Differentially expressed proteins in human MCF-7 breast cancer cells sensitive and resistant to paclitaxel
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61388971%3A_____%2F15%3A00451983" target="_blank" >RIV/61388971:_____/15:00451983 - isvavai.cz</a>
Alternative codes found
RIV/00216208:11120/15:43909252
Result on the web
<a href="http://dx.doi.org/10.1016/j.yexcr.2014.12.005" target="_blank" >http://dx.doi.org/10.1016/j.yexcr.2014.12.005</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1016/j.yexcr.2014.12.005" target="_blank" >10.1016/j.yexcr.2014.12.005</a>
Alternative languages
Result language
angličtina
Original language name
Differentially expressed proteins in human MCF-7 breast cancer cells sensitive and resistant to paclitaxel
Original language description
Resistance of cancer cells to chemotherapeutic agents is one of the main causes of treatment failure. In order to detect proteins potentially involved in the mechanism of resistance to taxanes, we assessed differences in protein expression in MCF-7 breast cancer cells that are sensitive to paclitaxel and in the same cells with acquired resistance to paclitaxel (established in our lab). Proteins were separated using two-dimensional electrophoresis. Changes in their expression were determined and proteinswith altered expression were identified using mass spectrometry. Changes in their expression were confirmed using western blot analysis. With these techniques, we found three proteins expressed differently in resistant MCF-7 cells, i.e., thyroid hormone-interacting protein 6 (TRIP6; upregulated to 650%), heat shock protein 27 (HSP27; downregulated to 50%) and cathepsin D (downregulated to 28%). Silencing of TRIP6 expression by specific siRNA leads to decreased number of grown resistant
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/NT13679" target="_blank" >NT13679: Study of mechanism of action of biomarkers correlating with breast cancer therapy outcome</a><br>
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
Experimental Cell Research
ISSN
0014-4827
e-ISSN
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Volume of the periodical
333
Issue of the periodical within the volume
1
Country of publishing house
US - UNITED STATES
Number of pages
10
Pages from-to
1-10
UT code for WoS article
000352823600001
EID of the result in the Scopus database
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