All

What are you looking for?

All
Projects
Results
Organizations

Quick search

  • Projects supported by TA ČR
  • Excellent projects
  • Projects with the highest public support
  • Current projects

Smart search

  • That is how I find a specific +word
  • That is how I leave the -word out of the results
  • “That is how I can find the whole phrase”

Identification of an AKT-dependent signalling pathway that mediates tamoxifen-dependent induction of the pro-metastatic protein anterior gradient-2

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00209805%3A_____%2F13%3A%230000407" target="_blank" >RIV/00209805:_____/13:#0000407 - isvavai.cz</a>

  • Result on the web

    <a href="http://www.sciencedirect.com/science/article/pii/S0304383513000773" target="_blank" >http://www.sciencedirect.com/science/article/pii/S0304383513000773</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.canlet.2013.01.034" target="_blank" >10.1016/j.canlet.2013.01.034</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Identification of an AKT-dependent signalling pathway that mediates tamoxifen-dependent induction of the pro-metastatic protein anterior gradient-2

  • Original language description

    The pro-metasta tic protein anterior gradient- 2 (AGR2) was previously demonstrated as a predictive factor of poor response to tamoxifen treatment . In this study we aimed to delineate the key signalling pathway that may contribute to regulation of AGR2protein induction in order to identify novel targets to overcome tamoxifen resistance in tumour cells. Together, our data identify PDPK1-AKT as a pro-oncogenic signalling pathway that triggers AGR2 protein induction in response to tamoxifen and suggest that AKT inhibitors could be used as part of a therapeutic strategy to treat tamoxifen resistant, AGR2 overexpressing cancers.

  • 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

    2013

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Cancer Letters

  • ISSN

    0304-3835

  • e-ISSN

  • Volume of the periodical

    333

  • Issue of the periodical within the volume

    27

  • Country of publishing house

    IE - IRELAND

  • Number of pages

    7

  • Pages from-to

    187-193

  • UT code for WoS article

    000318838700007

  • EID of the result in the Scopus database