-
1
-
-
30344477367
-
Histone deacetylase inhibitors and the promise of epigenetic (and more) treatments for cancer
-
Minucci S, Pelicci PG. Histone deacetylase inhibitors and the promise of epigenetic (and more) treatments for cancer. Nat Rev Cancer 2006;6:38-51.
-
(2006)
Nat Rev Cancer
, vol.6
, pp. 38-51
-
-
Minucci, S.1
Pelicci, P.G.2
-
2
-
-
34548526743
-
Chromatin remodeling and cancer. Part I. Covalent histone modifications
-
Wang GG, Allis CD, Chi P. Chromatin remodeling and cancer. Part I. Covalent histone modifications. Trends Mol Med 2007;13:363-72.
-
(2007)
Trends Mol Med
, vol.13
, pp. 363-372
-
-
Wang, G.G.1
Allis, C.D.2
Chi, P.3
-
3
-
-
33947313218
-
HDACs, histone deacetylation and gene transcription: From molecular biology to cancer therapeutics
-
Gallinari P, Di MS, Jones P, Pallaoro M, Steinkuhler 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, M.S.2
Jones, P.3
Pallaoro, M.4
Steinkuhler, C.5
-
4
-
-
34547864236
-
Histone deacetylase inhibitors: Molecular mechanisms of action
-
Xu WS, Parmigiani RB, Marks PA. Histone deacetylase inhibitors: molecular mechanisms of action. Oncogene 2007;26:5541-52.
-
(2007)
Oncogene
, vol.26
, pp. 5541-5552
-
-
Xu, W.S.1
Parmigiani, R.B.2
Marks, P.A.3
-
5
-
-
28044471827
-
Acetylation and deacetylation of non-histone proteins
-
Glozak MA, Sengupta N, Zhang X, Seto E. Acetylation and deacetylation of non-histone proteins. Gene 2005;363:15-23.
-
(2005)
Gene
, vol.363
, pp. 15-23
-
-
Glozak, M.A.1
Sengupta, N.2
Zhang, X.3
Seto, E.4
-
6
-
-
0034654011
-
Acetylation: A regulatory modification to rival phosphorylation?
-
Kouzarides T. Acetylation: a regulatory modification to rival phosphorylation? EMBO J 2000;19:1176-9.
-
(2000)
EMBO J
, vol.19
, pp. 1176-1179
-
-
Kouzarides, T.1
-
7
-
-
34547122494
-
HDAC inhibitors: Clinical update and mechanism-based potential
-
Glaser KB. HDAC inhibitors: clinical update and mechanism-based potential. Biochem Pharmacol 2007;74:659-71.
-
(2007)
Biochem Pharmacol
, vol.74
, pp. 659-671
-
-
Glaser, K.B.1
-
8
-
-
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
-
9
-
-
27744496468
-
Non-hydroxamate histone deacetylase inhibitors
-
Suzuki T, Miyata N. Non-hydroxamate histone deacetylase inhibitors. Curr Med Chem 2005;12:2867-80.
-
(2005)
Curr Med Chem
, vol.12
, pp. 2867-2880
-
-
Suzuki, T.1
Miyata, N.2
-
10
-
-
37849019672
-
Determination of the class and isoform selectivity of small molecule HDAC inhibitors
-
Khan N, Jeffers M, Kumar S, et al. Determination of the class and isoform selectivity of small molecule HDAC inhibitors. Biochem J 2008;409:581-9.
-
(2008)
Biochem J
, vol.409
, pp. 581-589
-
-
Khan, N.1
Jeffers, M.2
Kumar, S.3
-
11
-
-
0037444803
-
Histone deacetylases (HDACs): Characterization of the classical HDAC family
-
de Ruijter AJ, van Gennip AH, Caron HN, Kemp S, van Kuilenburg AB. Histone deacetylases (HDACs): characterization of the classical HDAC family. Biochem J 2003;370:737-49.
-
(2003)
Biochem J
, vol.370
, pp. 737-749
-
-
de Ruijter, A.J.1
van Gennip, A.H.2
Caron, H.N.3
Kemp, S.4
van Kuilenburg, A.B.5
-
12
-
-
0141570564
-
Role of class I and class II histone deacetylases in carcinoma cells using siRNA
-
Glaser KB, Li J, Staver MJ, Wei RQ, Albert DH, Davidsen SK. Role of class I and class II histone deacetylases in carcinoma cells using siRNA. Biochem Biophys Res Commun 2003;310:529-36.
-
(2003)
Biochem Biophys Res Commun
, vol.310
, pp. 529-536
-
-
Glaser, K.B.1
Li, J.2
Staver, M.J.3
Wei, R.Q.4
Albert, D.H.5
Davidsen, S.K.6
-
13
-
-
22844432021
-
Inhibition of histone deacetylase 6 acetylates and disrupts the chaperone function of heat shock protein 90: A novel basis for antileukemia activity of histone deacetylase inhibitors
-
Bali P, Pranpat M, Bradner J, et al. Inhibition of histone deacetylase 6 acetylates and disrupts the chaperone function of heat shock protein 90: a novel basis for antileukemia activity of histone deacetylase inhibitors. J Biol Chem 2005;280:26729-34.
-
(2005)
J Biol Chem
, vol.280
, pp. 26729-26734
-
-
Bali, P.1
Pranpat, M.2
Bradner, J.3
-
14
-
-
0346020435
-
The deacetylase HDAC6 regulates aggresome formation and cell viability in response to misfolded protein stress
-
Kawaguchi Y, Kovacs JJ, McLaurin A, Vance JM, Ito A, Yao TP. The deacetylase HDAC6 regulates aggresome formation and cell viability in response to misfolded protein stress. Cell 2003;115:727-38.
-
(2003)
Cell
, vol.115
, pp. 727-738
-
-
Kawaguchi, Y.1
Kovacs, J.J.2
McLaurin, A.3
Vance, J.M.4
Ito, A.5
Yao, T.P.6
-
15
-
-
33751172982
-
Aggresome induction by proteasome inhibitor bortezomib and α-tubulin hyperacetylation by tubulin deacetylase (TDAC) inhibitor LBH589 are synergistic in myeloma cells
-
Catley L, Weisberg E, Kiziltepe T, et al. Aggresome induction by proteasome inhibitor bortezomib and α-tubulin hyperacetylation by tubulin deacetylase (TDAC) inhibitor LBH589 are synergistic in myeloma cells. Blood 2006;108:3441-9.
-
(2006)
Blood
, vol.108
, pp. 3441-3449
-
-
Catley, L.1
Weisberg, E.2
Kiziltepe, T.3
-
16
-
-
20844435806
-
Small-molecule inhibition of proteasome and aggresome function induces synergistic antitumor activity in multiple myeloma
-
Hideshima T, Bradner JE, Wong J, et al. Small-molecule inhibition of proteasome and aggresome function induces synergistic antitumor activity in multiple myeloma. Proc Natl Acad Sci U S A 2005;102:8567-72.
-
(2005)
Proc Natl Acad Sci U S A
, vol.102
, pp. 8567-8572
-
-
Hideshima, T.1
Bradner, J.E.2
Wong, J.3
-
17
-
-
33645737411
-
Aggresome disruption: A novel strategy to enhance bortezomib-induced apoptosis in pancreatic cancer cells
-
Nawrocki ST, Carew JS, Pino MS, et al. Aggresome disruption: a novel strategy to enhance bortezomib-induced apoptosis in pancreatic cancer cells. Cancer Res 2006;66:3773-81.
-
(2006)
Cancer Res
, vol.66
, pp. 3773-3781
-
-
Nawrocki, S.T.1
Carew, J.S.2
Pino, M.S.3
-
18
-
-
33845514708
-
Will broad-spectrum histone deacetylase inhibitors be superseded by more specific compounds?
-
Karagiannis TC, El-Osta A. Will broad-spectrum histone deacetylase inhibitors be superseded by more specific compounds? Leukemia 2007;21:61-5.
-
(2007)
Leukemia
, vol.21
, pp. 61-65
-
-
Karagiannis, T.C.1
El-Osta, A.2
-
19
-
-
0032584224
-
A role for histone deacetylase activity in HDAC1-mediated transcriptional repression
-
Hassig CA, Tong JK, Fleischer TC, et al. A role for histone deacetylase activity in HDAC1-mediated transcriptional repression. Proc Natl Acad Sci U S A 1998;95:3519-24.
-
(1998)
Proc Natl Acad Sci U S A
, vol.95
, pp. 3519-3524
-
-
Hassig, C.A.1
Tong, J.K.2
Fleischer, T.C.3
-
20
-
-
12244295468
-
In vivo destabilization of dynamic microtubules by HDAC6-mediated deacetylation
-
Matsuyama A, Shimazu T, Sumida Y, et al. In vivo destabilization of dynamic microtubules by HDAC6-mediated deacetylation. EMBO J 2002;21:6820-31.
-
(2002)
EMBO J
, vol.21
, pp. 6820-6831
-
-
Matsuyama, A.1
Shimazu, T.2
Sumida, Y.3
-
21
-
-
0037161744
-
HDAC6 is a microtubule-associated deacetylase
-
Hubbert C, Guardiola A, Shao R, et al. HDAC6 is a microtubule-associated deacetylase. Nature 2002;417:455-8.
-
(2002)
Nature
, vol.417
, pp. 455-458
-
-
Hubbert, C.1
Guardiola, A.2
Shao, R.3
-
22
-
-
17744416444
-
Histone deacetylase inhibitor activates the WAF1/Cip1 gene promoter through the Sp1 sites
-
Sowa Y, Orita T, Minamikawa S, et al. Histone deacetylase inhibitor activates the WAF1/Cip1 gene promoter through the Sp1 sites. Biochem Biophys Res Commun 1997;241:142-50.
-
(1997)
Biochem Biophys Res Commun
, vol.241
, pp. 142-150
-
-
Sowa, Y.1
Orita, T.2
Minamikawa, S.3
-
23
-
-
33749011163
-
The NCI60 human tumour cell line anticancer drug screen
-
Shoemaker RH. The NCI60 human tumour cell line anticancer drug screen. Nat Rev Cancer 2006;6:813-23.
-
(2006)
Nat Rev Cancer
, vol.6
, pp. 813-823
-
-
Shoemaker, R.H.1
-
24
-
-
0141953928
-
The discovery of NVP-LAQ824: From concept to clinic
-
Remiszewski SW. The discovery of NVP-LAQ824: from concept to clinic. Curr Med Chem 2003;10:2393-402.
-
(2003)
Curr Med Chem
, vol.10
, pp. 2393-2402
-
-
Remiszewski, S.W.1
-
25
-
-
0034596309
-
Histone deacetylase inhibitors: Inducers of differentiation or apoptosis of transformed cells
-
Marks PA, Richon VM, Rifkind RA. Histone deacetylase inhibitors: inducers of differentiation or apoptosis of transformed cells. J Natl Cancer Inst 2000;92:1210-6.
-
(2000)
J Natl Cancer Inst
, vol.92
, pp. 1210-1216
-
-
Marks, P.A.1
Richon, V.M.2
Rifkind, R.A.3
-
26
-
-
0030612749
-
JC-1, but not DiOC6(3) or rhodamine 123, is a reliable fluorescent probe to assess yc changes in intact cells: Implications for studies on mitochondrial functionality during apoptosis
-
Salvioli S, Ardizzoni A, Franceschi C, Cossarizza A. JC-1, but not DiOC6(3) or rhodamine 123, is a reliable fluorescent probe to assess yc changes in intact cells: implications for studies on mitochondrial functionality during apoptosis. FEBS Lett 1997;411:77-82.
-
(1997)
FEBS Lett
, vol.411
, pp. 77-82
-
-
Salvioli, S.1
Ardizzoni, A.2
Franceschi, C.3
Cossarizza, A.4
-
27
-
-
27144477683
-
Epithelial to mesenchymal transition is a determinant of sensitivity of non-small-cell lung carcinoma cell lines and xenografts to epidermal growth factor receptor inhibition
-
Thomson S, Buck E, Petti F, et al. Epithelial to mesenchymal transition is a determinant of sensitivity of non-small-cell lung carcinoma cell lines and xenografts to epidermal growth factor receptor inhibition. Cancer Res 2005;65:9455-62.
-
(2005)
Cancer Res
, vol.65
, pp. 9455-9462
-
-
Thomson, S.1
Buck, E.2
Petti, F.3
-
28
-
-
33644753715
-
The application of epigenetic modifiers on the treatment of prostate and bladder cancer
-
Zhang Z, Karam J, Frenkel E, Sagalowsky A, Hsieh JT. The application of epigenetic modifiers on the treatment of prostate and bladder cancer. Urol Oncol 2006;24:152-60.
-
(2006)
Urol Oncol
, vol.24
, pp. 152-160
-
-
Zhang, Z.1
Karam, J.2
Frenkel, E.3
Sagalowsky, A.4
Hsieh, J.T.5
-
29
-
-
0032695910
-
Inhibition of epidermal growth factor receptor-associated tyrosine phosphorylation in human carcinomas with CP-358,774: Dynamics of receptor inhibition in situ and antitumor effects in athymic mice
-
Pollack VA, Savage DM, Baker DA, et al. Inhibition of epidermal growth factor receptor-associated tyrosine phosphorylation in human carcinomas with CP-358,774: dynamics of receptor inhibition in situ and antitumor effects in athymic mice. J Pharmacol Exp Ther 1999;291:739-48.
-
(1999)
J Pharmacol Exp Ther
, vol.291
, pp. 739-748
-
-
Pollack, V.A.1
Savage, D.M.2
Baker, D.A.3
-
30
-
-
33644696512
-
Chemical ablation of androgen receptor in prostate cancer cells by the histone deacetylase inhibitor LAQ824
-
Chen L, Meng S, Wang H, et al. Chemical ablation of androgen receptor in prostate cancer cells by the histone deacetylase inhibitor LAQ824. Mol Cancer Ther 2005;4:1311-9.
-
(2005)
Mol Cancer Ther
, vol.4
, pp. 1311-1319
-
-
Chen, L.1
Meng, S.2
Wang, H.3
-
31
-
-
0034665124
-
Suberoylanilide hydroxamic acid, an inhibitor of histone deacetylase, suppresses the growth of prostate cancer cells in vitro and in vivo
-
Butler LM, Agus DB, Scher HI, et al. Suberoylanilide hydroxamic acid, an inhibitor of histone deacetylase, suppresses the growth of prostate cancer cells in vitro and in vivo. Cancer Res 2000;60:5165-70.
-
(2000)
Cancer Res
, vol.60
, pp. 5165-5170
-
-
Butler, L.M.1
Agus, D.B.2
Scher, H.I.3
-
32
-
-
31544464120
-
Targeting tumor angiogenesis with histone deacetylase inhibitors: The hydroxamic acid derivative LBH589
-
Qian DZ, Kato Y, Shabbeer S, et al. Targeting tumor angiogenesis with histone deacetylase inhibitors: the hydroxamic acid derivative LBH589. Clin Cancer Res 2006;12:634-42.
-
(2006)
Clin Cancer Res
, vol.12
, pp. 634-642
-
-
Qian, D.Z.1
Kato, Y.2
Shabbeer, S.3
-
33
-
-
33746468951
-
Aberrant gene silencing in tumor progression: Implications for control of cancer
-
Baylin SB, Chen WY. Aberrant gene silencing in tumor progression: implications for control of cancer. Cold Spring Harb Symp Quant Biol 2005;70:427-33.
-
(2005)
Cold Spring Harb Symp Quant Biol
, vol.70
, pp. 427-433
-
-
Baylin, S.B.1
Chen, W.Y.2
-
34
-
-
0042905956
-
Gene expression profilingof multiple histone deacetylase (HDAC) inhibitors: Defininga common gene set produced by HDAC inhibition in T24 and MDA carcinoma cell lines
-
Glaser KB, Staver MJ, Waring JF, Stender J, Ulrich RG, Davidsen SK. Gene expression profilingof multiple histone deacetylase (HDAC) inhibitors: defininga common gene set produced by HDAC inhibition in T24 and MDA carcinoma cell lines. Mol Cancer Ther 2003;2:151-63.
-
(2003)
Mol Cancer Ther
, vol.2
, pp. 151-163
-
-
Glaser, K.B.1
Staver, M.J.2
Waring, J.F.3
Stender, J.4
Ulrich, R.G.5
Davidsen, S.K.6
-
35
-
-
9144220841
-
Transcriptional signature of histone deacetylase inhibition in multiple myeloma: Biological and clinical implications
-
Mitsiades CS, Mitsiades NS, McMullan CJ, et al. Transcriptional signature of histone deacetylase inhibition in multiple myeloma: biological and clinical implications. Proc Natl Acad Sci U S A 2004;101:540-5.
-
(2004)
Proc Natl Acad Sci U S A
, vol.101
, pp. 540-545
-
-
Mitsiades, C.S.1
Mitsiades, N.S.2
McMullan, C.J.3
-
36
-
-
14844353574
-
Identification and functional significance of genes regulated by structurally different histone deacetylase inhibitors
-
Peart MJ, Smyth GK, van Laar RK, et al. Identification and functional significance of genes regulated by structurally different histone deacetylase inhibitors. Proc Natl Acad Sci U S A 2005;102:3697-702.
-
(2005)
Proc Natl Acad Sci U S A
, vol.102
, pp. 3697-3702
-
-
Peart, M.J.1
Smyth, G.K.2
van Laar, R.K.3
-
37
-
-
0018168515
-
Captopril (SQ 14,225) (D-3-mercapto-2-methylpropranoyl-L-proline): A novel orally active inhibitor of angiotensin-converting enzyme and antihypertensive agent
-
Rubin B, Antonaccio MJ, Horovitz ZP. Captopril (SQ 14,225) (D-3-mercapto-2-methylpropranoyl-L-proline): a novel orally active inhibitor of angiotensin-converting enzyme and antihypertensive agent. Prog Cardiovasc Dis 1978;21:183-94.
-
(1978)
Prog Cardiovasc Dis
, vol.21
, pp. 183-194
-
-
Rubin, B.1
Antonaccio, M.J.2
Horovitz, Z.P.3
-
38
-
-
0035576820
-
Inhibition of angiogenesis and metastasis in two murine models by the matrix metalloproteinase inhibitor, BMS-275291
-
Naglich JG, Jure-Kunkel M, Gupta E, et al. Inhibition of angiogenesis and metastasis in two murine models by the matrix metalloproteinase inhibitor, BMS-275291. Cancer Res 2001;61:8480-5.
-
(2001)
Cancer Res
, vol.61
, pp. 8480-8485
-
-
Naglich, J.G.1
Jure-Kunkel, M.2
Gupta, E.3
-
39
-
-
18644379905
-
A phase I trial of depsipeptide (FR901228) in patients with advanced cancer
-
Marshall JL, Rizvi N, Kauh J, et al. A phase I trial of depsipeptide (FR901228) in patients with advanced cancer. J Exp Ther Oncol 2002;2:325-32.
-
(2002)
J Exp Ther Oncol
, vol.2
, pp. 325-332
-
-
Marshall, J.L.1
Rizvi, N.2
Kauh, J.3
-
40
-
-
2442597872
-
Thiol-based SAHA analogues as potent histone deacetylase inhibitors
-
Suzuki T, Kouketsu A, Matsuura A, et al. Thiol-based SAHA analogues as potent histone deacetylase inhibitors. Bioorg Med Chem Lett 2004;14:3313-7.
-
(2004)
Bioorg Med Chem Lett
, vol.14
, pp. 3313-3317
-
-
Suzuki, T.1
Kouketsu, A.2
Matsuura, A.3
-
41
-
-
84961981250
-
DFT-based ranking of zinc-bindingg roups in histone deacetylase inhibitors
-
Vanommeslaeghe K, Loverix S, Geerlings P, Tourwe D. DFT-based ranking of zinc-bindingg roups in histone deacetylase inhibitors. Bioorg Med Chem 2005;13:6070-82.
-
(2005)
Bioorg Med Chem
, vol.13
, pp. 6070-6082
-
-
Vanommeslaeghe, K.1
Loverix, S.2
Geerlings, P.3
Tourwe, D.4
-
42
-
-
38449100788
-
Expression profile of class I histone deacetylases in human cancer tissues
-
Nakagawa M, Oda Y, Eguchi T, et al. Expression profile of class I histone deacetylases in human cancer tissues. Oncol Rep 2007;18:769-74.
-
(2007)
Oncol Rep
, vol.18
, pp. 769-774
-
-
Nakagawa, M.1
Oda, Y.2
Eguchi, T.3
-
43
-
-
20544471104
-
Histone deacetylase inhibitors in programmed cell death and cancer therapy
-
Marks PA, Jiang X. Histone deacetylase inhibitors in programmed cell death and cancer therapy. Cell Cycle 2005;4:549-51.
-
(2005)
Cell Cycle
, vol.4
, pp. 549-551
-
-
Marks, P.A.1
Jiang, X.2
-
44
-
-
34250697605
-
MicroRNA expression profiles for the NCI-60 cancer cell panel
-
Blower PE, Verducci JS, Lin S, et al. MicroRNA expression profiles for the NCI-60 cancer cell panel. Mol Cancer Ther 2007;6:1483-91.
-
(2007)
Mol Cancer Ther
, vol.6
, pp. 1483-1491
-
-
Blower, P.E.1
Verducci, J.S.2
Lin, S.3
-
45
-
-
33845200848
-
Mutation analysis of 24 known cancer genes in the NCI-60 cell line set
-
Ikediobi ON, Davies H, Bignell G, et al. Mutation analysis of 24 known cancer genes in the NCI-60 cell line set. Mol Cancer Ther 2006;5:2606-12.
-
(2006)
Mol Cancer Ther
, vol.5
, pp. 2606-2612
-
-
Ikediobi, O.N.1
Davies, H.2
Bignell, G.3
-
46
-
-
33646541046
-
Integrating data on DNA copy number with gene expression levels and drug sensitivities in the NCI-60 cell line panel
-
Bussey KJ, Chin K, Lababidi S, et al. Integrating data on DNA copy number with gene expression levels and drug sensitivities in the NCI-60 cell line panel. Mol Cancer Ther 2006;5:853-67.
-
(2006)
Mol Cancer Ther
, vol.5
, pp. 853-867
-
-
Bussey, K.J.1
Chin, K.2
Lababidi, S.3
-
47
-
-
38449089087
-
Clinical potential of histone deacetylase inhibitors as stand alone therapeutics and in combination with other chemotherapeutics or radiotherapy for cancer
-
Karagiannis TC, El-Osta A. Clinical potential of histone deacetylase inhibitors as stand alone therapeutics and in combination with other chemotherapeutics or radiotherapy for cancer. Epigenetics 2006;1:121-6.
-
(2006)
Epigenetics
, vol.1
, pp. 121-126
-
-
Karagiannis, T.C.1
El-Osta, A.2
|