Multiple effects of iron chelators on molecules controlling cell cycle progression

Transfusion Science

Volumn 23, Issue 3, 2000, Pages 247-248

  Gao, J ^a   Richardson, D R ^a  

^a HEART RESEARCH INSTITUTE   (Australia)

Author keywords

[No Author keywords available]

Indexed keywords

2 HYDROXY 1 NAPHTHYLALDEHYDE ISONICOTINOYL HYDRAZONE; CYCLIN DEPENDENT KINASE; CYCLIN DEPENDENT KINASE INHIBITOR; CYCLIN DEPENDENT KINASE INHIBITOR 1; DEFEROXAMINE; GENE PRODUCT; GROWTH ARREST AND DNA DAMAGE INDUCIBLE PROTEIN 45; HYDRAZONE DERIVATIVE; IRON; IRON CHELATING AGENT; MESSENGER RNA; UNCLASSIFIED DRUG;

ANTINEOPLASTIC ACTIVITY; CELL CYCLE; CELL PROLIFERATION; CONFERENCE PAPER; DRUG MECHANISM; HUMAN; HUMAN CELL; IRON CHELATION; PROTEIN EXPRESSION;

CELL CYCLE; GENE EXPRESSION REGULATION; HUMANS; IRON CHELATING AGENTS;

EID: 0033693693     PISSN: 09553886     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0955-3886(00)00096-5     Document Type: Conference Paper

References (3)

1. The potential of iron chelators of the pyridoxal isonicotinoyl hydrazone class as effective anti-proliferative agents
2. The potential of iron chelators of the pyridoxal isonicotinoyl hydrazone class as effective antiproliferative agents. II. The mechanism of action of ligands derived from salicylaldehyde benzoyl hydrazone and 2-hydroxy-1-naphthylaldehyde benzoyl hydrazone
3. The potential of analogues of the pyridoxal isonicotinoyl hydrazone class as effective anti-proliferative agents. III: The effect of the ligands on molecular targets involved in proliferation