Nrf2 signaling pathway: Pivotal roles in inflammation

被引:1704
作者
Ahmed, Syed Minhaj Uddin [1 ]
Luo, Lin [2 ,3 ]
Namani, Akhileshwar [1 ]
Wang, Xiu Jun [2 ]
Tang, Xiuwen [1 ]
机构
[1] Zhejiang Univ, Sch Med, Dept Biochem, Hangzhou 310058, Zhejiang, Peoples R China
[2] Zhejiang Univ, Sch Med, Dept Pharmacol, Hangzhou 310058, Zhejiang, Peoples R China
[3] Nantong Univ, Sch Pharm, Nantong 226001, Peoples R China
来源
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE | 2017年 / 1863卷 / 02期
基金
中国国家自然科学基金;
关键词
Nrf2; Keap1; ARE; Inflammation; Oxidative stress; Phytochemical; NF-KAPPA-B; TRANSCRIPTION FACTOR NRF2; CUL3-BASED E3 LIGASE; ACUTE LUNG INJURY; OXIDATIVE STRESS; HEME OXYGENASE-1; NLRP3; INFLAMMASOME; ENDOTHELIAL-CELLS; LUPUS NEPHRITIS; ENHANCES SUSCEPTIBILITY;
D O I
10.1016/j.bbadis.2016.11.005
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Inflammation is the most common feature of many chronic diseases and complications, while playing critical roles in carcinogenesis. Several studies have demonstrated that Nrf2 contributes to the anti-inflammatory process by orchestrating the recruitment of inflammatory cells and regulating gene expression through the antioxidant response element (ARE).The Keap1 (Kelch-like ECH-associated protein)/Nrf2 (NF-E2 p45-related factor 2)/ARE signaling pathway mainly regulates anti-inflammatory gene expression and inhibits the progression of inflammation. Therefore, the identification of new Nrf2-dependent anti-inflammatory phytochemicals has become a key point in drug discovery. In this review, we discuss the members of the Keap1/Nrf2/ARE signal pathway and its downstream genes, the effects of this pathway on animal models of inflammatory diseases, and crosstalk with the NF-kappa B pathway. In addition we also discuss about the regulation of NLRP3 inflammasome by Nrf2. Besides this, we summarize the current scenario of the development of anti-inflammatory phytochemicals and others that mediate the Nrf2/ARE signaling pathway. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:585 / 597
页数:13
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