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转录因子 Nrf2 的致癌功能。

Oncogenic functions of the transcription factor Nrf2.

机构信息

Department of System Biology, Biochemistry and Molecular Biology Unit, University of Alcalá, 28871 Alcalá de Henares (Madrid), Spain.

Department of Leukemia, University of Texas M.D. Anderson Cancer Center, 77030 Houston, TX, USA.

出版信息

Free Radic Biol Med. 2013 Dec;65:750-764. doi: 10.1016/j.freeradbiomed.2013.06.041. Epub 2013 Jun 29.

Abstract

Nuclear factor E2-related factor 2 (Nrf2) is a transcription factor that controls the expression of a large pool of antioxidant and cytoprotective genes regulating the cellular response to oxidative and electrophilic stress. Nrf2 is negatively regulated by Kelch-like ECH-associated protein 1 (Keap1) and, upon stimulation by an oxidative or electrophilic insult, is rapidly activated by protein stabilization. Owing to its cytoprotective functions, Nrf2 has been traditionally studied in the field of chemoprevention; however, there is accumulated evidence that Keap1/Nrf2 mutations or unbalanced regulation that leads to overexpression or hyperactivation of Nrf2 may participate in tumorigenesis and be involved in chemoresistance of a wide number of solid cancers and leukemias. In addition to protecting cells from reactive oxygen species, Nrf2 seems to play a direct role in cell growth control and is related to apoptosis-regulating pathways. Moreover, Nrf2 activity is connected with oncogenic kinase pathways, structural proteins, hormonal regulation, other transcription factors, and epigenetic enzymes involved in the pathogenesis of various types of tumors. The aim of this review is to compile and summarize existing knowledge of the oncogenic functions of Nrf2 to provide a solid basis for its potential use as a molecular marker and pharmacological target in cancer.

摘要

核因子 E2 相关因子 2(Nrf2)是一种转录因子,可控制一大类抗氧化和细胞保护基因的表达,调节细胞对氧化和亲电应激的反应。Nrf2 受 Kelch 样 ECH 相关蛋白 1(Keap1)的负调控,在受到氧化或亲电损伤刺激后,其蛋白稳定性迅速增加而被激活。由于其细胞保护功能,Nrf2 传统上在化学预防领域进行研究;然而,越来越多的证据表明,Keap1/Nrf2 突变或不平衡的调节导致 Nrf2 的过度表达或过度激活可能参与肿瘤发生,并参与多种实体瘤和白血病的化疗耐药性。除了保护细胞免受活性氧的侵害外,Nrf2 似乎在细胞生长控制中发挥直接作用,并与凋亡调节途径有关。此外,Nrf2 活性与致癌激酶途径、结构蛋白、激素调节、其他参与各种类型肿瘤发病机制的转录因子和表观遗传酶有关。本综述的目的是总结和总结 Nrf2 的致癌功能的现有知识,为其作为癌症的分子标志物和药理学靶点的潜在用途提供坚实的基础。

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