-
1
-
-
0034614637
-
The hallmarks of cancer
-
Hanahan, D., and Weinberg, R. A. The hallmarks of cancer. Cell, 100: 57-70, 2000.
-
(2000)
Cell
, vol.100
, pp. 57-70
-
-
Hanahan, D.1
Weinberg, R.A.2
-
2
-
-
0033986112
-
Anticancer drug targets: Growth factors and growth factor signaling
-
Gibbs, J. B. Anticancer drug targets: growth factors and growth factor signaling. J. Clin. Investig., 105: 9-13, 2000.
-
(2000)
J. Clin. Investig.
, vol.105
, pp. 9-13
-
-
Gibbs, J.B.1
-
3
-
-
0034489914
-
Efficacy of cytotoxic agents against human tumor xenografts is markedly enhanced by coadministration of ZD1839 (Iressa), an inhibitor of EGFR tyrosine kinase
-
Sirotnak, F. M., Zakowski, M. F., Miller, V. A., Scher, H. I., and Kris, M. G. Efficacy of cytotoxic agents against human tumor xenografts is markedly enhanced by coadministration of ZD1839 (Iressa), an inhibitor of EGFR tyrosine kinase. Clin. Cancer Res., 6: 4885-4892, 2000.
-
(2000)
Clin. Cancer Res.
, vol.6
, pp. 4885-4892
-
-
Sirotnak, F.M.1
Zakowski, M.F.2
Miller, V.A.3
Scher, H.I.4
Kris, M.G.5
-
4
-
-
0036219609
-
Hsp90 inhibitors as novel chemotherapeutic agents
-
Neckers, L. Hsp90 inhibitors as novel chemotherapeutic agents. Trends Mol. Med., 8: S55-S61, 2002.
-
(2002)
Trends Mol. Med.
, vol.8
-
-
Neckers, L.1
-
5
-
-
0035989680
-
HSP90 as a new therapeutic target for cancer therapy: The story unfolds
-
Workman, P., and Maloney, A. HSP90 as a new therapeutic target for cancer therapy: the story unfolds. Expert Opin. Biol. Ther., 2: 3-24, 2002.
-
(2002)
Expert Opin. Biol. Ther.
, vol.2
, pp. 3-24
-
-
Workman, P.1
Maloney, A.2
-
6
-
-
0023940887
-
Inhibition of transforming activity of tyrosin kinase oncogenes by herbimycin A
-
Uehara, Y., Myrakawi, Y., Mizuno, S., and Kawai, S. Inhibition of transforming activity of tyrosin kinase oncogenes by herbimycin A. Virology. 164: 294-298, 1988.
-
(1988)
Virology
, vol.164
, pp. 294-298
-
-
Uehara, Y.1
Myrakawi, Y.2
Mizuno, S.3
Kawai, S.4
-
7
-
-
0028064940
-
Inhibition of heat-shock protein Hsp90-pp6βv-src heteroprotein complex formation by benzoquinone ansamycins: Essential role for stress proteins in oncogenic transformation
-
Whitesell, L., Mimnaugh, E. G., De Costa, B., Myers, C. E., and Neckers, L. M. Inhibition of heat-shock protein Hsp90-pp6βv-src heteroprotein complex formation by benzoquinone ansamycins: essential role for stress proteins in oncogenic transformation. Proc. Natl. Acad. Sci. USA, 91: 8324-8328, 1994.
-
(1994)
Proc. Natl. Acad. Sci. USA
, vol.91
, pp. 8324-8328
-
-
Whitesell, L.1
Mimnaugh, E.G.2
De Costa, B.3
Myers, C.E.4
Neckers, L.M.5
-
8
-
-
0034892432
-
Hsp90: Chaperoning signal transduction
-
Richter, K., and Buchner, J. Hsp90: Chaperoning signal transduction. J. Cell. Physiol., 188: 281-290, 2001.
-
(2001)
J. Cell. Physiol.
, vol.188
, pp. 281-290
-
-
Richter, K.1
Buchner, J.2
-
9
-
-
0030863995
-
The amino-terminal domain of heat shock protein 90 (hsp90) that binds geldanamycin is an ATP/ADP switch domain that regulates hsp90 conformation
-
Grenert, J. P., Sullivan, W. P., Fadden, P., Haystead, T. A. J., Clark, J., Mimnaugh, E., Krutzsch, H., Ochel, H. J., Schulle, T. W., Sausville, E., Neckers, L. M., and Toft, D. O. The amino-terminal domain of heat shock protein 90 (hsp90) that binds geldanamycin is an ATP/ADP switch domain that regulates hsp90 conformation. J. Biol. Chem., 272: 23843-23850, 1997.
-
(1997)
J. Biol. Chem.
, vol.272
, pp. 23843-23850
-
-
Grenert, J.P.1
Sullivan, W.P.2
Fadden, P.3
Haystead, T.A.J.4
Clark, J.5
Mimnaugh, E.6
Krutzsch, H.7
Ochel, H.J.8
Schulle, T.W.9
Sausville, E.10
Neckers, L.M.11
Toft, D.O.12
-
10
-
-
0030878952
-
Geldanamycin-stimulated destabilization of mutated p53 is mediated by proteasome in vivo
-
Whitesell, L., Sutphin, P., Wen, G. A., Schulte, T., Blagosklonny, M. V., and Neckers, L. Geldanamycin-stimulated destabilization of mutated p53 is mediated by proteasome in vivo. Oncogene, 14: 2809-2816, 1997.
-
(1997)
Oncogene
, vol.14
, pp. 2809-2816
-
-
Whitesell, L.1
Sutphin, P.2
Wen, G.A.3
Schulte, T.4
Blagosklonny, M.V.5
Neckers, L.6
-
11
-
-
0031590456
-
Geldanamycin-induced destabilization of Raf-1 involves the proteasome
-
Schulte, T. W., Won, G. A., and Neckers, L. M. Geldanamycin-induced destabilization of Raf-1 involves the proteasome. Biochem. Biophys. Res. Commun., 239: 655-659, 1997.
-
(1997)
Biochem. Biophys. Res. Commun.
, vol.239
, pp. 655-659
-
-
Schulte, T.W.1
Won, G.A.2
Neckers, L.M.3
-
12
-
-
0030612135
-
erB2, Raf- 1 and mutant p53 proteins by geldanamycin derivatives correlates with antiproliferative activity
-
erB2, Raf- 1 and mutant p53 proteins by geldanamycin derivatives correlates with antiproliferative activity. Cancer Chemother. Pharmacol., 40: 60-64, 1997.
-
(1997)
Cancer Chemother. Pharmacol.
, vol.40
, pp. 60-64
-
-
Won, G.A.1
Schnur, R.C.2
Neckers, L.3
Blagosklonny, M.V.4
-
13
-
-
0029056501
-
Preclinical pharmacological evaluation of geldanamycin as an antitumor agent
-
Supko, J. G., Hickman, R. L., Grever, M. R., and Malspeis, L. Preclinical pharmacological evaluation of geldanamycin as an antitumor agent. Cancer Chemother. Pharmacol., 36: 305-315, 1995.
-
(1995)
Cancer Chemother. Pharmacol.
, vol.36
, pp. 305-315
-
-
Supko, J.G.1
Hickman, R.L.2
Grever, M.R.3
Malspeis, L.4
-
14
-
-
0031875042
-
The benzoquinone ansamycin 17-allylamino-17-demethoxy-geldanamycin binds to HSP90 and shares important biologic activities with geldanamycin
-
Schulte, T., and Neckers, L. The benzoquinone ansamycin 17-allylamino-17-demethoxy-geldanamycin binds to HSP90 and shares important biologic activities with geldanamycin. Cancer Chemother. Pharmacol., 42: 273-279, 1998.
-
(1998)
Cancer Chemother. Pharmacol.
, vol.42
, pp. 273-279
-
-
Schulte, T.1
Neckers, L.2
-
15
-
-
0033579175
-
DT-Diaphorase expression and tumor cells sensitivity to 17-allylamino, 17-demethoxygeldanamycin, an inhibitor of heat shock protein 90
-
Kelland, L. R., Sharp, S. Y., Rogers, P. M., Myers, T. G., and Workman, P. DT-Diaphorase expression and tumor cells sensitivity to 17-allylamino, 17-demethoxygeldanamycin, an inhibitor of heat shock protein 90. J. Natl. Cancer Inst. (Bethesda), 91: 1940-1949, 1999.
-
(1999)
J. Natl. Cancer Inst. (Bethesda)
, vol.91
, pp. 1940-1949
-
-
Kelland, L.R.1
Sharp, S.Y.2
Rogers, P.M.3
Myers, T.G.4
Workman, P.5
-
16
-
-
0035872442
-
Inhibition of signal transduction by the Hsp90 inhibitor 17-allylamino-17-demethoxygeldanamycin results in cytostasis and apoptosis
-
Hostein, I., Robertson, D., DiStefano, F., Workman, P., and Clarke, P. A. Inhibition of signal transduction by the Hsp90 inhibitor 17-allylamino-17-demethoxygeldanamycin results in cytostasis and apoptosis. Cancer Res., 61: 4003-4009, 2001.
-
(2001)
Cancer Res.
, vol.61
, pp. 4003-4009
-
-
Hostein, I.1
Robertson, D.2
DiStefano, F.3
Workman, P.4
Clarke, P.A.5
-
17
-
-
0035872396
-
Disruption of the EF-2 kiaase/Hsp90 protein complex: A possible mechanism to inhibit glioblastoma by Geldanamycin
-
Yang, J., Yang, J-M., Iannone, M., Shih, J., Lin, Y., and Hait, W. N. Disruption of the EF-2 kiaase/Hsp90 protein complex: a possible mechanism to inhibit glioblastoma by Geldanamycin. Cancer Res., 61: 4010-4016, 2001.
-
(2001)
Cancer Res.
, vol.61
, pp. 4010-4016
-
-
Yang, J.1
Yang, J.-M.2
Iannone, M.3
Shih, J.4
Lin, Y.5
Hait, W.N.6
-
18
-
-
0035300564
-
Inhibition of heat shock protein 90 function by ansamycins causes the morphological and functional differentiation of breast cancer cells
-
Münster, P. N., Srethapakdi, M., Moasser, M. M., and Rosen, N. Inhibition of heat shock protein 90 function by ansamycins causes the morphological and functional differentiation of breast cancer cells. Cancer Res., 61: 2945-2952, 2001.
-
(2001)
Cancer Res.
, vol.61
, pp. 2945-2952
-
-
Münster, P.N.1
Srethapakdi, M.2
Moasser, M.M.3
Rosen, N.4
-
19
-
-
0000165431
-
Phase I pharmacological study of 17-(allylamino)-17-demethoxygeldanamycin (AAG) in adult patients with advanced solid tumors
-
Wilson, R. H., Takimoto, C. H., Agnew. E. B., Morrison, G., Grollman, F., Thomas, R. R., Saif, M. W., Hopkins, J., Allegra, C., Grochow, L., Szabo, E., Hamilton, J. M., Monhan B. P., Neckers, L., and Grem, J. L. Phase I pharmacological study of 17-(allylamino)-17-demethoxygeldanamycin (AAG) in adult patients with advanced solid tumors. Proc. Am. Soc. Clin. Oncol. Annu. Meet., 20: 82a, 2001.
-
(2001)
Proc. Am. Soc. Clin. Oncol. Annu. Meet.
, vol.20
-
-
Wilson, R.H.1
Takimoto, C.H.2
Agnew, E.B.3
Morrison, G.4
Grollman, F.5
Thomas, R.R.6
Saif, M.W.7
Hopkins, J.8
Allegra, C.9
Grochow, L.10
Szabo, E.11
Hamilton, J.M.12
Monhan, B.P.13
Neckers, L.14
Grem, J.L.15
-
20
-
-
0000235617
-
Phase 1 trial of 17-(allylamino)-17-demethoxygeldanamycin (17AAG) in patients (pts) with advanced solid malignancies
-
Münster, P. N., Tong, W., Schwartz, L., Larson, S., Keneson, K., De La Cruz, A., Rosen, N., and Scher, H. Phase 1 trial of 17-(allylamino)-17-demethoxygeldanamycin (17AAG) in patients (pts) with advanced solid malignancies. Proc. Am. Soc. Clin. Oncol. Annu. Meet., 20: 83a, 2001.
-
(2001)
Proc. Am. Soc. Clin. Oncol. Annu. Meet.
, vol.20
-
-
Münster, P.N.1
Tong, W.2
Schwartz, L.3
Larson, S.4
Keneson, K.5
De La Cruz, A.6
Rosen, N.7
Scher, H.8
-
21
-
-
0034902025
-
IV, Tabibi, E., and Schrump, D. S. Enhancement of paclitaxel-mediated cytotoxicity in lung cancer cells by 17-allylamino geldanamycin: In vitro and in vivo analysis
-
Nguyen, D. M., Logang, D., Chen, A., Stewart, J. H., IV, Tabibi, E., and Schrump, D. S. Enhancement of paclitaxel-mediated cytotoxicity in lung cancer cells by 17-allylamino geldanamycin: in vitro and in vivo analysis. Ann. Thorac. Surg., 72: 371-379, 2001.
-
(2001)
Ann. Thorac. Surg.
, vol.72
, pp. 371-379
-
-
Nguyen, D.M.1
Logang, D.2
Chen, A.3
Stewart, J.H.4
-
22
-
-
0034890377
-
Modulation of Hsp90 function by ansamycins sensitizes breast cancer cells to chemotherapy-induced apoptosis in RB- and schedule-dependent manner
-
Münster, P. N., Basso, A., Solit, D., Norton, L., and Rosen, N. Modulation of Hsp90 function by ansamycins sensitizes breast cancer cells to chemotherapy-induced apoptosis in RB- and schedule-dependent manner. Clin. Cancer Res., 7: 2228-2236, 2001.
-
(2001)
Clin. Cancer Res.
, vol.7
, pp. 2228-2236
-
-
Münster, P.N.1
Basso, A.2
Solit, D.3
Norton, L.4
Rosen, N.5
-
23
-
-
0021112076
-
Anthracycline-binding induced DNA stiffening, bending and elongation: Stereochemical implications from viscometric investigations
-
Reinert, K. E. Anthracycline-binding induced DNA stiffening, bending and elongation: stereochemical implications from viscometric investigations. Nucleic Acid Res., 11: 3411-3440, 1983.
-
(1983)
Nucleic Acid Res.
, vol.11
, pp. 3411-3440
-
-
Reinert, K.E.1
-
24
-
-
0002380701
-
Platinim complexes for the treatment of cancer: Why the search goes on
-
B. Lippert (ed.), Zurich, Switzerland: Verlag Helvetica Chimica Acta
-
Rosenberg, B. Platinim complexes for the treatment of cancer: why the search goes on. In: B. Lippert (ed.), Cisplatin: Chemistry and Biochemistry of a Leading Anticancer Drug, p. 3. Zurich, Switzerland: Verlag Helvetica Chimica Acta, 1999.
-
(1999)
Cisplatin: Chemistry and Biochemistry of a Leading Anticancer Drug
, pp. 3
-
-
Rosenberg, B.1
-
25
-
-
0001904644
-
Clinical status of cisplatin, carboplatin and other platinum-based antitumor drugs
-
B. Lippert (ed.), Zurich, Switzerland: Verlag Helvetica Chimica Acta
-
O'Dwyer, P., Stevenson, J., and Johnson, S. Clinical status of cisplatin, carboplatin and other platinum-based antitumor drugs. In: B. Lippert (ed.), Cisplatin: Chemistry and Biochemistry of a Leading Anticancer Drug, p. 31. Zurich, Switzerland: Verlag Helvetica Chimica Acta, 1999.
-
(1999)
Cisplatin: Chemistry and Biochemistry of a Leading Anticancer Drug
, pp. 31
-
-
O'Dwyer, P.1
Stevenson, J.2
Johnson, S.3
-
26
-
-
0001323706
-
Cisplatin and its analogues
-
V. T. DeVita, S. Hellman, and S. A. Rosenberg (eds.). Philadelphia: Lippincott, Williams & Wilkins
-
Johnson, S. W., Stevenson, P. J., and O'Dwyer, P. J. Cisplatin and its analogues. In: V. T. DeVita, S. Hellman, and S. A. Rosenberg (eds.). Cancer: Principles and Practice of Oncology, Ed. 6, pp. 377-388. Philadelphia: Lippincott, Williams & Wilkins, 2001.
-
(2001)
Cancer: Principles and Practice of Oncology, Ed. 6
, pp. 377-388
-
-
Johnson, S.W.1
Stevenson, P.J.2
O'Dwyer, P.J.3
-
27
-
-
0035060354
-
Is cisplatin-induced death always produced by apoptosis?
-
Gonzales, V. M., Fuertes, M. A., Alonso, C., and Perez, J. M. Is cisplatin-induced death always produced by apoptosis? Mol. Pharmacol., 59: 657-663, 2001.
-
(2001)
Mol. Pharmacol.
, vol.59
, pp. 657-663
-
-
Gonzales, V.M.1
Fuertes, M.A.2
Alonso, C.3
Perez, J.M.4
-
28
-
-
0031966318
-
Chemosensitivity of solid tumor cells in vitro related to activation of the CD95 system
-
Fulda, S., Los, M., Friesen, C., and Debatin, K-M. Chemosensitivity of solid tumor cells in vitro related to activation of the CD95 system. Int. J. Cancer, 76: 105-114, 1998.
-
(1998)
Int. J. Cancer
, vol.76
, pp. 105-114
-
-
Fulda, S.1
Los, M.2
Friesen, C.3
Debatin, K.-M.4
-
29
-
-
0032479165
-
Abrogation of mitochondrial cytochrome C release and caspase-3 activation in acquired multidrug resistance
-
Kojima, H., Eodo, K., Moriyama, H., Tanaka, Y., Alnemri, E. S., Slapak, C. A., Teicher, B., Kufe, D., and Datta, R. Abrogation of mitochondrial cytochrome C release and caspase-3 activation in acquired multidrug resistance. J. Biol. Chem., 273: 16647-16650, 1998.
-
(1998)
J. Biol. Chem.
, vol.273
, pp. 16647-16650
-
-
Kojima, H.1
Eodo, K.2
Moriyama, H.3
Tanaka, Y.4
Alnemri, E.S.5
Slapak, C.A.6
Teicher, B.7
Kufe, D.8
Datta, R.9
-
31
-
-
0034909622
-
Mechanism of growth-inhibitory effect of cisplatin on human pancreatic cancer cells and status of p53 gene
-
Seki, T., Ohba, N., Makino, R., Funatomi, H., and Mitamura, K. Mechanism of growth-inhibitory effect of cisplatin on human pancreatic cancer cells and status of p53 gene. Anticancer Res., 21: 1919-1924, 2001.
-
(2001)
Anticancer Res.
, vol.21
, pp. 1919-1924
-
-
Seki, T.1
Ohba, N.2
Makino, R.3
Funatomi, H.4
Mitamura, K.5
-
32
-
-
0032949934
-
Cisplatin-induced activation of mitogen-activated protein kinases in ovarian carcinoma cells: Inhibition of extracellular signal-regulated kinase activity increases sensitivity to cisplatin
-
Persons, D. L., Yazlovitskaya, E. M., Cui, W., and Pelling, J. C. Cisplatin-induced activation of mitogen-activated protein kinases in ovarian carcinoma cells: inhibition of extracellular signal-regulated kinase activity increases sensitivity to cisplatin. Clin. Cancer Res., 5: 1007-1014, 1999.
-
(1999)
Clin. Cancer Res.
, vol.5
, pp. 1007-1014
-
-
Persons, D.L.1
Yazlovitskaya, E.M.2
Cui, W.3
Pelling, J.C.4
-
33
-
-
0034671751
-
Requirement for ERK activation in cisplatin-induced apoptosis
-
Wang, X., Martindale, J. L., and Holbrook, N. J. Requirement for ERK activation in cisplatin-induced apoptosis. J. Biol. Chem., 275: 39435-39443, 2000.
-
(2000)
J. Biol. Chem.
, vol.275
, pp. 39435-39443
-
-
Wang, X.1
Martindale, J.L.2
Holbrook, N.J.3
-
34
-
-
0032576868
-
Cisplatin induces a persistent activation of JNK that is related to cell death
-
Sanchez-Perez, I., Murguia, J. R., and Perona, R. Cisplatin induces a persistent activation of JNK that is related to cell death. Oncogene, 16: 533-540, 1998.
-
(1998)
Oncogene
, vol.16
, pp. 533-540
-
-
Sanchez-Perez, I.1
Murguia, J.R.2
Perona, R.3
-
35
-
-
0033615657
-
Inhibition of extracellular signal-regulated protein kinase or c-Jun N-terminal protein kinase cascade, differentially activated by cisplatin, sensitized human ovarian cancer cell line
-
Hayakawa, J., Ohmich, M., Kurachi, H., Ikegami, H., Kimura, A., Matsuoka, T., Jikihara, H., Mercola, D., and Murata, Y. Inhibition of extracellular signal-regulated protein kinase or c-Jun N-terminal protein kinase cascade, differentially activated by cisplatin, sensitized human ovarian cancer cell line. J. Biol. Chem., 274: 31648-31654, 1999.
-
(1999)
J. Biol. Chem.
, vol.274
, pp. 31648-31654
-
-
Hayakawa, J.1
Ohmich, M.2
Kurachi, H.3
Ikegami, H.4
Kimura, A.5
Matsuoka, T.6
Jikihara, H.7
Mercola, D.8
Murata, Y.9
-
36
-
-
0034193343
-
A role for p38 mitogen-activated protein kinase pathway in the transcriptional activation of p53 on genotoxic stress by chemotherapeutic agents
-
Sanches-Prieto, R., Rojas, J. M., Taya, Y., and Gutkind, S. A role for p38 mitogen-activated protein kinase pathway in the transcriptional activation of p53 on genotoxic stress by chemotherapeutic agents. Cancer Res., 60: 2464-2472, 2000.
-
(2000)
Cancer Res.
, vol.60
, pp. 2464-2472
-
-
Sanches-Prieto, R.1
Rojas, J.M.2
Taya, Y.3
Gutkind, S.4
-
37
-
-
0033566822
-
Effects of geldanamycin on signaling through activator-protein 1 in hypoxic HT29 human colon adenocarcinoma cells
-
Vasilevskaya, I. A., and O'Dwyer, P. J. Effects of geldanamycin on signaling through activator-protein 1 in hypoxic HT29 human colon adenocarcinoma cells. Cancer Res., 59: 3935-3940, 1999.
-
(1999)
Cancer Res.
, vol.59
, pp. 3935-3940
-
-
Vasilevskaya, I.A.1
O'Dwyer, P.J.2
-
38
-
-
0021061819
-
Rapid colorimetric assay for cellular growth and survival: Application to proliferation and cytotoxicity assays
-
Mosmann, T. Rapid colorimetric assay for cellular growth and survival: application to proliferation and cytotoxicity assays. J. Immunol. Methods, 65: 55-63, 1983.
-
(1983)
J. Immunol. Methods
, vol.65
, pp. 55-63
-
-
Mosmann, T.1
-
39
-
-
0024582179
-
Lack of in vitro synergy between etoposide and cisdiammine-dichloroplatinum (II)
-
Tsai, C-M., Gazdar, A. F., Venzon, D. J., Steinberg, S. M., Dedrick, R. L., Mulshine, J. L., and Kramer, B. S. Lack of in vitro synergy between etoposide and cisdiammine-dichloroplatinum (II). Cancer Res., 49: 2390-2397, 1989.
-
(1989)
Cancer Res.
, vol.49
, pp. 2390-2397
-
-
Tsai, C.-M.1
Gazdar, A.F.2
Venzon, D.J.3
Steinberg, S.M.4
Dedrick, R.L.5
Mulshine, J.L.6
Kramer, B.S.7
-
40
-
-
0028153260
-
Computerized quantification of synergism and antagonism of taxol, topotecan, and cisplatin against human teratocarcinoma cell growth: A rational approach to clinical protocol design
-
Chou, T-C., Motzer, R. J., Tong, Y., and Bosl, G. J. Computerized quantification of synergism and antagonism of taxol, topotecan, and cisplatin against human teratocarcinoma cell growth: a rational approach to clinical protocol design. J. Natl. Cancer. Inst. (Bethesda), 86: 1517-1524, 1994.
-
(1994)
J. Natl. Cancer. Inst. (Bethesda)
, vol.86
, pp. 1517-1524
-
-
Chou, T.-C.1
Motzer, R.J.2
Tong, Y.3
Bosl, G.J.4
-
41
-
-
0034985847
-
p53 protein at the huh of cellular DNA damage response pathways through sequence-specific and non-sequence-specific DNA binding
-
Liu, Y., and Kulesz-Martin, M. p53 protein at the huh of cellular DNA damage response pathways through sequence-specific and non-sequence-specific DNA binding. Carcinogenesis (Lond.), 22: 851-860, 2001.
-
(2001)
Carcinogenesis (Lond.)
, vol.22
, pp. 851-860
-
-
Liu, Y.1
Kulesz-Martin, M.2
-
42
-
-
0032771826
-
Inhibition of Jun kinase pathway blocks DNA repair, enhances p53-mediated apoptosis and promotes gene amplification
-
Gjerset, R. A., Lebedeva, S., Haghigni, A. Turia, S. T., and Mercola, D. Inhibition of Jun kinase pathway blocks DNA repair, enhances p53-mediated apoptosis and promotes gene amplification. Cell Growth Differ., 10: 545-554, 1999.
-
(1999)
Cell Growth Differ.
, vol.10
, pp. 545-554
-
-
Gjerset, R.A.1
Lebedeva, S.2
Haghigni, A.3
Turia, S.T.4
Mercola, D.5
-
43
-
-
0036569631
-
Reversal of cisplatin resistance in human ovarian cancer cell lines by a c-jun oligodeoxynucleotide (ISIS 10582): Evidence for the role of transcription factor overexpression in determining resistant phenotype
-
Pan, B., Yao, K-S., Monia, B., Dean, N. M. McKay, R. A., Hamilton, T. C., and O'Dwyer, P. J. Reversal of cisplatin resistance in human ovarian cancer cell lines by a c-jun oligodeoxynucleotide (ISIS 10582): evidence for the role of transcription factor overexpression in determining resistant phenotype. Biochem. Pharmacol., 63: 1699-1707, 2002.
-
(2002)
Biochem. Pharmacol.
, vol.63
, pp. 1699-1707
-
-
Pan, B.1
Yao, K.-S.2
Monia, B.3
Dean, N.M.4
McKay, R.A.5
Hamilton, T.C.6
O'Dwyer, P.J.7
-
44
-
-
0036098552
-
AP-1 as a regulator of cell life and death
-
Shaulian, E., and Katin, M. AP-1 as a regulator of cell life and death. Nat. Cell Biol., 4: E131-E136, 2002.
-
(2002)
Nat. Cell Biol.
, vol.4
-
-
Shaulian, E.1
Katin, M.2
-
45
-
-
0032753492
-
Sequence-dependent enhancement of paclitaxel toxicity in non-small cell lung cancer by 17-allylamino 17-demethoxy-geldanamycin
-
Nguen, D. M., Chen, A., Mixon, A., and Schrump, D. S. Sequence-dependent enhancement of paclitaxel toxicity in non-small cell lung cancer by 17-allylamino 17-demethoxy-geldanamycin. J. Thorac. Cardiovasc. Surg., 118: 908-915, 1999.
-
(1999)
J. Thorac. Cardiovasc. Surg.
, vol.118
, pp. 908-915
-
-
Nguen, D.M.1
Chen, A.2
Mixon, A.3
Schrump, D.S.4
-
46
-
-
0033231024
-
A novel chaperone-activity-reducing mechanism of the 90-kDa molecular chaperone HSP90
-
Itoh, H., Ogura, M., Komatsuda, A., Wakui, H., Miura, A. B., and Tashima, Y. A novel chaperone-activity-reducing mechanism of the 90-kDa molecular chaperone HSP90. Biochem. J., 343: 697-703, 1999.
-
(1999)
Biochem. J.
, vol.343
, pp. 697-703
-
-
Itoh, H.1
Ogura, M.2
Komatsuda, A.3
Wakui, H.4
Miura, A.B.5
Tashima, Y.6
-
47
-
-
0034711270
-
The heat shock protein 90 antagonist novobiocin interacts with a previously unrecognized ATP-binding domain in the carboxyl-terminus of the chaperone
-
Marcu, M. G., Chadli, A., Bouhouche, I., Gatelli, M., and Neckers, L. M. The heat shock protein 90 antagonist novobiocin interacts with a previously unrecognized ATP-binding domain in the carboxyl-terminus of the chaperone. J. Biol. Chem., 275: 37181-37186, 2000.
-
(2000)
J. Biol. Chem.
, vol.275
, pp. 37181-37186
-
-
Marcu, M.G.1
Chadli, A.2
Bouhouche, I.3
Gatelli, M.4
Neckers, L.M.5
-
48
-
-
0036510547
-
A nucleotide-dependent molecular switch controls ATP binding at C-terminal dOmain of Hsp90: N-terminal nucleotide binding unmasks a C-terminal binding pocket
-
Soti, C., Racz, A., and Csermely, P. A nucleotide-dependent molecular switch controls ATP binding at C-terminal dOmain of Hsp90: N-terminal nucleotide binding unmasks a C-terminal binding pocket. J. Biol. Chem., 277: 7066-7075, 2002.
-
(2002)
J. Biol. Chem.
, vol.277
, pp. 7066-7075
-
-
Soti, C.1
Racz, A.2
Csermely, P.3
-
49
-
-
0033841622
-
Molecular mechanisms involved in cisplatin cytotoxicity
-
Jordan, P., and Carmo-Fonseca, M. Molecular mechanisms involved in cisplatin cytotoxicity. Cell. Mol. Life Sci., 57: 1229-1235, 2000.
-
(2000)
Cell. Mol. Life Sci.
, vol.57
, pp. 1229-1235
-
-
Jordan, P.1
Carmo-Fonseca, M.2
-
50
-
-
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
-
Münster, P. N., Marchion, D. C., Basso, A., and 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., 62: 3132-3137, 2002.
-
(2002)
Cancer Res.
, vol.62
, pp. 3132-3137
-
-
Münster, P.N.1
Marchion, D.C.2
Basso, A.3
Rosen, N.4
-
51
-
-
0034982174
-
Radicicol and geldanamycin prevent neurotoxic effects of anti-cancer drugs on cultured embryonic sensory neurons
-
Sano, M. Radicicol and geldanamycin prevent neurotoxic effects of anti-cancer drugs on cultured embryonic sensory neurons. Neuropharmacology, 40: 947-953, 2001.
-
(2001)
Neuropharmacology
, vol.40
, pp. 947-953
-
-
Sano, M.1
-
52
-
-
0034665461
-
p53 transcriptional activity is essential for p-53 dependent apoptosis following DNA damage
-
Chao, C. Saito, S., Kang, J., Anderson, C. W., Appella, E., and Xu, Y. p53 transcriptional activity is essential for p-53 dependent apoptosis following DNA damage. EMBO J., 19: 4967-4975, 2000.
-
(2000)
EMBO J.
, vol.19
, pp. 4967-4975
-
-
Chao, C.1
Saito, S.2
Kang, J.3
Anderson, C.W.4
Appella, E.5
Xu, Y.6
-
53
-
-
0032701521
-
Disruption of p53 in human cancer cells alters the responses to therapeutic agents
-
Bunz, F., Hwang, P. M., Torrance, C., Waldman, T., Zhang, Y. Dillehay, L., Williams, J. Lengauer, C., Kinzler, K. W., and Vogelstein, B. Disruption of p53 in human cancer cells alters the responses to therapeutic agents. J. Clin. Investig., 104: 263-269, 1999.
-
(1999)
J. Clin. Investig.
, vol.104
, pp. 263-269
-
-
Bunz, F.1
Hwang, P.M.2
Torrance, C.3
Waldman, T.4
Zhang, Y.5
Dillehay, L.6
Williams, J.7
Lengauer, C.8
Kinzler, K.W.9
Vogelstein, B.10
-
54
-
-
0031806708
-
Characterization of structural p53 mutants which show selective defects in apoptosis but not cell cycle arrest
-
Ryan, K. M., and Voudsen, K. H. Characterization of structural p53 mutants which show selective defects in apoptosis but not cell cycle arrest. Mol. Cell. Biol., 18: 3692-3698, 1998.
-
(1998)
Mol. Cell. Biol.
, vol.18
, pp. 3692-3698
-
-
Ryan, K.M.1
Voudsen, K.H.2
-
55
-
-
0033965487
-
p53 mutants have selective dominant-negative effects on apoptosis but not growth arrest in human cancer cell lines
-
Aurelio, O. N., Kong, X-T., Gupta, S., and Stanbridge, E. J. p53 mutants have selective dominant-negative effects on apoptosis but not growth arrest in human cancer cell lines. Mol. Cell. Biol., 20: 770-778, 2000.
-
(2000)
Mol. Cell. Biol.
, vol.20
, pp. 770-778
-
-
Aurelio, O.N.1
Kong, X.-T.2
Gupta, S.3
Stanbridge, E.J.4
-
56
-
-
0033971809
-
Drug-induced apoptosis in lung cancer cells is not mediated by the Fas/FasL (CD95/APO1) signaling pathway
-
Ferreira, C. G., Tolis, C., Span, S. W., Peters, G. J., van Lopik, T., Kummer, A. J., Pinedo, H. M., and Giaccone, G. Drug-induced apoptosis in lung cancer cells is not mediated by the Fas/FasL (CD95/APO1) signaling pathway. Clin. Cancer Res., 6: 203-212, 2000.
-
(2000)
Clin. Cancer Res.
, vol.6
, pp. 203-212
-
-
Ferreira, C.G.1
Tolis, C.2
Span, S.W.3
Peters, G.J.4
Van Lopik, T.5
Kummer, A.J.6
Pinedo, H.M.7
Giaccone, G.8
-
57
-
-
0033599527
-
STAT-1-independent up-regulation of procaspase -3 and -8 in cancer cells treated with cytotoxic drugs
-
Micheau, O., Hammann, A., Solary, E., and Dimanche-Boitrel, M-T. STAT-1-independent up-regulation of procaspase -3 and -8 in cancer cells treated with cytotoxic drugs. Biochem. Biophys. Res. Commun., 256: 603-607, 1999.
-
(1999)
Biochem. Biophys. Res. Commun.
, vol.256
, pp. 603-607
-
-
Micheau, O.1
Hammann, A.2
Solary, E.3
Dimanche-Boitrel, M.-T.4
-
58
-
-
0033583191
-
Fas ligandindependent, FADD-mediated activation of the Fas death pathway by anticancer drugs
-
Micheau, O., Solary, E., Hammann, A., and Dimanche-Boitrel, M-T. Fas ligandindependent, FADD-mediated activation of the Fas death pathway by anticancer drugs. J. Biol. Chem., 274: 7987-7992, 1999.
-
(1999)
J. Biol. Chem.
, vol.274
, pp. 7987-7992
-
-
Micheau, O.1
Solary, E.2
Hammann, A.3
Dimanche-Boitrel, M.-T.4
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