-
1
-
-
33745714230
-
Combined DNA methyltransferase and histone deacetylase inhibition in the treatment of myeloid neoplasms
-
Gore SD, Baylin S, Sugar E, et al. Combined DNA methyltransferase and histone deacetylase inhibition in the treatment of myeloid neoplasms. Cancer Res 2006;66:6361-9.
-
(2006)
Cancer Res
, vol.66
, pp. 6361-6369
-
-
Gore, S.D.1
Baylin, S.2
Sugar, E.3
-
3
-
-
34249033131
-
Histone deacetylase inhibitors: Molecular and biological activity as a premise to clinical application
-
Santini V, Gozzini A, Ferrari G. Histone deacetylase inhibitors: molecular and biological activity as a premise to clinical application. Curr Drug Metab 2007;8:383-93.
-
(2007)
Curr Drug Metab
, vol.8
, pp. 383-393
-
-
Santini, V.1
Gozzini, A.2
Ferrari, G.3
-
5
-
-
0036527775
-
Histone-deacetylase inhibitors: Novel drugs for the treatment of cancer
-
Johnstone RW. Histone-deacetylase inhibitors: novel drugs for the treatment of cancer. Nat Rev Drug Discov 2002;1:287-99.
-
(2002)
Nat Rev Drug Discov
, vol.1
, pp. 287-299
-
-
Johnstone, R.W.1
-
6
-
-
25144440127
-
Rational development of histone deacetylase inhibitors as anticancer agents: A review
-
Acharya MR, Sparreboom A, Venitz J, Figg WD. Rational development of histone deacetylase inhibitors as anticancer agents: a review. Mol Pharmacol 2005;68:917-32.
-
(2005)
Mol Pharmacol
, vol.68
, pp. 917-932
-
-
Acharya, M.R.1
Sparreboom, A.2
Venitz, J.3
Figg, W.D.4
-
7
-
-
34247109089
-
Histone deacetylase inhibitors for epigenetic therapy of cancer
-
Monneret C. Histone deacetylase inhibitors for epigenetic therapy of cancer. Anticancer Drugs 2007;18:363-70.
-
(2007)
Anticancer Drugs
, vol.18
, pp. 363-370
-
-
Monneret, C.1
-
8
-
-
33344456652
-
Histone deacetylase inhib itors: A review of their clinical status as antineoplastic agents
-
Garcia-Manero G, Issa JP. Histone deacetylase inhib itors: a review of their clinical status as antineoplastic agents. Cancer Invest 2005;23:635-42.
-
(2005)
Cancer Invest
, vol.23
, pp. 635-642
-
-
Garcia-Manero, G.1
Issa, J.P.2
-
9
-
-
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.
-
(2001)
Nat Rev Cancer
, vol.1
, pp. 194-202
-
-
Marks, P.1
Rifkind, R.A.2
Richon, V.M.3
Breslow, R.4
Miller, T.5
Kelly, W.K.6
-
10
-
-
33947313218
-
HDACs, histone deacetylation and gene transcription: From molecular biology to cancer therapeutics
-
Gallinari P, Di Marco S, Jones P, Pallaoro M, Stein-kuhler C HDACs, histone deacetylation and gene transcription: from molecular biology to cancer therapeutics. Cell Res 2007;17:195-211.
-
(2007)
Cell Res
, vol.17
, pp. 195-211
-
-
Gallinari, P.1
Di Marco, S.2
Jones, P.3
Pallaoro, M.4
Stein-kuhler, C.5
-
11
-
-
21244464349
-
Phase I study of an oral histone deacetylase inhibitor, suberoy-lanilide hydroxamic acid, in patients with advanced cancer
-
Kelly WK, O'Connor OA, Krug LM, et al. Phase I study of an oral histone deacetylase inhibitor, suberoy-lanilide hydroxamic acid, in patients with advanced cancer. J Clin Oncol 2005;23:3923-31.
-
(2005)
J Clin Oncol
, vol.23
, pp. 3923-3931
-
-
Kelly, W.K.1
O'Connor, O.A.2
Krug, L.M.3
-
12
-
-
33847258674
-
Discovery and development of SAHA as an anticancer agent
-
Marks PA. Discovery and development of SAHA as an anticancer agent. Oncogene 2007;26:1351-6.
-
(2007)
Oncogene
, vol.26
, pp. 1351-1356
-
-
Marks, P.A.1
-
13
-
-
34447509697
-
Vorinostat: A new oral histone deacetylase inhibitor approved for cutaneous T-cell lymphoma
-
Duvic M, Vu J. Vorinostat: a new oral histone deacetylase inhibitor approved for cutaneous T-cell lymphoma. Expert Opin Investig Drugs 2007;16:1111-20.
-
(2007)
Expert Opin Investig Drugs
, vol.16
, pp. 1111-1120
-
-
Duvic, M.1
Vu, J.2
-
14
-
-
33846804139
-
Antitumor effect of the histone deacetylase inhibitor LAQ824 in combination with 13-cis-retinoic acid in human malignant melanoma
-
Kato Y, Salumbides BC, Wang XF, et al. Antitumor effect of the histone deacetylase inhibitor LAQ824 in combination with 13-cis-retinoic acid in human malignant melanoma. Mol Cancer Ther 2007;6:70-81.
-
(2007)
Mol Cancer Ther
, vol.6
, pp. 70-81
-
-
Kato, Y.1
Salumbides, B.C.2
Wang, X.F.3
-
15
-
-
33748063974
-
A phase I study of intravenous LBH589, a novel cinnamic hydroxamic acid analogue histone deacetylase inhibitor, in patients with refractory hematologic malignancies
-
Giles F, Fischer T, Cortes J, et al. A phase I study of intravenous LBH589, a novel cinnamic hydroxamic acid analogue histone deacetylase inhibitor, in patients with refractory hematologic malignancies Clin Cancer Res 2006;12:4628-35.
-
(2006)
Clin Cancer Res
, vol.12
, pp. 4628-4635
-
-
Giles, F.1
Fischer, T.2
Cortes, J.3
-
16
-
-
33748353002
-
Activity of PXD101, a histone deacetylase inhibitor, in preclinical ovarian cancer studies
-
Qian X, LaRochelle WJ. Ara G, et al. Activity of PXD101, a histone deacetylase inhibitor, in preclinical ovarian cancer studies. Mol Cancer Ther 2006;5:2086-95.
-
(2006)
Mol Cancer Ther
, vol.5
, pp. 2086-2095
-
-
Qian, X.1
LaRochelle, W.J.2
Ara, G.3
-
17
-
-
1642453460
-
Pharmacodynamic response and inhibition of growth of human tumor xenografts by the novel histone deacetylase inhibitor PXD101
-
Plumb JA, Finn PW, Williams RJ, et al. Pharmacodynamic response and inhibition of growth of human tumor xenografts by the novel histone deacetylase inhibitor PXD101. Mol Cancer Ther 2003;2:721-8.
-
(2003)
Mol Cancer Ther
, vol.2
, pp. 721-728
-
-
Plumb, J.A.1
Finn, P.W.2
Williams, R.J.3
-
18
-
-
33947581039
-
Phase 1 and pharmacologic study of MS-275, a histone deacetylase inhibitor, in adults with refractory and relapsed acute leukemias
-
Gojo I, Jiemjit A, Trepel JB, et al. Phase 1 and pharmacologic study of MS-275, a histone deacetylase inhibitor, in adults with refractory and relapsed acute leukemias. Blood 2007;109:2781-90.
-
(2007)
Blood
, vol.109
, pp. 2781-2790
-
-
Gojo, I.1
Jiemjit, A.2
Trepel, J.B.3
-
19
-
-
34447101115
-
MS-275, a potent orally available inhibitor of histone deacetylases-the development of an anticancer agent
-
Hess-Stumpp H, Bracker TU, Henderson D, Politz O. MS-275, a potent orally available inhibitor of histone deacetylases-the development of an anticancer agent. Int J Biochem Cell Biol 2007;39:1388-405.
-
(2007)
Int J Biochem Cell Biol
, vol.39
, pp. 1388-1405
-
-
Hess-Stumpp, H.1
Bracker, T.U.2
Henderson, D.3
Politz, O.4
-
20
-
-
21244458052
-
Phase I and pharmacokinetic study of MS-275, a histone deacetylase inhibitor, in patients with advanced and refractory solid tumors or lymphoma
-
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;23:3912-22.
-
(2005)
J Clin Oncol
, vol.23
, pp. 3912-3922
-
-
Ryan, Q.C.1
Headlee, D.2
Acharya, M.3
-
21
-
-
33745164355
-
Substituted N-(2-aminophenyl)- benzamides, (E)-N-(2-aminophenyl)-acrylamides and their analogues: Novel classes of histone deacetylase inhibitors
-
Moradei O, Leit S, Zhou N, et al. Substituted N-(2-aminophenyl)- benzamides, (E)-N-(2-aminophenyl)-acrylamides and their analogues: novel classes of histone deacetylase inhibitors. Bioorg Med Chem Lett 2006;16:4048-52.
-
(2006)
Bioorg Med Chem Lett
, vol.16
, pp. 4048-4052
-
-
Moradei, O.1
Leit, S.2
Zhou, N.3
-
22
-
-
58349091060
-
-
Bonfils C, Kalita A, Liu J, Besterman JM, Li Z. Development of whole cell HDAC enzyme assay to analyze inhibitory activity of MGCD0103 in vitro and in vivo. 96th Annual Meeting of the AACR. Proc Am Assoc Cancer Res 2005;46:A606.
-
Bonfils C, Kalita A, Liu J, Besterman JM, Li Z. Development of whole cell HDAC enzyme assay to analyze inhibitory activity of MGCD0103 in vitro and in vivo. 96th Annual Meeting of the AACR. Proc Am Assoc Cancer Res 2005;46:A606.
-
-
-
-
23
-
-
58349099412
-
Antitumor activities of MGCD0103, a novel isotype-selective histone deacetylase inhibitor. 16th EORTC-NCI-AACR Symp Mol Targets Cancer Ther
-
Li Z, Zhou N, Fournel M, et al. Antitumor activities of MGCD0103, a novel isotype-selective histone deacetylase inhibitor. 16th EORTC-NCI-AACR Symp Mol Targets Cancer Ther. Eur J Cancer Suppl 2004;2:A83.
-
(2004)
Eur J Cancer Suppl
, vol.2
-
-
Li, Z.1
Zhou, N.2
Fournel, M.3
-
24
-
-
19944432566
-
A phase 1 and pharmacodynamic study of depsipeptide (FK228) in chronic lymphocytic leukemia and acute myeloid leukemia
-
Byrd JC, Marcucci G, Parthun MR, et al. A phase 1 and pharmacodynamic study of depsipeptide (FK228) in chronic lymphocytic leukemia and acute myeloid leukemia. Blood 2005;105:959-67.
-
(2005)
Blood
, vol.105
, pp. 959-967
-
-
Byrd, J.C.1
Marcucci, G.2
Parthun, M.R.3
-
27
-
-
0037086045
-
A microplate reader-based nonisotopic histone deacetylase activity assay
-
Heltweg B, Jung M. A microplate reader-based nonisotopic histone deacetylase activity assay. Anal Biochem 2002;302:175-83.
-
(2002)
Anal Biochem
, vol.302
, pp. 175-183
-
-
Heltweg, B.1
Jung, M.2
-
28
-
-
0017795309
-
Resolution of histones by poly-acrylamide gel electrophoresis in presence of nonionic detergents
-
Zweidler A. Resolution of histones by poly-acrylamide gel electrophoresis in presence of nonionic detergents. Methods Cell Biol 1978;17:223-33.
-
(1978)
Methods Cell Biol
, vol.17
, pp. 223-233
-
-
Zweidler, A.1
-
29
-
-
34748878324
-
Histone deacetylase inhibitors selectively suppress expression of HDAC7
-
Dokmanovic M, Perez G, Xu W, et al. Histone deacetylase inhibitors selectively suppress expression of HDAC7. Mol Cancer Ther 2007;6:2525-34.
-
(2007)
Mol Cancer Ther
, vol.6
, pp. 2525-2534
-
-
Dokmanovic, M.1
Perez, G.2
Xu, W.3
-
30
-
-
42949154252
-
A phase I study of MGCD0103 given as a three-weekly oral dose in patients with advanced solid tumors
-
Siu LL, Pili R, Duran I, et al. A phase I study of MGCD0103 given as a three-weekly oral dose in patients with advanced solid tumors. J Clin Oncol 2003;26:1940-7.
-
(2003)
J Clin Oncol
, vol.26
, pp. 1940-1947
-
-
Siu, L.L.1
Pili, R.2
Duran, I.3
-
31
-
-
34547864236
-
Histone deacetylase inhibitors: Molecular mechanisms of action. ncogene
-
Xu WS, Parmigiani RB, Marks PA. Histone deacetylase inhibitors: molecular mechanisms of action. ncogene 2007;26:5541-52.
-
(2007)
, vol.26
, pp. 5541-5552
-
-
Xu, W.S.1
Parmigiani, R.B.2
Marks, P.A.3
-
32
-
-
58349092082
-
Phase I study of isotype-selective histone deacetylase (HDAC) inhibitor MGCD0103 given as a three-times weekly oral dose in patients (pts) with advanced solid tumors
-
Siu LL, Carducci M, Patterson T, et al. Phase I study of isotype-selective histone deacetylase (HDAC) inhibitor MGCD0103 given as a three-times weekly oral dose in patients (pts) with advanced solid tumors. 18th EORTC-NCI-AACR Cancer Symposium. Eur J Cancer 2006;412:A300.
-
(2006)
18th EORTC-NCI-AACR Cancer Symposium. Eur J Cancer
, vol.412
-
-
Siu, L.L.1
Carducci, M.2
Patterson, T.3
-
33
-
-
34248370087
-
Phase I study of isotype-selective histone deacetylase (HDAC) inhibitor MGCD0103 given as three-times weekly oral dose in patients (pts) with advanced solid tumors
-
Proc Am Soc Clin Oncol
-
Carducci M, Siu LL, Sullivan R, et al. Phase I study of isotype-selective histone deacetylase (HDAC) inhibitor MGCD0103 given as three-times weekly oral dose in patients (pts) with advanced solid tumors. 2006 ASCO Annual Meeting. Proc Am Soc Clin Oncol 2006;25:A3007.
-
(2006)
2006 ASCO Annual Meeting
, vol.25
-
-
Carducci, M.1
Siu, L.L.2
Sullivan, R.3
-
34
-
-
58349090647
-
Phase I study of isotype-selective histone deacetylase (HDAC) inhibitor MGCD0103 given as three-times weekly oral dose in patients (pts) with advanced solid tumors. AACR-NCI-EORTC Intl Conf Mol Targ Cancer Ther
-
Siu LL, Carducci M, Pearce L, et al. Phase I study of isotype-selective histone deacetylase (HDAC) inhibitor MGCD0103 given as three-times weekly oral dose in patients (pts) with advanced solid tumors. AACR-NCI-EORTC Intl Conf Mol Targ Cancer Ther. Clin Cancer Res 2005;11:C77.
-
(2005)
Clin Cancer Res
, vol.11
-
-
Siu, L.L.1
Carducci, M.2
Pearce, L.3
-
35
-
-
0034641931
-
Corpse clearance defines the meaning of cell death
-
Savill J, Fadok V. Corpse clearance defines the meaning of cell death. Nature 2000;407:784-8.
-
(2000)
Nature
, vol.407
, pp. 784-788
-
-
Savill, J.1
Fadok, V.2
-
36
-
-
58349102512
-
-
Garcia-Manero G.Yang AS, Giles F, et al. Phase I/II study of the oral isotype-selective histone deacetylase (HDAC) inhibitor MGCD0103 in combination with azacitidine in patients (pts) with high-risk myelodys-plastic syndrome (MDS) or acute myelogenous leukemia (AML). 48th American Society of Hematology. Blood 2006;108:A1954.
-
Garcia-Manero G.Yang AS, Giles F, et al. Phase I/II study of the oral isotype-selective histone deacetylase (HDAC) inhibitor MGCD0103 in combination with azacitidine in patients (pts) with high-risk myelodys-plastic syndrome (MDS) or acute myelogenous leukemia (AML). 48th American Society of Hematology. Blood 2006;108:A1954.
-
-
-
|