From GC-rich DNA binding to the repression of survivin gene for quercetin nickel (II) complex: Implications for cancer therapy

BioMetals

Volumn 23, Issue 6, 2010, Pages 1075-1084

  Tan, Jun ^a,b   Zhu, Liancai ^a   Wang, Bochu ^a  

^a CHONGQING UNIVERSITY   (China)

^b CHONGQING UNIVERSITY OF EDUCATION   (China)

Author keywords

Antitumor activity; GC rich; Quercetin nickel (II) complex; Selective DNA binding; Survivin

Indexed keywords

ANTINEOPLASTIC METAL COMPLEX; CASPASE 3; CASPASE 8; CASPASE 9; PROTEIN BCL 2; PROTEIN P53; QUERCETIN; QUERCETIN NICKEL COMPLEX; SURVIVIN; UNCLASSIFIED DRUG;

ABSORPTION SPECTROSCOPY; ANTINEOPLASTIC ACTIVITY; APOPTOSIS; ARTICLE; CANCER THERAPY; CELL STRAIN HEPG2; CHROMATIN CONDENSATION; CONTROLLED STUDY; CYTOTOXICITY; DNA BASE COMPOSITION; DNA FRAGMENTATION; DRUG DNA BINDING; DRUG MECHANISM; DRUG SELECTIVITY; ENZYME ACTIVITY; FLUORESCENCE ANALYSIS; GENE REPRESSION; HUMAN; HUMAN CELL; IMMUNOCYTOCHEMISTRY; MOLECULAR MODEL; PROMOTER REGION; PROTEIN EXPRESSION;

ANTINEOPLASTIC AGENTS; APOPTOSIS; CELL LINE, TUMOR; COORDINATION COMPLEXES; DNA, NEOPLASM; DOWN-REGULATION; GC RICH SEQUENCE; HEP G2 CELLS; HUMANS; MICROTUBULE-ASSOCIATED PROTEINS; ORGANOMETALLIC COMPOUNDS; PROTO-ONCOGENE PROTEINS C-BCL-2; QUERCETIN;

EID: 78349313374     PISSN: 09660844     EISSN: None     Source Type: Journal    
DOI: 10.1007/s10534-010-9353-x     Document Type: Article

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