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Volumn 20, Issue 21, 2014, Pages 5547-5557

Canonical androstenedione reduction is the predominant source of signaling androgens in hormone-refractory prostate cancer

Author keywords

[No Author keywords available]

Indexed keywords

ANDROGEN; ANDROSTENEDIONE; CHOLESTEROL; HYDROXYSTEROID DEHYDROGENASE; PRASTERONE; PREGNENOLONE; PROGESTERONE; STEROID 17ALPHA MONOOXYGENASE; TESTOSTERONE; TESTOSTERONE 17BETA DEHYDROGENASE; 15 HYDROXYPROSTAGLANDIN DEHYDROGENASE; 3(OR 17)BETA HYDROXYSTEROID DEHYDROGENASE; AKR1C3 PROTEIN, HUMAN; ANDROGEN RECEPTOR; AR PROTEIN, HUMAN; ESTRADIOL 17BETA DEHYDROGENASE;

EID: 84907393368     PISSN: 10780432     EISSN: 15573265     Source Type: Journal    
DOI: 10.1158/1078-0432.CCR-13-3483     Document Type: Article
Times cited : (43)

References (37)
  • 3
    • 60149089419 scopus 로고    scopus 로고
    • Androgen deprivation therapy: Progress in understanding mechanisms of resistance and optimizing androgen depletion
    • Harris WP, Mostaghel EA, Nelson PS, Montgomery B. Androgen deprivation therapy: progress in understanding mechanisms of resistance and optimizing androgen depletion. Nat Clin Pract Urol 2009;6:76-85.
    • (2009) Nat Clin Pract Urol , vol.6 , pp. 76-85
    • Harris, W.P.1    Mostaghel, E.A.2    Nelson, P.S.3    Montgomery, B.4
  • 5
    • 70350244512 scopus 로고    scopus 로고
    • Increased expression of androgen receptor sensitizes prostate cancer cells to low levels of androgens
    • Waltering KK, Helenius MA, Sahu B, Manni V, Linja MJ, Janne OA, et al. Increased expression of androgen receptor sensitizes prostate cancer cells to low levels of androgens. Cancer Res 2009;69:8141-9.
    • (2009) Cancer Res , vol.69 , pp. 8141-8149
    • Waltering, K.K.1    Helenius, M.A.2    Sahu, B.3    Manni, V.4    Linja, M.J.5    Janne, O.A.6
  • 7
    • 34250331066 scopus 로고    scopus 로고
    • Intraprostatic androgens and androgen-regulated gene expression persist after testosterone suppression: Therapeutic implications for castration-resistant prostate cancer
    • Mostaghel EA, Page ST, Lin DW, Fazli L, Coleman IM, True LD, et al. Intraprostatic androgens and androgen-regulated gene expression persist after testosterone suppression: therapeutic implications for castration-resistant prostate cancer. Cancer Res 2007;67:5033-41.
    • (2007) Cancer Res , vol.67 , pp. 5033-5041
    • Mostaghel, E.A.1    Page, S.T.2    Lin, D.W.3    Fazli, L.4    Coleman, I.M.5    True, L.D.6
  • 8
    • 84871074337 scopus 로고    scopus 로고
    • Prostate cancer-from steroid transformations to clinical translation
    • Chang KH, Sharifi N. Prostate cancer-from steroid transformations to clinical translation. Nat Rev Urol 2012;9:721-4.
    • (2012) Nat Rev Urol , vol.9 , pp. 721-724
    • Chang, K.H.1    Sharifi, N.2
  • 9
    • 51049098138 scopus 로고    scopus 로고
    • 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, Wood CA, 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    Wood, C.A.6
  • 10
  • 11
    • 0034287545 scopus 로고    scopus 로고
    • Human 3alpha-hydroxysteroid dehydrogenase isoforms (AKR1C1-AKR1C4) of the aldo-keto reductase superfamily: Functional plasticity and tissue distribution reveals roles in the inactivation and formation of male and female sex hormones
    • Penning TM, Burczynski ME, Jez JM, Hung CF, Lin HK, Ma H, et al. Human 3alpha-hydroxysteroid dehydrogenase isoforms (AKR1C1-AKR1C4) of the aldo-keto reductase superfamily: functional plasticity and tissue distribution reveals roles in the inactivation and formation of male and female sex hormones. Biochem J 2000;351:67-77.
    • (2000) Biochem J , vol.351 , pp. 67-77
    • Penning, T.M.1    Burczynski, M.E.2    Jez, J.M.3    Hung, C.F.4    Lin, H.K.5    Ma, H.6
  • 12
    • 0027415714 scopus 로고
    • Metabolism of anabolic steroids in man: Synthesis and use of reference substances for identification of anabolic steroid metabolites
    • Schänzer W, Donike M. Metabolism of anabolic steroids in man: synthesis and use of reference substances for identification of anabolic steroid metabolites. Analytica Chimica Acta 1993;275:23-48.
    • (1993) Analytica Chimica Acta , vol.275 , pp. 23-48
    • Schänzer, W.1    Donike, M.2
  • 13
    • 4544341015 scopus 로고    scopus 로고
    • Linear models and empirical bayes methods for assessing differential expression in microarray experiments
    • Smyth GK. Linear models and empirical bayes methods for assessing differential expression in microarray experiments. Stat Appl Genet Mol Biol 2004;3:Article3.
    • (2004) Stat Appl Genet Mol Biol , vol.3
    • Smyth, G.K.1
  • 14
    • 33845432928 scopus 로고    scopus 로고
    • Adjusting batch effects in microarray expression data using empirical Bayes methods
    • Johnson WE, Li C, Rabinovic A. Adjusting batch effects in microarray expression data using empirical Bayes methods. Biostatistics 2007;8:118-27.
    • (2007) Biostatistics , vol.8 , pp. 118-127
    • Johnson, W.E.1    Li, C.2    Rabinovic, A.3
  • 15
    • 0025066941 scopus 로고
    • More powerful procedures for multiple significance testing
    • Hochberg Y, Benjamini Y. More powerful procedures for multiple significance testing. Stat Med 1990;9:811-8.
    • (1990) Stat Med , vol.9 , pp. 811-818
    • Hochberg, Y.1    Benjamini, Y.2
  • 16
    • 0029743674 scopus 로고    scopus 로고
    • Androgens markedly stimulate the accumulation of neutral lipids in the human prostatic adenocarcinoma cell line LNCaP
    • Swinnen JV, Van Veldhoven PP, Esquenet M, Heyns W, Verhoeven G. Androgens markedly stimulate the accumulation of neutral lipids in the human prostatic adenocarcinoma cell line LNCaP. Endocrinology 1996;137:4468-74.
    • (1996) Endocrinology , vol.137 , pp. 4468-4474
    • Swinnen, J.V.1    Van Veldhoven, P.P.2    Esquenet, M.3    Heyns, W.4    Verhoeven, G.5
  • 18
    • 84879671701 scopus 로고    scopus 로고
    • A coclinical approach identifies mechanisms and potential therapies for androgen deprivation resistance in prostate cancer
    • Lunardi A, Ala U, Epping MT, Salmena L, Clohessy JG, Webster KA, et al. A coclinical approach identifies mechanisms and potential therapies for androgen deprivation resistance in prostate cancer. Nat Genet 2013;45:747-55.
    • (2013) Nat Genet , vol.45 , pp. 747-755
    • Lunardi, A.1    Ala, U.2    Epping, M.T.3    Salmena, L.4    Clohessy, J.G.5    Webster, K.A.6
  • 21
    • 33645056171 scopus 로고    scopus 로고
    • Increased expression of genes converting adrenal androgens to testosterone in androgen-independent prostate cancer
    • Stanbrough M, Bubley GJ, Ross K, Golub TR, Rubin MA, Penning TM, 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    Penning, T.M.6
  • 22
    • 84870336847 scopus 로고    scopus 로고
    • Distinct patterns of dysregulated expression of enzymes involved in androgen synthesis and metabolism in metastatic prostate cancer tumors
    • Mitsiades N, Sung CC, Schultz N, Danila DC, He B, Eedunuri VK, et al. Distinct patterns of dysregulated expression of enzymes involved in androgen synthesis and metabolism in metastatic prostate cancer tumors. Cancer Res 2012;72:6142-52.
    • (2012) Cancer Res , vol.72 , pp. 6142-6152
    • Mitsiades, N.1    Sung, C.C.2    Schultz, N.3    Danila, D.C.4    He, B.5    Eedunuri, V.K.6
  • 23
    • 84888370246 scopus 로고    scopus 로고
    • Role of aldo-keto reductase family 1 (AKR1) enzymes in human steroid metabolism
    • Rizner TL, Penning TM. Role of aldo-keto reductase family 1 (AKR1) enzymes in human steroid metabolism. Steroids 2014;79:49-63.
    • (2014) Steroids , vol.79 , pp. 49-63
    • Rizner, T.L.1    Penning, T.M.2
  • 24
    • 49249119358 scopus 로고    scopus 로고
    • 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, Higano CS, 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    Higano, C.S.6
  • 26
    • 0028173882 scopus 로고
    • Steroid 5 alpha-reductase: Two genes/two enzymes
    • Russell DW, Wilson JD. Steroid 5 alpha-reductase: two genes/two enzymes. Ann Rev Biochem 1994;63:25-61.
    • (1994) Ann Rev Biochem , vol.63 , pp. 25-61
    • Russell, D.W.1    Wilson, J.D.2
  • 28
    • 0026723090 scopus 로고
    • Tissue distribution and kinetic characteristics of rat steroid 5 alpha-reductase isozymes. Evidence for distinct physiological functions
    • Normington K, Russell DW. Tissue distribution and kinetic characteristics of rat steroid 5 alpha-reductase isozymes. Evidence for distinct physiological functions. J Biol Chem 1992;267:19548-54.
    • (1992) J Biol Chem , vol.267 , pp. 19548-19554
    • Normington, K.1    Russell, D.W.2
  • 29
    • 0025873322 scopus 로고
    • Feed-forward control of prostate growth: Dihydrotestosterone induces expression of its own biosynthetic enzyme, steroid 5 alpha-reductase
    • George FW, Russell DW, Wilson JD. Feed-forward control of prostate growth: dihydrotestosterone induces expression of its own biosynthetic enzyme, steroid 5 alpha-reductase. Proc Natl Acad Sci U S A 1991;88:8044-7.
    • (1991) Proc Natl Acad Sci U S A , vol.88 , pp. 8044-8047
    • George, F.W.1    Russell, D.W.2    Wilson, J.D.3
  • 33
    • 61649103983 scopus 로고    scopus 로고
    • Steroid hormone transforming aldo-keto reductases and cancer
    • Penning TM, Byrns MC. Steroid hormone transforming aldo-keto reductases and cancer. Ann NY Acad Sci 2009;1155:33-42.
    • (2009) Ann NY Acad Sci , vol.1155 , pp. 33-42
    • Penning, T.M.1    Byrns, M.C.2
  • 34
    • 84863230589 scopus 로고    scopus 로고
    • Development of potent and selective inhibitors of aldo-keto reductase 1C3 (type 5 17beta-hydroxysteroid dehydrogenase) based on N-phenyl-aminobenzoates and their structure-activity relationships
    • Adeniji AO, Twenter BM, Byrns MC, Jin Y, Chen M, Winkler JD, et al. Development of potent and selective inhibitors of aldo-keto reductase 1C3 (type 5 17beta-hydroxysteroid dehydrogenase) based on N-phenyl-aminobenzoates and their structure-activity relationships. J Med Chem 2012;55:2311-23.
    • (2012) J Med Chem , vol.55 , pp. 2311-2323
    • Adeniji, A.O.1    Twenter, B.M.2    Byrns, M.C.3    Jin, Y.4    Chen, M.5    Winkler, J.D.6
  • 35
    • 79957722662 scopus 로고    scopus 로고
    • 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
  • 36
    • 37349047898 scopus 로고    scopus 로고
    • An indomethacin analogue, N-(4-chlorobenzoyl)-melatonin, is a selective inhibitor of aldo-keto reductase 1C3 (type 2 3alpha-HSD, type 5 17beta-HSD, and prostaglandin F synthase), a potential target for the treatment of hormone dependent and hormone independent malignancies
    • Byrns MC, Steckelbroeck S, Penning TM. An indomethacin analogue, N-(4-chlorobenzoyl)-melatonin, is a selective inhibitor of aldo-keto reductase 1C3 (type 2 3alpha-HSD, type 5 17beta-HSD, and prostaglandin F synthase), a potential target for the treatment of hormone dependent and hormone independent malignancies. Biochem Pharmacol 2008;75:484-93.
    • (2008) Biochem Pharmacol , vol.75 , pp. 484-493
    • Byrns, M.C.1    Steckelbroeck, S.2    Penning, T.M.3
  • 37
    • 84860493930 scopus 로고    scopus 로고
    • Crystal structures of AKR1C3 containing an N-(aryl) amino-benzoate inhibitor and a bifunctional AKR1C3 inhibitor and androgen receptor antagonist. Therapeutic leads for castrate-resistant prostate cancer
    • Chen M, Adeniji AO, Twenter BM, Winkler JD, Christianson DW, Penning TM. Crystal structures of AKR1C3 containing an N-(aryl) amino-benzoate inhibitor and a bifunctional AKR1C3 inhibitor and androgen receptor antagonist. Therapeutic leads for castrate-resistant prostate cancer. Bioorg Med Chem Lett 2012;22:3492-7.
    • (2012) Bioorg Med Chem Lett , vol.22 , pp. 3492-3497
    • Chen, M.1    Adeniji, A.O.2    Twenter, B.M.3    Winkler, J.D.4    Christianson, D.W.5    Penning, T.M.6


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