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Evaluation of MCF10A as a Reliable Model for Normal Human Mammary Epithelial Cells

Breast cancer is the most common cancer in women and a leading cause of cancer-related deaths for women worldwide. Various cell models have been developed to study breast cancer tumorigenesis, metastasis, and drug sensitivity. The MCF10A human mammary epithelial cell line is a widely used in vitro m...

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Autores principales: Qu, Ying, Han, Bingchen, Yu, Yi, Yao, Weiwu, Bose, Shikha, Karlan, Beth Y., Giuliano, Armando E., Cui, Xiaojiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4493126/
https://www.ncbi.nlm.nih.gov/pubmed/26147507
http://dx.doi.org/10.1371/journal.pone.0131285
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author Qu, Ying
Han, Bingchen
Yu, Yi
Yao, Weiwu
Bose, Shikha
Karlan, Beth Y.
Giuliano, Armando E.
Cui, Xiaojiang
author_facet Qu, Ying
Han, Bingchen
Yu, Yi
Yao, Weiwu
Bose, Shikha
Karlan, Beth Y.
Giuliano, Armando E.
Cui, Xiaojiang
author_sort Qu, Ying
collection PubMed
description Breast cancer is the most common cancer in women and a leading cause of cancer-related deaths for women worldwide. Various cell models have been developed to study breast cancer tumorigenesis, metastasis, and drug sensitivity. The MCF10A human mammary epithelial cell line is a widely used in vitro model for studying normal breast cell function and transformation. However, there is limited knowledge about whether MCF10A cells reliably represent normal human mammary cells. MCF10A cells were grown in monolayer, suspension (mammosphere culture), three-dimensional (3D) “on-top” Matrigel, 3D “cell-embedded” Matrigel, or mixed Matrigel/collagen I gel. Suspension culture was performed with the MammoCult medium and low-attachment culture plates. Cells grown in 3D culture were fixed and subjected to either immunofluorescence staining or embedding and sectioning followed by immunohistochemistry and immunofluorescence staining. Cells or slides were stained for protein markers commonly used to identify mammary progenitor and epithelial cells. MCF10A cells expressed markers representing luminal, basal, and progenitor phenotypes in two-dimensional (2D) culture. When grown in suspension culture, MCF10A cells showed low mammosphere-forming ability. Cells in mammospheres and 3D culture expressed both luminal and basal markers. Surprisingly, the acinar structure formed by MCF10A cells in 3D culture was positive for both basal markers and the milk proteins β-casein and α-lactalbumin. MCF10A cells exhibit a unique differentiated phenotype in 3D culture which may not exist or be rare in normal human breast tissue. Our results raise a question as to whether the commonly used MCF10A cell line is a suitable model for human mammary cell studies.
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spelling pubmed-44931262015-07-15 Evaluation of MCF10A as a Reliable Model for Normal Human Mammary Epithelial Cells Qu, Ying Han, Bingchen Yu, Yi Yao, Weiwu Bose, Shikha Karlan, Beth Y. Giuliano, Armando E. Cui, Xiaojiang PLoS One Research Article Breast cancer is the most common cancer in women and a leading cause of cancer-related deaths for women worldwide. Various cell models have been developed to study breast cancer tumorigenesis, metastasis, and drug sensitivity. The MCF10A human mammary epithelial cell line is a widely used in vitro model for studying normal breast cell function and transformation. However, there is limited knowledge about whether MCF10A cells reliably represent normal human mammary cells. MCF10A cells were grown in monolayer, suspension (mammosphere culture), three-dimensional (3D) “on-top” Matrigel, 3D “cell-embedded” Matrigel, or mixed Matrigel/collagen I gel. Suspension culture was performed with the MammoCult medium and low-attachment culture plates. Cells grown in 3D culture were fixed and subjected to either immunofluorescence staining or embedding and sectioning followed by immunohistochemistry and immunofluorescence staining. Cells or slides were stained for protein markers commonly used to identify mammary progenitor and epithelial cells. MCF10A cells expressed markers representing luminal, basal, and progenitor phenotypes in two-dimensional (2D) culture. When grown in suspension culture, MCF10A cells showed low mammosphere-forming ability. Cells in mammospheres and 3D culture expressed both luminal and basal markers. Surprisingly, the acinar structure formed by MCF10A cells in 3D culture was positive for both basal markers and the milk proteins β-casein and α-lactalbumin. MCF10A cells exhibit a unique differentiated phenotype in 3D culture which may not exist or be rare in normal human breast tissue. Our results raise a question as to whether the commonly used MCF10A cell line is a suitable model for human mammary cell studies. Public Library of Science 2015-07-06 /pmc/articles/PMC4493126/ /pubmed/26147507 http://dx.doi.org/10.1371/journal.pone.0131285 Text en © 2015 Qu et al http://creativecommons.org/licenses/by/4.0/ 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 properly credited.
spellingShingle Research Article
Qu, Ying
Han, Bingchen
Yu, Yi
Yao, Weiwu
Bose, Shikha
Karlan, Beth Y.
Giuliano, Armando E.
Cui, Xiaojiang
Evaluation of MCF10A as a Reliable Model for Normal Human Mammary Epithelial Cells
title Evaluation of MCF10A as a Reliable Model for Normal Human Mammary Epithelial Cells
title_full Evaluation of MCF10A as a Reliable Model for Normal Human Mammary Epithelial Cells
title_fullStr Evaluation of MCF10A as a Reliable Model for Normal Human Mammary Epithelial Cells
title_full_unstemmed Evaluation of MCF10A as a Reliable Model for Normal Human Mammary Epithelial Cells
title_short Evaluation of MCF10A as a Reliable Model for Normal Human Mammary Epithelial Cells
title_sort evaluation of mcf10a as a reliable model for normal human mammary epithelial cells
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4493126/
https://www.ncbi.nlm.nih.gov/pubmed/26147507
http://dx.doi.org/10.1371/journal.pone.0131285
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