Mesenchymal cell interaction with ovarian cancer cells triggers pro-metastatic properties.

Tumor microenvironment is an important actor of ovarian cancer progression but the relations between mesenchymal cells and ovarian cancer cells remain unclear. The objective of this study was to determine the ovarian cancer cells' biological modifications induced by mesenchymal cells. To addres...

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Main Authors: Raphael Lis, Cyril Touboul, Christophe M Raynaud, Joel A Malek, Karsten Suhre, Massoud Mirshahi, Arash Rafii
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2012-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3364218?pdf=render
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spelling doaj-c8c896d684f541009dd492db511639892020-11-25T01:23:40ZengPublic Library of Science (PLoS)PLoS ONE1932-62032012-01-0175e3834010.1371/journal.pone.0038340Mesenchymal cell interaction with ovarian cancer cells triggers pro-metastatic properties.Raphael LisCyril TouboulChristophe M RaynaudJoel A MalekKarsten SuhreMassoud MirshahiArash RafiiTumor microenvironment is an important actor of ovarian cancer progression but the relations between mesenchymal cells and ovarian cancer cells remain unclear. The objective of this study was to determine the ovarian cancer cells' biological modifications induced by mesenchymal cells. To address this issue, we used two different ovarian cancer cell lines (NIH:OVCAR3 and SKOV3) and co-cultured them with mesenchymal cells. Upon co-culture the different cell populations were sorted to study their transcriptome and biological properties. Transcriptomic analysis revealed three biological-function gene clusters were enriched upon contact with mesenchymal cells. These were related to the increase of metastatic abilities (adhesion, migration and invasion), proliferation and chemoresistance in vitro. Therefore, contact with the mesenchymal cell niche could increase metastatic initiation and expansion through modification of cancer cells. Taken together these findings suggest that pathways involved in hetero-cellular interaction may be targeted to disrupt the acquired pro-metastatic profile.http://europepmc.org/articles/PMC3364218?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Raphael Lis
Cyril Touboul
Christophe M Raynaud
Joel A Malek
Karsten Suhre
Massoud Mirshahi
Arash Rafii
spellingShingle Raphael Lis
Cyril Touboul
Christophe M Raynaud
Joel A Malek
Karsten Suhre
Massoud Mirshahi
Arash Rafii
Mesenchymal cell interaction with ovarian cancer cells triggers pro-metastatic properties.
PLoS ONE
author_facet Raphael Lis
Cyril Touboul
Christophe M Raynaud
Joel A Malek
Karsten Suhre
Massoud Mirshahi
Arash Rafii
author_sort Raphael Lis
title Mesenchymal cell interaction with ovarian cancer cells triggers pro-metastatic properties.
title_short Mesenchymal cell interaction with ovarian cancer cells triggers pro-metastatic properties.
title_full Mesenchymal cell interaction with ovarian cancer cells triggers pro-metastatic properties.
title_fullStr Mesenchymal cell interaction with ovarian cancer cells triggers pro-metastatic properties.
title_full_unstemmed Mesenchymal cell interaction with ovarian cancer cells triggers pro-metastatic properties.
title_sort mesenchymal cell interaction with ovarian cancer cells triggers pro-metastatic properties.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2012-01-01
description Tumor microenvironment is an important actor of ovarian cancer progression but the relations between mesenchymal cells and ovarian cancer cells remain unclear. The objective of this study was to determine the ovarian cancer cells' biological modifications induced by mesenchymal cells. To address this issue, we used two different ovarian cancer cell lines (NIH:OVCAR3 and SKOV3) and co-cultured them with mesenchymal cells. Upon co-culture the different cell populations were sorted to study their transcriptome and biological properties. Transcriptomic analysis revealed three biological-function gene clusters were enriched upon contact with mesenchymal cells. These were related to the increase of metastatic abilities (adhesion, migration and invasion), proliferation and chemoresistance in vitro. Therefore, contact with the mesenchymal cell niche could increase metastatic initiation and expansion through modification of cancer cells. Taken together these findings suggest that pathways involved in hetero-cellular interaction may be targeted to disrupt the acquired pro-metastatic profile.
url http://europepmc.org/articles/PMC3364218?pdf=render
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