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Myeloid-derived suppressor cells (MDSCs) in patients with solid tumors: considerations for granulocyte colony-stimulating factor treatment

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00209805%3A_____%2F18%3A00078001" target="_blank" >RIV/00209805:_____/18:00078001 - isvavai.cz</a>

  • Alternative codes found

    RIV/00216224:14110/18:00105319

  • Result on the web

    <a href="https://dx.doi.org/10.1007/s00262-018-2166-4" target="_blank" >https://dx.doi.org/10.1007/s00262-018-2166-4</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1007/s00262-018-2166-4" target="_blank" >10.1007/s00262-018-2166-4</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Myeloid-derived suppressor cells (MDSCs) in patients with solid tumors: considerations for granulocyte colony-stimulating factor treatment

  • Original language description

    Myeloid-derived suppressor cells (MDSCs) have been shown to contribute to tumor escape from host immune surveillance and to cancer progression by production of tumor-promoting soluble factors. Granulocyte colony-stimulating factor (G-CSF) is a principle cytokine controlling granulocyte number. Recombinant human G-CSF (rhG-CSF) has become the main therapeutic agent for the treatment of neutropenia and prophylaxis of febrile neutropenia in cancer patients. However, we show here that rhG-CSF triggers accumulation of granulocytic and monocytic subsets. Consequently, we discuss the pharmacological use of granulopoiesis stimulating factors not only in the context of febrile neutropenia but also from the perspective of MDSC-dependent and MDSC-independent mechanisms of immunosuppression and cancer angiogenesis.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    30204 - Oncology

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

    2018

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Cancer immunology, immunotherapy

  • ISSN

    0340-7004

  • e-ISSN

  • Volume of the periodical

    67

  • Issue of the periodical within the volume

    12

  • Country of publishing house

    DE - GERMANY

  • Number of pages

    11

  • Pages from-to

    1919-1929

  • UT code for WoS article

    000450811900011

  • EID of the result in the Scopus database

    2-s2.0-85046774605