Anderson William F, Umar Asad, Viner Jaye L, Hawk Ernest T
Gastrointestinal & Other Cancers Research Group, National Cancer Institute, Division of Cancer Prevention, EPN, Room 2141, 6130 Executive Boulevard, Bethesda, MD 20892-7317, USA.
Curr Pharm Des. 2002;8(12):1035-62. doi: 10.2174/1381612023394935.
Carcinogenesis results from the long-term accumulation of genetic and epigenetic aberrations at the molecular level, which are under constant selection pressure for growth advantage. Recognizing that cancer is the result of this long-term, multi-step process provides opportunities for molecularly targeted cancer prevention. Ideally, chemopreventive agents should be low in toxicity, morbidity, and cost. Several individual agents and agent combinations are currently under evaluation in the U.S. National Cancer Institute s (NCI) chemoprevention agent development program. Nonsteroidal anti-inflammatory drugs (NSAIDs) that inhibit cyclooxygenase (COX) -1 and -2 are among the most promising classes of agents for targeted molecular prevention.
癌症发生是由于分子水平上遗传和表观遗传异常的长期积累,这些异常在生长优势的持续选择压力下不断变化。认识到癌症是这一长期、多步骤过程的结果,为分子靶向癌症预防提供了机会。理想情况下,化学预防剂应具有低毒性、低发病率和低成本。目前,美国国立癌症研究所(NCI)的化学预防剂开发项目正在评估几种单独的药剂及其组合。抑制环氧化酶(COX)-1和-2的非甾体抗炎药(NSAIDs)是最有前景的靶向分子预防药剂类别之一。