-
1
-
-
0242610850
-
Inhibition of histone deacetylase increases cytotoxicity to anticancer drugs targeting DNA
-
Kim, M.S.; Blake, M.; Baek, J.H.; Kohlhagen, G.; Pommier, Y.; Carrier, F. Inhibition of histone deacetylase increases cytotoxicity to anticancer drugs targeting DNA. Cancer Res. 2003, 63, 7291-7300.
-
(2003)
Cancer Res.
, vol.63
, pp. 7291-7300
-
-
Kim, M.S.1
Blake, M.2
Baek, J.H.3
Kohlhagen, G.4
Pommier, Y.5
Carrier, F.6
-
2
-
-
70949083604
-
Synergistic antitumor effect between vorinostat and topotecan in small cell lung cancer cells is mediated by generation of reactive oxygen species and DNA damage-induced apoptosis
-
Bruzzese, F.; Rocco, M.; Castelli, S.; Di Gennaro, E.; Desideri, A.; Budillon, A. Synergistic antitumor effect between vorinostat and topotecan in small cell lung cancer cells is mediated by generation of reactive oxygen species and DNA damage-induced apoptosis. Mol. Cancer Ther. 2009, 8, 3075-3087.
-
(2009)
Mol. Cancer Ther.
, vol.8
, pp. 3075-3087
-
-
Bruzzese, F.1
Rocco, M.2
Castelli, S.3
Di Gennaro, E.4
Desideri, A.5
Budillon, A.6
-
3
-
-
23044487814
-
It's about time: Scheduling alters effect of histone deacetylase inhibitors on camptothecin-treated cells
-
Bevins, R.L.; Zimmer, S.G. It's about time: Scheduling alters effect of histone deacetylase inhibitors on camptothecin-treated cells. Cancer Res. 2005, 65, 6957-6966.
-
(2005)
Cancer Res.
, vol.65
, pp. 6957-6966
-
-
Bevins, R.L.1
Zimmer, S.G.2
-
4
-
-
18744408483
-
The histone-deacetylase inhibitor SAHA potentiates proapoptotic effects of 5-fluorouracil and irinotecan in hepatoma cells
-
Ocker, M.; Alajati, A.; Ganslmayer, M.; Zopf, S.; Luders, M.; Neureiter, D.; Hahn, E.G.; Schuppan, D.; Herold, C. The histone-deacetylase inhibitor SAHA potentiates proapoptotic effects of 5-fluorouracil and irinotecan in hepatoma cells. J. Cancer Res. Clin. Oncol. 2005, 131, 385-394.
-
(2005)
J. Cancer Res. Clin. Oncol.
, vol.131
, pp. 385-394
-
-
Ocker, M.1
Alajati, A.2
Ganslmayer, M.3
Zopf, S.4
Luders, M.5
Neureiter, D.6
Hahn, E.G.7
Schuppan, D.8
Herold, C.9
-
5
-
-
77956059770
-
Vorinostat enhances the cytotoxic effects of the topoisomerase i inhibitor SN38 in glioblastoma cell lines
-
Sarcar, B.; Kahali, S.; Chinnaiyan, P. Vorinostat enhances the cytotoxic effects of the topoisomerase I inhibitor SN38 in glioblastoma cell lines. J. Neurooncol. 2010, 99, 201-207.
-
(2010)
J. Neurooncol.
, vol.99
, pp. 201-207
-
-
Sarcar, B.1
Kahali, S.2
Chinnaiyan, P.3
-
6
-
-
36048958965
-
Histone deacetylase inhibitors: Overview and perspectives
-
Dokmanovic, M.; Clarke, C.; Marks, P.A. Histone deacetylase inhibitors: Overview and perspectives. Mol. Cancer Res. 2007, 5, 981-989.
-
(2007)
Mol. Cancer Res.
, vol.5
, pp. 981-989
-
-
Dokmanovic, M.1
Clarke, C.2
Marks, P.A.3
-
7
-
-
33745320974
-
Targeting histone deacetylase in cancer therapy
-
Lin, H.Y.; Chen, C.S.; Lin, S.P.; Weng, J.R.; Chen, C.S. Targeting histone deacetylase in cancer therapy. Med. Res. Rev. 2006, 26, 397-413.
-
(2006)
Med. Res. Rev.
, vol.26
, pp. 397-413
-
-
Lin, H.Y.1
Chen, C.S.2
Lin, S.P.3
Weng, J.R.4
Chen, C.S.5
-
8
-
-
55749101363
-
Histone deacetylase inhibitors in cancer therapy
-
Lee, M.J.; Kim, Y.S.; Kummar, S.; Giaccone, G.; Trepel, J.B. Histone deacetylase inhibitors in cancer therapy. Curr. Opin. Oncol. 2008, 20, 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
-
9
-
-
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.; Chen, C.S. Histone acetylation-independent effect of histone deacetylase inhibitors on Akt through the reshuffling of protein phosphatase 1 complexes. J. Biol. Chem. 2005, 280, 38879-38887.
-
(2005)
J. Biol. Chem.
, vol.280
, pp. 38879-38887
-
-
Chen, C.S.1
Weng, S.C.2
Tseng, P.H.3
Lin, H.P.4
Chen, C.S.5
-
10
-
-
77949353758
-
Discovery of 7-(4-(3-ethynylphenylamino)-7-methoxyquinazolin-6-yloxy)-N- hydroxyheptanamide (CUDc-101) as a potent multi-acting HDAC, EGFR, and HER2 inhibitor for the treatment of cancer
-
Cai, X.; Zhai, H.X.; Wang, J.; Forrester, J.; Qu, H.; Yin, L.; Lai, C.J.; Bao, R.; Qian, C. Discovery of 7-(4-(3-ethynylphenylamino)-7-methoxyquinazolin- 6-yloxy)-N-hydroxyheptanamide (CUDc-101) as a potent multi-acting HDAC, EGFR, and HER2 inhibitor for the treatment of cancer. J. Med. Chem. 2010, 53, 2000-2009.
-
(2010)
J. Med. Chem.
, vol.53
, pp. 2000-2009
-
-
Cai, X.1
Zhai, H.X.2
Wang, J.3
Forrester, J.4
Qu, H.5
Yin, L.6
Lai, C.J.7
Bao, R.8
Qian, C.9
-
11
-
-
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, C.J.; Bao, R.; Tao, X.; Wang, J.; Atoyan, R.; Qu, H.; Wang, D.G.; Yin, L.; Samson, M.; Forrester, J.; 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, 3647-3656.
-
(2010)
Cancer Res.
, vol.70
, pp. 3647-3656
-
-
Lai, C.J.1
Bao, R.2
Tao, X.3
Wang, J.4
Atoyan, R.5
Qu, H.6
Wang, D.G.7
Yin, L.8
Samson, M.9
Forrester, J.10
-
12
-
-
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.; Winkler, M.; Eichhorn, E.; Pongratz, H.; Ciossek, T.; Baer, T.; Maier, T.; Beckers, T. 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, 2265-2279.
-
(2009)
J. Med. Chem.
, vol.52
, pp. 2265-2279
-
-
Mahboobi, S.1
Dove, S.2
Sellmer, A.3
Winkler, M.4
Eichhorn, E.5
Pongratz, H.6
Ciossek, T.7
Baer, T.8
Maier, T.9
Beckers, T.10
-
13
-
-
78650321835
-
Novel chimeric histone deacetylase inhibitors: A series of lapatinib hybrides as potent inhibitors of epidermal growth factor receptor (EGFR), human epidermal growth factor receptor 2 (HER2), and histone deacetylase activity
-
Mahboobi, S.; Sellmer, A.; Winkler, M.; Eichhorn, E.; Pongratz, H.; Ciossek, T.; Baer, T.; Maier, T.; Beckers, T. Novel chimeric histone deacetylase inhibitors: A series of lapatinib hybrides as potent inhibitors of epidermal growth factor receptor (EGFR), human epidermal growth factor receptor 2 (HER2), and histone deacetylase activity. J. Med. Chem. 2010, 53, 8546-8555.
-
(2010)
J. Med. Chem.
, vol.53
, pp. 8546-8555
-
-
Mahboobi, S.1
Sellmer, A.2
Winkler, M.3
Eichhorn, E.4
Pongratz, H.5
Ciossek, T.6
Baer, T.7
Maier, T.8
Beckers, T.9
-
14
-
-
84877794404
-
The discovery of colchicine-SAHA hybrids as a new class of antitumor agents
-
Zhang, X.; Zhang, J.; Tong, L.; Luo, Y.; Su, M.; Zang, Y.; Li, J.; Lu, W.; Chen, Y., The discovery of colchicine-SAHA hybrids as a new class of antitumor agents. Bioorg. Med. Chem. 2013, 21, 3240-3244.
-
(2013)
Bioorg. Med. Chem.
, vol.21
, pp. 3240-3244
-
-
Zhang, X.1
Zhang, J.2
Tong, L.3
Luo, Y.4
Su, M.5
Zang, Y.6
Li, J.7
Lu, W.8
Chen, Y.9
-
15
-
-
62649103876
-
The ErbB kinase domain: Structural perspectives into kinase activation and inhibition
-
Bose, R.; Zhang, X. The ErbB kinase domain: structural perspectives into kinase activation and inhibition. Exp. Cell Res. 2009, 315, 649-658.
-
(2009)
Exp. Cell Res.
, vol.315
, pp. 649-658
-
-
Bose, R.1
Zhang, X.2
-
16
-
-
33847323129
-
Epidermal growth factor receptor mutations in lung cancer
-
Sharma, S.V.; Bell, D.W.; Settleman, J.; Haber, D.A. Epidermal growth factor receptor mutations in lung cancer. Nat. Rev. Cancer 2007, 7, 169-181.
-
(2007)
Nat. Rev. Cancer
, vol.7
, pp. 169-181
-
-
Sharma, S.V.1
Bell, D.W.2
Settleman, J.3
Haber, D.A.4
-
17
-
-
0033551152
-
A synthetic inhibitor of histone deacetylase, MS-27-275, with marked in vivo antitumor activity against human tumors
-
Saito, A.; Yamashita, T.; Mariko, Y.; Nosaka, Y.; Tsuchiya, K.; Ando, T.; Suzuki, T.; Tsuruo, T.; Nakanishi, O. 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, 4592-4297.
-
(1999)
Proc. Natl. Acad. Sci. USA
, vol.96
, pp. 4592-4297
-
-
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
-
-
0033199896
-
Hybrid polar histone deacetylase inhibitor induces apoptosis and CD95/CD95 ligand expression in human neuroblastoma
-
Glick, R.D.; Swendeman, S.L.; Coffey, D.C.; Rifkind, R.A.; Marks, P.A.; Richon, V.M.; La Quaglia, M.P. Hybrid polar histone deacetylase inhibitor induces apoptosis and CD95/CD95 ligand expression in human neuroblastoma. Cancer Res. 1999, 59, 4392-4399.
-
(1999)
Cancer Res.
, vol.59
, pp. 4392-4399
-
-
Glick, R.D.1
Swendeman, S.L.2
Coffey, D.C.3
Rifkind, R.A.4
Marks, P.A.5
Richon, V.M.6
La Quaglia, M.P.7
-
19
-
-
0034665124
-
Suberoylanilide hydroxamic acid, an inhibitor of histone deacetylase, suppresses the growth of prostate cancer cells in vitro and in vivo
-
Butler, L.M.; Agus, D.B.; Scher, H.I.; Higgins, B.; Rose, A.; Cordon-Cardo, C.; Thaler, H.T.; Rifkind, R.A.; Marks, P.A.; Richon, V.M. Suberoylanilide hydroxamic acid, an inhibitor of histone deacetylase, suppresses the growth of prostate cancer cells in vitro and in vivo. Cancer Res. 2000, 60, 5165-5170.
-
(2000)
Cancer Res.
, vol.60
, pp. 5165-5170
-
-
Butler, L.M.1
Agus, D.B.2
Scher, H.I.3
Higgins, B.4
Rose, A.5
Cordon-Cardo, C.6
Thaler, H.T.7
Rifkind, R.A.8
Marks, P.A.9
Richon, V.M.10
-
20
-
-
60549102514
-
Non-peptide macrocyclic histone deacetylase inhibitors
-
Oyelere, A.K.; Chen, P.C.; Guerrant, W.; Mwakwari, S.C.; Hood, R.; Zhang, Y.; Fan, Y. Non-peptide macrocyclic histone deacetylase inhibitors. J. Med. Chem. 2009, 52, 456-468.
-
(2009)
J. Med. Chem.
, vol.52
, pp. 456-468
-
-
Oyelere, A.K.1
Chen, P.C.2
Guerrant, W.3
Mwakwari, S.C.4
Hood, R.5
Zhang, Y.6
Fan, Y.7
-
21
-
-
36148950997
-
FDA approval summary: Vorinostat for treatment of advanced primary cutaneous T-cell lymphoma
-
Mann, B.S.; Johnson, J.R.; Cohen, M.H.; Justice, R.; Pazdur, R., FDA approval summary: vorinostat for treatment of advanced primary cutaneous T-cell lymphoma. Oncologist 2007, 12, 1247-1252.
-
(2007)
Oncologist
, vol.12
, pp. 1247-1252
-
-
Mann, B.S.1
Johnson, J.R.2
Cohen, M.H.3
Justice, R.4
Pazdur, R.5
-
22
-
-
77954884940
-
Romidepsin: A new therapy for cutaneous T-cell lymphoma and a potential therapy for solid tumors
-
Grant, C.; Rahman, F.; Piekarz, R.; Peer, C.; Frye, R.; Robey, R.W.; Gardner, E.R.; Figg, W.D.; Bates, S.E. Romidepsin: A new therapy for cutaneous T-cell lymphoma and a potential therapy for solid tumors. Expert Rev. Anticancer Ther. 2010, 10, 997-1008.
-
(2010)
Expert Rev. Anticancer Ther.
, vol.10
, pp. 997-1008
-
-
Grant, C.1
Rahman, F.2
Piekarz, R.3
Peer, C.4
Frye, R.5
Robey, R.W.6
Gardner, E.R.7
Figg, W.D.8
Bates, S.E.9
-
23
-
-
77955646151
-
Macrocyclic histone deacetylase inhibitors
-
Mwakwari, S.C.; Patil, V.; Guerrant, W.; Oyelere, A.K. Macrocyclic Histone Deacetylase Inhibitors. Curr. Top. Med. Chem. 2010, 10, 1423-1440.
-
(2010)
Curr. Top. Med. Chem.
, vol.10
, pp. 1423-1440
-
-
Mwakwari, S.C.1
Patil, V.2
Guerrant, W.3
Oyelere, A.K.4
-
24
-
-
77950640292
-
Inhibitors of HDACs-Effective drugs against cancer? Curr
-
Muller, S.; Kramer, O.H. Inhibitors of HDACs-Effective drugs against cancer? Curr. Cancer Drug Targets 2010, 10, 210-228.
-
(2010)
Cancer Drug Targets
, vol.10
, pp. 210-228
-
-
Muller, S.1
Kramer, O.H.2
-
25
-
-
84863649774
-
Chimerically designed HDAC- and tyrosine kinase inhibitors
-
Beckers, T.; Mahboobi, S.; Sellmer, A.; Winkler, M.; Eichhorn, E.; Pongratz, H.; Maier, T.; Ciossek, T.; Baer, T.; Kelter, G.; et al. Chimerically designed HDAC- and tyrosine kinase inhibitors. A series of erlotinib hybrids as dual-selective inhibitors of EGFR, HER2 and histone deacetylases. Med. Chem. Comm. 2012, 3, 829.
-
(2012)
A Series of Erlotinib Hybrids As Dual-selective Inhibitors of EGFR, HER2 and Histone Deacetylases. Med. Chem. Comm.
, vol.3
, pp. 829
-
-
Beckers, T.1
Mahboobi, S.2
Sellmer, A.3
Winkler, M.4
Eichhorn, E.5
Pongratz, H.6
Maier, T.7
Ciossek, T.8
Baer, T.9
Kelter, G.10
-
26
-
-
33947364274
-
One-pot conversion of 2-nitrobenzonitriles to quinazolin-4(3H)-ones and synthesis of gefitinib and erlotinib hydrochloride
-
Chandregowda, V.; Rao, G.V.; Reddy, G.C. One-pot conversion of 2-nitrobenzonitriles to quinazolin-4(3H)-ones and synthesis of gefitinib and erlotinib hydrochloride. Heterocycles 2007, 71, 39-48.
-
(2007)
Heterocycles
, vol.71
, pp. 39-48
-
-
Chandregowda, V.1
Rao, G.V.2
Reddy, G.C.3
-
27
-
-
77955463320
-
Chemical genetic strategy identifies histone deacetylase 1 (HDAC1) and HDAC2 as therapeutic targets in sickle cell disease
-
Bradner, J.E.; Mak, R.; Tanguturi, S.K.; Mazitschek, R.; Haggarty, S.J.; Ross, K.; Chang, C.Y.; Bosco, J.; West, N.; Morse, E.; et al. Chemical genetic strategy identifies histone deacetylase 1 (HDAC1) and HDAC2 as therapeutic targets in sickle cell disease. Proc. Natl. Acad. Sci. USA 2010, 107, 12617-12622.
-
(2010)
Proc. Natl. Acad. Sci. USA
, vol.107
, pp. 12617-12622
-
-
Bradner, J.E.1
Mak, R.2
Tanguturi, S.K.3
Mazitschek, R.4
Haggarty, S.J.5
Ross, K.6
Chang, C.Y.7
Bosco, J.8
West, N.9
Morse, E.10
-
28
-
-
70449675089
-
HDAC2: A critical factor in health and disease
-
Kramer, O.H. HDAC2: A critical factor in health and disease. Trends Pharmacol. Sci. 2009, 30, 647-655.
-
(2009)
Trends Pharmacol. Sci.
, vol.30
, pp. 647-655
-
-
Kramer, O.H.1
-
29
-
-
70350331905
-
BB, a new EGFR inhibitor, Exhibits prominent anti-angiogenesis and antitumor activities
-
Sun, Q.M.; Miao, Z.H.; Lin, L.P.; Gui, M.; Zhu, C.H.; Xie, H.; Duan, W.H.; Ding, J. BB, a new EGFR inhibitor, Exhibits prominent anti-angiogenesis and antitumor activities. Cancer Biol. Ther. 2009, 8, 1640-1647.
-
(2009)
Cancer Biol. Ther.
, vol.8
, pp. 1640-1647
-
-
Sun, Q.M.1
Miao, Z.H.2
Lin, L.P.3
Gui, M.4
Zhu, C.H.5
Xie, H.6
Duan, W.H.7
Ding, J.8
|