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Anterior gradient protein 3 is associated with less aggressive tumors and better outcome of 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_____%2F15%3A%230000627" target="_blank" >RIV/00209805:_____/15:#0000627 - isvavai.cz</a>

  • Result on the web

    <a href="http://dx.doi.org/10.2147/OTT.S82235" target="_blank" >http://dx.doi.org/10.2147/OTT.S82235</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.2147/OTT.S82235" target="_blank" >10.2147/OTT.S82235</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Anterior gradient protein 3 is associated with less aggressive tumors and better outcome of breast cancer patients

  • Original language description

    Anterior gradient protein (AGR) 3 is a highly related homologue of pro-oncogenic AGR2 and belongs to the family of protein disulfide isomerases. Although AGR3 was found in breast, ovary, prostate, and liver cancer, it remains of yet poorly defined function in tumo-rigenesis. This study aimed to determine AGR3 expression in a cohort of 129 primary breast carcinomas and evaluate the clinical and prognostic significance of AGR3 in these tumors. The immunohistochemical analysis revealed the presence of AGR3staining to varying degrees in 80% of analyzed specimens. The percentage of AGR3-positive cells significantly correlated with estrogen receptor, progesterone receptor (both P,0.0001) as well as low histological grade (P=0.003), and inversely correlatedwith the level of Ki-67 expression (P,0.0001). In the whole cohort, AGR3 expression was associated with longer progression-free survival (PFS), whereas AGR3-positive subgroup of low-histological grade tumors showed both significantly long

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>SC</sub> - Article in a specialist periodical, which is included in the SCOPUS database

  • CEP classification

    FD - Oncology and haematology

  • OECD FORD branch

    10608 - Biochemistry and molecular biology

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

    2015

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    OncoTargets and therapy

  • ISSN

    1178-6930

  • e-ISSN

  • Volume of the periodical

    8

  • Issue of the periodical within the volume

    June

  • Country of publishing house

    NZ - NEW ZEALAND

  • Number of pages

    10

  • Pages from-to

    1523-1532

  • UT code for WoS article

  • EID of the result in the Scopus database

    2-s2.0-84934273566