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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...

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Autores principales: Sunderland, Ashley, Williams, Jennifer, Andreou, Tereza, Rippaus, Nora, Fife, Christopher, James, Fiona, Kartika, Yolanda Dyah, Speirs, Valerie, Carr, Ian, Droop, Alastair, Lorger, Mihaela
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
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.
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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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