COX-2: A molecular target for colorectal cancer prevention

被引:443
作者
Brown, JR [1 ]
DuBois, RN [1 ]
机构
[1] Vanderbilt Univ, Ingram Canc Ctr, Nashville, TN 37232 USA
关键词
D O I
10.1200/JCO.2005.09.051
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Cyclooxygenase (COX), a key enzyme in the prostanoid biosynthetic pathway, has received considerable attention due to its role in human cancers. Observational and randomized controlled studies in many different population cohorts and settings have demonstrated protective effects of nonsteroidal anti-inflammatory drugs (NSAIDs; the inhibitors of COX activity) for colorectal cancers (CRCs). COX-2, the inducible isoform of cyclooxygenase, is overexpressed in early and advanced CRC tissues, which portends a poor prognosis. Experimental studies have thus identified important mechanisms and pathways by which COX-2 plays an important role in carcinogenesis. Selective COX-2 inhibitors have been approved for use as adjunctive therapy for patients with familial polyposis. The role of COX-2 inhibitors is currently being evaluated for use in wider populations,
引用
收藏
页码:2840 / 2855
页数:16
相关论文
共 215 条
[11]   MENINGITIS DUE TO MORAXELLA OSLOENSIS [J].
BERGER, U ;
KREISSEL, M .
INFECTION, 1974, 2 (03) :166-168
[12]  
Blanke CD, 2002, ONCOLOGY-NY, V16, P17
[13]   Comparison of upper gastrointestinal toxicity of rofecoxib and naproxen in patients with rheumatoid arthritis. [J].
Bombardier, C ;
Laine, L ;
Reicin, A ;
Shapiro, D ;
Burgos-Vargas, R ;
Davis, B ;
Day, R ;
Ferraz, MB ;
Hawkey, CJ ;
Hochberg, MC ;
Kvien, TK ;
Schnitzer, TJ ;
Weaver, A .
NEW ENGLAND JOURNAL OF MEDICINE, 2000, 343 (21) :1520-1528
[14]  
Boolbol SK, 1996, CANCER RES, V56, P2556
[15]  
BRAUN DP, 1993, CANCER RES, V53, P3362
[16]   Long-term use of nonsteroidal antiinflammatory drugs and the risk of colorectal adenomas [J].
Breuer-Katschinski, B ;
Nemes, K ;
Rump, B ;
Leiendecker, B ;
Marr, A ;
Breuer, N ;
Goebell, H .
DIGESTION, 2000, 61 (02) :129-134
[17]   APC, β-catenin and hTCF-4;: an unholy trinity in the genesis of colorectal cancer [J].
Bright-Thomas, RM ;
Hargest, R .
EUROPEAN JOURNAL OF SURGICAL ONCOLOGY, 2003, 29 (02) :107-117
[18]   INTEGRIN ALPHA(V)BETA(3) ANTAGONISTS PROMOTE TUMOR-REGRESSION BY INDUCING APOPTOSIS OF ANGIOGENIC BLOOD-VESSELS [J].
BROOKS, PC ;
MONTGOMERY, AMP ;
ROSENFELD, M ;
REISFELD, RA ;
HU, TH ;
KLIER, G ;
CHERESH, DA .
CELL, 1994, 79 (07) :1157-1164
[19]  
Brown JR, 2002, ADV EXP MED BIOL, V507, P409
[20]  
BRUNDA MJ, 1980, J IMMUNOL, V124, P2682