Transcription factors Hsf1 and Nrf2 engage in crosstalk for cytoprotection

Trends in Pharmacological Sciences

Volumn 36, Issue 1, 2015, Pages 6-14

  Dayalan Naidu, Sharadha ^a   Kostov, Rumen V ^a   Dinkova Kostova, Albena T ^a,b  

^a UNIVERSITY OF DUNDEE   (United Kingdom)

^b JOHNS HOPKINS UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

cysteine reactivity; glutathione; heat shock; Kelch like ECH associated protein 1 (Keap1); mitochondrial function; redox

Indexed keywords

1,2 DITHIOLE 3 THIONE DERIVATIVE; ACTIVATING TRANSCRIPTION FACTOR 3; ADENINE NUCLEOTIDE TRANSLOCASE; CELASTROL; CURCUMIN; CYCLOHEXANONE DERIVATIVE; GEDUNIN; GLUCOSE 6 PHOSPHATE DEHYDROGENASE; GLUTATHIONE PEROXIDASE; HEAT SHOCK PROTEIN 27; HEAT SHOCK PROTEIN 70; HEAT SHOCK PROTEIN 90; HEAT SHOCK TRANSCRIPTION FACTOR 1; HEME OXYGENASE 1; ISOCITRATE DEHYDROGENASE; KELCH LIKE ECH ASSOCIATED PROTEIN 1; MALATE DEHYDROGENASE (DECARBOXYLATING); MITOCHONDRIAL PROTEIN; PHOSPHOGLUCONATE DEHYDROGENASE; PROTEIN P62; REDUCED NICOTINAMIDE ADENINE DINUCLEOTIDE PHOSPHATE; RESVERATROL; SULFORAPHANE; TRANSCRIPTION FACTOR NRF2; WITHAFERIN A; DNA BINDING PROTEIN; HEAT SHOCK TRANSCRIPTION FACTOR; TRANSCRIPTION FACTOR;

CARDIOMYOPATHY; CELL PROTECTION; DISORDERS OF MITOCHONDRIAL FUNCTIONS; ENZYME ACTIVITY; GCLC GENE; GCLM GENE; GENE; GENE EXPRESSION REGULATION; HEART MITOCHONDRION; HEAT SHOCK; HUMAN; MITOCHONDRIAL PERMEABILITY; NONHUMAN; OXIDATION REDUCTION STATE; OXIDATIVE STRESS; PROTEIN DEPLETION; PROTEIN DNA BINDING; PROTEIN EXPRESSION; PROTEIN FUNCTION; PROTEIN INDUCTION; PROTEIN PROTEIN INTERACTION; PROTEIN TARGETING; REVIEW; SIGNAL TRANSDUCTION; SLC7A11 GENE; TRANSCRIPTION INITIATION; UPREGULATION; ANIMAL; METABOLISM; MITOCHONDRION; OXIDATION REDUCTION REACTION;

ANIMALS; CYTOPROTECTION; DNA-BINDING PROTEINS; HUMANS; MITOCHONDRIA; NF-E2-RELATED FACTOR 2; OXIDATION-REDUCTION; TRANSCRIPTION FACTORS;

EID: 84920129498     PISSN: 01656147     EISSN: 18733735     Source Type: Journal    
DOI: 10.1016/j.tips.2014.10.011     Document Type: Review

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