Nonsteroidal anti-inflammatory drugs as anticancer agents: Mechanistic, pharmacologic, and clinical issues

被引:1170
作者
Thun, MJ
Henley, SJ
Patrono, C
机构
[1] Amer Canc Soc, Dept Epidemiol & Surveillance Res, Natl Home Off, Atlanta, GA 30329 USA
[2] Univ G DAnnunzio, Ctr Excellence Aging, Chieti, Italy
来源
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE | 2002年 / 94卷 / 04期
关键词
D O I
10.1093/jnci/94.4.252
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Numerous experimental, epidemiologic, and clinical studies suggest that nonsteroidal anti-inflammatory drugs (NSAIDs), particularly the highly selective cyclooxygenase (COX)-2 inhibitors, have promise as anticancer agents. NSAIDs restore normal apoptosis in human adenomatous colorectal polyps and in various cancer cell lines that have lost adenomatous polyposis coli gene function. NSAIDs also inhibit angiogenesis in cell culture and rodent models of angiogenesis. Many epidemiologic studies have found that long-term use of NSAIDs is associated with a lower risk of colorectal cancer, adenomatous polyps, and, to some extent, other cancers. Two NSAIDs, sulindac and celecoxib, have been found to inhibit the growth of adenomatous polyps and cause regression of existing polyps in randomized trials of patients with familial adenomatous polyposis (FAP). However, unresolved questions about the safety, efficacy, optimal treatment regimen, and mechanism of action of NSAIDs currently limit their clinical application to the prevention of polyposis in FAP patients. Moreover, the development of safe and effective drugs for chemoprevention is complicated by the potential of even rare, serious toxicity to offset the benefit of treatment, particularly when the drug is administered to healthy people who have low annual risk of developing the disease for which treatment is intended. This review considers generic approaches to improve the balance between benefits and risks associated with the use of NSAIDs in chemoprevention. We critically examine the published experimental, clinical, and epidemiologic literature on NSAIDs and cancer, especially that regarding colorectal cancer, and identify strategies to overcome the various logistic and scientific barriers that impede clinical trials of NSAIDs for cancer prevention. Finally, we suggest research opportunities that may help to accelerate the future clinical application of NSAIDs for cancer prevention or treatment.
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收藏
页码:252 / 266
页数:15
相关论文
共 224 条
[1]   Apoptosis [J].
Afford, S ;
Randhawa, S .
JOURNAL OF CLINICAL PATHOLOGY-MOLECULAR PATHOLOGY, 2000, 53 (02) :55-63
[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, 2000, ONCOL REP, V7, P1377
[4]  
American Society of Clinical Oncology, 1998, CANC GEN CANC PRED T, V1
[5]  
[Anonymous], 1994, BMJ, V308, P81, DOI [10.1136/bmj.308.6921.81, DOI 10.1136/BMJ.308.6921.81]
[6]  
[Anonymous], 2001, The Pharmacological Basis of Therapeutics
[7]  
Baigent C, 2002, BMJ-BRIT MED J, V324, P71, DOI 10.1136/bmj.324.7329.71
[8]  
Bansal P, 1996, AM J GASTROENTEROL, V91, P44
[9]   Determination of an optimal dosing regimen for aspirin chemoprevention of 1,2-dimethylhydrazine-induced colon tumours in rats [J].
Barnes, CJ ;
Lee, M .
BRITISH JOURNAL OF CANCER, 1999, 79 (11-12) :1646-1650
[10]  
BEDI A, 1995, CANCER RES, V55, P1811