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Single-cell protein profiling defines cell populations associated with triple-negative breast cancer aggressiveness
B. Kvokačková, R. Fedr, D. Kužílková, J. Stuchlý, A. Vávrová, J. Navrátil, P. Fabian, R. Ondruššek, P. Ovesná, J. Remšík, J. Bouchal, T. Kalina, K. Souček
Jazyk angličtina Země Spojené státy americké
Typ dokumentu časopisecké články
Grantová podpora
NU21-08-00023
Agentura Pro Zdravotnický Výzkum České Republiky
NV18-08-00245
Agentura Pro Zdravotnický Výzkum České Republiky
20-22984S
Grantová Agentura České Republiky
21-11585S
Grantová Agentura České Republiky
CZ.02.1.01/0.0/0.0/16_025/0007381
Ministerstvo Školství, Mládeže a Tělovýchovy
NLK
Directory of Open Access Journals
od 2017
Free Medical Journals
od 2007 do Před 1 rokem
PubMed Central
od 2007
Europe PubMed Central
od 2007
ProQuest Central
od 2007-06-01
Wiley-Blackwell Open Access Titles
od 2007
PubMed
36550781
DOI
10.1002/1878-0261.13365
Knihovny.cz E-zdroje
- MeSH
- buňky stromatu metabolismus MeSH
- lidé MeSH
- nádorové buněčné linie MeSH
- nádorové mikroprostředí MeSH
- proteomika MeSH
- retrospektivní studie MeSH
- signální transdukce MeSH
- triple-negativní karcinom prsu * metabolismus MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
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.
Childhood Leukaemia Investigation Prague Czech Republic
Department of Comprehensive Cancer Care Masaryk Memorial Cancer Institute Brno Czech Republic
Department of Experimental Biology Faculty of Science Masaryk University Brno Czech Republic
Department of Oncological Pathology Masaryk Memorial Cancer Institute Brno Czech Republic
Department of Pathology EUC Laboratoře CGB a s Ostrava Czech Republic
Faculty of Science Charles University Prague Czech Republic
Human Oncology and Pathogenesis Program Memorial Sloan Kettering Cancer Center New York City NY USA
Institute of Biostatistics and Analyses Faculty of Medicine Masaryk University Brno Czech Republic
International Clinical Research Center St Anne's University Hospital Brno Czech Republic
Citace poskytuje Crossref.org
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