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ENDOGENOUS NITROSATION CHEMISTRY IN CARCINOGENESIS

致癌过程中的内源亚硝化化学

基本信息

批准号：
6710716
负责人：
Richard N Loeppky
金额：
$ 19.58万
依托单位：
UNIVERSITY OF MISSOURI-COLUMBIA
依托单位国家：
美国
项目类别：
财政年份：
2000
资助国家：
美国
起止时间：
2000-04-01 至 2006-03-31
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/6710716
关键词：
adduct aldehydes amidines aminoacid benzodiazepines chemical carcinogen chemical carcinogenesis cyanides dietary constituent food ketones mutagens nitric oxide nitrosamines nitroso compounds nutrition related neoplasm /cancer nutrition related tag

项目摘要

The goal of this research is to provide knowledge and practical strategies for the significant reduction of carcinogenesis which may arise from endogenous nitrosation processes which can generate electrophilic species capable of modifying DNA and causing mutations. The principle hypothesis of this proposal is that significant progress toward this goal can be achieved 1) by showing through logical experimentation what can be made; 2) by elucidating the chemistry of processes which may catalyze or otherwise facilitate, as well as block, the N-nitrosation of available substrates and the production of electrophiles, and 3) by providing available markers, such as DNA adducts or other products, of genotoxicity which could be used in epidemiological studies to make connections between endogenous nitrosation chemistry and cancer. Our focus is directed at revealing the role that nitrosation of compounds containing C-N double bonds may play in the generation of cell damaging electrophiles, and how this process, as well as the nitrosation of other substrates, may occur through the reaction of NO with radical cations produced by oxidation processes such as those which occur at inflammation sites. Model substrates and drugs containing the oxazoline, imidazoline, and benzodiazepine rings will be nitrosated under endogenous conditions and the nature of the electrophiles arising from these transformations identified and the nature of their DNA adducts determined when appropriate. Both acidic nitrosation and NO + O2 Dietary aldehydes and ketones, including sugars, will be examined for their ability to catalyze the nitrosative conversion of primary amines, including amino acids, to diazonium ions, alpha-acyloxynitrosamines, or alpha-hydroxynitrosamines. The ability of NO mediated damage to occur by its reaction with radical cations produced by other oxidative processes will be probed. Computational methods will be employed to reveal reaction paths of intermediates and lead to better predictions of the types of compounds which pose a carcinogenic threat through their endogenous nitrosation.

这项研究的目的是为显着减少内源性亚硝化过程可能引起的致癌提供知识和实用策略，内源亚硝化过程可以产生能够修饰DNA并导致突变的亲电物种。这一建议的主要假设是，可以实现这一目标的重大进展：1)通过逻辑实验表明可以取得什么；2)通过阐明可能催化或以其他方式促进和阻止可用底物的N-亚硝化和亲电体产生的过程的化学；以及3)通过提供可用于流行病学研究的遗传毒性的现有标记，如DNA加合物或其他产品，以建立内源亚硝化化学与癌症之间的联系。我们的重点是揭示含有C-N双键的化合物的亚硝化在产生细胞破坏性亲电体中可能起到的作用，以及这一过程以及其他底物的亚硝化如何通过NO与氧化过程产生的自由基阳离子反应而发生，这些过程发生在炎症部位。含有恶唑啉、咪唑啉和苯并二氮杂环的模型底物和药物将在内源条件下进行亚硝化，并在适当的情况下确定由这些转化产生的亲电性的性质及其DNA加合物的性质。酸性亚硝化和NO+O2膳食醛和酮，包括糖，将考察它们催化伯胺(包括氨基酸)亚硝化转化为重氮离子、α-酰氧基亚硝胺或α-羟基亚硝胺的能力。NO通过与其他氧化过程产生的自由基阳离子反应而发生损伤的能力将被探讨。计算方法将被用来揭示中间体的反应路径，并导致更好地预测通过内源亚硝化作用构成致癌威胁的化合物的类型。