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Biglycan and reduced glycolysis are associated with breast cancer cell dormancy in the brain
Exit of quiescent disseminated cancer cells from dormancy is thought to be responsible for metastatic relapse and a better understanding of dormancy could pave the way for novel therapeutic approaches. We used an in vivo model of triple negative breast cancer brain metastasis to identify differences...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10339804/ https://www.ncbi.nlm.nih.gov/pubmed/37456245 http://dx.doi.org/10.3389/fonc.2023.1191980 |
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author | Sunderland, Ashley Williams, Jennifer Andreou, Tereza Rippaus, Nora Fife, Christopher James, Fiona Kartika, Yolanda Dyah Speirs, Valerie Carr, Ian Droop, Alastair Lorger, Mihaela |
author_facet | Sunderland, Ashley Williams, Jennifer Andreou, Tereza Rippaus, Nora Fife, Christopher James, Fiona Kartika, Yolanda Dyah Speirs, Valerie Carr, Ian Droop, Alastair Lorger, Mihaela |
author_sort | Sunderland, Ashley |
collection | PubMed |
description | Exit of quiescent disseminated cancer cells from dormancy is thought to be responsible for metastatic relapse and a better understanding of dormancy could pave the way for novel therapeutic approaches. We used an in vivo model of triple negative breast cancer brain metastasis to identify differences in transcriptional profiles between dormant and proliferating cancer cells in the brain. BGN gene, encoding a small proteoglycan biglycan, was strongly upregulated in dormant cancer cells in vivo. BGN expression was significantly downregulated in patient brain metastases as compared to the matched primary breast tumors and BGN overexpression in cancer cells inhibited their growth in vitro and in vivo. Dormant cancer cells were further characterized by a reduced expression of glycolysis genes in vivo, and inhibition of glycolysis in vitro resulted in a reversible growth arrest reminiscent of dormancy. Our study identified mechanisms that could be targeted to induce/maintain cancer dormancy and thereby prevent metastatic relapse. |
format | Online Article Text |
id | pubmed-10339804 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-103398042023-07-14 Biglycan and reduced glycolysis are associated with breast cancer cell dormancy in the brain Sunderland, Ashley Williams, Jennifer Andreou, Tereza Rippaus, Nora Fife, Christopher James, Fiona Kartika, Yolanda Dyah Speirs, Valerie Carr, Ian Droop, Alastair Lorger, Mihaela Front Oncol Oncology Exit of quiescent disseminated cancer cells from dormancy is thought to be responsible for metastatic relapse and a better understanding of dormancy could pave the way for novel therapeutic approaches. We used an in vivo model of triple negative breast cancer brain metastasis to identify differences in transcriptional profiles between dormant and proliferating cancer cells in the brain. BGN gene, encoding a small proteoglycan biglycan, was strongly upregulated in dormant cancer cells in vivo. BGN expression was significantly downregulated in patient brain metastases as compared to the matched primary breast tumors and BGN overexpression in cancer cells inhibited their growth in vitro and in vivo. Dormant cancer cells were further characterized by a reduced expression of glycolysis genes in vivo, and inhibition of glycolysis in vitro resulted in a reversible growth arrest reminiscent of dormancy. Our study identified mechanisms that could be targeted to induce/maintain cancer dormancy and thereby prevent metastatic relapse. Frontiers Media S.A. 2023-06-29 /pmc/articles/PMC10339804/ /pubmed/37456245 http://dx.doi.org/10.3389/fonc.2023.1191980 Text en Copyright © 2023 Sunderland, Williams, Andreou, Rippaus, Fife, James, Kartika, Speirs, Carr, Droop and Lorger https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Oncology Sunderland, Ashley Williams, Jennifer Andreou, Tereza Rippaus, Nora Fife, Christopher James, Fiona Kartika, Yolanda Dyah Speirs, Valerie Carr, Ian Droop, Alastair Lorger, Mihaela Biglycan and reduced glycolysis are associated with breast cancer cell dormancy in the brain |
title | Biglycan and reduced glycolysis are associated with breast cancer cell dormancy in the brain |
title_full | Biglycan and reduced glycolysis are associated with breast cancer cell dormancy in the brain |
title_fullStr | Biglycan and reduced glycolysis are associated with breast cancer cell dormancy in the brain |
title_full_unstemmed | Biglycan and reduced glycolysis are associated with breast cancer cell dormancy in the brain |
title_short | Biglycan and reduced glycolysis are associated with breast cancer cell dormancy in the brain |
title_sort | biglycan and reduced glycolysis are associated with breast cancer cell dormancy in the brain |
topic | Oncology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10339804/ https://www.ncbi.nlm.nih.gov/pubmed/37456245 http://dx.doi.org/10.3389/fonc.2023.1191980 |
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