Redox mechanisms involved in the selective activation of Nrf2-mediated resistance versus p53-dependent apoptosis in adenocarcinoma cells

Journal of Biological Chemistry

Volumn 284, Issue 40, 2009, Pages 27721-27733

  Piccirillo, Sara ^c   Filomeni, Giuseppe ^a   Brüne, Bernhard ^b   Rotilio, Gluseppe ^a,c   Ciriolo, Maria R ^a,c  

^a UNIVERSITY OF ROME TOR VERGATA   (Italy)

^b GOETHE UNIVERSITY   (Germany)

^c IRCCS SAN RAFFAELE PISANA   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

ADENOCARCINOMA CELLS; APOPTOSIS; CARCINOMA CELL LINES; DIAMIDES; DNA DAMAGES; DNA-DEPENDENT PROTEIN KINASE; MITOCHONDRIAL PATHWAYS; OXIDATIVE DAMAGE; OXIDIZING AGENTS; REACTIVE OXYGEN SPECIES; REDOX MECHANISM; SELECTIVE ACTIVATION; SIGNALING PATHWAYS;

CELL CULTURE; CELL DEATH; CELL MEMBRANES; DNA; GENES; HYDROGEN; HYDROGEN PEROXIDE; NUCLEIC ACIDS; OXYGEN; PIGMENTS; PROTEINS; SIGNALING;

OXIDATION;

DIAMIDE; DNA DEPENDENT PROTEIN KINASE; GLUTATHIONE; GLUTATHIONE DISULFIDE; HISTONE H2AX; HYDROGEN PEROXIDE; KELCH LIKE ECH ASSOCIATED PROTEIN 1; MITOGEN ACTIVATED PROTEIN KINASE P38; PROTEIN P53; REACTIVE OXYGEN METABOLITE; THIOL OXIDASE; THIOREDOXIN REDUCTASE 1; TRANSCRIPTION FACTOR NRF2; THIOREDOXIN;

APOPTOSIS; ARTICLE; CANCER CELL CULTURE; CELL NUCLEUS; CELL STRAIN CACO 2; CONTROLLED STUDY; HUMAN; HUMAN CELL; MITOCHONDRION; OXIDATION REDUCTION REACTION; OXIDATIVE STRESS; PRIORITY JOURNAL; PROTEIN EXPRESSION; PROTEIN LOCALIZATION; SIGNAL TRANSDUCTION; STOMACH ADENOCARCINOMA; ADENOCARCINOMA; CELL SURVIVAL; DRUG EFFECT; ENZYME SPECIFICITY; INTRACELLULAR SPACE; METABOLISM; PATHOLOGY; PHOSPHORYLATION; TUMOR CELL LINE;

ADENOCARCINOMA; APOPTOSIS; CELL LINE, TUMOR; CELL SURVIVAL; DIAMIDE; HUMANS; HYDROGEN PEROXIDE; INTRACELLULAR SPACE; MITOCHONDRIA; NF-E2-RELATED FACTOR 2; OXIDATION-REDUCTION; OXIDATIVE STRESS; P38 MITOGEN-ACTIVATED PROTEIN KINASES; PHOSPHORYLATION; SIGNAL TRANSDUCTION; SUBSTRATE SPECIFICITY; THIOREDOXINS; TUMOR SUPPRESSOR PROTEIN P53;

EID: 70350068501     PISSN: 00219258     EISSN: 1083351X     Source Type: Journal    
DOI: 10.1074/jbc.M109.014837     Document Type: Article

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