메뉴 건너뛰기




Volumn 12, Issue 13, 2006, Pages 4072-4079

Pharmacologic basis for the enhanced efficacy of dutasteride against prostatic cancers

Author keywords

[No Author keywords available]

Indexed keywords

20ALPHA DIHYDROPROGESTERONE; ANDROGEN; DUTASTERIDE; EPRISTERIDE; FINASTERIDE; STEROID 5ALPHA REDUCTASE INHIBITOR; TESTOSTERONE;

EID: 33746047132     PISSN: 10780432     EISSN: None     Source Type: Journal    
DOI: 10.1158/1078-0432.CCR-06-0184     Document Type: Article
Times cited : (90)

References (45)
  • 1
    • 0038637317 scopus 로고    scopus 로고
    • Is the Achilles' heel for prostate cancer therapy a gain of function in androgen receptor signaling?
    • Litvinov IV, De Marzo AM, Isaacs JT. Is the Achilles' heel for prostate cancer therapy a gain of function in androgen receptor signaling? J Clin Endocrinol Metab 2003;88:2972-82.
    • (2003) J Clin Endocrinol Metab , vol.88 , pp. 2972-2982
    • Litvinov, I.V.1    De Marzo, A.M.2    Isaacs, J.T.3
  • 2
    • 0022361021 scopus 로고
    • Effectiveness of complete versus partial androgen withdrawal therapy for the treatment of prostatic cancer as studied in the Dunning R-3327 system of rat prostatic adenocarcinomas
    • Ellis WJ, Isaacs JT. Effectiveness of complete versus partial androgen withdrawal therapy for the treatment of prostatic cancer as studied in the Dunning R-3327 system of rat prostatic adenocarcinomas. Cancer Res 1985;45:6041-50.
    • (1985) Cancer Res , vol.45 , pp. 6041-6050
    • Ellis, W.J.1    Isaacs, J.T.2
  • 3
    • 0023555067 scopus 로고
    • Quantal relationship between prostatic dihydrotestosterone and prostatic cell content: Critical threshold concept
    • Kyprianou N, Isaacs JT. Quantal relationship between prostatic dihydrotestosterone and prostatic cell content: critical threshold concept. Prostate 1987;11:41-50.
    • (1987) Prostate , vol.11 , pp. 41-50
    • Kyprianou, N.1    Isaacs, J.T.2
  • 4
    • 0028696273 scopus 로고
    • Role of androgens in prostatic cancer
    • Isaacs JT. Role of androgens in prostatic cancer. Vitam Horm 1994;49:433-502.
    • (1994) Vitam Horm , vol.49 , pp. 433-502
    • Isaacs, J.T.1
  • 5
    • 0028173882 scopus 로고
    • Steroid 5α-reductase: Two genes/two enzymes
    • Russell DW, Wilson JD. Steroid 5α-reductase: two genes/two enzymes. Annu Rev Biochem 1994;63:25-61.
    • (1994) Annu Rev Biochem , vol.63 , pp. 25-61
    • Russell, D.W.1    Wilson, J.D.2
  • 6
    • 0025856103 scopus 로고
    • Assessment of the critical level of androgen for growth response of transplantable human prostatic carcinoma (PC-82) in nude mice
    • van Weerden WM, van Steenbrugge GJ, van Kreuningen A, Moerings EP, de Jong FH, Schroder FH. Assessment of the critical level of androgen for growth response of transplantable human prostatic carcinoma (PC-82) in nude mice. J Urol 1991;145:631-4.
    • (1991) J Urol , vol.145 , pp. 631-634
    • Van Weerden, W.M.1    Van Steenbrugge, G.J.2    Van Kreuningen, A.3    Moerings, E.P.4    De Jong, F.H.5    Schroder, F.H.6
  • 7
    • 0026744010 scopus 로고
    • Response of rat and human prostatic cancers to the novel 5α-reductase inhibitor, SK&F 105657
    • Lamb JC, Levy MA, Johnson RK, Isaacs JT. Response of rat and human prostatic cancers to the novel 5α-reductase inhibitor, SK&F 105657. Prostate 1992;21:15-34.
    • (1992) Prostate , vol.21 , pp. 15-34
    • Lamb, J.C.1    Levy, M.A.2    Johnson, R.K.3    Isaacs, J.T.4
  • 8
    • 0043184661 scopus 로고    scopus 로고
    • Pharmacokinetics of epristeride in rats and beagle dogs
    • Wei GL, Xiao SH, Liu CX. Pharmacokinetics of epristeride in rats and beagle dogs. Yao Xue Xue Bao 2000;35:721-4.
    • (2000) Yao Xue Xue Bao , vol.35 , pp. 721-724
    • Wei, G.L.1    Xiao, S.H.2    Liu, C.X.3
  • 10
    • 0028946134 scopus 로고
    • Cloning, expression and functional characterization of type 1 and type 2 steroid 5α-reductases from cynomolgus monkey: Comparisons with human and rat isoenzymes
    • Levy MA, Brandt M, Sheedy KM, et al. Cloning, expression and functional characterization of type 1 and type 2 steroid 5α-reductases from cynomolgus monkey: comparisons with human and rat isoenzymes. J Steroid Biochem Mol Biol 1995;52:307-19.
    • (1995) J Steroid Biochem Mol Biol , vol.52 , pp. 307-319
    • Levy, M.A.1    Brandt, M.2    Sheedy, K.M.3
  • 11
    • 0034071149 scopus 로고    scopus 로고
    • Kinetic analysis of LY320236: Competitive inhibitor of type I and non-competitive inhibitor of type II human steroid 5ct-reductase
    • McNulty AM, Audia JE, Bemis KG, Goode RL, Rocco VP, Neubauer BL. Kinetic analysis of LY320236: competitive inhibitor of type I and non-competitive inhibitor of type II human steroid 5ct-reductase. J Steroid Biochem Mol Biol 2000;72:13-21.
    • (2000) J Steroid Biochem Mol Biol , vol.72 , pp. 13-21
    • McNulty, A.M.1    Audia, J.E.2    Bemis, K.G.3    Goode, R.L.4    Rocco, V.P.5    Neubauer, B.L.6
  • 13
    • 0025808821 scopus 로고
    • Pharmacokinetics and biochemical efficacy after single and multiple oral administration of N-(2-methyl-2-propyl)-3-oxo-4-aza-5α-androst-1-ene- 17β-carboxamide, a new type of specific competitive inhibitor of testosterone 5α-reductase, in volunteers
    • Ohtawa M, Morikawa H, Shimazaki J. Pharmacokinetics and biochemical efficacy after single and multiple oral administration of N-(2-methyl-2-propyl)- 3-oxo-4-aza-5α-androst-1-ene-17β-carboxamide, a new type of specific competitive inhibitor of testosterone 5α-reductase, in volunteers. Eur J Drug Metab Pharmacokinet 1991;16:15-21.
    • (1991) Eur J Drug Metab Pharmacokinet , vol.16 , pp. 15-21
    • Ohtawa, M.1    Morikawa, H.2    Shimazaki, J.3
  • 14
    • 0028807269 scopus 로고
    • Mechanism of time-dependent inhibition of 5α-reductases by Δ1-4-azasteroids: Toward perfection of rates of time-dependent inhibition by using ligand-binding energies
    • Tian G, Mook RA, Jr., Moss ML, Frye SV. Mechanism of time-dependent inhibition of 5α-reductases by Δ1-4-azasteroids: toward perfection of rates of time-dependent inhibition by using ligand-binding energies. Biochemistry 1995;34:13453-9.
    • (1995) Biochemistry , vol.34 , pp. 13453-13459
    • Tian, G.1    Mook Jr., R.A.2    Moss, M.L.3    Frye, S.V.4
  • 15
    • 0032945558 scopus 로고    scopus 로고
    • The pharmacokinetic modelling of GI198745 (dutasteride), a compound with parallel linear and nonlinear elimination
    • Gisleskog PO, Hermann D, Hammarlund-Udenaes M, Karlsson MO. The pharmacokinetic modelling of GI198745 (dutasteride), a compound with parallel linear and nonlinear elimination. Br J Clin Pharmacol 1999;47:53-8.
    • (1999) Br J Clin Pharmacol , vol.47 , pp. 53-58
    • Gisleskog, P.O.1    Hermann, D.2    Hammarlund-Udenaes, M.3    Karlsson, M.O.4
  • 16
    • 0036046504 scopus 로고    scopus 로고
    • The clinical efficacy of epristeride in the treatment of benign prostatic hyperplasia
    • Ju XB, Wu HF, Hua LX, Zhang W, Li J. The clinical efficacy of epristeride in the treatment of benign prostatic hyperplasia. Zhonghua Nan Ke Xue 2002;8:42-4.
    • (2002) Zhonghua Nan Ke Xue , vol.8 , pp. 42-44
    • Ju, X.B.1    Wu, H.F.2    Hua, L.X.3    Zhang, W.4    Li, J.5
  • 17
    • 0005309240 scopus 로고    scopus 로고
    • Efficacy of finasteride is maintained in patients with benign prostatic hyperplasia treated for 5 years
    • The North American Finasteride Study Group
    • Hudson PB, Boake R, Trachtenberg J, et al. Efficacy of finasteride is maintained in patients with benign prostatic hyperplasia treated for 5 years. The North American Finasteride Study Group. Urology 1999;53:690-5.
    • (1999) Urology , vol.53 , pp. 690-695
    • Hudson, P.B.1    Boake, R.2    Trachtenberg, J.3
  • 18
    • 0026503988 scopus 로고
    • Finasteride, an inhibitor of 5α-reductase, suppresses prostatic dihydrotestosterone in men with benign prostatic hyperplasia
    • McConnell JD, Wilson JD, George FW, Geller J, Pappas F, Stoner E. Finasteride, an inhibitor of 5α-reductase, suppresses prostatic dihydrotestosterone in men with benign prostatic hyperplasia. J Clin Endocrinol Metab 1992;74:505-8.
    • (1992) J Clin Endocrinol Metab , vol.74 , pp. 505-508
    • McConnell, J.D.1    Wilson, J.D.2    George, F.W.3    Geller, J.4    Pappas, F.5    Stoner, E.6
  • 19
    • 4444336295 scopus 로고    scopus 로고
    • Efficacy and safety of long-term treatment with the dual 5α-reductase inhibitor dutasteride in men with symptomatic benign prostatic hyperplasia
    • discussion 495
    • Debruyne F, Barkin J, van Erps P, Reis M, Tammela TL, Roehrborn C. Efficacy and safety of long-term treatment with the dual 5α-reductase inhibitor dutasteride in men with symptomatic benign prostatic hyperplasia. Eur Urol 2004;46:488-94; discussion 495.
    • (2004) Eur Urol , vol.46 , pp. 488-494
    • Debruyne, F.1    Barkin, J.2    Van Erps, P.3    Reis, M.4    Tammela, T.L.5    Roehrborn, C.6
  • 20
    • 2442545242 scopus 로고    scopus 로고
    • Marked suppression of dihydrotestosterone in men with benign prostatic hyperplasia by dutasteride, a dual 5α-reductase inhibitor
    • Clark RV, Hermann DJ, Cunningham GR, Wilson TH, Morrill BB, Hobbs S. Marked suppression of dihydrotestosterone in men with benign prostatic hyperplasia by dutasteride, a dual 5α-reductase inhibitor. J Clin Endocrinol Metab 2004;89:2179-84.
    • (2004) J Clin Endocrinol Metab , vol.89 , pp. 2179-2184
    • Clark, R.V.1    Hermann, D.J.2    Cunningham, G.R.3    Wilson, T.H.4    Morrill, B.B.5    Hobbs, S.6
  • 21
    • 0026644386 scopus 로고
    • Multicenter, randomized, double-blind, placebo controlled study to investigate the effect of finasteride (MK-906) on stage D prostate cancer
    • Presti JC, Jr., Fair WR, Andriole G, et al. Multicenter, randomized, double-blind, placebo controlled study to investigate the effect of finasteride (MK-906) on stage D prostate cancer. J Urol 1992;148:1201-4.
    • (1992) J Urol , vol.148 , pp. 1201-1204
    • Presti Jr., J.C.1    Fair, W.R.2    Andriole, G.3
  • 22
    • 0028843851 scopus 로고
    • Treatment with finasteride following radical prostatectomy for prostate cancer
    • Andriole G, Lieber M, Smith J, et al. Treatment with finasteride following radical prostatectomy for prostate cancer. Urology 1995;45:491-7.
    • (1995) Urology , vol.45 , pp. 491-497
    • Andriole, G.1    Lieber, M.2    Smith, J.3
  • 23
    • 0035479907 scopus 로고    scopus 로고
    • Pharmacokinetic parameters and mechanisms of inhibition of rat type 1 and 2 steroid 5α-reductases: Determinants for different in vivo activities of GI198745 and finasteride in the rat
    • Stuart JD, Frank WL, Noel DS, et al. Pharmacokinetic parameters and mechanisms of inhibition of rat type 1 and 2 steroid 5α-reductases: determinants for different in vivo activities of GI198745 and finasteride in the rat. Biochem Pharmacol 2001;62:933-42.
    • (2001) Biochem Pharmacol , vol.62 , pp. 933-942
    • Stuart, J.D.1    Frank, W.L.2    Noel, D.S.3
  • 24
    • 0030071511 scopus 로고    scopus 로고
    • In vivo time-dependent inhibition of human steroid 5α-reductase by finasteride
    • Tian G. In vivo time-dependent inhibition of human steroid 5α-reductase by finasteride. J Pharm Sci 1996;85:106-11.
    • (1996) J Pharm Sci , vol.85 , pp. 106-111
    • Tian, G.1
  • 25
    • 0028158538 scopus 로고
    • In vitro biotransformation of finasteride in rat hepatic microsome: Isolation and characterization of metabolites
    • Ishii Y, Mukyama H, Ohtawa M. In vitro biotransformation of finasteride in rat hepatic microsome: isolation and characterization of metabolites. Drug Metab Dispos 1994;22:79-84.
    • (1994) Drug Metab Dispos , vol.22 , pp. 79-84
    • Ishii, Y.1    Mukyama, H.2    Ohtawa, M.3
  • 26
    • 0021914207 scopus 로고
    • Discrimination between normal, hyperplastic and malignant human prostatic tissues by enzymatic profiles
    • Brendler CB, Follansbee AL, Isaacs JT. Discrimination between normal, hyperplastic and malignant human prostatic tissues by enzymatic profiles. J Urol 1985;133:495-501.
    • (1985) J Urol , vol.133 , pp. 495-501
    • Brendler, C.B.1    Follansbee, A.L.2    Isaacs, J.T.3
  • 27
    • 0029910571 scopus 로고    scopus 로고
    • Differential expression of 5α-reductase isoenzymes in the human prostate and prostatic carcinomas
    • Bonkhoff H, Stein U, Aumuller G, Remberger K. Differential expression of 5α-reductase isoenzymes in the human prostate and prostatic carcinomas. Prostate 1996;29:261-7.
    • (1996) Prostate , vol.29 , pp. 261-267
    • Bonkhoff, H.1    Stein, U.2    Aumuller, G.3    Remberger, K.4
  • 28
    • 0141676080 scopus 로고    scopus 로고
    • Decreased gene expression of steroid 5α-reductase 2 in human prostate cancer: Implications for finasteride therapy of prostate carcinoma
    • Luo J, Dunn TA, Ewing CM, Walsh PC, Isaacs WB. Decreased gene expression of steroid 5α-reductase 2 in human prostate cancer: implications for finasteride therapy of prostate carcinoma. Prostate 2003;57:134-9.
    • (2003) Prostate , vol.57 , pp. 134-139
    • Luo, J.1    Dunn, T.A.2    Ewing, C.M.3    Walsh, P.C.4    Isaacs, W.B.5
  • 29
    • 17644362707 scopus 로고    scopus 로고
    • Differential alterations in 5α-reductase type 1 and type 2 levels during development and progression of prostate cancer
    • Thomas LN, Lazier CB, Gupta R, et al. Differential alterations in 5α-reductase type 1 and type 2 levels during development and progression of prostate cancer. Prostate 2005;63:231-9.
    • (2005) Prostate , vol.63 , pp. 231-239
    • Thomas, L.N.1    Lazier, C.B.2    Gupta, R.3
  • 31
    • 0026782628 scopus 로고
    • Testosterone and 5-αadihydrotestosterone interact differently with the androgen receptor to enhance transcription of the MMTA-CAT reporter gene
    • Deslypere JP, Young M, Wilson JD, McPhaul MJ. Testosterone and 5-αadihydrotestosterone interact differently with the androgen receptor to enhance transcription of the MMTA-CAT reporter gene. Mol Cell Endocrinol 1992;88:15-22.
    • (1992) Mol Cell Endocrinol , vol.88 , pp. 15-22
    • Deslypere, J.P.1    Young, M.2    Wilson, J.D.3    McPhaul, M.J.4
  • 32
    • 0025823093 scopus 로고
    • Effect of castration, DES, flutamide and the 5α-reductase inhibitor, MK906, on the growth of the Dunning rat prostatic carcinoma, R-3327
    • Brooks JR, Berman C, Nguyen H, et al. Effect of castration, DES, flutamide and the 5α-reductase inhibitor, MK906, on the growth of the Dunning rat prostatic carcinoma, R-3327. Prostate 1991;18:215-27.
    • (1991) Prostate , vol.18 , pp. 215-227
    • Brooks, J.R.1    Berman, C.2    Nguyen, H.3
  • 33
    • 0023025173 scopus 로고
    • Establishment and characterization of seven Dunning rat prostatic cancer cell lines and their use in developing methods for predicting metastatic abilities of prostatic cancers
    • Isaacs JT, Isaacs WB, Feitz WFJ, Scheres J. Establishment and characterization of seven Dunning rat prostatic cancer cell lines and their use in developing methods for predicting metastatic abilities of prostatic cancers. Prostate 1986;9:261-81.
    • (1986) Prostate , vol.9 , pp. 261-281
    • Isaacs, J.T.1    Isaacs, W.B.2    Feitz, W.F.J.3    Scheres, J.4
  • 34
    • 0142075168 scopus 로고    scopus 로고
    • Molecular characterization of human prostate carcinoma cell lines
    • van Bokhoven A, Varella-Garcia M, Korch C, et al. Molecular characterization of human prostate carcinoma cell lines. Prostate 2003;57:205-25.
    • (2003) Prostate , vol.57 , pp. 205-225
    • Van Bokhoven, A.1    Varella-Garcia, M.2    Korch, C.3
  • 35
    • 27144476439 scopus 로고    scopus 로고
    • Role of notch-1 and E-cadherin in the differential response to calcium in culturing normal versus malignant prostate cells
    • Dalrymple S, Antony L, Xu Y, et al. Role of notch-1 and E-cadherin in the differential response to calcium in culturing normal versus malignant prostate cells. Cancer Res 2005;65:9269-79.
    • (2005) Cancer Res , vol.65 , pp. 9269-9279
    • Dalrymple, S.1    Antony, L.2    Xu, Y.3
  • 37
    • 0035094483 scopus 로고    scopus 로고
    • Messenger ribonucleic acid levels of steroid 5α-reductase 2 in human prostate predict the enzyme activity
    • Soderstrom TG, Bjelfman C, Brekkan E, et al. Messenger ribonucleic acid levels of steroid 5α-reductase 2 in human prostate predict the enzyme activity. J Clin Endocrinol Metab 2001;86:855-8.
    • (2001) J Clin Endocrinol Metab , vol.86 , pp. 855-858
    • Soderstrom, T.G.1    Bjelfman, C.2    Brekkan, E.3
  • 38
    • 0347986651 scopus 로고    scopus 로고
    • Messenger RNA levels and enzyme activities of 5α-reductase types 1 and 2 in human benign prostatic hyperplasia (BPH) tissue
    • Shirakawa T, Okada H, Acharya B, et al. Messenger RNA levels and enzyme activities of 5α-reductase types 1 and 2 in human benign prostatic hyperplasia (BPH) tissue. Prostate 2004;58:33-40.
    • (2004) Prostate , vol.58 , pp. 33-40
    • Shirakawa, T.1    Okada, H.2    Acharya, B.3
  • 39
    • 0029926673 scopus 로고    scopus 로고
    • 5α-reductase expression by prostate cancer cell lines and benign prostatic hyperplasia in vitro
    • Smith CM, Ballard SA, Worman N, Buettner R, Masters JRW. 5α-Reductase expression by prostate cancer cell lines and benign prostatic hyperplasia in vitro. J Clin Endocrinol Metab 1996;81:1361-6.
    • (1996) J Clin Endocrinol Metab , vol.81 , pp. 1361-1366
    • Smith, C.M.1    Ballard, S.A.2    Worman, N.3    Buettner, R.4    Masters, J.R.W.5
  • 41
    • 0742287752 scopus 로고    scopus 로고
    • Dutasteride, the dual 5α-reductase inhibitor, inhibits androgen action and promotes cell death in the LNCaP prostate cancer cell line
    • Lazier CB, Thomas LN, Douglas RC, Vessey JP, Rittmaster RS. Dutasteride, the dual 5α-reductase inhibitor, inhibits androgen action and promotes cell death in the LNCaP prostate cancer cell line. Prostate 2004;58:130-44.
    • (2004) Prostate , vol.58 , pp. 130-144
    • Lazier, C.B.1    Thomas, L.N.2    Douglas, R.C.3    Vessey, J.P.4    Rittmaster, R.S.5
  • 42
    • 0035392953 scopus 로고    scopus 로고
    • Conversion from a paracrine to an autocrine mechanism of androgen-stimulated growth during malignant transformation of prostatic epithelial cells
    • Gao J, Arnold JT, Isaacs JT. Conversion from a paracrine to an autocrine mechanism of androgen-stimulated growth during malignant transformation of prostatic epithelial cells. Cancer Res 2001;61:5038-44.
    • (2001) Cancer Res , vol.61 , pp. 5038-5044
    • Gao, J.1    Arnold, J.T.2    Isaacs, J.T.3
  • 43
    • 0032402162 scopus 로고    scopus 로고
    • Biochemical response to testicular androgen ablation among patients with prostate cancer for whom flutamide and/or finasteride therapy failed
    • Ornstein DK, Smith DS, Andriole GL. Biochemical response to testicular androgen ablation among patients with prostate cancer for whom flutamide and/or finasteride therapy failed. Urology 1998;52:1094-7.
    • (1998) Urology , vol.52 , pp. 1094-1097
    • Ornstein, D.K.1    Smith, D.S.2    Andriole, G.L.3
  • 44
    • 27644452640 scopus 로고    scopus 로고
    • Testosterone and dihydrotestosterone tissue levels in recurrent prostate cancer
    • Titus MA, Schell MJ, Lih FB, Tomer KB, Mohler JL. Testosterone and dihydrotestosterone tissue levels in recurrent prostate cancer. Clin Cancer Res 2005;11:4653-7.
    • (2005) Clin Cancer Res , vol.11 , pp. 4653-4657
    • Titus, M.A.1    Schell, M.J.2    Lih, F.B.3    Tomer, K.B.4    Mohler, J.L.5
  • 45
    • 33746089137 scopus 로고    scopus 로고
    • Combinatorial androgen receptor targeted (i.e., CART) therapy for prostate cancer
    • In press
    • Singh P, Uzgare A, Litvinov I, Isaacs JT. Combinatorial androgen receptor targeted (i.e., CART) therapy for prostate cancer. Endocr Relat Cancer. In press 2006.
    • (2006) Endocr Relat Cancer
    • Singh, P.1    Uzgare, A.2    Litvinov, I.3    Isaacs, J.T.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.