-
1
-
-
77955635233
-
Cancer statistics
-
doi: 10.3322/caac.20073
-
Jemal A, Siegel R, Xu J, Ward E, (2010) Cancer statistics CA Cancer J Clin 60: 277-300. doi:10.3322/caac.20073. PubMed: 20610543.
-
(2010)
CA Cancer J Clin
, vol.60
, pp. 277-300
-
-
Jemal, A.1
Siegel, R.2
Xu, J.3
Ward, E.4
-
2
-
-
67349237892
-
Histone deacetylase inhibitor induced modulation of anti-estrogen therapy
-
doi: 10.1016/j.canlet.2008.12.026
-
Thomas S, Munster PN, (2009) Histone deacetylase inhibitor induced modulation of anti-estrogen therapy. Cancer Lett 280: 184-191. doi:10.1016/j.canlet.2008.12.026. PubMed: 19185986.
-
(2009)
Cancer Lett
, vol.280
, pp. 184-191
-
-
Thomas, S.1
Munster, P.N.2
-
3
-
-
79951519871
-
Invasive breast cancer
-
Carlson RW, Allred DC, Anderson BO, Burstein HJ, Carter WB, et al. (2011) Invasive breast cancer. J Natl Compr Canc Netw JNCCN 9: 136-222.
-
(2011)
J Natl Compr Canc Netw JNCCN
, vol.9
, pp. 136-222
-
-
Carlson, R.W.1
Allred, D.C.2
Anderson, B.O.3
Burstein, H.J.4
Carter, W.B.5
-
4
-
-
80052009896
-
Epigenetic modulation: a novel therapeutic target for overcoming hormonal therapy resistance
-
doi: 10.2217/epi.11.72
-
Raha P, Thomas S, Munster PN, (2011) Epigenetic modulation: a novel therapeutic target for overcoming hormonal therapy resistance. Epigenomics 3: 451-470. doi:10.2217/epi.11.72. PubMed: 22126205.
-
(2011)
Epigenomics
, vol.3
, pp. 451-470
-
-
Raha, P.1
Thomas, S.2
Munster, P.N.3
-
5
-
-
84863078767
-
Everolimus in postmenopausal hormone-receptor-positive advanced breast cancer
-
doi: 10.1056/NEJMoa1109653
-
Baselga J, Campone M, Piccart M, Burris HA 3rd, Rugo HS, et al. (2012) Everolimus in postmenopausal hormone-receptor-positive advanced breast cancer. N Engl J Med 366: 520-529. doi:10.1056/NEJMoa1109653. PubMed: 22149876.
-
(2012)
N Engl J Med
, vol.366
, pp. 520-529
-
-
Baselga, J.1
Campone, M.2
Piccart, M.3
Burris 3rd, H.A.4
Rugo, H.S.5
-
6
-
-
40449132791
-
Selective inhibition of histone deacetylase 2 silences progesterone receptor mediated signaling
-
doi: 10.1158/0008-5472.CAN-07-2822
-
Biçaku E, Marchion DC, Schmitt ML, Münster PN, (2008) Selective inhibition of histone deacetylase 2 silences progesterone receptor mediated signaling. Cancer Res 68: 1513-1519. doi:10.1158/0008-5472.CAN-07-2822. PubMed: 18316616.
-
(2008)
Cancer Res
, vol.68
, pp. 1513-1519
-
-
Biçaku, E.1
Marchion, D.C.2
Schmitt, M.L.3
Münster, P.N.4
-
7
-
-
82955170653
-
Addition of a histone deacetylase inhibitor redirects tamoxifen-treated breast cancer cells into apoptosis, which is opposed by the induction of autophagy
-
doi: 10.1007/s10549-011-1364-y
-
Thomas S, Thurn KT, Biçaku E, Marchion DC, Münster PN, (2011) Addition of a histone deacetylase inhibitor redirects tamoxifen-treated breast cancer cells into apoptosis, which is opposed by the induction of autophagy. Breast Cancer Res Treat 130: 437-447. doi:10.1007/s10549-011-1364-y. PubMed: 21298336.
-
(2011)
Breast Cancer Res Treat
, vol.130
, pp. 437-447
-
-
Thomas, S.1
Thurn, K.T.2
Biçaku, E.3
Marchion, D.C.4
Münster, P.N.5
-
9
-
-
79958084461
-
A phase II study of the histone deacetylase inhibitor vorinostat combined with tamoxifen for the treatment of patients with hormone therapy-resistant breast cancer
-
doi: 10.1038/bjc.2011.156
-
Munster PN, Thurn KT, Thomas S, Raha P, Lacevic M, et al. (2011) A phase II study of the histone deacetylase inhibitor vorinostat combined with tamoxifen for the treatment of patients with hormone therapy-resistant breast cancer. Br J Cancer 104: 1828-1835. doi:10.1038/bjc.2011.156. PubMed: 21559012.
-
(2011)
Br J Cancer
, vol.104
, pp. 1828-1835
-
-
Munster, P.N.1
Thurn, K.T.2
Thomas, S.3
Raha, P.4
Lacevic, M.5
-
10
-
-
79952259688
-
Gefitinib or placebo in combination with tamoxifen in patients with hormone receptor-positive metastatic breast cancer: a randomized phase II study
-
doi: 10.1158/1078-0432.CCR-10-1869
-
Osborne CK, Neven P, Dirix LY, Mackey JR, Robert J, et al. (2011) Gefitinib or placebo in combination with tamoxifen in patients with hormone receptor-positive metastatic breast cancer: a randomized phase II study. Clin Cancer Res 17: 1147-1159. doi:10.1158/1078-0432.CCR-10-1869. PubMed: 21220480.
-
(2011)
Clin Cancer Res
, vol.17
, pp. 1147-1159
-
-
Osborne, C.K.1
Neven, P.2
Dirix, L.Y.3
Mackey, J.R.4
Robert, J.5
-
11
-
-
51049118140
-
An integrative genomic and proteomic analysis of PIK3CA, PTEN, and AKT mutations in breast cancer
-
doi: 10.1158/0008-5472.CAN-07-6854
-
Stemke-Hale K, Gonzalez-Angulo AM, Lluch A, Neve RM, Kuo WL, et al. (2008) An integrative genomic and proteomic analysis of PIK3CA, PTEN, and AKT mutations in breast cancer. Cancer Res 68: 6084-6091. doi:10.1158/0008-5472.CAN-07-6854. PubMed: 18676830.
-
(2008)
Cancer Res
, vol.68
, pp. 6084-6091
-
-
Stemke-Hale, K.1
Gonzalez-Angulo, A.M.2
Lluch, A.3
Neve, R.M.4
Kuo, W.L.5
-
12
-
-
34547172596
-
A transforming mutation in the pleckstrin homology domain of AKT1 in cancer
-
doi: 10.1038/nature05933
-
Carpten JD, Faber AL, Horn C, Donoho GP, Briggs SL, et al. (2007) A transforming mutation in the pleckstrin homology domain of AKT1 in cancer. Nature 448: 439-444. doi:10.1038/nature05933. PubMed: 17611497.
-
(2007)
Nature
, vol.448
, pp. 439-444
-
-
Carpten, J.D.1
Faber, A.L.2
Horn, C.3
Donoho, G.P.4
Briggs, S.L.5
-
13
-
-
0029127042
-
Molecular alterations of the AKT2 oncogene in ovarian and breast carcinomas
-
doi: 10.1002/ijc.2910640412
-
Bellacosa A, de Feo D, Godwin AK, Bell DW, Cheng JQ, et al. (1995) Molecular alterations of the AKT2 oncogene in ovarian and breast carcinomas. Int J Cancer J Int Cancer 64: 280-285. doi:10.1002/ijc.2910640412. PubMed: 7657393.
-
(1995)
Int J Cancer J Int Cancer
, vol.64
, pp. 280-285
-
-
Bellacosa, A.1
de Feo, D.2
Godwin, A.K.3
Bell, D.W.4
Cheng, J.Q.5
-
14
-
-
0034742120
-
AKT1/PKBalpha kinase is frequently elevated in human cancers and its constitutive activation is required for oncogenic transformation in NIH3T3 cells
-
doi: 10.1016/S0002-9440(10)61714-2
-
Sun M, Wang G, Paciga JE, Feldman RI, Yuan ZQ, et al. (2001) AKT1/PKBalpha kinase is frequently elevated in human cancers and its constitutive activation is required for oncogenic transformation in NIH3T3 cells. Am J Pathol 159: 431-437. doi:10.1016/S0002-9440(10)61714-2. PubMed: 11485901.
-
(2001)
Am J Pathol
, vol.159
, pp. 431-437
-
-
Sun, M.1
Wang, G.2
Paciga, J.E.3
Feldman, R.I.4
Yuan, Z.Q.5
-
15
-
-
0036632368
-
The phosphatidylinositol 3-Kinase AKT pathway in human cancer
-
doi: 10.1038/nrc839
-
Vivanco I, Sawyers CL, (2002) The phosphatidylinositol 3-Kinase AKT pathway in human cancer. Nat Rev Cancer 2: 489-501. doi:10.1038/nrc839. PubMed: 12094235.
-
(2002)
Nat Rev Cancer
, vol.2
, pp. 489-501
-
-
Vivanco, I.1
Sawyers, C.L.2
-
16
-
-
13844312400
-
Phosphorylation and regulation of Akt/PKB by the rictor-mTOR complex
-
doi: 10.1126/science.1106148
-
Sarbassov DD, Guertin DA, Ali SM, Sabatini DM, (2005) Phosphorylation and regulation of Akt/PKB by the rictor-mTOR complex. Science 307: 1098-1101. doi:10.1126/science.1106148. PubMed: 15718470.
-
(2005)
Science
, vol.307
, pp. 1098-1101
-
-
Sarbassov, D.D.1
Guertin, D.A.2
Ali, S.M.3
Sabatini, D.M.4
-
17
-
-
0032578999
-
Protein kinase B kinases that mediate phosphatidylinositol 3,4,5-trisphosphate-dependent activation of protein kinase B
-
doi: 10.1126/science.279.5351.710
-
Stephens L, Anderson K, Stokoe D, Erdjument-Bromage H, Painter GF, et al. (1998) Protein kinase B kinases that mediate phosphatidylinositol 3,4,5-trisphosphate-dependent activation of protein kinase B. Science 279: 710-714. doi:10.1126/science.279.5351.710. PubMed: 9445477.
-
(1998)
Science
, vol.279
, pp. 710-714
-
-
Stephens, L.1
Anderson, K.2
Stokoe, D.3
Erdjument-Bromage, H.4
Painter, G.F.5
-
18
-
-
0030702123
-
Akt phosphorylation of BAD couples survival signals to the cell-intrinsic death machinery
-
doi: 10.1016/S0092-8674(00)80405-5
-
Datta SR, Dudek H, Tao X, Masters S, Fu H, et al. (1997) Akt phosphorylation of BAD couples survival signals to the cell-intrinsic death machinery. Cell 91: 231-241. doi:10.1016/S0092-8674(00)80405-5. PubMed: 9346240.
-
(1997)
Cell
, vol.91
, pp. 231-241
-
-
Datta, S.R.1
Dudek, H.2
Tao, X.3
Masters, S.4
Fu, H.5
-
19
-
-
0033582929
-
Akt promotes cell survival by phosphorylating and inhibiting a Forkhead transcription factor
-
doi: 10.1016/S0092-8674(00)80595-4
-
Brunet A, Bonni A, Zigmond MJ, Lin MZ, Juo P, et al. (1999) Akt promotes cell survival by phosphorylating and inhibiting a Forkhead transcription factor. Cell 96: 857-868. doi:10.1016/S0092-8674(00)80595-4. PubMed: 10102273.
-
(1999)
Cell
, vol.96
, pp. 857-868
-
-
Brunet, A.1
Bonni, A.2
Zigmond, M.J.3
Lin, M.Z.4
Juo, P.5
-
20
-
-
0029587224
-
Inhibition of glycogen synthase kinase-3 by insulin mediated by protein kinase B
-
doi: 10.1038/378785a0
-
Cross DA, Alessi DR, Cohen P, Andjelkovich M, Hemmings BA, (1995) Inhibition of glycogen synthase kinase-3 by insulin mediated by protein kinase B. Nature 378: 785-789. doi:10.1038/378785a0. PubMed: 8524413.
-
(1995)
Nature
, vol.378
, pp. 785-789
-
-
Cross, D.A.1
Alessi, D.R.2
Cohen, P.3
Andjelkovich, M.4
Hemmings, B.A.5
-
21
-
-
33644663872
-
Histone acetylation-independent effect of histone deacetylase inhibitors on Akt through the reshuffling of protein phosphatase 1 complexes
-
doi: 10.1074/jbc.M505733200
-
Chen CS, Weng SC, Tseng PH, Lin HP, (2005) Histone acetylation-independent effect of histone deacetylase inhibitors on Akt through the reshuffling of protein phosphatase 1 complexes. J Biol Chem 280: 38879-38887. doi:10.1074/jbc.M505733200. PubMed: 16186112.
-
(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
-
22
-
-
33644836891
-
Histone deacetylase inhibitor, trichostatin A induces ubiquitin-dependent cyclin D1 degradation in MCF-7 breast cancer cells
-
doi: 10.1186/1476-4598-5-8
-
Alao JP, Stavropoulou AV, Lam EW, Coombes RC, Vigushin DM, (2006) Histone deacetylase inhibitor, trichostatin A induces ubiquitin-dependent cyclin D1 degradation in MCF-7 breast cancer cells. Mol Cancer 5: 8. doi:10.1186/1476-4598-5-8. PubMed: 16504004.
-
(2006)
Mol Cancer
, vol.5
, pp. 8
-
-
Alao, J.P.1
Stavropoulou, A.V.2
Lam, E.W.3
Coombes, R.C.4
Vigushin, D.M.5
-
23
-
-
33749593863
-
Role of glycogen synthase kinase 3 beta (GSK3beta) in mediating the cytotoxic effects of the histone deacetylase inhibitor trichostatin A (TSA) in MCF-7 breast cancer cells
-
doi: 10.1186/1476-4598-5-40
-
Alao JP, Stavropoulou AV, Lam EW, Coombes RC, (2006) Role of glycogen synthase kinase 3 beta (GSK3beta) in mediating the cytotoxic effects of the histone deacetylase inhibitor trichostatin A (TSA) in MCF-7 breast cancer cells. Mol Cancer 5: 40. doi:10.1186/1476-4598-5-40. PubMed: 17018141.
-
(2006)
Mol Cancer
, vol.5
, pp. 40
-
-
Alao, J.P.1
Stavropoulou, A.V.2
Lam, E.W.3
Coombes, R.C.4
-
24
-
-
84875985004
-
Histone deacetylase 3 suppression increases PH domain and leucine-rich repeat phosphatase (Phlpp)1 expression in chondrocytes to suppress Akt signaling and matrix secretion
-
doi: 10.1074/jbc.M112.423723
-
Bradley EW, Carpio LR, Westendorf JJ, (2013) Histone deacetylase 3 suppression increases PH domain and leucine-rich repeat phosphatase (Phlpp)1 expression in chondrocytes to suppress Akt signaling and matrix secretion. J Biol Chem 288: 9572-9582. doi:10.1074/jbc.M112.423723. PubMed: 23408427.
-
(2013)
J Biol Chem
, vol.288
, pp. 9572-9582
-
-
Bradley, E.W.1
Carpio, L.R.2
Westendorf, J.J.3
-
25
-
-
33745087150
-
CRA-024781: a novel synthetic inhibitor of histone deacetylase enzymes with antitumor activity in vitro and in vivo
-
doi: 10.1158/1535-7163.MCT-05-0442
-
Buggy JJ, Cao ZA, Bass KE, Verner E, Balasubramanian S, et al. (2006) CRA-024781: a novel synthetic inhibitor of histone deacetylase enzymes with antitumor activity in vitro and in vivo. Mol Cancer Ther 5: 1309-1317. doi:10.1158/1535-7163.MCT-05-0442. PubMed: 16731764.
-
(2006)
Mol Cancer Ther
, vol.5
, pp. 1309-1317
-
-
Buggy, J.J.1
Cao, Z.A.2
Bass, K.E.3
Verner, E.4
Balasubramanian, S.5
-
26
-
-
66249095933
-
Phase I study of the safety, pharmacokinetics (PK) and pharmacodynamics (PD) of the histone deacetylase inhibitor (HDACi) PCI-24781
-
abstr 14514
-
Undevia SD, Janisch L, Schilsky RL, Loury D, Balasubramanian S, et al. (2008) Phase I study of the safety, pharmacokinetics (PK) and pharmacodynamics (PD) of the histone deacetylase inhibitor (HDACi) PCI-24781. J Clin Oncol 26 (suppl)(): abstr 14514.
-
(2008)
J Clin Oncol
, vol.26
, Issue.SUPPL.
-
-
Undevia, S.D.1
Janisch, L.2
Schilsky, R.L.3
Loury, D.4
Balasubramanian, S.5
-
27
-
-
21144444486
-
HDAC6 regulates Hsp90 acetylation and chaperone-dependent activation of glucocorticoid receptor
-
doi: 10.1016/j.molcel.2005.04.021
-
Kovacs JJ, Murphy PJ, Gaillard S, Zhao X, Wu JT, et al. (2005) HDAC6 regulates Hsp90 acetylation and chaperone-dependent activation of glucocorticoid receptor. Mol Cell 18: 601-607. doi:10.1016/j.molcel.2005.04.021. PubMed: 15916966.
-
(2005)
Mol Cell
, vol.18
, pp. 601-607
-
-
Kovacs, J.J.1
Murphy, P.J.2
Gaillard, S.3
Zhao, X.4
Wu, J.T.5
-
28
-
-
0037131187
-
Akt forms an intracellular complex with heat shock protein 90 (Hsp90) and Cdc37 and is destabilized by inhibitors of Hsp90 function
-
doi: 10.1074/jbc.M206322200
-
Basso AD, Solit DB, Chiosis G, Giri B, Tsichlis P, et al. (2002) Akt forms an intracellular complex with heat shock protein 90 (Hsp90) and Cdc37 and is destabilized by inhibitors of Hsp90 function. J Biol Chem 277: 39858-39866. doi:10.1074/jbc.M206322200. PubMed: 12176997.
-
(2002)
J Biol Chem
, vol.277
, pp. 39858-39866
-
-
Basso, A.D.1
Solit, D.B.2
Chiosis, G.3
Giri, B.4
Tsichlis, P.5
-
29
-
-
84861995114
-
Relative Expression Levels Rather Than Specific Activity Plays the Major Role in Determining In Vivo AKT Isoform Substrate Specificity
-
720985, 21869924
-
Lee RS, House CM, Cristiano BE, Hannan RD, Pearson RB, et al. (2011) Relative Expression Levels Rather Than Specific Activity Plays the Major Role in Determining In Vivo AKT Isoform Substrate Specificity. Enzyme Res, 2011(2011): 720985. PubMed: 21869924.
-
(2011)
Enzyme Res
, vol.2011
-
-
Lee, R.S.1
House, C.M.2
Cristiano, B.E.3
Hannan, R.D.4
Pearson, R.B.5
-
30
-
-
41949118169
-
Histone deacetylase inhibitor SAHA induces ERalpha degradation in breast cancer MCF-7 cells by CHIP-mediated ubiquitin pathway and inhibits survival signaling
-
doi: 10.1016/j.bcp.2007.10.035
-
Yi X, Wei W, Wang SY, Du ZY, Xu YJ, et al. (2008) Histone deacetylase inhibitor SAHA induces ERalpha degradation in breast cancer MCF-7 cells by CHIP-mediated ubiquitin pathway and inhibits survival signaling. Biochem Pharmacol 75: 1697-1705. doi:10.1016/j.bcp.2007.10.035. PubMed: 18342836.
-
(2008)
Biochem Pharmacol
, vol.75
, pp. 1697-1705
-
-
Yi, X.1
Wei, W.2
Wang, S.Y.3
Du, Z.Y.4
Xu, Y.J.5
-
31
-
-
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
-
doi: 10.1074/jbc.C500186200
-
Bali P, Pranpat M, Bradner J, Balasis M, Fiskus W, et al. (2005) 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 280: 26729-26734. doi:10.1074/jbc.C500186200. PubMed: 15937340.
-
(2005)
J Biol Chem
, vol.280
, pp. 26729-26734
-
-
Bali, P.1
Pranpat, M.2
Bradner, J.3
Balasis, M.4
Fiskus, W.5
-
32
-
-
34548075217
-
Hydroxamic acid analogue histone deacetylase inhibitors attenuate estrogen receptor-alpha levels and transcriptional activity: a result of hyperacetylation and inhibition of chaperone function of heat shock protein 90
-
doi: 10.1158/1078-0432.CCR-06-3093
-
Fiskus W, Ren Y, Mohapatra A, Bali P, Mandawat A, et al. (2007) Hydroxamic acid analogue histone deacetylase inhibitors attenuate estrogen receptor-alpha levels and transcriptional activity: a result of hyperacetylation and inhibition of chaperone function of heat shock protein 90. Clin Cancer Res 13: 4882-4890. doi:10.1158/1078-0432.CCR-06-3093. PubMed: 17699868.
-
(2007)
Clin Cancer Res
, vol.13
, pp. 4882-4890
-
-
Fiskus, W.1
Ren, Y.2
Mohapatra, A.3
Bali, P.4
Mandawat, A.5
-
33
-
-
32944462300
-
Rapid alteration of microRNA levels by histone deacetylase inhibition
-
doi: 10.1158/0008-5472.CAN-05-3632
-
Scott GK, Mattie MD, Berger CE, Benz SC, Benz CC, (2006) Rapid alteration of microRNA levels by histone deacetylase inhibition. Cancer Res 66: 1277-1281. doi:10.1158/0008-5472.CAN-05-3632. PubMed: 16452179.
-
(2006)
Cancer Res
, vol.66
, pp. 1277-1281
-
-
Scott, G.K.1
Mattie, M.D.2
Berger, C.E.3
Benz, S.C.4
Benz, C.C.5
-
34
-
-
84856413303
-
Histone deacetylase 1 enhances microRNA processing via deacetylation of DGCR8
-
doi: 10.1038/embor.2011.247
-
Wada T, Kikuchi J, Furukawa Y, (2012) Histone deacetylase 1 enhances microRNA processing via deacetylation of DGCR8. EMBO Rep 13: 142-149. doi:10.1038/embor.2011.247. PubMed: 22222205.
-
(2012)
EMBO Rep
, vol.13
, pp. 142-149
-
-
Wada, T.1
Kikuchi, J.2
Furukawa, Y.3
-
35
-
-
77956149872
-
miR-149* induces apoptosis by inhibiting Akt1 and E2F1 in human cancer cells
-
20623644
-
Lin RJ, Lin YC, Yu AL, (2010) miR-149* induces apoptosis by inhibiting Akt1 and E2F1 in human cancer cells. Mol Carcinog 49: 719-727. PubMed: 20623644.
-
(2010)
Mol Carcinog
, vol.49
, pp. 719-727
-
-
Lin, R.J.1
Lin, Y.C.2
Yu, A.L.3
-
36
-
-
77951030589
-
MicroRNA-184 inhibits neuroblastoma cell survival through targeting the serine/threonine kinase AKT2
-
doi: 10.1186/1476-4598-9-83
-
Foley NH, Bray IM, Tivnan A, Bryan K, Murphy DM, et al. (2010) MicroRNA-184 inhibits neuroblastoma cell survival through targeting the serine/threonine kinase AKT2. Mol Cancer 9: 83. doi:10.1186/1476-4598-9-83. PubMed: 20409325.
-
(2010)
Mol Cancer
, vol.9
, pp. 83
-
-
Foley, N.H.1
Bray, I.M.2
Tivnan, A.3
Bryan, K.4
Murphy, D.M.5
-
37
-
-
79952241662
-
miR-203 reverses chemoresistance in p53-mutated colon cancer cells through downregulation of Akt2 expression
-
doi: 10.1016/j.canlet.2011.02.003
-
Li J, Chen Y, Zhao J, Kong F, Zhang Y, (2011) miR-203 reverses chemoresistance in p53-mutated colon cancer cells through downregulation of Akt2 expression. Cancer Lett 304: 52-59. doi:10.1016/j.canlet.2011.02.003. PubMed: 21354697.
-
(2011)
Cancer Lett
, vol.304
, pp. 52-59
-
-
Li, J.1
Chen, Y.2
Zhao, J.3
Kong, F.4
Zhang, Y.5
-
38
-
-
4143087257
-
Histone deacetylase inhibition and estrogen signalling in human breast cancer cells
-
doi: 10.1016/j.bcp.2004.04.031
-
Margueron R, Duong V, Castet A, Cavaillès V, (2004) Histone deacetylase inhibition and estrogen signalling in human breast cancer cells. Biochem Pharmacol 68: 1239-1246. doi:10.1016/j.bcp.2004.04.031. PubMed: 15313422.
-
(2004)
Biochem Pharmacol
, vol.68
, pp. 1239-1246
-
-
Margueron, R.1
Duong, V.2
Castet, A.3
Cavaillès, V.4
-
39
-
-
0142122363
-
Overexpression of histone deacetylase HDAC1 modulates breast cancer progression by negative regulation of estrogen receptor alpha
-
doi: 10.1002/ijc.11403
-
Kawai H, Li H, Avraham S, Jiang S, Avraham HK, (2003) Overexpression of histone deacetylase HDAC1 modulates breast cancer progression by negative regulation of estrogen receptor alpha. Int J Cancer 107: 353-358. doi:10.1002/ijc.11403. PubMed: 14506733.
-
(2003)
Int J Cancer
, vol.107
, pp. 353-358
-
-
Kawai, H.1
Li, H.2
Avraham, S.3
Jiang, S.4
Avraham, H.K.5
-
40
-
-
9744223645
-
Histone deacetylase inhibitor trichostatin A represses estrogen receptor alpha-dependent transcription and promotes proteasomal degradation of cyclin D1 in human breast carcinoma cell lines
-
doi: 10.1158/1078-0432.CCR-04-1023
-
Alao JP, Lam EW, Ali S, Buluwela L, Bordogna W, et al. (2004) Histone deacetylase inhibitor trichostatin A represses estrogen receptor alpha-dependent transcription and promotes proteasomal degradation of cyclin D1 in human breast carcinoma cell lines. Clin Cancer Res 10: 8094-8104. doi:10.1158/1078-0432.CCR-04-1023. PubMed: 15585645.
-
(2004)
Clin Cancer Res
, vol.10
, pp. 8094-8104
-
-
Alao, J.P.1
Lam, E.W.2
Ali, S.3
Buluwela, L.4
Bordogna, W.5
-
41
-
-
33745087150
-
CRA-024781: a novel synthetic inhibitor of histone deacetylase enzymes with antitumor activity in vitro and in vivo
-
doi: 10.1158/1535-7163.MCT-05-0442
-
Buggy JJ, Cao ZA, Bass KE, Verner E, Balasubramanian S, et al. (2006) CRA-024781: a novel synthetic inhibitor of histone deacetylase enzymes with antitumor activity in vitro and in vivo. Mol Cancer Ther 5: 1309-1317. doi:10.1158/1535-7163.MCT-05-0442. PubMed: 16731764.
-
(2006)
Mol Cancer Ther
, vol.5
, pp. 1309-1317
-
-
Buggy, J.J.1
Cao, Z.A.2
Bass, K.E.3
Verner, E.4
Balasubramanian, S.5
-
42
-
-
15944406971
-
Coadministration of histone deacetylase inhibitors and perifosine synergistically induces apoptosis in human leukemia cells through Akt and ERK1/2 inactivation and the generation of ceramide and reactive oxygen species
-
doi: 10.1158/0008-5472.CAN-04-2440
-
Rahmani M, Reese E, Dai Y, Bauer C, Payne SG, et al. (2005) Coadministration of histone deacetylase inhibitors and perifosine synergistically induces apoptosis in human leukemia cells through Akt and ERK1/2 inactivation and the generation of ceramide and reactive oxygen species. Cancer Res 65: 2422-2432. doi:10.1158/0008-5472.CAN-04-2440. PubMed: 15781658.
-
(2005)
Cancer Res
, vol.65
, pp. 2422-2432
-
-
Rahmani, M.1
Reese, E.2
Dai, Y.3
Bauer, C.4
Payne, S.G.5
-
43
-
-
74449089863
-
Blockade of the ERK or PI3K-Akt signaling pathway enhances the cytotoxicity of histone deacetylase inhibitors in tumor cells resistant to gefitinib or imatinib
-
doi: 10.1016/j.bbrc.2009.12.086
-
Ozaki K, Kosugi M, Baba N, Fujio K, Sakamoto T, et al. (2010) Blockade of the ERK or PI3K-Akt signaling pathway enhances the cytotoxicity of histone deacetylase inhibitors in tumor cells resistant to gefitinib or imatinib. Biochem Biophys Res Commun 391: 1610-1615. doi:10.1016/j.bbrc.2009.12.086. PubMed: 20026060.
-
(2010)
Biochem Biophys Res Commun
, vol.391
, pp. 1610-1615
-
-
Ozaki, K.1
Kosugi, M.2
Baba, N.3
Fujio, K.4
Sakamoto, T.5
-
44
-
-
84855344629
-
Preclinical evaluation of dual PI3K-mTOR inhibitors and histone deacetylase inhibitors in head and neck squamous cell carcinoma
-
doi: 10.1038/bjc.2011.495
-
Erlich RB, Kherrouche Z, Rickwood D, Endo-Munoz L, Cameron S, et al. (2012) Preclinical evaluation of dual PI3K-mTOR inhibitors and histone deacetylase inhibitors in head and neck squamous cell carcinoma. Br J Cancer 106: 107-115. doi:10.1038/bjc.2011.495. PubMed: 22116303.
-
(2012)
Br J Cancer
, vol.106
, pp. 107-115
-
-
Erlich, R.B.1
Kherrouche, Z.2
Rickwood, D.3
Endo-Munoz, L.4
Cameron, S.5
-
45
-
-
84864558874
-
Randomized Phase II Trial of Everolimus in Combination With Tamoxifen in Patients With Hormone Receptor-Positive, Human Epidermal Growth Factor Receptor 2-Negative Metastatic Breast Cancer With Prior Exposure to Aromatase Inhibitors: A GINECO Study
-
22565002
-
Bachelot T, Bourgier C, Cropet C, Ray-Coquard I, Ferrero JM, et al. (2012) Randomized Phase II Trial of Everolimus in Combination With Tamoxifen in Patients With Hormone Receptor-Positive, Human Epidermal Growth Factor Receptor 2-Negative Metastatic Breast Cancer With Prior Exposure to Aromatase Inhibitors: A GINECO Study. J Clin Oncol Off J American Society Of Clinical Oncology, 30: 2718-24. PubMed: 22565002.
-
(2012)
J Clin Oncol Off J American Society Of Clinical Oncology
, vol.30
, pp. 2718-2724
-
-
Bachelot, T.1
Bourgier, C.2
Cropet, C.3
Ray-Coquard, I.4
Ferrero, J.M.5
|