Mechanisms of ellipticine-mediated resistance in UKF-NB-4 neuroblastoma cells
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11110%2F12%3A12958" target="_blank" >RIV/00216208:11110/12:12958 - isvavai.cz</a>
Alternative codes found
RIV/00216208:11310/12:10123193 RIV/00216208:11130/12:7995 RIV/00064203:_____/12:7995 RIV/00064165:_____/12:12958
Result on the web
<a href="http://dx.doi.org/10.1111/j.1349-7006.2011.02137.x" target="_blank" >http://dx.doi.org/10.1111/j.1349-7006.2011.02137.x</a>
DOI - Digital Object Identifier
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Alternative languages
Result language
angličtina
Original language name
Mechanisms of ellipticine-mediated resistance in UKF-NB-4 neuroblastoma cells
Original language description
Most high-risk neuroblastomas develop resistance to cytostatics and therefore there is a need to develop new drugs. In previous studies, we found that ellipticine induces apoptosis in human neuroblastoma cells. We also investigated whether ellipticine was able to induce resistance in the UKF-NB-4 neuroblastoma line and concluded that it may be possible after long-term treatment with increasing concentrations of ellipticine. The aim of the present study was to investigate the mechanisms responsible for ellipticine resistance. To elucidate the mechanisms involved, we used the ellipticine-resistant subline UKF-NB-4ELLI and performed comparative genomic hybridization, multicolor and interphase FISH, expression microarray, real-time RT-PCR, flow cytometry and western blotting analysis of proteins. On the basis of our results, it appears that ellipticine resistance in neuroblastoma is caused by a combination of overexpression of Bcl-2, efflux or degradation of the drug and downregulation of
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
EB - Genetics and molecular biology
OECD FORD branch
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Result continuities
Project
<a href="/en/project/GAP301%2F10%2F0356" target="_blank" >GAP301/10/0356: Study of contribution of different DNA-damaging mechanisms to toxicity of cytostatics to human chemosensitive and chemoresistant neuroblastomas</a><br>
Continuities
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Others
Publication year
2012
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
Cancer Science
ISSN
1347-9032
e-ISSN
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Volume of the periodical
103
Issue of the periodical within the volume
2
Country of publishing house
US - UNITED STATES
Number of pages
8
Pages from-to
334-341
UT code for WoS article
000299734000026
EID of the result in the Scopus database
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