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Metabolome Shift in Both Metastatic Breast Cancer Cells and Astrocytes Which May Contribute to the Tumor Microenvironment

The role of astrocytes in the periphery of metastatic brain tumors is unclear. Since astrocytes regulate central nervous metabolism, we hypothesized that changes in astrocytes induced by contact with cancer cells would appear in the metabolome of both cells and contribute to malignant transformation...

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Autores principales: Sato, Hiromi, Shimizu, Ayaka, Okawa, Toya, Uzu, Miaki, Goto, Momoko, Hisaka, Akihiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8308096/
https://www.ncbi.nlm.nih.gov/pubmed/34299050
http://dx.doi.org/10.3390/ijms22147430
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author Sato, Hiromi
Shimizu, Ayaka
Okawa, Toya
Uzu, Miaki
Goto, Momoko
Hisaka, Akihiro
author_facet Sato, Hiromi
Shimizu, Ayaka
Okawa, Toya
Uzu, Miaki
Goto, Momoko
Hisaka, Akihiro
author_sort Sato, Hiromi
collection PubMed
description The role of astrocytes in the periphery of metastatic brain tumors is unclear. Since astrocytes regulate central nervous metabolism, we hypothesized that changes in astrocytes induced by contact with cancer cells would appear in the metabolome of both cells and contribute to malignant transformation. Coculture of astrocytes with breast cancer cell supernatants altered glutamate (Glu)-centered arginine–proline metabolism. Similarly, the metabolome of cancer cells was also altered by astrocyte culture supernatants, and the changes were further amplified in astrocytes exposed to Glu. Inhibition of Glu uptake in astrocytes reduces the variability in cancer cells. Principal component analysis of the cancer cells revealed that all these changes were in the first principal component (PC1) axis, where the responsible metabolites were involved in the metabolism of the arginine–proline, pyrimidine, and pentose phosphate pathways. The contribution of these changes to the tumor microenvironment needs to be further pursued.
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spelling pubmed-83080962021-07-25 Metabolome Shift in Both Metastatic Breast Cancer Cells and Astrocytes Which May Contribute to the Tumor Microenvironment Sato, Hiromi Shimizu, Ayaka Okawa, Toya Uzu, Miaki Goto, Momoko Hisaka, Akihiro Int J Mol Sci Communication The role of astrocytes in the periphery of metastatic brain tumors is unclear. Since astrocytes regulate central nervous metabolism, we hypothesized that changes in astrocytes induced by contact with cancer cells would appear in the metabolome of both cells and contribute to malignant transformation. Coculture of astrocytes with breast cancer cell supernatants altered glutamate (Glu)-centered arginine–proline metabolism. Similarly, the metabolome of cancer cells was also altered by astrocyte culture supernatants, and the changes were further amplified in astrocytes exposed to Glu. Inhibition of Glu uptake in astrocytes reduces the variability in cancer cells. Principal component analysis of the cancer cells revealed that all these changes were in the first principal component (PC1) axis, where the responsible metabolites were involved in the metabolism of the arginine–proline, pyrimidine, and pentose phosphate pathways. The contribution of these changes to the tumor microenvironment needs to be further pursued. MDPI 2021-07-11 /pmc/articles/PMC8308096/ /pubmed/34299050 http://dx.doi.org/10.3390/ijms22147430 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Communication
Sato, Hiromi
Shimizu, Ayaka
Okawa, Toya
Uzu, Miaki
Goto, Momoko
Hisaka, Akihiro
Metabolome Shift in Both Metastatic Breast Cancer Cells and Astrocytes Which May Contribute to the Tumor Microenvironment
title Metabolome Shift in Both Metastatic Breast Cancer Cells and Astrocytes Which May Contribute to the Tumor Microenvironment
title_full Metabolome Shift in Both Metastatic Breast Cancer Cells and Astrocytes Which May Contribute to the Tumor Microenvironment
title_fullStr Metabolome Shift in Both Metastatic Breast Cancer Cells and Astrocytes Which May Contribute to the Tumor Microenvironment
title_full_unstemmed Metabolome Shift in Both Metastatic Breast Cancer Cells and Astrocytes Which May Contribute to the Tumor Microenvironment
title_short Metabolome Shift in Both Metastatic Breast Cancer Cells and Astrocytes Which May Contribute to the Tumor Microenvironment
title_sort metabolome shift in both metastatic breast cancer cells and astrocytes which may contribute to the tumor microenvironment
topic Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8308096/
https://www.ncbi.nlm.nih.gov/pubmed/34299050
http://dx.doi.org/10.3390/ijms22147430
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