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Biomarkers of NRF2 signalling: Current status and future challenges.

Authors :
Morgenstern C
Lastres-Becker I
Demirdöğen BC
Costa VM
Daiber A
Foresti R
Motterlini R
Kalyoncu S
Arioz BI
Genc S
Jakubowska M
Trougakos IP
Piechota-Polanczyk A
Mickael M
Santos M
Kensler TW
Cuadrado A
Copple IM
Source :
Redox biology [Redox Biol] 2024 Jun; Vol. 72, pp. 103134. Date of Electronic Publication: 2024 Mar 30.
Publication Year :
2024

Abstract

The cytoprotective transcription factor NRF2 regulates the expression of several hundred genes in mammalian cells and is a promising therapeutic target in a number of diseases associated with oxidative stress and inflammation. Hence, an ability to monitor basal and inducible NRF2 signalling is vital for mechanistic understanding in translational studies. Due to some caveats related to the direct measurement of NRF2 levels, the modulation of NRF2 activity is typically determined by measuring changes in the expression of one or more of its target genes and/or the associated protein products. However, there is a lack of consensus regarding the most relevant set of these genes/proteins that best represents NRF2 activity across cell types and species. We present the findings of a comprehensive literature search that according to stringent criteria identifies GCLC, GCLM, HMOX1, NQO1, SRXN1 and TXNRD1 as a robust panel of markers that are directly regulated by NRF2 in multiple cell and tissue types. We assess the relevance of these markers in clinically accessible biofluids and highlight future challenges in the development and use of NRF2 biomarkers in humans.<br />Competing Interests: Declaration of competing interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: Ian Copple reports article publishing charges was provided by European Cooperation in Science and Technology. Ian Copple reports financial support was provided by the Medical Research Council. If there are other authors, they declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.<br /> (Copyright © 2024 The Authors. Published by Elsevier B.V. All rights reserved.)

Details

Language :
English
ISSN :
2213-2317
Volume :
72
Database :
MEDLINE
Journal :
Redox biology
Publication Type :
Academic Journal
Accession number :
38643749
Full Text :
https://doi.org/10.1016/j.redox.2024.103134