-
1
-
-
1542348477
-
Cancer statistics, 2004
-
(a) Jemal, A.; Tiwari, R. C.; Murray, T.; Ghafoor, A.; Samuels, A.; Ward, E.; Feuer, E. J.; Thun, M. J. Cancer Statistics, 2004. CA Cancer J. Clin. 2004, 54, 8-29.
-
(2004)
CA Cancer J. Clin.
, vol.54
, pp. 8-29
-
-
Jemal, A.1
Tiwari, R.C.2
Murray, T.3
Ghafoor, A.4
Samuels, A.5
Ward, E.6
Feuer, E.J.7
Thun, M.J.8
-
2
-
-
0004312588
-
-
American Cancer Society: Atlanta, GA
-
(b) American Cancer Society. Cancer Facts and Figures 2003; American Cancer Society: Atlanta, GA.
-
Cancer Facts and Figures 2003
-
-
-
3
-
-
0025975824
-
Physiological basis of endocrine therapy for prostatic cancer
-
McConnell, J. D. Physiological basis of endocrine therapy for prostatic cancer. Urol. Clin. North Am. 1991, 18, 1-13.
-
(1991)
Urol. Clin. North Am.
, vol.18
, pp. 1-13
-
-
McConnell, J.D.1
-
4
-
-
0014429464
-
The conversion of testosterone to 5α-androstan-17β-ol-3-one by rat prostate in vivo and in vitro
-
Bruchovsky, N.; Wilson, J. D. The conversion of testosterone to 5α-androstan-17β-ol-3-one by rat prostate in vivo and in vitro. J. Biol. Chem. 1968, 243, 2012-2021.
-
(1968)
J. Biol. Chem.
, vol.243
, pp. 2012-2021
-
-
Bruchovsky, N.1
Wilson, J.D.2
-
5
-
-
0001189211
-
Studies on prostatic cancer: 2. The effects of castration on advanced carcinoma of the prostate gland
-
Huggins, C.; Stephens, R. C.; Hudges, C. V. Studies on prostatic cancer: 2. The effects of castration on advanced carcinoma of the prostate gland. Arch. Surg. 1941, 43, 209-212.
-
(1941)
Arch. Surg.
, vol.43
, pp. 209-212
-
-
Huggins, C.1
Stephens, R.C.2
Hudges, C.V.3
-
6
-
-
0036559864
-
A history of prostate cancer treatment
-
Denmeade, S. R.; Isaacs, J. T. A history of prostate cancer treatment. Nat. Rev. Cancer 2002, 2, 389-396.
-
(2002)
Nat. Rev. Cancer
, vol.2
, pp. 389-396
-
-
Denmeade, S.R.1
Isaacs, J.T.2
-
7
-
-
0024324367
-
A controlled trial of leuprolide with and without flutamide in prostatic carcinoma
-
Crawford, E. D.; Eisenberger, M. A.; McLeod, D. G.; Spaulding, J. T.; Benson, R.; Dorr, F. A.; Blumstein, B. A.; Davis, M. A.; Goodman, P. J. A controlled trial of leuprolide with and without flutamide in prostatic carcinoma. N. Engl. J. Med. 1989, 321, 419-424.
-
(1989)
N. Engl. J. Med.
, vol.321
, pp. 419-424
-
-
Crawford, E.D.1
Eisenberger, M.A.2
McLeod, D.G.3
Spaulding, J.T.4
Benson, R.5
Dorr, F.A.6
Blumstein, B.A.7
Davis, M.A.8
Goodman, P.J.9
-
8
-
-
0000139770
-
Treatment of newly diagnosed state D2 prostate cancer with leuprolide and flutamide or leuprolide alone, Phase III: Intergroup study 0036
-
Crawford, E. D.; Allen, J. A. Treatment of newly diagnosed state D2 prostate cancer with leuprolide and flutamide or leuprolide alone, Phase III: intergroup study 0036. J. Urol. 1992, 147, 417A.
-
(1992)
J. Urol.
, vol.147
-
-
Crawford, E.D.1
Allen, J.A.2
-
9
-
-
0028309781
-
Role of maximal androgen blockade in advanced prostate cancer
-
Denis, L. Role of maximal androgen blockade in advanced prostate cancer. Prostate 1994, 5 (Suppl.), 17s-22s.
-
(1994)
Prostate
, vol.5
, Issue.SUPPL.
-
-
Denis, L.1
-
10
-
-
0842311632
-
The androgen axis in recurrent prostate cancer
-
Mohler, J. L.; Gregory, C. W.; Ford, H. O., III; Kim, D.; Weaver, C. M.; Petrusz, P.; Wilson, E. M.; French, F. S. The androgen axis in recurrent prostate cancer. Clin. Cancer Res. 2004, 10, 440-448.
-
(2004)
Clin. Cancer Res.
, vol.10
, pp. 440-448
-
-
Mohler, J.L.1
Gregory, C.W.2
Ford III, H.O.3
Kim, D.4
Weaver, C.M.5
Petrusz, P.6
Wilson, E.M.7
French, F.S.8
-
11
-
-
1842612441
-
Molecular determinants of resistance to antiandrogen therapy
-
Chen, C. D.; Welsbie, D. S.; Tran, C.; Baek, S. H.; Chen, R.; Vessella, R.; Rosenfeld, G. M.; Sawyer, C. L. Molecular determinants of resistance to antiandrogen therapy. Nat. Med. 2004, 10, 33-39.
-
(2004)
Nat. Med.
, vol.10
, pp. 33-39
-
-
Chen, C.D.1
Welsbie, D.S.2
Tran, C.3
Baek, S.H.4
Chen, R.5
Vessella, R.6
Rosenfeld, G.M.7
Sawyer, C.L.8
-
12
-
-
0032587401
-
17,20-lyase (CYP17): Potential agents for the treatment of prostate cancer
-
17,20-lyase (CYP17): Potential agents for the treatment of prostate cancer. Curr. Pharm. Des. 1999, 5, 163-180.
-
(1999)
Curr. Pharm. Des.
, vol.5
, pp. 163-180
-
-
Njar, V.C.O.1
Brodie, A.M.H.2
-
13
-
-
0026052296
-
21scc: One enzyme with two actions: Hydroxylase and lyase
-
21scc: one enzyme with two actions: Hydroxylase and lyase, J. Steroid Biochem. Mol. Biol. 1991, 40, 527-532.
-
(1991)
J. Steroid Biochem. Mol. Biol.
, vol.40
, pp. 527-532
-
-
Hall, P.F.1
-
14
-
-
0020577565
-
Ketoconazole: A novel and rapid treatment for advanced prostatic cancer
-
Trachtenberg, J.; Halpern, N.; Pont, A. Ketoconazole: A novel and rapid treatment for advanced prostatic cancer. J. Urol. 1983, 130, 152-153.
-
(1983)
J. Urol.
, vol.130
, pp. 152-153
-
-
Trachtenberg, J.1
Halpern, N.2
Pont, A.3
-
15
-
-
0003117730
-
Optimal dosing of ketoconazole and hydrocrtisone leads to long responses in hormone refractory prostate cancer
-
Abstract
-
Muscato, J. J.; Ahmann, K. M.; Johnson, W.; Wilding, W.; Monaghan, G.; Schlossman, D. M. Optimal dosing of ketoconazole and hydrocrtisone leads to long responses in hormone refractory prostate cancer. Proc. Am. Assoc. Cancer Res. 1994, 13, 22 (Abstract).
-
(1994)
Proc. Am. Assoc. Cancer Res.
, vol.13
, pp. 22
-
-
Muscato, J.J.1
Ahmann, K.M.2
Johnson, W.3
Wilding, W.4
Monaghan, G.5
Schlossman, D.M.6
-
16
-
-
0030999075
-
Ketoconazole retains activity in advanced prostate cancer patients with progression despite flutamide withdrawal
-
Small, E. J.; Baron, A. D.; Fippin, L.; Apodaca, D. Ketoconazole retains activity in advanced prostate cancer patients with progression despite flutamide withdrawal. J. Urol. 1997, 157, 1204-1207.
-
(1997)
J. Urol.
, vol.157
, pp. 1204-1207
-
-
Small, E.J.1
Baron, A.D.2
Fippin, L.3
Apodaca, D.4
-
17
-
-
3042784503
-
Hormonal impact of the 17α-hydroxylase/C17, 20-lyase inhibitors abiraterone acetate (CB7630) in patients with prostate cancer
-
O'Donnell, A.; Judson, I.; Dowsett, M.; Raynaud, F.; Dearnaley, D.; Mason, M.; Harland, S.; Robbins, A.; Halbert, G.; Nutley, B.; Jarman, M. Hormonal impact of the 17α-hydroxylase/C17, 20-lyase inhibitors abiraterone acetate (CB7630) in patients with prostate cancer. Br. J. Cancer 2004, 90, 2317-2325.
-
(2004)
Br. J. Cancer
, vol.90
, pp. 2317-2325
-
-
O'Donnell, A.1
Judson, I.2
Dowsett, M.3
Raynaud, F.4
Dearnaley, D.5
Mason, M.6
Harland, S.7
Robbins, A.8
Halbert, G.9
Nutley, B.10
Jarman, M.11
-
18
-
-
0034541199
-
Antiandrogenic effects of novel androgen synthesis inhibitors on hormone-dependent prostate cancer
-
Long, B. J.; Grigoryev, D. N.; Nnane, I. P.; Liu, Y.; Ling, Y.-Z.; Brodie, A. M. Antiandrogenic effects of novel androgen synthesis inhibitors on hormone-dependent prostate cancer. Cancer Res. 2000, 60, 6630-6640.
-
(2000)
Cancer Res.
, vol.60
, pp. 6630-6640
-
-
Long, B.J.1
Grigoryev, D.N.2
Nnane, I.P.3
Liu, Y.4
Ling, Y.-Z.5
Brodie, A.M.6
-
19
-
-
0034684250
-
Natural product-like combinatorial libraries based on privileged structures. 1. General principles and solid-phase synthesis of benzopyrans
-
Nicolaou, K. C.; Pfefferkorn, J. A.; Roecker, J. A.; Cao, G.-Q.; Barluenga, S.; Mitchell, H. J. Natural product-like combinatorial libraries based on privileged structures. 1. General principles and solid-phase synthesis of benzopyrans. J. Am. Chem. Soc. 2000, 122, 9939-9953. "Privileged structures", a term originally introduced by Evans et al. (J. Med. Chem. 1988, 31, 2235-2246) to describe structural motifs capable of interacting with a variety of unrelated molecular targets.
-
(2000)
J. Am. Chem. Soc.
, vol.122
, pp. 9939-9953
-
-
Nicolaou, K.C.1
Pfefferkorn, J.A.2
Roecker, J.A.3
Cao, G.-Q.4
Barluenga, S.5
Mitchell, H.J.6
-
20
-
-
0024239320
-
-
Nicolaou, K. C.; Pfefferkorn, J. A.; Roecker, J. A.; Cao, G.-Q.; Barluenga, S.; Mitchell, H. J. Natural product-like combinatorial libraries based on privileged structures. 1. General principles and solid-phase synthesis of benzopyrans. J. Am. Chem. Soc. 2000, 122, 9939-9953. "Privileged structures", a term originally introduced by Evans et al. (J. Med. Chem. 1988, 31, 2235-2246) to describe structural motifs capable of interacting with a variety of unrelated molecular targets.
-
(1988)
J. Med. Chem.
, vol.31
, pp. 2235-2246
-
-
-
21
-
-
0035705824
-
Novel steroidal pyrimidyl inhibitors of P450 17 (17α-hydroxylase/ C17-20-lyase)
-
(a) Haidar, S.; Ehmer, P. B.; Hartmann, R. W. Novel steroidal pyrimidyl inhibitors of P450 17 (17α-hydroxylase/C17-20-lyase). Arch. Pharm. Med. Chem. 2001, 334, 373-374.
-
(2001)
Arch. Pharm. Med. Chem.
, vol.334
, pp. 373-374
-
-
Haidar, S.1
Ehmer, P.B.2
Hartmann, R.W.3
-
22
-
-
0038062686
-
Effects of novel 17α-hydroxylase/C17,20-lyase (P45017, CYP17) inhibitors on androgen biosynthesis in vitro and in vivo
-
(b) Haidar, S.; Ehmer, P. B.; Barassin, S.; Batzl-Hartmann, C.; Hartmann, R. W. Effects of novel 17α-hydroxylase/C17,20-lyase (P45017, CYP17) inhibitors on androgen biosynthesis in vitro and in vivo. J. Steroid Biochem. Mol. Biol. 2003, 84, 555-562.
-
(2003)
J. Steroid Biochem. Mol. Biol.
, vol.84
, pp. 555-562
-
-
Haidar, S.1
Ehmer, P.B.2
Barassin, S.3
Batzl-Hartmann, C.4
Hartmann, R.W.5
-
24
-
-
0032510321
-
17α): Potential agents for the treatment of prostate cancer
-
17α): Potential agents for the treatment of prostate cancer, J. Med. Chem. 1998, 41, 902-912.
-
(1998)
J. Med. Chem.
, vol.41
, pp. 902-912
-
-
Njar, V.C.O.1
Kato, K.2
Nnane, I.P.3
Grigoryev, D.N.4
Long, B.J.5
Brodie, A.M.H.6
-
25
-
-
0000559495
-
A convenient, large-scale synthesis of abiraterone acetate [3β-acetoxy-17(3-pyridyl)-androsta-5, 16-diene], a potential new drug for the treatment of prostate cancer
-
Potter, G. A.; Hardcastle, I. R.; Jarman, M. A convenient, large-scale synthesis of abiraterone acetate [3β-acetoxy-17(3-pyridyl)-androsta-5, 16-diene], a potential new drug for the treatment of prostate cancer. Org. Prep. Proc. Int. 1997, 29, 123-128.
-
(1997)
Org. Prep. Proc. Int.
, vol.29
, pp. 123-128
-
-
Potter, G.A.1
Hardcastle, I.R.2
Jarman, M.3
-
26
-
-
0029162015
-
Total synthesis of Grossularines-1 and -2
-
Choshi, T.; Yamada, S.; Sugino, E.; Kuwada, T.; Hibino, S. Total synthesis of Grossularines-1 and -2. J. Org. Chem. 1995, 60, 5899-5904.
-
(1995)
J. Org. Chem.
, vol.60
, pp. 5899-5904
-
-
Choshi, T.1
Yamada, S.2
Sugino, E.3
Kuwada, T.4
Hibino, S.5
-
27
-
-
0033557850
-
Cytochrome P450c17-expressing Escherichia coli as a first-step screening system for 17α-hydroxylase-C17,20-lyase inhibitors
-
Grigoryev, D. N.; Kato, K.; Njar, V. C. O.; Long, B. J.; Ling, Y.-Z.; Wang, X.; Mohler, J.; Brodie, A. M. H. Cytochrome P450c17-expressing Escherichia coli as a first-step screening system for 17α-hydroxylase-C17,20-lyase inhibitors. Anal. Biochem. 1999, 267, 319-330.
-
(1999)
Anal. Biochem.
, vol.267
, pp. 319-330
-
-
Grigoryev, D.N.1
Kato, K.2
Njar, V.C.O.3
Long, B.J.4
Ling, Y.-Z.5
Wang, X.6
Mohler, J.7
Brodie, A.M.H.8
-
28
-
-
0032589949
-
Effects of new 17α-hydroxylase/C17,20-lyase inhibitors on LNCaP prostate cancer cell growth in vitro and in vivo
-
Grigoryev, D. N.; Long, B. J.; Nnane, I. P.; Njar, V. C. O.; Liu, Y.; Brodie, A. M. H. Effects of new 17α-hydroxylase/C17,20-lyase inhibitors on LNCaP prostate cancer cell growth in vitro and in vivo. Br. J. Cancer 1999, 81, 622-630.
-
(1999)
Br. J. Cancer
, vol.81
, pp. 622-630
-
-
Grigoryev, D.N.1
Long, B.J.2
Nnane, I.P.3
Njar, V.C.O.4
Liu, Y.5
Brodie, A.M.H.6
-
29
-
-
0017794351
-
Measurement of substrate and inhibitor binding to microsomal cytochrome P450 by optical difference spectroscopy
-
Jefcoat, C. R. Measurement of substrate and inhibitor binding to microsomal cytochrome P450 by optical difference spectroscopy. Methods Enzymol. 1978, 52, 258-279.
-
(1978)
Methods Enzymol.
, vol.52
, pp. 258-279
-
-
Jefcoat, C.R.1
-
30
-
-
0036682372
-
Synthesis and evaluation of 2′-substituted 4-(4′-carboxy- or 4′-carboxymethylbenzylidene)-N-acylpiperidines: Highly potent and in vivo active steroid 5α-reductase type 2 inhibitors
-
Picard, F.; Barassin, S.; Mokhtarian, A.; Hartmann, R. W. Synthesis and evaluation of 2′-substituted 4-(4′-carboxy- or 4′- carboxymethylbenzylidene)-N-acylpiperidines: Highly potent and in vivo active steroid 5α-reductase type 2 inhibitors. J. Med. Chem. 2002, 45, 3406-3417.
-
(2002)
J. Med. Chem.
, vol.45
, pp. 3406-3417
-
-
Picard, F.1
Barassin, S.2
Mokhtarian, A.3
Hartmann, R.W.4
-
31
-
-
0034740808
-
Pharmacokinetic profile of 3β-hydroxy-17-(1H-123-triazol-1-yl) androsta-5,16-diene (VN/87-1), a potent androgen synthesis inhibitor in mice
-
Nnane, I. P.; Njar, V. C. O.; Brodie, A. M. H. Pharmacokinetic profile of 3β-hydroxy-17-(1H-123-triazol-1-yl)androsta-5,16-diene (VN/87-1), a potent androgen synthesis inhibitor in mice. J. Steroid Biochem. Mol. Biol. 2001, 71, 145-152.
-
(2001)
J. Steroid Biochem. Mol. Biol.
, vol.71
, pp. 145-152
-
-
Nnane, I.P.1
Njar, V.C.O.2
Brodie, A.M.H.3
-
32
-
-
9144242015
-
Potent CYP17 inhibitors: Improved syntheses, pharmacokinetics and anti-tumor activity in the LNCaP human prostate cancer model
-
Handratta, V. D.; Jelovac, D.; Long, B. J.; Kataria, R.; Nnane, I. V.; Njar, V. C. O.; Brodie, A. M. H. Potent CYP17 inhibitors: improved syntheses, pharmacokinetics and anti-tumor activity in the LNCaP human prostate cancer model. J. Steroid Biochem. Mol. Biol. 2004, 92, 155-165.
-
(2004)
J. Steroid Biochem. Mol. Biol.
, vol.92
, pp. 155-165
-
-
Handratta, V.D.1
Jelovac, D.2
Long, B.J.3
Kataria, R.4
Nnane, I.V.5
Njar, V.C.O.6
Brodie, A.M.H.7
-
33
-
-
1842429920
-
Synergism of cytoplasmic kinases in IL6-induced ligand-independent activation of androgen receptor in prostate cancer cells
-
Kim, O.; Jiang, T.; Xie, Y.; Guo, Z.; Chen, H.; Qiu, Y. Synergism of cytoplasmic kinases in IL6-induced ligand-independent activation of androgen receptor in prostate cancer cells. Oncogene 2004, 23, 1838-1844.
-
(2004)
Oncogene
, vol.23
, pp. 1838-1844
-
-
Kim, O.1
Jiang, T.2
Xie, Y.3
Guo, Z.4
Chen, H.5
Qiu, Y.6
-
34
-
-
0034520311
-
A small composite probasin promoter confers high levels of prostate-specific gene expression through regulation by androgens and glucocorticoids in Vitro and in Vivo
-
Zhang, J.; Thomas, T. Z.; Kasper, S.; Matusik, R. J. A Small composite probasin promoter confers high levels of prostate-specific gene expression through regulation by androgens and glucocorticoids in Vitro and in Vivo. Endocrinology 2000, 141, 4698-4710.
-
(2000)
Endocrinology
, vol.141
, pp. 4698-4710
-
-
Zhang, J.1
Thomas, T.Z.2
Kasper, S.3
Matusik, R.J.4
-
35
-
-
2342573753
-
Androgen antagonist activity by the antioxidant moiety of vitamin E, 2,2,5,7,8-pentamethyl-6-chromanol in human prostate carcinoma cells
-
Thompson, T. A.; Wilding, G. Androgen antagonist activity by the antioxidant moiety of vitamin E, 2,2,5,7,8-pentamethyl-6-chromanol in human prostate carcinoma cells. Mol. Caner Ther. 2003, 2, 797-803.
-
(2003)
Mol. Caner Ther.
, vol.2
, pp. 797-803
-
-
Thompson, T.A.1
Wilding, G.2
-
36
-
-
0024501136
-
Ketoconazole: A possible direct cytotoxic effect on prostate carcinoma cells
-
Eichenberger, T.; Trachtenberg, J.; Toor, P.; Keating, A. Ketoconazole: A possible direct cytotoxic effect on prostate carcinoma cells. J. Urol. 1989, 141, 190-191.
-
(1989)
J. Urol.
, vol.141
, pp. 190-191
-
-
Eichenberger, T.1
Trachtenberg, J.2
Toor, P.3
Keating, A.4
-
37
-
-
16944366096
-
Progression of metastatic human prostate cancer to androgen independence in immunodeficient SCID mice
-
Kline, K. A.; Reiter, R. E.; Redula, J.; Moradi, H.; Zhu, X. L.; Brothman, A. R.; Lamb, D. J.; Marcelli, M.; Belldegrun, A.; Witte, O. N.; Sawyer, C. L. Progression of metastatic human prostate cancer to androgen independence in immunodeficient SCID mice. Nat. Med. 1997, 3, 402-408.
-
(1997)
Nat. Med.
, vol.3
, pp. 402-408
-
-
Kline, K.A.1
Reiter, R.E.2
Redula, J.3
Moradi, H.4
Zhu, X.L.5
Brothman, A.R.6
Lamb, D.J.7
Marcelli, M.8
Belldegrun, A.9
Witte, O.N.10
Sawyer, C.L.11
-
38
-
-
4944235914
-
Symposium on androgen action in prostate cancer
-
Tindall, D.; McFarland Horne, F.; Hruszkewycz, A.; Mohla, S.; Shuman, M.; Wang, Z.; Kantoff, P. Symposium on androgen action in prostate cancer. Cancer Res. 2004, 64, 7178-7180.
-
(2004)
Cancer Res.
, vol.64
, pp. 7178-7180
-
-
Tindall, D.1
McFarland Horne, F.2
Hruszkewycz, A.3
Mohla, S.4
Shuman, M.5
Wang, Z.6
Kantoff, P.7
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