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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

  • Czech description

Classification

  • Type

    J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)

  • CEP classification

    FD - Oncology and haematology

  • OECD FORD branch

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

  • 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