclin-dependent kinases are crucial for maintaining genome integrity in S phase
-
H. Beck, V. Nahse, M.S. Larsen, P. Groth, T. Clancy, and M. Lees et al. Regulators of cyclin-dependent kinases are crucial for maintaining genome integrity in S phase J Cell Biol 188 2010 629 638
-
(2010)
J Cell Biol
, vol.188
, pp. 629-638
-
-
Beck, H.1
Nahse, V.2
Larsen, M.S.3
Groth, P.4
Clancy, T.5
Lees, M.6
-
7
-
-
84868689115
-
Cyclin-dependent kinase suppression by WEE1 kinase protects the genome through control of replication initiation and nucleotide consumption
-
H. Beck, V. Nahse-Kumpf, M.S. Larsen, K.A. O'Hanlon, S. Patzke, and C. Holmberg et al. Cyclin-dependent kinase suppression by WEE1 kinase protects the genome through control of replication initiation and nucleotide consumption Mol Cell Biol 32 2012 4226 4236
-
(2012)
Mol Cell Biol
, vol.32
, pp. 4226-4236
-
-
Beck, H.1
Nahse-Kumpf, V.2
Larsen, M.S.3
O'Hanlon, K.A.4
Patzke, S.5
Holmberg, C.6
-
8
-
-
84896709854
-
Dose and schedule determination of the Chk1/2 inhibitor LY2606368 in patients with solid tumors
-
AACR Washington, DC. Philadelphia (PA) (Abstract nr LB-200)
-
J. Bendell, F. Janku, J. Infante, S. Jones, H. Burris, and L. Golden et al. Dose and schedule determination of the Chk1/2 inhibitor LY2606368 in patients with solid tumors Proceedings of the 104th Annual Meeting of the American Association for Cancer Research; 2013 Apr 6-10 2013 AACR Washington, DC. Philadelphia (PA) (Abstract nr LB-200)
-
(2013)
Proceedings of the 104th Annual Meeting of the American Association for Cancer Research; 2013 Apr 6-10
-
-
Bendell, J.1
Janku, F.2
Infante, J.3
Jones, S.4
Burris, H.5
Golden, L.6
-
9
-
-
84879687956
-
Regulation of cell cycle checkpoint kinase WEE1 by miR-195 in malignant melanoma
-
A. Bhattacharya, U. Schmitz, O. Wolkenhauer, M. Schonherr, Y. Raatz, and M. Kunz Regulation of cell cycle checkpoint kinase WEE1 by miR-195 in malignant melanoma Oncogene 32 2013 3175 3183
-
(2013)
Oncogene
, vol.32
, pp. 3175-3183
-
-
Bhattacharya, A.1
Schmitz, U.2
Wolkenhauer, O.3
Schonherr, M.4
Raatz, Y.5
Kunz, M.6
-
10
-
-
53349156857
-
Breaching the DNA damage checkpoint via PF-00477736, a novel small-molecule inhibitor of checkpoint kinase 1
-
A. Blasina, J. Hallin, E. Chen, M.E. Arango, E. Kraynov, and J. Register et al. Breaching the DNA damage checkpoint via PF-00477736, a novel small-molecule inhibitor of checkpoint kinase 1 Mol Cancer Ther 7 2008 2394 2404
-
(2008)
Mol Cancer Ther
, vol.7
, pp. 2394-2404
-
-
Blasina, A.1
Hallin, J.2
Chen, E.3
Arango, M.E.4
Kraynov, E.5
Register, J.6
-
11
-
-
79958804691
-
Phase i clinical trial of gemcitabine (GEM) in combination with PF-00477736 (PF-736), a selective inhibitor of CHK1 kinase
-
(Suppl.; abstr 3062)
-
N. Brega, G. McArthur, C. Britten, S. Wong, E. Wang, and K. Wilner et al. Phase I clinical trial of gemcitabine (GEM) in combination with PF-00477736 (PF-736), a selective inhibitor of CHK1 kinase J Clin Oncol 28 15s 2010 (Suppl.; abstr 3062)
-
(2010)
J Clin Oncol
, vol.28
, Issue.15 S
-
-
Brega, N.1
McArthur, G.2
Britten, C.3
Wong, S.4
Wang, E.5
Wilner, K.6
-
12
-
-
84873739385
-
A potent Chk1 inhibitor is selectively cytotoxic in melanomas with high levels of replicative stress
-
K. Brooks, V. Oakes, B. Edwards, M. Ranall, P. Leo, and S. Pavey et al. A potent Chk1 inhibitor is selectively cytotoxic in melanomas with high levels of replicative stress Oncogene 32 2013 788 796
-
(2013)
Oncogene
, vol.32
, pp. 788-796
-
-
Brooks, K.1
Oakes, V.2
Edwards, B.3
Ranall, M.4
Leo, P.5
Pavey, S.6
-
14
-
-
38949147038
-
G2 checkpoint abrogation and checkpoint kinase-1 targeting in the treatment of cancer
-
N. Bucher, and C.D. Britten G2 checkpoint abrogation and checkpoint kinase-1 targeting in the treatment of cancer Br J Cancer 98 2008 523 528
-
(2008)
Br J Cancer
, vol.98
, pp. 523-528
-
-
Bucher, N.1
Britten, C.D.2
-
15
-
-
84896697039
-
Dose determination of LY2603618 administered in combination with pemetrexed and cisplatin in patients with advanced cancer
-
(abstract nbr 586)
-
E. Calvo, N. Dickgreber, S. Hynes, R. Decker, E. Kumm, and U. Ohnmacht et al. Dose determination of LY2603618 administered in combination with pemetrexed and cisplatin in patients with advanced cancer Poster presented at EORTC-NCI-AACR symposium on Molecular Targets and Cancer Therapeutics; November 6-9, 2012; Dublin, Ireland 2012 (abstract nbr 586)
-
(2012)
Poster Presented at EORTC-NCI-AACR Symposium on Molecular Targets and Cancer Therapeutics; November 6-9, 2012; Dublin, Ireland
-
-
Calvo, E.1
Dickgreber, N.2
Hynes, S.3
Decker, R.4
Kumm, E.5
Ohnmacht, U.6
-
16
-
-
84944047859
-
Dose determination of LY2603618, a Chk1 inhibitor, administered in combination with gemcitabine in patients with advanced cancer
-
Mol Cancer Ther (Abstract nr A94)
-
E. Calvo, D. Richards, F. Braiteh, D. Von Hoff, R. McWilliams, and C. Becerra et al. Dose determination of LY2603618, a Chk1 inhibitor, administered in combination with gemcitabine in patients with advanced cancer Proceedings of the AACR-NCI-EORTC International Conference: Molecular Targets and Cancer Therapeutics; 2011 Nov 12-16; San Francisco, CA Mol Cancer Ther 10 2011 (Abstract nr A94)
-
(2011)
Proceedings of the AACR-NCI-EORTC International Conference: Molecular Targets and Cancer Therapeutics; 2011 Nov 12-16; San Francisco, CA
, vol.10
-
-
Calvo, E.1
Richards, D.2
Braiteh, F.3
Von Hoff, D.4
McWilliams, R.5
Becerra, C.6
-
17
-
-
84863799519
-
Combined inhibition of Chk1 and Wee1: In vitro synergistic effect translates to tumor growth inhibition in vivo
-
L. Carrassa, R. Chila, M. Lupi, F. Ricci, C. Celenza, and M. Mazzoletti et al. Combined inhibition of Chk1 and Wee1: In vitro synergistic effect translates to tumor growth inhibition in vivo Cell Cycle 11 2012 2507 2517
-
(2012)
Cell Cycle
, vol.11
, pp. 2507-2517
-
-
Carrassa, L.1
Chila, R.2
Lupi, M.3
Ricci, F.4
Celenza, C.5
Mazzoletti, M.6
-
18
-
-
70349329673
-
U2OS cells lacking Chk1 undergo aberrant mitosis and fail to activate the spindle checkpoint
-
L. Carrassa, Y. Sanchez, E. Erba, and G. Damia U2OS cells lacking Chk1 undergo aberrant mitosis and fail to activate the spindle checkpoint J Cell Mol Med 13 2009 1565 1576
-
(2009)
J Cell Mol Med
, vol.13
, pp. 1565-1576
-
-
Carrassa, L.1
Sanchez, Y.2
Erba, E.3
Damia, G.4
-
19
-
-
65449142073
-
CHK1 inhibition as a strategy for targeting Fanconi Anemia (FA) DNA repair pathway deficient tumors
-
C.C. Chen, R.D. Kennedy, S. Sidi, A.T. Look, and A. D'Andrea CHK1 inhibition as a strategy for targeting Fanconi Anemia (FA) DNA repair pathway deficient tumors Mol Cancer 8 2009 24
-
(2009)
Mol Cancer
, vol.8
, pp. 24
-
-
Chen, C.C.1
Kennedy, R.D.2
Sidi, S.3
Look, A.T.4
D'Andrea, A.5
-
20
-
-
1542754615
-
Human Chk1 expression is dispensable for somatic cell death and critical for sustaining G2 DNA damage checkpoint
-
Z. Chen, Z. Xiao, J. Chen, S.C. Ng, T. Sowin, and H. Sham et al. Human Chk1 expression is dispensable for somatic cell death and critical for sustaining G2 DNA damage checkpoint Mol Cancer Ther 2 2003 543 548
-
(2003)
Mol Cancer Ther
, vol.2
, pp. 543-548
-
-
Chen, Z.1
Xiao, Z.2
Chen, J.3
Ng, S.C.4
Sowin, T.5
Sham, H.6
-
21
-
-
78649336706
-
The DNA damage response: Making it safe to play with knives
-
A. Ciccia, and S.J. Elledge The DNA damage response: Making it safe to play with knives Mol Cell 40 2010 179 204
-
(2010)
Mol Cell
, vol.40
, pp. 179-204
-
-
Ciccia, A.1
Elledge, S.J.2
-
22
-
-
79952775174
-
RNAi screen of the protein kinome identifies checkpoint kinase 1 (CHK1) as a therapeutic target in neuroblastoma
-
K.A. Cole, J. Huggins, M. Laquaglia, C.E. Hulderman, M.R. Russell, and K. Bosse et al. RNAi screen of the protein kinome identifies checkpoint kinase 1 (CHK1) as a therapeutic target in neuroblastoma Proc Natl Acad Sci U S A 108 2011 3336 3341
-
(2011)
Proc Natl Acad Sci U S A
, vol.108
, pp. 3336-3341
-
-
Cole, K.A.1
Huggins, J.2
Laquaglia, M.3
Hulderman, C.E.4
Russell, M.R.5
Bosse, K.6
-
23
-
-
0035941021
-
ATR and ATRIP: Partners in checkpoint signaling
-
D. Cortez, S. Guntuku, J. Qin, and S.J. Elledge ATR and ATRIP: Partners in checkpoint signaling Science 294 2001 1713 1716
-
(2001)
Science
, vol.294
, pp. 1713-1716
-
-
Cortez, D.1
Guntuku, S.2
Qin, J.3
Elledge, S.J.4
-
24
-
-
55249124825
-
Interruption of the Ras/MEK/ERK signaling cascade enhances Chk1 inhibitor-induced DNA damage in vitro and in vivo in human multiple myeloma cells
-
Y. Dai, S. Chen, X.Y. Pei, J.A. Almenara, L.B. Kramer, and C.A. Venditti et al. Interruption of the Ras/MEK/ERK signaling cascade enhances Chk1 inhibitor-induced DNA damage in vitro and in vivo in human multiple myeloma cells Blood 112 2008 2439 2449
-
(2008)
Blood
, vol.112
, pp. 2439-2449
-
-
Dai, Y.1
Chen, S.2
Pei, X.Y.3
Almenara, J.A.4
Kramer, L.B.5
Venditti, C.A.6
-
25
-
-
74549189337
-
New insights into checkpoint kinase 1 in the DNA damage response signaling network
-
Y. Dai, and S. Grant New insights into checkpoint kinase 1 in the DNA damage response signaling network Clin Cancer Res 16 2010 376 383
-
(2010)
Clin Cancer Res
, vol.16
, pp. 376-383
-
-
Dai, Y.1
Grant, S.2
-
26
-
-
34248352031
-
Statins synergistically potentiate 7-hydroxystaurosporine (UCN-01) lethality in human leukemia and myeloma cells by disrupting Ras farnesylation and activation
-
Y. Dai, P. Khanna, S. Chen, X.Y. Pei, P. Dent, and S. Grant Statins synergistically potentiate 7-hydroxystaurosporine (UCN-01) lethality in human leukemia and myeloma cells by disrupting Ras farnesylation and activation Blood 109 2007 4415 4423
-
(2007)
Blood
, vol.109
, pp. 4415-4423
-
-
Dai, Y.1
Khanna, P.2
Chen, S.3
Pei, X.Y.4
Dent, P.5
Grant, S.6
-
27
-
-
0035393498
-
Pharmacological inhibitors of the mitogen-activated protein kinase (MAPK) kinase/MAPK cascade interact synergistically with UCN-01 to induce mitochondrial dysfunction and apoptosis in human leukemia cells
-
Y. Dai, C. Yu, V. Singh, L. Tang, Z. Wang, and R. McInistry et al. Pharmacological inhibitors of the mitogen-activated protein kinase (MAPK) kinase/MAPK cascade interact synergistically with UCN-01 to induce mitochondrial dysfunction and apoptosis in human leukemia cells Cancer Res 61 2001 5106 5115
-
(2001)
Cancer Res
, vol.61
, pp. 5106-5115
-
-
Dai, Y.1
Yu, C.2
Singh, V.3
Tang, L.4
Wang, Z.5
McInistry, R.6
-
28
-
-
79651475663
-
A phase i dose-escalation study of Sch 900776, a selective inhibitor of checkpoint kinase 1 (CHK1), in combination with gemcitabine (Gem) in subjects with advanced solid tumors
-
(Suppl.; abstr 3064)
-
A. Daud, G. Springett, D. Mendelson, P. Munster, J. Goldman, and J. Strosberg et al. A phase I dose-escalation study of Sch 900776, a selective inhibitor of checkpoint kinase 1 (CHK1), in combination with gemcitabine (Gem) in subjects with advanced solid tumors J Clin Oncol 28 15s 2010 (Suppl.; abstr 3064)
-
(2010)
J Clin Oncol
, vol.28
, Issue.15 S
-
-
Daud, A.1
Springett, G.2
Mendelson, D.3
Munster, P.4
Goldman, J.5
Strosberg, J.6
-
29
-
-
80655141261
-
Chk1 inhibition and Wee1 inhibition combine synergistically to impede cellular proliferation
-
K.D. Davies, P.L. Cable, J.E. Garrus, F.X. Sullivan, I. von Carlowitz, and Y.L. Huerou et al. Chk1 inhibition and Wee1 inhibition combine synergistically to impede cellular proliferation Cancer Biol Ther 12 2011 788 796
-
(2011)
Cancer Biol Ther
, vol.12
, pp. 788-796
-
-
Davies, K.D.1
Cable, P.L.2
Garrus, J.E.3
Sullivan, F.X.4
Von Carlowitz, I.5
Huerou, Y.L.6
-
30
-
-
80051887747
-
Single-agent inhibition of Chk1 is antiproliferative in human cancer cell lines in vitro and inhibits tumor xenograft growth in vivo
-
K.D. Davies, M.J. Humphries, F.X. Sullivan, I. von Carlowitz, Y. Le Huerou, and P.J. Mohr et al. Single-agent inhibition of Chk1 is antiproliferative in human cancer cell lines in vitro and inhibits tumor xenograft growth in vivo Oncol Res 19 2011 349 363
-
(2011)
Oncol Res
, vol.19
, pp. 349-363
-
-
Davies, K.D.1
Humphries, M.J.2
Sullivan, F.X.3
Von Carlowitz, I.4
Le Huerou, Y.5
Mohr, P.J.6
-
31
-
-
34250705797
-
The Rad9-Hus1-Rad1 (9-1-1) clamp activates checkpoint signaling via TopBP1
-
S. Delacroix, J.M. Wagner, M. Kobayashi, K. Yamamoto, and L.M. Karnitz The Rad9-Hus1-Rad1 (9-1-1) clamp activates checkpoint signaling via TopBP1 Genes Dev 21 2007 1472 1477
-
(2007)
Genes Dev
, vol.21
, pp. 1472-1477
-
-
Delacroix, S.1
Wagner, J.M.2
Kobayashi, M.3
Yamamoto, K.4
Karnitz, L.M.5
-
32
-
-
79955686677
-
CHK1 inhibitors in combination chemotherapy: Thinking beyond the cell cycle
-
P. Dent, Y. Tang, A. Yacoub, Y. Dai, P.B. Fisher, and S. Grant CHK1 inhibitors in combination chemotherapy: Thinking beyond the cell cycle Mol Interv 11 2011 133 140
-
(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
-
33
-
-
80052632895
-
Wee1 controls genomic stability during replication by regulating the Mus81-Eme1 endonuclease
-
R. Dominguez-Kelly, Y. Martin, S. Koundrioukoff, M.E. Tanenbaum, V.A. Smits, and R.H. Medema et al. Wee1 controls genomic stability during replication by regulating the Mus81-Eme1 endonuclease J Cell Biol 194 2011 567 579
-
(2011)
J Cell Biol
, vol.194
, pp. 567-579
-
-
Dominguez-Kelly, R.1
Martin, Y.2
Koundrioukoff, S.3
Tanenbaum, M.E.4
Smits, V.A.5
Medema, R.H.6
-
34
-
-
0035802112
-
Activation of mammalian Chk1 during DNA replication arrest: A role for Chk1 in the intra-S phase checkpoint monitoring replication origin firing
-
C. Feijoo, C. Hall-Jackson, R. Wu, D. Jenkins, J. Leitch, and D.M. Gilbert 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 154 2001 913 923
-
(2001)
J Cell Biol
, vol.154
, pp. 913-923
-
-
Feijoo, C.1
Hall-Jackson, C.2
Wu, R.3
Jenkins, D.4
Leitch, J.5
Gilbert, D.M.6
-
35
-
-
80051758435
-
Structure-specific DNA endonuclease Mus81/Eme1 generates DNA damage caused by Chk1 inactivation
-
J.V. Forment, M. Blasius, I. Guerini, and S.P. Jackson Structure-specific DNA endonuclease Mus81/Eme1 generates DNA damage caused by Chk1 inactivation PLoS One 6 2011 e23517
-
(2011)
PLoS One
, vol.6
, pp. 23517
-
-
Forment, J.V.1
Blasius, M.2
Guerini, I.3
Jackson, S.P.4
-
36
-
-
84868654250
-
Unique functions of CHK1 and WEE1 underlie synergistic anti-tumor activity upon pharmacologic inhibition
-
A.D. Guertin, M.M. Martin, B. Roberts, M. Hurd, X. Qu, and N.R. Miselis et al. Unique functions of CHK1 and WEE1 underlie synergistic anti-tumor activity upon pharmacologic inhibition Cancer Cell Int 12 2012 45
-
(2012)
Cancer Cell Int
, vol.12
, pp. 45
-
-
Guertin, A.D.1
Martin, M.M.2
Roberts, B.3
Hurd, M.4
Qu, X.5
Miselis, N.R.6
-
37
-
-
79955735344
-
Targeting the replication checkpoint using Sch 900776, a potent and functionally selective CHK1 inhibitor identified via high content screening
-
T.J. Guzi, K. Paruch, M.P. Dwyer, M. Labroli, F. Shanahan, and N. Davis et al. Targeting the replication checkpoint using Sch 900776, a potent and functionally selective CHK1 inhibitor identified via high content screening Mol Cancer Ther 10 2011 591 602
-
(2011)
Mol Cancer Ther
, vol.10
, pp. 591-602
-
-
Guzi, T.J.1
Paruch, K.2
Dwyer, M.P.3
Labroli, M.4
Shanahan, F.5
Davis, N.6
-
38
-
-
35848930133
-
The structure-specific endonuclease Mus81 contributes to replication restart by generating double-strand DNA breaks
-
K. Hanada, M. Budzowska, S.L. Davies, E. van Drunen, H. Onizawa, and H.B. Beverloo et al. The structure-specific endonuclease Mus81 contributes to replication restart by generating double-strand DNA breaks Nat Struct Mol Biol 14 2007 1096 1104
-
(2007)
Nat Struct Mol Biol
, vol.14
, pp. 1096-1104
-
-
Hanada, K.1
Budzowska, M.2
Davies, S.L.3
Van Drunen, E.4
Onizawa, H.5
Beverloo, H.B.6
-
39
-
-
79952284127
-
Hallmarks of cancer: The next generation
-
D. Hanahan, and R.A. Weinberg Hallmarks of cancer: The next generation Cell 144 2011 646 674
-
(2011)
Cell
, vol.144
, pp. 646-674
-
-
Hanahan, D.1
Weinberg, R.A.2
-
40
-
-
34248218749
-
Cdc7-Dbf4 and the human S checkpoint response to UVC
-
T.P. Heffernan, K. Unsal-Kacmaz, A.N. Heinloth, D.A. Simpson, R.S. Paules, and A. Sancar et al. Cdc7-Dbf4 and the human S checkpoint response to UVC J Biol Chem 282 2007 9458 9468
-
(2007)
J Biol Chem
, vol.282
, pp. 9458-9468
-
-
Heffernan, T.P.1
Unsal-Kacmaz, K.2
Heinloth, A.N.3
Simpson, D.A.4
Paules, R.S.5
Sancar, A.6
-
41
-
-
84872494989
-
Phase I, open-label, dose-escalation study of AZD7762 in combination with irinotecan (irino) in patients (pts) with advanced solid tumors
-
(Suppl.; abstr 3033)
-
A. Ho, J. Bendell, J. Cleary, G. Schwartz, H. Burris, and P. Oakes et al. Phase I, open-label, dose-escalation study of AZD7762 in combination with irinotecan (irino) in patients (pts) with advanced solid tumors J Clin Oncol 29 2011 (Suppl.; abstr 3033)
-
(2011)
J Clin Oncol
, vol.29
-
-
Ho, A.1
Bendell, J.2
Cleary, J.3
Schwartz, G.4
Burris, H.5
Oakes, P.6
-
42
-
-
70350504453
-
The DNA-damage response in human biology and disease
-
S.P. Jackson, and J. Bartek The DNA-damage response in human biology and disease Nature 461 2009 1071 1078
-
(2009)
Nature
, vol.461
, pp. 1071-1078
-
-
Jackson, S.P.1
Bartek, J.2
-
43
-
-
84863347829
-
Replication fork dynamics and the DNA damage response
-
R.M. Jones, and E. Petermann Replication fork dynamics and the DNA damage response Biochem J 443 2012 13 26
-
(2012)
Biochem J
, vol.443
, pp. 13-26
-
-
Jones, R.M.1
Petermann, E.2
-
44
-
-
84871234067
-
Phase i and pharmacologic trial of cytosine arabinoside with the selective checkpoint 1 inhibitor Sch 900776 in refractory acute leukemias
-
J.E. Karp, B.M. Thomas, J.M. Greer, C. Sorge, S.D. Gore, and K.W. Pratz et al. Phase I and pharmacologic trial of cytosine arabinoside with the selective checkpoint 1 inhibitor Sch 900776 in refractory acute leukemias Clin Cancer Res 18 2012 6723 6731
-
(2012)
Clin Cancer Res
, vol.18
, pp. 6723-6731
-
-
Karp, J.E.1
Thomas, B.M.2
Greer, J.M.3
Sorge, C.4
Gore, S.D.5
Pratz, K.W.6
-
45
-
-
0344845197
-
Functions of mammalian Cdc7 kinase in initiation/monitoring of DNA replication and development
-
J.M. Kim, M. Yamada, and H. Masai Functions of mammalian Cdc7 kinase in initiation/monitoring of DNA replication and development Mutat Res 532 2003 29 40
-
(2003)
Mutat Res
, vol.532
, pp. 29-40
-
-
Kim, J.M.1
Yamada, M.2
Masai, H.3
-
46
-
-
0142231577
-
Structural basis for UCN-01 (7-hydroxystaurosporine) specificity and PDK1 (3-phosphoinositide-dependent protein kinase-1) inhibition
-
D. Komander, G.S. Kular, J. Bain, M. Elliott, D.R. Alessi, and D.M. Van Aalten Structural basis for UCN-01 (7-hydroxystaurosporine) specificity and PDK1 (3-phosphoinositide-dependent protein kinase-1) inhibition Biochem J 375 2003 255 262
-
(2003)
Biochem J
, vol.375
, pp. 255-262
-
-
Komander, D.1
Kular, G.S.2
Bain, J.3
Elliott, M.4
Alessi, D.R.5
Van Aalten, D.M.6
-
47
-
-
4444345565
-
Centrosome-associated Chk1 prevents premature activation of cyclin-B-Cdk1 kinase
-
A. Kramer, N. Mailand, C. Lukas, R.G. Syljuasen, C.J. Wilkinson, and E.A. Nigg et al. Centrosome-associated Chk1 prevents premature activation of cyclin-B-Cdk1 kinase Nat Cell Biol 6 2004 884 891
-
(2004)
Nat Cell Biol
, vol.6
, pp. 884-891
-
-
Kramer, A.1
Mailand, N.2
Lukas, C.3
Syljuasen, R.G.4
Wilkinson, C.J.5
Nigg, E.A.6
-
48
-
-
77953954908
-
How do Cdc7 and cyclin-dependent kinases trigger the initiation of chromosome replication in eukaryotic cells?
-
K. Labib How do Cdc7 and cyclin-dependent kinases trigger the initiation of chromosome replication in eukaryotic cells? Genes Dev 24 2010 1208 1219
-
(2010)
Genes Dev
, vol.24
, pp. 1208-1219
-
-
Labib, K.1
-
49
-
-
3142552523
-
Chk1 is haploinsufficient for multiple functions critical to tumor suppression
-
M.H. Lam, Q. Liu, S.J. Elledge, and J.M. Rosen Chk1 is haploinsufficient for multiple functions critical to tumor suppression Cancer Cell 6 2004 45 59
-
(2004)
Cancer Cell
, vol.6
, pp. 45-59
-
-
Lam, M.H.1
Liu, Q.2
Elledge, S.J.3
Rosen, J.M.4
-
50
-
-
36949013395
-
ATM and the Mre11 complex combine to recognize and signal DNA double-strand breaks
-
M.F. Lavin ATM and the Mre11 complex combine to recognize and signal DNA double-strand breaks Oncogene 26 2007 7749 7758
-
(2007)
Oncogene
, vol.26
, pp. 7749-7758
-
-
Lavin, M.F.1
-
51
-
-
0035158899
-
Positive regulation of Wee1 by Chk1 and 14-3-3 proteins
-
J. Lee, A. Kumagai, and W.G. Dunphy Positive regulation of Wee1 by Chk1 and 14-3-3 proteins Mol Biol Cell 12 2001 551 563
-
(2001)
Mol Biol Cell
, vol.12
, pp. 551-563
-
-
Lee, J.1
Kumagai, A.2
Dunphy, W.G.3
-
52
-
-
17644432403
-
Chk1 is an essential kinase that is regulated by Atr and required for the G(2)/M DNA damage checkpoint
-
Q. Liu, S. Guntuku, X.S. Cui, S. Matsuoka, D. Cortez, and K. Tamai et al. Chk1 is an essential kinase that is regulated by Atr and required for the G(2)/M DNA damage checkpoint Genes Dev 14 2000 1448 1459
-
(2000)
Genes Dev
, vol.14
, pp. 1448-1459
-
-
Liu, Q.1
Guntuku, S.2
Cui, X.S.3
Matsuoka, S.4
Cortez, D.5
Tamai, K.6
-
53
-
-
0034780430
-
Blocking Chk1 expression induces apoptosis and abrogates the G2 checkpoint mechanism
-
Y. Luo, S.K. Rockow-Magnone, P.E. Kroeger, L. Frost, Z. Chen, and E.K. Han et al. Blocking Chk1 expression induces apoptosis and abrogates the G2 checkpoint mechanism Neoplasia 3 2001 411 419
-
(2001)
Neoplasia
, vol.3
, pp. 411-419
-
-
Luo, Y.1
Rockow-Magnone, S.K.2
Kroeger, P.E.3
Frost, L.4
Chen, Z.5
Han, E.K.6
-
54
-
-
84859726248
-
Targeting Chk1 in p53-deficient triple-negative breast cancer is therapeutically beneficial in human-in-mouse tumor models
-
C.X. Ma, S. Cai, S. Li, C.E. Ryan, Z. Guo, and W.T. Schaiff et al. Targeting Chk1 in p53-deficient triple-negative breast cancer is therapeutically beneficial in human-in-mouse tumor models J Clin Invest 122 2012 1541 1552
-
(2012)
J Clin Invest
, vol.122
, pp. 1541-1552
-
-
Ma, C.X.1
Cai, S.2
Li, S.3
Ryan, C.E.4
Guo, Z.5
Schaiff, W.T.6
-
55
-
-
79651470785
-
Death by releasing the breaks: CHK1 inhibitors as cancer therapeutics
-
C.X. Ma, J.W. Janetka, and H. Piwnica-Worms Death by releasing the breaks: CHK1 inhibitors as cancer therapeutics Trends Mol Med 17 2011 88 96
-
(2011)
Trends Mol Med
, vol.17
, pp. 88-96
-
-
Ma, C.X.1
Janetka, J.W.2
Piwnica-Worms, H.3
-
56
-
-
84873076670
-
Characterization and preclinical development of LCI-1, a selective and potent Chk1 inhibitor in phase 1 clinical trials [abstract]
-
Mol Cancer Ther
-
M. Marshall, D. Barda, D. Barnard, K. Cox, H.B. Diaz, and C. King et al. Characterization and preclinical development of LCI-1, a selective and potent Chk1 inhibitor in phase 1 clinical trials [abstract] Proceedings of the AACR-NCI-EORTC International Conference: Molecular Targets and Cancer Therapeutics - Nov 15-19, 2009; Boston, MA Mol Cancer Ther 8 2009 B248
-
(2009)
Proceedings of the AACR-NCI-EORTC International Conference: Molecular Targets and Cancer Therapeutics - Nov 15-19, 2009; Boston, MA
, vol.8
, pp. 248
-
-
Marshall, M.1
Barda, D.2
Barnard, D.3
Cox, K.4
Diaz, H.B.5
King, C.6
-
57
-
-
84896725609
-
Characterization and preclinical development of LY2606368, a second generation Chk1 inhibitor
-
(Abstract nr 194)
-
M. Marshall, C. King, D. Barnard, H.B. Diaz, D. Barda, and A. Bence Characterization and preclinical development of LY2606368, a second generation Chk1 inhibitor Poster presented at EORTC-NCI-AACR symposium on Molecular Targets and Cancer Therapeutics; November 16-19, 2010; Berlin, Germany 2010 (Abstract nr 194)
-
(2010)
Poster Presented at EORTC-NCI-AACR Symposium on Molecular Targets and Cancer Therapeutics; November 16-19, 2010; Berlin, Germany
-
-
Marshall, M.1
King, C.2
Barnard, D.3
Diaz, H.B.4
Barda, D.5
Bence, A.6
-
58
-
-
33846567414
-
Pharmacological abrogation of S-phase checkpoint enhances the anti-tumor activity of gemcitabine in vivo
-
D.J. Matthews, F.M. Yakes, J. Chen, M. Tadano, L. Bornheim, and D.O. Clary et al. Pharmacological abrogation of S-phase checkpoint enhances the anti-tumor activity of gemcitabine in vivo Cell Cycle 6 2007 104 110
-
(2007)
Cell Cycle
, vol.6
, pp. 104-110
-
-
Matthews, D.J.1
Yakes, F.M.2
Chen, J.3
Tadano, M.4
Bornheim, L.5
Clary, D.O.6
-
59
-
-
34250010317
-
Chk1 regulates the density of active replication origins during the vertebrate S phase
-
A. Maya-Mendoza, E. Petermann, D.A. Gillespie, K.W. Caldecott, and D.A. Jackson Chk1 regulates the density of active replication origins during the vertebrate S phase EMBO J 26 2007 2719 2731
-
(2007)
EMBO J
, vol.26
, pp. 2719-2731
-
-
Maya-Mendoza, A.1
Petermann, E.2
Gillespie, D.A.3
Caldecott, K.W.4
Jackson, D.A.5
-
60
-
-
84867616967
-
Dormant origins, the licensing checkpoint, and the response to replicative stresses
-
D. McIntosh, and J.J. Blow Dormant origins, the licensing checkpoint, and the response to replicative stresses Cold Spring Harb Perspect Biol 4 2012
-
(2012)
Cold Spring Harb Perspect Biol
, vol.4
-
-
McIntosh, D.1
Blow, J.J.2
-
61
-
-
84896715257
-
LY2606368, a second generation Chk1 inhibitor, inhibits growth of ovarian carcinoma xenografts either as monotherapy or in combination with standard-of-care agents
-
Mol Cancer Ther (Abstract nr A108)
-
S. McNeely, T. Burke, S. Durland-Busbice, S. Barnard, M. Marshall, and A. Bence et al. LY2606368, a second generation Chk1 inhibitor, inhibits growth of ovarian carcinoma xenografts either as monotherapy or in combination with standard-of-care agents Proceedings of the AACR-NCI-EORTC International Conference: Molecular Targets and Cancer Therapeutics; 2011 Nov 12-16; San Francisco, CA Mol Cancer Ther 10 2011 (Abstract nr A108)
-
(2011)
Proceedings of the AACR-NCI-EORTC International Conference: Molecular Targets and Cancer Therapeutics; 2011 Nov 12-16; San Francisco, CA
, vol.10
-
-
McNeely, S.1
Burke, T.2
Durland-Busbice, S.3
Barnard, S.4
Marshall, M.5
Bence, A.6
-
62
-
-
77953506262
-
Chk1 inhibition after replicative stress activates a double strand break response mediated by ATM and DNA-dependent protein kinase
-
S. McNeely, C. Conti, T. Sheikh, H. Patel, S. Zabludoff, and Y. Pommier et al. Chk1 inhibition after replicative stress activates a double strand break response mediated by ATM and DNA-dependent protein kinase Cell Cycle 9 2010 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
-
63
-
-
77950650401
-
In vitro and in vivo radiation sensitization of human tumor cells by a novel checkpoint kinase inhibitor, AZD7762
-
J.B. Mitchell, R. Choudhuri, K. Fabre, A.L. Sowers, D. Citrin, and S.D. Zabludoff et al. In vitro and in vivo radiation sensitization of human tumor cells by a novel checkpoint kinase inhibitor, AZD7762 Clin Cancer Res 16 2010 2076 2084
-
(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
-
64
-
-
79961240240
-
Simultaneous exposure of transformed cells to SRC family inhibitors and CHK1 inhibitors causes cell death
-
C. Mitchell, H.A. Hamed, N. Cruickshanks, Y. Tang, M.D. Bareford, and N. Hubbard et al. Simultaneous exposure of transformed cells to SRC family inhibitors and CHK1 inhibitors causes cell death Cancer Biol Ther 12 2011 215 228
-
(2011)
Cancer Biol Ther
, vol.12
, pp. 215-228
-
-
Mitchell, C.1
Hamed, H.A.2
Cruickshanks, N.3
Tang, Y.4
Bareford, M.D.5
Hubbard, N.6
-
65
-
-
84856822207
-
Preclinical development of the novel Chk1 inhibitor SCH900776 in combination with DNA-damaging agents and antimetabolites
-
R. Montano, I. Chung, K.M. Garner, D. Parry, and A. Eastman Preclinical development of the novel Chk1 inhibitor SCH900776 in combination with DNA-damaging agents and antimetabolites Mol Cancer Ther 11 2012 427 438
-
(2012)
Mol Cancer Ther
, vol.11
, pp. 427-438
-
-
Montano, R.1
Chung, I.2
Garner, K.M.3
Parry, D.4
Eastman, A.5
-
66
-
-
82955203422
-
Exploiting oncogene-induced replicative stress for the selective killing of Myc-driven tumors
-
M. Murga, S. Campaner, A.J. Lopez-Contreras, L.I. Toledo, R. Soria, and M.F. Montana et al. Exploiting oncogene-induced replicative stress for the selective killing of Myc-driven tumors Nat Struct Mol Biol 18 2011 1331 1335
-
(2011)
Nat Struct Mol Biol
, vol.18
, pp. 1331-1335
-
-
Murga, M.1
Campaner, S.2
Lopez-Contreras, A.J.3
Toledo, L.I.4
Soria, R.5
Montana, M.F.6
-
67
-
-
79957690359
-
ATR signalling: More than meeting at the fork
-
E.A. Nam, and D. Cortez ATR signalling: More than meeting at the fork Biochem J 436 2011 527 536
-
(2011)
Biochem J
, vol.436
, pp. 527-536
-
-
Nam, E.A.1
Cortez, D.2
-
68
-
-
28244497051
-
Depletion of Chk1 leads to premature activation of Cdc2-cyclin B and mitotic catastrophe
-
H. Niida, S. Tsuge, Y. Katsuno, A. Konishi, N. Takeda, and M. Nakanishi Depletion of Chk1 leads to premature activation of Cdc2-cyclin B and mitotic catastrophe J Biol Chem 280 2005 39246 39252
-
(2005)
J Biol Chem
, vol.280
, pp. 39246-39252
-
-
Niida, H.1
Tsuge, S.2
Katsuno, Y.3
Konishi, A.4
Takeda, N.5
Nakanishi, M.6
-
69
-
-
0031035528
-
Chk1 is a wee1 kinase in the G2 DNA damage checkpoint inhibiting cdc2 by Y15 phosphorylation
-
M.J. O'Connell, J.M. Raleigh, H.M. Verkade, and P. Nurse Chk1 is a wee1 kinase in the G2 DNA damage checkpoint inhibiting cdc2 by Y15 phosphorylation EMBO J 16 1997 545 554
-
(1997)
EMBO J
, vol.16
, pp. 545-554
-
-
O'Connell, M.J.1
Raleigh, J.M.2
Verkade, H.M.3
Nurse, P.4
-
70
-
-
84862282465
-
Discovery of checkpoint kinase inhibitor (S)-5-(3-fluorophenyl)-N- (piperidin-3-yl)-3-ureidothiophene-2-carboxamide (AZD7762) by structure-based design and optimization of thiophenecarboxamide ureas
-
V. Oza, S. Ashwell, L. Almeida, P. Brassil, J. Breed, and C. Deng et al. Discovery of checkpoint kinase inhibitor (S)-5-(3-fluorophenyl)-N-(piperidin-3- yl)-3-ureidothiophene-2-carboxamide (AZD7762) by structure-based design and optimization of thiophenecarboxamide ureas J Med Chem 55 2012 5130 5142
-
(2012)
J Med Chem
, vol.55
, pp. 5130-5142
-
-
Oza, V.1
Ashwell, S.2
Almeida, L.3
Brassil, P.4
Breed, J.5
Deng, C.6
-
71
-
-
65249182632
-
The DNA-damage effector checkpoint kinase 1 is essential for chromosome segregation and cytokinesis
-
S. Peddibhotla, M.H. Lam, M. Gonzalez-Rimbau, and J.M. Rosen The DNA-damage effector checkpoint kinase 1 is essential for chromosome segregation and cytokinesis Proc Natl Acad Sci U S A 106 2009 5159 5164
-
(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
-
72
-
-
84896739126
-
The MEK1/2 inhibitor AZD6244 (ARRY-142886) interacts synergistically with the novel Chk1 inhibitor AZD7762 to induce apoptosis in human multiple myeloma cells
-
(LB-103)
-
X.-Y. Pei, Y. Dai, S. Chen, W. Bodie, L. Kramer, and P. Dent et al. The MEK1/2 inhibitor AZD6244 (ARRY-142886) interacts synergistically with the novel Chk1 inhibitor AZD7762 to induce apoptosis in human multiple myeloma cells AACR Meeting Abstracts 2008 (LB-103)
-
(2008)
AACR Meeting Abstracts
-
-
Pei, X.-Y.1
Dai, Y.2
Chen, S.3
Bodie, W.4
Kramer, L.5
Dent, P.6
-
73
-
-
34548821574
-
MEK1/2 inhibitors potentiate UCN-01 lethality in human multiple myeloma cells through a Bim-dependent mechanism
-
X.Y. Pei, Y. Dai, S. Tenorio, J. Lu, H. Harada, and P. Dent et al. MEK1/2 inhibitors potentiate UCN-01 lethality in human multiple myeloma cells through a Bim-dependent mechanism Blood 110 2007 2092 2101
-
(2007)
Blood
, vol.110
, pp. 2092-2101
-
-
Pei, X.Y.1
Dai, Y.2
Tenorio, S.3
Lu, J.4
Harada, H.5
Dent, P.6
-
74
-
-
81055147625
-
Cytokinetically quiescent (G0/G1) human multiple myeloma cells are susceptible to simultaneous inhibition of Chk1 and MEK1/2
-
X.Y. Pei, Y. Dai, L.E. Youssefian, S. Chen, W.W. Bodie, and Y. Takabatake et al. Cytokinetically quiescent (G0/G1) human multiple myeloma cells are susceptible to simultaneous inhibition of Chk1 and MEK1/2 Blood 118 2011 5189 5200
-
(2011)
Blood
, vol.118
, pp. 5189-5200
-
-
Pei, X.Y.1
Dai, Y.2
Youssefian, L.E.3
Chen, S.4
Bodie, W.W.5
Takabatake, Y.6
-
75
-
-
0030611095
-
Mitotic and G2 checkpoint control: Regulation of 14-3-3 protein binding by phosphorylation of Cdc25C on serine-216
-
C.Y. Peng, P.R. Graves, R.S. Thoma, Z. Wu, A.S. Shaw, and H. Piwnica-Worms Mitotic and G2 checkpoint control: Regulation of 14-3-3 protein binding by phosphorylation of Cdc25C on serine-216 Science 277 1997 1501 1505
-
(1997)
Science
, vol.277
, pp. 1501-1505
-
-
Peng, C.Y.1
Graves, P.R.2
Thoma, R.S.3
Wu, Z.4
Shaw, A.S.5
Piwnica-Worms, H.6
-
76
-
-
33645825609
-
Chk1 requirement for high global rates of replication fork progression during normal vertebrate S phase
-
E. Petermann, A. Maya-Mendoza, G. Zachos, D.A. Gillespie, D.A. Jackson, and K.W. Caldecott Chk1 requirement for high global rates of replication fork progression during normal vertebrate S phase Mol Cell Biol 26 2006 3319 3326
-
(2006)
Mol Cell Biol
, vol.26
, pp. 3319-3326
-
-
Petermann, E.1
Maya-Mendoza, A.2
Zachos, G.3
Gillespie, D.A.4
Jackson, D.A.5
Caldecott, K.W.6
-
77
-
-
77957982422
-
Chk1 promotes replication fork progression by controlling replication initiation
-
E. Petermann, M. Woodcock, and T. Helleday Chk1 promotes replication fork progression by controlling replication initiation Proc Natl Acad Sci U S A 107 2010 16090 16095
-
(2010)
Proc Natl Acad Sci U S A
, vol.107
, pp. 16090-16095
-
-
Petermann, E.1
Woodcock, M.2
Helleday, T.3
-
78
-
-
84872533885
-
Combination therapy targeting the Chk1 and Wee1 kinases shows therapeutic efficacy in neuroblastoma
-
M.R. Russell, K. Levin, J. Rader, L. Belcastro, Y. Li, and D. Martinez et al. Combination therapy targeting the Chk1 and Wee1 kinases shows therapeutic efficacy in neuroblastoma Cancer Res 73 2013 776 784
-
(2013)
Cancer Res
, vol.73
, pp. 776-784
-
-
Russell, M.R.1
Levin, K.2
Rader, J.3
Belcastro, L.4
Li, Y.5
Martinez, D.6
-
79
-
-
79960253104
-
Phase i dose-escalation study of AZD7762 in combination with gemcitabine (gem) in patients (pts) with advanced solid tumors
-
(Suppl.; abstr 3058)
-
E. Sausville, P. LoRusso, M. Carducci, P. Barker, F. Agbo, and P. Oakes Phase I dose-escalation study of AZD7762 in combination with gemcitabine (gem) in patients (pts) with advanced solid tumors J Clin Oncol 29 2011 (Suppl.; abstr 3058)
-
(2011)
J Clin Oncol
, vol.29
-
-
Sausville, E.1
Lorusso, P.2
Carducci, M.3
Barker, P.4
Agbo, F.5
Oakes, P.6
-
80
-
-
84866924927
-
Effects of selective checkpoint kinase 1 inhibition on cytarabine cytotoxicity in acute myelogenous leukemia cells in vitro
-
E.L. Schenk, B.D. Koh, K.S. Flatten, K.L. Peterson, D. Parry, and A.D. Hess et al. Effects of selective checkpoint kinase 1 inhibition on cytarabine cytotoxicity in acute myelogenous leukemia cells in vitro Clin Cancer Res 18 2012 5364 5373
-
(2012)
Clin Cancer Res
, vol.18
, pp. 5364-5373
-
-
Schenk, E.L.1
Koh, B.D.2
Flatten, K.S.3
Peterson, K.L.4
Parry, D.5
Hess, A.D.6
-
81
-
-
33751160547
-
CHK1 phosphorylates CDC25B during the cell cycle in the absence of DNA damage
-
E. Schmitt, R. Boutros, C. Froment, B. Monsarrat, B. Ducommun, and C. Dozier CHK1 phosphorylates CDC25B during the cell cycle in the absence of DNA damage J Cell Sci 119 2006 4269 4275
-
(2006)
J Cell Sci
, vol.119
, pp. 4269-4275
-
-
Schmitt, E.1
Boutros, R.2
Froment, C.3
Monsarrat, B.4
Ducommun, B.5
Dozier, C.6
-
82
-
-
84882716595
-
Phase i dose-escalation study of AZD7762 alone and in combination with gemcitabine in Japanese patients with advanced solid tumors
-
(Suppl.; abstr 3045)
-
T. Seto, T. Esaki, F. Hirai, S. Arita, K. Nosaki, and A. Makiyama et al. Phase I dose-escalation study of AZD7762 alone and in combination with gemcitabine in Japanese patients with advanced solid tumors J Clin Oncol 30 2012 (Suppl.; abstr 3045)
-
(2012)
J Clin Oncol
, vol.30
-
-
Seto, T.1
Esaki, T.2
Hirai, F.3
Arita, S.4
Nosaki, K.5
Makiyama, A.6
-
83
-
-
33846804136
-
Cell cycle phenotype-based optimization of G2-abrogating peptides yields CBP501 with a unique mechanism of action at the G2 checkpoint
-
S.K. Sha, T. Sato, H. Kobayashi, M. Ishigaki, S. Yamamoto, and H. Sato et al. Cell cycle phenotype-based optimization of G2-abrogating peptides yields CBP501 with a unique mechanism of action at the G2 checkpoint Mol Cancer Ther 6 2007 147 153
-
(2007)
Mol Cancer Ther
, vol.6
, pp. 147-153
-
-
Sha, S.K.1
Sato, T.2
Kobayashi, H.3
Ishigaki, M.4
Yamamoto, S.5
Sato, H.6
-
84
-
-
3242670803
-
ATR and ATM regulate the timing of DNA replication origin firing
-
D. Shechter, V. Costanzo, and J. Gautier ATR and ATM regulate the timing of DNA replication origin firing Nat Cell Biol 6 2004 648 655
-
(2004)
Nat Cell Biol
, vol.6
, pp. 648-655
-
-
Shechter, D.1
Costanzo, V.2
Gautier, J.3
-
85
-
-
13944266820
-
The cell-cycle checkpoint kinase Chk1 is required for mammalian homologous recombination repair
-
C.S. Sorensen, L.T. Hansen, J. Dziegielewski, R.G. Syljuasen, C. Lundin, and J. Bartek et al. The cell-cycle checkpoint kinase Chk1 is required for mammalian homologous recombination repair Nat Cell Biol 7 2005 195 201
-
(2005)
Nat Cell Biol
, vol.7
, pp. 195-201
-
-
Sorensen, C.S.1
Hansen, L.T.2
Dziegielewski, J.3
Syljuasen, R.G.4
Lundin, C.5
Bartek, J.6
-
86
-
-
84855908936
-
Safeguarding genome integrity: The checkpoint kinases ATR, CHK1 and WEE1 restrain CDK activity during normal DNA replication
-
C.S. Sorensen, and R.G. Syljuasen Safeguarding genome integrity: the checkpoint kinases ATR, CHK1 and WEE1 restrain CDK activity during normal DNA replication Nucleic Acids Res 40 2012 477 486
-
(2012)
Nucleic Acids Res
, vol.40
, pp. 477-486
-
-
Sorensen, C.S.1
Syljuasen, R.G.2
-
87
-
-
0012966157
-
Chk1 regulates the S phase checkpoint by coupling the physiological turnover and ionizing radiation-induced accelerated proteolysis of Cdc25A
-
C.S. Sorensen, R.G. Syljuasen, J. Falck, T. Schroeder, L. Ronnstrand, and K.K. Khanna et al. Chk1 regulates the S phase checkpoint by coupling the physiological turnover and ionizing radiation-induced accelerated proteolysis of Cdc25A Cancer Cell 3 2003 247 258
-
(2003)
Cancer Cell
, vol.3
, pp. 247-258
-
-
Sorensen, C.S.1
Syljuasen, R.G.2
Falck, J.3
Schroeder, T.4
Ronnstrand, L.5
Khanna, K.K.6
-
89
-
-
20244388673
-
Inhibition of human Chk1 causes increased initiation of DNA replication, phosphorylation of ATR targets, and DNA breakage
-
R.G. Syljuasen, C.S. Sorensen, L.T. Hansen, K. Fugger, C. Lundin, and F. Johansson et al. Inhibition of human Chk1 causes increased initiation of DNA replication, phosphorylation of ATR targets, and DNA breakage Mol Cell Biol 25 2005 3553 3562
-
(2005)
Mol Cell Biol
, vol.25
, pp. 3553-3562
-
-
Syljuasen, R.G.1
Sorensen, C.S.2
Hansen, L.T.3
Fugger, K.4
Lundin, C.5
Johansson, F.6
-
90
-
-
78649317232
-
Regulation of the initiation step of DNA replication by cyclin-dependent kinases
-
S. Tanaka, and H. Araki Regulation of the initiation step of DNA replication by cyclin-dependent kinases Chromosoma 119 2010 565 574
-
(2010)
Chromosoma
, vol.119
, pp. 565-574
-
-
Tanaka, S.1
Araki, H.2
-
91
-
-
33747083495
-
Checkpoint kinase 1 (Chk1) is required for mitotic progression through negative regulation of polo-like kinase 1 (Plk1)
-
J. Tang, R.L. Erikson, and X. Liu Checkpoint kinase 1 (Chk1) is required for mitotic progression through negative regulation of polo-like kinase 1 (Plk1) Proc Natl Acad Sci U S A 103 2006 11964 11969
-
(2006)
Proc Natl Acad Sci U S A
, vol.103
, pp. 11964-11969
-
-
Tang, J.1
Erikson, R.L.2
Liu, X.3
-
92
-
-
0035810054
-
Regulation of the G2/M transition by p53
-
W.R. Taylor, and G.R. Stark Regulation of the G2/M transition by p53 Oncogene 20 2001 1803 1815
-
(2001)
Oncogene
, vol.20
, pp. 1803-1815
-
-
Taylor, W.R.1
Stark, G.R.2
-
93
-
-
84882630267
-
The cancer therapeutic potential of Chk1 inhibitors: How mechanistic studies impact clinical trial design
-
R. Thompson, and A. Eastman The cancer therapeutic potential of Chk1 inhibitors: How mechanistic studies impact clinical trial design Br J Clin Pharmacol 76 2013 358 369
-
(2013)
Br J Clin Pharmacol
, vol.76
, pp. 358-369
-
-
Thompson, R.1
Eastman, A.2
-
94
-
-
84866612162
-
The Mre11 nuclease is critical for the sensitivity of cells to Chk1 inhibition
-
10.1371/journal.pone.0044021
-
R. Thompson, R. Montano, and A. Eastman The Mre11 nuclease is critical for the sensitivity of cells to Chk1 inhibition PLoS One 7 8 2012 e44021 10.1371/journal.pone.0044021
-
(2012)
PLoS One
, vol.7
, Issue.8
, pp. 44021
-
-
Thompson, R.1
Montano, R.2
Eastman, A.3
-
95
-
-
79953197948
-
Mutator activity induced by microRNA-155 (miR-155) links inflammation and cancer
-
E. Tili, J.J. Michaille, D. Wernicke, H. Alder, S. Costinean, and S. Volinia et al. Mutator activity induced by microRNA-155 (miR-155) links inflammation and cancer Proc Natl Acad Sci U S A 108 2011 4908 4913
-
(2011)
Proc Natl Acad Sci U S A
, vol.108
, pp. 4908-4913
-
-
Tili, E.1
Michaille, J.J.2
Wernicke, D.3
Alder, H.4
Costinean, S.5
Volinia, S.6
-
96
-
-
80052183228
-
Targeting ATR and Chk1 kinases for cancer treatment: A new model for new (and old) drugs
-
L.I. Toledo, M. Murga, and O. Fernandez-Capetillo Targeting ATR and Chk1 kinases for cancer treatment: A new model for new (and old) drugs Mol Oncol 5 2011 368 373
-
(2011)
Mol Oncol
, vol.5
, pp. 368-373
-
-
Toledo, L.I.1
Murga, M.2
Fernandez-Capetillo, O.3
-
97
-
-
34247481285
-
Targeting checkpoint kinase 1 in cancer therapeutics
-
A.N. Tse, R. Carvajal, and G.K. Schwartz Targeting checkpoint kinase 1 in cancer therapeutics Clin Cancer Res 13 2007 1955 1960
-
(2007)
Clin Cancer Res
, vol.13
, pp. 1955-1960
-
-
Tse, A.N.1
Carvajal, R.2
Schwartz, G.K.3
-
98
-
-
33846856967
-
CHIR-124, a novel potent inhibitor of Chk1, potentiates the cytotoxicity of topoisomerase i poisons in vitro and in vivo
-
A.N. Tse, K.G. Rendahl, T. Sheikh, H. Cheema, K. Aardalen, and M. Embry 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 13 2007 591 602
-
(2007)
Clin Cancer Res
, vol.13
, pp. 591-602
-
-
Tse, A.N.1
Rendahl, K.G.2
Sheikh, T.3
Cheema, H.4
Aardalen, K.5
Embry, M.6
-
99
-
-
67649842315
-
Cisplatin-induced DNA damage activates replication checkpoint signaling components that differentially affect tumor cell survival
-
J.M. Wagner, and L.M. Karnitz Cisplatin-induced DNA damage activates replication checkpoint signaling components that differentially affect tumor cell survival Mol Pharmacol 76 2009 208 214
-
(2009)
Mol Pharmacol
, vol.76
, pp. 208-214
-
-
Wagner, J.M.1
Karnitz, L.M.2
-
100
-
-
73949130389
-
The preclinical pharmacology and therapeutic activity of the novel CHK1 inhibitor SAR-020106
-
M.I. Walton, P.D. Eve, A. Hayes, M. Valenti, A. De Haven Brandon, and G. Box et al. The preclinical pharmacology and therapeutic activity of the novel CHK1 inhibitor SAR-020106 Mol Cancer Ther 9 2010 89 100
-
(2010)
Mol Cancer Ther
, vol.9
, pp. 89-100
-
-
Walton, M.I.1
Eve, P.D.2
Hayes, A.3
Valenti, M.4
De Haven Brandon, A.5
Box, G.6
-
101
-
-
34047190253
-
Chk1-mediated phosphorylation of FANCE is required for the Fanconi anemia/BRCA pathway
-
X. Wang, R.D. Kennedy, K. Ray, P. Stuckert, T. Ellenberger, and A.D. D'Andrea Chk1-mediated phosphorylation of FANCE is required for the Fanconi anemia/BRCA pathway Mol Cell Biol 27 2007 3098 3108
-
(2007)
Mol Cell Biol
, vol.27
, pp. 3098-3108
-
-
Wang, X.1
Kennedy, R.D.2
Ray, K.3
Stuckert, P.4
Ellenberger, T.5
D'Andrea, A.D.6
-
102
-
-
0033215306
-
Cdc7p-Dbf4p kinase binds to chromatin during S phase and is regulated by both the APC and the RAD53 checkpoint pathway
-
M. Weinreich, and B. Stillman Cdc7p-Dbf4p kinase binds to chromatin during S phase and is regulated by both the APC and the RAD53 checkpoint pathway EMBO J 18 1999 5334 5346
-
(1999)
EMBO J
, vol.18
, pp. 5334-5346
-
-
Weinreich, M.1
Stillman, B.2
-
103
-
-
84873100369
-
Phase i dose-escalation study to examine the safety and tolerability of LY2603618, a checkpoint 1 kinase inhibitor, administered 1 day after pemetrexed 500 mg/m(2) every 21 days in patients with cancer
-
G.J. Weiss, R.C. Donehower, T. Iyengar, R.K. Ramanathan, K. Lewandowski, and E. Westin et al. Phase I dose-escalation study to examine the safety and tolerability of LY2603618, a checkpoint 1 kinase inhibitor, administered 1 day after pemetrexed 500 mg/m(2) every 21 days in patients with cancer Invest New Drugs 31 2013 136 144
-
(2013)
Invest New Drugs
, vol.31
, pp. 136-144
-
-
Weiss, G.J.1
Donehower, R.C.2
Iyengar, T.3
Ramanathan, R.K.4
Lewandowski, K.5
Westin, E.6
-
104
-
-
58549089689
-
Essential function of Chk1 can be uncoupled from DNA damage checkpoint and replication control
-
D. Wilsker, E. Petermann, T. Helleday, and F. Bunz Essential function of Chk1 can be uncoupled from DNA damage checkpoint and replication control Proc Natl Acad Sci U S A 105 2008 20752 20757
-
(2008)
Proc Natl Acad Sci U S A
, vol.105
, pp. 20752-20757
-
-
Wilsker, D.1
Petermann, E.2
Helleday, T.3
Bunz, F.4
-
105
-
-
84896697658
-
Antitumor activity of Chk1 inhibitor LY2606368 as a single agent in SW1990 human pancreas orthotopic tumor model
-
(Abstract nr 177)
-
W. Wu, B. Chen, A. Bence, S. Um, B. Yan, and J. Starling et al. Antitumor activity of Chk1 inhibitor LY2606368 as a single agent in SW1990 human pancreas orthotopic tumor model Cancer Res 72 2012 (Abstract nr 177)
-
(2012)
Cancer Res
, vol.72
-
-
Wu, W.1
Chen, B.2
Bence, A.3
Um, S.4
Yan, B.5
Starling, J.6
-
106
-
-
52949139387
-
AZD7762, a novel checkpoint kinase inhibitor, drives checkpoint abrogation and potentiates DNA-targeted therapies
-
S.D. Zabludoff, C. Deng, M.R. Grondine, A.M. Sheehy, S. Ashwell, and B.L. Caleb et al. AZD7762, a novel checkpoint kinase inhibitor, drives checkpoint abrogation and potentiates DNA-targeted therapies Mol Cancer Ther 7 2008 2955 2966
-
(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
-
107
-
-
33846636785
-
Chk1 is required for spindle checkpoint function
-
G. Zachos, E.J. Black, M. Walker, M.T. Scott, P. Vagnarelli, and W.C. Earnshaw et al. Chk1 is required for spindle checkpoint function Dev Cell 12 2007 247 260
-
(2007)
Dev Cell
, vol.12
, pp. 247-260
-
-
Zachos, G.1
Black, E.J.2
Walker, M.3
Scott, M.T.4
Vagnarelli, P.5
Earnshaw, W.C.6
-
108
-
-
0037415735
-
Chk1-deficient tumour cells are viable but exhibit multiple checkpoint and survival defects
-
G. Zachos, M.D. Rainey, and D.A. Gillespie Chk1-deficient tumour cells are viable but exhibit multiple checkpoint and survival defects EMBO J 22 2003 713 723
-
(2003)
EMBO J
, vol.22
, pp. 713-723
-
-
Zachos, G.1
Rainey, M.D.2
Gillespie, D.A.3
-
109
-
-
78650208984
-
Status of p53 in human cancer cells does not predict efficacy of CHK1 kinase inhibitors combined with chemotherapeutic agents
-
S. Zenvirt, N. Kravchenko-Balasha, and A. Levitzki Status of p53 in human cancer cells does not predict efficacy of CHK1 kinase inhibitors combined with chemotherapeutic agents Oncogene 29 2010 6149 6159
-
(2010)
Oncogene
, vol.29
, pp. 6149-6159
-
-
Zenvirt, S.1
Kravchenko-Balasha, N.2
Levitzki, A.3
-
110
-
-
0037069326
-
Disruption of the checkpoint kinase 1/cell division cycle 25A pathway abrogates ionizing radiation-induced S and G2 checkpoints
-
H. Zhao, J.L. Watkins, and H. Piwnica-Worms Disruption of the checkpoint kinase 1/cell division cycle 25A pathway abrogates ionizing radiation-induced S and G2 checkpoints Proc Natl Acad Sci U S A 99 2002 14795 14800
-
(2002)
Proc Natl Acad Sci U S A
, vol.99
, pp. 14795-14800
-
-
Zhao, H.1
Watkins, J.L.2
Piwnica-Worms, H.3
-
111
-
-
72249123144
-
Fanconi anemia complementation group FANCD2 protein serine 331 phosphorylation is important for fanconi anemia pathway function and BRCA2 interaction
-
G. Zhi, J.B. Wilson, X. Chen, D.S. Krause, Y. Xiao, and N.J. Jones et al. Fanconi anemia complementation group FANCD2 protein serine 331 phosphorylation is important for fanconi anemia pathway function and BRCA2 interaction Cancer Res 69 2009 8775 8783
-
(2009)
Cancer Res
, vol.69
, pp. 8775-8783
-
-
Zhi, G.1
Wilson, J.B.2
Chen, X.3
Krause, D.S.4
Xiao, Y.5
Jones, N.J.6
|