Matches in SemOpenAlex for { <https://semopenalex.org/work/W2022631908> ?p ?o ?g. }
- W2022631908 endingPage "359" @default.
- W2022631908 startingPage "351" @default.
- W2022631908 abstract "An antitumor drug N-[2-(dimethylamino)ethyl]acridine-4-carboxamide (DACA) and its three close structural analogs N-[2-(hydroxyethylamino)ethyl]acridine-4-carboxamide (DACAH), N-[2-(dimethylamino)ethyl]-9-aminoacridine-4-carboxamide (amino-DACA), and N-[2-(hydroxyethylamino)ethyl]-9-aminoacridine-4-carboxamide (amino-DACAH) were studied for their ability to inhibit RNA synthesis in vitro and to form topoisomerase II-mediated DNA lesions in relation to cell-killing activity. All tested compounds induced chromatin lesions characteristic of topoisomerase II-blocking drugs (DNA breaks and DNA-protein cross-links) in treated cells, but were much less active than reference antileukemic acridine m-AMSA (4'-(9-acridinylamino)-methanesulfon-m-anisidide). The ability to form these lesions was dependent on the structure of the 4-carboxamide side-chain, which seems to be an important factor affecting the drug transport rate through cell membrane. A 4-carboxamide chain with an N-2-(dimethylamino)ethyl moiety resulted in more efficient transport through cell membranes, higher cytotoxicity, and DNA-damaging activity. The mode of action of acridine-4-carboxamides was further elucidated by their incubation with cells in the presence of antitopoisomerase II agents of a known mechanism of inhibition. These were: bisdioxopiperazine (ICRF-187), a catalytic inhibitor of topoisomerase II, and etoposide (VP-16), an inducer of a cleavable complex of the enzyme with DNA. The cytotoxicity of DACA and its analogs was not antagonized by preincubating cells with ICRF-187. All tested acridines protected cells against DNA breakage induced by VP-16, but the extent of protection varied significantly. Amino-DACA, which easily penetrates cell membrane, fully inhibited DNA break formation, whereas other analogs exhibited a low degree of protection when used at high concentration. Our results suggest that the acridine-4-carboxamides discussed here are poor topoisomerase II poisons and that this enzyme is not their main target." @default.
- W2022631908 created "2016-06-24" @default.
- W2022631908 creator A5017930480 @default.
- W2022631908 creator A5018292794 @default.
- W2022631908 creator A5023901201 @default.
- W2022631908 creator A5027234988 @default.
- W2022631908 creator A5029114214 @default.
- W2022631908 creator A5056222311 @default.
- W2022631908 date "1998-08-01" @default.
- W2022631908 modified "2023-10-16" @default.
- W2022631908 title "Cytotoxic and DNA-Damaging Properties of N-[2-(Dimethylamino)ethyl]acridine-4-Carboxamide (DACA) and Its Analogues" @default.
- W2022631908 cites W1022873875 @default.
- W2022631908 cites W1568313491 @default.
- W2022631908 cites W1586111039 @default.
- W2022631908 cites W1964639478 @default.
- W2022631908 cites W1967552836 @default.
- W2022631908 cites W1970841446 @default.
- W2022631908 cites W1971730609 @default.
- W2022631908 cites W1972227366 @default.
- W2022631908 cites W1974839286 @default.
- W2022631908 cites W1980782542 @default.
- W2022631908 cites W1984651948 @default.
- W2022631908 cites W1993283812 @default.
- W2022631908 cites W2007335376 @default.
- W2022631908 cites W2007838632 @default.
- W2022631908 cites W2009722630 @default.
- W2022631908 cites W2010511880 @default.
- W2022631908 cites W2020104207 @default.
- W2022631908 cites W2026542838 @default.
- W2022631908 cites W2028302196 @default.
- W2022631908 cites W2040390348 @default.
- W2022631908 cites W2052411412 @default.
- W2022631908 cites W2058537071 @default.
- W2022631908 cites W2061163224 @default.
- W2022631908 cites W2069256784 @default.
- W2022631908 cites W2077421856 @default.
- W2022631908 cites W2080010039 @default.
- W2022631908 cites W2086527685 @default.
- W2022631908 cites W2093993014 @default.
- W2022631908 cites W2952072637 @default.
- W2022631908 doi "https://doi.org/10.1016/s0006-2952(98)00030-6" @default.
- W2022631908 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/9744573" @default.
- W2022631908 hasPublicationYear "1998" @default.
- W2022631908 type Work @default.
- W2022631908 sameAs 2022631908 @default.
- W2022631908 citedByCount "7" @default.
- W2022631908 countsByYear W20226319082018 @default.
- W2022631908 crossrefType "journal-article" @default.
- W2022631908 hasAuthorship W2022631908A5017930480 @default.
- W2022631908 hasAuthorship W2022631908A5018292794 @default.
- W2022631908 hasAuthorship W2022631908A5023901201 @default.
- W2022631908 hasAuthorship W2022631908A5027234988 @default.
- W2022631908 hasAuthorship W2022631908A5029114214 @default.
- W2022631908 hasAuthorship W2022631908A5056222311 @default.
- W2022631908 hasConcept C109316439 @default.
- W2022631908 hasConcept C147897179 @default.
- W2022631908 hasConcept C178790620 @default.
- W2022631908 hasConcept C185592680 @default.
- W2022631908 hasConcept C202751555 @default.
- W2022631908 hasConcept C2776120743 @default.
- W2022631908 hasConcept C2776924795 @default.
- W2022631908 hasConcept C2778327999 @default.
- W2022631908 hasConcept C2780500152 @default.
- W2022631908 hasConcept C54355233 @default.
- W2022631908 hasConcept C552990157 @default.
- W2022631908 hasConcept C55493867 @default.
- W2022631908 hasConcept C71240020 @default.
- W2022631908 hasConcept C81885089 @default.
- W2022631908 hasConcept C86803240 @default.
- W2022631908 hasConceptScore W2022631908C109316439 @default.
- W2022631908 hasConceptScore W2022631908C147897179 @default.
- W2022631908 hasConceptScore W2022631908C178790620 @default.
- W2022631908 hasConceptScore W2022631908C185592680 @default.
- W2022631908 hasConceptScore W2022631908C202751555 @default.
- W2022631908 hasConceptScore W2022631908C2776120743 @default.
- W2022631908 hasConceptScore W2022631908C2776924795 @default.
- W2022631908 hasConceptScore W2022631908C2778327999 @default.
- W2022631908 hasConceptScore W2022631908C2780500152 @default.
- W2022631908 hasConceptScore W2022631908C54355233 @default.
- W2022631908 hasConceptScore W2022631908C552990157 @default.
- W2022631908 hasConceptScore W2022631908C55493867 @default.
- W2022631908 hasConceptScore W2022631908C71240020 @default.
- W2022631908 hasConceptScore W2022631908C81885089 @default.
- W2022631908 hasConceptScore W2022631908C86803240 @default.
- W2022631908 hasIssue "3" @default.
- W2022631908 hasLocation W20226319081 @default.
- W2022631908 hasLocation W20226319082 @default.
- W2022631908 hasOpenAccess W2022631908 @default.
- W2022631908 hasPrimaryLocation W20226319081 @default.
- W2022631908 hasRelatedWork W1497508512 @default.
- W2022631908 hasRelatedWork W2010511880 @default.
- W2022631908 hasRelatedWork W2022631908 @default.
- W2022631908 hasRelatedWork W2039474772 @default.
- W2022631908 hasRelatedWork W2055388274 @default.
- W2022631908 hasRelatedWork W2058537071 @default.
- W2022631908 hasRelatedWork W2165968169 @default.
- W2022631908 hasRelatedWork W2169456841 @default.
- W2022631908 hasRelatedWork W2407144342 @default.