Kansanen Emilia, Kuosmanen Suvi M, Leinonen Hanna, Levonen Anna-Liisa
Department of Biotechnology and Molecular Medicine, A. I. Virtanen Institute for Molecular Sciences, University of Eastern Finland, P.O. Box 1627, FIN-70211, Kuopio, Finland.
Redox Biol. 2013 Jan 18;1(1):45-9. doi: 10.1016/j.redox.2012.10.001.
The Keap1-Nrf2 pathway is the major regulator of cytoprotective responses to oxidative and electrophilic stress. Although cell signaling pathways triggered by the transcription factor Nrf2 prevent cancer initiation and progression in normal and premalignant tissues, in fully malignant cells Nrf2 activity provides growth advantage by increasing cancer chemoresistance and enhancing tumor cell growth. In this graphical review, we provide an overview of the Keap1-Nrf2 pathway and its dysregulation in cancer cells. We also briefly summarize the consequences of constitutive Nrf2 activation in cancer cells and how this can be exploited in cancer gene therapy.
Keap1-Nrf2通路是细胞对氧化应激和亲电应激产生细胞保护反应的主要调节因子。尽管转录因子Nrf2触发的细胞信号通路可预防正常组织和癌前组织中的癌症起始和进展,但在完全恶性的细胞中,Nrf2活性通过增加癌症化疗耐药性和促进肿瘤细胞生长而提供生长优势。在本篇图文综述中,我们概述了Keap1-Nrf2通路及其在癌细胞中的失调。我们还简要总结了癌细胞中Nrf2组成型激活的后果以及如何在癌症基因治疗中利用这一点。