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TUSC3 Loss Alters the ER Stress Response and Accelerates Prostate Cancer Growth in vivo

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216224%3A14110%2F14%3A00075600" target="_blank" >RIV/00216224:14110/14:00075600 - isvavai.cz</a>

  • Result on the web

    <a href="http://dx.doi.org/10.1038/srep03739" target="_blank" >http://dx.doi.org/10.1038/srep03739</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1038/srep03739" target="_blank" >10.1038/srep03739</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    TUSC3 Loss Alters the ER Stress Response and Accelerates Prostate Cancer Growth in vivo

  • Original language description

    Prostate cancer is the most prevalent cancer in males in developed countries. Tumor suppressor candidate 3 (TUSC3) has been identified as a putative tumor suppressor gene in prostate cancer, though its function has not been characterized. TUSC3 shares homologies with the yeast oligosaccharyltransferase (OST) complex subunit Ost3p, suggesting a role in protein glycosylation. We provide evidence that TUSC3 is part of the OST complex and affects N-linked glycosylation in mammalian cells. Loss of TUSC3 expression in DU145 and PC3 prostate cancer cell lines leads to increased proliferation, migration and invasion as well as accelerated xenograft growth in a PTEN negative background. TUSC3 downregulation also affects endoplasmic reticulum (ER) structure andstress response, which results in increased Akt signaling. Together, our findings provide first mechanistic insight in TUSC3 function in prostate carcinogenesis in general and N-glycosylation in particular.

  • 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/7AMB12AT019" target="_blank" >7AMB12AT019: Molecular mechanisms of novel tumor markers in ovarian and prostate cancers</a><br>

  • Continuities

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Others

  • Publication year

    2014

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Scientific Reports

  • ISSN

    2045-2322

  • e-ISSN

  • Volume of the periodical

    4

  • Issue of the periodical within the volume

    "3739"

  • Country of publishing house

    GB - UNITED KINGDOM

  • Number of pages

    9

  • Pages from-to

    1-9

  • UT code for WoS article

    000329849100005

  • EID of the result in the Scopus database