-
1
-
-
0033760789
-
Inhibitors of cyclin-dependent kinases as anticancer therapeutics
-
Fischer PM, Lane DP. Inhibitors of cyclin-dependent kinases as anticancer therapeutics. Curr Med Chem 2000;7:1213-45.
-
(2000)
Curr Med Chem
, vol.7
, pp. 1213-1245
-
-
Fischer, P.M.1
Lane, D.P.2
-
2
-
-
0032511893
-
Interaction with cyclin-dependent kinases and PCNA modulates proteasome-dependent degradation of p21
-
Cayrol C, Ducommun B. Interaction with cyclin-dependent kinases and PCNA modulates proteasome-dependent degradation of p21. Oncogene 1998;17:2437-44.
-
(1998)
Oncogene
, vol.17
, pp. 2437-2444
-
-
Cayrol, C.1
Ducommun, B.2
-
3
-
-
31544440126
-
Cell cycle control in breast cancer cells
-
DOI 10.1002/jcb.20690
-
Caldon CE, Daly RJ, Sutherland RL, Musgrove EA. Cell cycle control in breast cancer cells. J Cell Biochem 2006;97:261-74. (Pubitemid 43167144)
-
(2006)
Journal of Cellular Biochemistry
, vol.97
, Issue.2
, pp. 261-274
-
-
Caldon, C.E.1
Daly, R.J.2
Sutherland, R.L.3
Musgrove, E.A.4
-
4
-
-
0034238115
-
Down-regulation of p21(WAF1/CIP1) or p27(Kip1) abrogates antiestrogen-mediated cell cycle arrest in human breast cancer cells
-
DOI 10.1073/pnas.160016897
-
Cariou S, Donovan JC, Flanagan WM, Milic A, Bhattacharya N, Slingerland JM. Down-regulation of p21WAF1/CIP1 or p27Kip1 abrogates antiestrogen-mediated cell cycle arrest in human breast cancer cells. Proc Natl Acad Sci U S A 2000;97:9042-6. (Pubitemid 30626670)
-
(2000)
Proceedings of the National Academy of Sciences of the United States of America
, vol.97
, Issue.16
, pp. 9042-9046
-
-
Cariou, S.1
Donovan, J.C.H.2
Flanagan, W.M.3
Milic, A.4
Bhattacharya, N.5
Slingerland, J.M.6
-
5
-
-
40449117681
-
WAF1)
-
DOI 10.1096/fj.07-9322com
-
Maynadier M, Ramirez JM, Cathiard AM, Platet N, Gras D, Gleizes M, et al. Unliganded estrogen receptor alpha inhibits breast cancer cell growth through interaction with a cyclin-dependent kinase inhibitor (p21(WAF1)). FASEB J 2008;22:671-81. (Pubitemid 351348120)
-
(2008)
FASEB Journal
, vol.22
, Issue.3
, pp. 671-681
-
-
Maynadier, M.1
Ramirez, J.-M.2
Cathiard, A.-M.3
Platet, N.4
Gras, D.5
Gleizes, M.6
Sheikh, M.S.7
Nirde, P.8
Garcia, M.9
-
6
-
-
16944363001
-
Decreased levels of the cell-cycle inhibitor p27(Kip1) protein: Prognostic implications in primary breast cancer
-
DOI 10.1038/nm0297-227
-
Catzavelos C, Bhattacharya N, Ung YC, Wilson JA, Roncari L, Sandhu C, et al. Decreased levels of the cell-cycle inhibitor p27Kip1 protein: prognostic implications in primary breast cancer. Nat Med 1997;3:227-30. (Pubitemid 27064710)
-
(1997)
Nature Medicine
, vol.3
, Issue.2
, pp. 227-230
-
-
Catzavelos, C.1
Bhattacharya, N.2
Ung, Y.C.3
Wilson, J.A.4
Roncari, L.5
Sandhu, C.6
Shaw, P.7
Yeger, H.8
Morava-Protzner, I.9
Kapusta, L.10
Franssen, E.11
Pritchard, K.I.12
Slingerland, J.M.13
-
7
-
-
0031004664
-
p21(Waf1/Cip1) and p53 protein expression in breast cancer
-
Wakasugi E, Kobayashi T, Tamaki Y, Ito Y, Miyashiro I, Komoike Y, et al. p21(Waf1/Cip1) and p53 protein expression in breast cancer. Am J Clin Pathol 1997;107:684-91. (Pubitemid 27220527)
-
(1997)
American Journal of Clinical Pathology
, vol.107
, Issue.6
, pp. 684-691
-
-
Wakasugi, E.1
Kobayashi, T.2
Tamaki, Y.3
Ito, Y.4
Miyashiro, I.5
Komoike, Y.6
Takeda, T.7
Shin, E.8
Takatsuka, Y.9
Kikkawa, N.10
Monden, T.11
Monden, M.12
-
8
-
-
0030667191
-
p21/waf1/cip1 and mdm-2 expression in breast carcinoma patients as related to prognosis
-
DOI 10.1002/(SICI)1097-0215(19971021)74:5<529::AID-IJC9>3.0.CO;2-5
-
Jiang M, Shao ZM, Wu J, Lu JS, Yu LM, Yuan JD, et al. p21/waf1/cip1 and mdm-2 expression in breast carcinoma patients as related to prognosis. Int J Cancer 1997;74:529-34. (Pubitemid 27486511)
-
(1997)
International Journal of Cancer
, vol.74
, Issue.5
, pp. 529-534
-
-
Jiang, M.1
Shao, Z.-M.2
Wu, J.3
Lu, J.-S.4
Yu, L.-M.5
Yuan, J.-D.6
Han, Q.-X.7
Shen, Z.-Z.8
Fontana, J.A.9
-
9
-
-
0032589191
-
p27(KIP1) is abnormally expressed in diffuse large B-cell lymphomas and is associated with an adverse clinical outcome
-
DOI 10.1038/sj.bjc.6690539
-
Saez A, Sanchez E, Sanchez-Beato M, Cruz MA, Chacon I, Munoz E, et al. p27KIP1 is abnormally expressed in diffuse large B-cell lymphomas and is associated with an adverse clinical outcome. Br J Cancer 1999;80:1427-34. (Pubitemid 29308613)
-
(1999)
British Journal of Cancer
, vol.80
, Issue.9
, pp. 1427-1434
-
-
Saez, A.I.1
Sanchez, E.2
Sanchez-Beato, M.3
Cruz, M.A.4
Chacon, I.5
Munoz, E.6
Camacho, F.I.7
Martinez-Montero, J.C.8
Mollejo, M.9
Garcia, J.F.10
Piris, M.A.11
-
10
-
-
0032980308
-
The prognostic significance of altered cyclin-dependent kinase inhibitors in human cancer
-
DOI 10.1146/annurev.med.50.1.401
-
Tsihlias J, Kapusta L, Slingerland J. The prognostic significance of altered cyclin-dependent kinase inhibitors in human cancer. Annu Rev Med 1999;50:401-23. (Pubitemid 29117075)
-
(1999)
Annual Review of Medicine
, vol.50
, pp. 401-423
-
-
Tsihlias, J.1
Kapusta, L.2
Slingerland, J.3
-
11
-
-
0141987892
-
Proteasome-mediated degradation of p21 via N-terminal ubiquitinylation
-
DOI 10.1016/S0092-8674(03)00755-4
-
Bloom J, Amador V, Bartolini F, DeMartino G, Pagano M. Proteasome-mediated degradation of p21 via N-terminal ubiquitinylation. Cell 2003;115:71-82. (Pubitemid 37255319)
-
(2003)
Cell
, vol.115
, Issue.1
, pp. 71-82
-
-
Bloom, J.1
Amador, V.2
Bartolini, F.3
DeMartino, G.4
Pagano, M.5
-
12
-
-
0029024015
-
Role of the ubiquitin-proteasome pathway in regulating abundance of the cyclin-dependent kinase inhibitor p27
-
Pagano M, Tam SW, Theodoras AM, Beer-Romero P, Del Sal G, Chau V, et al. Role of the ubiquitin-proteasome pathway in regulating abundance of the cyclin-dependent kinase inhibitor p27. Science 1995;269:682-5.
-
(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
-
14
-
-
0035072563
-
P53-dependent apoptosis induced by proteasome inhibition in mammary epithelial cells
-
DOI 10.1038/sj.cdd.4400801
-
MacLaren AP, Chapman RS, Wyllie AH, Watson CJ. p53-dependent apoptosis induced by proteasome inhibition in mammary epithelial cells. Cell Death Differ 2001;8:210-8. (Pubitemid 32288166)
-
(2001)
Cell Death and Differentiation
, vol.8
, Issue.3
, pp. 210-218
-
-
MacLaren, A.P.1
Chapman, R.S.2
Wyllie, A.H.3
Watson, C.J.4
-
15
-
-
9144264926
-
Induction of proteasome expression in skeletal muscle is attenuated by inhibitors of NF-κB activation
-
DOI 10.1038/sj.bjc.6602165
-
Wyke SM, Russell ST, Tisdale MJ. Induction of proteasome expression in skeletal muscle is attenuated by inhibitors of NF-kappaB activation. Br J Cancer 2004;91:1742-50. (Pubitemid 39546149)
-
(2004)
British Journal of Cancer
, vol.91
, Issue.9
, pp. 1742-1750
-
-
Wyke, S.M.1
Russell, S.T.2
Tisdale, M.J.3
-
16
-
-
4644352784
-
Inhibitory effect of ubiquitin-proteasome pathway on proliferation of esophageal carcinoma cells
-
Zhang WG, Yu JP, Wu QM, Tong Q, Li SB, Wang XH, et al. Inhibitory effect of ubiquitin-proteasome pathway on proliferation of esophageal carcinoma cells. World J Gastroenterol 2004;10:2779-84. (Pubitemid 39302988)
-
(2004)
World Journal of Gastroenterology
, vol.10
, Issue.19
, pp. 2779-2784
-
-
Zhang, W.-G.1
Yu, J.-P.2
Wu, Q.-M.3
Tong, Q.4
Li, S.-B.5
Wang, X.-H.6
Xie, G.-J.7
-
19
-
-
0032587495
-
p27(kip1): A multifunctional cyclin-dependent kinase inhibitor with prognostic significance in human cancers
-
Lloyd RV, Erickson LA, Jin L, Kulig E, Qian X, Cheville JC, et al. p27kip1: a multifunctional cyclin-dependent kinase inhibitor with prognostic significance in human cancers. Am J Pathol 1999;154:313-23. (Pubitemid 29094081)
-
(1999)
American Journal of Pathology
, vol.154
, Issue.2
, pp. 313-323
-
-
Lloyd, R.V.1
Erickson, L.A.2
Jin, L.3
Kulig, E.4
Qian, X.5
Cheville, J.C.6
Scheithauer, B.W.7
-
20
-
-
0037973279
-
A phase 2 study of Bortezomib in relapsed, refractory myeloma
-
DOI 10.1056/NEJMoa030288
-
Richardson PG, Barlogie B, Berenson J, Singhal S, Jagannath S, Irwin D, et al.Aphase 2 study of bortezomib in relapsed, refractory myeloma. N Engl J Med 2003;348:2609-17. (Pubitemid 36741588)
-
(2003)
New England Journal of Medicine
, vol.348
, Issue.26
, 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..
-
21
-
-
0032539702
-
Potent and selective inhibitors of the proteasome: Dipeptidyl boronic acids
-
DOI 10.1016/S0960-894X(98)00029-8, PII S0960894X98000298
-
Adams J, Behnke M, Chen S, Cruickshank AA, Dick LR, Grenier L, et al. Potent and selective inhibitors of the proteasome: dipeptidyl boronic acids. Bioorg Med Chem Lett 1998;8:333-8. (Pubitemid 28072702)
-
(1998)
Bioorganic and Medicinal Chemistry Letters
, vol.8
, Issue.4
, pp. 333-338
-
-
Adams, J.1
Behnke, M.2
Chen, S.3
Cruickshank, A.A.4
Dick, L.R.5
Grenier, L.6
Klunder, J.M.7
Ma, Y.-T.8
Plamondon, L.9
Stein, R.L.10
-
22
-
-
36849013003
-
A phase II study of single agent bortezomib in patients with metastatic breast cancer: A single institution experience
-
DOI 10.1080/07357900701506573, PII 783100851
-
Engel RH, Brown JA, Von Roenn JH, O'Regan RM, Bergan R, Badve S, et al. A phase II study of single agent bortezomib in patients with metastatic breast cancer: a single institution experience. Cancer Invest 2007;25:733-7. (Pubitemid 350223168)
-
(2007)
Cancer Investigation
, vol.25
, Issue.8
, 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
-
23
-
-
34447618562
-
Farnesyltransferase inhibitor R115,777 enhances tamoxifen inhibition of MCF-7 cell growth through estrogen receptor dependent and independent pathways
-
Dalenc F, Giamarchi C, Petit M, Poirot M, Favre G, Faye JC. Farnesyltransferase inhibitor R115,777 enhances tamoxifen inhibition of MCF-7 cell growth through estrogen receptor dependent and independent pathways. Breast Cancer Res 2005;7:R1159-67.
-
(2005)
Breast Cancer Res
, vol.7
-
-
Dalenc, F.1
Giamarchi, C.2
Petit, M.3
Poirot, M.4
Favre, G.5
Faye, J.C.6
-
24
-
-
0032429122
-
Novel dipeptidyl proteasome inhibitors overcome Bcl-2 protective function and selectively accumulate the cyclin-dependent kinase inhibitor p27 and induce apoptosis in transformed, but not normal, human fibroblasts
-
An B, Goldfarb RH, Siman R, Dou QP. Novel dipeptidyl proteasome inhibitors overcome Bcl-2 protective function and selectively accumulate the cyclin-dependent kinase inhibitor p27 and induce apoptosis in transformed, but not normal, human fibroblasts. Cell Death Differ 1998;5:1062-75. (Pubitemid 29008220)
-
(1998)
Cell Death and Differentiation
, vol.5
, Issue.12
, pp. 1062-1075
-
-
An, B.1
Goldfarb, R.H.2
Siman, R.3
Ping, D.Q.4
-
25
-
-
0033152760
-
Proteasome inhibitors: A novel class of potent and effective antitumor agents
-
Adams J, Palombella VJ, Sausville EA, Johnson J, Destree A, Lazarus DD, et al. Proteasome inhibitors: a novel class of potent and effective antitumor agents. Cancer Res 1999;59:2615-22. (Pubitemid 29269108)
-
(1999)
Cancer Research
, vol.59
, Issue.11
, 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
-
26
-
-
44849083172
-
Bortezomib (Velcade) induces p27Kip1 expression through S-phase kinase protein 2 degradation in colorectal cancer
-
Uddin S, Ahmed M, Bavi P, El-Sayed R, Al-Sanea N, AbdulJabbar A, et al. Bortezomib (Velcade) induces p27Kip1 expression through S-phase kinase protein 2 degradation in colorectal cancer. Cancer Res 2008;68:3379-88.
-
(2008)
Cancer Res
, vol.68
, pp. 3379-3388
-
-
Uddin, S.1
Ahmed, M.2
Bavi, P.3
El-Sayed, R.4
Al-Sanea, N.5
AbdulJabbar, A.6
-
27
-
-
0031594705
-
2/M-phase transition
-
Dulic V, Stein GH, Far DF, Reed SI. Nuclear accumulation of p21Cip1 at the onset of mitosis: a role at the G2/M-phase transition. Mol Cell Biol 1998;18:546-57. (Pubitemid 28021065)
-
(1998)
Molecular and Cellular Biology
, vol.18
, Issue.1
, pp. 546-557
-
-
Dulic, V.1
Stein, G.H.2
Far, D.F.3
Reed, S.I.4
-
28
-
-
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 VJ, Elliott PJ, Adams J, et al. The proteasome inhibitor PS-341 inhibits growth, induces apoptosis, and overcomes drug resistance in human multiple myeloma cells. Cancer Res 2001;61:3071-6. (Pubitemid 32691956)
-
(2001)
Cancer Research
, vol.61
, Issue.7
, 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
-
29
-
-
14844354335
-
kip1 protein levels through both increased transcriptional activity and inhibition of proteasome degradation
-
DOI 10.1016/j.cellsig.2004.11.002
-
Chen F, Harrison LE. Ciglitazone-induced cellular anti-proliferation increases p27kip1 protein levels through both increased transcriptional activity and inhibition of proteasome degradation. Cell Signal 2005;17:809-16. (Pubitemid 40353651)
-
(2005)
Cellular Signalling
, vol.17
, Issue.7
, pp. 809-816
-
-
Chen, F.1
Harrison, L.E.2
-
30
-
-
0032553485
-
2 arrest after DNA damage
-
Bunz F, Dutriaux A, Lengauer C, Waldman T, Zhou S, Brown JP, et al. Requirement for p53 and p21 to sustain G2 arrest after DNA damage. Science 1998;282:1497-501. (Pubitemid 28538613)
-
(1998)
Science
, vol.282
, Issue.5393
, pp. 1497-1501
-
-
Bunz, F.1
Dutriaux, A.2
Lengauer, C.3
Waldman, T.4
Zhou, S.5
Brown, J.P.6
Sedivy, J.M.7
Kinzler, K.W.8
Vogelstein, B.9
-
31
-
-
42549148850
-
MDA-MB-435: The questionable use of a melanoma cell line as a model for human breast cancer is ongoing
-
Christgen M, Lehmann U. MDA-MB-435: the questionable use of a melanoma cell line as a model for human breast cancer is ongoing. Cancer Biol Ther 2007;6:1355-7. (Pubitemid 351590342)
-
(2007)
Cancer Biology and Therapy
, vol.6
, Issue.9
, pp. 1355-1357
-
-
Christgen, M.1
Lehmann, U.2
-
32
-
-
78149487540
-
Breast cancer stem-like cells are inhibited by a non-toxic aryl hydrocarbon receptor agonist
-
Prud'homme GJ, Glinka Y, Toulina A, Ace O, Subramaniam V, Jothy S. Breast cancer stem-like cells are inhibited by a non-toxic aryl hydrocarbon receptor agonist. PLoS ONE 2010;5:e13831.
-
(2010)
PLoS ONE
, vol.5
-
-
Prud'homme, G.J.1
Glinka, Y.2
Toulina, A.3
Ace, O.4
Subramaniam, V.5
Jothy, S.6
-
33
-
-
77949422964
-
Proteasome inhibition represses ERalpha gene expression in ER+ cells: A new link between proteasome activity and estrogen signaling in breast cancer
-
Powers GL, Ellison-Zelski SJ, Casa AJ, Lee AV, Alarid ET. Proteasome inhibition represses ERalpha gene expression in ER+ cells: a new link between proteasome activity and estrogen signaling in breast cancer. Oncogene 2010;29:1509-18.
-
(2010)
Oncogene
, vol.29
, pp. 1509-1518
-
-
Powers, G.L.1
Ellison-Zelski, S.J.2
Casa, A.J.3
Lee, A.V.4
Alarid, E.T.5
-
34
-
-
75149129645
-
Bortezomib blocks the catabolic process of autophagy via a cathepsin-dependent mechanism, affects endoplasmic reticulum stress and induces caspase-dependent cell death in antiestrogen-sensitive and resistant ER+ breast cancer cells
-
Periyasamy-Thandavan S, Jackson WH, Samaddar JS, Erickson B, Barrett JR, Raney L, et al. Bortezomib blocks the catabolic process of autophagy via a cathepsin-dependent mechanism, affects endoplasmic reticulum stress and induces caspase-dependent cell death in antiestrogen-sensitive and resistant ER+ breast cancer cells. Autophagy 2010;6:19-35.
-
(2010)
Autophagy
, vol.6
, pp. 19-35
-
-
Periyasamy-Thandavan, S.1
Jackson, W.H.2
Samaddar, J.S.3
Erickson, B.4
Barrett, J.R.5
Raney, L.6
-
36
-
-
34248377893
-
Bortezomib activity and in vitro interactions with anthracyclines and cytarabine in acute myeloid leukemia cells are independent of multidrug resistance mechanisms and p53 status
-
DOI 10.1007/s00280-006-0367-6
-
Minderman H, Zhou Y, O'Loughlin KL, Baer MR. Bortezomib activity and in vitro interactions with anthracyclines and cytarabine in acute myeloid leukemia cells are independent of multidrug resistance mechanisms and p53 status. Cancer Chemother Pharmacol 2007;60:245-55. (Pubitemid 46742540)
-
(2007)
Cancer Chemotherapy and Pharmacology
, vol.60
, Issue.2
, pp. 245-255
-
-
Minderman, H.1
Zhou, Y.2
O'Loughlin, K.L.3
Baer, M.R.4
-
37
-
-
22244452016
-
Proteasome inhibitors trigger NOXA-mediated apoptosis in melanoma and myeloma cells
-
DOI 10.1158/0008-5472.CAN-05-0676
-
Qin JZ, Ziffra J, Stennett L, Bodner B, Bonish BK, Chaturvedi V, et al. Proteasome inhibitors trigger NOXA-mediated apoptosis in melanoma and myeloma cells. Cancer Res 2005;65:6282-93. (Pubitemid 40994414)
-
(2005)
Cancer Research
, vol.65
, Issue.14
, 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.C.10
Rizzo, P.11
Miele, L.12
Nickoloff, B.J.13
-
38
-
-
30144442233
-
The proteasome inhibitor bortezomib induces apoptosis in mantle-cell lymphoma through generation of ROS and Noxa activation independent of p53 status
-
DOI 10.1182/blood-2005-05-2091
-
Perez-Galan P, Roue G, Villamor N, Montserrat E, Campo E, Colomer D. The proteasome inhibitor bortezomib induces apoptosis in mantlecell lymphoma through generation of ROS and Noxa activation independent of p53 status. Blood 2006;107:257-64. (Pubitemid 43053550)
-
(2006)
Blood
, vol.107
, Issue.1
, pp. 257-264
-
-
Perez-Galan, P.1
Roue, G.2
Villamor, N.3
Montserrat, E.4
Campo, E.5
Colomer, D.6
-
39
-
-
30344441540
-
Sensitization of DNA damage-induced apoptosis by the proteasome inhibitor PS-341 is p53 dependent and involves target proteins 14-3-3σ and survivin
-
DOI 10.1158/1535-7163.MCT-05-0222
-
Vaziri SA, Hill J, Chikamori K, Grabowski DR, Takigawa N, Chawla-Sarkar M, et al. Sensitization of DNA damage-induced apoptosis by the proteasome inhibitor PS-341 is p53 dependent and involves target proteins 14-3-3 sigma and survivin. Mol Cancer Ther 2005;4:1880-90. (Pubitemid 43056971)
-
(2005)
Molecular Cancer Therapeutics
, vol.4
, Issue.12
, pp. 1880-1890
-
-
Vaziri, S.A.J.1
Hill, J.2
Chikamori, K.3
Grabowski, D.R.4
Takigawa, N.5
Chawla-Sarkar, M.6
Rybicki, L.R.7
Gudkov, A.V.8
Mekhail, T.9
Bukowski, R.M.10
Ganapathi, M.K.11
Ganapathi, R.12
-
40
-
-
0038189917
-
Rationale for the treatment of solid tumors with the proteasome inhibitor bortezomib
-
Cusack JC. Rationale for the treatment of solid tumors with the proteasome inhibitor bortezomib. Cancer Treat Rev 2003;29(Suppl 1):21-31.
-
(2003)
Cancer Treat Rev
, vol.29
, Issue.SUPPL. 1
, pp. 21-31
-
-
Cusack, J.C.1
-
41
-
-
50549090299
-
Enhanced anti-cancer effect of a phosphatidylinositol-3 kinase inhibitor and doxorubicin on human breast epithelial cell lines with different p53 and oestrogen receptor status
-
Wang YA, Johnson SK, Brown BL, McCarragher LM, Al-Sakkaf K, Royds JA, et al. Enhanced anti-cancer effect of a phosphatidylinositol-3 kinase inhibitor and doxorubicin on human breast epithelial cell lines with different p53 and oestrogen receptor status. Int J Cancer 2008;123:1536-44.
-
(2008)
Int J Cancer
, vol.123
, pp. 1536-1544
-
-
Wang, Y.A.1
Johnson, S.K.2
Brown, B.L.3
McCarragher, L.M.4
Al-Sakkaf, K.5
Royds, J.A.6
-
42
-
-
0032189685
-
Tumor growth inhibition induced in a murine model of human Burkitt's lymphoma by a proteasome inhibitor
-
Orlowski RZ, Eswara JR, Lafond-Walker A, Grever MR, Orlowski M, Dang CV. Tumor growth inhibition induced in a murine model of human Burkitt's lymphoma by a proteasome inhibitor. Cancer Res 1998;58:4342-8. (Pubitemid 28450035)
-
(1998)
Cancer Research
, vol.58
, Issue.19
, 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
-
43
-
-
13244262655
-
Proteasome inhibitor PS-341 causes cell growth arrest and apoptosis in human glioblastoma multiforme (GBM)
-
DOI 10.1038/sj.onc.1208225
-
Yin D, Zhou H, Kumagai T, Liu G, Ong JM, Black KL, et al. Proteasome inhibitor PS-341 causes cell growth arrest and apoptosis in human glioblastoma multiforme (GBM). Oncogene 2005;24:344-54. (Pubitemid 40188583)
-
(2005)
Oncogene
, vol.24
, Issue.3
, pp. 344-354
-
-
Yin, D.1
Zhou, H.2
Kumagai, T.3
Liu, G.4
Ong, J.M.5
Black, K.L.6
Koeffler, H.P.7
-
44
-
-
60249101252
-
Bortezomib arrests the proliferation of hepatocellular carcinoma cells HepG2 and JHH6 by differentially affecting E2F1, p21 and p27 levels
-
Baiz D, Pozzato G, Dapas B, Farra R, Scaggiante B, Grassi M, et al. Bortezomib arrests the proliferation of hepatocellular carcinoma cells HepG2 and JHH6 by differentially affecting E2F1, p21 and p27 levels. Biochimie 2009;91:373-82.
-
(2009)
Biochimie
, vol.91
, pp. 373-382
-
-
Baiz, D.1
Pozzato, G.2
Dapas, B.3
Farra, R.4
Scaggiante, B.5
Grassi, M.6
-
45
-
-
77951985216
-
Examination of the expanding pathways for the regulation of p21 expression and activity
-
Jung YS, Qian Y, Chen X. Examination of the expanding pathways for the regulation of p21 expression and activity. Cell Signal 2010;22:1003-12.
-
(2010)
Cell Signal
, vol.22
, pp. 1003-1012
-
-
Jung, Y.S.1
Qian, Y.2
Chen, X.3
-
46
-
-
0033080402
-
Transcriptional regulation of the p21((WAF1/CIP1)) gene
-
DOI 10.1006/excr.1998.4319
-
Gartel AL, Tyner AL. Transcriptional regulation of the p21((WAF1/CIP1)) gene. Exp Cell Res 1999;246:280-9. (Pubitemid 29393989)
-
(1999)
Experimental Cell Research
, vol.246
, Issue.2
, pp. 280-289
-
-
Gartel, A.L.1
Tyner, A.L.2
-
47
-
-
4644248931
-
Phase II study of the proteasome inhibitor bortezomib (PS-341) in patients with metastatic neuroendocrine tumors
-
DOI 10.1158/1078-0432.CCR-04-0422
-
Shah MH, Young D, Kindler HL,Webb I, Kleiber B, Wright J, et al. Phase II study of the proteasome inhibitor bortezomib (PS-341) in patients with metastatic neuroendocrine tumors. Clin Cancer Res 2004;10:6111-8. (Pubitemid 39287516)
-
(2004)
Clinical Cancer Research
, vol.10
, Issue.18 I
, 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
-
48
-
-
33646186160
-
Bortezomib (VELCADE) in metastatic breast cancer: Pharmacodynamics, biological effects, and prediction of clinical benefits
-
Yang CH, Gonzalez-Angulo AM, Reuben JM, Booser DJ, Pusztai L, Krishnamurthy S, et al. Bortezomib (VELCADE) in metastatic breast cancer: pharmacodynamics, biological effects, and prediction of clinical benefits. Ann Oncol 2006;17:813-7.
-
(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
-
49
-
-
33846216907
-
Bortezomib (PS-341, Velcade) increases the efficacy of trastuzumab (Herceptin) in HER-2-positive breast cancer cells in a synergistic manner
-
DOI 10.1158/1535-7163.MCT-06-0104
-
Cardoso F, Durbecq V, Laes JF, Badran B, Lagneaux L, Bex F, et al. Bortezomib (PS-341, Velcade) increases the efficacy of trastuzumab (Herceptin) in HER-2-positive breast cancer cells in a synergistic manner. Mol Cancer Ther 2006;5:3042-51. (Pubitemid 46092045)
-
(2006)
Molecular Cancer Therapeutics
, vol.5
, Issue.12
, pp. 3042-3051
-
-
Cardoso, F.1
Durbecq, V.2
Laes, J.-F.3
Badran, B.4
Lagneaux, L.5
Bex, F.6
Desmedt, C.7
Willard-Gallo, K.8
Ross, J.S.9
Burny, A.10
Piccart, M.11
Sotiriou, C.12
-
50
-
-
34347352213
-
Proteasome-regulated ERBB2 and estrogen receptor pathways in breast cancer
-
DOI 10.1124/mol.107.034090
-
Marx C, Yau C, Banwait S, Zhou Y, Scott GK, Hann B, et al. Proteasome-regulated ERBB2 and estrogen receptor pathways in breast cancer. Mol Pharmacol 2007;71:1525-34. (Pubitemid 47010905)
-
(2007)
Molecular Pharmacology
, vol.71
, Issue.6
, pp. 1525-1534
-
-
Marx, C.1
Yau, C.2
Banwait, S.3
Zhou, Y.4
Scott, G.K.5
Hann, B.6
Park, J.W.7
Benz, C.C.8
|