Reaction pathways of lipid oxyl radicals and DNA damage

脂氧自由基与DNA损伤的反应途径

• 批准号: 7234707
• 负责人: VLADIMIR SHAFIROVICH
• 金额: $ 28.95万
• 依托单位: NEW YORK UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2002
• 资助国家: 美国
• 起止时间: 2002-04-01 至 2010-02-28
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7234707
• 关键词: 8-oxoguanine; Anions; Biological Markers; Biological Models; Cancer Etiology; Carbon; Carbonates; Cells; Chemicals; Chronic; Clinical; Colon Carcinoma; Complex; Condition; Cyclization; DNA; DNA Damage; Data; Development; Electrons; Etiology; Fatty Acids; Goals; Guanine; High Pressure Liquid Chromatography; Human; Infection; Inflammation; Inflammatory; Kinetics; Knowledge; Lasers; Lesion; Lipid Peroxidation; Lipids; Malignant Neoplasms; Malignant neoplasm of pancreas; Malignant neoplasm of prostate; Mass Spectrum Analysis; Membrane Lipids; Methods; Nitrogen; Nitrogen Dioxide; Nucleic Acids; Numbers; Oligonucleotides; Oxidants; Oxidation-Reduction; Oxygen; Pathway interactions; Personal Satisfaction; Play; Polyunsaturated Fatty Acids; Prevention strategy; Primary carcinoma of the liver cells; Purpose; Reaction; Reaction Time; Reactive Oxygen Species; Recruitment Activity; Relative (related person); Renal Cell Carcinoma; Research Personnel; Role; Solutions; Spectrum Analysis; Superoxides; Testing; Time; absorption; alkoxyl radical; analytical method; aqueous; base; cancer cell; cell transformation; chemical reaction; ds-DNA; in vivo; insight; macrophage; neutrophil; novel strategies; nucleobase; oxidation; oxidative DNA damage; perhydroxyl radical; programs; response; study characteristics

DESCRIPTION (provided by applicant): A growing body of epidemiological data suggests that chronic inflammation and infection induce malignant cell transformations and thus play a critical role in the etiology of human cancers. The overproduction of radicals (carbonate, nitrogen dioxide, superoxide radicals) in response to chronic infection and cellular inflammation is accompanied by the reactions of these radicals with polyunsaturated fatty acids (PUFA) in lipid membranes that generate highly reactive, genotoxic oxyl intermediates (peroxyl and alkoxyl radicals). In turn, these radicals contribute to oxidative DNA damage that contributes to the etiology of cancer by poorly defined pathways. Guanine is the most easily oxidizable nucleic acid base in DNA and is therefore a primary target of attack of reactive radical species. The guanine radicals formed undergo a cascade of reactions that culminate in the formation of stable and unstable, genotoxic chemical end-products. However, the reaction pathways, particularly the mechanisms of reaction of peroxyl and alkoxyl radicals with DNA are poorly understood. We have developed new approaches for studying in real time the reactions of unstable nucleobase radicals in DNA with reactive intermediates such as the peroxyl and alkoxyl radicals derived from lipid peroxidation, in aqueous solutions. The analysis of intermediate and final reaction products by a complex of analytical methods including HPLC, MALDI-TOF/MS, and HPLC-ESI-MS/MS, will provide insights into the mechanism of DNA reaction and oxidation pathways. In specific Aim 1, the mechanisms of radical-radical reactions of PUFA peroxyl radicals and guanine radicals in DNA will be investigated. In specific Aim 2, the further oxidation initiated by PUFA peroxyl radicals of 8-oxoguanine, a ubiquitous and well known form of cellular oxidative DNA damage, will be assessed. In specific Aim 3, the detailed mechanisms of the still poorly understood oxidation pathways of PUFA molecules with reactive oxygen species (carbonate radical anion, nitrogen dioxide, superoxide radicals) will be investigated. The development of a variety of cancers including hepatocellular carcinoma, prostate cancer, pancreatic cancer, renal cell carcinoma, and colon cancer, have been correlated with chronic inflammation and infection. A better understanding of the oxidative lipid peroxidation pathways of DNA damage should provide a rational basis for the development of new strategies for the prevention and/or progression of these types of malignancies.

描述（由申请人提供）：越来越多的流行病学数据表明，慢性炎症和感染诱导恶性细胞转化，因此在人类癌症的病因学中起关键作用。在慢性感染和细胞炎症反应中，自由基（碳酸盐、二氧化氮、超氧自由基）的过量产生伴随着这些自由基与脂质膜中的多不饱和脂肪酸（PUFA）的反应，这些多不饱和脂肪酸产生高活性、遗传毒性的氧中间体（过氧基和烷氧基自由基）。反过来，这些自由基通过不明确的途径导致DNA氧化损伤，从而导致癌症的病因。鸟嘌呤是DNA中最易氧化的核酸碱基，因此是活性自由基攻击的主要目标。形成的鸟嘌呤自由基经过一连串的反应，最终形成稳定和不稳定的遗传毒性化学最终产物。然而，人们对过氧基和烷氧基自由基与DNA的反应途径，特别是反应机制了解甚少。我们开发了新的方法来实时研究DNA中不稳定的核碱基自由基与活性中间体（如脂质过氧化产生的过氧基和烷氧基自由基）在水溶液中的反应。通过HPLC、MALDI-TOF/MS和HPLC- esi -MS/MS等分析方法对中间和最终反应产物进行分析，将有助于深入了解DNA反应的机理和氧化途径。在特定的Aim 1中，将研究DNA中PUFA过氧自由基和鸟嘌呤自由基的自由基-自由基反应机制。在特定的Aim 2中，将评估8-氧鸟嘌呤的PUFA过氧自由基（一种普遍存在且众所周知的细胞氧化DNA损伤形式）引发的进一步氧化。在特定的Aim 3中，将研究PUFA分子与活性氧（碳酸盐自由基阴离子，二氧化氮，超氧自由基）氧化途径的详细机制。包括肝细胞癌、前列腺癌、胰腺癌、肾细胞癌和结肠癌在内的各种癌症的发展都与慢性炎症和感染有关。更好地了解DNA损伤的氧化脂质过氧化途径将为开发预防和/或发展这些类型的恶性肿瘤的新策略提供合理的基础。