Please use this identifier to cite or link to this item: https://hdl.handle.net/20.500.11851/11559
Title: Biomarkers of Nrf2 Signalling: Current Status and Future Challenges
Authors: Morgenstern, C.
Lastres-Becker, I.
Demirdögen, B.C.
Costa, V.M.
Daiber, A.
Foresti, R.
Motterlini, R.
Keywords: Biomarker
NRF2
Oxidative stress response
Target genes
Transcription factor
biological marker
glutamate cysteine ligase
glutamate cysteine ligase catalytic subunit
glutamate cysteine ligase modifier subunit
heme oxygenase 1
nicotinamide adenine dinucleotide phosphate quinone dehydrogenase 1
reduced nicotinamide adenine dinucleotide phosphate dehydrogenase
sulfiredoxin 1
thioredoxin reductase 1
transcription factor Nrf2
unclassified drug
body fluid
cell protection
GCLC gene
GCLM gene
gene targeting
HMOX1 gene
human
nonhuman
NQO1 gene
Nrf2 signaling
oxidative stress
protein function
Review
SRXN1 gene
translational research
TXNRD1 gene
Publisher: Elsevier B.V.
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. © 2024 The Authors
URI: https://doi.org/10.1016/j.redox.2024.103134
https://hdl.handle.net/20.500.11851/11559
ISSN: 2213-2317
Appears in Collections:Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection

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