Baek Seung Joon, Eling Thomas E
University of Tennessee, Department of Pathobiology, College of Veterinary Medicine Knoxville, TN 37996, USA.
Prog Lipid Res. 2006 Jan;45(1):1-16. doi: 10.1016/j.plipres.2005.10.001. Epub 2005 Nov 21.
Non-steroidal anti-inflammatory drugs (NSAIDs) are used primarily for the treatment of inflammatory diseases. However, certain NSAIDs also have a chemopreventive effect on the development of human colorectal and other cancers. NSAIDs inhibit cyclooxygenase-1 (COX-1) and/or cyclooxygenase-2 (COX-2) activity and considerable evidence supports a role for prostaglandins in cancer development. However, the chemopreventive effect of NSAIDs on colorectal and other cancers appears also to be partially independent of COX activity. COX inhibitors also alter the expression of a number of genes that influence cancer development. One such gene is NAG-1 (NSAID-Activated Gene), a critical gene regulated by a number of COX inhibitors and chemopreventive chemicals. Therefore, this article will discuss the evidence supporting the conclusion that the chemo-preventive activity of COX inhibitors is mediated, in part, by altered gene expression with an emphasis on NAG-1 studies. This review may also provide new insights into how chemicals and environmental factors influence cancer development. In view of the cardiovascular and gastrointestinal toxic side effects of COX-2 inhibitors and non-selective COX inhibitors, respectively, the results presented here may provide the basis for the development of a new family of anti-tumorigenic compounds acting independent of COX inhibition.
非甾体抗炎药(NSAIDs)主要用于治疗炎症性疾病。然而,某些NSAIDs对人类结直肠癌和其他癌症的发生也具有化学预防作用。NSAIDs抑制环氧化酶-1(COX-1)和/或环氧化酶-2(COX-2)的活性,并且大量证据支持前列腺素在癌症发生中起作用。然而,NSAIDs对结直肠癌和其他癌症的化学预防作用似乎也部分独立于COX活性。COX抑制剂还会改变许多影响癌症发生的基因的表达。其中一个这样的基因是NAG-1(NSAID激活基因),它是一个受多种COX抑制剂和化学预防剂调控的关键基因。因此,本文将讨论支持COX抑制剂的化学预防活性部分是由基因表达改变介导这一结论的证据,重点是NAG-1的研究。这篇综述还可能为化学物质和环境因素如何影响癌症发生提供新的见解。鉴于COX-2抑制剂和非选择性COX抑制剂分别具有心血管和胃肠道毒性副作用,本文给出的结果可能为开发一类独立于COX抑制作用的新型抗肿瘤化合物提供依据。