Long chain acyl-CoA synthetase-3 is a molecular target for peroxisome proliferator-activated receptor δ in HepG2 hepatoma cells

Journal of Biological Chemistry

Volumn 285, Issue 22, 2010, Pages 16664-16674

  Cao, Aiqin ^a   Li, Hai ^a   Zhou, Yue ^a   Wu, Minhao ^a   Liu, Jingwen ^a  

^a NONE

Author keywords

[No Author keywords available]

Indexed keywords

ACYL-COA SYNTHETASE; CHROMATIN IMMUNOPRECIPITATION ASSAY; CYTOKINES; DIRECT INTERACTIONS; FATTY ACID METABOLISM; GEL MOBILITY; GENE TRANSCRIPTIONS; HEPATOMA CELLS; HEPG2 CELLS; IN-VIVO; LIVER TISSUE; LONG CHAINS; MOLECULAR MECHANISM; MOLECULAR TARGETS; MRNA EXPRESSION; MRNA LEVEL; PEROXISOME PROLIFERATOR-ACTIVATED RECEPTOR; PROMOTER ACTIVITIES; PROMOTER REGION; PROMOTER SEQUENCES; PROTEIN LEVEL; REGULATORY MECHANISM; TRANSCRIPTION START SITE; UP-REGULATION;

BINDING ENERGY; BINDING SITES; BIOCHEMISTRY; COMPUTER SOFTWARE MAINTENANCE; CYTOLOGY; FATTY ACIDS; GELS; LAWS AND LEGISLATION; LIVER; PROTEINS;

TRANSCRIPTION;

4 [4 [3 (4 ACETYL 3 HYDROXY 2 PROPYLPHENOXY)PROPOXY]PHENOXY]ACETIC ACID; LONG CHAIN FATTY ACID COENZYME A LIGASE; LONG CHAIN FATTY ACID COENZYME A LIGASE 3; MESSENGER RNA; PEROXISOME PROLIFERATOR ACTIVATED RECEPTOR DELTA; SMALL INTERFERING RNA; UNCLASSIFIED DRUG;

ANIMAL EXPERIMENT; ARTICLE; BINDING SITE; CELL STRAIN HEPG2; CHROMATIN IMMUNOPRECIPITATION; CONTROLLED STUDY; GEL MOBILITY SHIFT ASSAY; GENE MUTATION; GENETIC TRANSCRIPTION; GENETIC TRANSFECTION; HAMSTER; HUMAN; HUMAN CELL; IN VIVO STUDY; MALE; MOLECULAR MECHANICS; NONHUMAN; PLASMID; PRIORITY JOURNAL; PROMOTER REGION; PROTEIN DEPLETION; PROTEIN INTERACTION; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; RNA ISOLATION; TRANSCRIPTION INITIATION SITE; UPREGULATION; WESTERN BLOTTING;

ANIMALS; BASE SEQUENCE; CARCINOMA, HEPATOCELLULAR; CELL LINE, TUMOR; COENZYME A LIGASES; CRICETINAE; CYTOKINES; HUMANS; LIVER; LIVER NEOPLASMS; MOLECULAR SEQUENCE DATA; ONCOSTATIN M; PPAR DELTA; PROMOTER REGIONS, GENETIC; RESPONSE ELEMENTS; TRANSCRIPTION, GENETIC;

CRICETINAE;

EID: 77952766021     PISSN: 00219258     EISSN: 1083351X     Source Type: Journal    
DOI: 10.1074/jbc.M110.112805     Document Type: Article

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