生物
重编程
癌细胞
转录因子
粒体自噬
癌症干细胞
串扰
细胞生物学
KEAP1型
线粒体
线粒体生物发生
干细胞
背景(考古学)
癌症
细胞适应
自噬
遗传学
细胞
细胞凋亡
基因
古生物学
物理
光学
作者
Emiliano Panieri,Sónia Pinho,Gonçalo J. M. Afonso,Paulo J. Oliveira,Teresa Cunha‐Oliveira,Luciano Saso
出处
期刊:Cells
[MDPI AG]
日期:2022-08-04
卷期号:11 (15): 2401-2401
被引量:35
标识
DOI:10.3390/cells11152401
摘要
The NRF2–KEAP1 system is a fundamental component of the cellular response that controls a great variety of transcriptional targets that are mainly involved in the regulation of redox homeostasis and multiple cytoprotective mechanisms that confer adaptation to the stress conditions. The pleiotropic response orchestrated by NRF2 is particularly relevant in the context of oncogenic activation, wherein this transcription factor acts as a key driver of tumor progression and cancer cells’ resistance to treatment. For this reason, NRF2 has emerged as a promising therapeutic target in cancer cells, stimulating extensive research aimed at the identification of natural, as well as chemical, NRF2 inhibitors. Excitingly, the influence of NRF2 on cancer cells’ biology extends far beyond its mere antioxidant function and rather encompasses a functional crosstalk with the mitochondrial network that can influence crucial aspects of mitochondrial homeostasis, including biogenesis, oxidative phosphorylation, metabolic reprogramming, and mitophagy. In the present review, we summarize the current knowledge of the reciprocal interrelation between NRF2 and mitochondria, with a focus on malignant tumors and cancer stem cells.
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