Androgen ablation therapy for prostate carcinoma suppresses the immunoreactive telomerase subunit hTERT

被引:17
作者
Iczkowski, KA
Huang, W
Mazzucchelli, R
Pantazis, CG
Stevens, GR
Montironi, R
机构
[1] VA Med Ctr, Pathol & Lab Med Serv 113, Dept Pathol & Lab Med, Gainesville, FL 32608 USA
[2] Univ Florida, Dept Pathol & Lab Med, Gainesville, FL 32611 USA
[3] Univ Ancona Hosp, Dept Pathol & Lab Med, Ancona, Italy
[4] Univ Florida, Biostat Consulting Lab, Gainesville, FL 32611 USA
关键词
telomerase; hTERT; prostate carcinoma; androgen ablation; immunohistochemistry;
D O I
10.1002/cncr.20002
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BACKGROUND. Telomerase is a ribonucleoprotein complex that protects the ends of chromosomes from degradation. Its catalytic subunit, hTERT, controls its activity. Prior data in prostate carcinoma cases indicated that immunohistochemical hTERT reactivity increases with tumor grade and may be absent in lower grade cases. The effect of complete androgen ablation (CAA) on tumor hTERT expression was uncertain. METHODS. hTERT immunostaining was performed on the cancerous pretreatment biopsy tissue of 30 men who consecutively underwent CAA with bicalutamide and goserelin acetate for 30 days prior to undergoing radical prostatectomy, and on their tumor tissue from radical prostatectomy. As controls, biopsy and prostatectomy samples from 30 untreated men were studied. Nuclear staining was evaluated by two observers, and the change in staining between biopsy and prostatectomy samples was evaluated using the Student t test in both groups. RESULTS. The percent of reactive tumor nuclei in treated men declined from 36.7% to 13.2% (P = 0.0001), and declined from 19.8% to 16.1% in untreated men (P = 0.4). The greater mean hTERT reactivity in the treated men's biopsy specimens was attributed to an increased proportion of higher (Gleason score greater than or equal to 7) grade tumors. The decline in hTERT immunostaining remained significant after normalizing it to that of the untreated group (P = 0.002). The original Gleason scores, corresponding declines in the percentage of reactive tumor nuclei, and significance were: Gleason score less than or equal to 6: 11% (P = 0.03); Gleason score of 7:23% (P < 0.006); and Gleason score less than or equal to 8: 46% (P < 0.005) (from a mean 63% to 17%). CONCLUSIONS. CAA for prostate carcinoma can be considered an antitelomerase therapy. The steepest reduction in telomerase activity was noted in the highest grade tumors. (C) 2003 American Cancer Society.
引用
收藏
页码:294 / 299
页数:6
相关论文
共 35 条
[1]   bcl-2 Overexpression combined with p53 protein accumulation correlates with hormone-refractory prostate cancer [J].
Apakama, I ;
Robinson, MC ;
Walter, NM ;
Charlton, RG ;
Royds, JA ;
Fuller, CE ;
Neal, DE ;
Hamdy, FC .
BRITISH JOURNAL OF CANCER, 1996, 74 (08) :1258-1262
[2]   Gleason score predicts androgen independent progression after androgen deprivation therapy [J].
Benaim, EA ;
Pace, CM ;
Roehrborn, CG .
EUROPEAN UROLOGY, 2002, 42 (01) :12-17
[3]   Expression-patterns of the RNA component (hTR) and the catalytic subunit (hTERT) of human telomerase in nonneoplastic prostate tissue, prostatic intraepithelial neoplasia, and prostate cancer [J].
Bettendorf, O ;
Heine, B ;
Kneif, S ;
Eltze, E ;
Semjonow, A ;
Herbst, H ;
Stein, H ;
Böcker, W ;
Poremba, C .
PROSTATE, 2003, 55 (02) :99-104
[4]   The effects of natural ligands of hormone receptors and their antagonists on telomerase activity in the androgen sensitive prostatic cancer cell line LNCaP [J].
Bouchal, J ;
Kolár, Z ;
Mad'arová, J ;
Hlobilková, A ;
von Angerer, E .
BIOCHEMICAL PHARMACOLOGY, 2002, 63 (06) :1177-1181
[5]   Pathologic effects of Neoadjuvant cyproterone acetate on nonneoplastic prostate, prostatic intraepithelial neoplasia, and adenocarcinoma - A detailed analysis of radical prostatectomy specimens from a randomized trial [J].
Bullock, MJ ;
Srigley, JR ;
Klotz, LH ;
Goldenberg, SL .
AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 2002, 26 (11) :1400-1413
[6]   Telomerase activity is restored in human cells by ectopic expression of hTERT (hEST2), the catalytic subunit of telomerase [J].
Counter, CM ;
Meyerson, M ;
Eaton, EN ;
Ellisen, LW ;
Caddle, SD ;
Haber, DA ;
Weinberg, RA .
ONCOGENE, 1998, 16 (09) :1217-1222
[7]   THE RNA COMPONENT OF HUMAN TELOMERASE [J].
FENG, JL ;
FUNK, WD ;
WANG, SS ;
WEINRICH, SL ;
AVILION, AA ;
CHIU, CP ;
ADAMS, RR ;
CHANG, E ;
ALLSOPP, RC ;
YU, JH ;
LE, SY ;
WEST, MD ;
HARLEY, CB ;
ANDREWS, WH ;
GREIDER, CW ;
VILLEPONTEAU, B .
SCIENCE, 1995, 269 (5228) :1236-1241
[8]  
Hisatake J, 1999, CANCER RES, V59, P4023
[9]   Telomerase reverse transcriptase subunit immunoreactivity - A marker for high-grade prostate carcinoma [J].
Iczkowski, KA ;
Pantazis, CG ;
McGregor, DH ;
Wu, YP ;
Tawfik, OW .
CANCER, 2002, 95 (12) :2487-2493
[10]  
Johnson MI, 1998, PROSTATE, V37, P223, DOI 10.1002/(SICI)1097-0045(19981201)37:4<223::AID-PROS3>3.0.CO