-
1
-
-
2342613652
-
The proteasome: A suitable antineoplastic target
-
Adams, J. The proteasome: a suitable antineoplastic target. Nat. Rev. Cancer 2004, 4, 349-360
-
(2004)
Nat. Rev. Cancer
, vol.4
, pp. 349-360
-
-
Adams, J.1
-
2
-
-
0028018268
-
The ubiquitin-proteasome proteolytic pathway
-
Ciechanover, A. The ubiquitin-proteasome proteolytic pathway. Cell 1994, 79, 13-21
-
(1994)
Cell
, vol.79
, pp. 13-21
-
-
Ciechanover, A.1
-
3
-
-
0028935165
-
Ubiquitin, proteasomes, and the regulation of intracellular protein degradation
-
Hochstrasser, M. Ubiquitin, proteasomes, and the regulation of intracellular protein degradation. Curr. Opin. Cell Biol. 1995, 7, 215-223
-
(1995)
Curr. Opin. Cell Biol
, vol.7
, pp. 215-223
-
-
Hochstrasser, M.1
-
4
-
-
0038743111
-
The role of the ubiquitination- proteasome pathway in breast cancer: Applying drugs that affect the ubiquitin-proteasome pathway to the therapy of breast cancer
-
Orlowski, R. Z.; Dees, E. C. The role of the ubiquitination- proteasome pathway in breast cancer: applying drugs that affect the ubiquitin-proteasome pathway to the therapy of breast cancer. Breast Cancer Res. 2003, 5, 1-7
-
(2003)
Breast Cancer Res
, vol.5
, pp. 1-7
-
-
Orlowski, R.Z.1
Dees, E.C.2
-
5
-
-
33644916110
-
Phase I/II trial assessing bortezomib and melphalan combination therapy for the treatment of patients with relapsed or refractory multiple myeloma
-
Berenson, J. R.; Yang, H. H.; Sadler, K.; Jarutirasarn, S. G.; Vescio, R. A.; Mapes, R.; Purner, M.; Lee, S. P.; Wilson, J.; Morrison, B.; Adams, J.; Schenkein, D.; Swift, R. Phase I/II trial assessing bortezomib and melphalan combination therapy for the treatment of patients with relapsed or refractory multiple myeloma. J. Clin. Oncol. 2006, 24, 937-944
-
(2006)
J. Clin. Oncol
, vol.24
, pp. 937-944
-
-
Berenson, J.R.1
Yang, H.H.2
Sadler, K.3
Jarutirasarn, S.G.4
Vescio, R.A.5
Mapes, R.6
Purner, M.7
Lee, S.P.8
Wilson, J.9
Morrison, B.10
Adams, J.11
Schenkein, D.12
Swift, R.13
-
6
-
-
33744832401
-
United States Food and Drug Administration approval summary: Bortezomib for the treatment of progressive multiple myeloma after one prior therapy
-
Kane, R. C.; Farrell, A. T.; Sridhara, R.; Pazdur, R. United States Food and Drug Administration approval summary: bortezomib for the treatment of progressive multiple myeloma after one prior therapy. Clin. Cancer Res. 2006, 12, 2955-2960
-
(2006)
Clin. Cancer Res
, vol.12
, pp. 2955-2960
-
-
Kane, R.C.1
Farrell, A.T.2
Sridhara, R.3
Pazdur, R.4
-
7
-
-
0345447210
-
Velcade: U.S. FDA approval for the treatment of multiple myeloma progressing on prior therapy
-
Kane, R. C.; Bross, P. F.; Farrell, A. T.; Pazdur, R. Velcade: U.S. FDA approval for the treatment of multiple myeloma progressing on prior therapy. Oncologist 2003, 8, 508-513
-
(2003)
Oncologist
, vol.8
, pp. 508-513
-
-
Kane, R.C.1
Bross, P.F.2
Farrell, A.T.3
Pazdur, R.4
-
8
-
-
34848870352
-
Bortezomib for the treatment of mantle cell lymphoma
-
Kane, R. C.; Dagher, R.; Farrell, A.; Ko, C. W.; Sridhara, R.; Justice, R.; Pazdur, R. Bortezomib for the treatment of mantle cell lymphoma. Clin. Cancer Res. 2007, 13, 5291-5294
-
(2007)
Clin. Cancer Res
, vol.13
, pp. 5291-5294
-
-
Kane, R.C.1
Dagher, R.2
Farrell, A.3
Ko, C.W.4
Sridhara, R.5
Justice, R.6
Pazdur, R.7
-
9
-
-
0032189685
-
Tumor growth inhibition induced in a murine model of human Burkitt's lymphoma by a proteasome inhibitor
-
Orlowski, R. Z.; Eswara, J. R.; Lafond-Walker, A.; Grever, M. R.; Orlowski, M.; Dang, C. V. Tumor growth inhibition induced in a murine model of human Burkitt's lymphoma by a proteasome inhibitor. Cancer Res. 1998, 58, 4342-4348
-
(1998)
Cancer Res
, vol.58
, pp. 4342-4348
-
-
Orlowski, R.Z.1
Eswara, J.R.2
Lafond-Walker, A.3
Grever, M.R.4
Orlowski, M.5
Dang, C.V.6
-
10
-
-
0033152760
-
Proteasome inhibitors: A novel class of potent and effective antitumor agents
-
Adams, J.; Palombella, V. J.; Sausville, E. A.; Johnson, J.; Destree, A.; Lazarus, D. D.; Maas, J.; Pien, C. S.; Prakash, S.; Elliott, P. J. Proteasome inhibitors: a novel class of potent and effective antitumor agents. Cancer Res. 1999, 59, 2615-2622
-
(1999)
Cancer Res
, vol.59
, pp. 2615-2622
-
-
Adams, J.1
Palombella, V.J.2
Sausville, E.A.3
Johnson, J.4
Destree, A.5
Lazarus, D.D.6
Maas, J.7
Pien, C.S.8
Prakash, S.9
Elliott, P.J.10
-
11
-
-
0037111832
-
Phase I trial of the proteasome inhibitor PS-341 in patients with refractory hematologic malignancies
-
Orlowski, R. Z.; Stinchcombe, T. E.; Mitchell, B. S.; Shea, T. C.; Baldwin, A. S.; Stahl, S.; Adams, J.; Esseltine, D. L.; Elliott, P. J.; Pien, C. S.; Guerciolini, R.; Anderson, J. K.; Depcik-Smith, N. D.; Bhagat, R.; Lehman, M. J.; Novick, S. C.; O'Connor, O. A.; Soignet, S. L. Phase I trial of the proteasome inhibitor PS-341 in patients with refractory hematologic malignancies. J. Clin. Oncol. 2002, 20, 4420-4427
-
(2002)
J. Clin. Oncol
, vol.20
, pp. 4420-4427
-
-
Orlowski, R.Z.1
Stinchcombe, T.E.2
Mitchell, B.S.3
Shea, T.C.4
Baldwin, A.S.5
Stahl, S.6
Adams, J.7
Esseltine, D.L.8
Elliott, P.J.9
Pien, C.S.10
Guerciolini, R.11
Anderson, J.K.12
Depcik-Smith, N.D.13
Bhagat, R.14
Lehman, M.J.15
Novick, S.C.16
O'Connor, O.A.17
Soignet, S.L.18
-
12
-
-
0346692671
-
Bortezomib (millennium pharmaceuticals)
-
Dou, Q. P.; Goldfarb, R. H. Bortezomib (millennium pharmaceuticals). IDrugs 2002, 5, 828-834
-
(2002)
IDrugs
, vol.5
, pp. 828-834
-
-
Dou, Q.P.1
Goldfarb, R.H.2
-
13
-
-
33750625445
-
Multicenter phase II study of bortezomib in patients with relapsed or refractory mantle cell lymphoma
-
Fisher, R. I.; Bernstein, S. H.; Kahl, B. S.; Djulbegovic, B.; Robertson, M. J.; de Vos, S.; Epner, E.; Krishnan, A.; Leonard, J. P.; Lonial, S.; Stadtmauer, E. A.; O'Connor, O. A.; Shi, H.; Boral, A. L.; Goy, A. Multicenter phase II study of bortezomib in patients with relapsed or refractory mantle cell lymphoma. J. Clin. Oncol. 2006, 24, 4867-4874
-
(2006)
J. Clin. Oncol
, vol.24
, pp. 4867-4874
-
-
Fisher, R.I.1
Bernstein, S.H.2
Kahl, B.S.3
Djulbegovic, B.4
Robertson, M.J.5
de Vos, S.6
Epner, E.7
Krishnan, A.8
Leonard, J.P.9
Lonial, S.10
Stadtmauer, E.A.11
O'Connor, O.A.12
Shi, H.13
Boral, A.L.14
Goy, A.15
-
14
-
-
2942692143
-
Phase I trial of the proteasome inhibitor bortezomib in patients with advanced solid tumors with observations in androgen-independent prostate cancer
-
Papandreou, C. N.; Daliani, D. D.; Nix, D.; Yang, H.; Madden, T.; Wang, X.; Pien, C. S.; Millikan, R. E.; Tu, S. M.; Pagliaro, L.; Kim, J.; Adams, J.; Elliott, P.; Esseltine, D.; Petrusich, A.; Dieringer, P.; Perez, C.; Logothetis, C. J. Phase I trial of the proteasome inhibitor bortezomib in patients with advanced solid tumors with observations in androgen-independent prostate cancer. J. Clin. Oncol. 2004, 22, 2108-2121
-
(2004)
J. Clin. Oncol
, vol.22
, pp. 2108-2121
-
-
Papandreou, C.N.1
Daliani, D.D.2
Nix, D.3
Yang, H.4
Madden, T.5
Wang, X.6
Pien, C.S.7
Millikan, R.E.8
Tu, S.M.9
Pagliaro, L.10
Kim, J.11
Adams, J.12
Elliott, P.13
Esseltine, D.14
Petrusich, A.15
Dieringer, P.16
Perez, C.17
Logothetis, C.J.18
-
15
-
-
77952555794
-
Generating a generation of proteasome inhibitors: From microbial fermentation to total synthesis of salinosporamide a (marizomib) and other salinosporamides
-
Potts, B. C.; Lam, K. S. Generating a generation of proteasome inhibitors: from microbial fermentation to total synthesis of salinosporamide a (marizomib) and other salinosporamides. Mar. Drugs 2010, 8, 835-880
-
(2010)
Mar. Drugs
, vol.8
, pp. 835-880
-
-
Potts, B.C.1
Lam, K.S.2
-
16
-
-
77951682116
-
Pharmacodynamic and efficacy studies of the novel proteasome inhibitor NPI-0052 (marizomib) in a human plasmacytoma xenograft murine model
-
Singh, A. V.; Palladino, M. A.; Lloyd, G. K.; Potts, B. C.; Chauhan, D.; Anderson, K. C. Pharmacodynamic and efficacy studies of the novel proteasome inhibitor NPI-0052 (marizomib) in a human plasmacytoma xenograft murine model. Br. J. Haematol. 2010, 149, 550-559
-
(2010)
Br. J. Haematol
, vol.149
, pp. 550-559
-
-
Singh, A.V.1
Palladino, M.A.2
Lloyd, G.K.3
Potts, B.C.4
Chauhan, D.5
Anderson, K.C.6
-
17
-
-
62149103377
-
Discovery and development of the anticancer agent salinosporamide A (NPI-0052)
-
Fenical, W.; Jensen, P. R.; Palladino, M. A.; Lam, K. S.; Lloyd, G. K.; Potts, B. C. Discovery and development of the anticancer agent salinosporamide A (NPI-0052). Bioorg. Med. Chem. 2009, 17, 2175-2180
-
(2009)
Bioorg. Med. Chem
, vol.17
, pp. 2175-2180
-
-
Fenical, W.1
Jensen, P.R.2
Palladino, M.A.3
Lam, K.S.4
Lloyd, G.K.5
Potts, B.C.6
-
18
-
-
36148944490
-
Potent activity of carfilzomib, a novel, irreversible inhibitor of the ubiquitin- proteasome pathway, against preclinical models of multiple myeloma
-
Kuhn, D. J.; Chen, Q.; Voorhees, P. M.; Strader, J. S.; Shenk, K. D.; Sun, C. M.; Demo, S. D.; Bennett, M. K.; van Leeuwen, F. W.; Chanan-Khan, A. A.; Orlowski, R. Z. Potent activity of carfilzomib, a novel, irreversible inhibitor of the ubiquitin- proteasome pathway, against preclinical models of multiple myeloma. Blood 2007, 110, 3281-3290
-
(2007)
Blood
, vol.110
, pp. 3281-3290
-
-
Kuhn, D.J.1
Chen, Q.2
Voorhees, P.M.3
Strader, J.S.4
Shenk, K.D.5
Sun, C.M.6
Demo, S.D.7
Bennett, M.K.8
van Leeuwen, F.W.9
Chanan-Khan, A.A.10
Orlowski, R.Z.11
-
19
-
-
72549116835
-
A phase 1 dose escalation study of the safety and pharmacokinetics of the novel proteasome inhibitor carfilzomib (PR-171) in patients with hematologic malignancies
-
O'Connor, O. A.; Stewart, A. K.; Vallone, M.; Molineaux, C. J.; Kunkel, L. A.; Gerecitano, J. F.; Orlowski, R. Z. A phase 1 dose escalation study of the safety and pharmacokinetics of the novel proteasome inhibitor carfilzomib (PR-171) in patients with hematologic malignancies. Clin. Cancer Res. 2009, 15, 7085-7091
-
(2009)
Clin. Cancer Res
, vol.15
, pp. 7085-7091
-
-
O'Connor, O.A.1
Stewart, A.K.2
Vallone, M.3
Molineaux, C.J.4
Kunkel, L.A.5
Gerecitano, J.F.6
Orlowski, R.Z.7
-
20
-
-
0346727127
-
Protein degradation and protection against misfolded or damaged proteins
-
Goldberg, A. L. Protein degradation and protection against misfolded or damaged proteins. Nature 2003, 426, 895-899
-
(2003)
Nature
, vol.426
, pp. 895-899
-
-
Goldberg, A.L.1
-
21
-
-
41549133200
-
Proteasome inhibitors in cancer therapy: Lessons from the first decade
-
Orlowski, R. Z.; Kuhn, D. J. Proteasome inhibitors in cancer therapy: lessons from the first decade. Clin. Cancer Res. 2008, 14, 1649-1657
-
(2008)
Clin. Cancer Res
, vol.14
, pp. 1649-1657
-
-
Orlowski, R.Z.1
Kuhn, D.J.2
-
22
-
-
0034065822
-
Ubiquitin-mediated proteolysis: Biological regulation via destruction
-
Ciechanover, A.; Orian, A.; Schwartz, A. L. Ubiquitin-mediated proteolysis: biological regulation via destruction. Bioessays 2000, 22, 442-451
-
(2000)
Bioessays
, vol.22
, pp. 442-451
-
-
Ciechanover, A.1
Orian, A.2
Schwartz, A.L.3
-
23
-
-
0032535483
-
The ubiquitin-proteasome pathway: On protein death and cell life
-
Ciechanover, A. The ubiquitin-proteasome pathway: on protein death and cell life. EMBO J. 1998, 17, 7151-7160
-
(1998)
EMBO J
, vol.17
, pp. 7151-7160
-
-
Ciechanover, A.1
-
24
-
-
0027771443
-
Structural features of the 26 S proteasome complex
-
Peters, J. M.; Cejka, Z.; Harris, J. R.; Kleinschmidt, J. A.; Baumeister, W. Structural features of the 26 S proteasome complex. J. Mol. Biol. 1993, 234, 932-937
-
(1993)
J. Mol. Biol
, vol.234
, pp. 932-937
-
-
Peters, J.M.1
Cejka, Z.2
Harris, J.R.3
Kleinschmidt, J.A.4
Baumeister, W.5
-
25
-
-
0032488846
-
The proteasome: Paradigm of a self-compartmentalizing protease
-
Baumeister, W.; Walz, J.; Zuhl, F.; Seemuller, E. The proteasome: paradigm of a self-compartmentalizing protease. Cell 1998, 92, 367-380
-
(1998)
Cell
, vol.92
, pp. 367-380
-
-
Baumeister, W.1
Walz, J.2
Zuhl, F.3
Seemuller, E.4
-
26
-
-
0030897031
-
Structure of 20S proteasome from yeast at 2.4 A resolution
-
Groll, M.; Ditzel, L.; Lowe, J.; Stock, D.; Bochtler, M.; Bartunik, H. D.; Huber, R. Structure of 20S proteasome from yeast at 2.4 A resolution. Nature 1997, 386, 463-471
-
(1997)
Nature
, vol.386
, pp. 463-471
-
-
Groll, M.1
Ditzel, L.2
Lowe, J.3
Stock, D.4
Bochtler, M.5
Bartunik, H.D.6
Huber, R.7
-
27
-
-
0033613196
-
The catalytic sites of 20S proteasomes and their role in subunit maturation: A mutational and crystallographic study
-
Groll, M.; Heinemeyer, W.; Jager, S.; Ullrich, T.; Bochtler, M.; Wolf, D. H.; Huber, R. The catalytic sites of 20S proteasomes and their role in subunit maturation: a mutational and crystallographic study. Proc. Natl. Acad. Sci. U. S. A. 1999, 96, 10976-10983
-
(1999)
Proc. Natl. Acad. Sci. U. S. A
, vol.96
, pp. 10976-10983
-
-
Groll, M.1
Heinemeyer, W.2
Jager, S.3
Ullrich, T.4
Bochtler, M.5
Wolf, D.H.6
Huber, R.7
-
28
-
-
0033529596
-
The proteasome, a novel protease regulated by multiple mechanisms
-
DeMartino, G. N.; Slaughter, C. A. The proteasome, a novel protease regulated by multiple mechanisms. J. Biol. Chem. 1999, 274, 22123-22126
-
(1999)
J. Biol. Chem
, vol.274
, pp. 22123-22126
-
-
Demartino, G.N.1
Slaughter, C.A.2
-
29
-
-
0036777957
-
The importance of the proteasome and subsequent proteolytic steps in the generation of antigenic peptides
-
Goldberg, A. L.; Cascio, P.; Saric, T.; Rock, K. L. The importance of the proteasome and subsequent proteolytic steps in the generation of antigenic peptides. Mol. Immunol. 2002, 39, 147-164
-
(2002)
Mol. Immunol
, vol.39
, pp. 147-164
-
-
Goldberg, A.L.1
Cascio, P.2
Saric, T.3
Rock, K.L.4
-
30
-
-
0030016595
-
Structure and functions of the 20S and 26S proteasomes
-
Coux, O.; Tanaka, K.; Goldberg, A. L. Structure and functions of the 20S and 26S proteasomes. Annu. Rev. Biochem. 1996, 65, 801-847
-
(1996)
Annu. Rev. Biochem
, vol.65
, pp. 801-847
-
-
Coux, O.1
Tanaka, K.2
Goldberg, A.L.3
-
31
-
-
33645669213
-
The ubiquitin- proteasome system
-
Nandi, D.; Tahiliani, P.; Kumar, A.; Chandu, D. The ubiquitin- proteasome system. J. Biosci. 2006, 31, 137-155
-
(2006)
J. Biosci
, vol.31
, pp. 137-155
-
-
Nandi, D.1
Tahiliani, P.2
Kumar, A.3
Chandu, D.4
-
33
-
-
0037852202
-
The proteasome: Structure, function, and role in the cell
-
Adams, J. The proteasome: structure, function, and role in the cell. Cancer Treat Rev. 2003, 29 Suppl 1, 3-9
-
(2003)
Cancer Treat Rev
, vol.29
, Issue.SUPPL. 1
, pp. 3-9
-
-
Adams, J.1
-
34
-
-
3242732010
-
Ubiquitin-free routes into the proteasome
-
Hoyt, M. A.; Coffino, P. Ubiquitin-free routes into the proteasome. Cell Mol Life Sci. 2004, 61, 1596-1600
-
(2004)
Cell Mol Life Sci
, vol.61
, pp. 1596-1600
-
-
Hoyt, M.A.1
Coffino, P.2
-
35
-
-
34447522124
-
Constitutive/hypoxic degradation of HIF-alpha proteins by the proteasome is independent of von Hippel Lindau protein ubiquitylation and the transactivation activity of the protein
-
Kong, X.; Alvarez-Castelao, B.; Lin, Z.; Castano, J. G.; Caro, J. Constitutive/hypoxic degradation of HIF-alpha proteins by the proteasome is independent of von Hippel Lindau protein ubiquitylation and the transactivation activity of the protein. J. Biol. Chem. 2007, 282, 15498-15505
-
(2007)
J. Biol. Chem
, vol.282
, pp. 15498-15505
-
-
Kong, X.1
Alvarez-Castelao, B.2
Lin, Z.3
Castano, J.G.4
Caro, J.5
-
36
-
-
2542623585
-
Proteasome-mediated destruction of the cyclin a/cyclin-dependent kinase 2 complex suppresses tumor cell growth in vitro and in vivo
-
Chen, W.; Lee, J.; Cho, S. Y.; Fine, H. A. Proteasome-mediated destruction of the cyclin a/cyclin-dependent kinase 2 complex suppresses tumor cell growth in vitro and in vivo. Cancer Res. 2004, 64, 3949-3957
-
(2004)
Cancer Res
, vol.64
, pp. 3949-3957
-
-
Chen, W.1
Lee, J.2
Cho, S.Y.3
Fine, H.A.4
-
37
-
-
0030916209
-
Inhibition of cyclin D1 phosphorylation on threonine-286 prevents its rapid degradation via the ubiquitin-proteasome pathway
-
Diehl, J. A.; Zindy, F.; Sherr, C. J. Inhibition of cyclin D1 phosphorylation on threonine-286 prevents its rapid degradation via the ubiquitin-proteasome pathway. Genes Dev. 1997, 11, 957-972
-
(1997)
Genes Dev
, vol.11
, pp. 957-972
-
-
Diehl, J.A.1
Zindy, F.2
Sherr, C.J.3
-
38
-
-
0029737650
-
Activation of cyclin E/CDK2 is coupled to site-specific autophosphorylation and ubiquitin-dependent degradation of cyclin
-
Won, K. A.; Reed, S. I. Activation of cyclin E/CDK2 is coupled to site-specific autophosphorylation and ubiquitin-dependent degradation of cyclin E. EMBO J. 1996, 15, 4182-4193
-
(1996)
E. EMBO J
, vol.15
, pp. 4182-4193
-
-
Won, K.A.1
Reed, S.I.2
-
39
-
-
0037051095
-
P53: An ubiquitous target of anticancer drugs
-
Blagosklonny, M. V. P53: an ubiquitous target of anticancer drugs. Int. J. Cancer. 2002, 98, 161-166
-
(2002)
Int. J. Cancer
, vol.98
, pp. 161-166
-
-
Blagosklonny, M.V.1
-
40
-
-
0037452979
-
Proteasome-dependent, ubiquitin- independent degradation of the Rb family of tumor suppressors by the human cytomegalovirus pp71 protein
-
Kalejta, R. F.; Shenk, T. Proteasome-dependent, ubiquitin- independent degradation of the Rb family of tumor suppressors by the human cytomegalovirus pp71 protein. Proc. Natl. Acad. Sci. USA 2003, 100, 3263-3268
-
(2003)
Proc. Natl. Acad. Sci. USA
, vol.100
, pp. 3263-3268
-
-
Kalejta, R.F.1
Shenk, T.2
-
41
-
-
0034635952
-
Bax degradation by the ubiquitin/proteasomedependent pathway: Involvement in tumor survival and progression
-
Li, B.; Dou, Q. P. Bax degradation by the ubiquitin/proteasomedependent pathway: involvement in tumor survival and progression. Proc. Natl. Acad. Sci. U. S. A. 2000, 97, 3850-3855
-
(2000)
Proc. Natl. Acad. Sci. U. S. A
, vol.97
, pp. 3850-3855
-
-
Li, B.1
Dou, Q.P.2
-
42
-
-
0029024015
-
Role of the ubiquitin-proteasome pathway in regulating abundance of the cyclin-dependent kinase inhibitor p27
-
Pagano, M.; Tam, S. W.; Theodoras, A. M.; Beer-Romero, P.; Del Sal, G.; Chau, V.; Yew, P. R.; Draetta, G. F.; Rolfe, M. Role of the ubiquitin-proteasome pathway in regulating abundance of the cyclin-dependent kinase inhibitor p27. Science 1995, 269, 682-685
-
(1995)
Science
, vol.269
, pp. 682-685
-
-
Pagano, M.1
Tam, S.W.2
Theodoras, A.M.3
Beer-Romero, P.4
Del Sal, G.5
Chau, V.6
Yew, P.R.7
Draetta, G.F.8
Rolfe, M.9
-
43
-
-
23144449789
-
Ubiquitin signalling in the NF-kappaB pathway
-
Chen, Z. J. Ubiquitin signalling in the NF-kappaB pathway. Nat. Cell Biol. 2005, 7, 758-765
-
(2005)
Nat. Cell Biol
, vol.7
, pp. 758-765
-
-
Chen, Z.J.1
-
44
-
-
0031048236
-
Increased proteasome- dependent degradation of the cyclin-dependent kinase inhibitor p27 in aggressive colorectal carcinomas
-
Loda, M.; Cukor, B.; Tam, S. W.; Lavin, P.; Fiorentino, M.; Draetta, G. F.; Jessup, J. M.; Pagano, M. Increased proteasome- dependent degradation of the cyclin-dependent kinase inhibitor p27 in aggressive colorectal carcinomas. Nat. Med. 1997, 3, 231-234
-
(1997)
Nat. Med
, vol.3
, pp. 231-234
-
-
Loda, M.1
Cukor, B.2
Tam, S.W.3
Lavin, P.4
Fiorentino, M.5
Draetta, G.F.6
Jessup, J.M.7
Pagano, M.8
-
45
-
-
0025115736
-
Abnormally high expression of proteasomes in human leukemic cells
-
Kumatori, A.; Tanaka, K.; Inamura, N.; Sone, S.; Ogura, T.; Matsumoto, T.; Tachikawa, T.; Shin, S.; Ichihara, A. Abnormally high expression of proteasomes in human leukemic cells. Proc. Natl. Acad. Sci. U. S. A. 1990, 87, 7071-7075
-
(1990)
Proc. Natl. Acad. Sci. U. S. A
, vol.87
, pp. 7071-7075
-
-
Kumatori, A.1
Tanaka, K.2
Inamura, N.3
Sone, S.4
Ogura, T.5
Matsumoto, T.6
Tachikawa, T.7
Shin, S.8
Ichihara, A.9
-
46
-
-
0033178142
-
Proteasome inhibitors as potential novel anticancer agents
-
Dou, Q. P.; Li, B. Proteasome inhibitors as potential novel anticancer agents. Drug Resist. Updat. 1999, 2, 215-223
-
(1999)
Drug Resist. Updat
, vol.2
, pp. 215-223
-
-
Dou, Q.P.1
Li, B.2
-
47
-
-
0036240701
-
The proteasome: A novel target for cancer chemotherapy
-
Almond, J. B.; Cohen, G. M. The proteasome: a novel target for cancer chemotherapy. Leukemia 2002, 16, 433-443
-
(2002)
Leukemia
, vol.16
, pp. 433-443
-
-
Almond, J.B.1
Cohen, G.M.2
-
48
-
-
0035866355
-
CEP1612, a dipeptidyl proteasome inhibitor, induces p21WAF1 and p27KIP1 expression and apoptosis and inhibits the growth of the human lung adenocarcinoma A-549 in nude mice
-
Sun, J.; Nam, S.; Lee, C. S.; Li, B.; Coppola, D.; Hamilton, A. D.; Dou, Q. P.; Sebti, S. M. CEP1612, a dipeptidyl proteasome inhibitor, induces p21WAF1 and p27KIP1 expression and apoptosis and inhibits the growth of the human lung adenocarcinoma A-549 in nude mice. Cancer Res. 2001, 61, 1280-1284
-
(2001)
Cancer Res
, vol.61
, pp. 1280-1284
-
-
Sun, J.1
Nam, S.2
Lee, C.S.3
Li, B.4
Coppola, D.5
Hamilton, A.D.6
Dou, Q.P.7
Sebti, S.M.8
-
49
-
-
33646406554
-
Celastrol, a triterpene extracted from the Chinese Thunder of God Vine, is a potent proteasome inhibitor and suppresses human prostate cancer growth in nude mice
-
Yang, H.; Chen, D.; Cui, Q. C.; Yuan, X.; Dou, Q. P. Celastrol, a triterpene extracted from the Chinese Thunder of God Vine, is a potent proteasome inhibitor and suppresses human prostate cancer growth in nude mice. Cancer Res. 2006, 66, 4758-4765
-
(2006)
Cancer Res
, vol.66
, pp. 4758-4765
-
-
Yang, H.1
Chen, D.2
Cui, Q.C.3
Yuan, X.4
Dou, Q.P.5
-
50
-
-
0032919345
-
The role of the ubiquitin-proteasome pathway in apoptosis
-
Orlowski, R. Z. The role of the ubiquitin-proteasome pathway in apoptosis. Cell Death Differ. 1999, 6, 303-313
-
(1999)
Cell Death Differ
, vol.6
, pp. 303-313
-
-
Orlowski, R.Z.1
-
51
-
-
0033376668
-
Proteasomes in apoptosis: Villains or guardians?
-
Wojcik, C. Proteasomes in apoptosis: villains or guardians? Cell Mol. Life Sci. 1999, 56, 908-917
-
(1999)
Cell Mol. Life Sci
, vol.56
, pp. 908-917
-
-
Wojcik, C.1
-
52
-
-
0033817518
-
Lack of multicellular drug resistance observed in human ovarian and prostate carcinoma treated with the proteasome inhibitor PS-341
-
Frankel, A.; Man, S.; Elliott, P.; Adams, J.; Kerbel, R. S. Lack of multicellular drug resistance observed in human ovarian and prostate carcinoma treated with the proteasome inhibitor PS-341. Clin. Cancer Res. 2000, 6, 3719-3728
-
(2000)
Clin. Cancer Res
, vol.6
, pp. 3719-3728
-
-
Frankel, A.1
Man, S.2
Elliott, P.3
Adams, J.4
Kerbel, R.S.5
-
53
-
-
0035300479
-
The proteasome inhibitor PS-341 inhibits growth, induces apoptosis, and overcomes drug resistance in human multiple myeloma cells
-
Hideshima, T.; Richardson, P.; Chauhan, D.; Palombella, V. J.; Elliott, P. J.; Adams, J.; Anderson, K. C. The proteasome inhibitor PS-341 inhibits growth, induces apoptosis, and overcomes drug resistance in human multiple myeloma cells. Cancer Res. 2001, 61, 3071-3076
-
(2001)
Cancer Res
, vol.61
, pp. 3071-3076
-
-
Hideshima, T.1
Richardson, P.2
Chauhan, D.3
Palombella, V.J.4
Elliott, P.J.5
Adams, J.6
Anderson, K.C.7
-
54
-
-
17644379385
-
Pharmacology, pharmacokinetics, and practical applications of bortezomib
-
Schwartz, R.; Davidson, T. Pharmacology, pharmacokinetics, and practical applications of bortezomib. Oncology (Williston Park). 2004, 18, 14-21
-
(2004)
Oncology (Williston Park)
, vol.18
, pp. 14-21
-
-
Schwartz, R.1
Davidson, T.2
-
55
-
-
43049115407
-
Bortezomib in mantle cell lymphoma
-
Suh, K. S.; Goy, A. Bortezomib in mantle cell lymphoma. Future Oncol. 2008, 4, 149-168
-
(2008)
Future Oncol
, vol.4
, pp. 149-168
-
-
Suh, K.S.1
Goy, A.2
-
56
-
-
33747517230
-
The proteasome: A novel target for anticancer therapy
-
Montagut, C.; Rovira, A.; Albanell, J. The proteasome: a novel target for anticancer therapy. Clin. Transl. Oncol. 2006, 8, 313-317
-
(2006)
Clin. Transl. Oncol
, vol.8
, pp. 313-317
-
-
Montagut, C.1
Rovira, A.2
Albanell, J.3
-
57
-
-
46049100809
-
Bortezomib: A novel chemotherapeutic agent for hematologic malignancies
-
Utecht, K. N.; Kolesar, J. Bortezomib: a novel chemotherapeutic agent for hematologic malignancies. Am. J. Health Syst. Pharm. 2008, 65, 1221-1231
-
(2008)
Am. J. Health Syst. Pharm
, vol.65
, pp. 1221-1231
-
-
Utecht, K.N.1
Kolesar, J.2
-
58
-
-
0036023407
-
A phase I trial of the novel proteasome inhibitor PS341 in advanced solid tumor malignancies
-
Aghajanian, C.; Soignet, S.; Dizon, D. S.; Pien, C. S.; Adams, J.; Elliott, P. J.; Sabbatini, P.; Miller, V.; Hensley, M. L.; Pezzulli, S.; Canales, C.; Daud, A.; Spriggs, D. R. A phase I trial of the novel proteasome inhibitor PS341 in advanced solid tumor malignancies. Clin. Cancer Res. 2002, 8, 2505-2511
-
(2002)
Clin. Cancer Res
, vol.8
, pp. 2505-2511
-
-
Aghajanian, C.1
Soignet, S.2
Dizon, D.S.3
Pien, C.S.4
Adams, J.5
Elliott, P.J.6
Sabbatini, P.7
Miller, V.8
Hensley, M.L.9
Pezzulli, S.10
Canales, C.11
Daud, A.12
Spriggs, D.R.13
-
59
-
-
24944514626
-
Proteasome inhibition with bortezomib (PS-341): A phase I study with pharmacodynamic end points using a day 1 and day 4 schedule in a 14-day cycle
-
Hamilton, A. L.; Eder, J. P.; Pavlick, A. C.; Clark, J. W.; Liebes, L.; Garcia-Carbonero, R.; Chachoua, A.; Ryan, D. P.; Soma, V.; Farrell, K.; Kinchla, N.; Boyden, J.; Yee, H.; Zeleniuch-Jacquotte, A.; Wright, J.; Elliott, P.; Adams, J.; Muggia, F. M. Proteasome inhibition with bortezomib (PS-341): a phase I study with pharmacodynamic end points using a day 1 and day 4 schedule in a 14-day cycle. J. Clin. Oncol. 2005, 23, 6107-6116
-
(2005)
J. Clin. Oncol
, vol.23
, pp. 6107-6116
-
-
Hamilton, A.L.1
Eder, J.P.2
Pavlick, A.C.3
Clark, J.W.4
Liebes, L.5
Garcia-Carbonero, R.6
Chachoua, A.7
Ryan, D.P.8
Soma, V.9
Farrell, K.10
Kinchla, N.11
Boyden, J.12
Yee, H.13
Zeleniuch-Jacquotte, A.14
Wright, J.15
Elliott, P.16
Adams, J.17
Muggia, F.M.18
-
60
-
-
33745728140
-
Comparative selectivity and specificity of the proteasome inhibitors BzLLLCOCHO, PS-341, and MG-132
-
Crawford, L. J.; Walker, B.; Ovaa, H.; Chauhan, D.; Anderson, K. C.; Morris, T. C.; Irvine, A. E. Comparative selectivity and specificity of the proteasome inhibitors BzLLLCOCHO, PS-341, and MG-132. Cancer Res. 2006, 66, 6379-6386
-
(2006)
Cancer Res
, vol.66
, pp. 6379-6386
-
-
Crawford, L.J.1
Walker, B.2
Ovaa, H.3
Chauhan, D.4
Anderson, K.C.5
Morris, T.C.6
Irvine, A.E.7
-
61
-
-
78651321769
-
The ubiquitin-proteasome system as a prospective molecular target for cancer treatment and prevention
-
Chen, D.; Dou, Q. P. The ubiquitin-proteasome system as a prospective molecular target for cancer treatment and prevention. Curr. Protein Pept. Sci. 2010, 11, 459-470
-
(2010)
Curr. Protein Pept. Sci
, vol.11
, pp. 459-470
-
-
Chen, D.1
Dou, Q.P.2
-
62
-
-
36849013003
-
A phase II study of single agent bortezomib in patients with metastatic breast cancer: A single institution experience
-
Engel, R. H.; Brown, J. A.; Von Roenn, J. H.; O'Regan, R. M.; Bergan, R.; Badve, S.; Rademaker, A.; Gradishar, W. J. A phase II study of single agent bortezomib in patients with metastatic breast cancer: a single institution experience. Cancer Invest. 2007, 25, 733-737
-
(2007)
Cancer Invest
, vol.25
, pp. 733-737
-
-
Engel, R.H.1
Brown, J.A.2
von Roenn, J.H.3
O'Regan, R.M.4
Bergan, R.5
Badve, S.6
Rademaker, A.7
Gradishar, W.J.8
-
63
-
-
33646186160
-
Bortezomib (VELCADE) in metastatic breast cancer: Pharmacodynamics, biological effects, and prediction of clinical benefits
-
Yang, C. H.; Gonzalez-Angulo, A. M.; Reuben, J. M.; Booser, D. J.; Pusztai, L.; Krishnamurthy, S.; Esseltine, D.; Stec, J.; Broglio, K. R.; Islam, R.; Hortobagyi, G. N.; Cristofanilli, M. Bortezomib (VELCADE) in metastatic breast cancer: pharmacodynamics, biological effects, and prediction of clinical benefits. Ann. Oncol. 2006, 17, 813-817
-
(2006)
Ann. Oncol
, vol.17
, pp. 813-817
-
-
Yang, C.H.1
Gonzalez-Angulo, A.M.2
Reuben, J.M.3
Booser, D.J.4
Pusztai, L.5
Krishnamurthy, S.6
Esseltine, D.7
Stec, J.8
Broglio, K.R.9
Islam, R.10
Hortobagyi, G.N.11
Cristofanilli, M.12
-
64
-
-
33644701684
-
The potential role of bortezomib in combination with chemotherapy and radiation in non-small-cell lung cancer
-
Edelman, M. J. The potential role of bortezomib in combination with chemotherapy and radiation in non-small-cell lung cancer. Clin. Lung Cancer 2005, 7 Suppl 2, S64-66
-
(2005)
Clin. Lung Cancer
, vol.7
, Issue.SUPPL. 2
-
-
Edelman, M.J.1
-
65
-
-
0035341494
-
Enhancement of radiosensitivity by proteasome inhibition: Implications for a role of NF-kappaB
-
Russo, S. M.; Tepper, J. E.; Baldwin, A. S., Jr.; Liu, R.; Adams, J.; Elliott, P.; Cusack, J. C., Jr. Enhancement of radiosensitivity by proteasome inhibition: implications for a role of NF-kappaB. Int. J. Radiat. Oncol. Biol. Phys. 2001, 50, 183-193
-
(2001)
Int. J. Radiat. Oncol. Biol. Phys
, vol.50
, pp. 183-193
-
-
Russo, S.M.1
Tepper, J.E.2
Baldwin Jr., A.S.3
Liu, R.4
Adams, J.5
Elliott, P.6
Cusack Jr., J.C.7
-
66
-
-
33644785935
-
Phase I trial of bortezomib in combination with docetaxel in patients with advanced solid tumors
-
Messersmith, W. A.; Baker, S. D.; Lassiter, L.; Sullivan, R. A.; Dinh, K.; Almuete, V. I.; Wright, J. J.; Donehower, R. C.; Carducci, M. A.; Armstrong, D. K. Phase I trial of bortezomib in combination with docetaxel in patients with advanced solid tumors. Clin. Cancer Res. 2006, 12, 1270-1275
-
(2006)
Clin. Cancer Res
, vol.12
, pp. 1270-1275
-
-
Messersmith, W.A.1
Baker, S.D.2
Lassiter, L.3
Sullivan, R.A.4
Dinh, K.5
Almuete, V.I.6
Wright, J.J.7
Donehower, R.C.8
Carducci, M.A.9
Armstrong, D.K.10
-
67
-
-
20144387627
-
Phase 1 trial of the proteasome inhibitor bortezomib and pegylated liposomal doxorubicin in patients with advanced hematologic malignancies
-
Orlowski, R. Z.; Voorhees, P. M.; Garcia, R. A.; Hall, M. D.; Kudrik, F. J.; Allred, T.; Johri, A. R.; Jones, P. E.; Ivanova, A.; Van Deventer, H. W.; Gabriel, D. A.; Shea, T. C.; Mitchell, B. S.; Adams, J.; Esseltine, D. L.; Trehu, E. G.; Green, M.; Lehman, M. J.; Natoli, S.; Collins, J. M.; Lindley, C. M.; Dees, E. C. Phase 1 trial of the proteasome inhibitor bortezomib and pegylated liposomal doxorubicin in patients with advanced hematologic malignancies. Blood 2005, 105, 3058-3065
-
(2005)
Blood
, vol.105
, pp. 3058-3065
-
-
Orlowski, R.Z.1
Voorhees, P.M.2
Garcia, R.A.3
Hall, M.D.4
Kudrik, F.J.5
Allred, T.6
Johri, A.R.7
Jones, P.E.8
Ivanova, A.9
van Deventer, H.W.10
Gabriel, D.A.11
Shea, T.C.12
Mitchell, B.S.13
Adams, J.14
Esseltine, D.L.15
Trehu, E.G.16
Green, M.17
Lehman, M.J.18
Natoli, S.19
Collins, J.M.20
Lindley, C.M.21
Dees, E.C.22
more..
-
68
-
-
70349303770
-
Ascorbic acid inhibits antitumor activity of bortezomib in vivo
-
Perrone, G.; Hideshima, T.; Ikeda, H.; Okawa, Y.; Calabrese, E.; Gorgun, G.; Santo, L.; Cirstea, D.; Raje, N.; Chauhan, D.; Baccarani, M.; Cavo, M.; Anderson, K. C. Ascorbic acid inhibits antitumor activity of bortezomib in vivo. Leukemia 2009, 23, 1679-1686
-
(2009)
Leukemia
, vol.23
, pp. 1679-1686
-
-
Perrone, G.1
Hideshima, T.2
Ikeda, H.3
Okawa, Y.4
Calabrese, E.5
Gorgun, G.6
Santo, L.7
Cirstea, D.8
Raje, N.9
Chauhan, D.10
Baccarani, M.11
Cavo, M.12
Anderson, K.C.13
-
69
-
-
33751563004
-
A Phase I study of bortezomib plus irinotecan in patients with advanced solid tumors
-
Ryan, D. P.; O'Neil, B. H.; Supko, J. G.; Rocha Lima, C. M.; Dees, E. C.; Appleman, L. J.; Clark, J.; Fidias, P.; Orlowski, R. Z.; Kashala, O.; Eder, J. P.; Cusack, J. C., Jr. A Phase I study of bortezomib plus irinotecan in patients with advanced solid tumors. Cancer 2006, 107, 2688-2697
-
(2006)
Cancer
, vol.107
, pp. 2688-2697
-
-
Ryan, D.P.1
O'Neil, B.H.2
Supko, J.G.3
Rocha Lima, C.M.4
Dees, E.C.5
Appleman, L.J.6
Clark, J.7
Fidias, P.8
Orlowski, R.Z.9
Kashala, O.10
Eder, J.P.11
Cusack Jr., J.C.12
-
70
-
-
0346505340
-
The IKK NF-kappa B system: A treasure trove for drug development
-
Karin, M.; Yamamoto, Y.; Wang, Q. M. The IKK NF-kappa B system: a treasure trove for drug development. Nat. Rev. Drug Discov. 2004, 3, 17-26
-
(2004)
Nat. Rev. Drug Discov
, vol.3
, pp. 17-26
-
-
Karin, M.1
Yamamoto, Y.2
Wang, Q.M.3
-
71
-
-
0042167462
-
Mechanisms of cell death and survival in multiple myeloma (MM): Therapeutic implications
-
Chauhan, D.; Anderson, K. C. Mechanisms of cell death and survival in multiple myeloma (MM): Therapeutic implications. Apoptosis 2003, 8, 337-343
-
(2003)
Apoptosis
, vol.8
, pp. 337-343
-
-
Chauhan, D.1
Anderson, K.C.2
-
72
-
-
0037342894
-
The proteasome inhibitor PS-341 markedly enhances sensitivity of multiple myeloma tumor cells to chemotherapeutic agents
-
Ma, M. H.; Yang, H. H.; Parker, K.; Manyak, S.; Friedman, J. M.; Altamirano, C.; Wu, Z. Q.; Borad, M. J.; Frantzen, M.; Roussos, E.; Neeser, J.; Mikail, A.; Adams, J.; Sjak-Shie, N.; Vescio, R. A.; Berenson, J. R. The proteasome inhibitor PS-341 markedly enhances sensitivity of multiple myeloma tumor cells to chemotherapeutic agents. Clin. Cancer Res. 2003, 9, 1136-1144
-
(2003)
Clin. Cancer Res
, vol.9
, pp. 1136-1144
-
-
Ma, M.H.1
Yang, H.H.2
Parker, K.3
Manyak, S.4
Friedman, J.M.5
Altamirano, C.6
Wu, Z.Q.7
Borad, M.J.8
Frantzen, M.9
Roussos, E.10
Neeser, J.11
Mikail, A.12
Adams, J.13
Sjak-Shie, N.14
Vescio, R.A.15
Berenson, J.R.16
-
73
-
-
0033121314
-
Role of NF-kappaB in the rescue of multiple myeloma cells from glucocorticoid-induced apoptosis by bcl-2
-
Feinman, R.; Koury, J.; Thames, M.; Barlogie, B.; Epstein, J.; Siegel, D. S. Role of NF-kappaB in the rescue of multiple myeloma cells from glucocorticoid-induced apoptosis by bcl-2. Blood 1999, 93, 3044-3052
-
(1999)
Blood
, vol.93
, pp. 3044-3052
-
-
Feinman, R.1
Koury, J.2
Thames, M.3
Barlogie, B.4
Epstein, J.5
Siegel, D.S.6
-
74
-
-
70349243697
-
Bortezomib induces canonical nuclear factor-kappaB activation in multiple myeloma cells
-
Hideshima, T.; Ikeda, H.; Chauhan, D.; Okawa, Y.; Raje, N.; Podar, K.; Mitsiades, C.; Munshi, N. C.; Richardson, P. G.; Carrasco, R. D.; Anderson, K. C. Bortezomib induces canonical nuclear factor-kappaB activation in multiple myeloma cells. Blood 2009, 114, 1046-1052
-
(2009)
Blood
, vol.114
, pp. 1046-1052
-
-
Hideshima, T.1
Ikeda, H.2
Chauhan, D.3
Okawa, Y.4
Raje, N.5
Podar, K.6
Mitsiades, C.7
Munshi, N.C.8
Richardson, P.G.9
Carrasco, R.D.10
Anderson, K.C.11
-
75
-
-
22244452016
-
Proteasome inhibitors trigger NOXA-mediated apoptosis in melanoma and myeloma cells
-
Qin, J. Z.; Ziffra, J.; Stennett, L.; Bodner, B.; Bonish, B. K.; Chaturvedi, V.; Bennett, F.; Pollock, P. M.; Trent, J. M.; Hendrix, M. J.; Rizzo, P.; Miele, L.; Nickoloff, B. J. Proteasome inhibitors trigger NOXA-mediated apoptosis in melanoma and myeloma cells. Cancer Res. 2005, 65, 6282-6293
-
(2005)
Cancer Res
, vol.65
, pp. 6282-6293
-
-
Qin, J.Z.1
Ziffra, J.2
Stennett, L.3
Bodner, B.4
Bonish, B.K.5
Chaturvedi, V.6
Bennett, F.7
Pollock, P.M.8
Trent, J.M.9
Hendrix, M.J.10
Rizzo, P.11
Miele, L.12
Nickoloff, B.J.13
-
76
-
-
0034640281
-
Noxa, a BH3- only member of the Bcl-2 family and candidate mediator of p53- induced apoptosis
-
Oda, E.; Ohki, R.; Murasawa, H.; Nemoto, J.; Shibue, T.; Yamashita, T.; Tokino, T.; Taniguchi, T.; Tanaka, N. Noxa, a BH3- only member of the Bcl-2 family and candidate mediator of p53- induced apoptosis. Science 2000, 288, 1053-1058
-
(2000)
Science
, vol.288
, pp. 1053-1058
-
-
Oda, E.1
Ohki, R.2
Murasawa, H.3
Nemoto, J.4
Shibue, T.5
Yamashita, T.6
Tokino, T.7
Taniguchi, T.8
Tanaka, N.9
-
77
-
-
0032575688
-
The Bcl-2 protein family: Arbiters of cell survival
-
Adams, J. M.; Cory, S. The Bcl-2 protein family: arbiters of cell survival. Science 1998, 281, 1322-1326
-
(1998)
Science
, vol.281
, pp. 1322-1326
-
-
Adams, J.M.1
Cory, S.2
-
78
-
-
0033179760
-
BCL-2 family members and the mitochondria in apoptosis
-
Gross, A.; McDonnell, J. M.; Korsmeyer, S. J. BCL-2 family members and the mitochondria in apoptosis. Genes Dev. 1999, 13, 1899-1911
-
(1999)
Genes Dev
, vol.13
, pp. 1899-1911
-
-
Gross, A.1
McDonnell, J.M.2
Korsmeyer, S.J.3
-
79
-
-
37649000950
-
Tumor cell- selective regulation of NOXA by c-MYC in response to proteasome inhibition
-
Nikiforov, M. A.; Riblett, M.; Tang, W. H.; Gratchouck, V.; Zhuang, D.; Fernandez, Y.; Verhaegen, M.; Varambally, S.; Chinnaiyan, A. M.; Jakubowiak, A. J.; Soengas, M. S. Tumor cell- selective regulation of NOXA by c-MYC in response to proteasome inhibition. Proc. Natl. Acad. Sci. U. S. A. 2007, 104, 19488-19493
-
(2007)
Proc. Natl. Acad. Sci. U. S. A
, vol.104
, pp. 19488-19493
-
-
Nikiforov, M.A.1
Riblett, M.2
Tang, W.H.3
Gratchouck, V.4
Zhuang, D.5
Fernandez, Y.6
Verhaegen, M.7
Varambally, S.8
Chinnaiyan, A.M.9
Jakubowiak, A.J.10
Soengas, M.S.11
-
80
-
-
2342667387
-
The development of proteasome inhibitors as anticancer drugs
-
Adams, J. The development of proteasome inhibitors as anticancer drugs. Cancer Cell. 2004, 5, 417-421
-
(2004)
Cancer Cell
, vol.5
, pp. 417-421
-
-
Adams, J.1
-
81
-
-
33745855438
-
Bortezomib: Efficacy comparisons in solid tumors and hematologic malignancies
-
Caravita, T.; de Fabritiis, P.; Palumbo, A.; Amadori, S.; Boccadoro, M. Bortezomib: efficacy comparisons in solid tumors and hematologic malignancies. Nat. Clin. Pract. Oncol. 2006, 3, 374-387
-
(2006)
Nat. Clin. Pract. Oncol
, vol.3
, pp. 374-387
-
-
Caravita, T.1
de Fabritiis, P.2
Palumbo, A.3
Amadori, S.4
Boccadoro, M.5
-
82
-
-
22244454745
-
Differential regulation of noxa in normal melanocytes and melanoma cells by proteasome inhibition: Therapeutic implications
-
Fernandez, Y.; Verhaegen, M.; Miller, T. P.; Rush, J. L.; Steiner, P.; Opipari, A. W., Jr.; Lowe, S. W.; Soengas, M. S. Differential regulation of noxa in normal melanocytes and melanoma cells by proteasome inhibition: therapeutic implications. Cancer Res. 2005, 65, 6294-6304
-
(2005)
Cancer Res
, vol.65
, pp. 6294-6304
-
-
Fernandez, Y.1
Verhaegen, M.2
Miller, T.P.3
Rush, J.L.4
Steiner, P.5
Opipari Jr., A.W.6
Lowe, S.W.7
Soengas, M.S.8
-
83
-
-
33750312678
-
Enhanced killing of melanoma cells by simultaneously targeting Mcl-1 and NOXA
-
Qin, J. Z.; Xin, H.; Sitailo, L. A.; Denning, M. F.; Nickoloff, B. J. Enhanced killing of melanoma cells by simultaneously targeting Mcl-1 and NOXA. Cancer Res. 2006, 66, 9636-9645
-
(2006)
Cancer Res
, vol.66
, pp. 9636-9645
-
-
Qin, J.Z.1
Xin, H.2
Sitailo, L.A.3
Denning, M.F.4
Nickoloff, B.J.5
-
84
-
-
0036680037
-
Preclinical and clinical evaluation of proteasome inhibitor PS-341 for the treatment of cancer
-
Adams, J. Preclinical and clinical evaluation of proteasome inhibitor PS-341 for the treatment of cancer. Curr. Opin. Chem. Biol. 2002, 6, 493-500
-
(2002)
Curr. Opin. Chem. Biol
, vol.6
, pp. 493-500
-
-
Adams, J.1
-
85
-
-
21344469223
-
Bortezomib therapy alone and in combination with dexamethasone for previously untreated symptomatic multiple myeloma
-
Jagannath, S.; Durie, B. G.; Wolf, J.; Camacho, E.; Irwin, D.; Lutzky, J.; McKinley, M.; Gabayan, E.; Mazumder, A.; Schenkein, D.; Crowley, J. Bortezomib therapy alone and in combination with dexamethasone for previously untreated symptomatic multiple myeloma. Br. J. Haematol. 2005, 129, 776-783
-
(2005)
Br. J. Haematol
, vol.129
, pp. 776-783
-
-
Jagannath, S.1
Durie, B.G.2
Wolf, J.3
Camacho, E.4
Irwin, D.5
Lutzky, J.6
McKinley, M.7
Gabayan, E.8
Mazumder, A.9
Schenkein, D.10
Crowley, J.11
-
86
-
-
4644304196
-
Phase II trial of bortezomib for patients with advanced renal cell carcinoma
-
Kondagunta, G. V.; Drucker, B.; Schwartz, L.; Bacik, J.; Marion, S.; Russo, P.; Mazumdar, M.; Motzer, R. J. Phase II trial of bortezomib for patients with advanced renal cell carcinoma. J. Clin. Oncol. 2004, 22, 3720-3725
-
(2004)
J. Clin. Oncol
, vol.22
, pp. 3720-3725
-
-
Kondagunta, G.V.1
Drucker, B.2
Schwartz, L.3
Bacik, J.4
Marion, S.5
Russo, P.6
Mazumdar, M.7
Motzer, R.J.8
Phase, I.I.9
-
87
-
-
20444433230
-
Bortezomib or high-dose dexamethasone for relapsed multiple myeloma
-
Richardson, P. G.; Sonneveld, P.; Schuster, M. W.; Irwin, D.; Stadtmauer, E. A.; Facon, T.; Harousseau, J. L.; Ben-Yehuda, D.; Lonial, S.; Goldschmidt, H.; Reece, D.; San-Miguel, J. F.; Blade, J.; Boccadoro, M.; Cavenagh, J.; Dalton, W. S.; Boral, A. L.; Esseltine, D. L.; Porter, J. B.; Schenkein, D.; Anderson, K. C. Bortezomib or high-dose dexamethasone for relapsed multiple myeloma. N. Engl. J. Med. 2005, 352, 2487-2498
-
(2005)
N. Engl. J. Med
, vol.352
, pp. 2487-2498
-
-
Richardson, P.G.1
Sonneveld, P.2
Schuster, M.W.3
Irwin, D.4
Stadtmauer, E.A.5
Facon, T.6
Harousseau, J.L.7
Ben-Yehuda, D.8
Lonial, S.9
Goldschmidt, H.10
Reece, D.11
San-Miguel, J.F.12
Blade, J.13
Boccadoro, M.14
Cavenagh, J.15
Dalton, W.S.16
Boral, A.L.17
Esseltine, D.L.18
Porter, J.B.19
Schenkein, D.20
Anderson, K.C.21
more..
-
88
-
-
0034981649
-
26S proteasome inhibition induces apoptosis and limits growth of human pancreatic cancer
-
Shah, S. A.; Potter, M. W.; McDade, T. P.; Ricciardi, R.; Perugini, R. A.; Elliott, P. J.; Adams, J.; Callery, M. P. 26S proteasome inhibition induces apoptosis and limits growth of human pancreatic cancer. J. Cell Biochem. 2001, 82, 110-122
-
(2001)
J. Cell Biochem
, vol.82
, pp. 110-122
-
-
Shah, S.A.1
Potter, M.W.2
McDade, T.P.3
Ricciardi, R.4
Perugini, R.A.5
Elliott, P.J.6
Adams, J.7
Callery, M.P.8
-
89
-
-
0034902354
-
Novel proteasome inhibitor PS-341 inhibits activation of nuclear factor- kappa B, cell survival, tumor growth, and angiogenesis in squamous cell carcinoma
-
Sunwoo, J. B.; Chen, Z.; Dong, G.; Yeh, N.; Crowl Bancroft, C.; Sausville, E.; Adams, J.; Elliott, P.; Van Waes, C. Novel proteasome inhibitor PS-341 inhibits activation of nuclear factor- kappa B, cell survival, tumor growth, and angiogenesis in squamous cell carcinoma. Clin. Cancer Res. 2001, 7, 1419-1428
-
(2001)
Clin. Cancer Res
, vol.7
, pp. 1419-1428
-
-
Sunwoo, J.B.1
Chen, Z.2
Dong, G.3
Yeh, N.4
Crowl Bancroft, C.5
Sausville, E.6
Adams, J.7
Elliott, P.8
van Waes, C.9
-
90
-
-
0035207110
-
The role of nuclear factor- kappaB in the biology and treatment of multiple myeloma
-
Berenson, J. R.; Ma, H. M.; Vescio, R. The role of nuclear factor- kappaB in the biology and treatment of multiple myeloma. Semin. Oncol. 2001, 28, 626-633
-
(2001)
Semin. Oncol
, vol.28
, pp. 626-633
-
-
Berenson, J.R.1
Ma, H.M.2
Vescio, R.3
-
91
-
-
0036735298
-
Proteasome inhibitor PS-341 inhibits human myeloma cell growth in vivo and prolongs survival in a murine model
-
LeBlanc, R.; Catley, L. P.; Hideshima, T.; Lentzsch, S.; Mitsiades, C. S.; Mitsiades, N.; Neuberg, D.; Goloubeva, O.; Pien, C. S.; Adams, J.; Gupta, D.; Richardson, P. G.; Munshi, N. C.; Anderson, K. C. Proteasome inhibitor PS-341 inhibits human myeloma cell growth in vivo and prolongs survival in a murine model. Cancer Res. 2002, 62, 4996-5000
-
(2002)
Cancer Res
, vol.62
, pp. 4996-5000
-
-
Leblanc, R.1
Catley, L.P.2
Hideshima, T.3
Lentzsch, S.4
Mitsiades, C.S.5
Mitsiades, N.6
Neuberg, D.7
Goloubeva, O.8
Pien, C.S.9
Adams, J.10
Gupta, D.11
Richardson, P.G.12
Munshi, N.C.13
Anderson, K.C.14
-
92
-
-
0012433771
-
Effects of the proteasome inhibitor PS-341 on apoptosis and angiogenesis in orthotopic human pancreatic tumor xenografts
-
Nawrocki, S. T.; Bruns, C. J.; Harbison, M. T.; Bold, R. J.; Gotsch, B. S.; Abbruzzese, J. L.; Elliott, P.; Adams, J.; McConkey, D. J. Effects of the proteasome inhibitor PS-341 on apoptosis and angiogenesis in orthotopic human pancreatic tumor xenografts. Mol. Cancer Ther. 2002, 1, 1243-1253
-
(2002)
Mol. Cancer Ther
, vol.1
, pp. 1243-1253
-
-
Nawrocki, S.T.1
Bruns, C.J.2
Harbison, M.T.3
Bold, R.J.4
Gotsch, B.S.5
Abbruzzese, J.L.6
Elliott, P.7
Adams, J.8
McConkey, D.J.9
-
93
-
-
33845496508
-
Bortezomib disrupts tumour-dendritic cell interactions in myeloma and lymphoma: Therapeutic implications
-
Kukreja, A.; Hutchinson, A.; Mazumder, A.; Vesole, D.; Angitapalli, R.; Jagannath, S.; O'Connor O. A.; Dhodapkar, M. V. Bortezomib disrupts tumour-dendritic cell interactions in myeloma and lymphoma: therapeutic implications. Br. J. Haematol. 2007, 136, 106-110
-
(2007)
Br. J. Haematol
, vol.136
, pp. 106-110
-
-
Kukreja, A.1
Hutchinson, A.2
Mazumder, A.3
Vesole, D.4
Angitapalli, R.5
Jagannath, S.6
O'Connor, O.A.7
Dhodapkar, M.V.8
-
94
-
-
0242496212
-
Molecular sequelae of proteasome inhibition in human multiple myeloma cells
-
Mitsiades, N.; Mitsiades, C. S.; Poulaki, V.; Chauhan, D.; Fanourakis, G.; Gu, X.; Bailey, C.; Joseph, M.; Libermann, T. A.; Treon, S. P.; Munshi, N. C.; Richardson, P. G.; Hideshima, T.; Anderson, K. C. Molecular sequelae of proteasome inhibition in human multiple myeloma cells. Proc. Natl. Acad. Sci. U. S. A. 2002, 99, 14374-14379
-
(2002)
Proc. Natl. Acad. Sci. U. S. A
, vol.99
, pp. 14374-14379
-
-
Mitsiades, N.1
Mitsiades, C.S.2
Poulaki, V.3
Chauhan, D.4
Fanourakis, G.5
Gu, X.6
Bailey, C.7
Joseph, M.8
Libermann, T.A.9
Treon, S.P.10
Munshi, N.C.11
Richardson, P.G.12
Hideshima, T.13
Anderson, K.C.14
-
95
-
-
34047257880
-
The proteasome inhibitor bortezomib acts independently of p53 and induces cell death via apoptosis and mitotic catastrophe in B-cell lymphoma cell lines
-
Strauss, S. J.; Higginbottom, K.; Juliger, S.; Maharaj, L.; Allen, P.; Schenkein, D.; Lister, T. A.; Joel, S. P. The proteasome inhibitor bortezomib acts independently of p53 and induces cell death via apoptosis and mitotic catastrophe in B-cell lymphoma cell lines. Cancer Res. 2007, 67, 2783-2790
-
(2007)
Cancer Res
, vol.67
, pp. 2783-2790
-
-
Strauss, S.J.1
Higginbottom, K.2
Juliger, S.3
Maharaj, L.4
Allen, P.5
Schenkein, D.6
Lister, T.A.7
Joel, S.P.8
-
96
-
-
33751189389
-
Proteasome inhibitor induces apoptosis through induction of endoplasmic reticulum stress
-
Fribley, A.; Wang, C. Y. Proteasome inhibitor induces apoptosis through induction of endoplasmic reticulum stress. Cancer Biol. Ther. 2006, 5, 745-748
-
(2006)
Cancer Biol. Ther
, vol.5
, pp. 745-748
-
-
Fribley, A.1
Wang, C.Y.2
-
97
-
-
7644242953
-
Proteasome inhibitor PS-341 induces apoptosis through induction of endoplasmic reticulum stress-reactive oxygen species in head and neck squamous cell carcinoma cells
-
Fribley, A.; Zeng, Q.; Wang, C. Y. Proteasome inhibitor PS-341 induces apoptosis through induction of endoplasmic reticulum stress-reactive oxygen species in head and neck squamous cell carcinoma cells. Mol. Cell Biol. 2004, 24, 9695-9704
-
(2004)
Mol. Cell Biol
, vol.24
, pp. 9695-9704
-
-
Fribley, A.1
Zeng, Q.2
Wang, C.Y.3
-
98
-
-
54049085820
-
Bortezomib induces apoptosis in esophageal squamous cell carcinoma cells through activation of the p38 mitogen-activated protein kinase pathway
-
Lioni, M.; Noma, K.; Snyder, A.; Klein-Szanto, A.; Diehl, J. A.; Rustgi, A. K.; Herlyn, M.; Smalley, K. S. Bortezomib induces apoptosis in esophageal squamous cell carcinoma cells through activation of the p38 mitogen-activated protein kinase pathway. Mol. Cancer Ther. 2008, 7, 2866-2875
-
(2008)
Mol. Cancer Ther
, vol.7
, pp. 2866-2875
-
-
Lioni, M.1
Noma, K.2
Snyder, A.3
Klein-Szanto, A.4
Diehl, J.A.5
Rustgi, A.K.6
Herlyn, M.7
Smalley, K.S.8
-
99
-
-
20444364475
-
A phase II study of bortezomib in the treatment of metastatic malignant melanoma
-
Markovic, S. N.; Geyer, S. M.; Dawkins, F.; Sharfman, W.; Albertini, M.; Maples, W.; Fracasso, P. M.; Fitch, T.; Lorusso, P.; Adjei, A. A.; Erlichman, C. A phase II study of bortezomib in the treatment of metastatic malignant melanoma. Cancer 2005, 103, 2584-2589
-
(2005)
Cancer
, vol.103
, pp. 2584-2589
-
-
Markovic, S.N.1
Geyer, S.M.2
Dawkins, F.3
Sharfman, W.4
Albertini, M.5
Maples, W.6
Fracasso, P.M.7
Fitch, T.8
Lorusso, P.9
Adjei, A.A.10
Erlichman, C.11
-
100
-
-
34250770091
-
A parallel dose-escalation study of weekly and twice-weekly bortezomib in combination with gemcitabine and cisplatin in the first-line treatment of patients with advanced solid tumors. Clin
-
Voortman, J.; Smit, E. F.; Honeywell, R.; Kuenen, B. C.; Peters, G. J.; van de Velde, H.; Giaccone, G. A parallel dose-escalation study of weekly and twice-weekly bortezomib in combination with gemcitabine and cisplatin in the first-line treatment of patients with advanced solid tumors. Clin. Cancer Res. 2007, 13, 3642-3651
-
(2007)
Cancer Res
, vol.13
, pp. 3642-3651
-
-
Voortman, J.1
Smit, E.F.2
Honeywell, R.3
Kuenen, B.C.4
Peters, G.J.5
van de Velde, H.6
Giaccone, G.7
-
101
-
-
33947196412
-
Phase I/II study of bortezomib plus docetaxel in patients with advanced androgen-independent prostate cancer
-
Dreicer, R.; Petrylak, D.; Agus, D.; Webb, I.; Roth, B. Phase I/II study of bortezomib plus docetaxel in patients with advanced androgen-independent prostate cancer. Clin. Cancer Res. 2007, 13, 1208-1215
-
(2007)
Clin. Cancer Res
, vol.13
, pp. 1208-1215
-
-
Dreicer, R.1
Petrylak, D.2
Agus, D.3
Webb, I.4
Roth, B.5
-
102
-
-
34249910962
-
Weekly docetaxel and bortezomib as first-line treatment for patients with hormone- refractory prostate cancer: A Minnie Pearl Cancer Research Network phase II trial
-
Hainsworth, J. D.; Meluch, A. A.; Spigel, D. R.; Barton, J., Jr.; Simons, L.; Meng, C.; Gould, B.; Greco, F. A. Weekly docetaxel and bortezomib as first-line treatment for patients with hormone- refractory prostate cancer: a Minnie Pearl Cancer Research Network phase II trial. Clin. Genitourin. Cancer 2007, 5, 278-283
-
(2007)
Clin. Genitourin. Cancer
, vol.5
, pp. 278-283
-
-
Hainsworth, J.D.1
Meluch, A.A.2
Spigel, D.R.3
Barton Jr., J.4
Simons, L.5
Meng, C.6
Gould, B.7
Greco, F.A.8
-
103
-
-
35948969806
-
A phase II trial of bortezomib and prednisone for castration resistant metastatic prostate cancer
-
discussion 2383-2374
-
Morris, M. J.; Kelly, W. K.; Slovin, S.; Ryan, C.; Eicher, C.; Heller, G.; Scher, H. I. A phase II trial of bortezomib and prednisone for castration resistant metastatic prostate cancer. J. Urol. 2007, 178, 2378-2383; discussion 2383-2374
-
(2007)
J. Urol
, vol.178
, pp. 2378-2383
-
-
Morris, M.J.1
Kelly, W.K.2
Slovin, S.3
Ryan, C.4
Eicher, C.5
Heller, G.6
Scher, H.I.7
-
104
-
-
0037973279
-
A phase 2 study of bortezomib in relapsed, refractory myeloma
-
Richardson, P. G.; Barlogie, B.; Berenson, J.; Singhal, S.; Jagannath, S.; Irwin, D.; Rajkumar, S. V.; Srkalovic, G.; Alsina, M.; Alexanian, R.; Siegel, D.; Orlowski, R. Z.; Kuter, D.; Limentani, S. A.; Lee, S.; Hideshima, T.; Esseltine, D. L.; Kauffman, M.; Adams, J.; Schenkein, D. P.; Anderson, K. C. A phase 2 study of bortezomib in relapsed, refractory myeloma. N. Engl. J. Med. 2003, 348, 2609-2617
-
(2003)
N. Engl. J. Med
, vol.348
, pp. 2609-2617
-
-
Richardson, P.G.1
Barlogie, B.2
Berenson, J.3
Singhal, S.4
Jagannath, S.5
Irwin, D.6
Rajkumar, S.V.7
Srkalovic, G.8
Alsina, M.9
Alexanian, R.10
Siegel, D.11
Orlowski, R.Z.12
Kuter, D.13
Limentani, S.A.14
Lee, S.15
Hideshima, T.16
Esseltine, D.L.17
Kauffman, M.18
Adams, J.19
Schenkein, D.P.20
Anderson, K.C.21
more..
-
105
-
-
5644250621
-
A phase 2 study of two doses of bortezomib in relapsed or refractory myeloma
-
Jagannath, S.; Barlogie, B.; Berenson, J.; Siegel, D.; Irwin, D.; Richardson, P. G.; Niesvizky, R.; Alexanian, R.; Limentani, S. A.; Alsina, M.; Adams, J.; Kauffman, M.; Esseltine, D. L.; Schenkein, D. P.; Anderson, K. C. A phase 2 study of two doses of bortezomib in relapsed or refractory myeloma. Br. J. Haematol. 2004, 127, 165-172
-
(2004)
Br. J. Haematol
, vol.127
, pp. 165-172
-
-
Jagannath, S.1
Barlogie, B.2
Berenson, J.3
Siegel, D.4
Irwin, D.5
Richardson, P.G.6
Niesvizky, R.7
Alexanian, R.8
Limentani, S.A.9
Alsina, M.10
Adams, J.11
Kauffman, M.12
Esseltine, D.L.13
Schenkein, D.P.14
Anderson, K.C.15
-
106
-
-
21344435052
-
PAD combination therapy (PS-341/bortezomib, doxorubicin and dexamethasone) for previously untreated patients with multiple myeloma
-
Oakervee, H. E.; Popat, R.; Curry, N.; Smith, P.; Morris, C.; Drake, M.; Agrawal, S.; Stec, J.; Schenkein, D.; Esseltine, D. L.; Cavenagh, J. D. PAD combination therapy (PS-341/bortezomib, doxorubicin and dexamethasone) for previously untreated patients with multiple myeloma. Br. J. Haematol. 2005, 129, 755-762
-
(2005)
Br. J. Haematol
, vol.129
, pp. 755-762
-
-
Oakervee, H.E.1
Popat, R.2
Curry, N.3
Smith, P.4
Morris, C.5
Drake, M.6
Agrawal, S.7
Stec, J.8
Schenkein, D.9
Esseltine, D.L.10
Cavenagh, J.D.11
-
107
-
-
33846530661
-
A phase II study of bortezomib in mantle cell lymphoma: The National Cancer Institute of Canada Clinical Trials Group trial IND.150
-
Belch, A.; Kouroukis, C. T.; Crump, M.; Sehn, L.; Gascoyne, R. D.; Klasa, R.; Powers, J.; Wright, J.; Eisenhauer, E. A. A phase II study of bortezomib in mantle cell lymphoma: the National Cancer Institute of Canada Clinical Trials Group trial IND.150. Ann. Oncol. 2007, 18, 116-121
-
(2007)
Ann. Oncol
, vol.18
, pp. 116-121
-
-
Belch, A.1
Kouroukis, C.T.2
Crump, M.3
Sehn, L.4
Gascoyne, R.D.5
Klasa, R.6
Powers, J.7
Wright, J.8
Eisenhauer, E.A.9
-
108
-
-
20044376092
-
Phase II clinical experience with the novel proteasome inhibitor bortezomib in patients with indolent non-Hodgkin's lymphoma and mantle cell lymphoma
-
O'Connor, O. A.; Wright, J.; Moskowitz, C.; Muzzy, J.; MacGregor-Cortelli, B.; Stubblefield, M.; Straus, D.; Portlock, C.; Hamlin, P.; Choi, E.; Dumetrescu, O.; Esseltine, D.; Trehu, E.; Adams, J.; Schenkein, D.; Zelenetz, A. D. Phase II clinical experience with the novel proteasome inhibitor bortezomib in patients with indolent non-Hodgkin's lymphoma and mantle cell lymphoma. J. Clin. Oncol. 2005, 23, 676-684
-
(2005)
J. Clin. Oncol
, vol.23
, pp. 676-684
-
-
O'Connor, O.A.1
Wright, J.2
Moskowitz, C.3
Muzzy, J.4
Macgregor-Cortelli, B.5
Stubblefield, M.6
Straus, D.7
Portlock, C.8
Hamlin, P.9
Choi, E.10
Dumetrescu, O.11
Esseltine, D.12
Trehu, E.13
Adams, J.14
Schenkein, D.15
Zelenetz, A.D.16
-
109
-
-
77952548567
-
A randomized phase II study of bortezomib and pemetrexed, in combination or alone, in patients with previously treated advanced non-small-cell lung cancer
-
Scagliotti, G. V.; Germonpre, P.; Bosquee, L.; Vansteenkiste, J.; Gervais, R.; Planchard, D.; Reck, M.; De Marinis, F.; Lee, J. S.; Park, K.; Biesma, B.; Gans, S.; Ramlau, R.; Szczesna, A.; Makhson, A.; Manikhas, G.; Morgan, B.; Zhu, Y.; Chan, K. C.; von Pawel, J. A randomized phase II study of bortezomib and pemetrexed, in combination or alone, in patients with previously treated advanced non-small-cell lung cancer. Lung Cancer 2010, 68, 420-426
-
(2010)
Lung Cancer
, vol.68
, pp. 420-426
-
-
Scagliotti, G.V.1
Germonpre, P.2
Bosquee, L.3
Vansteenkiste, J.4
Gervais, R.5
Planchard, D.6
Reck, M.7
de Marinis, F.8
Lee, J.S.9
Park, K.10
Biesma, B.11
Gans, S.12
Ramlau, R.13
Szczesna, A.14
Makhson, A.15
Manikhas, G.16
Morgan, B.17
Zhu, Y.18
Chan, K.C.19
von Pawel, J.20
more..
-
110
-
-
60749125815
-
Reversibility of symptomatic peripheral neuropathy with bortezomib in the phase III APEX trial in relapsed multiple myeloma: Impact of a dose-modification guideline
-
Richardson, P. G.; Sonneveld, P.; Schuster, M. W.; Stadtmauer, E. A.; Facon, T.; Harousseau, J. L.; Ben-Yehuda, D.; Lonial, S.; Goldschmidt, H.; Reece, D.; Blade, J.; Boccadoro, M.; Cavenagh, J. D.; Boral, A. L.; Esseltine, D. L.; Wen, P. Y.; Amato, A. A.; Anderson, K. C.; San Miguel, J. Reversibility of symptomatic peripheral neuropathy with bortezomib in the phase III APEX trial in relapsed multiple myeloma: impact of a dose-modification guideline. Br. J. Haematol. 2009, 144, 895-903
-
(2009)
Br. J. Haematol
, vol.144
, pp. 895-903
-
-
Richardson, P.G.1
Sonneveld, P.2
Schuster, M.W.3
Stadtmauer, E.A.4
Facon, T.5
Harousseau, J.L.6
Ben-Yehuda, D.7
Lonial, S.8
Goldschmidt, H.9
Reece, D.10
Blade, J.11
Boccadoro, M.12
Cavenagh, J.D.13
Boral, A.L.14
Esseltine, D.L.15
Wen, P.Y.16
Amato, A.A.17
Anderson, K.C.18
San Miguel, J.19
-
111
-
-
58149086029
-
High response rate to bortezomib with or without dexamethasone in patients with relapsed or refractory multiple myeloma: Results of a global phase 3b expanded access program
-
Mikhael, J. R.; Belch, A. R.; Prince, H. M.; Lucio, M. N.; Maiolino, A.; Corso, A.; Petrucci, M. T.; Musto, P.; Komarnicki, M.; Stewart, A. K. High response rate to bortezomib with or without dexamethasone in patients with relapsed or refractory multiple myeloma: results of a global phase 3b expanded access program. Br. J. Haematol. 2009, 144, 169-175
-
(2009)
Br. J. Haematol
, vol.144
, pp. 169-175
-
-
Mikhael, J.R.1
Belch, A.R.2
Prince, H.M.3
Lucio, M.N.4
Maiolino, A.5
Corso, A.6
Petrucci, M.T.7
Musto, P.8
Komarnicki, M.9
Stewart, A.K.10
-
112
-
-
58149350310
-
Consolidation therapy with bortezomib/lenalidomide/dexamethasone versus bortezomib/dexa- methasone after a dexamethasone-based induction regimen in patients with multiple myeloma: A randomized phase III trial
-
Fonseca, R.; Rajkumar, S. V. Consolidation therapy with bortezomib/lenalidomide/dexamethasone versus bortezomib/dexa- methasone after a dexamethasone-based induction regimen in patients with multiple myeloma: a randomized phase III trial. Clin. Lymphoma Myeloma 2008, 8, 315-317
-
(2008)
Clin. Lymphoma Myeloma
, vol.8
, pp. 315-317
-
-
Fonseca, R.1
Rajkumar, S.V.2
-
113
-
-
50449086728
-
Bortezomib plus melphalan and prednisone for initial treatment of multiple myeloma
-
San Miguel, J. F.; Schlag, R.; Khuageva, N. K.; Dimopoulos, M. A.; Shpilberg, O.; Kropff, M.; Spicka, I.; Petrucci, M. T.; Palumbo, A.; Samoilova, O. S.; Dmoszynska, A.; Abdulkadyrov, K. M.; Schots, R.; Jiang, B.; Mateos, M. V.; Anderson, K. C.; Esseltine, D. L.; Liu, K.; Cakana, A.; van de Velde, H.; Richardson, P. G. Bortezomib plus melphalan and prednisone for initial treatment of multiple myeloma. N. Engl. J. Med. 2008, 359, 906-917
-
(2008)
N. Engl. J. Med
, vol.359
, pp. 906-917
-
-
San Miguel, J.F.1
Schlag, R.2
Khuageva, N.K.3
Dimopoulos, M.A.4
Shpilberg, O.5
Kropff, M.6
Spicka, I.7
Petrucci, M.T.8
Palumbo, A.9
Samoilova, O.S.10
Dmoszynska, A.11
Abdulkadyrov, K.M.12
Schots, R.13
Jiang, B.14
Mateos, M.V.15
Anderson, K.C.16
Esseltine, D.L.17
Liu, K.18
Cakana, A.19
van de Velde, H.20
Richardson, P.G.21
more..
-
114
-
-
77952310929
-
Bortezomib plus melphalan and prednisone compared with melphalan and prednisone in previously untreated multiple myeloma: Updated follow-up and impact of subsequent therapy in the phase III VISTA trial
-
Mateos, M. V.; Richardson, P. G.; Schlag, R.; Khuageva, N. K.; Dimopoulos, M. A.; Shpilberg, O.; Kropff, M.; Spicka, I.; Petrucci, M. T.; Palumbo, A.; Samoilova, O. S.; Dmoszynska, A.; Abdulkadyrov, K. M.; Schots, R.; Jiang, B.; Esseltine, D. L.; Liu, K.; Cakana, A.; van de Velde, H.; San Miguel, J. F. Bortezomib plus melphalan and prednisone compared with melphalan and prednisone in previously untreated multiple myeloma: updated follow-up and impact of subsequent therapy in the phase III VISTA trial. J. Clin. Oncol. 2010, 28, 2259-2266
-
(2010)
J. Clin. Oncol
, vol.28
, pp. 2259-2266
-
-
Mateos, M.V.1
Richardson, P.G.2
Schlag, R.3
Khuageva, N.K.4
Dimopoulos, M.A.5
Shpilberg, O.6
Kropff, M.7
Spicka, I.8
Petrucci, M.T.9
Palumbo, A.10
Samoilova, O.S.11
Dmoszynska, A.12
Abdulkadyrov, K.M.13
Schots, R.14
Jiang, B.15
Esseltine, D.L.16
Liu, K.17
Cakana, A.18
van de Velde, H.19
San Miguel, J.F.20
more..
-
116
-
-
70449674487
-
Increased proteasome subunit protein expression and proteasome activity in colon cancer relate to an enhanced activation of nuclear factor E2-related factor 2 (Nrf2)
-
Arlt, A.; Bauer, I.; Schafmayer, C.; Tepel, J.; Muerkoster, S. S.; Brosch, M.; Roder, C.; Kalthoff, H.; Hampe, J.; Moyer, M. P.; Folsch, U. R.; Schafer, H. Increased proteasome subunit protein expression and proteasome activity in colon cancer relate to an enhanced activation of nuclear factor E2-related factor 2 (Nrf2). Oncogene 2009, 28, 3983-3996
-
(2009)
Oncogene
, vol.28
, pp. 3983-3996
-
-
Arlt, A.1
Bauer, I.2
Schafmayer, C.3
Tepel, J.4
Muerkoster, S.S.5
Brosch, M.6
Roder, C.7
Kalthoff, H.8
Hampe, J.9
Moyer, M.P.10
Folsch, U.R.11
Schafer, H.12
-
117
-
-
66649101365
-
Proteasome enzymatic activities in plasma as risk stratification of patients with acute myeloid leukemia and advanced-stage myelodysplastic syndrome
-
Ma, W.; Kantarjian, H.; Bekele, B.; Donahue, A. C.; Zhang, X.; Zhang, Z. J.; O'Brien, S.; Estey, E.; Estrov, Z.; Cortes, J.; Keating, M.; Giles, F.; Albitar, M. Proteasome enzymatic activities in plasma as risk stratification of patients with acute myeloid leukemia and advanced-stage myelodysplastic syndrome. Clin. Cancer Res. 2009, 15, 3820-3826
-
(2009)
Clin. Cancer Res
, vol.15
, pp. 3820-3826
-
-
Ma, W.1
Kantarjian, H.2
Bekele, B.3
Donahue, A.C.4
Zhang, X.5
Zhang, Z.J.6
O'Brien, S.7
Estey, E.8
Estrov, Z.9
Cortes, J.10
Keating, M.11
Giles, F.12
Albitar, M.13
-
118
-
-
33645731530
-
Ubiquitin-proteasome system stress sensitizes ovarian cancer to proteasome inhibitor-induced apoptosis
-
Bazzaro, M.; Lee, M. K.; Zoso, A.; Stirling, W. L.; Santillan, A.; Shih Ie, M.; Roden, R. B. Ubiquitin-proteasome system stress sensitizes ovarian cancer to proteasome inhibitor-induced apoptosis. Cancer Res. 2006, 66, 3754-3763
-
(2006)
Cancer Res
, vol.66
, pp. 3754-3763
-
-
Bazzaro, M.1
Lee, M.K.2
Zoso, A.3
Stirling, W.L.4
Santillan, A.5
Shih Ie, M.6
Roden, R.B.7
-
119
-
-
33751285781
-
Disulfiram, a clinically used anti-alcoholism drug and copper-binding agent, induces apoptotic cell death in breast cancer cultures and xenografts via inhibition of the proteasome activity
-
Chen, D.; Cui, Q. C.; Yang, H.; Dou, Q. P. Disulfiram, a clinically used anti-alcoholism drug and copper-binding agent, induces apoptotic cell death in breast cancer cultures and xenografts via inhibition of the proteasome activity. Cancer Res. 2006, 66, 10425-10433
-
(2006)
Cancer Res
, vol.66
, pp. 10425-10433
-
-
Chen, D.1
Cui, Q.C.2
Yang, H.3
Dou, Q.P.4
-
120
-
-
18044383342
-
Dietary flavonoids as proteasome inhibitors and apoptosis inducers in human leukemia cells
-
Chen, D.; Daniel, K. G.; Chen, M. S.; Kuhn, D. J.; Landis-Piwowar, K. R.; Dou, Q. P. Dietary flavonoids as proteasome inhibitors and apoptosis inducers in human leukemia cells. Biochem. Pharmacol. 2005, 69, 1421-1432
-
(2005)
Biochem. Pharmacol
, vol.69
, pp. 1421-1432
-
-
Chen, D.1
Daniel, K.G.2
Chen, M.S.3
Kuhn, D.J.4
Landis-Piwowar, K.R.5
Dou, Q.P.6
-
121
-
-
1442355024
-
Activity-based ubiquitin-specific protease (USP) profiling of virus-infected and malignant human cells
-
Ovaa, H.; Kessler, B. M.; Rolen, U.; Galardy, P. J.; Ploegh, H. L.; Masucci, M. G. Activity-based ubiquitin-specific protease (USP) profiling of virus-infected and malignant human cells. Proc. Natl. Acad. Sci. U. S. A. 2004, 101, 2253-2258
-
(2004)
Proc. Natl. Acad. Sci. U. S. A
, vol.101
, pp. 2253-2258
-
-
Ovaa, H.1
Kessler, B.M.2
Rolen, U.3
Galardy, P.J.4
Ploegh, H.L.5
Masucci, M.G.6
-
122
-
-
0035000515
-
The apoptogenic response of human myeloid leukaemia cell lines and of normal and malignant haematopoietic progenitor cells to the proteasome inhibitor PSI
-
Soligo, D.; Servida, F.; Delia, D.; Fontanella, E.; Lamorte, G.; Caneva, L.; Fumiatti, R.; Lambertenghi Deliliers, G. The apoptogenic response of human myeloid leukaemia cell lines and of normal and malignant haematopoietic progenitor cells to the proteasome inhibitor PSI. Br. J. Haematol. 2001, 113, 126-135
-
(2001)
Br. J. Haematol
, vol.113
, pp. 126-135
-
-
Soligo, D.1
Servida, F.2
Delia, D.3
Fontanella, E.4
Lamorte, G.5
Caneva, L.6
Fumiatti, R.7
Lambertenghi Deliliers, G.8
-
123
-
-
0000612742
-
Multiple Myeloma: New Insights and Therapeutic Approaches
-
Anderson, K. C.; Kyle, R. A.; Dalton, W. S.; Landowski, T.; Shain, K.; Jove, R.; Hazlehurst, L.; Berenson, J. Multiple Myeloma: New Insights and Therapeutic Approaches. Hematology Am. Soc. Hematol. Educ. Program 2000, 147-165
-
(2000)
Hematology Am. Soc. Hematol. Educ. Program
, pp. 147-165
-
-
Anderson, K.C.1
Kyle, R.A.2
Dalton, W.S.3
Landowski, T.4
Shain, K.5
Jove, R.6
Hazlehurst, L.7
Berenson, J.8
-
124
-
-
0142054051
-
Bortezomib (PS-341): A novel, first-in-class proteasome inhibitor for the treatment of multiple myeloma and other cancers
-
Richardson, P. G.; Hideshima, T.; Anderson, K. C. Bortezomib (PS-341): a novel, first-in-class proteasome inhibitor for the treatment of multiple myeloma and other cancers. Cancer Control 2003, 10, 361-369
-
(2003)
Cancer Control
, vol.10
, pp. 361-369
-
-
Richardson, P.G.1
Hideshima, T.2
Anderson, K.C.3
-
125
-
-
33847610748
-
The proteasome as a potential target for novel anticancer drugs and chemosensitizers
-
Landis-Piwowar, K. R.; Milacic, V.; Chen, D.; Yang, H.; Zhao, Y.; Chan, T. H.; Yan, B.; Dou, Q. P. The proteasome as a potential target for novel anticancer drugs and chemosensitizers. Drug Resist. Updat. 2006, 9, 263-273
-
(2006)
Drug Resist. Updat
, vol.9
, pp. 263-273
-
-
Landis-Piwowar, K.R.1
Milacic, V.2
Chen, D.3
Yang, H.4
Zhao, Y.5
Chan, T.H.6
Yan, B.7
Dou, Q.P.8
-
126
-
-
77950300115
-
Proteasome inhibitor bortezomib increases radiation sensitivity in androgen independent human prostate cancer cells
-
Goktas, S.; Baran, Y.; Ural, A. U.; Yazici, S.; Aydur, E.; Basal, S.; Avcu, F.; Pekel, A.; Dirican, B.; Beyzadeoglu, M. Proteasome inhibitor bortezomib increases radiation sensitivity in androgen independent human prostate cancer cells. Urology 2010, 75, 793-798
-
(2010)
Urology
, vol.75
, pp. 793-798
-
-
Goktas, S.1
Baran, Y.2
Ural, A.U.3
Yazici, S.4
Aydur, E.5
Basal, S.6
Avcu, F.7
Pekel, A.8
Dirican, B.9
Beyzadeoglu, M.10
-
127
-
-
0034788065
-
Molecular pathways that modify tumor radiation response
-
Pervan, M.; Pajonk, F.; Sun, J. R.; Withers, H. R.; McBride, W. H. Molecular pathways that modify tumor radiation response. Am. J. Clin. Oncol. 2001, 24, 481-485
-
(2001)
Am. J. Clin. Oncol
, vol.24
, pp. 481-485
-
-
Pervan, M.1
Pajonk, F.2
Sun, J.R.3
Withers, H.R.4
McBride, W.H.5
-
128
-
-
66149146607
-
Bortezomib: A review of its use in patients with multiple myeloma
-
Curran, M. P.; McKeage, K. Bortezomib: a review of its use in patients with multiple myeloma. Drugs 2009, 69, 859-888
-
(2009)
Drugs
, vol.69
, pp. 859-888
-
-
Curran, M.P.1
McKeage, K.2
-
129
-
-
2542523228
-
Synergistic induction of oxidative injury and apoptosis in human multiple myeloma cells by the proteasome inhibitor bortezomib and histone deacetylase inhibitors
-
Pei, X. Y.; Dai, Y.; Grant, S. Synergistic induction of oxidative injury and apoptosis in human multiple myeloma cells by the proteasome inhibitor bortezomib and histone deacetylase inhibitors. Clin. Cancer Res. 2004, 10, 3839-3852
-
(2004)
Clin. Cancer Res
, vol.10
, pp. 3839-3852
-
-
Pei, X.Y.1
Dai, Y.2
Grant, S.3
-
130
-
-
18144431710
-
Mitochondrial-mediated disregulation of Ca2+ is a critical determinant of Velcade (PS-341/bortezomib) cytotoxicity in myeloma cell lines
-
Landowski, T. H.; Megli, C. J.; Nullmeyer, K. D.; Lynch, R. M.; Dorr, R. T. Mitochondrial-mediated disregulation of Ca2+ is a critical determinant of Velcade (PS-341/bortezomib) cytotoxicity in myeloma cell lines. Cancer Res. 2005, 65, 3828-3836
-
(2005)
Cancer Res
, vol.65
, pp. 3828-3836
-
-
Landowski, T.H.1
Megli, C.J.2
Nullmeyer, K.D.3
Lynch, R.M.4
Dorr, R.T.5
-
131
-
-
20044396543
-
Phase II study of proteasome inhibitor bortezomib in relapsed or refractory B-cell non-Hodgkin's lymphoma
-
Goy, A.; Younes, A.; McLaughlin, P.; Pro, B.; Romaguera, J. E.; Hagemeister, F.; Fayad, L.; Dang, N. H.; Samaniego, F.; Wang, M.; Broglio, K.; Samuels, B.; Gilles, F.; Sarris, A. H.; Hart, S.; Trehu, E.; Schenkein, D.; Cabanillas, F.; Rodriguez, A. M. Phase II study of proteasome inhibitor bortezomib in relapsed or refractory B-cell non-Hodgkin's lymphoma. J. Clin. Oncol. 2005, 23, 667-675
-
(2005)
J. Clin. Oncol
, vol.23
, pp. 667-675
-
-
Goy, A.1
Younes, A.2
McLaughlin, P.3
Pro, B.4
Romaguera, J.E.5
Hagemeister, F.6
Fayad, L.7
Dang, N.H.8
Samaniego, F.9
Wang, M.10
Broglio, K.11
Samuels, B.12
Gilles, F.13
Sarris, A.H.14
Hart, S.15
Trehu, E.16
Schenkein, D.17
Cabanillas, F.18
Rodriguez, A.M.19
Phase, I.I.20
more..
-
132
-
-
52049086674
-
Overexpression of the PSMB5 gene contributes to bortezomib resistance in T-lymphoblastic lymphoma/leukemia cells derived from Jurkat line
-
Lu, S.; Chen, Z.; Yang, J.; Chen, L.; Gong, S.; Zhou, H.; Guo, L.; Wang, J. Overexpression of the PSMB5 gene contributes to bortezomib resistance in T-lymphoblastic lymphoma/leukemia cells derived from Jurkat line. Exp. Hematol. 2008, 36, 1278-1284
-
(2008)
Exp. Hematol
, vol.36
, pp. 1278-1284
-
-
Lu, S.1
Chen, Z.2
Yang, J.3
Chen, L.4
Gong, S.5
Zhou, H.6
Guo, L.7
Wang, J.8
-
133
-
-
67049107847
-
Different mutants of PSMB5 confer varying bortezomib resistance in T lymphoblastic lymphoma/leukemia cells derived from the Jurkat cell line
-
Lu, S.; Yang, J.; Chen, Z.; Gong, S.; Zhou, H.; Xu, X.; Wang, J. Different mutants of PSMB5 confer varying bortezomib resistance in T lymphoblastic lymphoma/leukemia cells derived from the Jurkat cell line. Exp. Hematol. 2009, 37, 831-837
-
(2009)
Exp. Hematol
, vol.37
, pp. 831-837
-
-
Lu, S.1
Yang, J.2
Chen, Z.3
Gong, S.4
Zhou, H.5
Xu, X.6
Wang, J.7
-
134
-
-
47949089799
-
Point mutation of the proteasome beta5 subunit gene is an important mechanism of bortezomib resistance in bortezomib-selected variants of Jurkat T cell lymphoblastic lymphoma/leukemia line
-
Lu, S.; Yang, J.; Song, X.; Gong, S.; Zhou, H.; Guo, L.; Song, N.; Bao, X.; Chen, P.; Wang, J. Point mutation of the proteasome beta5 subunit gene is an important mechanism of bortezomib resistance in bortezomib-selected variants of Jurkat T cell lymphoblastic lymphoma/leukemia line. J. Pharmacol. Exp. Ther. 2008, 326, 423-431
-
(2008)
J. Pharmacol. Exp. Ther
, vol.326
, pp. 423-431
-
-
Lu, S.1
Yang, J.2
Song, X.3
Gong, S.4
Zhou, H.5
Guo, L.6
Song, N.7
Bao, X.8
Chen, P.9
Wang, J.10
-
135
-
-
53049106912
-
Molecular basis of bortezomib resistance: Proteasome subunit beta5 (PSMB5) gene mutation and overexpression of PSMB5 protein
-
Oerlemans, R.; Franke, N. E.; Assaraf, Y. G.; Cloos, J.; van Zantwijk, I.; Berkers, C. R.; Scheffer, G. L.; Debipersad, K.; Vojtekova, K.; Lemos, C.; van der Heijden, J. W.; Ylstra, B.; Peters, G. J.; Kaspers, G. L.; Dijkmans, B. A.; Scheper, R. J.; Jansen, G. Molecular basis of bortezomib resistance: proteasome subunit beta5 (PSMB5) gene mutation and overexpression of PSMB5 protein. Blood 2008, 112, 2489-2499
-
(2008)
Blood
, vol.112
, pp. 2489-2499
-
-
Oerlemans, R.1
Franke, N.E.2
Assaraf, Y.G.3
Cloos, J.4
van Zantwijk, I.5
Berkers, C.R.6
Scheffer, G.L.7
Debipersad, K.8
Vojtekova, K.9
Lemos, C.10
van der Heijden, J.W.11
Ylstra, B.12
Peters, G.J.13
Kaspers, G.L.14
Dijkmans, B.A.15
Scheper, R.J.16
Jansen, G.17
-
136
-
-
66949155833
-
Green tea polyphenols block the anticancer effects of bortezomib and other boronic acid-based proteasome inhibitors
-
Golden, E. B.; Lam, P. Y.; Kardosh, A.; Gaffney, K. J.; Cadenas, E.; Louie, S. G.; Petasis, N. A.; Chen, T. C.; Schonthal, A. H. Green tea polyphenols block the anticancer effects of bortezomib and other boronic acid-based proteasome inhibitors. Blood 2009, 113, 5927-5937
-
(2009)
Blood
, vol.113
, pp. 5927-5937
-
-
Golden, E.B.1
Lam, P.Y.2
Kardosh, A.3
Gaffney, K.J.4
Cadenas, E.5
Louie, S.G.6
Petasis, N.A.7
Chen, T.C.8
Schonthal, A.H.9
-
137
-
-
67650475322
-
Natural polyphenols antagonize the antimyeloma activity of proteasome inhibitor bortezomib by direct chemical interaction
-
Kim, T. Y.; Park, J.; Oh, B.; Min, H. J.; Jeong, T. S.; Lee, J. H.; Suh, C.; Cheong, J. W.; Kim, H. J.; Yoon, S. S.; Park, S. B.; Lee, D. S. Natural polyphenols antagonize the antimyeloma activity of proteasome inhibitor bortezomib by direct chemical interaction. Br. J. Haematol. 2009, 146, 270-281
-
(2009)
Br. J. Haematol
, vol.146
, pp. 270-281
-
-
Kim, T.Y.1
Park, J.2
Oh, B.3
Min, H.J.4
Jeong, T.S.5
Lee, J.H.6
Suh, C.7
Cheong, J.W.8
Kim, H.J.9
Yoon, S.S.10
Park, S.B.11
Lee, D.S.12
-
138
-
-
55749090958
-
Dietary flavonoids inhibit the anticancer effects of the proteasome inhibitor bortezomib
-
Liu, F. T.; Agrawal, S. G.; Movasaghi, Z.; Wyatt, P. B.; Rehman, I. U.; Gribben, J. G.; Newland, A. C.; Jia, L. Dietary flavonoids inhibit the anticancer effects of the proteasome inhibitor bortezomib. Blood 2008, 112, 3835-3846
-
(2008)
Blood
, vol.112
, pp. 3835-3846
-
-
Liu, F.T.1
Agrawal, S.G.2
Movasaghi, Z.3
Wyatt, P.B.4
Rehman, I.U.5
Gribben, J.G.6
Newland, A.C.7
Jia, L.8
-
139
-
-
4644248931
-
Phase II study of the proteasome inhibitor bortezomib (PS-341) in patients with metastatic neuroendocrine tumors
-
Shah, M. H.; Young, D.; Kindler, H. L.; Webb, I.; Kleiber, B.; Wright, J.; Grever, M. Phase II study of the proteasome inhibitor bortezomib (PS-341) in patients with metastatic neuroendocrine tumors. Clin. Cancer Res. 2004, 10, 6111-6118
-
(2004)
Clin. Cancer Res
, vol.10
, pp. 6111-6118
-
-
Shah, M.H.1
Young, D.2
Kindler, H.L.3
Webb, I.4
Kleiber, B.5
Wright, J.6
Grever, M.7
-
140
-
-
67650462779
-
Clinical development of novel proteasome inhibitors for cancer treatment
-
Yang, H.; Zonder, J. A.; Dou, Q. P. Clinical development of novel proteasome inhibitors for cancer treatment. Expert Opin. Investig. Drugs 2009, 18, 957-971
-
(2009)
Expert Opin. Investig. Drugs
, vol.18
, pp. 957-971
-
-
Yang, H.1
Zonder, J.A.2
Dou, Q.P.3
-
141
-
-
34548539381
-
Randomized phase III study of pegylated liposomal doxorubicin plus bortezomib compared with bortezomib alone in relapsed or refractory multiple myeloma: Combination therapy improves time to progression
-
Orlowski, R. Z.; Nagler, A.; Sonneveld, P.; Blade, J.; Hajek, R.; Spencer, A.; San Miguel, J.; Robak, T.; Dmoszynska, A.; Horvath, N.; Spicka, I.; Sutherland, H. J.; Suvorov, A. N.; Zhuang, S. H.; Parekh, T.; Xiu, L.; Yuan, Z.; Rackoff, W.; Harousseau, J. L. Randomized phase III study of pegylated liposomal doxorubicin plus bortezomib compared with bortezomib alone in relapsed or refractory multiple myeloma: combination therapy improves time to progression. J. Clin. Oncol. 2007, 25, 3892-3901
-
(2007)
J. Clin. Oncol
, vol.25
, pp. 3892-3901
-
-
Orlowski, R.Z.1
Nagler, A.2
Sonneveld, P.3
Blade, J.4
Hajek, R.5
Spencer, A.6
San Miguel, J.7
Robak, T.8
Dmoszynska, A.9
Horvath, N.10
Spicka, I.11
Sutherland, H.J.12
Suvorov, A.N.13
Zhuang, S.H.14
Parekh, T.15
Xiu, L.16
Yuan, Z.17
Rackoff, W.18
Harousseau, J.L.19
-
142
-
-
60649085451
-
Bortezomib, low-dose intravenous melphalan, and dexamethasone for patients with relapsed multiple myeloma
-
Popat, R.; Oakervee, H.; Williams, C.; Cook, M.; Craddock, C.; Basu, S.; Singer, C.; Harding, S.; Foot, N.; Hallam, S.; Odeh, L.; Joel, S.; Cavenagh, J. Bortezomib, low-dose intravenous melphalan, and dexamethasone for patients with relapsed multiple myeloma. Br. J. Haematol. 2009, 144, 887-894
-
(2009)
Br. J. Haematol
, vol.144
, pp. 887-894
-
-
Popat, R.1
Oakervee, H.2
Williams, C.3
Cook, M.4
Craddock, C.5
Basu, S.6
Singer, C.7
Harding, S.8
Foot, N.9
Hallam, S.10
Odeh, L.11
Joel, S.12
Cavenagh, J.13
-
143
-
-
54249122860
-
Phase I-II trial of bortezomib plus oral cyclophosphamide and prednisone in relapsed and refractory multiple myeloma
-
Reece, D. E.; Rodriguez, G. P.; Chen, C.; Trudel, S.; Kukreti, V.; Mikhael, J.; Pantoja, M.; Xu, W.; Stewart, A. K. Phase I-II trial of bortezomib plus oral cyclophosphamide and prednisone in relapsed and refractory multiple myeloma. J. Clin. Oncol. 2008, 26, 4777-4783
-
(2008)
J. Clin. Oncol
, vol.26
, pp. 4777-4783
-
-
Reece, D.E.1
Rodriguez, G.P.2
Chen, C.3
Trudel, S.4
Kukreti, V.5
Mikhael, J.6
Pantoja, M.7
Xu, W.8
Stewart, A.K.9
-
144
-
-
57849161431
-
The combination of bortezomib, melphalan, dexamethasone and intermittent thalidomide is an effective regimen for relapsed/refractory myeloma and is associated with improvement of abnormal bone metabolism and angiogenesis
-
Terpos, E.; Kastritis, E.; Roussou, M.; Heath, D.; Christoulas, D.; Anagnostopoulos, N.; Eleftherakis-Papaiakovou, E.; Tsionos, K.; Croucher, P.; Dimopoulos, M. A. The combination of bortezomib, melphalan, dexamethasone and intermittent thalidomide is an effective regimen for relapsed/refractory myeloma and is associated with improvement of abnormal bone metabolism and angiogenesis. Leukemia 2008, 22, 2247-2256
-
(2008)
Leukemia
, vol.22
, pp. 2247-2256
-
-
Terpos, E.1
Kastritis, E.2
Roussou, M.3
Heath, D.4
Christoulas, D.5
Anagnostopoulos, N.6
Eleftherakis-Papaiakovou, E.7
Tsionos, K.8
Croucher, P.9
Dimopoulos, M.A.10
-
145
-
-
34250194653
-
A phase I/II study of arsenic trioxide/bortezomib/ ascorbic acid combination therapy for the treatment of relapsed or refractory multiple myeloma
-
Berenson, J. R.; Matous, J.; Swift, R. A.; Mapes, R.; Morrison, B.; Yeh, H. S. A phase I/II study of arsenic trioxide/bortezomib/ ascorbic acid combination therapy for the treatment of relapsed or refractory multiple myeloma. Clin. Cancer Res. 2007, 13, 1762-1768
-
(2007)
Clin. Cancer Res
, vol.13
, pp. 1762-1768
-
-
Berenson, J.R.1
Matous, J.2
Swift, R.A.3
Mapes, R.4
Morrison, B.5
Yeh, H.S.6
-
146
-
-
33750945704
-
Randomized phase II study of bortezomib alone and bortezomib in combination with docetaxel in previously treated advanced non-small-cell lung cancer
-
Fanucchi, M. P.; Fossella, F. V.; Belt, R.; Natale, R.; Fidias, P.; Carbone, D. P.; Govindan, R.; Raez, L. E.; Robert, F.; Ribeiro, M.; Akerley, W.; Kelly, K.; Limentani, S. A.; Crawford, J.; Reimers, H. J.; Axelrod, R.; Kashala, O.; Sheng, S.; Schiller, J. H. Randomized phase II study of bortezomib alone and bortezomib in combination with docetaxel in previously treated advanced non-small-cell lung cancer. J. Clin. Oncol. 2006, 24, 5025-5033
-
(2006)
J. Clin. Oncol
, vol.24
, pp. 5025-5033
-
-
Fanucchi, M.P.1
Fossella, F.V.2
Belt, R.3
Natale, R.4
Fidias, P.5
Carbone, D.P.6
Govindan, R.7
Raez, L.E.8
Robert, F.9
Ribeiro, M.10
Akerley, W.11
Kelly, K.12
Limentani, S.A.13
Crawford, J.14
Reimers, H.J.15
Axelrod, R.16
Kashala, O.17
Sheng, S.18
Schiller, J.H.19
-
147
-
-
78049428148
-
Marine antitumor drugs: Status, shortfalls and strategies
-
Bhatnagar, I.; Kim, S. K. Marine antitumor drugs: status, shortfalls and strategies. Mar. Drugs 2010, 8, 2702-2720
-
(2010)
Mar. Drugs
, vol.8
, pp. 2702-2720
-
-
Bhatnagar, I.1
Kim, S.K.2
-
148
-
-
33750209537
-
A novel proteasome inhibitor NPI-0052 as an anticancer therapy
-
Chauhan, D.; Hideshima, T.; Anderson, K. C. A novel proteasome inhibitor NPI-0052 as an anticancer therapy. Br. J. Cancer 2006, 95, 961-965
-
(2006)
Br. J. Cancer
, vol.95
, pp. 961-965
-
-
Chauhan, D.1
Hideshima, T.2
Anderson, K.C.3
-
149
-
-
84864322479
-
Tea polyphenols, their biological effects and potential molecular targets
-
Chen, D.; Milacic, V.; Chen, M. S.; Wan, S. B.; Lam, W. H.; Huo, C.; Landis-Piwowar, K. R.; Cui, Q. C.; Wali, A.; Chan, T. H.; Dou, Q. P. Tea polyphenols, their biological effects and potential molecular targets. Histol. Histopathol. 2008, 23, 487-496
-
(2008)
Histol. Histopathol
, vol.23
, pp. 487-496
-
-
Chen, D.1
Milacic, V.2
Chen, M.S.3
Wan, S.B.4
Lam, W.H.5
Huo, C.6
Landis-Piwowar, K.R.7
Cui, Q.C.8
Wali, A.9
Chan, T.H.10
Dou, Q.P.11
-
150
-
-
0035918278
-
Ester bond-containing tea polyphenols potently inhibit proteasome activity in vitro and in vivo
-
Nam, S.; Smith, D. M.; Dou, Q. P. Ester bond-containing tea polyphenols potently inhibit proteasome activity in vitro and in vivo. J. Biol. Chem. 2001, 276, 13322-13330
-
(2001)
J. Biol. Chem
, vol.276
, pp. 13322-13330
-
-
Nam, S.1
Smith, D.M.2
Dou, Q.P.3
-
151
-
-
0042261670
-
Inhibition of the proteasome activity, a novel mechanism associated with the tumor cell apoptosis-inducing ability of genistein
-
Kazi, A.; Daniel, K. G.; Smith, D. M.; Kumar, N. B.; Dou, Q. P. Inhibition of the proteasome activity, a novel mechanism associated with the tumor cell apoptosis-inducing ability of genistein. Biochem. Pharmacol. 2003, 66, 965-976
-
(2003)
Biochem. Pharmacol
, vol.66
, pp. 965-976
-
-
Kazi, A.1
Daniel, K.G.2
Smith, D.M.3
Kumar, N.B.4
Dou, Q.P.5
-
152
-
-
1642564603
-
Inhibition of proteasomal function by curcumin induces apoptosis through mitochondrial pathway
-
Jana, N. R.; Dikshit, P.; Goswami, A.; Nukina, N. Inhibition of proteasomal function by curcumin induces apoptosis through mitochondrial pathway. J. Biol. Chem. 2004, 279, 11680-11685
-
(2004)
J. Biol. Chem
, vol.279
, pp. 11680-11685
-
-
Jana, N.R.1
Dikshit, P.2
Goswami, A.3
Nukina, N.4
-
153
-
-
54749132655
-
Curcumin inhibits the proteasome activity in human colon cancer cells in vitro and in vivo
-
Milacic, V.; Banerjee, S.; Landis-Piwowar, K. R.; Sarkar, F. H.; Majumdar, A. P.; Dou, Q. P. Curcumin inhibits the proteasome activity in human colon cancer cells in vitro and in vivo. Cancer Res. 2008, 68, 7283-7292
-
(2008)
Cancer Res
, vol.68
, pp. 7283-7292
-
-
Milacic, V.1
Banerjee, S.2
Landis-Piwowar, K.R.3
Sarkar, F.H.4
Majumdar, A.P.5
Dou, Q.P.6
-
154
-
-
40349111004
-
Inhibition of proteasome activity by the dietary flavonoid apigenin is associated with growth inhibition in cultured breast cancer cells and xenografts
-
Chen, D.; Landis-Piwowar, K. R.; Chen, M. S.; Dou, Q. P. Inhibition of proteasome activity by the dietary flavonoid apigenin is associated with growth inhibition in cultured breast cancer cells and xenografts. Breast Cancer Res. 2007, 9, R80
-
(2007)
Breast Cancer Res
, vol.9
-
-
Chen, D.1
Landis-Piwowar, K.R.2
Chen, M.S.3
Dou, Q.P.4
-
155
-
-
77951745289
-
Gemcitabine sensitivity can be induced in pancreatic cancer cells through modulation of miR-200 and miR-21 expression by curcumin or its analogue CDF
-
Ali, S.; Ahmad, A.; Banerjee, S.; Padhye, S.; Dominiak, K.; Schaffert, J. M.; Wang, Z.; Philip, P. A.; Sarkar, F. H. Gemcitabine sensitivity can be induced in pancreatic cancer cells through modulation of miR-200 and miR-21 expression by curcumin or its analogue CDF. Cancer Res. 2010, 70, 3606-3617
-
(2010)
Cancer Res
, vol.70
, pp. 3606-3617
-
-
Ali, S.1
Ahmad, A.2
Banerjee, S.3
Padhye, S.4
Dominiak, K.5
Schaffert, J.M.6
Wang, Z.7
Philip, P.A.8
Sarkar, F.H.9
-
156
-
-
34249299083
-
A novel prodrug of the green tea polyphenol (-)-epigallocatechin-3-gallate as a potential anticancer agent
-
Landis-Piwowar, K. R.; Huo, C.; Chen, D.; Milacic, V.; Shi, G.; Chan, T. H.; Dou, Q. P. A novel prodrug of the green tea polyphenol (-)-epigallocatechin-3-gallate as a potential anticancer agent. Cancer Res. 2007, 67, 4303-4310
-
(2007)
Cancer Res
, vol.67
, pp. 4303-4310
-
-
Landis-Piwowar, K.R.1
Huo, C.2
Chen, D.3
Milacic, V.4
Shi, G.5
Chan, T.H.6
Dou, Q.P.7
-
157
-
-
70350217623
-
Fluorocurcumins as cyclooxygenase-2 inhibitor: Molecular docking, pharmacokinetics and tissue distribution in mice. Pharm
-
Padhye, S.; Banerjee, S.; Chavan, D.; Pandye, S.; Swamy, K. V.; Ali, S.; Li, J.; Dou, Q. P.; Sarkar, F. H. Fluorocurcumins as cyclooxygenase-2 inhibitor: molecular docking, pharmacokinetics and tissue distribution in mice. Pharm. Res. 2009, 26, 2438-2445
-
(2009)
Res
, vol.26
, pp. 2438-2445
-
-
Padhye, S.1
Banerjee, S.2
Chavan, D.3
Pandye, S.4
Swamy, K.V.5
Ali, S.6
Li, J.7
Dou, Q.P.8
Sarkar, F.H.9
-
158
-
-
67650032601
-
New difluoro Knoevenagel condensates of curcumin, their Schiff bases and copper complexes as proteasome inhibitors and apoptosis inducers in cancer cells
-
Padhye, S.; Yang, H.; Jamadar, A.; Cui, Q. C.; Chavan, D.; Dominiak, K.; McKinney, J.; Banerjee, S.; Dou, Q. P.; Sarkar, F. H. New difluoro Knoevenagel condensates of curcumin, their Schiff bases and copper complexes as proteasome inhibitors and apoptosis inducers in cancer cells. Pharm. Res. 2009, 26, 1874-1880
-
(2009)
Pharm. Res
, vol.26
, pp. 1874-1880
-
-
Padhye, S.1
Yang, H.2
Jamadar, A.3
Cui, Q.C.4
Chavan, D.5
Dominiak, K.6
McKinney, J.7
Banerjee, S.8
Dou, Q.P.9
Sarkar, F.H.10
-
159
-
-
77951239011
-
Antitumor activity of novel fluoro-substituted (-)-epigallocatechin-3-gallate analogs
-
Yang, H.; Sun, D. K.; Chen, D.; Cui, Q. C.; Gu, Y. Y.; Jiang, T.; Chen, W.; Wan, S. B.; Dou, Q. P. Antitumor activity of novel fluoro-substituted (-)-epigallocatechin-3-gallate analogs. Cancer Lett. 2010, 292, 48-53
-
(2010)
Cancer Lett
, vol.292
, pp. 48-53
-
-
Yang, H.1
Sun, D.K.2
Chen, D.3
Cui, Q.C.4
Gu, Y.Y.5
Jiang, T.6
Chen, W.7
Wan, S.B.8
Dou, Q.P.9
-
160
-
-
0036968468
-
Cell cycle regulatory E3 ubiquitin ligases as anticancer targets
-
Pray, T. R.; Parlati, F.; Huang, J.; Wong, B. R.; Payan, D. G.; Bennett, M. K.; Issakani, S. D.; Molineaux, S.; Demo, S. D. Cell cycle regulatory E3 ubiquitin ligases as anticancer targets. Drug Resist. Updat. 2002, 5, 249-258
-
(2002)
Drug Resist. Updat
, vol.5
, pp. 249-258
-
-
Pray, T.R.1
Parlati, F.2
Huang, J.3
Wong, B.R.4
Payan, D.G.5
Bennett, M.K.6
Issakani, S.D.7
Molineaux, S.8
Demo, S.D.9
-
161
-
-
76049102305
-
Validation of SAG/RBX2/ROC2 E3 ubiquitin ligase as an anticancer and radiosensitizing target
-
Jia, L.; Yang, J.; Hao, X.; Zheng, M.; He, H.; Xiong, X.; Xu, L.; Sun, Y. Validation of SAG/RBX2/ROC2 E3 ubiquitin ligase as an anticancer and radiosensitizing target. Clin. Cancer Res. 2010, 16, 814-824
-
(2010)
Clin. Cancer Res
, vol.16
, pp. 814-824
-
-
Jia, L.1
Yang, J.2
Hao, X.3
Zheng, M.4
He, H.5
Xiong, X.6
Xu, L.7
Sun, Y.8
-
162
-
-
0031583962
-
Oncoprotein MDM2 is a ubiquitin ligase E3 for tumor suppressor p53
-
Honda, R.; Tanaka, H.; Yasuda, H. Oncoprotein MDM2 is a ubiquitin ligase E3 for tumor suppressor p53. FEBS Lett. 1997, 420, 25-27
-
(1997)
FEBS Lett
, vol.420
, pp. 25-27
-
-
Honda, R.1
Tanaka, H.2
Yasuda, H.3
-
163
-
-
64749098830
-
An inhibitor of NEDD8- activating enzyme as a new approach to treat cancer
-
Soucy, T. A.; Smith, P. G.; Milhollen, M. A.; Berger, A. J.; Gavin, J. M.; Adhikari, S.; Brownell, J. E.; Burke, K. E.; Cardin, D. P.; Critchley, S.; Cullis, C. A.; Doucette, A.; Garnsey, J. J.; Gaulin, J. L.; Gershman, R. E.; Lublinsky, A. R.; McDonald, A.; Mizutani, H.; Narayanan, U.; Olhava, E. J.; Peluso, S.; Rezaei, M.; Sintchak, M. D.; Talreja, T.; Thomas, M. P.; Traore, T.; Vyskocil, S.; Weatherhead, G. S.; Yu, J.; Zhang, J.; Dick, L. R.; Claiborne, C. F.; Rolfe, M.; Bolen, J. B.; Langston, S. P. An inhibitor of NEDD8- activating enzyme as a new approach to treat cancer. Nature 2009, 458, 732-736
-
(2009)
Nature
, vol.458
, pp. 732-736
-
-
Soucy, T.A.1
Smith, P.G.2
Milhollen, M.A.3
Berger, A.J.4
Gavin, J.M.5
Adhikari, S.6
Brownell, J.E.7
Burke, K.E.8
Cardin, D.P.9
Critchley, S.10
Cullis, C.A.11
Doucette, A.12
Garnsey, J.J.13
Gaulin, J.L.14
Gershman, R.E.15
Lublinsky, A.R.16
McDonald, A.17
Mizutani, H.18
Narayanan, U.19
Olhava, E.J.20
Peluso, S.21
Rezaei, M.22
Sintchak, M.D.23
Talreja, T.24
Thomas, M.P.25
Traore, T.26
Vyskocil, S.27
Weatherhead, G.S.28
Yu, J.29
Zhang, J.30
Dick, L.R.31
Claiborne, C.F.32
Rolfe, M.33
Bolen, J.B.34
Langston, S.P.35
more..
|