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Single-cell protein profiling defines cell populations associated with triple-negative breast cancer aggressiveness

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F68081707%3A_____%2F23%3A00574522" target="_blank" >RIV/68081707:_____/23:00574522 - isvavai.cz</a>

  • Alternative codes found

    RIV/00216224:14310/23:00130413 RIV/00216208:11130/23:10452827 RIV/00216208:11310/23:10452827 RIV/61989592:15110/23:73624727 and 4 more

  • Result on the web

    <a href="https://febs.onlinelibrary.wiley.com/doi/10.1002/1878-0261.13365" target="_blank" >https://febs.onlinelibrary.wiley.com/doi/10.1002/1878-0261.13365</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1002/1878-0261.13365" target="_blank" >10.1002/1878-0261.13365</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Single-cell protein profiling defines cell populations associated with triple-negative breast cancer aggressiveness

  • Original language description

    Triple-negative breast cancer (TNBC) is an aggressive and complex subtype of breast cancer that lacks targeted therapy. TNBC manifests characteristic, extensive intratumoral heterogeneity that promotes disease progression and influences drug response. Single-cell techniques in combination with next-generation computation provide an unprecedented opportunity to identify molecular events with therapeutic potential. Here, we describe the generation of a comprehensive mass cytometry panel for multiparametric detection of 23 phenotypic markers and 13 signaling molecules. This single-cell proteomic approach allowed us to explore the landscape of TNBC heterogeneity, with particular emphasis on the tumor microenvironment. We prospectively profiled freshly resected tumors from 26 TNBC patients. These tumors contained phenotypically distinct subpopulations of cancer and stromal cells that were associated with the patient's clinical status at the time of surgery. We further classified the epithelial-mesenchymal plasticity of tumor cells, and molecularly defined phenotypically diverse populations of tumor-associated stroma. Furthermore, in a retrospective tissue-microarray TNBC cohort, we showed that the level of CD97 at the time of surgery has prognostic potential.

  • 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

    30102 - Immunology

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

    2023

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Molecular Oncology

  • ISSN

    1574-7891

  • e-ISSN

    1878-0261

  • Volume of the periodical

    17

  • Issue of the periodical within the volume

    6

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    17

  • Pages from-to

    1024-1040

  • UT code for WoS article

    000926769000001

  • EID of the result in the Scopus database

    2-s2.0-85147231039