-
1
-
-
0033000990
-
Histone acetylases and deacetylases in cell proliferation
-
DOI 10.1016/S0959-437X(99)80006-9
-
Kouzarides T. Histone acetylases and deacetylases in cell proliferation. Curr Opin Genet Dev 1999;9(1):40-8 (Pubitemid 29080385)
-
(1999)
Current Opinion in Genetics and Development
, vol.9
, Issue.1
, pp. 40-48
-
-
Kouzarides, T.1
-
3
-
-
0034654011
-
Acetylation: A regulatory modification to rival phosphorylation
-
Kouzarides T. Acetylation: a regulatory modification to rival phosphorylation? EMBO J 2000;19(6):1176-9 (Pubitemid 30151013)
-
(2000)
EMBO Journal
, vol.19
, Issue.6
, pp. 1176-1179
-
-
Kouzarides, T.1
-
4
-
-
68949212379
-
Lysine acetylation targets protein complexes and co-regulates major cellular functions
-
Choudhary C, Kumar C, Gnad F, et al. Lysine acetylation targets protein complexes and co-regulates major cellular functions. Science 2009;325(5942):834-40
-
(2009)
Science
, vol.325
, Issue.5942
, pp. 834-40
-
-
Choudhary, C.1
Kumar, C.2
Gnad, F.3
-
5
-
-
30344477367
-
Histone deacetylase inhibitors and the promise of epigenetic (and more) treatments for cancer
-
DOI 10.1038/nrc1779
-
Minucci S, Pelicci PG. Histone deacetylase inhibitors and the promise of epigenetic (and more) treatments for cancer. Nat Rev Cancer 2006;6(1):38-51 (Pubitemid 43054973)
-
(2006)
Nature Reviews Cancer
, vol.6
, Issue.1
, pp. 38-51
-
-
Minucci, S.1
Pelicci, P.G.2
-
6
-
-
77952853306
-
Histone deacetylases and epigenetic therapies of hematological malignancies
-
Mercurio C, Minucci S, Pelicci PG. Histone deacetylases and epigenetic therapies of hematological malignancies. Pharmacol Res 2010;62(1):18-34
-
(2010)
Pharmacol Res
, vol.62
, Issue.1
, pp. 18-34
-
-
Mercurio, C.1
Minucci, S.2
Pelicci, P.G.3
-
7
-
-
77649171884
-
Novel histone deacetylase inhibitors in clinical trials as anti-cancer agents
-
Tan J, Cang S, Ma Y, et al. Novel histone deacetylase inhibitors in clinical trials as anti-cancer agents.J Hematol Oncol 2010;3:5
-
(2010)
J Hematol Oncol
, vol.3
, pp. 5
-
-
Tan, J.1
Cang, S.2
Ma, Y.3
-
8
-
-
77955413261
-
Histone deacetylase inhibitors in lymphoma
-
Copeland A, Buglio D, Younes A. Histone deacetylase inhibitors in lymphoma. Curr Opin Oncol 2010;22(5):431-6
-
(2010)
Curr Opin Oncol
, vol.22
, Issue.5
, pp. 431-6
-
-
Copeland, A.1
Buglio, D.2
Younes, A.3
-
9
-
-
67449127082
-
Clinical studies of histone deacetylase inhibitors
-
Prince HM, Bishton MJ, Harrison SJ. Clinical studies of histone deacetylase inhibitors. Clin Cancer Res 2009;15(12):3958-69
-
(2009)
Clin Cancer Res
, vol.15
, Issue.12
, pp. 3958-69
-
-
Prince, H.M.1
Bishton, M.J.2
Harrison, S.J.3
-
10
-
-
73949128107
-
Histone deacetylase inhibitors in cancer therapy
-
Lane AA, Chabner BA. Histone deacetylase inhibitors in cancer therapy. J Clin Oncol 2009;27(32):5459-68
-
(2009)
J Clin Oncol
, vol.27
, Issue.32
, pp. 5459-68
-
-
Lane, A.A.1
Chabner, B.A.2
-
11
-
-
34547122494
-
HDAC inhibitors: Clinical update and mechanism-based potential
-
DOI 10.1016/j.bcp.2007.04.007, PII S0006295207002262
-
Glaser KB. HDAC inhibitors: clinical update and mechanism-based potential. Biochem Pharmacol 2007;74(5):659-71 (Pubitemid 47096639)
-
(2007)
Biochemical Pharmacology
, vol.74
, Issue.5
, pp. 659-671
-
-
Glaser, K.B.1
-
12
-
-
33847258674
-
Discovery and development of SAHA as an anticancer agent
-
DOI 10.1038/sj.onc.1210204, PII 1210204
-
Marks PA. Discovery and development of SAHA as an anticancer agent. Oncogene 2007;26(9):1351-6 (Pubitemid 46328465)
-
(2007)
Oncogene
, vol.26
, Issue.9
, pp. 1351-1356
-
-
Marks, P.A.1
-
13
-
-
73949149251
-
Phase II multi-institutional trial of the histone deacetylase inhibitor romidepsin as monotherapy for patients with cutaneous T-cell lymphoma
-
Piekarz RL, Frye R, Turner M, et al. Phase II multi-institutional trial of the histone deacetylase inhibitor romidepsin as monotherapy for patients with cutaneous T-cell lymphoma. J Clin Oncol 2009:5410-17
-
(2009)
J Clin Oncol
, pp. 5410-17
-
-
Piekarz, R.L.1
Frye, R.2
Turner, M.3
-
14
-
-
3042576479
-
Valproic acid: An old drug newly discovered as inhibitor of histone deacetylases
-
Gottlicher M. Valproic acid: an old drug newly discovered as inhibitor of histone deacetylases. Ann Hematol 2004;83(Suppl 1):S91-2
-
(2004)
Ann Hematol
, vol.83
, Issue.SUPPL. 1
-
-
Gottlicher, M.1
-
15
-
-
42649109021
-
Valproic acid as epigenetic cancer drug: Preclinical, clinical and transcriptional effects on solid tumors
-
Duenas-Gonzalez A, Candelaria M, Perez-Plascencia C, et al. Valproic acid as epigenetic cancer drug: preclinical, clinical and transcriptional effects on solid tumors. Cancer Treat Rev 2008;34(3):206-22
-
(2008)
Cancer Treat Rev
, vol.34
, Issue.3
, pp. 206-22
-
-
Duenas-Gonzalez, A.1
Candelaria, M.2
Perez-Plascencia, C.3
-
16
-
-
0036721055
-
Anti-tumor mechanisms of valproate: A novel role for an old drug
-
Blaheta RA, Cinatl J Jr. Anti-tumor mechanisms of valproate: a novel role for an old drug. Med Res Rev 2002;22(5):492-511
-
(2002)
Med Res Rev
, vol.22
, Issue.5
, pp. 492-511
-
-
Blaheta, R.A.1
Cinatl Jr., J.2
-
17
-
-
64049097640
-
The promises and pitfalls of epigenetic therapies in solid tumours
-
Graham JS, Kaye SB, Brown R. The promises and pitfalls of epigenetic therapies in solid tumours. Eur J Cancer 2009;45(7):1129-36
-
(2009)
Eur J Cancer
, vol.45
, Issue.7
, pp. 1129-36
-
-
Graham, J.S.1
Kaye, S.B.2
Brown, R.3
-
18
-
-
49249116407
-
A work in progress: The clinical development of histone deacetylase inhibitors
-
Marsoni S, Damia G, Camboni G. A work in progress: the clinical development of histone deacetylase inhibitors. Epigenetics 2008;3(3):164-71
-
(2008)
Epigenetics
, vol.3
, Issue.3
, pp. 164-71
-
-
Marsoni, S.1
Damia, G.2
Camboni, G.3
-
19
-
-
67349208442
-
Histone deacetylase inhibitors as a new weapon in the arsenal of differentiation therapies of cancer
-
Botrugno OA, Santoro F, Minucci S. Histone deacetylase inhibitors as a new weapon in the arsenal of differentiation therapies of cancer. Cancer Lett 2009;280(2):134-44
-
(2009)
Cancer Lett
, vol.280
, Issue.2
, pp. 134-44
-
-
Botrugno, O.A.1
Santoro, F.2
Minucci, S.3
-
20
-
-
49349098483
-
Histone deacetylase inhibitors: Mechanisms of cell death and promise in combination cancer therapy
-
Carew JS, Giles FJ, Nawrocki ST. Histone deacetylase inhibitors: Mechanisms of cell death and promise in combination cancer therapy. Cancer Lett 2008;269(1):7-17
-
(2008)
Cancer Lett
, vol.269
, Issue.1
, pp. 7-17
-
-
Carew, J.S.1
Giles, F.J.2
Nawrocki, S.T.3
-
21
-
-
50249175241
-
Will histone deacetylase inhibitors require combination with other agents to fulfil their therapeutic potential?
-
Nolan L, Johnson PW, Ganesan A, et al. Will histone deacetylase inhibitors require combination with other agents to fulfil their therapeutic potential? Br J Cancer 2008;99(5):689-94
-
(2008)
Br J Cancer
, vol.99
, Issue.5
, pp. 689-94
-
-
Nolan, L.1
Johnson, P.W.2
Ganesan, A.3
-
22
-
-
65249135408
-
Design of chimeric histone deacetylase-and tyrosine kinase-inhibitors: A series of imatinib hybrides as potent inhibitors of wild-type and mutant BCR-ABL, PDGF-Rbeta, and histone deacetylases
-
Mahboobi S, Dove S, Sellmer A, et al. Design of chimeric histone deacetylase-and tyrosine kinase-inhibitors: a series of imatinib hybrides as potent inhibitors of wild-type and mutant BCR-ABL, PDGF-Rbeta, and histone deacetylases.J Med Chem 2009;52(8):2265-79
-
(2009)
J Med Chem
, vol.52
, Issue.8
, pp. 2265-79
-
-
Mahboobi, S.1
Dove, S.2
Sellmer, A.3
-
23
-
-
77949353758
-
Discovery of 7-(4-(3-ethynylphenylamino)-7-methoxyquinazolin-6-yloxy)-N- hydroxyheptanam ide (CUDc-101) as a potent multi-acting HDAC, EGFR, and HER2 inhibitor for the treatment of cancer
-
Cai X, Zhai HX, Wang J, et al. Discovery of 7-(4-(3-ethynylphenylamino)- 7-methoxyquinazolin-6-yloxy)-N-hydroxyheptanam ide (CUDc-101) as a potent multi-acting HDAC, EGFR, and HER2 inhibitor for the treatment of cancer. J Med Chem 2010;53(5):2000-9
-
(2010)
J Med Chem
, vol.53
, Issue.5
, pp. 2000-9
-
-
Cai, X.1
Zhai, H.X.2
Wang, J.3
-
24
-
-
77951708371
-
CUDC-101 a multitargeted inhibitor of histone deacetylase epidermal growth factor receptor and human epidermal growth factor receptor 2 exerts potent anticancer activity
-
Lai CJ, Bao R, Tao X, et al. CUDC-101, a multitargeted inhibitor of histone deacetylase, epidermal growth factor receptor, and human epidermal growth factor receptor 2, exerts potent anticancer activity. Cancer Res 2010;70(9):3647-56
-
(2010)
Cancer Res
, vol.70
, Issue.9
, pp. 3647-56
-
-
Lai, C.J.1
Bao, R.2
Tao, X.3
-
25
-
-
79953146669
-
364 the first-in-human, first-in-class study of CUDC-101, a multi-targeted inhibitor of HDAC, EGFR, and HER2: A Phase i study in patients with advanced cancer
-
Shimizu T, Tolcher AW, LoRusso P, et al. 364 The first-in-human, first-in-class study of CUDC-101, a multi-targeted inhibitor of HDAC, EGFR, and HER2: a Phase I study in patients with advanced cancer. Eur J Cancer Suppl 2010;8(7):115
-
(2010)
Eur J Cancer Suppl
, vol.8
, Issue.7
, pp. 115
-
-
Shimizu, T.1
Tolcher, A.W.2
Lorusso, P.3
-
26
-
-
77958610661
-
An integrated genomic and epigenomic approach predicts therapeutic response to zebularine in human liver cancer
-
Andersen JB, Factor VM, Marquardt JU, et al. An integrated genomic and epigenomic approach predicts therapeutic response to zebularine in human liver cancer. Sci Transl Med 2010;2(54):54ra77
-
(2010)
Sci Transl Med
, vol.2
, Issue.54
-
-
Andersen, J.B.1
Factor, V.M.2
Marquardt, J.U.3
-
27
-
-
64049094851
-
Epigenetic therapies in haematological malignancies: Searching for true targets
-
Altucci L, Minucci S. Epigenetic therapies in haematological malignancies: searching for true targets. Eur J Cancer 2009;45(7):1137-45
-
(2009)
Eur J Cancer
, vol.45
, Issue.7
, pp. 1137-45
-
-
Altucci, L.1
Minucci, S.2
-
28
-
-
55949105474
-
Epigenomic profiling of cancer cells
-
Gargiulo G, Minucci S. Epigenomic profiling of cancer cells. Int J Biochem Cell Biol 2009;41(1):127-35
-
(2009)
Int J Biochem Cell Biol
, vol.41
, Issue.1
, pp. 127-35
-
-
Gargiulo, G.1
Minucci, S.2
-
29
-
-
77249087051
-
Chemical phylogenetics of histone deacetylases
-
Bradner JE, West N, Grachan ML, et al. Chemical phylogenetics of histone deacetylases. Nat Chem Biol 2010;6(3):238-43
-
(2010)
Nat Chem Biol
, vol.6
, Issue.3
, pp. 238-43
-
-
Bradner, J.E.1
West, N.2
Grachan, M.L.3
-
30
-
-
34548748173
-
The pharmaceutical potential of histone deacetylase inhibitors
-
DOI 10.2174/138161207781663064
-
Elaut G, Rogiers V, Vanhaecke T. The pharmaceutical potential of histone deacetylase inhibitors. Curr Pharm Des 2007;13(25):2584-620 (Pubitemid 47430437)
-
(2007)
Current Pharmaceutical Design
, vol.13
, Issue.25
, pp. 2584-2620
-
-
Elaut, G.1
Rogiers, V.2
Vanhaecke, T.3
-
31
-
-
21244458052
-
Phase I and pharmacokinetic study of MS-275, a histone deacetylase inhibitor, in patients with advanced and refractory solid tumors or lymphoma
-
DOI 10.1200/JCO.2005.02.188
-
Ryan QC, Headlee D, Acharya M, et al. Phase I and pharmacokinetic study of MS-275, a histone deacetylase inhibitor, in patients with advanced and refractory solid tumors or lymphoma. J Clin Oncol 2005;23(17):3912-22 (Pubitemid 46218694)
-
(2005)
Journal of Clinical Oncology
, vol.23
, Issue.17
, pp. 3912-3922
-
-
Ryan, Q.C.1
Headlee, D.2
Acharya, M.3
Sparreboom, A.4
Trepel, J.B.5
Ye, J.6
Figg, W.D.7
Hwang, K.8
Chung, E.J.9
Murgo, A.10
Melillo, G.11
Elsayed, Y.12
Monga, M.13
Kalnitskiy, M.14
Zwiebel, J.15
Sausville, E.A.16
-
32
-
-
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, 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(8):4592-7 (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
-
33
-
-
71449109387
-
New patented histone deacetylase inhibitors
-
Wang H, Dymock BW. New patented histone deacetylase inhibitors. Expert Opin Ther Pat 2009;19(12):1727-57
-
(2009)
Expert Opin Ther Pat
, vol.19
, Issue.12
, pp. 1727-57
-
-
Wang, H.1
Dymock, B.W.2
-
34
-
-
33847043595
-
Development and validation of high-performance liquid chromatography-tandem mass spectrometry assay for 6-(3-benzoyl-ureido)-hexanoic acid hydroxyamide, a novel HDAC inhibitor, in mouse plasma for pharmacokinetic studies
-
Yeo P, Xin L, Goh E, et al. Development and validation of high-performance liquid chromatography-tandem mass spectrometry assay for 6-(3-benzoyl-ureido)-hexanoic acid hydroxyamide, a novel HDAC inhibitor, in mouse plasma for pharmacokinetic studies. Biomed Chromatogr 2007;21(2):184-9
-
(2007)
Biomed Chromatogr
, vol.21
, Issue.2
, pp. 184-9
-
-
Yeo, P.1
Xin, L.2
Goh, E.3
-
35
-
-
77249090313
-
ADME and PK/PD attributes of SB939, a potent orally active HDAC inhibitor
-
Sangthongpitag K, Wang H, Yeo P, et al. ADME and PK/PD attributes of SB939, a potent orally active HDAC inhibitor Eur J Cancer Suppl 2006;4(12):53
-
(2006)
Eur J Cancer Suppl
, vol.4
, Issue.12
, pp. 53
-
-
Sangthongpitag, K.1
Wang, H.2
Yeo, P.3
-
36
-
-
77949714263
-
SB939 a novel potent and orally active histone deacetylase inhibitor with high tumor exposure and efficacy in mouse models of colorectal cancer
-
Novotny-Diermayr V, Sangthongpitag K, Hu CY, et al. SB939, a novel potent and orally active histone deacetylase inhibitor with high tumor exposure and efficacy in mouse models of colorectal cancer. Mol Cancer Ther 2010;9(3):642-52
-
(2010)
Mol Cancer Ther
, vol.9
, Issue.3
, pp. 642-52
-
-
Novotny-Diermayr, V.1
Sangthongpitag, K.2
Hu, C.Y.3
-
37
-
-
71449084715
-
Phase i study of SB939 three times weekly for 3 weeks every 4 weeks in patients with advanced solid malignancies
-
abstract 2560
-
Yong W, Goh B, Toh H, et al. Phase I study of SB939 three times weekly for 3 weeks every 4 weeks in patients with advanced solid malignancies. J Clin Oncol 2009;27(15):abstract 2560
-
(2009)
J Clin Oncol
, vol.27
, Issue.15
-
-
Yong, W.1
Goh, B.2
Toh, H.3
-
38
-
-
77951685547
-
The novel inhibitor of histone deacetylase resminostat (RAS2410) inhibits proliferation and induces apoptosis in multiple myeloma (MM) cells
-
Mandl-Weber S, Meinel FG, Jankowsky R, et al. The novel inhibitor of histone deacetylase resminostat (RAS2410) inhibits proliferation and induces apoptosis in multiple myeloma (MM) cells. Br J Haematol 2010;149(4):518-28
-
(2010)
Br J Haematol
, vol.149
, Issue.4
, pp. 518-28
-
-
Mandl-Weber, S.1
Meinel, F.G.2
Jankowsky, R.3
-
39
-
-
79953160130
-
A first-in-human phase i study of 4SC-201, an oral histone deacetylase (HDAC) inhibitor, in patients with advanced solid tumors [abstr 3530]
-
Brunetto AT, Ang JE, Lal R, et al. A first-in-human phase I study of 4SC-201, an oral histone deacetylase (HDAC) inhibitor, in patients with advanced solid tumors [abstr 3530]. J Clin Oncol 2009;27:15s
-
(2009)
J Clin Oncol
, vol.27
-
-
Brunetto, A.T.1
Ang, J.E.2
Lal, R.3
-
40
-
-
79953158660
-
Centralised analysis of phase i ECG dataset of resminostat, a new oral histone deacetylase inhibitor (HDACi)
-
Hauns B, Mais A, Jankowsky R, et al. Centralised analysis of phase I ECG dataset of resminostat, a new oral histone deacetylase inhibitor (HDACi). Eur J Cancer Suppl 2010;8(7):172
-
(2010)
Eur J Cancer Suppl
, vol.8
, Issue.7
, pp. 172
-
-
Hauns, B.1
Mais, A.2
Jankowsky, R.3
-
42
-
-
72549086620
-
JNJ-26481585, a novel 'second-generation' oral histone deacetylase inhibitor, shows broad-spectrum preclinical antitumoral activity
-
Arts J, King P, Marien A, et al. JNJ-26481585, a novel 'second-generation' oral histone deacetylase inhibitor, shows broad-spectrum preclinical antitumoral activity. Clin Cancer Res 2009;15(22):6841-51
-
(2009)
Clin Cancer Res
, vol.15
, Issue.22
, pp. 6841-51
-
-
Arts, J.1
King, P.2
Marien, A.3
-
43
-
-
79953155349
-
Preclinical assessment of the HDAC inhibitor JNJ-26481585: Potent in vivo activity across a broad spectrum of human tumor xenografts
-
Hickson I, King P, Marien A, et al. Preclinical assessment of the HDAC inhibitor JNJ-26481585: potent in vivo activity across a broad spectrum of human tumor xenografts. AACR Meeting Abstracts 2010;2010:5441
-
(2010)
AACR Meeting Abstracts
, vol.2010
, pp. 5441
-
-
Hickson, I.1
King, P.2
Marien, A.3
-
44
-
-
77954105581
-
Preliminary results of an open-label phase i pharmacokinetic/ pharmacodynamic study of JNJ26481585: Early evidence of antitumor activity
-
Postel-Vinay S, Kristeleit R, Fong P, et al. Preliminary results of an open-label phase I pharmacokinetic/pharmacodynamic study of JNJ26481585: early evidence of antitumor activity. J Clin Oncol 2009;27(20 Suppl 15S):e13504
-
(2009)
J Clin Oncol
, vol.27
, Issue.20 SUPPL. 15S
-
-
Postel-Vinay, S.1
Kristeleit, R.2
Fong, P.3
-
45
-
-
79953128085
-
The discovery and Anti-Tumor Activity CHR-3996-A Novel Orally Available Inhibitor of Class 1 Histone Deacetylases. EFMC-ISMC (European Federation for Medicinal Chemistry) 2010
-
Brussels
-
Donald A, Belfield A, Day F, et al. The discovery and Anti-Tumor Activity CHR-3996-A Novel, Orally Available Inhibitor of Class 1 Histone Deacetylases. EFMC-ISMC (European Federation for Medicinal Chemistry) 2010, XXIst International Symposium on Medicinal Chemistry. Brussels 2010:PC 365
-
(2010)
XXIst International Symposium on Medicinal Chemistry
-
-
Donald, A.1
Belfield, A.2
Day, F.3
-
46
-
-
79953155698
-
A phase i pharmacokinetic (PK) and pharmacodynamic (PD) study of CHR-3996, a class 1 selective histone deacetylase inhibitor (HDACi), in patients with advanced solid tumors
-
Banerji U, van Doorn L, Papadatos-Pastos D, et al. A phase I pharmacokinetic (PK) and pharmacodynamic (PD) study of CHR-3996, a class 1 selective histone deacetylase inhibitor (HDACi), in patients with advanced solid tumors. J Clin Oncol 2010;28(15 Suppl):2552
-
(2010)
J Clin Oncol
, vol.28
, Issue.15 SUPPL.
, pp. 2552
-
-
Banerji, U.1
Van Doorn, L.2
Papadatos-Pastos, D.3
-
47
-
-
23944487678
-
Structure-based optimization of phenylbutyrate-derived histone deacetylase inhibitors
-
DOI 10.1021/jm0503749
-
Lu Q, Wang DS, Chen CS, et al. Structure-based optimization of phenylbutyrate-derived histone deacetylase inhibitors. J Med Chem 2005;48(17):5530-5 (Pubitemid 41209250)
-
(2005)
Journal of Medicinal Chemistry
, vol.48
, Issue.17
, pp. 5530-5535
-
-
Lu, Q.1
Wang, D.-S.2
Chen, C.-S.3
Hu, Y.-D.4
Chen, C.-S.5
-
48
-
-
77956194142
-
The novel deacetylase inhibitor AR-42 demonstrates pre-clinical activity in B-cell malignancies in vitro and in vivo
-
Lucas DM, Alinari L, West DA, et al. The novel deacetylase inhibitor AR-42 demonstrates pre-clinical activity in B-cell malignancies in vitro and in vivo. PLoS One 2010;5(6):e10941
-
(2010)
PLoS One
, vol.5
, Issue.6
-
-
Lucas, D.M.1
Alinari, L.2
West, D.A.3
-
49
-
-
33749029926
-
Antitumor effects of a novel phenylbutyrate-based histone deacetylase inhibitor, (S)-HDAC-42, in prostate cancer
-
DOI 10.1158/1078-0432.CCR-06-0429
-
Kulp SK, Chen CS, Wang DS, et al. Antitumor effects of a novel phenylbutyrate-based histone deacetylase inhibitor, (S)-HDAC-42, in prostate cancer. Clin Cancer Res 2006;12(17):5199-206 (Pubitemid 44453349)
-
(2006)
Clinical Cancer Research
, vol.12
, Issue.17
, pp. 5199-5206
-
-
Kulp, S.K.1
Chen, C.-S.2
Wang, D.-S.3
Chen, C.-Y.4
Chen, C.-S.5
-
50
-
-
79953128957
-
Preclinical pharmacokinetic studies with s-HDAC-42 (NSC 736012), an inhibitor of histone deacetylase, by LC-MS/MS
-
abstract 3091
-
Cheng H, Liu Z, Kulp SK, et al. Preclinical pharmacokinetic studies with s-HDAC-42 (NSC 736012), an inhibitor of histone deacetylase, by LC-MS/MS. Proc Am Assoc Cancer Res 2006;47:abstract 3091
-
(2006)
Proc Am Assoc Cancer Res
, vol.47
-
-
Cheng, H.1
Liu, Z.2
Kulp, S.K.3
-
51
-
-
79953154995
-
Preclinical pharmacokinetics studies of R-and S-enantiomers of the histone deacetylase inhibitor, HDAC-42 (NSC 731438), in the rat
-
abstract 686
-
Cheng H, Jones W, Wei X, et al. Preclinical pharmacokinetics studies of R-and S-enantiomers of the histone deacetylase inhibitor, HDAC-42 (NSC 731438), in the rat. Proc Am Assoc Cancer Res 2006;47:abstract 686
-
(2006)
Proc Am Assoc Cancer Res
, vol.47
-
-
Cheng, H.1
Jones, W.2
Wei, X.3
-
52
-
-
84862265924
-
Novel histone deacetylase inhibitor CG200745 induces clonogenic cell death by modulating acetylation of p53 in cancer cells
-
published online 27 October 2010. doi:10.1007/s10637-010-9568-2
-
Oh ET, Park MT, Choi BH, et al. Novel histone deacetylase inhibitor CG200745 induces clonogenic cell death by modulating acetylation of p53 in cancer cells. Invest New Drugs 2010 published online 27 October 2010, doi:10.1007/s10637-010-9568-2
-
(2010)
Invest New Drugs
-
-
Oh, E.T.1
Park, M.T.2
Choi, B.H.3
-
53
-
-
79953156134
-
Preclinical studies of CG200745, novel histone deacetylase inhibitor discovered using structure-based drug discovery technologies
-
Hyun Y-L, Kim HJ, Kim YE, et al. Preclinical studies of CG200745, novel histone deacetylase inhibitor discovered using structure-based drug discovery technologies. AACR Meeting Abstracts 2009 2009;2009:4561
-
(2009)
AACR Meeting Abstracts 2009
, vol.2009
, pp. 4561
-
-
Hyun, Y.-L.1
Kim, H.J.2
Kim, Y.E.3
-
55
-
-
75749143069
-
A novel histone deacetylase inhibitor Chidamide induces apoptosis of human colon cancer cells
-
Liu L, Chen B, Qin S, et al. A novel histone deacetylase inhibitor Chidamide induces apoptosis of human colon cancer cells. Biochem Biophys Res Commun 2010;392(2):190-5
-
(2010)
Biochem Biophys Res Commun
, vol.392
, Issue.2
, pp. 190-5
-
-
Liu, L.1
Chen, B.2
Qin, S.3
-
56
-
-
77952889966
-
Phase i study of chidamide (CS055/HBI-8000), a novel histone deacetylase inhibitor, in patients with advanced solid tumors and lymphomas [abstract 3529]
-
Dong M, Ning Z, Newman MJ, et al. Phase I study of chidamide (CS055/HBI-8000), a novel histone deacetylase inhibitor, in patients with advanced solid tumors and lymphomas [abstract 3529]. J Clin Oncol 2009;27:15s
-
(2009)
J Clin Oncol
, vol.27
-
-
Dong, M.1
Ning, Z.2
Newman, M.J.3
-
57
-
-
69849110970
-
Panobinostat (LBH589): A potent pan-deacetylase inhibitor with promising activity against hematologic and solid tumors
-
Prince HM, Bishton MJ, Johnstone RW. Panobinostat (LBH589): a potent pan-deacetylase inhibitor with promising activity against hematologic and solid tumors. Future Oncol 2009;5(5):601-12
-
(2009)
Future Oncol
, vol.5
, Issue.5
, pp. 601-12
-
-
Prince, H.M.1
Bishton, M.J.2
Johnstone, R.W.3
-
58
-
-
67349228774
-
Development of the pan-DAC inhibitor panobinostat (LBH589): Successes and challenges
-
Atadja P. Development of the pan-DAC inhibitor panobinostat (LBH589): successes and challenges. Cancer Lett 2009;280(2):233-41
-
(2009)
Cancer Lett
, vol.280
, Issue.2
, pp. 233-41
-
-
Atadja, P.1
-
59
-
-
33846122993
-
Dimethyl sulfoxide to vorinostat: Development of this histone deacetylase inhibitor as an anticancer drug
-
DOI 10.1038/nbt1272, PII NBT1272
-
Marks PA, Breslow R. Dimethyl sulfoxide to vorinostat: development of this histone deacetylase inhibitor as an anticancer drug. Nat Biotechnol 2007;25(1):84-90 (Pubitemid 46087907)
-
(2007)
Nature Biotechnology
, vol.25
, Issue.1
, pp. 84-90
-
-
Marks, P.A.1
Breslow, R.2
-
60
-
-
36849004821
-
Unraveling the hidden catalytic activity of vertebrate class IIa histone deacetylases
-
DOI 10.1073/pnas.0706487104
-
Lahm A, Paolini C, Pallaoro M, et al. Unraveling the hidden catalytic activity of vertebrate class IIa histone deacetylases. Proc Natl Acad Sci USA 2007;104(44):17335-40 (Pubitemid 350219843)
-
(2007)
Proceedings of the National Academy of Sciences of the United States of America
, vol.104
, Issue.44
, pp. 17335-17340
-
-
Lahm, A.1
Paolini, C.2
Pallaoro, M.3
Nardi, M.C.4
Jones, P.5
Neddermann, P.6
Sambucini, S.7
Bottomley, M.J.8
Lo Surdo, P.9
Carfi, A.10
Koch, U.11
De Francesco, R.12
Steinkuhler, C.13
Gallinari, P.14
-
61
-
-
0033539092
-
Structures of a histone deacetylase homologue bound to the TSA and SAHA inhibitors
-
DOI 10.1038/43710
-
Finnin MS, Donigian JR, Cohen A, et al. Structures of a histone deacetylase homologue bound to the TSA and SAHA inhibitors. Nature 1999;401(6749):188-93 (Pubitemid 29436325)
-
(1999)
Nature
, vol.401
, Issue.6749
, pp. 188-193
-
-
Finnin, M.S.1
Donigian, J.R.2
Cohen, A.3
Richon, V.M.4
Rifkind, R.A.5
Marks, P.A.6
Breslow, R.7
Pavletich, N.P.8
-
63
-
-
55549094833
-
Structural and functional analysis of the human HDAC4 catalytic domain reveals a regulatory structural zinc-binding domain
-
Bottomley MJ, Lo Surdo P, Di Giovine P, et al. Structural and functional analysis of the human HDAC4 catalytic domain reveals a regulatory structural zinc-binding domain. J Biol Chem 2008;283(39):26694-704
-
(2008)
J Biol Chem
, vol.283
, Issue.39
, pp. 26694-704
-
-
Bottomley, M.J.1
Lo Surdo, P.2
Di Giovine, P.3
-
64
-
-
45549095066
-
Human HDAC7 harbors a class IIa histone deacetylase-specific zinc binding motif and cryptic deacetylase activity
-
Schuetz A, Min J, Allali-Hassani A, et al. Human HDAC7 harbors a class IIa histone deacetylase-specific zinc binding motif and cryptic deacetylase activity. J Biol Chem 2008;283(17):11355-63
-
(2008)
J Biol Chem
, vol.283
, Issue.17
, pp. 11355-63
-
-
Schuetz, A.1
Min, J.2
Allali-Hassani, A.3
-
65
-
-
3142562372
-
Structural snapshots of human HDAC8 provide insights into the class I histone deacetylases
-
DOI 10.1016/j.str.2004.04.012, PII S0969212604001595
-
Somoza JR, Skene RJ, Katz BA, et al. Structural snapshots of human HDAC8 provide insights into the class I histone deacetylases. Structure 2004;12(7):1325-34 (Pubitemid 38900774)
-
(2004)
Structure
, vol.12
, Issue.7
, pp. 1325-1334
-
-
Somoza, J.R.1
Skene, R.J.2
Katz, B.A.3
Mol, C.4
Ho, J.D.5
Jennings, A.J.6
Luong, C.7
Arvai, A.8
Buggy, J.J.9
Chi, E.10
Tang, J.11
Sang, B.-C.12
Verner, E.13
Wynands, R.14
Leahy, E.M.15
Dougan, D.R.16
Snell, G.17
Navre, M.18
Knuth, M.W.19
Swanson, R.V.20
McRee, D.E.21
Tari, L.W.22
more..
-
66
-
-
6344222799
-
Crystal structure of a eukaryotic zinc-dependent histone deacetylase, human HDAC8, complexed with a hydroxamic acid inhibitor
-
DOI 10.1073/pnas.0404603101
-
Vannini A, Volpari C, Filocamo G, et al. Crystal structure of a eukaryotic zinc-dependent histone deacetylase, human HDAC8, complexed with a hydroxamic acid inhibitor. Proc Natl Acad Sci USA 2004;101(42):15064-9 (Pubitemid 39391719)
-
(2004)
Proceedings of the National Academy of Sciences of the United States of America
, vol.101
, Issue.42
, pp. 15064-15069
-
-
Vannini, A.1
Volpari, C.2
Filocamo, G.3
Casavola, E.C.4
Brunetti, M.5
Renzoni, D.6
Chakravarty, P.7
Paolini, C.8
De Francesco, R.9
Gallinari, P.10
Steinkuhler, C.11
Di Marco, S.12
-
69
-
-
40849114307
-
Phenylglycine and phenylalanine derivatives as potent and selective HDAC1 inhibitors (SHI-1)
-
Wilson KJ, Witter DJ, Grimm JB, et al. Phenylglycine and phenylalanine derivatives as potent and selective HDAC1 inhibitors (SHI-1). Bioorg Med Chem Lett 2008;18(6):1859-63
-
(2008)
Bioorg Med Chem Lett
, vol.18
, Issue.6
, pp. 1859-63
-
-
Wilson, K.J.1
Witter, D.J.2
Grimm, J.B.3
-
70
-
-
38149079799
-
Optimization of biaryl Selective HDAC1&2 Inhibitors (SHI-1:2)
-
Witter DJ, Harrington P, Wilson KJ, et al. Optimization of biaryl Selective HDAC1&2 Inhibitors (SHI-1:2). Bioorg Med Chem Lett 2008;18(2):726-31
-
(2008)
Bioorg Med Chem Lett
, vol.18
, Issue.2
, pp. 726-31
-
-
Witter, D.J.1
Harrington, P.2
Wilson, K.J.3
-
71
-
-
38749136234
-
Exploration of the internal cavity of histone deacetylase (HDAC) with selective HDAC1/HDAC2 inhibitors (SHI-1:2)
-
DOI 10.1016/j.bmcl.2007.12.031, PII S0960894X0701476X
-
Methot JL, Chakravarty PK, Chenard M, et al. Exploration of the internal cavity of histone deacetylase (HDAC) with selective HDAC1/HDAC2 inhibitors (SHI-1:2). Bioorg Med Chem Lett 2008;18(3):973-8 (Pubitemid 351179353)
-
(2008)
Bioorganic and Medicinal Chemistry Letters
, vol.18
, Issue.3
, pp. 973-978
-
-
Methot, J.L.1
Chakravarty, P.K.2
Chenard, M.3
Close, J.4
Cruz, J.C.5
Dahlberg, W.K.6
Fleming, J.7
Hamblett, C.L.8
Hamill, J.E.9
Harrington, P.10
Harsch, A.11
Heidebrecht, R.12
Hughes, B.13
Jung, J.14
Kenific, C.M.15
Kral, A.M.16
Meinke, P.T.17
Middleton, R.E.18
Ozerova, N.19
Sloman, D.L.20
Stanton, M.G.21
Szewczak, A.A.22
Tyagarajan, S.23
Witter, D.J.24
Paul Secrist, J.25
Miller, T.A.26
more..
-
72
-
-
77952100365
-
Exploration of the HDAC2 foot pocket: Synthesis and SAR of substituted N-(2-aminophenyl)benzamides
-
Bressi JC, Jennings AJ, Skene R, et al. Exploration of the HDAC2 foot pocket: Synthesis and SAR of substituted N-(2-aminophenyl)benzamides. Bioorg Med Chem Lett 2010;20(10):3142-5
-
(2010)
Bioorg Med Chem Lett
, vol.20
, Issue.10
, pp. 3142-5
-
-
Bressi, J.C.1
Jennings, A.J.2
Skene, R.3
-
73
-
-
69949090550
-
Diphenylmethylene hydroxamic acids as selective class IIa histone deacetylase inhibitors
-
Tessier P, Smil DV, Wahhab A, et al. Diphenylmethylene hydroxamic acids as selective class IIa histone deacetylase inhibitors. Bioorg Med Chem Lett 2009;19(19):5684-8
-
(2009)
Bioorg Med Chem Lett
, vol.19
, Issue.19
, pp. 5684-8
-
-
Tessier, P.1
Smil, D.V.2
Wahhab, A.3
-
74
-
-
42049118549
-
Isoform-selective histone deacetylase inhibitors
-
DOI 10.2174/138161208783885335
-
Itoh Y, Suzuki T, Miyata N. Isoform-selective histone deacetylase inhibitors. Curr Pharm Des 2008;14(6):529-44 (Pubitemid 351516877)
-
(2008)
Current Pharmaceutical Design
, vol.14
, Issue.6
, pp. 529-544
-
-
Itoh, Y.1
Suzuki, T.2
Miyata, N.3
-
75
-
-
42049096372
-
Chemical origins of isoform selectivity in histone deacetylase inhibitors
-
DOI 10.2174/138161208783885353
-
Butler KV, Kozikowski AP. Chemical origins of isoform selectivity in histone deacetylase inhibitors. Curr Pharm Des 2008;14(6):505-28 (Pubitemid 351516876)
-
(2008)
Current Pharmaceutical Design
, vol.14
, Issue.6
, pp. 505-528
-
-
Butler, K.V.1
Kozikowski, A.P.2
-
77
-
-
34948875686
-
Quantitative chemical proteomics reveals mechanisms of action of clinical ABL kinase inhibitors
-
DOI 10.1038/nbt1328, PII NBT1328
-
Bantscheff M, Eberhard D, Abraham Y, et al. Quantitative chemical proteomics reveals mechanisms of action of clinical ABL kinase inhibitors. Nat Biotechnol 2007;25(9):1035-44 (Pubitemid 47517638)
-
(2007)
Nature Biotechnology
, vol.25
, Issue.9
, pp. 1035-1044
-
-
Bantscheff, M.1
Eberhard, D.2
Abraham, Y.3
Bastuck, S.4
Boesche, M.5
Hobson, S.6
Mathieson, T.7
Perrin, J.8
Raida, M.9
Rau, C.10
Reader, V.11
Sweetman, G.12
Bauer, A.13
Bouwmeester, T.14
Hopf, C.15
Kruse, U.16
Neubauer, G.17
Ramsden, N.18
Rick, J.19
Kuster, B.20
Drewes, G.21
more..
-
78
-
-
78650847770
-
Selective inhibition of BET bromodomains
-
Filippakopoulos P, Qi J, Picaud S, et al. Selective inhibition of BET bromodomains. Nature 2010;468(7327):1067-73
-
(2010)
Nature
, vol.468
, Issue.7327
, pp. 1067-73
-
-
Filippakopoulos, P.1
Qi, J.2
Picaud, S.3
-
79
-
-
77952105211
-
Effective targeting of quiescent chronic myelogenous leukemia stem cells by histone deacetylase inhibitors in combination with imatinib mesylate
-
Zhang B, Strauss AC, Chu S, et al. Effective targeting of quiescent chronic myelogenous leukemia stem cells by histone deacetylase inhibitors in combination with imatinib mesylate. Cancer Cell 2010;17(5):427-42
-
(2010)
Cancer Cell
, vol.17
, Issue.5
, pp. 427-42
-
-
Zhang, B.1
Strauss, A.C.2
Chu, S.3
-
80
-
-
77958612597
-
Epigenetic drugs can stimulate metastasis through enhanced expression of the pro-metastatic Ezrin gene
-
Yu Y, Zeng P, Xiong J, et al. Epigenetic drugs can stimulate metastasis through enhanced expression of the pro-metastatic Ezrin gene. PLoS One 2010;5(9):e12710
-
(2010)
PLoS One
, vol.5
, Issue.9
-
-
Yu, Y.1
Zeng, P.2
Xiong, J.3
-
81
-
-
68749108259
-
LSD1 is a subunit of the NuRD complex and targets the metastasis programs in breast cancer
-
Wang Y, Zhang H, Chen Y, et al. LSD1 is a subunit of the NuRD complex and targets the metastasis programs in breast cancer. Cell 2009;138(4):660-72
-
(2009)
Cell
, vol.138
, Issue.4
, pp. 660-72
-
-
Wang, Y.1
Zhang, H.2
Chen, Y.3
-
82
-
-
7444256739
-
Overexpression of histone deacetylase 1 confers resistance to sodium butyrate-mediated apoptosis in melanoma cells through a p53-mediated pathway
-
DOI 10.1158/0008-5472.CAN-03-3897
-
Bandyopadhyay D, Mishra A, Medrano EE. Overexpression of histone deacetylase 1 confers resistance to sodium butyrate-mediated apoptosis in melanoma cells through a p53-mediated pathway. Cancer Res 2004;64(21):7706-10 (Pubitemid 39446901)
-
(2004)
Cancer Research
, vol.64
, Issue.21
, pp. 7706-7710
-
-
Bandyopadhyay, D.1
Mishra, A.2
Medrano, E.E.3
-
83
-
-
45549083112
-
Constitutive activation of signal transducers and activators of transcription predicts vorinostat resistance in cutaneous T-cell lymphoma
-
Fantin VR, Loboda A, Paweletz CP, et al. Constitutive activation of signal transducers and activators of transcription predicts vorinostat resistance in cutaneous T-cell lymphoma. Cancer Res 2008;68(10):3785-94
-
(2008)
Cancer Res
, vol.68
, Issue.10
, pp. 3785-94
-
-
Fantin, V.R.1
Loboda, A.2
Paweletz, C.P.3
-
84
-
-
67349157687
-
Biomarkers for predicting clinical responses to HDAC inhibitors
-
Stimson L, La Thangue NB. Biomarkers for predicting clinical responses to HDAC inhibitors. Cancer Lett 2009;280(2):177-83
-
(2009)
Cancer Lett
, vol.280
, Issue.2
, pp. 177-83
-
-
Stimson, L.1
La Thangue, N.B.2
-
85
-
-
51649126046
-
Destabilization of ERBB2 transcripts by targeting 3' untranslated region messenger RNA associated HuR and histone deacetylase-6
-
Scott GK, Marx C, Berger CE, et al. Destabilization of ERBB2 transcripts by targeting 3' untranslated region messenger RNA associated HuR and histone deacetylase-6. Mol Cancer Res 2008;6(7):1250-8
-
(2008)
Mol Cancer Res
, vol.6
, Issue.7
, pp. 1250-8
-
-
Scott, G.K.1
Marx, C.2
Berger, C.E.3
|