-
1
-
-
80052936044
-
Androgen quantitation in prostate cancer tissue using liquid chromatography tandem mass spectrometry
-
Titus M, Tomer KB. Androgen quantitation in prostate cancer tissue using liquid chromatography tandem mass spectrometry. Methods Mol Biol 2011; 776: 47-57
-
(2011)
Methods Mol Biol
, vol.776
, pp. 47-57
-
-
Titus, M.1
Tomer, K.B.2
-
2
-
-
10844235652
-
Androgen-independent prostate cancer is a heterogeneous group of diseases: Lessons from a rapid autopsy program
-
Shah RB, Mehra R, Chinnaiyan AM, Shen R, Ghosh D, et al. Androgen-independent prostate cancer is a heterogeneous group of diseases: lessons from a rapid autopsy program. Cancer Res 2004; 64: 9209-16
-
(2004)
Cancer Res
, vol.64
, pp. 9209-9216
-
-
Shah, R.B.1
Mehra, R.2
Chinnaiyan, A.M.3
Shen, R.4
Ghosh, D.5
-
3
-
-
42949144171
-
Intracrine androgen metabolism in prostate cancer progression: Mechanisms of castration resistance and therapeutic implications
-
Mostaghel EA, Nelson PS. Intracrine androgen metabolism in prostate cancer progression: mechanisms of castration resistance and therapeutic implications. Best Pract Res Clin Endocrinol Metab 2008; 22: 243-58
-
(2008)
Best Pract Res Clin Endocrinol Metab
, vol.22
, pp. 243-258
-
-
Mostaghel, E.A.1
Nelson, P.S.2
-
4
-
-
51049098138
-
Androgen levels increase by intratumoral de novo steroidogenesis during progression of castration-resistant prostate cancer
-
Locke JA, Guns ES, Lubik AA, Adomat HH, Hendy SC, et al. Androgen levels increase by intratumoral de novo steroidogenesis during progression of castration-resistant prostate cancer. Cancer Res 2008; 68: 6407-15
-
(2008)
Cancer Res
, vol.68
, pp. 6407-6415
-
-
Locke, J.A.1
Guns, E.S.2
Lubik, A.A.3
Adomat, H.H.4
Hendy, S.C.5
-
5
-
-
49249119358
-
Maintenance of intratumoral androgens in metastatic prostate cancer: A mechanism for castration-resistant tumor growth
-
Montgomery RB, Mostaghel EA, Vessella R, Hess DL, Kalhorn TF, et al. Maintenance of intratumoral androgens in metastatic prostate cancer: a mechanism for castration-resistant tumor growth. Cancer Res 2008; 68: 4447-54
-
(2008)
Cancer Res
, vol.68
, pp. 4447-4454
-
-
Montgomery, R.B.1
Mostaghel, E.A.2
Vessella, R.3
Hess, D.L.4
Kalhorn, T.F.5
-
6
-
-
84858000846
-
Abiraterone acetate: Redefining hormone treatment for advanced prostate cancer
-
Pezaro CJ, Mukherji D, De Bono JS. Abiraterone acetate: redefining hormone treatment for advanced prostate cancer. Drug Discov Today 2012; 17: 221-6
-
(2012)
Drug Discov Today
, vol.17
, pp. 221-226
-
-
Pezaro, C.J.1
Mukherji, D.2
De Bono, J.S.3
-
7
-
-
84857071455
-
Abiraterone acetate: Oral androgen biosynthesis inhibitor for treatment of castration-resistant prostate cancer
-
Rehman Y, Rosenberg JE. Abiraterone acetate: oral androgen biosynthesis inhibitor for treatment of castration-resistant prostate cancer. Drug Des Devel Ther 2012; 6: 13-8
-
(2012)
Drug des Devel Ther
, vol.6
, pp. 13-18
-
-
Rehman, Y.1
Rosenberg, J.E.2
-
8
-
-
79957443342
-
Abiraterone and increased survival in metastatic prostate cancer
-
de Bono JS, Logothetis CJ, Molina A, Fizazi K, North S, et al. Abiraterone and increased survival in metastatic prostate cancer. N Engl J Med 2011; 364: 1995-2005
-
(2011)
N Engl J Med
, vol.364
, pp. 1995-2005
-
-
De Bono, J.S.1
Logothetis, C.J.2
Molina, A.3
Fizazi, K.4
North, S.5
-
9
-
-
53749090666
-
Phase i clinical trial of a selective inhibitor of CYP17, abiraterone acetate, confirms that castration-resistant prostate cancer commonly remains hormone driven
-
Attard G, Reid AH, Yap TA, Raynaud F, Dowsett M, et al. Phase I clinical trial of a selective inhibitor of CYP17, abiraterone acetate, confirms that castration-resistant prostate cancer commonly remains hormone driven. J Clin Oncol 2008; 26: 4563-71
-
(2008)
J Clin Oncol
, vol.26
, pp. 4563-4571
-
-
Attard, G.1
Reid, A.H.2
Yap, T.A.3
Raynaud, F.4
Dowsett, M.5
-
10
-
-
3042784503
-
Hormonal impact of the 17alpha-hydroxylase/C (17,20)-lyase inhibitor abiraterone acetate (CB7630) in patients with prostate cancer
-
O'Donnell A, Judson I, Dowsett M, Raynaud F, Dearnaley D, et al. Hormonal impact of the 17alpha-hydroxylase/C (17,20)-lyase inhibitor abiraterone acetate (CB7630) in patients with prostate cancer. Br J Cancer 2004; 90: 2317-25
-
(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
-
12
-
-
20144389477
-
In situ androgen producing enzymes in human prostate cancer
-
Nakamura Y, Suzuki T, Nakabayashi M, Endoh M, Sakamoto K, et al. In situ androgen producing enzymes in human prostate cancer. Endocr Relat Cancer 2005; 12: 101-7
-
(2005)
Endocr Relat Cancer
, vol.12
, pp. 101-107
-
-
Nakamura, Y.1
Suzuki, T.2
Nakabayashi, M.3
Endoh, M.4
Sakamoto, K.5
-
13
-
-
0035140497
-
Immunoelectron microscopic localization of 3beta-hydroxysteroid dehydrogenase and type 5 17beta-hydroxysteroid dehydrogenase in the human prostate and mammary gland
-
Pelletier G, Luu-The V, El-Alfy M, Li S, Labrie F. Immunoelectron microscopic localization of 3beta-hydroxysteroid dehydrogenase and type 5 17beta-hydroxysteroid dehydrogenase in the human prostate and mammary gland. J Mol Endocrinol 2001; 26: 11-9
-
(2001)
J Mol Endocrinol
, vol.26
, pp. 11-19
-
-
Pelletier, G.1
Luu-The, V.2
El-Alfy, M.3
Li, S.4
Labrie, F.5
-
14
-
-
46749097968
-
Specific properties of a C-terminal truncated androgen receptor detected in hormone refractory prostate cancer
-
Lapouge G, Marcias G, Erdmann E, Kessler P, Cruchant M, et al. Specific properties of a C-terminal truncated androgen receptor detected in hormone refractory prostate cancer. Adv Exp Med Biol 2008; 617: 529-34
-
(2008)
Adv Exp Med Biol
, vol.617
, pp. 529-534
-
-
Lapouge, G.1
Marcias, G.2
Erdmann, E.3
Kessler, P.4
Cruchant, M.5
-
15
-
-
84895141227
-
AKR1C3 overexpression may serve as a promising biomarker for prostate cancer progression
-
Tian Y, Zhao L, Zhang H, Liu X, Zhao X, et al. AKR1C3 overexpression may serve as a promising biomarker for prostate cancer progression. Diagn Pathol 2014; 9: 42
-
(2014)
Diagn Pathol
, vol.9
, pp. 42
-
-
Tian, Y.1
Zhao, L.2
Zhang, H.3
Liu, X.4
Zhao, X.5
-
16
-
-
84858036972
-
Overexpression of aldo-keto reductase 1C3 (AKR1C3) in LNCaP cells diverts androgen metabolism towards testosterone resulting in resistance to the 5alpha-reductase inhibitor finasteride
-
Byrns MC, Mindnich R, Duan L, Penning TM. Overexpression of aldo-keto reductase 1C3 (AKR1C3) in LNCaP cells diverts androgen metabolism towards testosterone resulting in resistance to the 5alpha-reductase inhibitor finasteride. J Steroid Biochem Mol Biol 2012; 130: 7-15
-
(2012)
J Steroid Biochem Mol Biol
, vol.130
, pp. 7-15
-
-
Byrns, M.C.1
Mindnich, R.2
Duan, L.3
Penning, T.M.4
-
17
-
-
79957722662
-
Inhibitors of type 5 17beta-hydroxysteroid dehydrogenase (AKR1C3): Overview and structural insights
-
Byrns MC, Jin Y, Penning TM. Inhibitors of type 5 17beta-hydroxysteroid dehydrogenase (AKR1C3): overview and structural insights. J Steroid Biochem Mol Biol 2011; 125: 95-104
-
(2011)
J Steroid Biochem Mol Biol
, vol.125
, pp. 95-104
-
-
Byrns, M.C.1
Jin, Y.2
Penning, T.M.3
-
18
-
-
84862006905
-
Berberine, a genotoxic alkaloid, induces ATM-Chk1 mediated G2 arrest in prostate cancer cells
-
Wang Y, Liu Q, Liu Z, Li B, Sun Z, et al. Berberine, a genotoxic alkaloid, induces ATM-Chk1 mediated G2 arrest in prostate cancer cells. Mutat Res 2012; 734: 20-9
-
(2012)
Mutat Res
, vol.734
, pp. 20-29
-
-
Wang, Y.1
Liu, Q.2
Liu, Z.3
Li, B.4
Sun, Z.5
-
19
-
-
80051591737
-
Berberine suppresses androgen receptor signaling in prostate cancer
-
Li J, Cao B, Liu X, Fu X, Xiong Z, et al. Berberine suppresses androgen receptor signaling in prostate cancer. Mol Cancer Ther 2011; 10: 1346-56
-
(2011)
Mol Cancer Ther
, vol.10
, pp. 1346-1356
-
-
Li, J.1
Cao, B.2
Liu, X.3
Fu, X.4
Xiong, Z.5
-
20
-
-
33644984254
-
Berberine, a natural product, induces G1-phase cell cycle arrest and caspase-3-dependent apoptosis in human prostate carcinoma cells
-
Mantena SK, Sharma SD, Katiyar SK. Berberine, a natural product, induces G1-phase cell cycle arrest and caspase-3-dependent apoptosis in human prostate carcinoma cells. Mol Cancer Ther 2006; 5: 296-308
-
(2006)
Mol Cancer Ther
, vol.5
, pp. 296-308
-
-
Mantena, S.K.1
Sharma, S.D.2
Katiyar, S.K.3
-
21
-
-
84927652789
-
Safety, tolerability and anti-tumour activity of the androgen biosynthesis inhibitor ASP9521 in patients with metastatic castration-resistant prostate cancer: Multi-centre phase I/II study
-
Loriot Y, Fizazi K, Jones RJ, Van den Brande J, Molife RL, et al. Safety, tolerability and anti-tumour activity of the androgen biosynthesis inhibitor ASP9521 in patients with metastatic castration-resistant prostate cancer: multi-centre phase I/II study. Invest New Drugs 2014; 32: 995-1004
-
(2014)
Invest New Drugs
, vol.32
, pp. 995-1004
-
-
Loriot, Y.1
Fizazi, K.2
Jones, R.J.3
Van Den Brande, J.4
Molife, R.L.5
-
22
-
-
84904660980
-
The activity of SN33638, an inhibitor of AKR1C3, on testosterone and 17beta-estradiol production and function in castration-resistant prostate cancer and ER-positive breast cancer
-
Yin YD, Fu M, Brooke DG, Heinrich DM, Denny WA, et al. The activity of SN33638, an inhibitor of AKR1C3, on testosterone and 17beta-estradiol production and function in castration-resistant prostate cancer and ER-positive breast cancer. Front Oncol 2014; 4: 159
-
(2014)
Front Oncol
, vol.4
, pp. 159
-
-
Yin, Y.D.1
Fu, M.2
Brooke, D.G.3
Heinrich, D.M.4
Denny, W.A.5
-
23
-
-
67649438659
-
Berberine inhibits p53-dependent cell growth through induction of apoptosis of prostate cancer cells
-
Choi MS, Oh JH, Kim SM, Jung HY, Yoo HS, et al. Berberine inhibits p53-dependent cell growth through induction of apoptosis of prostate cancer cells. Int J Oncol 2009; 34: 1221-30
-
(2009)
J Oncol
, vol.34
, pp. 1221-1230
-
-
Choi, M.S.1
Oh, J.H.2
Kim, S.M.3
Jung, H.Y.4
Yoo, H.S.5
-
24
-
-
33645056171
-
Increased expression of genes converting adrenal androgens to testosterone in androgen-independent prostate cancer
-
Stanbrough M, Bubley GJ, Ross K, Golub TR, Rubin MA, et al. Increased expression of genes converting adrenal androgens to testosterone in androgen-independent prostate cancer. Cancer Res 2006; 66: 2815-25
-
(2006)
Cancer Res
, vol.66
, pp. 2815-2825
-
-
Stanbrough, M.1
Bubley, G.J.2
Ross, K.3
Golub, T.R.4
Rubin, M.A.5
-
25
-
-
0032502245
-
Mutagenesis of 3 alpha-hydroxysteroid dehydrogenase reveals a "push-pull" mechanism for proton transfer in aldo-keto reductases
-
Schlegel BP, Jez JM, Penning TM. Mutagenesis of 3 alpha-hydroxysteroid dehydrogenase reveals a "push-pull" mechanism for proton transfer in aldo-keto reductases. Biochemistry 1998; 37: 3538-48
-
(1998)
Biochemistry
, vol.37
, pp. 3538-3548
-
-
Schlegel, B.P.1
Jez, J.M.2
Penning, T.M.3
-
26
-
-
11244348953
-
Development of nonsteroidal anti-inflammatory drug analogs and steroid carboxylates selective for human aldo-keto reductase isoforms: Potential antineoplastic agents that work independently of cyclooxygenase isozymes
-
Bauman DR, Rudnick SI, Szewczuk LM, Jin Y, Gopishetty S, et al. Development of nonsteroidal anti-inflammatory drug analogs and steroid carboxylates selective for human aldo-keto reductase isoforms: potential antineoplastic agents that work independently of cyclooxygenase isozymes. Mol Pharmacol 2005; 67: 60-8
-
(2005)
Mol Pharmacol
, vol.67
, pp. 60-68
-
-
Bauman, D.R.1
Rudnick, S.I.2
Szewczuk, L.M.3
Jin, Y.4
Gopishetty, S.5
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