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Anterior Gradient-3: a novel biomarker for ovarian cancer that mediates cisplatin resistance in xenograft models

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00209805%3A_____%2F12%3A%230000288" target="_blank" >RIV/00209805:_____/12:#0000288 - isvavai.cz</a>

  • Result on the web

    <a href="http://www.sciencedirect.com/science/article/pii/S002217591200035X" target="_blank" >http://www.sciencedirect.com/science/article/pii/S002217591200035X</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.jim.2012.01.013" target="_blank" >10.1016/j.jim.2012.01.013</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Anterior Gradient-3: a novel biomarker for ovarian cancer that mediates cisplatin resistance in xenograft models

  • Original language description

    The Anterior Gradient genes AGR2 and AGR3 are part of Protein Disulfide Isomerase (PDI) family and harbour core thioredoxin folds (CxxS motifs) that have the potential to regulate protein folding and maturation. Despite the fact that AGR2 and AGR3 genesare contiguous on chromosome 7p21.1-3, AGR3 protein has rarely been identified along with AGR2 protein. Therefore there is little information on how AGR3 protein is expressed in normal and diseased states. A panel of three monoclonal antibodies was generated towards AGR3 protein for identifying novel clinical models that can be used to define whether AGR3 protein could play a positive or negative role in human cancer development. One monoclonal antibody was AGR3-specific and bound a linear epitope thatcould be defined using both pep-scan and phage-peptide library screening. Using this antibody, endogenous AGR3 protein expression was shown to be cytosolic in four human ovarian cancer subtypes; serous, endometrioid, clear cell, and mucin

  • 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

    Result was created during the realization of more than one project. More information in the Projects tab.

  • 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

    Journal of immunological methods

  • ISSN

    0022-1759

  • e-ISSN

  • Volume of the periodical

    378

  • Issue of the periodical within the volume

    1-2

  • Country of publishing house

    NL - THE KINGDOM OF THE NETHERLANDS

  • Number of pages

    13

  • Pages from-to

    20-32

  • UT code for WoS article

    000304285900003

  • EID of the result in the Scopus database