Langenbach R, Loftin C D, Lee C, Tiano H
National Institute of Environmental Health Sciences, Research Triangle Park, North Carolina 27709, USA.
Ann N Y Acad Sci. 1999;889:52-61. doi: 10.1111/j.1749-6632.1999.tb08723.x.
Cyclooxygenase (COX)-1- and COX-2-deficient mice have unique physiological differences that have allowed investigation into the individual biological roles of the COX isoforms. In the following, the phenotypes of the two COX knockout mice are summarized, and recent studies to investigate the effects of COX deficiency on inflammatory responses and cancer susceptibility are discussed. The data suggest that both isoforms have important roles in the maintenance of physiological homeostasis and that such designations as house-keeping and/or response gene may not be entirely accurate. Furthermore, data from COX-deficient mice indicate that both isoforms can contribute to the inflammatory response and that both isoforms have significant roles in carcinogenesis.
环氧化酶(COX)-1和COX-2基因敲除小鼠具有独特的生理差异,这使得对COX同工型的个体生物学作用进行研究成为可能。以下总结了两种COX基因敲除小鼠的表型,并讨论了最近关于研究COX缺乏对炎症反应和癌症易感性影响的研究。数据表明,这两种同工型在维持生理稳态中都具有重要作用,并且诸如管家基因和/或反应基因这样的命名可能并不完全准确。此外,来自COX基因敲除小鼠的数据表明,这两种同工型都可促成炎症反应,并且在致癌过程中都具有重要作用。