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Volumn 8, Issue 11, 2001, Pages 1033-1049
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The inefficiency of incisions of ecteinascidin 743-DNA adducts by the UvrABC nuclease and the unique structural feature of the DNA adducts can be used to explain the repair-dependent toxicities of this antitumor agent
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Author keywords
Alkylating agent; Anticancer drug; DNA repair; Ecteinascidin
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Indexed keywords
1,3 DIOXOLANE DERIVATIVE;
ALKYLATING AGENT;
DEOXYRIBONUCLEASE;
DNA;
ENDODEOXYRIBONUCLEASE UVRABC;
ESCHERICHIA COLI PROTEIN;
ISOQUINOLINE DERIVATIVE;
TRABECTEDIN;
ANIMAL;
ARTICLE;
BINDING SITE;
CELL SURVIVAL;
CHEMICAL STRUCTURE;
CHEMISTRY;
CHO CELL;
DNA ADDUCT;
DNA REPAIR;
DRUG DELIVERY SYSTEM;
DRUG EFFECT;
GENE EXPRESSION REGULATION;
GENE TARGETING;
GENETICS;
HAMSTER;
HUMAN;
METABOLISM;
METHODOLOGY;
MOLECULAR GENETICS;
NUCLEOTIDE SEQUENCE;
ANIMAL;
ANTINEOPLASTIC AGENTS, ALKYLATING;
BASE SEQUENCE;
BINDING SITES;
CELL SURVIVAL;
CHO CELLS;
DIOXOLES;
DNA;
DNA ADDUCTS;
DNA REPAIR;
DRUG DELIVERY SYSTEMS;
ENDODEOXYRIBONUCLEASES;
ESCHERICHIA COLI PROTEINS;
GENE TARGETING;
HAMSTERS;
HUMAN;
ISOQUINOLINES;
MODELS, MOLECULAR;
MOLECULAR SEQUENCE DATA;
MUTAGENESIS, INSERTIONAL;
SUPPORT, NON-U.S. GOV'T;
SUPPORT, U.S. GOV'T, P.H.S.;
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EID: 0035199322
PISSN: 10745521
EISSN: None
Source Type: Journal
DOI: 10.1016/S1074-5521(01)00071-0 Document Type: Article |
Times cited : (86)
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References (48)
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