-
1
-
-
0032055037
-
Covalent modification of histones: expression from chromatin templates
-
Davie J.R. Covalent modification of histones: expression from chromatin templates. Curr. Opin. Genet. Dev. 8 (1998) 173-178
-
(1998)
Curr. Opin. Genet. Dev.
, vol.8
, pp. 173-178
-
-
Davie, J.R.1
-
3
-
-
34248631385
-
The role of histone deacetylases (HDACs) in human cancer
-
Ropero S., and Esteller M. The role of histone deacetylases (HDACs) in human cancer. Mol. Oncol. 1 (2007) 19-25
-
(2007)
Mol. Oncol.
, vol.1
, pp. 19-25
-
-
Ropero, S.1
Esteller, M.2
-
4
-
-
55749103404
-
Histone deacetylation: an attractive target for cancer therapy?
-
Al-Janadi A., Chandana S.R., and Conley B.A. Histone deacetylation: an attractive target for cancer therapy?. Drugs R D 9 (2008) 369-383
-
(2008)
Drugs R D
, vol.9
, pp. 369-383
-
-
Al-Janadi, A.1
Chandana, S.R.2
Conley, B.A.3
-
5
-
-
55749101363
-
Histone deacetylase inhibitors in cancer therapy
-
Lee M.J., Kim Y.S., Kummar S., Giaccone G., and Trepel J.B. Histone deacetylase inhibitors in cancer therapy. Curr. Opin. Oncol. 20 (2008) 639-649
-
(2008)
Curr. Opin. Oncol.
, vol.20
, pp. 639-649
-
-
Lee, M.J.1
Kim, Y.S.2
Kummar, S.3
Giaccone, G.4
Trepel, J.B.5
-
6
-
-
20544471104
-
Histone deacetylase inhibitors in programmed cell death and cancer therapy
-
Marks P.A., and Jiang X. Histone deacetylase inhibitors in programmed cell death and cancer therapy. Cell Cycle 4 (2005) 549-551
-
(2005)
Cell Cycle
, vol.4
, pp. 549-551
-
-
Marks, P.A.1
Jiang, X.2
-
7
-
-
34247880441
-
Development of histone deacetylase inhibitors for cancer treatment
-
Marchion D., and Munster P. Development of histone deacetylase inhibitors for cancer treatment. Expert Rev. Anticancer Ther. 7 (2007) 583-598
-
(2007)
Expert Rev. Anticancer Ther.
, vol.7
, pp. 583-598
-
-
Marchion, D.1
Munster, P.2
-
8
-
-
53749087120
-
Histone deacetylase inhibitors: mechanism of action and therapeutic use in cancer
-
Martínez-Iglesias O., Ruiz-Llorente L., Sánchez-Martínez R., García L., Zambrano A., and Aranda A. Histone deacetylase inhibitors: mechanism of action and therapeutic use in cancer. Clin. Transl. Oncol. 10 (2008) 395-398
-
(2008)
Clin. Transl. Oncol.
, vol.10
, pp. 395-398
-
-
Martínez-Iglesias, O.1
Ruiz-Llorente, L.2
Sánchez-Martínez, R.3
García, L.4
Zambrano, A.5
Aranda, A.6
-
9
-
-
34547864236
-
Histone deacetylase inhibitors: molecular mechanisms of action
-
Xu W.S., Parmigiani R.B., and Marks P.A. Histone deacetylase inhibitors: molecular mechanisms of action. Oncogene 26 (2007) 5541-5552
-
(2007)
Oncogene
, vol.26
, pp. 5541-5552
-
-
Xu, W.S.1
Parmigiani, R.B.2
Marks, P.A.3
-
10
-
-
34250643993
-
Histone deacetylase inhibitors: biology and mechanism of action
-
Mehnert J.M., and Kelly W.K. Histone deacetylase inhibitors: biology and mechanism of action. Cancer J. 13 (2007) 23-29
-
(2007)
Cancer J.
, vol.13
, pp. 23-29
-
-
Mehnert, J.M.1
Kelly, W.K.2
-
11
-
-
67651153048
-
New clinical developments in histone deacetylase inhibitors for epigenetic therapy of cancer
-
Cang S., Ma Y., and Liu D. New clinical developments in histone deacetylase inhibitors for epigenetic therapy of cancer. J. Hematol. Oncol. 1 (2009) 22
-
(2009)
J. Hematol. Oncol.
, vol.1
, pp. 22
-
-
Cang, S.1
Ma, Y.2
Liu, D.3
-
12
-
-
67650090545
-
Histone deacetylase inhibitors: potential in cancer therapy
-
Marks P.A., and Xu W.S. Histone deacetylase inhibitors: potential in cancer therapy. J. Cell Biochem. 107 (2009) 600-608
-
(2009)
J. Cell Biochem.
, vol.107
, pp. 600-608
-
-
Marks, P.A.1
Xu, W.S.2
-
13
-
-
0142179154
-
Identification of novel isoform-selective inhibitors within class I histone deacetylases
-
Hu E., Dul E., Sung C.M., Chen Z., Kirkpatrick R., Zhang G.F., Johanson K., Liu R., Lago A., Hofmann G., Macarron R., de los Frailes M., Perez P., Krawiec J., Winkler J., and Jaye M. Identification of novel isoform-selective inhibitors within class I histone deacetylases. J. Pharmacol. Exp. Ther. 307 (2003) 720-728
-
(2003)
J. Pharmacol. Exp. Ther.
, vol.307
, 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
-
14
-
-
6344222799
-
Crystal structure of a eukaryotic zinc-dependent histone deacetylase, human HDAC8, complexed with a hydroxamic acid inhibitor
-
Vannini A., Volpari C., Filocamo G., Casavola E.C., Brunetti M., Renzoni D., Chakravarty P., Paolini C., De Francesco R., Gallinari P., Steinkühler C., and Di Marco S. Crystal structure of a eukaryotic zinc-dependent histone deacetylase, human HDAC8, complexed with a hydroxamic acid inhibitor. Proc. Natl. Acad. Sci. USA 101 (2004) 15064-15069
-
(2004)
Proc. Natl. Acad. Sci. USA
, vol.101
, 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
Steinkühler, C.11
Di Marco, S.12
-
15
-
-
27444435580
-
Toward selective histone deacetylase inhibitor design: homology modeling, docking studies, and molecular dynamics simulations of human class I histone deacetylases
-
Wang D.F., Helquist P., Wiech N.L., and Wiest O. Toward selective histone deacetylase inhibitor design: homology modeling, docking studies, and molecular dynamics simulations of human class I histone deacetylases. J. Med. Chem. 48 (2005) 6936-6947
-
(2005)
J. Med. Chem.
, vol.48
, pp. 6936-6947
-
-
Wang, D.F.1
Helquist, P.2
Wiech, N.L.3
Wiest, O.4
-
16
-
-
33644663872
-
Histone acetylation-independent effect of histone deacetylase inhibitors on Akt through the reshuffling of protein phosphatase 1 complexes
-
Chen C.S., Weng S.C., Tseng P.H., Lin H.P., and Chen C.S. Histone acetylation-independent effect of histone deacetylase inhibitors on Akt through the reshuffling of protein phosphatase 1 complexes. J. Biol. Chem. 46 (2005) 38879-38887
-
(2005)
J. Biol. Chem.
, vol.46
, pp. 38879-38887
-
-
Chen, C.S.1
Weng, S.C.2
Tseng, P.H.3
Lin, H.P.4
Chen, C.S.5
-
17
-
-
31544455853
-
Histone deacetylase inhibitor FK228 suppresses the Ras-MAP kinase signaling pathway by upregulating Rap1 and induces apoptosis in malignant melanoma
-
Kobayashi Y., Ohtsuki M., Murakami T., Kobayashi T., Sutheesophon K., Kitayama H., Kano Y., Kusano E., Nakagawa H., and Furukawa Y. Histone deacetylase inhibitor FK228 suppresses the Ras-MAP kinase signaling pathway by upregulating Rap1 and induces apoptosis in malignant melanoma. Oncogene 4 (2006) 512-524
-
(2006)
Oncogene
, vol.4
, pp. 512-524
-
-
Kobayashi, Y.1
Ohtsuki, M.2
Murakami, T.3
Kobayashi, T.4
Sutheesophon, K.5
Kitayama, H.6
Kano, Y.7
Kusano, E.8
Nakagawa, H.9
Furukawa, Y.10
-
18
-
-
0035522657
-
Inhibition of Kirsten-ras expression in human colorectal cancer using rationally selected Kirsten-ras antisense oligonucleotides
-
Ross P.J., George M., Cunningham D., DiStefano F., Andreyev H.J., Workman P., and Clarke P.A. Inhibition of Kirsten-ras expression in human colorectal cancer using rationally selected Kirsten-ras antisense oligonucleotides. Mol. Cancer Ther. 1 (2001) 29-41
-
(2001)
Mol. Cancer Ther.
, vol.1
, pp. 29-41
-
-
Ross, P.J.1
George, M.2
Cunningham, D.3
DiStefano, F.4
Andreyev, H.J.5
Workman, P.6
Clarke, P.A.7
-
19
-
-
4444333268
-
Identification of 4-anilino-3-quinolinecarbonitrile inhibitors of mitogen-activated protein/extracellular signal-regulated kinase 1 kinase
-
Mallon R., Feldberg L., Kim S., Collins K., Wojciechowicz D., Kohler C., Kovacs D., Discafani C., Zhang N., Wu B., Floyd B., Powell D., and Berger D. Identification of 4-anilino-3-quinolinecarbonitrile inhibitors of mitogen-activated protein/extracellular signal-regulated kinase 1 kinase. Mol. Cancer Ther. 3 (2004) 755-762
-
(2004)
Mol. Cancer Ther.
, vol.3
, pp. 755-762
-
-
Mallon, R.1
Feldberg, L.2
Kim, S.3
Collins, K.4
Wojciechowicz, D.5
Kohler, C.6
Kovacs, D.7
Discafani, C.8
Zhang, N.9
Wu, B.10
Floyd, B.11
Powell, D.12
Berger, D.13
-
20
-
-
34548336384
-
Low-dose BBR3610 toxicity in colon cancer cells is p53-independent and enhanced by inhibition of epidermal growth factor receptor (ERBB1)-phosphatidyl inositol 3 kinase signaling
-
Mitchell C., Kabolizadeh P., Ryan J., Roberts J.D., Yacoub A., Curiel D.T., Fisher P.B., Hagan M.P., Farrell N.P., Grant S., and Dent P. Low-dose BBR3610 toxicity in colon cancer cells is p53-independent and enhanced by inhibition of epidermal growth factor receptor (ERBB1)-phosphatidyl inositol 3 kinase signaling. Mol. Pharmacol. 72 (2007) 704-714
-
(2007)
Mol. Pharmacol.
, vol.72
, pp. 704-714
-
-
Mitchell, C.1
Kabolizadeh, P.2
Ryan, J.3
Roberts, J.D.4
Yacoub, A.5
Curiel, D.T.6
Fisher, P.B.7
Hagan, M.P.8
Farrell, N.P.9
Grant, S.10
Dent, P.11
-
21
-
-
34250171437
-
Histone deacetylase inhibitors: signalling towards p21cip1/waf1
-
Ocker M., and Schneider-Stock R. Histone deacetylase inhibitors: signalling towards p21cip1/waf1. Int. J. Biochem. Cell Biol. 39 (2007) 1367-1374
-
(2007)
Int. J. Biochem. Cell Biol.
, vol.39
, pp. 1367-1374
-
-
Ocker, M.1
Schneider-Stock, R.2
-
22
-
-
58449111523
-
Apoptotic mechanism of paclitaxel-induced cell death in human head and neck tumor cell lines
-
Hsiao J.R., Leu S.F., and Huang B.M. Apoptotic mechanism of paclitaxel-induced cell death in human head and neck tumor cell lines. J. Oral. Pathol. Med. 38 (2009) 188-197
-
(2009)
J. Oral. Pathol. Med.
, vol.38
, pp. 188-197
-
-
Hsiao, J.R.1
Leu, S.F.2
Huang, B.M.3
-
23
-
-
0035666958
-
Cell cycle arrest is sufficient for p53-mediated tumor regression
-
Dubrez L., Coll J.L., Hurbin A., de Fraipont F., Lantejoul S., and Favrot M.C. Cell cycle arrest is sufficient for p53-mediated tumor regression. Gene. Ther. 8 (2001) 1705-1712
-
(2001)
Gene. Ther.
, vol.8
, pp. 1705-1712
-
-
Dubrez, L.1
Coll, J.L.2
Hurbin, A.3
de Fraipont, F.4
Lantejoul, S.5
Favrot, M.C.6
-
24
-
-
24744434639
-
Induction of polyploidy by histone deacetylase inhibitor: a pathway for antitumor effects
-
Xu W.S., Perez G., Ngo L., Gui C.Y., and Marks P.A. Induction of polyploidy by histone deacetylase inhibitor: a pathway for antitumor effects. Cancer Res. 65 (2005) 7832-7839
-
(2005)
Cancer Res.
, vol.65
, pp. 7832-7839
-
-
Xu, W.S.1
Perez, G.2
Ngo, L.3
Gui, C.Y.4
Marks, P.A.5
-
25
-
-
0032743259
-
Annexin V used for measuring apoptosis in the early events of cellular cytotoxicity
-
Aubry J.P., Blaecke A., Lecoanet-Henchoz S., Jeannin P., Herbault N., Caron G., Moine V., and Bonnefoy J.Y. Annexin V used for measuring apoptosis in the early events of cellular cytotoxicity. Cytometry 37 (1999) 197-204
-
(1999)
Cytometry
, vol.37
, pp. 197-204
-
-
Aubry, J.P.1
Blaecke, A.2
Lecoanet-Henchoz, S.3
Jeannin, P.4
Herbault, N.5
Caron, G.6
Moine, V.7
Bonnefoy, J.Y.8
-
27
-
-
68849110181
-
The HDAC inhibitor panobinostat (LBH589) inhibits mesothelioma and lung cancer cells in vitro and in vivo with particular efficacy for small cell lung cancer
-
Crisanti M.C., Wallace A.F., Kapoor V., Vandermeers F., Dowling M.L., Pereira L.P., Coleman K., Campling B.G., Fridlender Z.G., Kao G.D., and Albelda S.M. The HDAC inhibitor panobinostat (LBH589) inhibits mesothelioma and lung cancer cells in vitro and in vivo with particular efficacy for small cell lung cancer. Mol. Cancer Ther. 8 (2009) 2221-2231
-
(2009)
Mol. Cancer Ther.
, vol.8
, pp. 2221-2231
-
-
Crisanti, M.C.1
Wallace, A.F.2
Kapoor, V.3
Vandermeers, F.4
Dowling, M.L.5
Pereira, L.P.6
Coleman, K.7
Campling, B.G.8
Fridlender, Z.G.9
Kao, G.D.10
Albelda, S.M.11
-
29
-
-
67349142662
-
HDAC inhibitors in models of inflammation-related tumorigenesis
-
Glauben R., Sonnenberg E., Zeitz M., and Siegmund B. HDAC inhibitors in models of inflammation-related tumorigenesis. Cancer Lett. 280 (2009) 154-159
-
(2009)
Cancer Lett.
, vol.280
, pp. 154-159
-
-
Glauben, R.1
Sonnenberg, E.2
Zeitz, M.3
Siegmund, B.4
-
30
-
-
67649774358
-
A novel delta-lactam-based histone deacetylase inhibitor, KBH-A42, induces cell cycle arrest and apoptosis in colon cancer cells
-
Kang M.R., Kang J.S., Han S.B., Kim J.H., Kim D.M., Lee K., Lee C.W., Lee K.H., Lee C.H., Han G., Kang J.S., Kim H.M., and Park S.K. A novel delta-lactam-based histone deacetylase inhibitor, KBH-A42, induces cell cycle arrest and apoptosis in colon cancer cells. Biochem. Pharmacol. 78 (2009) 486-494
-
(2009)
Biochem. Pharmacol.
, vol.78
, pp. 486-494
-
-
Kang, M.R.1
Kang, J.S.2
Han, S.B.3
Kim, J.H.4
Kim, D.M.5
Lee, K.6
Lee, C.W.7
Lee, K.H.8
Lee, C.H.9
Han, G.10
Kang, J.S.11
Kim, H.M.12
Park, S.K.13
-
31
-
-
49349098483
-
Histone deacetylase inhibitors: mechanisms of cell death and promise in combination cancer therapy
-
Carew J.S., Giles F.J., and Nawrocki S.T. Histone deacetylase inhibitors: mechanisms of cell death and promise in combination cancer therapy. Cancer Lett. 269 (2008) 7-17
-
(2008)
Cancer Lett.
, vol.269
, pp. 7-17
-
-
Carew, J.S.1
Giles, F.J.2
Nawrocki, S.T.3
-
32
-
-
4344639284
-
Cell growth inhibition and gene expression induced by the histone deacetylase inhibitor, trichostatin A, on human hepatoma cells
-
Chiba T., Yokosuka O., Fukai K., Kojima H., Tada M., Arai M., Imazeki F., and Saisho H. Cell growth inhibition and gene expression induced by the histone deacetylase inhibitor, trichostatin A, on human hepatoma cells. Oncology 66 (2004) 481-491
-
(2004)
Oncology
, vol.66
, pp. 481-491
-
-
Chiba, T.1
Yokosuka, O.2
Fukai, K.3
Kojima, H.4
Tada, M.5
Arai, M.6
Imazeki, F.7
Saisho, H.8
-
33
-
-
24944585561
-
Gene expression profiling in response to the histone deacetylase inhibitor BL1521 in neuroblastoma
-
de Ruijter A.J., Meinsma R.J., Bosma P., Kemp S., Caron H.N., and van Kuilenburg A.B. Gene expression profiling in response to the histone deacetylase inhibitor BL1521 in neuroblastoma. Exp. Cell Res. 309 (2005) 451-467
-
(2005)
Exp. Cell Res.
, vol.309
, pp. 451-467
-
-
de Ruijter, A.J.1
Meinsma, R.J.2
Bosma, P.3
Kemp, S.4
Caron, H.N.5
van Kuilenburg, A.B.6
-
34
-
-
68949212379
-
Lysine acetylation targets protein complexes and co-regulates major cellular functions
-
Choudhary C., Kumar C., Gnad F., Nielsen M.L., Rehman M., Walther T., Olsen J.V., and Mann M. Lysine acetylation targets protein complexes and co-regulates major cellular functions. Science 325 (2009) 834-840
-
(2009)
Science
, vol.325
, pp. 834-840
-
-
Choudhary, C.1
Kumar, C.2
Gnad, F.3
Nielsen, M.L.4
Rehman, M.5
Walther, T.6
Olsen, J.V.7
Mann, M.8
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