Cargando…

The diverse metabolic heterogeneity of stem cells in a BRCA+/-breast cancer population

Breast cancers are very heterogeneous tissues constituted by epithelial cancer cells and an abnormal tumor microenvironment – cancer-associated fibroblasts (CAFs), activated adipocytes, mesenchymal stem cells (MSCs), and others. The aim of the study is to cancer cells and their microenvironment, whi...

Descripción completa

Detalles Bibliográficos
Autores principales: Gramatiuk, Svetlana Mykolaivna, Bagmut, Irina Yuriivna, Sheremet, Michael Ivanovich, Maksymyuk, Vitaliy Vasilyevich, Tarabanchuk, Volodimir Volodimirovich, Moroz, Petro Vasilyevich
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Carol Davila University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8321609/
https://www.ncbi.nlm.nih.gov/pubmed/34377198
http://dx.doi.org/10.25122/jml-2020-0105
_version_ 1783730886121881600
author Gramatiuk, Svetlana Mykolaivna
Bagmut, Irina Yuriivna
Sheremet, Michael Ivanovich
Maksymyuk, Vitaliy Vasilyevich
Tarabanchuk, Volodimir Volodimirovich
Moroz, Petro Vasilyevich
author_facet Gramatiuk, Svetlana Mykolaivna
Bagmut, Irina Yuriivna
Sheremet, Michael Ivanovich
Maksymyuk, Vitaliy Vasilyevich
Tarabanchuk, Volodimir Volodimirovich
Moroz, Petro Vasilyevich
author_sort Gramatiuk, Svetlana Mykolaivna
collection PubMed
description Breast cancers are very heterogeneous tissues constituted by epithelial cancer cells and an abnormal tumor microenvironment – cancer-associated fibroblasts (CAFs), activated adipocytes, mesenchymal stem cells (MSCs), and others. The aim of the study is to cancer cells and their microenvironment, which behave like a complex and heterogeneous metabolic ecosystem, where cancer cells can reprogram their metabolism as a result of interaction with the components of the microenvironment. The study was based on cancer stem cells (CSC) that were isolated from breast tumors by magnetic separation (AutoMACS). We used spectrophotometric methods for the measurement of aldehyde dehydrogenase (ALDH) enzymatic activity. For these experiments, we used breast cancer and normal stem cell lines. Analyses showed that the proportion of BRCA+ CSC cells was in accordance with the relatively low percentages of CSCs in BRCA+ tumors. ALHD was significantly higher in the CSCs-high BRCA+ breast cancer and CSCs-low BRCA- breast cancer cells, compared with the CSCs-low BRCA+ breast cancer. Breast cancer from BRCA mutation carriers harbor more “high-energy” cell sub-populations than “low-energy” and have their more aggressive phenotype. Key oncogenic pathways known to be dysregulated in breast cancer also regulate stem-cell behavior.
format Online
Article
Text
id pubmed-8321609
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Carol Davila University Press
record_format MEDLINE/PubMed
spelling pubmed-83216092021-08-09 The diverse metabolic heterogeneity of stem cells in a BRCA+/-breast cancer population Gramatiuk, Svetlana Mykolaivna Bagmut, Irina Yuriivna Sheremet, Michael Ivanovich Maksymyuk, Vitaliy Vasilyevich Tarabanchuk, Volodimir Volodimirovich Moroz, Petro Vasilyevich J Med Life Original Article Breast cancers are very heterogeneous tissues constituted by epithelial cancer cells and an abnormal tumor microenvironment – cancer-associated fibroblasts (CAFs), activated adipocytes, mesenchymal stem cells (MSCs), and others. The aim of the study is to cancer cells and their microenvironment, which behave like a complex and heterogeneous metabolic ecosystem, where cancer cells can reprogram their metabolism as a result of interaction with the components of the microenvironment. The study was based on cancer stem cells (CSC) that were isolated from breast tumors by magnetic separation (AutoMACS). We used spectrophotometric methods for the measurement of aldehyde dehydrogenase (ALDH) enzymatic activity. For these experiments, we used breast cancer and normal stem cell lines. Analyses showed that the proportion of BRCA+ CSC cells was in accordance with the relatively low percentages of CSCs in BRCA+ tumors. ALHD was significantly higher in the CSCs-high BRCA+ breast cancer and CSCs-low BRCA- breast cancer cells, compared with the CSCs-low BRCA+ breast cancer. Breast cancer from BRCA mutation carriers harbor more “high-energy” cell sub-populations than “low-energy” and have their more aggressive phenotype. Key oncogenic pathways known to be dysregulated in breast cancer also regulate stem-cell behavior. Carol Davila University Press 2021 /pmc/articles/PMC8321609/ /pubmed/34377198 http://dx.doi.org/10.25122/jml-2020-0105 Text en ©2021 JOURNAL of MEDICINE and LIFE https://creativecommons.org/licenses/by/3.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/ (https://creativecommons.org/licenses/by/3.0/) ), which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Original Article
Gramatiuk, Svetlana Mykolaivna
Bagmut, Irina Yuriivna
Sheremet, Michael Ivanovich
Maksymyuk, Vitaliy Vasilyevich
Tarabanchuk, Volodimir Volodimirovich
Moroz, Petro Vasilyevich
The diverse metabolic heterogeneity of stem cells in a BRCA+/-breast cancer population
title The diverse metabolic heterogeneity of stem cells in a BRCA+/-breast cancer population
title_full The diverse metabolic heterogeneity of stem cells in a BRCA+/-breast cancer population
title_fullStr The diverse metabolic heterogeneity of stem cells in a BRCA+/-breast cancer population
title_full_unstemmed The diverse metabolic heterogeneity of stem cells in a BRCA+/-breast cancer population
title_short The diverse metabolic heterogeneity of stem cells in a BRCA+/-breast cancer population
title_sort diverse metabolic heterogeneity of stem cells in a brca+/-breast cancer population
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8321609/
https://www.ncbi.nlm.nih.gov/pubmed/34377198
http://dx.doi.org/10.25122/jml-2020-0105
work_keys_str_mv AT gramatiuksvetlanamykolaivna thediversemetabolicheterogeneityofstemcellsinabrcabreastcancerpopulation
AT bagmutirinayuriivna thediversemetabolicheterogeneityofstemcellsinabrcabreastcancerpopulation
AT sheremetmichaelivanovich thediversemetabolicheterogeneityofstemcellsinabrcabreastcancerpopulation
AT maksymyukvitaliyvasilyevich thediversemetabolicheterogeneityofstemcellsinabrcabreastcancerpopulation
AT tarabanchukvolodimirvolodimirovich thediversemetabolicheterogeneityofstemcellsinabrcabreastcancerpopulation
AT morozpetrovasilyevich thediversemetabolicheterogeneityofstemcellsinabrcabreastcancerpopulation
AT gramatiuksvetlanamykolaivna diversemetabolicheterogeneityofstemcellsinabrcabreastcancerpopulation
AT bagmutirinayuriivna diversemetabolicheterogeneityofstemcellsinabrcabreastcancerpopulation
AT sheremetmichaelivanovich diversemetabolicheterogeneityofstemcellsinabrcabreastcancerpopulation
AT maksymyukvitaliyvasilyevich diversemetabolicheterogeneityofstemcellsinabrcabreastcancerpopulation
AT tarabanchukvolodimirvolodimirovich diversemetabolicheterogeneityofstemcellsinabrcabreastcancerpopulation
AT morozpetrovasilyevich diversemetabolicheterogeneityofstemcellsinabrcabreastcancerpopulation