Catalase protects HepG2 cells from apoptosis induced by DNA-damaging agents by accelerating the degradation of p53

Journal of Biological Chemistry

Volumn 278, Issue 7, 2003, Pages 4660-4667

  Bai, Jingxiang ^b   Cederbaum, Arthur I ^a  

^a MOUNT SINAI SCHOOL OF MEDICINE   (United States)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

BIOSYNTHESIS; CATALYST ACTIVITY; CATALYSTS; DNA; TUMORS; VIRUSES;

OXIDANTS;

CELLS;

ADENOVIRUS VECTOR; ANTINEOPLASTIC AGENT; CALPEPTIN; CATALASE; ETOPOSIDE; HYDROGEN PEROXIDE; MITOMYCIN C; OKADAIC ACID; OXIDIZING AGENT; PHOSPHATASE; PROTEASOME INHIBITOR; PROTEIN P21; PROTEIN P53; COMPLEMENTARY DNA; MITOMYCIN; NUCLEIC ACID SYNTHESIS INHIBITOR;

APOPTOSIS; ARTICLE; CANCER CHEMOTHERAPY; CANCER RESISTANCE; CELL STRAIN HEPG2; CONTROLLED STUDY; DNA DAMAGE; ENZYME ACTIVATION; ENZYME ACTIVITY; ENZYME INHIBITION; HUMAN; HUMAN CELL; OXIDATION; PRIORITY JOURNAL; PROTEIN DEGRADATION; PROTEIN EXPRESSION; PROTEIN FUNCTION; PROTEIN PHOSPHORYLATION; PROTEIN SYNTHESIS; UPREGULATION; ADENOVIRUS; CELL LINE; DRUG EFFECT; GENE EXPRESSION REGULATION; GENETIC TRANSFECTION; GENETICS; OXIDATIVE STRESS; TUMOR SUPPRESSOR GENE;

ADENOVIRIDAE; FELIS CATUS;

ADENOVIRIDAE; APOPTOSIS; CATALASE; CELL LINE; DNA DAMAGE; DNA, COMPLEMENTARY; ETOPOSIDE; GENE EXPRESSION REGULATION, ENZYMOLOGIC; GENES, P53; HUMANS; MITOMYCIN; NUCLEIC ACID SYNTHESIS INHIBITORS; OXIDATIVE STRESS; TRANSFECTION;

EID: 0038813711     PISSN: 00219258     EISSN: None     Source Type: Journal    
DOI: 10.1074/jbc.M206273200     Document Type: Article

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