Crowell James A, Steele Vernon E, Sigman Caroline C, Fay Judith R
National Cancer Institute, Division of Cancer Prevention, Chemopreventive Agent Development Research Group, Bethesda, Maryland 20892, USA.
Mol Cancer Ther. 2003 Aug;2(8):815-23.
The molecular messenger nitric oxide (NO) is synthesized endogenously from L-arginine by three isoforms of the enzyme NO synthase. The isoform most consistently associated with neoplasia is the inducible form, inducible nitric oxide synthase (iNOS). However, the role played by the NO/iNOS system in tumor development is complex, and both promoting and inhibitory effects on neoplasia have been reported. This review attempts to clarify the role of iNOS in carcinogenesis, with particular emphasis on the early stages of tumor development, offers possible explanations for the confused picture presented in the literature regarding the association of the NO/iNOS pathway with neoplasia, and identifies selective iNOS inhibitors that may have chemopreventive potential.
分子信使一氧化氮(NO)由一氧化氮合酶的三种同工型从L-精氨酸内源性合成。与肿瘤形成最始终相关的同工型是诱导型,即诱导型一氧化氮合酶(iNOS)。然而,NO/iNOS系统在肿瘤发展中所起的作用是复杂的,并且已经报道了对肿瘤形成既有促进作用又有抑制作用。本综述试图阐明iNOS在致癌作用中的作用,特别强调肿瘤发展的早期阶段,为文献中关于NO/iNOS途径与肿瘤形成关联所呈现的混乱情况提供可能的解释,并确定可能具有化学预防潜力的选择性iNOS抑制剂。