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Therapeutic targeting of the NRF2 and KEAP1 partnership in chronic diseases
by
Rojo, Ana I
, Kensler, Thomas W
, Dinkova-Kostova, Albena T
, Hayes, John D
, Attucks, Otis C
, Cousin, Sharon P
, Rumsey, William L
, Cuadrado, Antonio
, Wells, Geoffrey
, Franklin, Stephen
, Levonen, Anna-Liisa
in
Autophagy
/ Cancer
/ Gene expression
/ Grants
/ Ligands
/ Lung cancer
/ Medical research
/ Proteins
2019
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Therapeutic targeting of the NRF2 and KEAP1 partnership in chronic diseases
by
Rojo, Ana I
, Kensler, Thomas W
, Dinkova-Kostova, Albena T
, Hayes, John D
, Attucks, Otis C
, Cousin, Sharon P
, Rumsey, William L
, Cuadrado, Antonio
, Wells, Geoffrey
, Franklin, Stephen
, Levonen, Anna-Liisa
in
Autophagy
/ Cancer
/ Gene expression
/ Grants
/ Ligands
/ Lung cancer
/ Medical research
/ Proteins
2019
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While trying to remove the title from your shelf something went wrong :( Kindly try again later!
Do you wish to request the book?
Therapeutic targeting of the NRF2 and KEAP1 partnership in chronic diseases
by
Rojo, Ana I
, Kensler, Thomas W
, Dinkova-Kostova, Albena T
, Hayes, John D
, Attucks, Otis C
, Cousin, Sharon P
, Rumsey, William L
, Cuadrado, Antonio
, Wells, Geoffrey
, Franklin, Stephen
, Levonen, Anna-Liisa
in
Autophagy
/ Cancer
/ Gene expression
/ Grants
/ Ligands
/ Lung cancer
/ Medical research
/ Proteins
2019
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Therapeutic targeting of the NRF2 and KEAP1 partnership in chronic diseases
Journal Article
Therapeutic targeting of the NRF2 and KEAP1 partnership in chronic diseases
2019
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Overview
The transcription factor NF-E2 p45-related factor 2 (NRF2; encoded by NFE2L2) and its principal negative regulator, the E3 ligase adaptor Kelch-like ECH-associated protein 1 (KEAP1), are critical in the maintenance of redox, metabolic and protein homeostasis, as well as the regulation of inflammation. Thus, NRF2 activation provides cytoprotection against numerous pathologies including chronic diseases of the lung and liver; autoimmune, neurodegenerative and metabolic disorders; and cancer initiation. One NRF2 activator has received clinical approval and several electrophilic modifiers of the cysteine-based sensor KEAP1 and inhibitors of its interaction with NRF2 are now in clinical development. However, challenges regarding target specificity, pharmacodynamic properties, efficacy and safety remain.
Publisher
Nature Publishing Group
Subject
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