-
1
-
-
28944432804
-
Multidrug resistance/P-glycoprotein and breast cancer: review and meta-analysis
-
Clarke R., Leonessa F., and Trock B. Multidrug resistance/P-glycoprotein and breast cancer: review and meta-analysis. Semin. Oncol. 32 (2005) S9-S15
-
(2005)
Semin. Oncol.
, vol.32
-
-
Clarke, R.1
Leonessa, F.2
Trock, B.3
-
2
-
-
0035902115
-
Proliferation, cell cycle and apoptosis in cancer
-
Evan G.I., and Vousden K.H. Proliferation, cell cycle and apoptosis in cancer. Nature 411 (2001) 245-248
-
(2001)
Nature
, vol.411
, pp. 245-248
-
-
Evan, G.I.1
Vousden, K.H.2
-
4
-
-
0041347519
-
Histone deacetylase inhibitors in cancer therapy: is transcription the primary target?
-
Johnstone R.W., and Licht J.D. Histone deacetylase inhibitors in cancer therapy: is transcription the primary target?. Cancer Cell 4 (2003) 13-18
-
(2003)
Cancer Cell
, vol.4
, pp. 13-18
-
-
Johnstone, R.W.1
Licht, J.D.2
-
5
-
-
0035839136
-
Translating the histone code
-
Jenuwein T., and Alli's C.D. Translating the histone code. Science 293 (2001) 1074-1080
-
(2001)
Science
, vol.293
, pp. 1074-1080
-
-
Jenuwein, T.1
Alli's, C.D.2
-
7
-
-
0032694596
-
Inhibitors of histone deacetylase suppress the growth of MCF-7 breast cancer cells
-
Schmidt K., Gust R., and Jung M. Inhibitors of histone deacetylase suppress the growth of MCF-7 breast cancer cells. Arch. Pharm. 332 (1999) 353-357
-
(1999)
Arch. Pharm.
, vol.332
, pp. 353-357
-
-
Schmidt, K.1
Gust, R.2
Jung, M.3
-
8
-
-
0033740191
-
Histone deacetylase inhibitors decrease proliferation and modulate cell cycle gene expression in normal mammary epithelial cells
-
Davis T., Kennedy C., Chiew Y.-E., Clarke C.L., and DeFazio A. Histone deacetylase inhibitors decrease proliferation and modulate cell cycle gene expression in normal mammary epithelial cells. Clin. Cancer Res. 6 (2000) 4334-4342
-
(2000)
Clin. Cancer Res.
, vol.6
, pp. 4334-4342
-
-
Davis, T.1
Kennedy, C.2
Chiew, Y.-E.3
Clarke, C.L.4
DeFazio, A.5
-
9
-
-
0034901985
-
Trichostatin A is a histone deacetylase inhibitor with potent antitumor activity against breast cancer in vivo
-
Vigushin D.M., Ali A., Pace P.E., Mirsaidi N., Ito K., Adcock I., and Coombes R.C. Trichostatin A is a histone deacetylase inhibitor with potent antitumor activity against breast cancer in vivo. Clin. Cancer Res. 7 (2001) 971-976
-
(2001)
Clin. Cancer Res.
, vol.7
, pp. 971-976
-
-
Vigushin, D.M.1
Ali, A.2
Pace, P.E.3
Mirsaidi, N.4
Ito, K.5
Adcock, I.6
Coombes, R.C.7
-
10
-
-
0035965343
-
Histone deacetylase is a direct target of valproic acid, a potent anticonvulsant, mood stabilizer, and teratogen
-
Phiel C.J., Zhang F., Huang E.Y., Guenther M.G., Lazar M.A., and Klein P.S. Histone deacetylase is a direct target of valproic acid, a potent anticonvulsant, mood stabilizer, and teratogen. J. Biol. Chem. 276 (2001) 36734-36741
-
(2001)
J. Biol. Chem.
, vol.276
, pp. 36734-36741
-
-
Phiel, C.J.1
Zhang, F.2
Huang, E.Y.3
Guenther, M.G.4
Lazar, M.A.5
Klein, P.S.6
-
12
-
-
35348961982
-
Inhibition of histone deacetylase enhances the anti-proliferative action of antiestrogens on breast cancer cells and blocks tamoxifen-induced proliferation of uterine cells
-
Hodges-Gallagher L., Valentine C.D., Bader S.E., and Kushner P.J. Inhibition of histone deacetylase enhances the anti-proliferative action of antiestrogens on breast cancer cells and blocks tamoxifen-induced proliferation of uterine cells. Breast Cancer Res. Treat. 105 (2007) 297-309
-
(2007)
Breast Cancer Res. Treat.
, vol.105
, pp. 297-309
-
-
Hodges-Gallagher, L.1
Valentine, C.D.2
Bader, S.E.3
Kushner, P.J.4
-
13
-
-
17444373424
-
Cytochrome C is released from mitochondria into the cytosol after cerebral anoxia or ischemia
-
Perez-Pinzon M.A., Xu G.P., Born J., Lorenzo J., Busto R., Rosenthal M., and Sick T.J. Cytochrome C is released from mitochondria into the cytosol after cerebral anoxia or ischemia. J. Cer. Blood Flow Met. 19 (1999) 39-43
-
(1999)
J. Cer. Blood Flow Met.
, vol.19
, pp. 39-43
-
-
Perez-Pinzon, M.A.1
Xu, G.P.2
Born, J.3
Lorenzo, J.4
Busto, R.5
Rosenthal, M.6
Sick, T.J.7
-
14
-
-
0028283303
-
Animal models and molecular markers for cerebral ischemia- reperfusion injury in brain
-
Ravindranath V. Animal models and molecular markers for cerebral ischemia- reperfusion injury in brain. Methods Enzymol. 233 (1994) 610-619
-
(1994)
Methods Enzymol.
, vol.233
, pp. 610-619
-
-
Ravindranath, V.1
-
15
-
-
0027411268
-
Identification of an NADH plus iron dependent, Ca2+ activated hydrogen peroxide production in synaptosomes
-
Zoccarato F., Valente M., and Alexandre A. Identification of an NADH plus iron dependent, Ca2+ activated hydrogen peroxide production in synaptosomes. Biochim. Biophys. Acta 1176 (1993) 208-214
-
(1993)
Biochim. Biophys. Acta
, vol.1176
, pp. 208-214
-
-
Zoccarato, F.1
Valente, M.2
Alexandre, A.3
-
16
-
-
0023277545
-
Single step method of RNA isolation by guanidinium thiocyanate-phenol-chloroform extraction
-
Chomczynski P., and Sacchi N. Single step method of RNA isolation by guanidinium thiocyanate-phenol-chloroform extraction. Anal. Biochem. 162 (1987) 156-159
-
(1987)
Anal. Biochem.
, vol.162
, pp. 156-159
-
-
Chomczynski, P.1
Sacchi, N.2
-
17
-
-
3242690866
-
Pharmacokinetics, drug interactions, and tolerability of valproate
-
DeVane C.L. Pharmacokinetics, drug interactions, and tolerability of valproate. Psychopharmacol. Bull. 37 (2003) 25-42
-
(2003)
Psychopharmacol. Bull.
, vol.37
, pp. 25-42
-
-
DeVane, C.L.1
-
18
-
-
0344306402
-
Apoptotic pathways activated by histone deacetylase inhibitors: implications for the drug-resistant phenotype
-
Henderson C., and Brancolini C. Apoptotic pathways activated by histone deacetylase inhibitors: implications for the drug-resistant phenotype. Drug Res. Update 6 (2003) 247-256
-
(2003)
Drug Res. Update
, vol.6
, pp. 247-256
-
-
Henderson, C.1
Brancolini, C.2
-
20
-
-
0036176617
-
Histone deacetylase inhibitors in cancer treatment
-
Vigushin D.M., and Coombes R.C. Histone deacetylase inhibitors in cancer treatment. Anticancer Drugs 13 (2002) 1-13
-
(2002)
Anticancer Drugs
, vol.13
, pp. 1-13
-
-
Vigushin, D.M.1
Coombes, R.C.2
-
21
-
-
0035577768
-
The histone deacetylase inhibitor suberoylanilide hydroxamic acid induces differentiation of human breast cancer cells
-
Munster P.N., Troso-Sandoval T., Rosen N., Rifkind R., Marks P.A., and Richon V.M. The histone deacetylase inhibitor suberoylanilide hydroxamic acid induces differentiation of human breast cancer cells. Cancer Res. 61 (2001) 8492-8497
-
(2001)
Cancer Res.
, vol.61
, pp. 8492-8497
-
-
Munster, P.N.1
Troso-Sandoval, T.2
Rosen, N.3
Rifkind, R.4
Marks, P.A.5
Richon, V.M.6
-
22
-
-
0034730127
-
Histone deacetylase inhibitors selectively induce p21WAF expression and gene-associated histone acetylation
-
Richon V.M., Sandhoff T.W., Rifkind R.A., and Marks P.A. Histone deacetylase inhibitors selectively induce p21WAF expression and gene-associated histone acetylation. Proc. Natl. Acad. Sci. USA 97 (2000) 10014-10019
-
(2000)
Proc. Natl. Acad. Sci. USA
, vol.97
, pp. 10014-10019
-
-
Richon, V.M.1
Sandhoff, T.W.2
Rifkind, R.A.3
Marks, P.A.4
-
23
-
-
0033520944
-
Histone deacetylase inhibition selectively alters the activity and expression of the cell cycle proteins leading to specific chromatin acetylation and antiproliferative effects
-
Sambucetti L.C., Fisher D.D., Zabludoff S., Known P.O., Chamberlin H., Trogani N., Xu H., and Cohen D. Histone deacetylase inhibition selectively alters the activity and expression of the cell cycle proteins leading to specific chromatin acetylation and antiproliferative effects. J. Biol. Chem. 274 (1999) 34940-34947
-
(1999)
J. Biol. Chem.
, vol.274
, pp. 34940-34947
-
-
Sambucetti, L.C.1
Fisher, D.D.2
Zabludoff, S.3
Known, P.O.4
Chamberlin, H.5
Trogani, N.6
Xu, H.7
Cohen, D.8
-
24
-
-
0033551152
-
A synthetic inhibitor of histone deacetylase, MS-27-275, with marked in vitro antitumor activity against human tumors
-
Saito A., Yamashita T., Makiro Y., Nosaka Y., Tsuchiya K., Ando T., Suzuki T., Tsuruo T., and Nakanishi O. A synthetic inhibitor of histone deacetylase, MS-27-275, with marked in vitro antitumor activity against human tumors. Proc. Natl. Acad. Sci. USA 96 (1999) 4592-4597
-
(1999)
Proc. Natl. Acad. Sci. USA
, vol.96
, pp. 4592-4597
-
-
Saito, A.1
Yamashita, T.2
Makiro, Y.3
Nosaka, Y.4
Tsuchiya, K.5
Ando, T.6
Suzuki, T.7
Tsuruo, T.8
Nakanishi, O.9
-
25
-
-
0034930374
-
Apoptosis is critical for drug response in vivo
-
Schmitt C.A., and Lowe S.W. Apoptosis is critical for drug response in vivo. Drug. Resist. Updat. 4 (2001) 132-134
-
(2001)
Drug. Resist. Updat.
, vol.4
, pp. 132-134
-
-
Schmitt, C.A.1
Lowe, S.W.2
-
26
-
-
0038485588
-
Role of caspases, Bid, and p53 in the apoptotic response triggered by histone deacetylase inhibitors Trichostatin-A (TSA) and Suberoylanilide Hidroxamic Acid (SAHA)
-
Henderson C., Mizzau M., Paroni G., Maestro R., Schneider C., and Brancolini C. Role of caspases, Bid, and p53 in the apoptotic response triggered by histone deacetylase inhibitors Trichostatin-A (TSA) and Suberoylanilide Hidroxamic Acid (SAHA). J. Biol. Chem. 278 (2003) 12579-12589
-
(2003)
J. Biol. Chem.
, vol.278
, pp. 12579-12589
-
-
Henderson, C.1
Mizzau, M.2
Paroni, G.3
Maestro, R.4
Schneider, C.5
Brancolini, C.6
-
27
-
-
0035845541
-
The histone deacetylase inhibitor and chemotherapeutic agent suberoylanilide hydroxamic acid (SAHA) induces a cell-death pathway characterized by cleavage of Bid and production of reactive oxygen species
-
Ruefli A.A., Ausserlechner M.J., Bernhard D., Sutton V.R., Tainton K.M., Kofler R., Smyth M.J., and Johnstone R.W. The histone deacetylase inhibitor and chemotherapeutic agent suberoylanilide hydroxamic acid (SAHA) induces a cell-death pathway characterized by cleavage of Bid and production of reactive oxygen species. Proc. Natl. Acad. Sci. USA 98 (2001) 10833-10838
-
(2001)
Proc. Natl. Acad. Sci. USA
, vol.98
, pp. 10833-10838
-
-
Ruefli, A.A.1
Ausserlechner, M.J.2
Bernhard, D.3
Sutton, V.R.4
Tainton, K.M.5
Kofler, R.6
Smyth, M.J.7
Johnstone, R.W.8
-
28
-
-
0037421221
-
Caspase-mediated loss of mitochondrial function and generation of reactive oxygen species during apoptosis
-
Ricci J.E., Gottlieb R.A., and Green D.R. Caspase-mediated loss of mitochondrial function and generation of reactive oxygen species during apoptosis. J. Cell Biol. 160 (2003) 65-75
-
(2003)
J. Cell Biol.
, vol.160
, pp. 65-75
-
-
Ricci, J.E.1
Gottlieb, R.A.2
Green, D.R.3
-
29
-
-
0035877605
-
Caspase-2-induced apoptosis is dependent on caspase-9, but its processing during UV- or tumor necrosis factor-dependent cell death requires caspase-3
-
Paroni G., Henderson C., Schneider C., and Brancolini C. Caspase-2-induced apoptosis is dependent on caspase-9, but its processing during UV- or tumor necrosis factor-dependent cell death requires caspase-3. J. Biol. Chem. 276 (2001) 21907-21915
-
(2001)
J. Biol. Chem.
, vol.276
, pp. 21907-21915
-
-
Paroni, G.1
Henderson, C.2
Schneider, C.3
Brancolini, C.4
-
30
-
-
10544250250
-
Cell cycle independent regulation of p21Waf1/Cip1 and retinoblastoma protein during okadaic acid-induced apoptosis is coupled with induction of Bax protein in human breast carcinoma cells
-
Sheikh M.S., Garcia M., Zhan Q., Liu Y., and Fornace A.J. Cell cycle independent regulation of p21Waf1/Cip1 and retinoblastoma protein during okadaic acid-induced apoptosis is coupled with induction of Bax protein in human breast carcinoma cells. Cell Growth Differ. 7 (1996) 1599-1607
-
(1996)
Cell Growth Differ.
, vol.7
, pp. 1599-1607
-
-
Sheikh, M.S.1
Garcia, M.2
Zhan, Q.3
Liu, Y.4
Fornace, A.J.5
-
31
-
-
0142182098
-
Oestrogen receptor alpha increases p21(WAF1/CIP1) gene expression and the antiproliferative activity of histone deacetylase inhibitors in human breast cancer cells
-
Margueron R., Licznar A., Lazennec G., Vignon F., and Cavaillès V. Oestrogen receptor alpha increases p21(WAF1/CIP1) gene expression and the antiproliferative activity of histone deacetylase inhibitors in human breast cancer cells. J. Endocrinol. 179 (2003) 41-53
-
(2003)
J. Endocrinol.
, vol.179
, pp. 41-53
-
-
Margueron, R.1
Licznar, A.2
Lazennec, G.3
Vignon, F.4
Cavaillès, V.5
-
32
-
-
33746842309
-
DNA damage-dependent cell cycle checkpoints and genomic stability
-
Ishikawa K., Ishii H., and Saito T. DNA damage-dependent cell cycle checkpoints and genomic stability. DNA Cell Biol. 25 (2006) 406-411
-
(2006)
DNA Cell Biol.
, vol.25
, pp. 406-411
-
-
Ishikawa, K.1
Ishii, H.2
Saito, T.3
-
33
-
-
1442352159
-
Valproic acid induces the expression of the Na symporter and iodine uptake in poorly differentiated thyroid cancer cells
-
Fortunati N., Catalano M.G., Arena K., Brignardello E., Piovesan A., and Boccuzzi G. Valproic acid induces the expression of the Na symporter and iodine uptake in poorly differentiated thyroid cancer cells. J. Clin. Endocrinol. Metab. 89 (2004) 1006-1009
-
(2004)
J. Clin. Endocrinol. Metab.
, vol.89
, pp. 1006-1009
-
-
Fortunati, N.1
Catalano, M.G.2
Arena, K.3
Brignardello, E.4
Piovesan, A.5
Boccuzzi, G.6
-
34
-
-
15944372866
-
Valproic acid induces apoptosis and cell cycle arrest in poorly differentiated thyroid cancer cells
-
Catalano M.G., Fortunati N., Pugliese M., Costantino L., Poli R., Bosco O., and Boccuzzi G. Valproic acid induces apoptosis and cell cycle arrest in poorly differentiated thyroid cancer cells. J. Clin. Endocrinol. Metab. 90 (2005) 383-1389
-
(2005)
J. Clin. Endocrinol. Metab.
, vol.90
, pp. 383-1389
-
-
Catalano, M.G.1
Fortunati, N.2
Pugliese, M.3
Costantino, L.4
Poli, R.5
Bosco, O.6
Boccuzzi, G.7
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