Understanding the Epidemiology, Natural History, and Key Pathways Involved in Prostate Cancer

被引:135
作者
Crawford, E. David [1 ]
机构
[1] Univ Colorado, Hlth Sci Ctr, Sect Urol Oncol, Aurora, CO 80045 USA
基金
美国国家卫生研究院;
关键词
STEROID; 5-ALPHA-REDUCTASE; ANDROGEN RECEPTOR; UNITED-STATES; MALE PSEUDOHERMAPHRODITISM; WHITE MEN; RISK; EXPRESSION; ISOENZYMES; TYPE-1; BLACK;
D O I
10.1016/j.urology.2009.03.001
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Prostate cancer accounts for about 25% of all the newly diagnosed cancers in American men and was projected to cause >28 000 deaths in 2008. Black men are disproportionately affected; their incidence rate is about 1.6 times greater than the rate for white men. As the population ages, the number of new cases per year is expected to increase by >60% and reach 300 000 by 2015. This high incidence, coupled with the protracted onset of the disease, makes PCa a particularly appropriate candidate for prevention and early intervention strategies. Potential disease precursors, particularly high-grade prostatic intraepithelial neoplasia, might help identify men at high risk of developing PCa. Dihydrotestosterone, a product converted from testosterone by 5 alpha-reductases, plays an important role in normal prostate growth and in the development of PCa. The 5 alpha-reductase levels, particularly type 1, appear to increase during the disease course of prostatic intraepithelial neoplasia and PCa, with greater expression occurring as the disease progresses. Therefore, the inhibition of 5 alpha-reductase could potentially reduce the risk of PCa development, slow or prevent disease progression, and/or treat existing disease. A substantial research effort has recently focused on understanding the pathways involved in the disease's emergence and progression, particularly the 5a-reductase pathway. UROLOGY 73 (Suppl 5A): 4-10, 2009. (C) 2009 Published by Elsevier Inc.
引用
收藏
页码:4 / 10
页数:7
相关论文
共 57 条
[1]   STRUCTURAL AND BIOCHEMICAL-PROPERTIES OF CLONED AND EXPRESSED HUMAN AND RAT STEROID 5-ALPHA-REDUCTASES [J].
ANDERSSON, S ;
RUSSELL, DW .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (10) :3640-3644
[2]   DELETION OF STEROID 5-ALPHA-REDUCTASE 2-GENE IN MALE PSEUDOHERMAPHRODITISM [J].
ANDERSSON, S ;
BERMAN, DM ;
JENKINS, EP ;
RUSSELL, DW .
NATURE, 1991, 354 (6349) :159-161
[3]   The effects of 5α-reductase inhibitors on the natural history, detection and grading of prostate cancer:: Current state of knowledge [J].
Andriole, G ;
Bostwick, D ;
Civantos, F ;
Epstein, J ;
Lucia, MS ;
McConnell, J ;
Roehrborn, CG .
JOURNAL OF UROLOGY, 2005, 174 (06) :2098-2104
[4]   Chemoprevention of prostate cancer in men at high risk: Rationale and design of the reduction by dutasteride of prostate cancer events (reduce) trial [J].
Andriole, G ;
Bostwick, D ;
Brawley, O ;
Gomella, L ;
Tindall, D ;
Breed, S ;
Somerville, M ;
Rittmaster, R .
JOURNAL OF UROLOGY, 2004, 172 (04) :1314-1317
[5]  
[Anonymous], GLOBAL CANC FACTS FI
[6]   International trends in prostate-cancer mortality: the decrease is continuing and spreading [J].
Baade, PD ;
Coory, MD ;
Aitken, JF .
CANCER CAUSES & CONTROL, 2004, 15 (03) :237-241
[7]  
Balk Steven P, 2008, Nucl Recept Signal, V6, pe001, DOI 10.1621/nrs.06001
[8]  
Bonkhoff H, 1996, PROSTATE, V29, P261, DOI 10.1002/(SICI)1097-0045(199610)29:4<261::AID-PROS7>3.0.CO
[9]  
2-E
[10]   Human prostate cancer risk factors [J].
Bostwick, DG ;
Burke, HB ;
Djakiew, D ;
Euling, S ;
Ho, SM ;
Landolph, J ;
Morrison, H ;
Sonawane, B ;
Shifflett, T ;
Waters, DJ ;
Timms, B .
CANCER, 2004, 101 (10) :2371-2490