Nickel-induced histone hypoacetylation: The role of reactive oxygen species

Toxicological Sciences

Volumn 74, Issue 2, 2003, Pages 279-286

  Kang, Jiuhong ^a   Zhang, Yuntao ^a   Chen, Jie ^b   Chen, Haifeng ^c   Lin, Changjun ^a   Wang, Qing ^a   Ou, Yingxian ^b  

^a LANZHOU UNIVERSITY   (China)

^b LANZHOU GENERAL HOSPITAL   (China)

^c EUROPEAN SPACE AGENCY   (France)

Author keywords

Carcinogenesis; Histone acetylation; Histone acetyltransferase (HAT); Histone deacetylase (HDAC); Nickel; Reactive oxygen species (ROS)

Indexed keywords

ACETYLCYSTEINE; ANTIOXIDANT; HISTIDINE; HISTONE ACETYLTRANSFERASE; HISTONE DEACETYLASE INHIBITOR; HISTONE H4; HYDROGEN PEROXIDE; MERCAPTOETHANOL; NICKEL; REACTIVE OXYGEN METABOLITE; TRICHOSTATIN A;

ACETYLATION; AMINO TERMINAL SEQUENCE; ARTICLE; CARCINOGENICITY; CHEMICAL CARCINOGENESIS; CONCENTRATION (PARAMETERS); CONTROLLED STUDY; ENZYME ACTIVITY; ENZYME ASSAY; GENE REPRESSION; GENE SILENCING; GENETIC TRANSCRIPTION; HEPATOMA CELL; HUMAN; HUMAN CELL; IN VITRO STUDY; IN VIVO STUDY; MAMMAL; MAMMAL CELL; PROTEIN BINDING;

ACETYLATION; ACETYLTRANSFERASES; ANTIOXIDANTS; CARCINOGENS; CARCINOMA, HEPATOCELLULAR; CELL LINE, TUMOR; DOSE-RESPONSE RELATIONSHIP, DRUG; DRUG COMBINATIONS; ENZYME INHIBITORS; HEPATOCYTES; HISTONE ACETYLTRANSFERASES; HISTONE DEACETYLASES; HISTONES; HUMANS; HYDROGEN PEROXIDE; HYDROXAMIC ACIDS; NICKEL; REACTIVE OXYGEN SPECIES;

MAMMALIA;

EID: 0042591402     PISSN: 10966080     EISSN: None     Source Type: Journal    
DOI: 10.1093/toxsci/kfg137     Document Type: Article

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