Neuroblastoma stem cells - mechanisms of chemoresistance and histonedeacetylase inhibitors
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11310%2F12%3A10126299" target="_blank" >RIV/00216208:11310/12:10126299 - isvavai.cz</a>
Alternative codes found
RIV/00216208:11130/12:8252 RIV/00064203:_____/12:8252
Result on the web
<a href="http://dx.doi.org/10.4149/neo_2012_093" target="_blank" >http://dx.doi.org/10.4149/neo_2012_093</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.4149/neo_2012_093" target="_blank" >10.4149/neo_2012_093</a>
Alternative languages
Result language
angličtina
Original language name
Neuroblastoma stem cells - mechanisms of chemoresistance and histonedeacetylase inhibitors
Original language description
Cancer stem cells (CSCs) form a small proportion of tumor cells that have stem cell properties: self-renewal capacity, the ability to develop into different lineages and proliferative potential. The interest in CSCs emerged from their expected role in initiation, progression and recurrence of many tumors. They are generally resistant to conventional chemotherapy and radiotherapy. There are two hypotheses about their origin: The first assumes that CSCs may arise from normal stem cells, and the second supposes that differentiated cells acquire the properties of CSCs. Both hypotheses are not mutually exclusive, as it is possible that CSCs have a diverse origin in different tumors. CD133+ cells (CD133 is marker of CSC in some tumors) isolated from NBL, osteosarcoma and Ewing sarcoma cell lines are resistant to cisplatin, carboplatin, etoposide and doxorubicin than the CD133- ones. Being resistant to chemotherapy, there were many attempts to target CSCs epigenetically including the use of h
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
<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
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)<br>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
Neoplasma
ISSN
0028-2685
e-ISSN
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Volume of the periodical
59
Issue of the periodical within the volume
6
Country of publishing house
SK - SLOVAKIA
Number of pages
10
Pages from-to
737-746
UT code for WoS article
000310820200018
EID of the result in the Scopus database
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