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TGF beta: A player on multiple fronts in the tumor microenvironment

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61388971%3A_____%2F15%3A00445710" target="_blank" >RIV/61388971:_____/15:00445710 - isvavai.cz</a>

  • Alternative codes found

    RIV/67985904:_____/15:00457798

  • Result on the web

    <a href="http://dx.doi.org/10.3109/1547691X.2014.945667" target="_blank" >http://dx.doi.org/10.3109/1547691X.2014.945667</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.3109/1547691X.2014.945667" target="_blank" >10.3109/1547691X.2014.945667</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    TGF beta: A player on multiple fronts in the tumor microenvironment

  • Original language description

    The physiological functions of transforming growth factor (TGF)-beta in cell signaling include regulation of developmental processes and cell growth. Tumor cells very often display altered regulation of the TGF beta signaling pathway, either by defects in TGF beta itself or in downstream components of the pathway. TGF beta can play a dual role in tumorigenesis, i.e. it can be either tumor-suppressive or tumor-promoting. TGF beta suppresses the growth of tumor cells; however, in advanced tumors, it is associated with induction of progression, resulting in poor prognosis for patients. The TGF beta negative regulation of cytotoxic cell function, together with the promotion of T-regulatory cell maturation, impairs anti-tumor responses. Recent studies haveelucidated new roles for TGF beta signaling in the tumor microenvironment. Abrogation of proper signaling induces epithelial-to-mesenchymal transition with pro-metastatic functions, resulting in cancer progression. Thus, TGF beta signalin

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)

  • CEP classification

    EC - Immunology

  • OECD FORD branch

Result continuities

  • Project

    <a href="/en/project/IAA500200917" target="_blank" >IAA500200917: Genetics and immunity in early stages of colorectal adenocarcinoma: inflammatory environment inconventional vs germ-free animal models, and in human samples</a><br>

  • 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

    Journal of Immunotoxicology

  • ISSN

    1547-691X

  • e-ISSN

  • Volume of the periodical

    12

  • Issue of the periodical within the volume

    3

  • Country of publishing house

    GB - UNITED KINGDOM

  • Number of pages

    8

  • Pages from-to

    300-307

  • UT code for WoS article

    000353580200012

  • EID of the result in the Scopus database