-
1
-
-
0142179154
-
Identification of Novel Isoform-Selective Inhibitors within Class I Histone Deacetylases
-
DOI 10.1124/jpet.103.055541
-
Hu E, Dul E, Sung CM, et al. Identification of novel isoform-selective inhibitors within class I histone deacetylases. J Pharmacol Exp Ther 2003;307(2):720-8 (Pubitemid 37310689)
-
(2003)
Journal of Pharmacology and Experimental Therapeutics
, vol.307
, Issue.2
, pp. 720-728
-
-
Hu, E.1
Dul, E.2
Sung, C.-M.3
Chen, Z.4
Kirkpatrick, R.5
Zhang, G.-F.6
Johanson, K.7
Liu, R.8
Lago, A.9
Hofmann, G.10
Macarron, R.11
De Los Frailes, M.12
Perez, P.13
Krawiec, J.14
Winkler, J.15
Jaye, M.16
-
2
-
-
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(37):5541-52 (Pubitemid 47255934)
-
(2007)
Oncogene
, vol.26
, Issue.37
, pp. 5541-5552
-
-
Xu, W.S.1
Parmigiani, R.B.2
Marks, P.A.3
-
3
-
-
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
-
4
-
-
34848883438
-
Phase I trial of MS-275, a histone deacetylase inhibitor, administered weekly in refractory solid tumors and lymphoid malignancies
-
DOI 10.1158/1078-0432.CCR-07-0791
-
Kummar S, Gutierrez M, Gardner ER, et al. Phase I trial of MS-275, a histone deacetylase inhibitor, administered weekly in refractory solid tumors and lymphoid malignancies. Clin Cancer Res 2007;13(18 Pt 1):5411-17. (Pubitemid 47510368)
-
(2007)
Clinical Cancer Research
, vol.13
, Issue.18
, pp. 5411-5417
-
-
Kummar, S.1
Gutierrez, M.2
Gardner, E.R.3
Donovan, E.4
Hwang, K.5
Eun, J.C.6
Lee, M.-J.7
Maynard, K.8
Kalnitskiy, M.9
Chen, A.10
Melillo, G.11
Ryan, Q.C.12
Conley, B.13
Figg, W.D.14
Trepel, J.B.15
Zwiebel, J.16
Doroshow, J.H.17
Murgo, A.J.18
-
5
-
-
33947581039
-
Phase 1 and pharmacologic study of MS-275, a histone deacetylase inhibitor, in adults with refractory and relapsed acute leukemias
-
DOI 10.1182/blood-2006-05-021873
-
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(7):2781-90. (Pubitemid 46482071)
-
(2007)
Blood
, vol.109
, Issue.7
, pp. 2781-2790
-
-
Gojo, I.1
Jiemjit, A.2
Trepel, J.B.3
Sparreboom, A.4
Figg, W.D.5
Rollins, S.6
Tidwell, M.L.7
Greer, J.8
Eun, J.C.9
Lee, M.-J.10
Gore, S.D.11
Sausville, E.A.12
Zwiebel, J.13
Karp, J.E.14
-
6
-
-
51649091668
-
A phase i and pharmacokinetic study of the oral histone deacetylase inhibitor, MS-275, in patients with refractory solid tumors and lymphomas
-
Gore L, Rothenberg ML, O'Bryant CL, et al. A phase I and pharmacokinetic study of the oral histone deacetylase inhibitor, MS-275, in patients with refractory solid tumors and lymphomas. Clin Cancer Res 2008;14(14):4517-25.
-
(2008)
Clin Cancer Res
, vol.14
, Issue.14
, pp. 4517-4525
-
-
Gore, L.1
Rothenberg, M.L.2
O'Bryant, C.L.3
-
7
-
-
58149377828
-
Multicenter phase II trial of the histone deacetylase inhibitor pyridylmethyl-N-{4-[(2-aminophenyl)-carbamoyl]-benzyl}-carbamate in pretreated metastatic melanoma
-
Hauschild A, Trefzer U, Garbe C, et al. Multicenter phase II trial of the histone deacetylase inhibitor pyridylmethyl-N-{4-[(2-aminophenyl)-carbamoyl]- benzyl}-carbamate in pretreated metastatic melanoma. Melanoma Res 2008;18(4):274-8.
-
(2008)
Melanoma Res
, vol.18
, Issue.4
, pp. 274-278
-
-
Hauschild, A.1
Trefzer, U.2
Garbe, C.3
-
8
-
-
34547897023
-
Histone deacetylases and cancer
-
DOI 10.1038/sj.onc.1210610, PII 1210610
-
Glozak MA, Seto E. Histone deacetylases and cancer. Oncogene 2007;26(37):5420-32 (Pubitemid 47255924)
-
(2007)
Oncogene
, vol.26
, Issue.37
, pp. 5420-5432
-
-
Glozak, M.A.1
Seto, E.2
-
9
-
-
33750036141
-
Histone deacetylase inhibitors in cancer therapy
-
DOI 10.1080/07357900600814979, PII W7P41387608366P0
-
Fouladi M. Histone deacetylase inhibitors in cancer therapy. Cancer Invest 2006;24(5):521-7 (Pubitemid 44576406)
-
(2006)
Cancer Investigation
, vol.24
, Issue.5
, pp. 521-527
-
-
Fouladi, M.1
-
10
-
-
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. 3958-3969
-
-
Prince, H.M.1
Bishton, M.J.2
Harrison, S.J.3
-
11
-
-
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
-
12
-
-
33845996135
-
Phase 2 trial of oral vorinostat (suberoylanilide hydroxamic acid, SAHA) for refractory cutaneous T-cell lymphoma (CTCL)
-
DOI 10.1182/blood-2006-06-025999
-
Duvic M, Talpur R, Ni X, et al. Phase 2 trial of oral vorinostat (suberoylanilide hydroxamic acid, SAHA) for refractory cutaneous T-cell lymphoma (CTCL). Blood 2007;109(1):31-9. (Pubitemid 46053039)
-
(2007)
Blood
, vol.109
, Issue.1
, pp. 31-39
-
-
Duvic, M.1
Talpur, R.2
Ni, X.3
Zhang, C.4
Hazarika, P.5
Kelly, C.6
Chiao, J.H.7
Reilly, J.F.8
Ricker, J.L.9
Richon, V.M.10
Frankel, S.R.11
-
13
-
-
36148950997
-
FDA approval summary: Vorinostat for treatment of advanced primary cutaneous T-cell lymphoma
-
DOI 10.1634/theoncologist.12-10-1247
-
Mann BS, Johnson JR, Cohen MH, et al. FDA approval summary: vorinostat for treatment of advanced primary cutaneous T-cell lymphoma. Oncologist 2007;12(10):1247-52 (Pubitemid 350106355)
-
(2007)
Oncologist
, vol.12
, Issue.10
, pp. 1247-1252
-
-
Mann, B.S.1
Johnson, J.R.2
Cohen, M.H.3
Justice, R.4
Pazdur, R.5
-
14
-
-
77749309291
-
Romidepsin for the treatment of cutaneous T-cell lymphoma
-
Campas-Moya C. Romidepsin for the treatment of cutaneous T-cell lymphoma. Drugs Today (Barc) 2009;45(11):787-95
-
(2009)
Drugs Today (Barc)
, vol.45
, Issue.11
, pp. 787-795
-
-
Campas-Moya, C.1
-
15
-
-
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;27(32):5410-17.
-
(2009)
J Clin Oncol
, vol.27
, Issue.32
, pp. 5410-5417
-
-
Piekarz, R.L.1
Frye, R.2
Turner, M.3
-
16
-
-
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. 431-436
-
-
Copeland, A.1
Buglio, D.2
Younes, A.3
-
17
-
-
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
-
18
-
-
0033614993
-
Synthesis and histone deacetylase inhibitory activity of new benzamide derivatives
-
DOI 10.1021/jm980565u
-
Suzuki T, Ando T, Tsuchiya K, et al. Synthesis and histone deacetylase inhibitory activity of new benzamide derivatives. J Med Chem 1999;42(15):3001-3. (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
-
19
-
-
31944444233
-
The benzamide MS-275 is a potent, long-lasting brain region-selective inhibitor of histone deacetylases
-
DOI 10.1073/pnas.0510341103
-
Simonini MV, Camargo LM, Dong E, et al. The benzamide MS-275 is a potent, long-lasting brain region-selective inhibitor of histone deacetylases. Proc Natl Acad Sci USA 2006;103(5):1587-92 (Pubitemid 43191209)
-
(2006)
Proceedings of the National Academy of Sciences of the United States of America
, vol.103
, Issue.5
, pp. 1587-1592
-
-
Simonini, M.V.1
Camargo, L.M.2
Dong, E.3
Maloku, E.4
Veldic, M.5
Costa, E.6
Guidotti, A.7
-
20
-
-
29244453236
-
Interspecies differences in plasma protein binding of MS-275, a novel histone deacetylase inhibitor
-
DOI 10.1007/s00280-005-0058-8
-
Acharya MR, Sparreboom A, Sausville EA, et al. Interspecies differences in plasma protein binding of MS-275, a novel histone deacetylase inhibitor. Cancer Chemother Pharmacol 2006;57(3):275-81 (Pubitemid 41827349)
-
(2006)
Cancer Chemotherapy and Pharmacology
, vol.57
, Issue.3
, pp. 275-281
-
-
Acharya, M.R.1
Sparreboom, A.2
Sausville, E.A.3
Conley, B.A.4
Doroshow, J.H.5
Venitz, J.6
Figg, W.D.7
-
21
-
-
33745031006
-
Factors affecting the pharmacokinetic profile of MS-275, a novel histone deacetylase inhibitor, in patients with cancer
-
DOI 10.1007/s10637-005-5707-6
-
Acharya MR, Karp JE, Sausville EA, et al. Factors affecting the pharmacokinetic profile of MS-275, a novel histone deacetylase inhibitor, in patients with cancer. Invest New Drugs 2006;24(5):367-75 (Pubitemid 43876072)
-
(2006)
Investigational New Drugs
, vol.24
, Issue.5
, pp. 367-375
-
-
Acharya, M.R.1
Karp, J.E.2
Sausville, E.A.3
Hwang, K.4
Ryan, Q.5
Gojo, I.6
Venitz, J.7
Figg, W.D.8
Sparreboom, A.9
-
22
-
-
70349395570
-
Anti-leukemia activity of MS-275 histone deacetylase inhibitor implicates 4-1BBL/4-1BB immunomodulatory functions
-
Vire B, de Walque S, Restouin A, et al. Anti-leukemia activity of MS-275 histone deacetylase inhibitor implicates 4-1BBL/4-1BB immunomodulatory functions. PLoS One 2009;4(9):e7085
-
(2009)
PLoS One
, vol.4
, Issue.9
-
-
Vire, B.1
De Walque, S.2
Restouin, A.3
-
23
-
-
20744449274
-
Blockade of histone deacetylase inhibitor-induced RelA/p65 acetylation and NF-κB activation potentiates apoptosis in leukemia cells through a process mediated by oxidative damage, XIAP downregulation, and c-Jun N-terminal kinase 1 activation
-
DOI 10.1128/MCB.25.13.5429-5444.2005
-
Dai Y, Rahmani M, Dent P, Grant S. Blockade of histone deacetylase inhibitor-induced RelA/p65 acetylation and NF-kappaB activation potentiates apoptosis in leukemia cells through a process mediated by oxidative damage, XIAP downregulation, and c-Jun Nterminal kinase 1 activation. Mol Cell Biol 2005;25(13):5429-44 (Pubitemid 40853579)
-
(2005)
Molecular and Cellular Biology
, vol.25
, Issue.13
, pp. 5429-5444
-
-
Dai, Y.1
Rahmani, M.2
Dent, P.3
Grant, S.4
-
24
-
-
57849141586
-
Blockade of mTOR signaling potentiates the ability of histone deacetylase inhibitor to induce growth arrest and differentiation of acute myelogenous leukemia cells
-
Nishioka C, Ikezoe T, Yang J, et al. Blockade of mTOR signaling potentiates the ability of histone deacetylase inhibitor to induce growth arrest and differentiation of acute myelogenous leukemia cells. Leukemia 2008;22(12):2159-68.
-
(2008)
Leukemia
, vol.22
, Issue.12
, pp. 2159-2168
-
-
Nishioka, C.1
Ikezoe, T.2
Yang, J.3
-
25
-
-
34447096461
-
HDAC inhibitors induce apoptosis in glucocorticoid-resistant acute lymphatic leukemia cells despite a switch from the extrinsic to the intrinsic death pathway
-
DOI 10.1016/j.biocel.2007.03.009, PII S1357272507000866
-
Tsapis M, Lieb M, Manzo F, et al. HDAC inhibitors induce apoptosis in glucocorticoid-resistant acute lymphatic leukemia cells despite a switch from the extrinsic to the intrinsic death pathway. Int J Biochem Cell Biol 2007;39(7-8):1500-9 (Pubitemid 47031039)
-
(2007)
International Journal of Biochemistry and Cell Biology
, vol.39
, Issue.7-8
, pp. 1500-1509
-
-
Tsapis, M.1
Lieb, M.2
Manzo, F.3
Shankaranarayanan, P.4
Herbrecht, R.5
Lutz, P.6
Gronemeyer, H.7
-
26
-
-
3142689788
-
The histone deacetylase inhibitor MS-275 induces caspase-dependent apoptosis in B-cell chronic lymphocytic leukemia cells
-
DOI 10.1038/sj.leu.2403388
-
Lucas DM, Davis ME, Parthun MR, et al. The histone deacetylase inhibitor MS-275 induces caspase-dependent apoptosis in B-cell chronic lymphocytic leukemia cells. Leukemia 2004;18(7):1207-14 (Pubitemid 39023130)
-
(2004)
Leukemia
, vol.18
, Issue.7
, pp. 1207-1214
-
-
Lucas, D.M.1
Davis, M.E.2
Parthun, M.R.3
Mone, A.P.4
Kitada, S.5
Cunningham, K.D.6
Flax, E.L.7
Wickham, J.8
Reed, J.C.9
Byrd, J.C.10
Grever, M.R.11
-
27
-
-
11144356134
-
The histone deacetylase inhibitor MS-275 interacts synergistically with fludarabine to induce apoptosis in human leukemia cells
-
DOI 10.1158/0008-5472.CAN-03-2631
-
Maggio SC, Rosato RR, Kramer LB, et al. The histone deacetylase inhibitor MS-275 interacts synergistically with fludarabine to induce apoptosis in human leukemia cells. Cancer Res 2004;64(7):2590-600 (Pubitemid 38523917)
-
(2004)
Cancer Research
, vol.64
, Issue.7
, pp. 2590-2600
-
-
Maggio, S.C.1
Rosato, R.R.2
Kramer, L.B.3
Dai, Y.4
Rahmani, M.5
Paik, D.S.6
Czarnik, A.C.7
Payne, S.G.8
Spiegel, S.9
Grant, S.10
-
28
-
-
0038079767
-
CIP1/WAF1
-
Rosato RR, Almenara JA, Grant S. The histone deacetylase inhibitor MS-275 promotes differentiation or apoptosis in human leukemia cells through a process regulated by generation of reactive oxygen species and induction of p21CIP1/WAF1 1. Cancer Res 2003;63(13):3637-45 (Pubitemid 36793047)
-
(2003)
Cancer Research
, vol.63
, Issue.13
, pp. 3637-3645
-
-
Rosato, R.R.1
Almenara, J.A.2
Grant, S.3
-
29
-
-
47549090091
-
waf1 promoter in acute myelogenous leukemia cell
-
DOI 10.1038/sj.leu.2405079, PII 2405079
-
Nishioka C, Ikezoe T, Yang J, et al. Inhibition of MEK/ERK signaling synergistically potentiates histone deacetylase inhibitor-induced growth arrest, apoptosis and acetylation of histone H3 on p21waf1 promoter in acute myelogenous leukemia cell. Leukemia 2008;22(7):1449-52 (Pubitemid 352006093)
-
(2008)
Leukemia
, vol.22
, Issue.7
, pp. 1449-1452
-
-
Nishioka, C.1
Ikezoe, T.2
Yang, J.3
Koeffler, H.P.4
Yokoyama, A.5
-
30
-
-
43049173740
-
MS-275, a novel histone deacetylase inhibitor with selectivity against HDAC1, induces degradation of FLT3 via inhibition of chaperone function of heat shock protein 90 in AML cells
-
Nishioka C, Ikezoe T, Yang J, et al. MS-275, a novel histone deacetylase inhibitor with selectivity against HDAC1, induces degradation of FLT3 via inhibition of chaperone function of heat shock protein 90 in AML cells. Leuk Res 2008;32(9):1382-92
-
(2008)
Leuk Res
, vol.32
, Issue.9
, pp. 1382-1392
-
-
Nishioka, C.1
Ikezoe, T.2
Yang, J.3
-
31
-
-
34347375499
-
NPI-0052, a novel proteasome inhibitor, induces caspase-8 and ROS-dependent apoptosis alone and in combination with HDAC inhibitors in leukemia cells
-
DOI 10.1182/blood-2006-03-013128
-
Miller CP, Ban K, Dujka ME, et al. NPI-0052, a novel proteasome inhibitor, induces caspase-8 and ROS-dependent apoptosis alone and in combination with HDAC inhibitors in leukemia cells. Blood 2007;110(1):267-77 (Pubitemid 47026844)
-
(2007)
Blood
, vol.110
, Issue.1
, pp. 267-277
-
-
Miller, C.P.1
Ban, K.2
Dujka, M.E.3
McConkey, D.J.4
Munsell, M.5
Palladino, M.6
Chandra, J.7
-
32
-
-
40049097050
-
Potentiation of reactive oxygen species is a marker for synergistic cytotoxicity of MS-275 and 5-azacytidine in leukemic cells
-
DOI 10.1016/j.leukres.2007.09.007, PII S0145212607003463
-
Gao S, Mobley A, Miller C, et al. Potentiation of reactive oxygen species is a marker for synergistic cytotoxicity of MS-275 and 5-azacytidine in leukemic cells. Leuk Res 2008;32(5):771-80 (Pubitemid 351323931)
-
(2008)
Leukemia Research
, vol.32
, Issue.5
, pp. 771-780
-
-
Gao, S.1
Mobley, A.2
Miller, C.3
Boklan, J.4
Chandra, J.5
-
33
-
-
77955675650
-
HDAC inhibition synergistically enhances alkylator-induced DNA damage responses and apoptosis in multiple myeloma cells
-
Lee CK, Wang S, Huang X, et al. HDAC inhibition synergistically enhances alkylator-induced DNA damage responses and apoptosis in multiple myeloma cells. Cancer Lett 2010;296(2):233-40
-
(2010)
Cancer Lett
, vol.296
, Issue.2
, pp. 233-240
-
-
Lee, C.K.1
Wang, S.2
Huang, X.3
-
34
-
-
33646839799
-
Sequence-dependent interaction between cisplatin and histone deacetylase inhibitors in human oral squamous cell carcinoma cells
-
Sato T, Suzuki M, Sato Y, et al. Sequence-dependent interaction between cisplatin and histone deacetylase inhibitors in human oral squamous cell carcinoma cells. Int J Oncol 2006;28(5):1233-41
-
(2006)
Int J Oncol
, vol.28
, Issue.5
, pp. 1233-1241
-
-
Sato, T.1
Suzuki, M.2
Sato, Y.3
-
35
-
-
70449367075
-
Efficacy of MS-275, a selective inhibitor of class i histone deacetylases, in human colon cancer models
-
Bracker TU, Sommer A, Fichtner I, et al. Efficacy of MS-275, a selective inhibitor of class I histone deacetylases, in human colon cancer models. Int J Oncol 2009;35(4):909-20
-
(2009)
Int J Oncol
, vol.35
, Issue.4
, pp. 909-920
-
-
Bracker, T.U.1
Sommer, A.2
Fichtner, I.3
-
36
-
-
67949123074
-
HDAC inhibitors, MS275 and SBHA, enhances cytotoxicity induced by oxaliplatin in the colorectal cancer cell lines
-
Flis S, Gnyszka A, Splawinski J. HDAC inhibitors, MS275 and SBHA, enhances cytotoxicity induced by oxaliplatin in the colorectal cancer cell lines. Biochem Biophys Res Commun 2009;387(2):336-41
-
(2009)
Biochem Biophys Res Commun
, vol.387
, Issue.2
, pp. 336-341
-
-
Flis, S.1
Gnyszka, A.2
Splawinski, J.3
-
37
-
-
73449126835
-
MS275 enhances cytotoxicity induced by 5-fluorouracil in the colorectal cancer cells
-
Flis S, Gnyszka A, Flis K, Splawinski J. MS275 enhances cytotoxicity induced by 5-fluorouracil in the colorectal cancer cells. Eur J Pharmacol 2010;627(1-3):26-32
-
(2010)
Eur J Pharmacol
, vol.627
, Issue.1-3
, pp. 26-32
-
-
Flis, S.1
Gnyszka, A.2
Flis, K.3
Splawinski, J.4
-
38
-
-
2342564962
-
Histone deacetylase inhibitors FK228, N-(2-aminophenyl)-4-[N-(pyridin-3- yl-methoxycarbonyl)amino-methyl]benzamide and m-carboxycinnamic acid bis-hydroxamide augment radiation-induced cell death in gastrointestinal adenocarcinoma cells
-
DOI 10.1002/ijc.20117
-
Zhang Y, Adachi M, Zhao X, et al. Histone deacetylase inhibitors FK228, N-(2-aminophenyl)-4-[N-(pyridin-3-ylmethoxycarbonyl) amino-methyl] benzamide and m-carboxycinnamic acid bis-hydroxamide augment radiation-induced cell death in gastrointestinal adenocarcinoma cells. Int J Cancer 2004;110(2):301-8 (Pubitemid 38580407)
-
(2004)
International Journal of Cancer
, vol.110
, Issue.2
, pp. 301-308
-
-
Zhang, Y.1
Adachi, M.2
Zhao, X.3
Kawamura, R.4
Imai, K.5
-
39
-
-
78751512281
-
Combination therapy with Vidaza and entinostat suppresses tumor growth and reprograms the epigenome in an orthotopic lung cancer model
-
Belinsky SA, Grimes MJ, Picchi MA, et al. Combination therapy with Vidaza and entinostat suppresses tumor growth and reprograms the epigenome in an orthotopic lung cancer model. Cancer Res 2011;71(2):454-62.
-
(2011)
Cancer Res
, vol.71
, Issue.2
, pp. 454-462
-
-
Belinsky, S.A.1
Grimes, M.J.2
Picchi, M.A.3
-
40
-
-
63549083115
-
ErbB-3 expression is associated with E-cadherin and their coexpression restores response to gefitinib in non-small-cell lung cancer (NSCLC)
-
Witta SE, Dziadziuszko R, Yoshida K, et al. ErbB-3 expression is associated with E-cadherin and their coexpression restores response to gefitinib in non-small-cell lung cancer (NSCLC). Ann Oncol 2009;20(4):689-95
-
(2009)
Ann Oncol
, vol.20
, Issue.4
, pp. 689-695
-
-
Witta, S.E.1
Dziadziuszko, R.2
Yoshida, K.3
-
41
-
-
78650791916
-
Histone deacetylase inhibitors downregulate checkpoint kinase 1 expression to induce cell death in non-small cell lung cancer cells
-
Brazelle W, Kreahling JM, Gemmer J, et al. Histone deacetylase inhibitors downregulate checkpoint kinase 1 expression to induce cell death in non-small cell lung cancer cells. PLoS ONE 2010;5(12):e14335
-
(2010)
PLoS ONE
, vol.5
, Issue.12
-
-
Brazelle, W.1
Kreahling, J.M.2
Gemmer, J.3
-
42
-
-
74249112953
-
Induction of E-cadherin in lung cancer and interaction with growth suppression by histone deacetylase inhibition
-
Kakihana M, Ohira T, Chan D, et al. Induction of E-cadherin in lung cancer and interaction with growth suppression by histone deacetylase inhibition. J Thorac Oncol 2009;4(12):1455-65
-
(2009)
J Thorac Oncol
, vol.4
, Issue.12
, pp. 1455-1465
-
-
Kakihana, M.1
Ohira, T.2
Chan, D.3
-
43
-
-
31544452076
-
Restoring E-cadherin expression increases sensitivity to epidermal growth factor receptor inhibitors in lung cancer cell lines
-
DOI 10.1158/0008-5472.CAN-05-1988
-
Witta SE, Gemmill RM, Hirsch FR, et al. Restoring E-cadherin expression increases sensitivity to epidermal growth factor receptor inhibitors in lung cancer cell lines. Cancer Res 2006;66(2):944-50 (Pubitemid 43165962)
-
(2006)
Cancer Research
, vol.66
, Issue.2
, pp. 944-950
-
-
Witta, S.E.1
Gemmill, R.M.2
Hirsch, F.R.3
Coldren, C.D.4
Hedman, K.5
Ravdel, L.6
Helfrich, B.7
Dziadziuszko, R.8
Chan, D.C.9
Sugita, M.10
Chan, Z.11
Baron, A.12
Franklin, W.13
Drabkin, H.A.14
Girard, L.15
Gazdar, A.F.16
Minna, J.D.17
Bunn Jr., P.A.18
-
44
-
-
34547662889
-
Antitumor activity of the histone deacetylase inhibitor MS-275 in prostate cancer models
-
DOI 10.1002/pros.20611
-
Qian DZ, Wei YF, Wang X, et al. Antitumor activity of the histone deacetylase inhibitor MS-275 in prostate cancer models. Prostate 2007;67(11):1182-93 (Pubitemid 47221885)
-
(2007)
Prostate
, vol.67
, Issue.11
, pp. 1182-1193
-
-
Qian, D.Z.1
Wei, Y.-F.2
Wang, X.3
Kato, Y.4
Cheng, L.5
Pili, R.6
-
45
-
-
54449089024
-
Chemical targeting of the innate antiviral response by histone deacetylase inhibitors renders refractory cancers sensitive to viral oncolysis
-
Nguyen TL, Abdelbary H, Arguello M, et al. Chemical targeting of the innate antiviral response by histone deacetylase inhibitors renders refractory cancers sensitive to viral oncolysis. Proc Natl Acad Sci USA 2008;105(39):14981-6
-
(2008)
Proc Natl Acad Sci USA
, vol.105
, Issue.39
, pp. 14981-6
-
-
Nguyen, T.L.1
Abdelbary, H.2
Arguello, M.3
-
46
-
-
57349093914
-
Defining the molecular action of HDAC inhibitors and synergism with androgen deprivation in ERG-positive prostate cancer
-
Bjorkman M, Iljin K, Halonen P, et al. Defining the molecular action of HDAC inhibitors and synergism with androgen deprivation in ERG-positive prostate cancer. Int J Cancer 2008;123(12):2774-81
-
(2008)
Int J Cancer
, vol.123
, Issue.12
, pp. 2774-2781
-
-
Bjorkman, M.1
Iljin, K.2
Halonen, P.3
-
47
-
-
1642576220
-
Enhanced Radiation-Induced Cell Killing and Prolongation of γH2AX Foci Expression by the Histone Deacetylase Inhibitor MS-275
-
DOI 10.1158/0008-5472.CAN-03-2630
-
Camphausen K, Burgan W, Cerra M, et al. Enhanced radiation-induced cell killing and prolongation of gammaH2AX foci expression by the histone deacetylase inhibitor MS-275. Cancer Res 2004;64(1):316-21 (Pubitemid 38114113)
-
(2004)
Cancer Research
, vol.64
, Issue.1
, pp. 316-321
-
-
Camphausen, K.1
Burgan, W.2
Cerra, M.3
Oswald, K.A.4
Trepel, J.B.5
Lee, M.-J.6
Tofilon, P.J.7
-
48
-
-
4644259264
-
Enhancement of xenograft tumor radiosensitivity by the histone deacetylase inhibitor MS-275 and correlation with histone hyperacetylation
-
DOI 10.1158/1078-0432.CCR-04-0537
-
Camphausen K, Scott T, Sproull M, Tofilon PJ. Enhancement of xenograft tumor radiosensitivity by the histone deacetylase inhibitor MS-275 and correlation with histone hyperacetylation. Clin Cancer Res 2004;10(18 Pt 1):6066-71 (Pubitemid 39302609)
-
(2004)
Clinical Cancer Research
, vol.10
, Issue.18
, pp. 6066-6071
-
-
Camphausen, K.1
Scott, T.2
Sproull, M.3
Tofilon, P.J.4
-
49
-
-
34347206854
-
Histone deacetylase inhibitors sensitize prostate cancer cells to agents that produce DNA double-strand breaks by targeting Ku70 acetylation
-
Chen CS, Wang YC, Yang HC, et al. Histone deacetylase inhibitors sensitize prostate cancer cells to agents that produce DNA double-strand breaks by targeting Ku70 acetylation. Cancer Res 2007;67(11):5318-27.
-
(2007)
Cancer Res
, vol.67
, Issue.11
, pp. 5318-5327
-
-
Chen, C.S.1
Wang, Y.C.2
Yang, H.C.3
-
50
-
-
53949108746
-
Histone deacetylase inhibitors sensitize tumour cells for cytotoxic effects of natural killer cells
-
Schmudde M, Braun A, Pende D, et al. Histone deacetylase inhibitors sensitize tumour cells for cytotoxic effects of natural killer cells. Cancer Lett 2008;272(1):110-21
-
(2008)
Cancer Lett
, vol.272
, Issue.1
, pp. 110-121
-
-
Schmudde, M.1
Braun, A.2
Pende, D.3
-
51
-
-
40949102209
-
Improved synthesis of histone deacetylase inhibitors (HDIs) (MS-275 and CI-994) and inhibitory effects of HDIs alone or in combination with RAMBAs or retinoids on growth of human LNCaP prostate cancer cells and tumor xenografts
-
DOI 10.1016/j.bmc.2007.12.007, PII S0968089607010577
-
Gediya LK, Belosay A, Khandelwal A, et al. Improved synthesis of histone deacetylase inhibitors (HDIs) (MS-275 and CI-994) and inhibitory effects of HDIs alone or in combination with RAMBAs or retinoids on growth of human LNCaP prostate cancer cells and tumor xenografts. Bioorg Med Chem 2008;16(6):3352-60 (Pubitemid 351418177)
-
(2008)
Bioorganic and Medicinal Chemistry
, vol.16
, Issue.6
, pp. 3352-3360
-
-
Gediya, L.K.1
Belosay, A.2
Khandelwal, A.3
Purushottamachar, P.4
Njar, V.C.O.5
-
52
-
-
41649115195
-
MS-275 synergistically enhances the growth inhibitory effects of RAMBA VN/66-1 in hormone-insensitive PC-3 prostate cancer cells and tumours
-
DOI 10.1038/sj.bjc.6604295, PII 6604295
-
Khandelwal A, Gediya L, Njar V. MS-275 synergistically enhances the growth inhibitory effects of RAMBA VN/66-1 in hormone-insensitive PC-3 prostate cancer cells and tumours. Br J Cancer 2008;98(7):1234-43 (Pubitemid 351481680)
-
(2008)
British Journal of Cancer
, vol.98
, Issue.7
, pp. 1234-1243
-
-
Khandelwal, A.1
Gediya, L.K.2
Njar, V.C.O.3
-
53
-
-
68049121594
-
DNER, an epigenetically modulated gene, regulates glioblastoma-derived neurosphere cell differentiation and tumor propagation
-
Sun P, Xia S, Lal B, et al. DNER, an epigenetically modulated gene, regulates glioblastoma-derived neurosphere cell differentiation and tumor propagation. Stem Cells 2009;27(7):1473-86
-
(2009)
Stem Cells
, vol.27
, Issue.7
, pp. 1473-1486
-
-
Sun, P.1
Xia, S.2
Lal, B.3
-
54
-
-
33745073751
-
Experimental therapy of malignant gliomas using the inhibitor of histone deacetylase MS-275
-
DOI 10.1158/1535-7163.MCT-05-0533
-
Eyupoglu IY, Hahnen E, Trankle C, et al. Experimental therapy of malignant gliomas using the inhibitor of histone deacetylase MS-275. Mol Cancer Ther 2006;5(5):1248-55 (Pubitemid 43881317)
-
(2006)
Molecular Cancer Therapeutics
, vol.5
, Issue.5
, pp. 1248-1255
-
-
Eyupoglu, I.Y.1
Hahnen, E.2
Trankle, C.3
Savaskan, N.E.4
Siebzehnrubl, F.A.5
Buslei, R.6
Lemke, D.7
Wick, W.8
Fahlbusch, R.9
Blumcke, I.10
-
55
-
-
79952237710
-
Functional activation of the Estrogen Receptor-alpha and aromatase by the HDAC inhibitor entinostat sensitizes ER-negative tumors to letrozole
-
Sabnis GJ, Goloubeva O, Chumsri S, et al. Functional activation of the Estrogen Receptor-alpha and aromatase by the HDAC inhibitor entinostat sensitizes ER-negative tumors to letrozole. Cancer Res 2011;71(5):1893-903.
-
(2011)
Cancer Res
, vol.71
, Issue.5
, pp. 1893-903
-
-
Sabnis, G.J.1
Goloubeva, O.2
Chumsri, S.3
-
56
-
-
70350540711
-
HDAC inhibitor SNDX-275 induces apoptosis in erbB2-overexpressing breast cancer cells via down-regulation of erbB3 expression
-
Huang X, Gao L, Wang S, et al. HDAC inhibitor SNDX-275 induces apoptosis in erbB2-overexpressing breast cancer cells via down-regulation of erbB3 expression. Cancer Res 2009;69(21):8403-11
-
(2009)
Cancer Res
, vol.69
, Issue.21
, pp. 8403-8411
-
-
Huang, X.1
Gao, L.2
Wang, S.3
-
57
-
-
22744437647
-
HDAC inhibitors enhance the apoptosis-inducing potential of TRAIL in breast carcinoma
-
DOI 10.1038/sj.onc.1208585
-
Singh TR, Shankar S, Srivastava RK. HDAC inhibitors enhance the apoptosis-inducing potential of TRAIL in breast carcinoma. Oncogene 2005;24(29):4609-23 (Pubitemid 41032599)
-
(2005)
Oncogene
, vol.24
, Issue.29
, pp. 4609-4623
-
-
Singh, T.R.1
Shankar, S.2
Srivastava, R.K.3
-
58
-
-
78650443648
-
MS-275 sensitizes TRAIL-resistant breast cancer cells inhibits angiogenesis and metastasis and reverses epithelial-mesenchymal transition in vivo
-
Srivastava RK, Kurzrock R, Shankar S. MS-275 sensitizes TRAIL-resistant breast cancer cells, inhibits angiogenesis and metastasis, and reverses epithelial-mesenchymal transition in vivo. Mol Cancer Ther 2010;9(12):3254-66.
-
(2010)
Mol Cancer Ther
, vol.9
, Issue.12
, pp. 3254-3266
-
-
Srivastava, R.K.1
Kurzrock, R.2
Shankar, S.3
-
59
-
-
0035113602
-
MS-275, a histone deacetylase inhibitor, selectively induces transforming growth factor β type II receptor expression in human breast cancer cells
-
Lee BI, Park SH, Kim JW, et al. MS-275, a histone deacetylase inhibitor, selectively induces transforming growth factor beta type II receptor expression in human breast cancer cells. Cancer Res 2001;61(3):931-4 (Pubitemid 32174406)
-
(2001)
Cancer Research
, vol.61
, Issue.3
, pp. 931-934
-
-
Lee, B.I.1
Park, S.H.2
Kim, J.W.3
Sausville, E.A.4
Kim, H.T.5
Nakanishi, O.6
Trepel, J.B.7
Kim, S.-J.8
-
60
-
-
53049107304
-
Sp1-mediated TRAIL induction in chemosensitization
-
Xu J, Zhou JY, Wei WZ, et al. Sp1-mediated TRAIL induction in chemosensitization. Cancer Res 2008;68(16):6718-26
-
(2008)
Cancer Res
, vol.68
, Issue.16
, pp. 6718-6726
-
-
Xu, J.1
Zhou, J.Y.2
Wei, W.Z.3
-
61
-
-
78149397645
-
Experimental study on inhibitory effects of histone deacetylase inhibitor MS-275 and TSA on bladder cancer cells
-
Qu W, Kang YD, Zhou MS, et al. Experimental study on inhibitory effects of histone deacetylase inhibitor MS-275 and TSA on bladder cancer cells. Urol Oncol 2010;28(6):648-54
-
(2010)
Urol Oncol
, vol.28
, Issue.6
, pp. 648-654
-
-
Qu, W.1
Kang, Y.D.2
Zhou, M.S.3
-
62
-
-
33846813964
-
Antiproliferative and proapoptotic effects of histone deacetylase inhibitors on gastrointestinal neuroendocrine tumor cells
-
DOI 10.1677/erc.1.01249
-
Baradari V, Huether A, Hopfner M, et al. Antiproliferative and proapoptotic effects of histone deacetylase inhibitors on gastrointestinal neuroendocrine tumor cells. Endocr Relat Cancer 2006;13(4):1237-50 (Pubitemid 46212577)
-
(2006)
Endocrine-Related Cancer
, vol.13
, Issue.4
, pp. 1237-1250
-
-
Baradari, V.1
Huether, A.2
Hopfner, M.3
Schuppan, D.4
Scherubl, H.5
-
63
-
-
49749146742
-
Differential responsiveness of human hepatoma cells versus normal hepatocytes to TRAIL in combination with either histone deacetylase inhibitors or conventional cytostatics
-
Dzieran J, Beck JF, Sonnemann J. Differential responsiveness of human hepatoma cells versus normal hepatocytes to TRAIL in combination with either histone deacetylase inhibitors or conventional cytostatics. Cancer Sci 2008;99(8):1685-92.
-
(2008)
Cancer Sci
, vol.99
, Issue.8
, pp. 1685-1692
-
-
Dzieran, J.1
Beck, J.F.2
Sonnemann, J.3
-
64
-
-
58149359340
-
The histone-deacetylase inhibitor MS-275 and the CDK-inhibitor CYC-202 promote anti-tumor effects in hepatoma cell lines
-
Gahr S, Peter G, Wissniowski TT, et al. The histone-deacetylase inhibitor MS-275 and the CDK-inhibitor CYC-202 promote anti-tumor effects in hepatoma cell lines. Oncol Rep 2008;20(5):1249-56
-
(2008)
Oncol Rep
, vol.20
, Issue.5
, pp. 1249-1256
-
-
Gahr, S.1
Peter, G.2
Wissniowski, T.T.3
-
65
-
-
20944436158
-
Epigenetic modulation of retinoic acid receptor β2 by the histone deacetylase inhibitor MS-275 in human renal cell carcinoma
-
DOI 10.1158/1078-0432.CCR-04-1092
-
Wang XF, Qian DZ, Ren M, et al. Epigenetic modulation of retinoic acid receptor beta2 by the histone deacetylase inhibitor MS-275 in human renal cell carcinoma. Clin Cancer Res 2005;11(9):3535-42 (Pubitemid 40627909)
-
(2005)
Clinical Cancer Research
, vol.11
, Issue.9
, pp. 3535-3542
-
-
Wang, X.-F.1
Qian, D.Z.2
Ren, M.3
Kato, Y.4
Wei, Y.5
Zhang, L.6
Fansler, Z.7
Clark, D.8
Nakanishi, O.9
Pili, R.10
-
66
-
-
34547653955
-
Synergistic in vivo antitumor effect of the histone deacetylase inhibitor MS-275 in combination with interleukin 2 in a murine model of renal cell carcinoma
-
DOI 10.1158/1078-0432.CCR-07-0014
-
Kato Y, Yoshimura K, Shin T, et al. Synergistic in vivo antitumor effect of the histone deacetylase inhibitor MS-275 in combination with interleukin 2 in a murine model of renal cell carcinoma. Clin Cancer Res 2007;13(15 Pt 1):4538-46. (Pubitemid 47219724)
-
(2007)
Clinical Cancer Research
, vol.13
, Issue.15
, pp. 4538-4546
-
-
Kato, Y.1
Yoshimura, K.2
Shin, T.3
Verheul, H.4
Hammers, H.5
Sanni, T.B.6
Salumbides, B.C.7
Van Erp, K.8
Schulick, R.9
Pili, R.10
-
67
-
-
37349022318
-
Ex vivo therapy of malignant melanomas transplanted into organotypic brain slice cultures using inhibitors of histone deacetylases
-
Holsken A, Eyupoglu IY, Lueders M, et al. Ex vivo therapy of malignant melanomas transplanted into organotypic brain slice cultures using inhibitors of histone deacetylases. Acta Neuropathol 2006;112(2):205-15
-
(2006)
Acta Neuropathol
, vol.112
, Issue.2
, pp. 205-215
-
-
Holsken, A.1
Eyupoglu, I.Y.2
Lueders, M.3
-
68
-
-
49849098245
-
Histone deacetylase inhibitors induce growth arrest, apoptosis, and differentiation in clear cell sarcoma models
-
Liu S, Cheng H, Kwan W, et al. Histone deacetylase inhibitors induce growth arrest, apoptosis, and differentiation in clear cell sarcoma models. Mol Cancer Ther 2008;7(6):1751-61
-
(2008)
Mol Cancer Ther
, vol.7
, Issue.6
, pp. 1751-1761
-
-
Liu, S.1
Cheng, H.2
Kwan, W.3
-
69
-
-
34548668194
-
Histone deacetylase inhibitor MS-275 alone or combined with bortezomib or sorafenib exhibits strong antiproliferative action in human cholangiocarcinoma cells
-
Baradari V, Hopfner M, Huether A, et al. Histone deacetylase inhibitor MS-275 alone or combined with bortezomib or sorafenib exhibits strong antiproliferative action in human cholangiocarcinoma cells. World J Gastroenterol 2007;13(33):4458-66 (Pubitemid 47412408)
-
(2007)
World Journal of Gastroenterology
, vol.13
, Issue.33
, pp. 4458-4466
-
-
Baradari, V.1
Hopfner, M.2
Huether, A.3
Schuppan, D.4
Scherubl, H.5
-
70
-
-
78649774178
-
Therapy of thyroid carcinoma with the histone deacetylase inhibitor MS-275
-
Altmann A, Eisenhut M, Bauder-Wust U, et al. Therapy of thyroid carcinoma with the histone deacetylase inhibitor MS-275. Eur J Nucl Med Mol Imaging 2010;37(12):2286-97
-
(2010)
Eur J Nucl Med Mol Imaging
, vol.37
, Issue.12
, pp. 2286-2297
-
-
Altmann, A.1
Eisenhut, M.2
Bauder-Wust, U.3
-
71
-
-
69849094949
-
Histone deacetylase inhibitors cooperate with IFN-gamma to restore caspase-8 expression and overcome TRAIL resistance in cancers with silencing of caspase-8
-
Hacker S, Dittrich A, Mohr A, et al. Histone deacetylase inhibitors cooperate with IFN-gamma to restore caspase-8 expression and overcome TRAIL resistance in cancers with silencing of caspase-8. Oncogene 2009;28(35):3097-110
-
(2009)
Oncogene
, vol.28
, Issue.35
, pp. 3097-110
-
-
Hacker, S.1
Dittrich, A.2
Mohr, A.3
-
72
-
-
33947153003
-
Inhibitors of histone deacetylases as potential therapeutic tools for high-risk embryonal tumors of the nervous system of childhood
-
DOI 10.1002/ijc.22401
-
Furchert SE, Lanvers-Kaminsky C, Juurgens H, et al. Inhibitors of histone deacetylases as potential therapeutic tools for high-risk embryonal tumors of the nervous system of childhood. Int J Cancer 2007;120(8):1787-94 (Pubitemid 46399367)
-
(2007)
International Journal of Cancer
, vol.120
, Issue.8
, pp. 1787-1794
-
-
Furchert, S.E.1
Lanvers-Kaminsky, C.2
Jurgens, H.3
Jung, M.4
Loidl, A.5
Fruhwald, M.C.6
-
73
-
-
0036828101
-
MS-27-275, an inhibitor of histone deacetylase, has marked in vitro and in vivo antitumor activity against pediatric solid tumors
-
Jaboin J, Wild J, Hamidi H, et al. MS-27-275, an inhibitor of histone deacetylase, has marked in vitro and in vivo antitumor activity against pediatric solid tumors. Cancer Res 2002;62(21):6108-15. (Pubitemid 35244459)
-
(2002)
Cancer Research
, vol.62
, Issue.21
, pp. 6108-6115
-
-
Jaboin, J.1
Wild, J.2
Hamidi, H.3
Khanna, C.4
Kim, C.J.5
Robey, R.6
Bates, S.E.7
Thiele, C.J.8
-
74
-
-
67349128584
-
Reactivation of death receptor 4 (DR4) expression sensitizes medulloblastoma cell lines to TRAIL
-
Aguilera DG, Das CM, Sinnappah-Kang ND, et al. Reactivation of death receptor 4 (DR4) expression sensitizes medulloblastoma cell lines to TRAIL. J Neurooncol 2009;93(3):303-18
-
(2009)
J Neurooncol
, vol.93
, Issue.3
, pp. 303-318
-
-
Aguilera, D.G.1
Das, C.M.2
Sinnappah-Kang, N.D.3
-
75
-
-
49649085534
-
Evaluation of the in vitro and in vivo antitumor activity of histone deacetylase inhibitors for the therapy of retinoblastoma
-
Dalgard CL, Van Quill KR, O'Brien JM. Evaluation of the in vitro and in vivo antitumor activity of histone deacetylase inhibitors for the therapy of retinoblastoma. Clin Cancer Res 2008;14(10):3113-23
-
(2008)
Clin Cancer Res
, vol.14
, Issue.10
, pp. 3113-3123
-
-
Dalgard, C.L.1
Van Quill, K.R.2
O'Brien, J.M.3
-
76
-
-
36849016900
-
Histone deacetylase inhibitors induce cell death and enhance the apoptosis-inducing activity of TRAIL in Ewing's sarcoma cells
-
DOI 10.1007/s00432-007-0227-8
-
Sonnemann J, Dreyer L, Hartwig M, et al. Histone deacetylase inhibitors induce cell death and enhance the apoptosis-inducing activity of TRAIL in Ewing's sarcoma cells. J Cancer Res Clin Oncol 2007;133(11):847-58 (Pubitemid 350218911)
-
(2007)
Journal of Cancer Research and Clinical Oncology
, vol.133
, Issue.11
, pp. 847-858
-
-
Sonnemann, J.1
Dreyer, L.2
Hartwig, M.3
Palani, C.D.4
Hong, L.T.T.5
Klier, U.6
Broker, B.7
Volker, U.8
Beck, J.F.9
-
77
-
-
57749179753
-
Preclinical evaluation of the antineoplastic action of 5-aza-2'-deoxycytidine and different histone deacetylase inhibitors on human Ewing's sarcoma cells
-
Hurtubise A, Bernstein ML, Momparler RL. Preclinical evaluation of the antineoplastic action of 5-aza-2'-deoxycytidine and different histone deacetylase inhibitors on human Ewing's sarcoma cells. Cancer Cell Int 2008;8:16
-
(2008)
Cancer Cell Int
, vol.8
, pp. 16
-
-
Hurtubise, A.1
Bernstein, M.L.2
Momparler, R.L.3
-
78
-
-
79952998700
-
Deacetylation of the DNA-binding Domain Regulates p53-mediated Apoptosis
-
Mellert HS, Stanek TJ, Sykes SM, et al. Deacetylation of the DNA-binding Domain Regulates p53-mediated Apoptosis. J Biol Chem 2011;286(6):4264-70.
-
(2011)
J Biol Chem
, vol.286
, Issue.6
, pp. 4264-4270
-
-
Mellert, H.S.1
Stanek, T.J.2
Sykes, S.M.3
-
79
-
-
0042905956
-
Gene expression profiling of multiple histone deacetylase (HDAC) inhibitors: Defining a common gene set produced by HDAC inhibition in T24 and MDA carcinoma cell lines
-
Glaser KB, Staver MJ, Waring JF, et al. Gene expression profiling of multiple histone deacetylase (HDAC) inhibitors: defining a common gene set produced by HDAC inhibition in T24 and MDA carcinoma cell lines. Mol Cancer Ther 2003;2(2):151-63
-
(2003)
Mol Cancer Ther
, vol.2
, Issue.2
, pp. 151-163
-
-
Glaser, K.B.1
Staver, M.J.2
Waring, J.F.3
-
80
-
-
20044390016
-
Role of thioredoxin in the response of normal and transformed cells to histone deacetylase inhibitors
-
DOI 10.1073/pnas.0408732102
-
Ungerstedt JS, Sowa Y, Xu WS, et al. Role of thioredoxin in the response of normal and transformed cells to histone deacetylase inhibitors. Proc Natl Acad Sci USA 2005;102(3):673-8 (Pubitemid 40282724)
-
(2005)
Proceedings of the National Academy of Sciences of the United States of America
, vol.102
, Issue.3
, pp. 673-678
-
-
Ungerstedt, J.S.1
Sowa, Y.2
Xu, W.-S.3
Shao, Y.4
Dokmanovic, M.5
Perez, G.6
Ngo, L.7
Holmgren, A.8
Jiang, X.9
Marks, P.A.10
-
81
-
-
33746144518
-
Inhibition of histone deacetylase class I but not class II is critical for the sensitization of leukemic cells to tumor necrosis factor-related apoptosis-inducing ligand-induced apoptosis
-
DOI 10.1158/0008-5472.CAN-05-4563
-
Inoue S, Mai A, Dyer MJ, Cohen GM. Inhibition of histone deacetylase class I but not class II is critical for the sensitization of leukemic cells to tumor necrosis factor-related apoptosis-inducing ligand-induced apoptosis. Cancer Res 2006;66(13):6785-92 (Pubitemid 44085638)
-
(2006)
Cancer Research
, vol.66
, Issue.13
, pp. 6785-6792
-
-
Inoue, S.1
Mai, A.2
Dyer, M.J.S.3
Cohen, G.M.4
-
82
-
-
77956526517
-
Impact of histone deacetylase inhibitors SAHA and MS-275 on DNA repair pathways in human mesenchymal stem cells
-
Di Bernardo G, Alessio N, Dell'Aversana C, et al. Impact of histone deacetylase inhibitors SAHA and MS-275 on DNA repair pathways in human mesenchymal stem cells. J Cell Physiol 2010;225(2):537-44
-
(2010)
J Cell Physiol
, vol.225
, Issue.2
, pp. 537-544
-
-
Di Bernardo, G.1
Alessio, N.2
Dell'Aversana, C.3
-
83
-
-
63149187235
-
Rescue of major histocompatibility-DR surface expression in retinoblastoma-defective, non-small cell lung carcinoma cells by the MS-275 histone deacetylase inhibitor
-
Niesen MI, Blanck G. Rescue of major histocompatibility-DR surface expression in retinoblastoma-defective, non-small cell lung carcinoma cells by the MS-275 histone deacetylase inhibitor. Biol Pharm Bull 2009;32(3):480-2
-
(2009)
Biol Pharm Bull
, vol.32
, Issue.3
, pp. 480-482
-
-
Niesen, M.I.1
Blanck, G.2
-
84
-
-
80052741042
-
Phase i trial of 5-azacitidine (5AC) and SNDX-275 in advanced lung cancer (NSCLC)
-
abstract #19036
-
Juergens RAVF, Coleman B, Sebree RS, et al. Phase I trial of 5-azacitidine (5AC) and SNDX-275 in advanced lung cancer (NSCLC). J Clin Oncol 2008;26:abstract #19036.
-
(2008)
J Clin Oncol
, vol.26
-
-
Ravf, J.1
Coleman, B.2
Sebree, R.S.3
-
85
-
-
70350506791
-
Early epigenetic changes and DNA damage do not predict clinical response in an overlapping schedule of 5-azacytidine and entinostat in patients with myeloid malignancies
-
Fandy TE, Herman JG, Kerns P, et al. Early epigenetic changes and DNA damage do not predict clinical response in an overlapping schedule of 5-azacytidine and entinostat in patients with myeloid malignancies. Blood 2009;114(13):2764-73.
-
(2009)
Blood
, vol.114
, Issue.13
, pp. 2764-2773
-
-
Fandy, T.E.1
Herman, J.G.2
Kerns, P.3
-
86
-
-
33746035691
-
Cardiotoxicity of histone deacetylase inhibitor depsipeptide in patients with metastatic neuroendocrine tumors
-
DOI 10.1158/1078-0432.CCR-05-2689
-
Shah MH, Binkley P, Chan K, et al. Cardiotoxicity of histone deacetylase inhibitor depsipeptide in patients with metastatic neuroendocrine tumors. Clin Cancer Res 2006;12(13):3997-4003 (Pubitemid 44078086)
-
(2006)
Clinical Cancer Research
, vol.12
, Issue.13
, pp. 3997-4003
-
-
Shah, M.H.1
Binkley, P.2
Chan, K.3
Xiao, J.4
Arbogast, D.5
Collamore, M.6
Farra, Y.7
Young, D.8
Grever, M.9
|