Development of COX inhibitors in cancer prevention and therapy

被引:26
作者
Umar, A
Viner, JL
Anderson, WF
Hawk, ET
机构
[1] NCI, Div Canc Prevent, EPN, Bethesda, MD 20892 USA
[2] NCI, Gastrointestinal & Other Canc Res Grp, Div Canc Prevent, Bethesda, MD 20892 USA
来源
AMERICAN JOURNAL OF CLINICAL ONCOLOGY-CANCER CLINICAL TRIALS | 2003年 / 26卷 / 04期
关键词
cyclooxygenases; COX-1; COX-2; cancer prevention; cancer therapy; molecular target; clinical trials; nonsteroidal antiinflammatory drugs (NSAIDs); celecoxib; sulindac; aspirin;
D O I
10.1097/00000421-200308002-00003
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
dOn the strength of in vitro, in vivo, observational, and clinical data, nonsteroidal antiinflammatory drugs (NSAIDs)-also referred to as COX inhibitors-have emerged as lead compounds for cancer prevention, and possible adjuncts to cancer therapy. Thus far, the routine use of NSAIDs for these indications is limited, largely owing to toxicity concerns, the paucity of efficacy data for any specific target organ, and uncertainties with regard to the most appropriate regimen (i.e., the best agent, formulation, dose, route of administration, and duration). Strategies to address these concerns primarily aim to improve the therapeutic index (i.e., benefit:risk ratio) of COX inhibitors by 1) minimizing systemic exposures whenever feasible, 2) achieving greater mechanistic specificity, 3) coadministering agents that provide prophylaxis against common toxicities, and 4) coadministering other effective anticancer agents. Clinical trials testing most of these strategies have been completed or are under way. The National Cancer Institute has a substantial research portfolio dedicated to the identification, testing, and development of NSAIDs as preventive and therapeutic anticancer agents. Discovering how to apply NSAIDs in persons with-or at risk for-cancer, although challenging, has the potential for considerable clinical and public health benefits.
引用
收藏
页码:S48 / S57
页数:10
相关论文
共 210 条
[1]  
Achiwa H, 1999, CLIN CANCER RES, V5, P1001
[2]   Lovastatin augments sulindac-induced apoptosis in colon cancer cells and potentiates chemopreventive effects of sulindac [J].
Agarwal, B ;
Rao, CV ;
Bhendwal, S ;
Ramey, WR ;
Shirin, H ;
Reddy, BS ;
Holt, PR .
GASTROENTEROLOGY, 1999, 117 (04) :838-847
[3]  
Alshafie GA, 1999, ANTICANCER RES, V19, P3031
[4]  
Alshafie GA, 2000, ONCOL REP, V7, P1377
[5]  
[Anonymous], 1998, Am J Med
[6]   Epithelial cyclooxygenase-2 expression: A model for pathogenesis of colon cancer [J].
Arbabi, S ;
Rosengart, MR ;
Garcia, I ;
Jelacic, S ;
Maier, RV .
JOURNAL OF SURGICAL RESEARCH, 2001, 97 (01) :60-64
[7]  
Bae SH, 2001, CLIN CANCER RES, V7, P1410
[8]  
BALCH CM, 1984, SURGERY, V95, P71
[9]  
Bamba H, 1999, INT J CANCER, V83, P470, DOI 10.1002/(SICI)1097-0215(19991112)83:4<470::AID-IJC6>3.3.CO
[10]  
2-6