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Breast Cancer Classification Based on Proteotypes Obtained by SWATH Mass Spectrometry

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00209805%3A_____%2F19%3A00078216" target="_blank" >RIV/00209805:_____/19:00078216 - isvavai.cz</a>

  • Alternative codes found

    RIV/00216224:14310/19:00107609

  • Result on the web

    <a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6656695/" target="_blank" >https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6656695/</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.celrep.2019.06.046" target="_blank" >10.1016/j.celrep.2019.06.046</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Breast Cancer Classification Based on Proteotypes Obtained by SWATH Mass Spectrometry

  • Original language description

    Accurate classification of breast tumors is vital for patient management decisions and enables more precise cancer treatment. Here, we present a quantitative proteotyping approach based on sequential windowed acquisition of all theoretical fragment ion spectra (SWATH) mass spectrometry and establish key proteins for breast tumor classification. The study is based on 96 tissue samples representing five conventional breast cancer subtypes. SWATH proteotype patterns largely recapitulate these subtypes; however, they also reveal varying heterogeneity within the conventional subtypes, with triple negative tumors being the most heterogeneous. Proteins that contribute most strongly to the proteotypebased classification include INPP4B, CDK1, and ERBB2 and are associated with estrogen receptor (ER) status, tumor grade status, and HER2 status. Although these three key proteins exhibit high levels of correlation with transcript levels (R &gt; 0.67), general correlation did not exceed R = 0.29, indicating the value of protein-level measurements of diseaseregulated genes. Overall, this study highlights how cancer tissue proteotyping can lead to more accurate patient stratification.

  • 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

    2019

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Cell Reports

  • ISSN

    2211-1247

  • e-ISSN

  • Volume of the periodical

    28

  • Issue of the periodical within the volume

    3

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    20

  • Pages from-to

    "832–843.e1–e7"

  • UT code for WoS article

    000475582000021

  • EID of the result in the Scopus database

    2-s2.0-85068466554