Mitochondrially targeted vitamin E succinate efficiently kills breast tumour-initiating cells in a complex II-dependent manner
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F60461373%3A22330%2F15%3A43899518" target="_blank" >RIV/60461373:22330/15:43899518 - isvavai.cz</a>
Alternative codes found
RIV/86652036:_____/15:00446714
Result on the web
<a href="http://dx.doi.org/10.1186/s12885-015-1394-7" target="_blank" >http://dx.doi.org/10.1186/s12885-015-1394-7</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1186/s12885-015-1394-7" target="_blank" >10.1186/s12885-015-1394-7</a>
Alternative languages
Result language
angličtina
Original language name
Mitochondrially targeted vitamin E succinate efficiently kills breast tumour-initiating cells in a complex II-dependent manner
Original language description
Background: Accumulating evidence suggests that breast cancer involves tumour-initiating cells (TICs), which play a role in initiation, metastasis, therapeutic resistance and relapse of the disease. Emerging drugs that target TICs are becoming a focus ofcontemporary research. Mitocans, a group of compounds that induce apoptosis of cancer cells by destabilising their mitochondria, are showing their potential in killing TICs. In this project, we investigated mitochondrially targeted vitamin E succinate (MitoVES), a recently developed mitocan, for its in vitro and in vivo efficacy against TICs. Methods: The mammosphere model of breast TICs was established by culturing murine NeuTL and human MCF7 cells as spheres. This model was verified by stem cell marker expression, tumour initiation capacity and chemotherapeutic resistance. Cell susceptibility to MitoVES was assessed and the cell death pathway investigated. In vivo efficacy was studied by grafting NeuTL TICs to form syngeneic tumours.
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
FD - Oncology and haematology
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
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Others
Publication year
2015
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
BMC CANCER
ISSN
1471-2407
e-ISSN
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Volume of the periodical
15
Issue of the periodical within the volume
MAY 13 2015
Country of publishing house
GB - UNITED KINGDOM
Number of pages
12
Pages from-to
"Article Number: 401"
UT code for WoS article
000354932800001
EID of the result in the Scopus database
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