Alteration of the HSP70/HSP90 chaperone and the HOP/CHIP co-chaperone system in cancer
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00209805%3A_____%2F12%3A%230000328" target="_blank" >RIV/00209805:_____/12:#0000328 - isvavai.cz</a>
Result on the web
<a href="http://www.springerlink.com/content/j27772813123n887/" target="_blank" >http://www.springerlink.com/content/j27772813123n887/</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.2478/s11658-012-0021-8" target="_blank" >10.2478/s11658-012-0021-8</a>
Alternative languages
Result language
angličtina
Original language name
Alteration of the HSP70/HSP90 chaperone and the HOP/CHIP co-chaperone system in cancer
Original language description
Activation of the Hsp90 chaperone system is a characteristic of cancer cells. The regulation of chaperone activities involves their interaction with cochaperones; therefore we investigated the expression of Hsp70 and Hsp90 and their specific co-chaperones HOP and CHIP in cancer cell lines and primary cancers. Inhibition of Hsp90 by 17AAG increased the levels of Hsp70, Hsp90 and HOP but not CHIP mRNA in cancer cells. These changes are linked to activation of the HSF1 transcription factor and we show thatthe HOP promoter contains HSF1 binding sites, and that HSF1 binding to the HOP promoter is increased following 17AAG. The lack of alteration in the co-chaperone CHIP is explained by a lack of HSF response elements in the CHIP promoter. Nonproliferatingcells expressed higher levels of CHIP and lower HOP, Hsp70 and Hsp90 levels compared to proliferating cells. Decreased expression of CHIP in proliferating cancer cells is in keeping with its proposed tumor suppressor properties, while ove
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
<a href="/en/project/NS9812" target="_blank" >NS9812: Elucidating the role of ubiquitin-chaperone degradation machinery in cancer and modulating its biochemical functions using targeted chaperone inhibitors</a><br>
Continuities
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)
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
Cellular and molecular biology letters
ISSN
1425-8153
e-ISSN
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Volume of the periodical
17
Issue of the periodical within the volume
3
Country of publishing house
PL - POLAND
Number of pages
13
Pages from-to
446-458
UT code for WoS article
000305349300009
EID of the result in the Scopus database
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