Modulation of iron on mitochondrial aconitase expression in human prostatic carcinoma cells

Molecular and Cellular Biochemistry

Volumn 265, Issue 1-2, 2004, Pages 185-194

  Juang, Horng Heng ^a  

^a CHANG GUNG UNIVERSITY   (Taiwan)

Author keywords

ATP; Citrate; Deferoxamine mesylate; FAC; Hemin; IRE; Transferrin

Indexed keywords

ACONITATE HYDRATASE; ASCORBIC ACID; CITRIC ACID; DEFEROXAMINE MESYLATE; FERRIC AMMONIUM CITRATE; HEMIN; IRON CHELATING AGENT; LUCIFERASE; MITOCHONDRIAL ACONITASE; MITOCHONDRIAL ENZYME; UNCLASSIFIED DRUG; ADENOSINE TRIPHOSPHATE; CHELATING AGENT; DEFEROXAMINE; FERRIC ION; IRON; QUATERNARY AMMONIUM DERIVATIVE;

ANTIOXIDANT ACTIVITY; ANTIOXIDANT RESPONSIVE ELEMENT; ARTICLE; CARCINOMA CELL; CONTROLLED STUDY; CYTOMEGALOVIRUS; ENZYME ACTIVITY; GENE EXPRESSION; HUMAN; HUMAN CELL; IN VITRO STUDY; IRON METABOLISM; IRON RESPONSIVE ELEMENT; MALE; PROSTATE CARCINOMA; PROTEIN EXPRESSION; RNA TRANSLATION; SIGNAL TRANSDUCTION; UPREGULATION; BIOSYNTHESIS; CELL PROLIFERATION; CHEMISTRY; DOSE RESPONSE; ENZYMOLOGY; GENE EXPRESSION REGULATION; GENE VECTOR; GENETIC TRANSCRIPTION; IMMUNOBLOTTING; METABOLISM; MITOCHONDRION; MOLECULAR GENETICS; NUCLEOTIDE SEQUENCE; PROSTATE TUMOR; PROTEIN SYNTHESIS; REPORTER GENE; SITE DIRECTED MUTAGENESIS; TUMOR CELL LINE;

CYTOMEGALOVIRUS;

ACONITATE HYDRATASE; ADENOSINE TRIPHOSPHATE; ASCORBIC ACID; BASE SEQUENCE; CELL LINE, TUMOR; CELL PROLIFERATION; CHELATING AGENTS; CITRATES; DEFEROXAMINE; DOSE-RESPONSE RELATIONSHIP, DRUG; FERRIC COMPOUNDS; GENE EXPRESSION REGULATION, NEOPLASTIC; GENES, REPORTER; GENETIC VECTORS; HEMIN; HUMANS; IMMUNOBLOTTING; IRON; MALE; MITOCHONDRIA; MOLECULAR SEQUENCE DATA; MUTAGENESIS, SITE-DIRECTED; PROSTATIC NEOPLASMS; PROTEIN BIOSYNTHESIS; QUATERNARY AMMONIUM COMPOUNDS; SIGNAL TRANSDUCTION; TRANSCRIPTION, GENETIC; UP-REGULATION;

EID: 16644399910     PISSN: 03008177     EISSN: 15734919     Source Type: Journal    
DOI: 10.1023/B:MCBI.0000044395.59739.1f     Document Type: Article

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