메뉴 건너뛰기




Volumn 141, Issue , 2014, Pages 44-51

In vitro and in vivo evaluation of a 3β-androsterone derivative as inhibitor of 17β-hydroxysteroid dehydrogenase type 3

Author keywords

17 Hydroxysteroid dehydrogenase; Androgen; Enzyme; Hormone; Inhibitor; Prostate cancer; Steroid

Indexed keywords

17 BETA HYDROXYSTEROID DEHYDROGENASE TYPE 3; ANDROSTERONE DERIVATIVE; RM 532 105; TESTOSTERONE 17BETA DEHYDROGENASE; UNCLASSIFIED DRUG;

EID: 84893451149     PISSN: 09600760     EISSN: 18791220     Source Type: Journal    
DOI: 10.1016/j.jsbmb.2013.12.019     Document Type: Article
Times cited : (12)

References (45)
  • 2
    • 0025975824 scopus 로고
    • Physiologic basis of endocrine therapy for prostatic cancer
    • J.D. McConnell Physiologic basis of endocrine therapy for prostatic cancer Urol. Clin. North Am. 18 1991 1 13
    • (1991) Urol. Clin. North Am. , vol.18 , pp. 1-13
    • Mcconnell, J.D.1
  • 4
    • 0034066457 scopus 로고    scopus 로고
    • Screening and early hormonal treatment of prostate cancer are accumulating strong evidence and support
    • DOI 10.1002/(SICI)1097-0045(20000515)43:3<215::AID-PROS7>3.0.CO;2-G
    • F. Labrie Screening and early hormonal treatment of prostate cancer are accumulating strong evidence and support Prostate 40 2000 215 222 (Pubitemid 30230457)
    • (2000) Prostate , vol.43 , Issue.3 , pp. 215-222
    • Labrie, F.1
  • 6
    • 0034207640 scopus 로고    scopus 로고
    • Current concepts in androgen deprivation therapy - is there a best endocrine treatment?
    • E.L. Gheiler, and R. Tiguert Current concepts in androgen deprivation therapy - is there a best endocrine treatment? World J. Urol. 18 2000 190 193
    • (2000) World J. Urol. , vol.18 , pp. 190-193
    • Gheiler, E.L.1    Tiguert, R.2
  • 7
    • 0033900377 scopus 로고    scopus 로고
    • Failure to achieve castrate levels of testosterone during luteinizing hormone releasing hormone agonist therapy: The case for monitoring serum testosterone and a treatment decision algorithm
    • M.G. Oefelein, and R. Cornum Failure to achieve castrate levels of testosterone during luteinizing hormone releasing hormone agonist therapy: the case for monitoring serum testosterone and a treatment decision algorithm J. Urol. 164 2000 726 729 (Pubitemid 30637611)
    • (2000) Journal of Urology , vol.164 , Issue.I3 , pp. 726-729
    • Oefelein, M.G.1    Cornum, R.2
  • 8
    • 0032866280 scopus 로고    scopus 로고
    • Serum testosterone-based luteinizing hormone-releasing hormone agonist redosing schedule for chronic androgen ablation: A phase I assessment
    • DOI 10.1016/S0090-4295(99)00316-7, PII S0090429599003167
    • M.G. Oefelein Serum testosterone-based luteinizing hormone-releasing hormone agonist redosing schedule for chronic androgen ablation: a phase I assessment Urology 54 1999 694 699 (Pubitemid 29449432)
    • (1999) Urology , vol.54 , Issue.4 , pp. 694-699
    • Oefelein, M.G.1
  • 9
    • 0022639044 scopus 로고
    • Characteristics of interaction of the antiandrogen flutamide with the androgen receptor in various target tissues
    • DOI 10.1016/0303-7207(86)90132-2
    • J. Simard, I. Luthy, J. Guay, A. Bélanger, and F. Labrie Characteristics of interaction of the antiandrogen flutamide with the androgen receptor in various target tissues Mol. Cell. Endocrinol. 44 1986 261 270 (Pubitemid 16165779)
    • (1986) Molecular and Cellular Endocrinology , vol.44 , Issue.3 , pp. 261-270
    • Simard, J.1    Luthy, I.2    Guay, J.3
  • 10
    • 57749106633 scopus 로고    scopus 로고
    • New cancer drugs targeting the biosynthesis of estrogens and androgens
    • D. Poirier New cancer drugs targeting the biosynthesis of estrogens and androgens Drug Dev. Res. 69 2008 304 318
    • (2008) Drug Dev. Res. , vol.69 , pp. 304-318
    • Poirier, D.1
  • 11
    • 60249089957 scopus 로고    scopus 로고
    • Integrated view on 17beta-hydroxysteroid dehydrogenases
    • G. Moeller, and J. Adamski Integrated view on 17beta-hydroxysteroid dehydrogenases Mol. Cell. Endocrinol. 301 2009 7 19
    • (2009) Mol. Cell. Endocrinol. , vol.301 , pp. 7-19
    • Moeller, G.1    Adamski, J.2
  • 13
    • 77955507711 scopus 로고    scopus 로고
    • The intracrine sex steroid biosynthesis pathways
    • L. Martini, (Chap. 10)
    • V. Luu-The, and F. Labrie The intracrine sex steroid biosynthesis pathways L. Martini, Progress in Brain Research 181 2010 177 192 (Chap. 10)
    • (2010) Progress in Brain Research , vol.181 , pp. 177-192
    • Luu-The, V.1    Labrie, F.2
  • 14
    • 0031023049 scopus 로고    scopus 로고
    • The key role of 17β-hydroxysteroid dehydrogenases in sex steroid biology
    • DOI 10.1016/S0039-128X(96)00174-2, PII S0039128X96001747
    • F. Labrie, V. Luu-The, S.X. Lin, C. Labrie, J. Simard, R. Breton, and A. Bélanger The key role of 17β-hydroxysteroid dehydrogenases in sex steroid biology Steroids 62 1997 148 158 (Pubitemid 27066999)
    • (1997) Steroids , vol.62 , Issue.1 , pp. 148-158
    • Labrie, F.1    Luu-The, V.2    Lin, S.-X.3    Labrie, C.4    Simard, J.5    Breton, R.6    Belanger, A.7
  • 15
    • 84871309352 scopus 로고    scopus 로고
    • Regulation of 17β-hydroxysteroid dehydrogenases in cancer: Regulating steroid receptor at pre-receptor stage
    • M. Rotinen, J. Villar, and I. Encio Regulation of 17β-hydroxysteroid dehydrogenases in cancer: regulating steroid receptor at pre-receptor stage J. Physiol. Biochem. 68 2012 461 473
    • (2012) J. Physiol. Biochem. , vol.68 , pp. 461-473
    • Rotinen, M.1    Villar, J.2    Encio, I.3
  • 16
    • 0037396439 scopus 로고    scopus 로고
    • Endocrine and intracrine sources of androgens in women: Inhibition of breast cancer and other roles of androgens and their precursor dehydroepiandrosterone
    • DOI 10.1210/er.2001-0031
    • F. Labrie, V. Luu-The, C. Labrie, A. Bélanger, J. Simard, S.X. Lin, and G. Pelletier Endocrine and intracrine sources of androgens in women: inhibition of breast cancer and other roles of androgens and their precursor dehydroepiandrosterone Endrocr. Rev. 24 2003 152 182 (Pubitemid 36515283)
    • (2003) Endocrine Reviews , vol.24 , Issue.2 , pp. 152-182
    • Labrie, F.1    Luu-The, V.2    Labrie, C.3    Belanger, A.4    Simard, J.5    Lin, S.-X.6    Pelletier, G.7
  • 17
    • 38649108152 scopus 로고    scopus 로고
    • Proliferative effect of androst-4-ene-3,17-dione and its metabolites in the androgen-sensitive LNCaP cell line
    • Y. Laplante, and D. Poirier Proliferative effect of androst-4-ene-3,17- dione and its metabolites in the androgen-sensitive LNCaP cell line Steroids 73 2008 266 271
    • (2008) Steroids , vol.73 , pp. 266-271
    • Laplante, Y.1    Poirier, D.2
  • 18
    • 0030925341 scopus 로고    scopus 로고
    • Molecular endocrinology of hydroxysteroid dehydrogenases
    • DOI 10.1210/er.18.3.281
    • T.M. Penning Molecular endocrinology of hydroxysteroid dehydrogenases Endocr. Rev. 18 1997 281 305 (Pubitemid 27246879)
    • (1997) Endocrine Reviews , vol.18 , Issue.3 , pp. 281-305
    • Penning, T.M.1
  • 19
    • 57749091994 scopus 로고    scopus 로고
    • Hydroxysteroid dehydrogenase (17β-HSD3, 17β-HSD5, and 3α-HSD3) inhibitors: Extragonadal regulation of intracellular sex steroid hormone levels
    • M.L. Mohler, R. Narayanan, Y. He, D.D. Miller, and J.T. Dalton Hydroxysteroid dehydrogenase (17β-HSD3, 17β-HSD5, and 3α-HSD3) inhibitors: extragonadal regulation of intracellular sex steroid hormone levels Recent Patents Endocr. Metab. Immune Drug Discov. 1 2007 103 118
    • (2007) Recent Patents Endocr. Metab. Immune Drug Discov. , vol.1 , pp. 103-118
    • Mohler, M.L.1    Narayanan, R.2    He, Y.3    Miller, D.D.4    Dalton, J.T.5
  • 22
    • 0036771843 scopus 로고    scopus 로고
    • Differential expression of 17β-hydroxysteroid dehydrogenase isozyme genes in prostate cancer and noncancer tissues
    • E. Koh, T. Noda, J. Kanaya, and M. Namiki Differential expression of 17β-hydroxysteroid dehydrogenase isozyme genes in prostate cancer and noncancer tissues Prostate 53 2002 154 159
    • (2002) Prostate , vol.53 , pp. 154-159
    • Koh, E.1    Noda, T.2    Kanaya, J.3    Namiki, M.4
  • 24
  • 27
    • 0001429526 scopus 로고    scopus 로고
    • Characteristics of a highly labile human type 5 17β-hydroxysteroid dehydrogenase
    • DOI 10.1210/en.140.2.568
    • I. Dufort, P. Rheault, X.F. Huang, and P. Soucy Characteristics of a highly labile human type 5 17β-hydroxysteroid dehydrogenase Endocrinology 140 1999 568 574 (Pubitemid 29058186)
    • (1999) Endocrinology , vol.140 , Issue.2 , pp. 568-574
    • Dufort, I.1    Rheault, P.2    Huang, X.-F.3    Soucy, P.4    Luu-The, V.5
  • 28
    • 79957722662 scopus 로고    scopus 로고
    • Inhibitors of type 5 17β-hydroxysteroid dehydrogenase (AKR1C3): Overview and structural insights
    • M.C. Byrns, Y.T. Jin, and T.M. Penning Inhibitors of type 5 17β-hydroxysteroid dehydrogenase (AKR1C3): overview and structural insights J. Steroid Biochem. Mol. Biol. 125 2011 95 114
    • (2011) J. Steroid Biochem. Mol. Biol. , vol.125 , pp. 95-114
    • Byrns, M.C.1    Jin, Y.T.2    Penning, T.M.3
  • 30
    • 84886586041 scopus 로고    scopus 로고
    • Assessment of steroidogenesis and steroidogenic enzyme functions
    • V. Luu-The Assessment of steroidogenesis and steroidogenic enzyme functions J. Steroid Biochem. Mol. Biol. 137 2013 176 182
    • (2013) J. Steroid Biochem. Mol. Biol. , vol.137 , pp. 176-182
    • Luu-The, V.1
  • 31
    • 80052846905 scopus 로고    scopus 로고
    • Potential prostate cancer drug target: Bioactivation of androstanediol by conversion to dihydrotestosterone
    • J.L. Mohler, M.A. Titus, and E.M. Wilson Potential prostate cancer drug target: bioactivation of androstanediol by conversion to dihydrotestosterone Clin. Cancer Res. 17 2011 5844 5849
    • (2011) Clin. Cancer Res. , vol.17 , pp. 5844-5849
    • Mohler, J.L.1    Titus, M.A.2    Wilson, E.M.3
  • 32
    • 84861197052 scopus 로고    scopus 로고
    • Steroid biosynthesis and prostate cancer
    • N. Sharifi, and R.J. Auchus Steroid biosynthesis and prostate cancer Steroids 77 2012 719 726
    • (2012) Steroids , vol.77 , pp. 719-726
    • Sharifi, N.1    Auchus, R.J.2
  • 33
    • 77955836270 scopus 로고    scopus 로고
    • 17β-Hydroxysteroid dehydrogenase inhibitors: A patent review
    • D. Poirier 17β-Hydroxysteroid dehydrogenase inhibitors: a patent review Exp. Opin. Ther. Patents 20 2010 1123 1145
    • (2010) Exp. Opin. Ther. Patents , vol.20 , pp. 1123-1145
    • Poirier, D.1
  • 34
    • 53849119147 scopus 로고    scopus 로고
    • Design and validation of specific inhibitors of 17β-hydroxysteroid dehydrogenases for therapeutic application in breast and prostate cancer, and in endometriosis
    • J.M. Day, H.J. Tutill, A. Purohit, and M.J. Reed Design and validation of specific inhibitors of 17β-hydroxysteroid dehydrogenases for therapeutic application in breast and prostate cancer, and in endometriosis Endocr. Relat. Cancer 15 2008 665 692
    • (2008) Endocr. Relat. Cancer , vol.15 , pp. 665-692
    • Day, J.M.1    Tutill, H.J.2    Purohit, A.3    Reed, M.J.4
  • 36
    • 23444434382 scopus 로고    scopus 로고
    • Androsterone 3α-ether-3β-substituted and androsterone 3β-substituted derivatives as inhibitors of type 3 17β-hydroxysteroid dehydrogenase: Chemical synthesis and structure - Activity relationship
    • DOI 10.1021/jm058179h
    • B. Tchédam-Ngatcha, V. Luu-The, F. Labrie, and D. Poirier Androsterone 3α-ether-3β-substituted and androsterone 3β-substituted derivatives as inhibitors of type 3 17β-hydroxysteroid dehydrogenase: chemical synthesis and structure-activity relationship J. Med. Chem. 48 2005 5257 5268 (Pubitemid 41113912)
    • (2005) Journal of Medicinal Chemistry , vol.48 , Issue.16 , pp. 5257-5268
    • Ngatcha, B.T.1    Luu-The, V.2    Labrie, F.3    Poirier, D.4
  • 37
    • 0037203996 scopus 로고    scopus 로고
    • Synthesis and optimization of a new family of type 3 17β- hydroxysteroid dehydrogenase inhibitors by parallel liquid-phase chemistry
    • DOI 10.1021/jm010286y
    • R. Maltais, V. Luu-The, and D. Poirier Synthesis and optimization of a new family of type 3 17 β-hydroxysteroid dehydrogenase inhibitors by parallel liquid-phase chemistry J. Med. Chem. 45 2002 640 653 (Pubitemid 34145710)
    • (2002) Journal of Medicinal Chemistry , vol.45 , Issue.3 , pp. 640-653
    • Maltais, R.1    Luu-The, V.2    Poirier, D.3
  • 38
    • 79960564976 scopus 로고    scopus 로고
    • Development of 3β-substituted androsterone derivatives as potent inhibitors of 17β-hydroxysteroid dehydrogenase type 3
    • R. Maltais, M.A. Fournier, and D. Poirier Development of 3β-substituted androsterone derivatives as potent inhibitors of 17β-hydroxysteroid dehydrogenase type 3 Bioorg. Med. Chem. 19 2011 4652 4668
    • (2011) Bioorg. Med. Chem. , vol.19 , pp. 4652-4668
    • Maltais, R.1    Fournier, M.A.2    Poirier, D.3
  • 39
    • 0029593494 scopus 로고
    • Characteristics of human types 1, 2 and 3 17β-hydroxysteroid dehydrogenase activities: Oxidation/reduction and inhibition
    • DOI 10.1016/0960-0760(95)00209-X
    • V. Luu-The, Y. Zhang, D. Poirier, and F. Labrie Characteristics of human types 1, 2 and 3 17β-hydroxysteroid dehydrogenase activities: oxidation/reduction and inhibition J. Steroid Biochem. Mol. Biol. 55 1995 581 587 (Pubitemid 26019342)
    • (1995) Journal of Steroid Biochemistry and Molecular Biology , vol.55 , Issue.5-6 , pp. 581-587
    • Luu-The, V.1    Zhang, Y.2    Poirier, D.3    Labrie, F.4
  • 41
    • 0017184389 scopus 로고
    • A rapid and sensitive method for the quantification of microgram quantities of protein utilizing the principle of protein-dye binding
    • M.M. Bradford A rapid and sensitive method for the quantification of microgram quantities of protein utilizing the principle of protein-dye binding Anal. Biochem. 72 1976 248 254
    • (1976) Anal. Biochem. , vol.72 , pp. 248-254
    • Bradford, M.M.1
  • 42
    • 0000882795 scopus 로고
    • Extension of multiple range tests to group with unique numbers of replications
    • C.Y. Kramer Extension of multiple range tests to group with unique numbers of replications Biometrics 12 1956 307 310
    • (1956) Biometrics , vol.12 , pp. 307-310
    • Kramer, C.Y.1
  • 43
    • 0032586817 scopus 로고    scopus 로고
    • 17β-Hydroxysteroid dehydrogenase (HSD)/17-ketosteroid reductase (KSR) family; nomenclature and main characteristics of the 17HSD/KSR enzymes
    • DOI 10.1677/jme.0.0230001
    • H. Peltoketo, V. Luu-The, J. Simard, and J. Adamski 17β- Hydroxysteroid dehydrogenase (HSD)/17-ketosteroid reductase (KSR) family; nomenclature and main characteristics of the 17HSD/KSR enzymes J. Mol. Endocrinol. 23 1999 1 11 (Pubitemid 29369554)
    • (1999) Journal of Molecular Endocrinology , vol.23 , Issue.1 , pp. 1-11
    • Peltoketo, H.1    Luu-The, V.2    Simard, J.3    Adamski, J.4
  • 44
    • 0023215471 scopus 로고
    • Effect of adrenal steroids on testosterone and luteinizing hormone secretion in the ram
    • P.E. Juniewicz, B.H. Johnson, and D.J. Bolt Effect of adrenal steroid on testosterone and luteinizing hormone secretion in the ram J. Androl. 30 1987 190 196 (Pubitemid 17110752)
    • (1987) Journal of Andrology , vol.8 , Issue.3 , pp. 190-196
    • Juniewicz, P.E.1    Johnson, B.H.2    Bolt, D.J.3
  • 45
    • 28544432178 scopus 로고    scopus 로고
    • Selective blockade of androgenic steroid synthesis by novel lyase inhibitors as a therapeutic strategy for treating metastatic prostate cancer
    • DOI 10.1111/j.1464-410X.2005.05821.x
    • G. Attard, A.S. Belldegrun, and J.S. De Bono Selective blockade of androgenic steroid synthesis by novel lyase inhibitors as a therapeutic strategy for treating metastatic prostate cancer BJU Int. 96 2005 1241 1246 (Pubitemid 41743917)
    • (2005) BJU International , vol.96 , Issue.9 , pp. 1241-1246
    • Attard, G.1    Belldegrun, A.S.2    De Bono, J.S.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.