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AGR2 predicts tamoxifen resistance in postmenopausal breast cancer patients

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00209805%3A_____%2F13%3A%230000428" target="_blank" >RIV/00209805:_____/13:#0000428 - isvavai.cz</a>

  • Result on the web

    <a href="http://dx.doi.org/10.1155/2013/761537" target="_blank" >http://dx.doi.org/10.1155/2013/761537</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1155/2013/761537" target="_blank" >10.1155/2013/761537</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    AGR2 predicts tamoxifen resistance in postmenopausal breast cancer patients

  • Original language description

    Endocrine resistance is a significant problem in breast cancer treatment. Thus identification and validation of novel resistance determinants is important to improve treatment efficacy and patient outcome. In our work, AGR2 expression was determined by qRT-PCR in Tru-Cut needle biopsies from tamoxifen-treated postmenopausal breast cancer patients. Our results showed inversed association of AGR2 mRNA levels with primary treatment response (P = 0.0011) and progression-free survival (P = 0.0366) in 61 ER-positive breast carcinomas. As shown by our experimental and clinical evaluations, elevated AGR2 expression predicts decreased efficacy of tamoxifen treatment. From this perspective, AGR2 is a potential predictive biomarker enabling selection of an optimal algorithm for adjuvant hormonal therapy in postmenopausal ER-positive breast cancer patients.

  • 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)<br>I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

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

    Disease Markers

  • ISSN

    0278-0240

  • e-ISSN

  • Volume of the periodical

    35

  • Issue of the periodical within the volume

    4

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    6

  • Pages from-to

    207-212

  • UT code for WoS article

    000324981400001

  • EID of the result in the Scopus database