Selection of topically applied non-steroidal anti-inflammatory drugs for oral cancer chemoprevention

被引:21
作者
Sood, S
Shiff, SJ
Yang, CS
Chen, XX
机构
[1] Rutgers State Univ, Susan Lehman Cullman Lab Canc Res, Dept Biol Chem, Ernest Mario Sch Pharm, Piscataway, NJ 08854 USA
[2] Canc Inst New Jersey, New Brunswick, NJ 08903 USA
关键词
oral cancer; NSAIDs;
D O I
10.1016/j.oraloncology.2005.01.003
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Topical delivery of non-steroidal anti-inflammatory drugs through the oral mucosa has been used for oral cancer chemoprevention. Local permeation of these agents has been one of the major concerns. Here we propose an approach to predict the permeability of topically applied agents for oral cancer chemoprevention. In theory, the total flux through the oral mucosa (J(max)) can be estimated by adding the transcellutar flux (J(TC)) and the paracettutar flux (J(PC)). To target the Cox-2 enzyme in oral epithelial cells, it is desirable to maximize the theoretical activity index, the ratio of J(TC) and IC50 of a Cox-2 inhibitor (J(TC)/IC50-Cox-2). Among the 12 commonly used NSAIDs, cetecoxib, nimesulide and ibuprofen had the highest values and may be the agents of choice to target Cox-2 in oral epithelial cells through topical application. Based on these calculations, a tong-term chemopreventive experiment using celecoxib (3% or 6%) through topical application was performed in a DMBA induced hamster oral cancer model. Both 3% and 6% reduced the incidence of squamous cell carcinoma at the post-initiation stage. (c) 2005 Elsevier Ltd. All rights reserved.
引用
收藏
页码:562 / 567
页数:6
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