-
1
-
-
18444404925
-
Drug-induced ubiquitylation and degradation of ErbB receptor tyrosine kinases: Implications for cancer therapy
-
Citri A, Alroy I, Lavi S, et al. Drug-induced ubiquitylation and degradation of ErbB receptor tyrosine kinases: implications for cancer therapy. EMBO J 2002;21:2407-17.
-
(2002)
EMBO J
, vol.21
, pp. 2407-2417
-
-
Citri, A.1
Alroy, I.2
Lavi, S.3
-
2
-
-
0029813620
-
Destabilization of Raf-1 by geldanamycin leads to disruption of the Raf-1-MEK-mitogen-activated protein kinase signalling pathway
-
Schulte TW, Blagosklonny MV, Romanova L, et al. Destabilization of Raf-1 by geldanamycin leads to disruption of the Raf-1-MEK-mitogen-activated protein kinase signalling pathway. Mol Cell Biol 1996;16:5839-45.
-
(1996)
Mol Cell Biol
, vol.16
, pp. 5839-5845
-
-
Schulte, T.W.1
Blagosklonny, M.V.2
Romanova, L.3
-
3
-
-
0037131187
-
Akt forms an intracellular complex with heat shock protein 90 (Hsp90) and Cdc37 and is destabilized by inhibitors of Hsp90 function
-
Basso AD, Solit DB, Chiosis G, Giri B, Tsichlis P, Rosen N. Akt forms an intracellular complex with heat shock protein 90 (Hsp90) and Cdc37 and is destabilized by inhibitors of Hsp90 function. J Biol Chem 2002;277:39858-66.
-
(2002)
J Biol Chem
, vol.277
, pp. 39858-39866
-
-
Basso, A.D.1
Solit, D.B.2
Chiosis, G.3
Giri, B.4
Tsichlis, P.5
Rosen, N.6
-
4
-
-
0029665779
-
Mammalian p50Cdc37 is a protein kinase-targeting subunit of Hsp90 that binds and stabilizes Cdk4
-
Stepanova L, Leng X, Parker SB, Harper JW. Mammalian p50Cdc37 is a protein kinase-targeting subunit of Hsp90 that binds and stabilizes Cdk4. Genes Dev 1996;10:1491-502.
-
(1996)
Genes Dev
, vol.10
, pp. 1491-1502
-
-
Stepanova, L.1
Leng, X.2
Parker, S.B.3
Harper, J.W.4
-
5
-
-
0036091221
-
17-Allylamino-17- demethoxygeldanamycin induces the degradation of androgen receptor and HER-2/neu and inhibits the growth of prostate cancer xenografts
-
Solit DB, Zheng FF, Drobnjak M, et al. 17-Allylamino-17- demethoxygeldanamycin induces the degradation of androgen receptor and HER-2/neu and inhibits the growth of prostate cancer xenografts. Clin Cancer Res 2002;8:986-93.
-
(2002)
Clin Cancer Res
, vol.8
, pp. 986-993
-
-
Solit, D.B.1
Zheng, F.F.2
Drobnjak, M.3
-
6
-
-
0142188139
-
Hormone-refractory breast cancer remains sensitive to the antitumor activity of heat shock protein 90 inhibitors
-
Beliakoff J, Bagatell R, Paine-Murrieta G, Taylor CW, Lykkesfeldt AE, Whitesell L. Hormone-refractory breast cancer remains sensitive to the antitumor activity of heat shock protein 90 inhibitors. Clin Cancer Res 2003;9:4961-71.
-
(2003)
Clin Cancer Res
, vol.9
, pp. 4961-4971
-
-
Beliakoff, J.1
Bagatell, R.2
Paine-Murrieta, G.3
Taylor, C.W.4
Lykkesfeldt, A.E.5
Whitesell, L.6
-
7
-
-
0036569704
-
Geldanamycin induces degradation of hypoxia-inducible factor1α protein via the proteosome pathway in prostate cancer cells
-
Mabjeesh NJ, Post DE, Willard MT, et al. Geldanamycin induces degradation of hypoxia-inducible factor1α protein via the proteosome pathway in prostate cancer cells. Cancer Res 2002;62:2478- 82.
-
(2002)
Cancer Res
, vol.62
, pp. 2478-2482
-
-
Mabjeesh, N.J.1
Post, D.E.2
Willard, M.T.3
-
8
-
-
0028064940
-
Inhibition of heat shock protein HSP90-60v-src heteroprotein complex formation by benzoquinone ansamycins: Essential role for stress proteins in oncogenic transformation
-
Whitesell L, Mimnaugh EG, De Costa B, Myers CE, Neckers LM. Inhibition of heat shock protein HSP90-60v-src heteroprotein complex formation by benzoquinone ansamycins: essential role for stress proteins in oncogenic transformation. Proc Natl Acad Sci U S A 1994;91:8324-8.
-
(1994)
Proc Natl Acad Sci U S A
, vol.91
, pp. 8324-8328
-
-
Whitesell, L.1
Mimnaugh, E.G.2
De Costa, B.3
Myers, C.E.4
Neckers, L.M.5
-
9
-
-
0027291238
-
Heat-shock protein hsp90 governs the activity of pp60v-src kinase
-
Xu Y, Lindquist S. Heat-shock protein hsp90 governs the activity of pp60v-src kinase. Proc Natl Acad Sci U S A 1993;90:7074-8.
-
(1993)
Proc Natl Acad Sci U S A
, vol.90
, pp. 7074-7078
-
-
Xu, Y.1
Lindquist, S.2
-
10
-
-
22244485706
-
Epidermal growth factor receptors harboring kinase domain mutations associate with the heat shock protein 90 chaperone and are destabilized following exposure to geldanamycins
-
Shimamura T, Lowell AM, Engelman JA, Shapiro GI. Epidermal growth factor receptors harboring kinase domain mutations associate with the heat shock protein 90 chaperone and are destabilized following exposure to geldanamycins. Cancer Res 2005;65:6401-8.
-
(2005)
Cancer Res
, vol.65
, pp. 6401-6408
-
-
Shimamura, T.1
Lowell, A.M.2
Engelman, J.A.3
Shapiro, G.I.4
-
11
-
-
30444441778
-
V600EB-Raf requires the Hsp90 chaperone for stability and is degraded in response to Hsp90 inhibitors
-
Grbovic OM, Basso AD, Sawai A, et al. V600EB-Raf requires the Hsp90 chaperone for stability and is degraded in response to Hsp90 inhibitors. Proc Natl Acad Sci US A 2006;103:57-62.
-
(2006)
Proc Natl Acad Sci US A
, vol.103
, pp. 57-62
-
-
Grbovic, O.M.1
Basso, A.D.2
Sawai, A.3
-
12
-
-
28244444919
-
Activated B-RAF is an Hsp90 client protein that is targeted by the anticancer drug 17-allylamino-17-demethoxygeldanamycin
-
da Rocha Dias S, Friedlos F, Light Y, Springer C, Workman P, Marais R. Activated B-RAF is an Hsp90 client protein that is targeted by the anticancer drug 17-allylamino-17-demethoxygeldanamycin. Cancer Res 2005;65:10686-91.
-
(2005)
Cancer Res
, vol.65
, pp. 10686-10691
-
-
da Rocha Dias, S.1
Friedlos, F.2
Light, Y.3
Springer, C.4
Workman, P.5
Marais, R.6
-
13
-
-
33645471864
-
Reaction of geldanamycin and C17-substituted analogues with glutathione: Product identifications and pharmacological implications
-
Cysyk RL, Parker RJ, Barchi JJ, Jr., Steeg PS, Hartman NR, Strong JM. Reaction of geldanamycin and C17-substituted analogues with glutathione: product identifications and pharmacological implications. Chem Res Toxicol 2006;19:376-81.
-
(2006)
Chem Res Toxicol
, vol.19
, pp. 376-381
-
-
Cysyk, R.L.1
Parker, R.J.2
Barchi Jr., J.J.3
Steeg, P.S.4
Hartman, N.R.5
Strong, J.M.6
-
14
-
-
0033579175
-
DT-diaphorase expression and tumor cell sensitivity to 17-allylamino, 17- demethoxygeldanamycin, an inhibitor of heat shock protein 90
-
Kelland LR, Sharp SY, Rogers PM, Myers TG, Workman P. DT-diaphorase expression and tumor cell sensitivity to 17-allylamino, 17- demethoxygeldanamycin, an inhibitor of heat shock protein 90. J Natl Cancer Inst 1999;91:1940-9.
-
(1999)
J Natl Cancer Inst
, vol.91
, pp. 1940-1949
-
-
Kelland, L.R.1
Sharp, S.Y.2
Rogers, P.M.3
Myers, T.G.4
Workman, P.5
-
15
-
-
27544446054
-
Formation of 17-allylamino-demethoxygeldanamycin (17-AAG) hydroquinone by NAD(P)H:quinone oxidoreductase 1: Role of 17-AAG hydroquinone in heat shock protein 90 inhibition
-
Guo W, Reigan P, Siegel D, Zirrolli J, Gustafson D, Ross D. Formation of 17-allylamino-demethoxygeldanamycin (17-AAG) hydroquinone by NAD(P)H:quinone oxidoreductase 1: role of 17-AAG hydroquinone in heat shock protein 90 inhibition. Cancer Res 2005;65:10006-15.
-
(2005)
Cancer Res
, vol.65
, pp. 10006-10015
-
-
Guo, W.1
Reigan, P.2
Siegel, D.3
Zirrolli, J.4
Gustafson, D.5
Ross, D.6
-
16
-
-
40749157803
-
Chemoproteomics-driven drug discovery: Identification of novel hsp90 inhibitors
-
April 14-18, Los Angeles, CA
-
Hall S, Barbasz A, Barta T, et al. Chemoproteomics-driven drug discovery: identification of novel hsp90 inhibitors. American Association for Cancer Research Annual Meeting 2007, April 14-18, Los Angeles, CA.
-
(2007)
American Association for Cancer Research Annual Meeting
-
-
Hall, S.1
Barbasz, A.2
Barta, T.3
-
17
-
-
0025076484
-
2/M-phase subpopulations in mammalian cell nuclei using side scatter and DNA content measurements
-
2/M-phase subpopulations in mammalian cell nuclei using side scatter and DNA content measurements. Cytometry 1990;11:813-21.
-
(1990)
Cytometry
, vol.11
, pp. 813-821
-
-
Nusse, M.1
Beisker, W.2
Hoffmann, C.3
Tarnok, A.4
-
18
-
-
33744525496
-
The use of high-content screening for the discovery and characterization of compounds that modulate mitotic index and cell cycle progression by differing mechanisms of action
-
Barabasz A, Foley B, Otto JC, Scott A, Rice J. The use of high-content screening for the discovery and characterization of compounds that modulate mitotic index and cell cycle progression by differing mechanisms of action. Assay Drug Dev Technol 2006;4:153-63.
-
(2006)
Assay Drug Dev Technol
, vol.4
, pp. 153-163
-
-
Barabasz, A.1
Foley, B.2
Otto, J.C.3
Scott, A.4
Rice, J.5
-
19
-
-
0026694947
-
In-gel digestion of proteins for internal sequence analysis after one- or two-dimensional gel electrophoresis
-
Rosenfeld J, Capdevielle J, Guillemot JC, Ferrara P. In-gel digestion of proteins for internal sequence analysis after one- or two-dimensional gel electrophoresis. Anal Biochem 1992;203:173-9.
-
(1992)
Anal Biochem
, vol.203
, pp. 173-179
-
-
Rosenfeld, J.1
Capdevielle, J.2
Guillemot, J.C.3
Ferrara, P.4
-
20
-
-
0032961627
-
Mass spectrometric identification of proteins from silver-stained polyacrylamide gel: A method for the removal of silver ions to enhance sensitivity
-
Gharahdaghi F, Weinberg CR, Meagher DA, Imai BS, Mische SM. Mass spectrometric identification of proteins from silver-stained polyacrylamide gel: a method for the removal of silver ions to enhance sensitivity. Electrophoresis 1999;20:601-5.
-
(1999)
Electrophoresis
, vol.20
, pp. 601-605
-
-
Gharahdaghi, F.1
Weinberg, C.R.2
Meagher, D.A.3
Imai, B.S.4
Mische, S.M.5
-
21
-
-
0036892305
-
Discovery of novel targets of quinoline drugs in the human purine binding proteome
-
Graves PR, Kwiek JJ, Fadden P, et al. Discovery of novel targets of quinoline drugs in the human purine binding proteome. Mol Pharmacol 2002;62:1364-72.
-
(2002)
Mol Pharmacol
, vol.62
, pp. 1364-1372
-
-
Graves, P.R.1
Kwiek, J.J.2
Fadden, P.3
-
22
-
-
33746334186
-
The purinome, a complex mix of drug and toxicity targets
-
Haystead TA. The purinome, a complex mix of drug and toxicity targets. Curr Top Med Chem 2006;6:1117-27.
-
(2006)
Curr Top Med Chem
, vol.6
, pp. 1117-1127
-
-
Haystead, T.A.1
-
24
-
-
0036606332
-
Degradation of HER2 by ansamycins induces growth arrest and apoptosis in cells with HER2 overexpression via a HER3, phosphatidylinositol 3′-kinase-AKT-dependent pathway
-
Munster PN, Marchion DC, Basso AD, Rosen N. Degradation of HER2 by ansamycins induces growth arrest and apoptosis in cells with HER2 overexpression via a HER3, phosphatidylinositol 3′-kinase-AKT-dependent pathway. Cancer Res 2002;62:3132-7.
-
(2002)
Cancer Res
, vol.62
, pp. 3132-3137
-
-
Munster, P.N.1
Marchion, D.C.2
Basso, A.D.3
Rosen, N.4
-
25
-
-
3042553538
-
Targeting wide-range oncogenic transformation via PU24FCl, a specific inhibitor of tumor Hsp90
-
Vilenchik M, Solit D, Basso A, et al. Targeting wide-range oncogenic transformation via PU24FCl, a specific inhibitor of tumor Hsp90. Chem Biol 2004;11:787-97.
-
(2004)
Chem Biol
, vol.11
, pp. 787-797
-
-
Vilenchik, M.1
Solit, D.2
Basso, A.3
-
26
-
-
0038404927
-
Inhibition of heat shock protein 90 function down-regulates akt kinase and sensitizes tumors to Taxol
-
Solit DB, Basso AD, Olshen AB, Scher HI, Rosen N. Inhibition of heat shock protein 90 function down-regulates akt kinase and sensitizes tumors to Taxol. Cancer Res 2003;63:2139-44.
-
(2003)
Cancer Res
, vol.63
, pp. 2139-2144
-
-
Solit, D.B.1
Basso, A.D.2
Olshen, A.B.3
Scher, H.I.4
Rosen, N.5
-
27
-
-
0142027766
-
Angiogenesis impairment in Id-deficient mice cooperates with an Hsp90 inhibitor to completely suppress HER2/neu-dependent breast tumors
-
de Candia P, Solit DB, Giri D, et al. Angiogenesis impairment in Id-deficient mice cooperates with an Hsp90 inhibitor to completely suppress HER2/neu-dependent breast tumors. Proc Natl Acad Sci U S A 2003;100:12337-42.
-
(2003)
Proc Natl Acad Sci U S A
, vol.100
, pp. 12337-12342
-
-
de Candia, P.1
Solit, D.B.2
Giri, D.3
-
28
-
-
33746899628
-
Association with HSP90 inhibits Cbl-mediated down-regulation of mutant epidermal growth factor receptors
-
Yang S, Qu S, Perez-Tores M, et al. Association with HSP90 inhibits Cbl-mediated down-regulation of mutant epidermal growth factor receptors. Cancer Res 2006;66:6990-7.
-
(2006)
Cancer Res
, vol.66
, pp. 6990-6997
-
-
Yang, S.1
Qu, S.2
Perez-Tores, M.3
-
29
-
-
0141484615
-
A high-affinity conformation of Hsp90 confers tumour selectivity on Hsp90 inhibitors
-
Kamal A, Thao L, Sensintaffar J, et al. A high-affinity conformation of Hsp90 confers tumour selectivity on Hsp90 inhibitors. Nature 2003;425:407-10.
-
(2003)
Nature
, vol.425
, pp. 407-410
-
-
Kamal, A.1
Thao, L.2
Sensintaffar, J.3
-
30
-
-
2442464375
-
Role of the cytosolic chaperones Hsp70 and Hsp90 in maturation of the cardiac potassium channel HERG
-
Ficker E, Dennis AT, Wang L, Brown AM. Role of the cytosolic chaperones Hsp70 and Hsp90 in maturation of the cardiac potassium channel HERG. Circ Res 2003;92:e87-100.
-
(2003)
Circ Res
, vol.92
-
-
Ficker, E.1
Dennis, A.T.2
Wang, L.3
Brown, A.M.4
-
31
-
-
20144375312
-
Phase I and pharmacologic study of 17-(allylamino)-17-demethoxygeldanamycin in adult patients with solid tumors
-
Grem JL, Morrison G, Guo XD, et al. Phase I and pharmacologic study of 17-(allylamino)-17-demethoxygeldanamycin in adult patients with solid tumors. J Clin Oncol 2005;23:1885-93.
-
(2005)
J Clin Oncol
, vol.23
, pp. 1885-1893
-
-
Grem, J.L.1
Morrison, G.2
Guo, X.D.3
-
32
-
-
20044384168
-
Phase I trial of 17-allylamino-17- demethoxygeldanamycin in patients with advanced cancer
-
Goetz MP, Toft D, Reid J, et al. Phase I trial of 17-allylamino-17- demethoxygeldanamycin in patients with advanced cancer. J Clin Oncol 2005;23:1078-87.
-
(2005)
J Clin Oncol
, vol.23
, pp. 1078-1087
-
-
Goetz, M.P.1
Toft, D.2
Reid, J.3
-
33
-
-
23044441106
-
Phase I pharmacokinetic and pharmacodynamic study of 17-allylamino, 17-demethoxygeldanamycin in patients with advanced malignancies
-
Banerji U, O'Donnell A, Scurr M, et al. Phase I pharmacokinetic and pharmacodynamic study of 17-allylamino, 17-demethoxygeldanamycin in patients with advanced malignancies. J Clin Oncol 2005;23:4152-61.
-
(2005)
J Clin Oncol
, vol.23
, pp. 4152-4161
-
-
Banerji, U.1
O'Donnell, A.2
Scurr, M.3
-
34
-
-
20944444881
-
Phase I pharmacokinetic- pharmacodynamic study of 17-(allylamino)-17-demethoxygeldanamycin (17AAG, NSC 330507), a novel inhibitor of heat shock protein 90, in patients with refractory advanced cancers
-
Ramanathan RK, Trump DL, Eiseman JL, et al. Phase I pharmacokinetic- pharmacodynamic study of 17-(allylamino)-17-demethoxygeldanamycin (17AAG, NSC 330507), a novel inhibitor of heat shock protein 90, in patients with refractory advanced cancers. Clin Cancer Res 2005;11:3385-91.
-
(2005)
Clin Cancer Res
, vol.11
, pp. 3385-3391
-
-
Ramanathan, R.K.1
Trump, D.L.2
Eiseman, J.L.3
-
35
-
-
34250197902
-
Phase I trial of 17-allylamino-17- demethoxygeldanamycin in patients with advanced cancer
-
Solit DB, Ivy SP, Kopil C, et al. Phase I trial of 17-allylamino-17- demethoxygeldanamycin in patients with advanced cancer. Clin Cancer Res 2007;13:1775-82.
-
(2007)
Clin Cancer Res
, vol.13
, pp. 1775-1782
-
-
Solit, D.B.1
Ivy, S.P.2
Kopil, C.3
-
36
-
-
21244462689
-
In vivo antitumor efficacy of 17-DMAG (17-dimethylaminoethylamino-17-demethoxygeldanamycin hydrochloride), a water-soluble geldanamycin derivative
-
Hollingshead M, Alley M, Burger AM, et al. In vivo antitumor efficacy of 17-DMAG (17-dimethylaminoethylamino-17-demethoxygeldanamycin hydrochloride), a water-soluble geldanamycin derivative. Cancer Chemother Pharmacol 2005;56:115-25.
-
(2005)
Cancer Chemother Pharmacol
, vol.56
, pp. 115-125
-
-
Hollingshead, M.1
Alley, M.2
Burger, A.M.3
-
37
-
-
33746662241
-
Design, synthesis, and biological evaluation of hydroquinone derivatives of 17-amino-17-demethoxygeldanamycin as potent, water-soluble inhibitors of Hsp90
-
Ge J, Normant E, Porter JR, et al. Design, synthesis, and biological evaluation of hydroquinone derivatives of 17-amino-17-demethoxygeldanamycin as potent, water-soluble inhibitors of Hsp90. J Med Chem 2006;49:4606-15.
-
(2006)
J Med Chem
, vol.49
, pp. 4606-4615
-
-
Ge, J.1
Normant, E.2
Porter, J.R.3
|