Nrf2 signaling pathway: current status and potential therapeutic targetable role in human cancers

癌症 癌症研究 氧化应激 转录因子 信号转导 调节器 癌细胞 生物 机制(生物学) 癌变 戒毒(替代医学) 癌症预防 生物信息学 医学 基因 细胞生物学 遗传学 病理 生物化学 替代医学 哲学 认识论
作者
Lin Li,Qing Wu,Feifei Lu,Jiaming Lei,Yanhong Zhou,Yifei Liu,Ni Zhu,Yu You,Zhifeng Ning,Tonghui She,Meichun Hu
出处
期刊:Frontiers in Oncology [Frontiers Media]
卷期号:13 被引量:53
标识
DOI:10.3389/fonc.2023.1184079
摘要

Cancer is a borderless global health challenge that continues to threaten human health. Studies have found that oxidative stress (OS) is often associated with the etiology of many diseases, especially the aging process and cancer. Involved in the OS reaction as a key transcription factor, Nrf2 is a pivotal regulator of cellular redox state and detoxification. Nrf2 can prevent oxidative damage by regulating gene expression with antioxidant response elements (ARE) to promote the antioxidant response process. OS is generated with an imbalance in the redox state and promotes the accumulation of mutations and genome instability, thus associated with the establishment and development of different cancers. Nrf2 activation regulates a plethora of processes inducing cellular proliferation, differentiation and death, and is strongly associated with OS-mediated cancer. What’s more, Nrf2 activation is also involved in anti-inflammatory effects and metabolic disorders, neurodegenerative diseases, and multidrug resistance. Nrf2 is highly expressed in multiple human body parts of digestive system, respiratory system, reproductive system and nervous system. In oncology research, Nrf2 has emerged as a promising therapeutic target. Therefore, certain natural compounds and drugs can exert anti-cancer effects through the Nrf2 signaling pathway, and blocking the Nrf2 signaling pathway can reduce some types of tumor recurrence rates and increase sensitivity to chemotherapy. However, Nrf2’s dual role and controversial impact in cancer are inevitable consideration factors when treating Nrf2 as a therapeutic target. In this review, we summarized the current state of biological characteristics of Nrf2 and its dual role and development mechanism in different tumor cells, discussed Keap1/Nrf2/ARE signaling pathway and its downstream genes, elaborated the expression of related signaling pathways such as AMPK/mTOR and NF-κB. Besides, the main mechanism of Nrf2 as a cancer therapeutic target and the therapeutic strategies using Nrf2 inhibitors or activators, as well as the possible positive and negative effects of Nrf2 activation were also reviewed. It can be concluded that Nrf2 is related to OS and serves as an important factor in cancer formation and development, thus provides a basis for targeted therapy in human cancers.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
更新
PDF的下载单位、IP信息已删除 (2025-6-4)

科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
充电宝应助健忘傲柏采纳,获得10
刚刚
洛神发布了新的文献求助10
1秒前
1秒前
XSY发布了新的文献求助10
1秒前
3秒前
善学以致用应助ardejiang采纳,获得10
4秒前
张张小白发布了新的文献求助30
4秒前
传奇3应助DRYAN采纳,获得10
5秒前
阿龙发布了新的文献求助10
5秒前
5秒前
SciGPT应助多发文章采纳,获得10
6秒前
6秒前
汉堡包应助猴丫丫采纳,获得10
6秒前
高大的千柳完成签到,获得积分10
7秒前
想发SCI的小钰完成签到,获得积分10
8秒前
XSY完成签到,获得积分10
10秒前
wangbq发布了新的文献求助10
10秒前
Hello应助binxman采纳,获得10
12秒前
心想事成完成签到,获得积分20
12秒前
Alvin完成签到,获得积分10
13秒前
13秒前
花南星发布了新的文献求助10
14秒前
小石头完成签到,获得积分10
14秒前
15秒前
SYLH应助HBXAurora采纳,获得20
15秒前
博修发布了新的文献求助10
16秒前
17秒前
17秒前
18秒前
19秒前
19秒前
20秒前
20秒前
20秒前
DRYAN发布了新的文献求助10
20秒前
四夕水窖完成签到 ,获得积分10
21秒前
linuo完成签到,获得积分10
22秒前
fczs发布了新的文献求助10
22秒前
xiaoshuwang发布了新的文献求助10
22秒前
22秒前
高分求助中
【请各位用户详细阅读此贴后再求助】科研通的精品贴汇总(请勿应助) 10000
【提示信息,请勿应助】关于scihub 10000
Les Mantodea de Guyane: Insecta, Polyneoptera [The Mantids of French Guiana] 3000
徐淮辽南地区新元古代叠层石及生物地层 3000
The Mother of All Tableaux: Order, Equivalence, and Geometry in the Large-scale Structure of Optimality Theory 3000
Research on Disturbance Rejection Control Algorithm for Aerial Operation Robots 1000
Global Eyelash Assessment scale (GEA) 1000
热门求助领域 (近24小时)
化学 材料科学 医学 生物 工程类 有机化学 生物化学 物理 内科学 纳米技术 计算机科学 化学工程 复合材料 遗传学 基因 物理化学 催化作用 冶金 细胞生物学 免疫学
热门帖子
关注 科研通微信公众号,转发送积分 4047090
求助须知:如何正确求助?哪些是违规求助? 3584921
关于积分的说明 11393661
捐赠科研通 3312285
什么是DOI,文献DOI怎么找? 1822513
邀请新用户注册赠送积分活动 894507
科研通“疑难数据库(出版商)”最低求助积分说明 816316