Ellipticine cytotoxicity to cancer cell lines - a comparative study
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11310%2F11%3A10106313" target="_blank" >RIV/00216208:11310/11:10106313 - isvavai.cz</a>
Alternative codes found
RIV/62156489:43210/11:00177572 RIV/00216208:11130/11:7258 RIV/00064203:_____/11:7258
Result on the web
<a href="http://www.intertox.sav.sk/ITX_pdf/04_02_2011/10102-Volume4_Issue_2-06_paper.pdf" target="_blank" >http://www.intertox.sav.sk/ITX_pdf/04_02_2011/10102-Volume4_Issue_2-06_paper.pdf</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.2478/v10102-011-0017-7" target="_blank" >10.2478/v10102-011-0017-7</a>
Alternative languages
Result language
angličtina
Original language name
Ellipticine cytotoxicity to cancer cell lines - a comparative study
Original language description
Ellipticine is a potent antineoplastic agent exhibiting multiple mechanisms of action. This anticancer agent should be considered a pro-drug, whose pharmacological efficiency and/or genotoxic side effects are dependent on its cytochrome P450 (CYP)- and/or peroxidase-mediated activation to species forming covalent DNA adducts. Ellipticine can also act as an inhibitor or inducer of biotransformation enzymes, thereby modulating its own metabolism leading to its genotoxic and pharmacological effects. Here,a comparison of the toxicity of ellipticine to human breast adenocarcinoma MCF-7 cells, leukemia HL-60 and CCRF-CEM cells, neu- roblastoma IMR-32, UKF-NB-3 and UKF-NB-4 cells and U87MG glioblastoma cells and mechanisms of its action to these cells wereevaluated. Treatment of all cells tested with ellipticine resulted in inhibition of cell growth and proliferation. This effect was associated with formation of two covalent ellipticine-derived DNA adducts, identical to those formed by 13-
Czech name
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Czech description
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Classification
Type
J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)
CEP classification
CE - Biochemistry
OECD FORD branch
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Result continuities
Project
Result was created during the realization of more than one project. More information in the Projects tab.
Continuities
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)<br>Z - Vyzkumny zamer (s odkazem do CEZ)
Others
Publication year
2011
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
Interdisciplinary toxicology
ISSN
1337-6853
e-ISSN
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Volume of the periodical
4
Issue of the periodical within the volume
2
Country of publishing house
SK - SLOVAKIA
Number of pages
8
Pages from-to
98-105
UT code for WoS article
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EID of the result in the Scopus database
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