Regulation of NRF2 by Na+/K+-ATPase: implication of tyrosine phosphorylation of Src

• Published in: Free radical research Vol. 54; no. 11-12; pp. 883 - 893
• Main Authors: Nam, Le Ba, Keum, Young-Sam
• Format: Journal Article
• Language: English
• Published: England Taylor & Francis 01.12.2020
• Subjects: Adenosine Triphosphatases - metabolism; Animals; Antioxidant response element (ARE); C-terminal kinase 1 (CSK1); Cell Line, Tumor; Fireflies; Humans; Na+/K+-translocating adenosine triphosphatase (Na+/K+-ATPase); NF-E2-related factor 2 (NRF2); NF-E2-Related Factor 2 - metabolism; Oxidative Stress; Phosphorylation; Reactive oxygen species (ROS); Signal Transduction; src-Family Kinases - metabolism; Transfection; Tyrosine - metabolism; C-terminal kinase 1 (CSK1); Antioxidant response element (ARE); Na+/K+-translocating adenosine triphosphatase (Na+/K+-ATPase); NF-E2-related factor 2 (NRF2); Reactive oxygen species (ROS)
• ISSN: 1071-5762; 1029-2470
• DOI: 10.1080/10715762.2020.1735633

Tumors adapt well to the imbalanced redox status created by rapid growth and limited nutrient availability because they highly express high levels of NRF2 to counteract oxidative stress. Therefore, inhibition of NRF2 is currently considered a feasible strategy for development of chemotherapeutic agents. In the present study, we identified that Na + /K + -ATPase regulates NRF2 in A549 cells. Suppression of Na + /K + -ATPase by convallatoxin or siRNAs downregulates NRF2 in A549 cells, and this event is mediated by Ca 2+ -dependent induction of CSK1 and subsequent phosphorylation of SRC at Tyr 527. Consistent with this finding, knocking down the α1 or β1 subunit of Na + /K + -ATPase promotes the generation of intracellular ROS by cisplatin and potentiates cisplatin-induced apoptosis and autophagy in A549 cells. Our study reveals that the signaling axis composed of Na + /K + -ATPase, CSK1, and tyrosine phosphorylation of Src could be a useful target for development of NRF2 inhibitors.