Testosterone and dihydrotestosterone tissue levels in recurrent prostate cancer

被引:421
作者
Titus, MA [1 ]
Schell, MJ
Lih, FB
Tomer, KB
Mohler, JL
机构
[1] Univ N Carolina, Sch Med, Lineberger Comprehens Canc Ctr, Dept Pathol & Lab Med, Chapel Hill, NC 27599 USA
[2] Univ N Carolina, Sch Med, Lineberger Comprehens Canc Ctr, Dept Surg, Chapel Hill, NC 27599 USA
[3] Univ N Carolina, Sch Med, Lineberger Comprehens Canc Ctr, Dept Biostat, Chapel Hill, NC 27599 USA
[4] Natl Inst Environm Hlth Sci, Struct Biol Lab, Res Triangle Pk, NC USA
[5] Roswell Pk Canc Inst, Dept Urol Oncol, Buffalo, NY 14263 USA
[6] SUNY Buffalo, Sch Med & Biotechnol, Dept Urol, Buffalo, NY 14260 USA
关键词
D O I
10.1158/1078-0432.CCR-05-0525
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: Prostate cancer eventually recurs during androgen deprivation therapy despite castrate levels of serum androgens. Expression of androgen receptor and androgen receptor-regulated proteins suggests androgen receptor activation in recurrent prostate cancer. Many groups have pursued mechanisms of ligand-independent androgen receptor activation but we found high levels of testicular androgens in recurrent prostate cancer tissue using RIA. Experimental Designs: Prostate specimens from 36 men were procured preserving blood flow to prevent ischemia and cyropreserved immediately. Recurrent prostate cancer specimens from 18 men whose cancer recurred locally during androgen deprivation therapy and androgen-stimulated benign prostate specimens from 18 men receiving no hormonal treatments were studied. Tissue levels of testosterone and dihydrotestosterone were measured in each specimen using liquid chromatography/electrospray tandem mass spectrometry.Testosterone and dihydrotestosterone levels were compared with clinical variables and treatment received. Results: Testosterone levels were similar in recurrent prostate cancer (3.75 pmol/g tissue) and androgen-stimulated benign prostate (2.75 pmol/g tissue, Wilcoxon two-sided, P = 0.30). Dihydrotestosterone levels decreased 91 % in recurrent prostate cancer (1.25 pmol/g tissue) compared with androgen-stimulated benign prostate (13.7 pmol/g tissue; Wilcoxon two-sided, P < 0.0001) although dihydrotestosterone levels in most specimens of recurrent prostate cancer were sufficient for androgen receptor activation. Testosterone or dihydrotestosterone levels were not related to metastatic status, antiandrogen treatment, or survival (Wilcoxon rank sum, all P > 0.2). Conclusions: Recurrent prostate cancer may develop the capacity to biosynthesize testicular androgens from adrenal androgens or cholesterol. This surprising finding suggests intracrine production of dihydrotestosterone and should be exploited for novel treatment of recurrent prostate cancer.
引用
收藏
页码:4653 / 4657
页数:5
相关论文
共 31 条
[1]   COMPARISON OF RESIDUAL C-19 STEROIDS IN PLASMA AND PROSTATIC TISSUE OF HUMAN, RAT AND GUINEA-PIG AFTER CASTRATION - UNIQUE IMPORTANCE OF EXTRATESTICULAR ANDROGENS IN MEN [J].
BELANGER, B ;
BELANGER, A ;
LABRIE, F ;
DUPONT, A ;
CUSAN, L ;
MONFETTE, G .
JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 1989, 32 (05) :695-698
[2]   Amplification of the androgen receptor gene in bone metastases from hormone-refractory prostate cancer [J].
Brown, RSD ;
Edwards, J ;
Dogan, A ;
Payne, H ;
Harland, SJ ;
Bartlett, JMS ;
Masters, JRW .
JOURNAL OF PATHOLOGY, 2002, 198 (02) :237-244
[3]   Molecular determinants of resistance to antiandrogen therapy [J].
Chen, CD ;
Welsbie, DS ;
Tran, C ;
Baek, SH ;
Chen, R ;
Vessella, R ;
Rosenfeld, MG ;
Sawyers, CL .
NATURE MEDICINE, 2004, 10 (01) :33-39
[4]   Switch from antagonist to agonist of the androgen receptor blocker bicalutamide is associated with prostate tumour progression in a new model system [J].
Culig Z. ;
Hoffmann J. ;
Erdel M. ;
Eder I.E. ;
Hobisch A. ;
Hittmair A. ;
Bartsch G. ;
Utermann G. ;
Schneider M.R. ;
Parczyk K. ;
Klocker H. .
British Journal of Cancer, 1999, 81 (2) :242-251
[5]   Androgen receptor gene amplification and protein expression in hormone refractory prostate cancer [J].
Edwards, J ;
Krishna, NS ;
Grigor, KM ;
Bartlett, JMS .
BRITISH JOURNAL OF CANCER, 2003, 89 (03) :552-556
[6]   The development of androgen-independent prostate cancer [J].
Feldman, BJ ;
Feldman, D .
NATURE REVIEWS CANCER, 2001, 1 (01) :34-45
[7]   Cholesterol and prostate cancer [J].
Freeman, MR ;
Solomon, KR .
JOURNAL OF CELLULAR BIOCHEMISTRY, 2004, 91 (01) :54-69
[8]   STEROID-LEVELS IN CANCER OF THE PROSTATE - MARKERS OF TUMOR DIFFERENTIATION AND ADEQUACY OF ANTI-ANDROGEN THERAPY [J].
GELLER, J ;
ALBERT, J ;
LOZA, D .
JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 1979, 11 (01) :631-636
[9]  
GELLER J, 1988, SEMIN ONCOL, V15, P53
[10]  
GELLER J, 1978, J CLIN ENDOCR METAB, V46, P440