-
1
-
-
33751267902
-
Acute myeloid leukaemia
-
DOI 10.1016/S0140-6736(06)69780-8, PII S0140673606697808
-
Estey E, Dohner H. Acute myeloid leukaemia. Lancet 2006; 368: 1894-1907. (Pubitemid 44794525)
-
(2006)
Lancet
, vol.368
, Issue.9550
, pp. 1894-1907
-
-
Estey, E.1
Dohner, H.2
-
2
-
-
23644455476
-
Drug therapy for acute myeloid leukemia
-
DOI 10.1182/blood-2005-01-0178
-
Tallman MS, Gilliland DG, Rowe JM. Drug therapy for acute myeloid leukemia. Blood 2005; 106: 1154-1163. (Pubitemid 41130866)
-
(2005)
Blood
, vol.106
, Issue.4
, pp. 1154-1163
-
-
Tallman, M.S.1
Gilliland, D.G.2
Rowe, J.M.3
-
3
-
-
0015721940
-
Cytosine arabinoside (NSC-63878) and daunorubicin (NSC-83142) therapy in acute nonlymphocytic leukemia
-
Yates JW, Wallace Jr HJ, Ellison RR, Holland JF. Cytosine arabinoside (NSC-63878) and daunorubicin (NSC-83142) therapy in acute nonlymphocytic leukemia. Cancer Chemother Rep 1973; 57: 485-488.
-
(1973)
Cancer Chemother Rep
, vol.57
, pp. 485-488
-
-
Yates, J.W.1
Wallace Jr., H.J.2
Ellison, R.R.3
Holland, J.F.4
-
4
-
-
0036040215
-
Chromatin modification, leukaemia and implications for therapy
-
DOI 10.1046/j.1365-2141.2002.03586.x
-
Jones LK, Saha V. Chromatin modification, leukaemia and implications for therapy. Br J Haematol 2002; 118: 714-727. (Pubitemid 35007375)
-
(2002)
British Journal of Haematology
, vol.118
, Issue.3
, pp. 714-727
-
-
Jones, L.K.1
Saha, V.2
-
5
-
-
17844385784
-
Regulatory cross-talk between lysine acetylation and ubiquitination: Role in control of protein stability
-
DOI 10.1002/bies.20210
-
Caron C, Boyault C, Khochbin S. Regulatory cross-talk between lysine acetylation and ubiquitination: role in the control of protein stability. Bioessays 2005; 27: 408-415. (Pubitemid 40592597)
-
(2005)
BioEssays
, vol.27
, Issue.4
, pp. 408-415
-
-
Caron, C.1
Boyault, C.2
Khochbin, S.3
-
6
-
-
13844252820
-
Regulation of histone deacetylase activities
-
Sengupta N, Seto E. Regulation of histone deacetylase activities. J Cell Biochem 2004; 93: 57-67.
-
(2004)
J Cell Biochem
, vol.93
, pp. 57-67
-
-
Sengupta, N.1
Seto, E.2
-
7
-
-
0035755974
-
Histone deacetylases and cancer: Causes and therapies
-
Marks P, Rifkind RA, Richon VM, Breslow R, Miller T, Kelly WK. Histone deacetylases and cancer: causes and therapies. Nat Rev Cancer 2001; 1: 194-202. (Pubitemid 33741894)
-
(2001)
Nature Reviews Cancer
, vol.1
, Issue.3
, pp. 194-202
-
-
Marks, P.A.1
Rifkind, R.A.2
Richon, V.M.3
Breslow, R.4
Miller, T.5
Kelly, W.K.6
-
8
-
-
0034968671
-
Histone acetylation and disease
-
Timmermann S, Lehrmann H, Polesskaya A, Harel-Bellan A. Histone acetylation and disease. Cell Mol Life Sci 2001; 58: 728-736. (Pubitemid 32553030)
-
(2001)
Cellular and Molecular Life Sciences
, vol.58
, Issue.5-6
, pp. 728-736
-
-
Timmermann, S.1
Lehrmann, H.2
Polesskaya, A.3
Harel-Bellan, A.4
-
9
-
-
36048958965
-
Histone deacetylase inhibitors: Overview and perspectives
-
DOI 10.1158/1541-7786.MCR-07-0324
-
Dokmanovic M, Clarke C, Marks PA. Histone deacetylase inhibitors: overview and perspectives. Mol Cancer Res 2007; 5: 981-989. (Pubitemid 350080267)
-
(2007)
Molecular Cancer Research
, vol.5
, Issue.10
, pp. 981-989
-
-
Dokmanovic, M.1
Clarke, C.2
Marks, P.A.3
-
10
-
-
34547864236
-
Histone deacetylase inhibitors: Molecular mechanisms of action
-
DOI 10.1038/sj.onc.1210620, PII 1210620
-
Xu WS, Parmigiani RB, Marks PA. Histone deacetylase inhibitors: molecular mechanisms of action. Oncogene 2007; 26: 5541-5552. (Pubitemid 47255934)
-
(2007)
Oncogene
, vol.26
, Issue.37
, pp. 5541-5552
-
-
Xu, W.S.1
Parmigiani, R.B.2
Marks, P.A.3
-
11
-
-
38949096781
-
Phase 1 study of the histone deacetylase inhibitor vorinostat (suberoylanilide hydroxamic acid [SAHA]) in patients with advanced leukemias and myelodysplastic syndromes
-
DOI 10.1182/blood-2007-06-098061
-
Garcia-Manero G, Yang H, Bueso-Ramos C, Ferrajoli A, Cortes J, Wierda WG et al. Phase 1 study of the histone deacetylase inhibitor vorinostat (suberoylanilide hydroxamic acid [SAHA]) in patients with advanced leukemias and myelodysplastic syndromes. Blood 2008; 111: 1060-1066. (Pubitemid 351213383)
-
(2008)
Blood
, vol.111
, Issue.3
, pp. 1060-1066
-
-
Garcia-Manero, G.1
Yang, H.2
Bueso-Ramos, C.3
Ferrajoli, A.4
Cortes, J.5
Wierda, W.G.6
Faderl, S.7
Koller, C.8
Morris, G.9
Rosner, G.10
Loboda, A.11
Fantin, V.R.12
Randolph, S.S.13
Hardwick, J.S.14
Reilly, J.F.15
Chen, C.16
Ricker, J.L.17
Secrist, J.P.18
Richon, V.M.19
Frankel, S.R.20
Kantarjian, H.M.21
more..
-
12
-
-
13844309711
-
Clinical development of histone deacetylase inhibitors as anticancer agents
-
DOI 10.1146/annurev.pharmtox.45.120403.095825
-
Drummond DC, Noble CO, Kirpotin DB, Guo Z, Scott GK, Benz CC. Clinical development of histone deacetylase inhibitors as anticancer agents. Annu Rev Pharmacol Toxicol 2005; 45: 495-528. (Pubitemid 40261815)
-
(2005)
Annual Review of Pharmacology and Toxicology
, vol.45
, pp. 495-528
-
-
Drummond, D.C.1
Noble, C.O.2
Kirpotin, D.B.3
Guo, Z.4
Scott, G.K.5
Benz, C.C.6
-
13
-
-
33745258655
-
The histone deacetylase inhibitor LBH589 is a potent antimyeloma agent that overcomes drug resistance
-
DOI 10.1158/0008-5472.CAN-05-4186
-
Maiso P, Carvajal-Vergara X, Ocio EM, Lopez-Perez R, Mateo G, Gutierrez N et al. The histone deacetylase inhibitor LBH589 is a potent antimyeloma agent that overcomes drug resistance. Cancer Res 2006; 66: 5781-5789. (Pubitemid 43927132)
-
(2006)
Cancer Research
, vol.66
, Issue.11
, pp. 5781-5789
-
-
Maiso, P.1
Carvajal-Vergara, X.2
Ocio, E.M.3
Lopez-Perez, R.4
Mateo, G.5
Gutierrez, N.6
Atadja, P.7
Pandiella, A.8
San Miguel, J.F.9
-
15
-
-
38549170488
-
+ immature phenotype
-
DOI 10.3324/haematol.11666
-
Colado E, varez-Fernandez S, Maiso P, Martin-Sanchez J, Vidriales MB, Garayoa M et al. The effect of the proteasome inhibitor bortezomib on acute myeloid leukemia cells and drug resistance associated with the CD34+ immature phenotype. Haematologica 2008; 93: 57-66. (Pubitemid 351156152)
-
(2008)
Haematologica
, vol.93
, Issue.1
, pp. 57-66
-
-
Colado, E.1
Alvarez-Fernandez, S.2
Maiso, P.3
Martin-Sanchez, J.4
Vidriales, M.B.5
Garayoa, M.6
Ocio, E.M.7
Montero, J.C.8
Pandiella, A.9
San Miguel, J.F.10
-
16
-
-
0021118703
-
Quantitative analysis of dose-effect relationships: The combined effects of multiple drugs or enzyme inhibitors
-
Chou TC, Talalay P. Quantitative analysis of dose-effect relationships: the combined effects of multiple drugs or enzyme inhibitors. Adv Enzyme Regul 1984; 22: 27-55.
-
(1984)
Adv Enzyme Regul
, vol.22
, pp. 27-55
-
-
Chou, T.C.1
Talalay, P.2
-
17
-
-
0033635266
-
Aven, a novel inhibitor of caspase activation, binds Bcl-xL and Apaf-1
-
Chau BN, Cheng EH, Kerr DA, Hardwick JM. Aven, a novel inhibitor of caspase activation, binds Bcl-xL and Apaf-1. Mol Cell 2000; 6: 31-40.
-
(2000)
Mol Cell
, vol.6
, pp. 31-40
-
-
Chau, B.N.1
Cheng, E.H.2
Kerr, D.A.3
Hardwick, J.M.4
-
18
-
-
0028847003
-
The biochemistry of programmed cell death
-
Kroemer G, Petit P, Zamzami N, Vayssiere JL, Mignotte B. The biochemistry of programmed cell death. FASEB J 1995; 9: 1277-1287.
-
(1995)
FASEB J
, vol.9
, pp. 1277-1287
-
-
Kroemer, G.1
Petit, P.2
Zamzami, N.3
Vayssiere, J.L.4
Mignotte, B.5
-
19
-
-
0032949351
-
Role for caspase-mediated cleavage of Rad51 in induction of apoptosis by DNA damage
-
Huang Y, Nakada S, Ishiko T, Utsugisawa T, Datta R, Kharbanda S et al. Role for caspase-mediated cleavage of Rad51 in induction of apoptosis by DNA damage. Mol Cell Biol 1999; 19: 2986-2997. (Pubitemid 29144544)
-
(1999)
Molecular and Cellular Biology
, vol.19
, Issue.4
, pp. 2986-2997
-
-
Huang, Y.1
Nakada, S.2
Ishiko, T.3
Utsugisawa, T.4
Datta, R.5
Kharbanda, S.6
Yoshida, K.7
Talanian, R.V.8
Weichselbaum, R.9
Kufe, D.10
Yuan, Z.-M.11
-
20
-
-
0035724488
-
Histone deacetylase inhibitors induce caspase-dependent apoptosis and downregulation of daxx in acute promyelocytic leukaemia with t(15;17)
-
DOI 10.1046/j.1365-2141.2001.03123.x
-
Amin HM, Saeed S, Alkan S. Histone deacetylase inhibitors induce caspase-dependent apoptosis and downregulation of daxx in acute promyelocytic leukaemia with t(15;17). Br J Haematol 2001; 115: 287-297. (Pubitemid 34203490)
-
(2001)
British Journal of Haematology
, vol.115
, Issue.2
, pp. 287-297
-
-
Amin, H.M.1
Saeed, S.2
Alkan, S.3
-
21
-
-
13444306459
-
Tumor-selective action of HDAC inhibitors involves TRAIL induction in acute myeloid leukemia cells
-
DOI 10.1038/nm1161
-
Nebbioso A, Clarke N, Voltz E, Germain E, Ambrosino C, Bontempo P et al. Tumor-selective action of HDAC inhibitors involves TRAIL induction in acute myeloid leukemia cells. Nat Med 2005; 11: 77-84. (Pubitemid 40215841)
-
(2005)
Nature Medicine
, vol.11
, Issue.1
, pp. 77-84
-
-
Nebbioso, A.1
Clarke, N.2
Voltz, E.3
Germain, E.4
Ambrosino, C.5
Bontempo, P.6
Alvarez, R.7
Schiavone, E.M.8
Ferrara, F.9
Bresciani, F.10
Weisz, A.11
De Lera, A.R.12
Gronemeyer, H.13
Altucci, L.14
-
22
-
-
0033551152
-
A synthetic inhibitor of histone deacetylase, MS-27-275, with marked in vivo antitumor activity against human tumors
-
DOI 10.1073/pnas.96.8.4592
-
Saito A, Yamashita T, Mariko Y, Nosaka Y, Tsuchiya K, Ando T et al. A synthetic inhibitor of histone deacetylase, MS-27-275, with marked in vivo antitumor activity against human tumors. Proc Natl Acad Sci USA 1999; 96: 4592-4597. (Pubitemid 29190381)
-
(1999)
Proceedings of the National Academy of Sciences of the United States of America
, vol.96
, Issue.8
, pp. 4592-4597
-
-
Saito, A.1
Yamashita, T.2
Mariko, Y.3
Nosaka, Y.4
Tsuchiya, K.5
Ando, T.6
Suzuki, T.7
Tsuruo, T.8
Nakanishi, O.9
-
23
-
-
0033614993
-
Synthesis and histone deacetylase inhibitory activity of new benzamide derivatives
-
DOI 10.1021/jm980565u
-
Suzuki T, Ando T, Tsuchiya K, Fukazawa N, Saito A, Mariko Y et al. Synthesis and histone deacetylase inhibitory activity of new benzamide derivatives. J Med Chem 1999; 42: 3001-3003. (Pubitemid 29370445)
-
(1999)
Journal of Medicinal Chemistry
, vol.42
, Issue.15
, pp. 3001-3003
-
-
Suzuki, T.1
Ando, T.2
Tsuchiya, K.3
Fukazawa, N.4
Saito, A.5
Mariko, Y.6
Yamashita, T.7
Nakanishi, O.8
-
24
-
-
18244383806
-
Valproic acid defines a novel class of HDAC inhibitors inducing differentiation of transformed cells
-
DOI 10.1093/emboj/20.24.6969
-
Gottlicher M, Minucci S, Zhu P, Kramer OH, Schimpf A, Giavara S et al. Valproic acid defines a novel class of HDAC inhibitors inducing differentiation of transformed cells. EMBO J 2001; 20: 6969-6978. (Pubitemid 34062289)
-
(2001)
EMBO Journal
, vol.20
, Issue.24
, pp. 6969-6978
-
-
Gottlicher, M.1
Minucci, S.2
Zhu, P.3
Kramer, O.H.4
Schimpf, A.5
Giavara, S.6
Sleeman, J.P.7
Lo Coco, F.8
Nervi, C.9
Pelicci, P.G.10
Heinzel, T.11
-
25
-
-
0035965343
-
Histone deacetylase is a direct target of valproic acid, a potent anticonvulsant, mood stabilizer, and teratogen
-
Phiel CJ, Zhang F, Huang EY, Guenther MG, Lazar MA, Klein PS. Histone deacetylase is a direct target of valproic acid, a potent anticonvulsant, mood stabilizer, and teratogen. J Biol Chem 2001; 276: 36734-36741.
-
(2001)
J Biol Chem
, vol.276
, pp. 36734-36741
-
-
Phiel, C.J.1
Zhang, F.2
Huang, E.Y.3
Guenther, M.G.4
Lazar, M.A.5
Klein, P.S.6
-
26
-
-
40749113668
-
Selective anti-leukaemic activity of low-dose histone deacetylase inhibitor ITF2357 on AML1/ETO-positive cells
-
DOI 10.1038/sj.onc.1210820, PII 1210820
-
Barbetti V, Gozzini A, Rovida E, Morandi A, Spinelli E, Fossati G et al. Selective anti-leukaemic activity of low-dose histone deacetylase inhibitor ITF2357 on AML1/ETO-positive cells. Oncogene 2008; 27: 1767-1778. (Pubitemid 351380272)
-
(2008)
Oncogene
, vol.27
, Issue.12
, pp. 1767-1778
-
-
Barbetti, V.1
Gozzini, A.2
Rovida, E.3
Morandi, A.4
Spinelli, E.5
Fossati, G.6
Mascagni, P.7
Lubbert, M.8
Dello Sbarba, P.9
Santini, V.10
-
27
-
-
0038485588
-
Role of caspases, Bid, and p53 in the apoptotic response triggered by histone deacetylase inhibitors trichostatin-A (TSA) and suberoylanilide hydroxamic acid (SAHA)
-
DOI 10.1074/jbc.M213093200
-
Henderson C, Mizzau M, Paroni G, Maestro R, Schneider C, Brancolini C. Role of caspases, Bid, and p53 in the apoptotic response triggered by histone deacetylase inhibitors trichostatin-A (TSA) and suberoylanilide hydroxamic acid (SAHA). J Biol Chem 2003; 278: 12579-12589. (Pubitemid 36800248)
-
(2003)
Journal of Biological Chemistry
, vol.278
, Issue.14
, pp. 12579-12589
-
-
Henderson, C.1
Mizzau, M.2
Paroni, G.3
Maestro, R.4
Schneider, C.5
Brancolini, C.6
-
28
-
-
33745280074
-
Synergistic induction of folate receptor β by all-trans retinoic acid and histone deacetylase inhibitors in acute myelogenous leukemia cells: Mechanism and utility in enhancing selective growth inhibition by antifolates
-
DOI 10.1158/0008-5472.CAN-05-4048
-
Qi H, Ratnam M. Synergistic induction of folate receptor beta by all-trans retinoic acid and histone deacetylase inhibitors in acute myelogenous leukemia cells: mechanism and utility in enhancing selective growth inhibition by antifolates. Cancer Res 2006; 66: 5875-5882. (Pubitemid 43927142)
-
(2006)
Cancer Research
, vol.66
, Issue.11
, pp. 5875-5882
-
-
Qi, H.1
Ratnam, M.2
-
29
-
-
34547094822
-
Distinct pharmacological properties of second generation HDAC inhibitors with the benzamide or hydroxamate head group
-
DOI 10.1002/ijc.22751
-
Beckers T, Burkhardt C, Wieland H, Gimmnich P, Ciossek T, Maier T et al. Distinct pharmacological properties of second generation HDAC inhibitors with the benzamide or hydroxamate head group. Int J Cancer 2007; 121: 1138-1148. (Pubitemid 47101654)
-
(2007)
International Journal of Cancer
, vol.121
, Issue.5
, pp. 1138-1148
-
-
Beckers, T.1
Burkhardt, C.2
Wieland, H.3
Gimmnich, P.4
Ciossek, T.5
Maier, T.6
Sanders, K.7
-
30
-
-
0842281645
-
Cell death: Critical control points
-
DOI 10.1016/S0092-8674(04)00046-7
-
Danial NN, Korsmeyer SJ. Cell death: critical control points. Cell 2004; 116: 205-219. (Pubitemid 38167313)
-
(2004)
Cell
, vol.116
, Issue.2
, pp. 205-219
-
-
Danial, N.N.1
Korsmeyer, S.J.2
|