Distinct effects of EGFR ligands on human mammary epithelial cell differentiation.

Based on gene expression patterns, breast cancers can be divided into subtypes that closely resemble various developmental stages of normal mammary epithelial cells (MECs). Thus, understanding molecular mechanisms of MEC development is expected to provide critical insights into initiation and progre...

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Main Authors: Chandrani Mukhopadhyay, Xiangshan Zhao, Dulce Maroni, Vimla Band, Mayumi Naramura
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3790811?pdf=render
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author Chandrani Mukhopadhyay
Xiangshan Zhao
Dulce Maroni
Vimla Band
Mayumi Naramura
author_facet Chandrani Mukhopadhyay
Xiangshan Zhao
Dulce Maroni
Vimla Band
Mayumi Naramura
author_sort Chandrani Mukhopadhyay
collection DOAJ
description Based on gene expression patterns, breast cancers can be divided into subtypes that closely resemble various developmental stages of normal mammary epithelial cells (MECs). Thus, understanding molecular mechanisms of MEC development is expected to provide critical insights into initiation and progression of breast cancer. Epidermal growth factor receptor (EGFR) and its ligands play essential roles in normal and pathological mammary gland. Signals through EGFR is required for normal mammary gland development. Ligands for EGFR are over-expressed in a significant proportion of breast cancers, and elevated expression of EGFR is associated with poorer clinical outcome. In the present study, we examined the effect of signals through EGFR on MEC differentiation using the human telomerase reverse transcriptase (hTERT)-immortalized human stem/progenitor MECs which express cytokeratin 5 but lack cytokeratin 19 (K5(+)K19(-) hMECs). As reported previously, these cells can be induced to differentiate into luminal and myoepithelial cells under appropriate culture conditions. K5(+)K19(-) hMECs acquired distinct cell fates in response to EGFR ligands epidermal growth factor (EGF), amphiregulin (AREG) and transforming growth factor alpha (TGFα) in differentiation-promoting MEGM medium. Specifically, presence of EGF during in vitro differentiation supported development into both luminal and myoepithelial lineages, whereas cells differentiated only towards luminal lineage when EGF was replaced with AREG. In contrast, substitution with TGFα led to differentiation only into myoepithelial lineage. Chemical inhibition of the MEK-Erk pathway, but not the phosphatidylinositol 3-kinase (PI3K)-AKT pathway, interfered with K5(+)K19(-) hMEC differentiation. The present data validate the utility of the K5(+)K19(-) hMEC cells for modeling key features of human MEC differentiation. This system should be useful in studying molecular/biochemical mechanisms of human MEC differentiation.
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spelling doaj.art-c1b26e3326e4453aaac73630367401e12022-12-21T19:08:39ZengPublic Library of Science (PLoS)PLoS ONE1932-62032013-01-01810e7590710.1371/journal.pone.0075907Distinct effects of EGFR ligands on human mammary epithelial cell differentiation.Chandrani MukhopadhyayXiangshan ZhaoDulce MaroniVimla BandMayumi NaramuraBased on gene expression patterns, breast cancers can be divided into subtypes that closely resemble various developmental stages of normal mammary epithelial cells (MECs). Thus, understanding molecular mechanisms of MEC development is expected to provide critical insights into initiation and progression of breast cancer. Epidermal growth factor receptor (EGFR) and its ligands play essential roles in normal and pathological mammary gland. Signals through EGFR is required for normal mammary gland development. Ligands for EGFR are over-expressed in a significant proportion of breast cancers, and elevated expression of EGFR is associated with poorer clinical outcome. In the present study, we examined the effect of signals through EGFR on MEC differentiation using the human telomerase reverse transcriptase (hTERT)-immortalized human stem/progenitor MECs which express cytokeratin 5 but lack cytokeratin 19 (K5(+)K19(-) hMECs). As reported previously, these cells can be induced to differentiate into luminal and myoepithelial cells under appropriate culture conditions. K5(+)K19(-) hMECs acquired distinct cell fates in response to EGFR ligands epidermal growth factor (EGF), amphiregulin (AREG) and transforming growth factor alpha (TGFα) in differentiation-promoting MEGM medium. Specifically, presence of EGF during in vitro differentiation supported development into both luminal and myoepithelial lineages, whereas cells differentiated only towards luminal lineage when EGF was replaced with AREG. In contrast, substitution with TGFα led to differentiation only into myoepithelial lineage. Chemical inhibition of the MEK-Erk pathway, but not the phosphatidylinositol 3-kinase (PI3K)-AKT pathway, interfered with K5(+)K19(-) hMEC differentiation. The present data validate the utility of the K5(+)K19(-) hMEC cells for modeling key features of human MEC differentiation. This system should be useful in studying molecular/biochemical mechanisms of human MEC differentiation.http://europepmc.org/articles/PMC3790811?pdf=render
spellingShingle Chandrani Mukhopadhyay
Xiangshan Zhao
Dulce Maroni
Vimla Band
Mayumi Naramura
Distinct effects of EGFR ligands on human mammary epithelial cell differentiation.
PLoS ONE
title Distinct effects of EGFR ligands on human mammary epithelial cell differentiation.
title_full Distinct effects of EGFR ligands on human mammary epithelial cell differentiation.
title_fullStr Distinct effects of EGFR ligands on human mammary epithelial cell differentiation.
title_full_unstemmed Distinct effects of EGFR ligands on human mammary epithelial cell differentiation.
title_short Distinct effects of EGFR ligands on human mammary epithelial cell differentiation.
title_sort distinct effects of egfr ligands on human mammary epithelial cell differentiation
url http://europepmc.org/articles/PMC3790811?pdf=render
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AT dulcemaroni distincteffectsofegfrligandsonhumanmammaryepithelialcelldifferentiation
AT vimlaband distincteffectsofegfrligandsonhumanmammaryepithelialcelldifferentiation
AT mayuminaramura distincteffectsofegfrligandsonhumanmammaryepithelialcelldifferentiation