Effective Prostate Cancer Chemopreventive Intervention with Green Tea Polyphenols in the TRAMP Model Depends on the Stage of the Disease

被引:73
作者
Adhami, Vaclar Mustafa [1 ]
Siddiqui, Imtiaz Ahmad [1 ]
Sarfaraz, Sami [1 ]
Khwaja, Sabih Islam [1 ]
Bin Hafeez, Bilal [1 ]
Ahmad, Nihal [1 ]
Mukhtar, Hasan [1 ]
机构
[1] Univ Wisconsin, Dept Dermatol, Madison, WI 53706 USA
关键词
GROWTH-FACTOR-I; INTRAEPITHELIAL NEOPLASIA; BINDING PROTEIN-3; MOUSE MODEL; CATECHINS; MICE; PREVENTION; TRIAL; CARCINOGENESIS; EPIDEMIOLOGY;
D O I
10.1158/1078-0432.CCR-08-2332
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: We have shown previously that oral feeding of green tea polyphenols (GTP) to transgenic adenocarcinoma of the mouse prostate mice in a purely chemopreventive setting significantly inhibits prostate cancer development. To translate this to a human situation, the present study was designed to identify the stage of prostate cancer that is most vulnerable to chemopreventive intervention by GTP. Experimental Design: GTP infusion (0.1% in drinking water) to transgenic adenocarcinoma of the mouse prostate was initiated at ages representing different stage of the disease: (a) 6 weeks (group 1, normal prostate), (b) 12 weeks (group 2, prostatic intraepithelial neoplasia), (c) 18 weeks (group 3, well-differentiated adenocarcinoma), and (b) 28 weeks (group 4, moderately differentiated adenocarcinoma). At age 32 weeks, subsets of animals were evaluated by magnetic resonance imaging, ultrasound, and prostate weight and for serum insulin-like growth factor (IGF)-I/IGF binding protein-3 and IGF signaling. Results: Tumor-free survival was extended to 38 weeks (P < 0.001) in group 1, 31 weeks (P < 0.01) in group 2, and 24 weeks (P < 0.05) in group 3 compared with 19 weeks in water-fed controls. Median life expectancy was 68 weeks in group 1, 63 weeks in group 2, 56 weeks in group 3, and 51 weeks in group 4 compared with 42 weeks in the control mice. IGF-I and its downstream targets including phosphaticlylinositol 3-kinase, pAkt, and phosphorylated extracellular signal-regulated kinase were significantly inhibited only when intervention was initiated early when prostatic intraepithelial neoplasia lesions were common. Conclusions: Our studies indicate that chemopreventive potential of GTP decreases with advancing stage of the disease and underscore the need to design appropriate chemoprevention clinical trails.
引用
收藏
页码:1947 / 1953
页数:7
相关论文
共 39 条
  • [1] Anti-oxidants from green tea and pomegranate for chemoprevention of prostate cancer
    Adhami, Vaqar Mustafa
    Mukhtar, Hasan
    [J]. MOLECULAR BIOTECHNOLOGY, 2007, 37 (01) : 52 - 57
  • [2] Insulin-like growth factor-I axis as a pathway for cancer chemoprevention
    Adhami, Vaqar Mustafa
    Afaq, Farrukh
    Mukhtar, Hasan
    [J]. CLINICAL CANCER RESEARCH, 2006, 12 (19) : 5611 - 5614
  • [3] Oral consumption of green tea polyphenols inhibits insulin-like growth factor-i-induced signaling in an autochthonous mouse model of prostate cancer
    Adhami, VM
    Siddiqui, IA
    Ahmad, N
    Gupta, S
    Mukhtar, H
    [J]. CANCER RESEARCH, 2004, 64 (23) : 8715 - 8722
  • [4] Angwafo FF, 1998, J NATL MED ASSOC, V90, pS720
  • [5] Chemoprevention of human prostate cancer by oral administration of green tea catechins in volunteers with high-grade prostate intraepithelial neoplasia: A preliminary report from a one-year proof-of-principle study
    Bettuzzi, S
    Brausi, M
    Rizzi, F
    Castagnetti, G
    Peracchia, G
    Corti, A
    [J]. CANCER RESEARCH, 2006, 66 (02) : 1234 - 1240
  • [6] Epidemiology of prostate cancer chemoprevention
    Boyle, P
    Severi, G
    [J]. EUROPEAN UROLOGY, 1999, 35 (5-6) : 370 - 376
  • [7] Chemoprevention of human prostate cancer by Green Tea Catechins: Two years later. A follow-up update
    Brausi, Maurizio
    Rizzi, Federica
    Bettuzzi, Saverio
    [J]. EUROPEAN UROLOGY, 2008, 54 (02) : 472 - 473
  • [8] The chemopreventive action of catechins in the TRAMP mouse model of prostate carcinogenesis is accompanied by clusterin over-expression
    Caporali, A
    Davalli, P
    Astancolle, S
    D'Arca, D
    Brausi, M
    Bettuzzi, S
    Corti, A
    [J]. CARCINOGENESIS, 2004, 25 (11) : 2217 - 2224
  • [9] Chan JM, 2002, J NATL CANCER I, V94, P1099
  • [10] A prospective clinical trial of green tea for hormone refractory prostate cancer: An evaluation of the complementary/alternative therapy approach
    Choan, E
    Segal, R
    Jonker, D
    Malone, S
    Reaume, N
    Eapen, L
    Gallant, V
    [J]. UROLOGIC ONCOLOGY-SEMINARS AND ORIGINAL INVESTIGATIONS, 2005, 23 (02) : 108 - 113