Longevity PapersAbout
← All papers
RESEARCH PAPER / 2026-05-19

NRF2 as a guardian of health: from an ancient survival pathway to a modern therapeutic target.

Sandra Tenreiro, Ana Sofia Falcão, Nicole Bender, Iveta Bernatova, Alessandra Berry, Antonio Cuadrado, Patrick Eppenberger, Letizia Giona, Anna Grochot-Przeczek, Elke Heiss, Monika Jakubowska, Paul F Long, Asya Makhro, Mojgan Masoodi, Christina Morgenstern, Luciano Saso, Miguel C Seabra, Alicja Sznarkowska, Gerasimos Sykiotis, Ioannis P Trougakos

iNOVA4Health, NOVA Medical School|Faculdade de Ciências Médicas, NMS|FCM, Universidade Nova de Lisboa, Lisboa, Portugal. Electronic address: [email protected], NOVA Medical School|Faculdade de Ciências Médicas, NMS|FCM, Universidade Nova de Lisboa, Lisboa, Portugal. Electronic address: [email protected]. · pubmed

Abstract

NRF2 (Nuclear Factor Erythroid 2-Related Factor 2) has traditionally been viewed as a master regulator of the antioxidant response. However, emerging evidence redefines NRF2 as a pleiotropic and evolutionarily conserved systems-level integrator of redox, metabolic, proteostatic, and inflammatory homeostasis, i.e., an evolutionarily conserved guardian of health. From its origins as an adaptive response to rising atmospheric oxygen in early metazoans to its role in orchestrating complex cytoprotective networks in humans, NRF2 exemplifies the biological transition from stress resistance to adaptive resilience. Understanding its regulation across species, tissues, life stages and gender offers novel perspectives for combating age-related cellular dysfunction and reframing the dynamic process of redox regulation as a component of adaptive homeostasis in a precision medicine perspective. This review summarizes and integrates essential concepts currently being developed regarding the evolutionary roots of NRF2, its molecular and regulatory complexity, its dualistic role in health and disease, and its potential as a biomarker of resilience and therapeutic target. We highlight NRF2's function as a rheostat rather than a binary stress switch, including the role of hormetic activation through lifestyle and environmental stimuli. By maintaining redox homeostasis and dynamic adaptive stress responses, NRF2 bridges molecular defense mechanisms with strategies for healthspan extension and preventive medicine from very early life stages until senescence.

The following analysis is generated by AI and may contain errors. It is separate from the authors’ abstract and is not peer review.

Research summary

This review proposes that NRF2 functions as a systemic rheostat for adaptive resilience rather than a simple antioxidant switch, suggesting that its evolutionary conservation and role in integrating redox, metabolic, and proteostatic homeostasis provide a mechanistic framework for targeting fundamental aging processes. The paper is relevant because it addresses the root causes of aging by framing NRF2 as a central integrator of cellular healthspan and resilience, moving beyond symptom management to discuss the biological transition from stress resistance to adaptive resilience across the lifespan.

Author of this paper? Send a correction.