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Volumn 18, Issue 3, 2004, Pages 565-567
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Plasmin-activated doxorubicin prodrugs containing a spacer reduce tumor growth and angiogenesis without systemic toxicity.
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Author keywords
[No Author keywords available]
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Indexed keywords
DOXORUBICIN;
DRUG DERIVATIVE;
PLASMIN;
PRODRUG;
ST 9802;
ST 9905;
TUMOR PROTEIN;
UROKINASE;
ADENOCARCINOMA;
ANIMAL;
ARTICLE;
BAGG ALBINO MOUSE;
BIOTRANSFORMATION;
BODY WEIGHT;
BREAST TUMOR;
CHEMICAL STRUCTURE;
CHEMISTRY;
COMPARATIVE STUDY;
DRUG EFFECT;
DRUG SCREENING;
ENZYMOLOGY;
EXPERIMENTAL NEOPLASM;
FEMALE;
HUMAN;
MAXIMUM TOLERATED DOSE;
METABOLISM;
MOUSE;
NEOVASCULARIZATION (PATHOLOGY);
NUDE MOUSE;
PATHOLOGY;
TRANSPLANTATION;
TUMOR CELL LINE;
VASCULARIZATION;
ADENOCARCINOMA;
ANIMALS;
BIOTRANSFORMATION;
BODY WEIGHT;
BREAST NEOPLASMS;
CELL LINE, TUMOR;
DOXORUBICIN;
FEMALE;
HUMANS;
MAMMARY NEOPLASMS, EXPERIMENTAL;
MAXIMUM TOLERATED DOSE;
MICE;
MICE, INBRED BALB C;
MICE, NUDE;
MOLECULAR STRUCTURE;
NEOPLASM PROTEINS;
NEOVASCULARIZATION, PATHOLOGIC;
PLASMIN;
PRODRUGS;
URINARY PLASMINOGEN ACTIVATOR;
XENOGRAFT MODEL ANTITUMOR ASSAYS;
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EID: 2442715459
PISSN: None
EISSN: 15306860
Source Type: Journal
DOI: 10.1096/fj.03-0462fje Document Type: Article |
Times cited : (39)
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References (0)
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