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 > 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
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Czech description
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Classification
Type
J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database
CEP classification
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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
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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