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Mammary gland stem cells and their application in breast cancer

The mammary gland is an organ comprising two primary lineages, specifically the inner luminal and the outer myoepithelial cell layers. Mammary gland stem cells (MaSCs) are highly dynamic and self-renewing, and can give rise to these mammary gland lineages. The lineages are responsible for gland gene...

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Detalles Bibliográficos
Autores principales: Yang, Xing, Wang, Hui, Jiao, Baowei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5354691/
https://www.ncbi.nlm.nih.gov/pubmed/27793013
http://dx.doi.org/10.18632/oncotarget.12893
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author Yang, Xing
Wang, Hui
Jiao, Baowei
author_facet Yang, Xing
Wang, Hui
Jiao, Baowei
author_sort Yang, Xing
collection PubMed
description The mammary gland is an organ comprising two primary lineages, specifically the inner luminal and the outer myoepithelial cell layers. Mammary gland stem cells (MaSCs) are highly dynamic and self-renewing, and can give rise to these mammary gland lineages. The lineages are responsible for gland generation during puberty as well as expansion during pregnancy. In recent years, researchers have focused on understanding how MaSCs are regulated during mammary gland development and transformation of breast cancer. Here, we summarize the identification of MaSCs, and how they are regulated by the signaling transduction pathways, mammary gland microenvironment, and non-coding RNAs (ncRNAs). Moreover, we debate the evidence for their serving as the origin of breast cancer, and discuss the therapeutic perspectives of targeting breast cancer stem cells (BCSCs). In conclusion, a better understanding of the key regulators of MaSCs is crucial for the clinical treatment of breast cancer.
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spelling pubmed-53546912017-04-14 Mammary gland stem cells and their application in breast cancer Yang, Xing Wang, Hui Jiao, Baowei Oncotarget Review The mammary gland is an organ comprising two primary lineages, specifically the inner luminal and the outer myoepithelial cell layers. Mammary gland stem cells (MaSCs) are highly dynamic and self-renewing, and can give rise to these mammary gland lineages. The lineages are responsible for gland generation during puberty as well as expansion during pregnancy. In recent years, researchers have focused on understanding how MaSCs are regulated during mammary gland development and transformation of breast cancer. Here, we summarize the identification of MaSCs, and how they are regulated by the signaling transduction pathways, mammary gland microenvironment, and non-coding RNAs (ncRNAs). Moreover, we debate the evidence for their serving as the origin of breast cancer, and discuss the therapeutic perspectives of targeting breast cancer stem cells (BCSCs). In conclusion, a better understanding of the key regulators of MaSCs is crucial for the clinical treatment of breast cancer. Impact Journals LLC 2016-10-25 /pmc/articles/PMC5354691/ /pubmed/27793013 http://dx.doi.org/10.18632/oncotarget.12893 Text en Copyright: © 2017 Yang et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Review
Yang, Xing
Wang, Hui
Jiao, Baowei
Mammary gland stem cells and their application in breast cancer
title Mammary gland stem cells and their application in breast cancer
title_full Mammary gland stem cells and their application in breast cancer
title_fullStr Mammary gland stem cells and their application in breast cancer
title_full_unstemmed Mammary gland stem cells and their application in breast cancer
title_short Mammary gland stem cells and their application in breast cancer
title_sort mammary gland stem cells and their application in breast cancer
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5354691/
https://www.ncbi.nlm.nih.gov/pubmed/27793013
http://dx.doi.org/10.18632/oncotarget.12893
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