Role of Nrf2 Cross-Talk in Cancer Chemoprevention

Nrf2 串扰在癌症化学预防中的作用

• 批准号: 8635981
• 负责人: THOMAS W KENSLER
• 金额: $ 36.2万
• 依托单位: UNIVERSITY OF PITTSBURGH AT PITTSBURGH
• 依托单位国家: 美国
• 财政年份: 2001
• 资助国家: 美国
• 起止时间: 2001-12-21 至 2017-03-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8635981
• 关键词: Acetaminophen; Affect; Albumins; Animals; Anti-Inflammatory Agents; Anti-inflammatory; Antioxidants; Autophagocytosis; Benefits and Risks; Binding; Carcinogens; Cell Survival; Cells; Chemicals; Chemoprevention; Chemopreventive Agent; Chemoprotection; Chemoprotective Agent; Chronic; DNA Repair; Excision; Food; Gene Targeting; Genes; Genetic; Goals; Heat shock proteins; Hepatocarcinogenesis; Hepatocyte; Human; Kinetics; Liver; Liver Regeneration; Liver diseases; Luciferases; Mediating; Molecular; Molecular Genetics; Mus; Natural regeneration; Nucleotides; Oncogenes; Outcome; Partial Hepatectomy; Pathway interactions; Pharmacodynamics; Prevention; Promoter Regions; Recovery; Reporter; Research; Resistance; Response Elements; Role; Rosa; Signal Pathway; Signal Transduction; Stress; Sulforaphane; System; Testing; Toxic effect; Transgenic Mice; Transgenic Model; Transplantation; Urokinase; Wild Type Mouse; Work; base; cancer chemoprevention; carcinogenesis; chemical carcinogenesis; chemical genetics; detoxication; in vivo; liver injury; major urinary proteins; multicatalytic endopeptidase complex; neoplastic cell; promoter; protective effect; protein misfolding; repaired; research study; response; small molecule; stress protein; tissue repair; transcription factor; tumor growth

DESCRIPTION (provided by applicant): Activation of the Keap1-Nrf2 signaling pathway is an adaptive response to environmental and endogenous stresses and serves to render animals resistant to chemical carcinogenesis and other forms of toxicity, whereas disruption of the pathway exacerbates these outcomes. This pathway, which can be activated by sulfhydryl reactive, small-molecule pharmacologic and food-based agents used in chemoprevention, regulates the inducible expression of an extended battery of cytoprotective genes, often by direct binding of the transcription factor Nrf2 to antioxidant response elements in the promoter regions of target genes. However, our recent work indicates that some of the protective effects may be mediated indirectly through cross-talk with additional pathways affecting cell survival and other aspects of cell fate. These interactions provide a multi-tiered, integrated response to chemical stresses through: (i) prevention of macromolecular damage through induction of antioxidative, anti-inflammatory and carcinogen detoxication genes; (ii) induction of macromolecular damage recognition, repair/removal systems; and (iii) activation of tissue repair/regeneration pathways. In this project we seek to use molecular, genetic and chemical approaches to test the hypothesis that chemoprotection mediated by Nrf2 reflects both activation of its direct target genes but importantly cross- talk with other adaptive response signaling networks affecting cell fate, such as Notch1. The overall goals of the proposed studies are two-fold: to assess the underlying mechanisms and consequences of pathway cross-talk and to assess the functional significance and possible untoward effects of chronic induction of the Nrf2 response in order to facilitate the identification and utilization of safe, efficacious chemopreventive agents.

描述（由申请人提供）：Keap 1-Nrf 2信号通路的激活是对环境和内源性应激的适应性反应，可使动物对化学致癌作用和其他形式的毒性具有抗性，而该通路的破坏会加剧这些结果。该途径可被化学预防中使用的巯基反应性、小分子药理学和基于食物的试剂激活，通常通过转录因子Nrf 2与靶基因启动子区中的抗氧化反应元件直接结合来调节细胞保护基因的扩展电池的诱导表达。然而，我们最近的工作表明，一些保护作用可能是通过与影响细胞存活和细胞命运其他方面的其他途径的串扰间接介导的。这些相互作用通过以下方式提供了对化学应激的多层次综合反应：（i）通过诱导抗氧化、抗炎和致癌物解毒基因来预防大分子损伤;（ii）诱导大分子损伤识别、修复/去除系统;和（iii）激活组织修复/再生途径。在这个项目中，我们试图使用分子，遗传和化学方法来测试的假设，即Nrf 2介导的化学保护反映了其直接靶基因的激活，但重要的是与影响细胞命运的其他适应性反应信号网络，如Notch 1的串扰。拟议研究的总体目标有两个方面：评估通路串扰的潜在机制和后果，并评估慢性诱导Nrf 2应答的功能意义和可能的不良影响，以促进安全有效的化学预防剂的鉴定和利用。