Cyclooxygenase-2 as a potential target in the prevention and treatment of genitourinary tumors: A review

被引:62
作者
Pruthi, RS [1 ]
Derksen, E [1 ]
Gaston, K [1 ]
机构
[1] Univ N Carolina, Div Urol Surg, Chapel Hill, NC 27599 USA
关键词
prostatic neoplasms; bladder neoplasms; kidney neoplasms; cyclooxygenase inhibitors; prostaglandins;
D O I
10.1097/01.ju.0000047364.56051.74
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
Purpose: Recent years have seen a dramatic expansion in our discovery and knowledge of the molecular mechanisms of cancer development and progression. The discovery and elucidation of prostaglandin pathways, in particular the molecular and clinical role of cyclooxygenase (COX)-2 function, has had important application to neoplasms. Current understanding of the role of COX-2 activity and, thereby, the potential clinical usefulness of COX-2 specific inhibitors as they apply to urological oncology are discussed. Materials and Methods: The discovery of prostaglandin pathways, the molecular and clinical role of COX-2 function, and the corresponding application to neoplasms were reviewed in the scientific literature (MEDLINE from 1960 to the present). In particular, a thorough review of the current literature and recent abstract presentations at scientific meetings was done regarding the potential role of COX-2 in urological cancers (MEDLINE from 1960 to the present, and American Urological Association and American Society of Clinical Oncology annual meeting abstracts from 1998 to the present). Results: Decreased apoptosis, increased angiogenesis and immunosuppression are just some of the known sequelae of COX-2 over expression and each effect may have an important role in tumor formation and progression. Preclinical research and pilot clinical studies in urological oncology, in particular prostate, bladder and kidney cancer, have proved to be quite promising to date. Conclusions: Currently we are just beginning to understand the molecular mechanisms and clinical effects of COX-2 function and inhibition, and the potential for COX-2 specific inhibitors to affect potentially tumor biology and growth and, thereby, serve as antitumor drugs with therapeutic and chemopreventive roles for urological cancers. The absence of complete scientific understanding in these areas provides a generous opportunity for innovative and important scientific study.
引用
收藏
页码:2352 / 2359
页数:8
相关论文
共 75 条
[1]  
Almer G, 2001, ANN NEUROL, V49, P176, DOI 10.1002/1531-8249(20010201)49:2<176::AID-ANA37>3.0.CO
[2]  
2-X
[3]  
[Anonymous], CAMPBELLS UROLOGY
[4]   STRUCTURE OF THE HUMAN CYCLO-OXYGENASE-2 GENE [J].
APPLEBY, SB ;
RISTIMAKI, A ;
NEILSON, K ;
NARKO, K ;
HLA, T .
BIOCHEMICAL JOURNAL, 1994, 302 :723-727
[5]  
Attiga FA, 2000, CANCER RES, V60, P4629
[6]   Interaction of cyclooxygenases with an apoptosis- and autoimmunity-associated protein [J].
Ballif, BA ;
Mincek, NV ;
Barratt, JT ;
Wilson, ML ;
Simmons, DL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (11) :5544-5549
[7]  
BARNA BP, 1991, ONCOLOGY, V48, P464
[9]   Expression of cyclooxygenase-1 and-2 in urinary bladder carcinoma in vivo and in vitro and prostaglandin E2 synthesis in cultured bladder cancer cells [J].
Boström, PJ ;
Aaltonen, V ;
Söderstrom, KO ;
Uotila, P ;
Laato, M .
PATHOLOGY, 2001, 33 (04) :469-474
[10]  
Brzozowski T, 2000, J PHYSIOL PHARMACOL, V51, P751