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Mesenchymal Stem Cells Shed Amphiregulin at the Surface of Lung Carcinoma Cells in a Juxtacrine Manner()()
Solid tumors comprise cancer cells and different supportive stromal cells, including mesenchymal stem cells (MSCs), which have recently been shown to enhance tumor growth and metastasis. We provide new mechanistic insights into how bone marrow (BM)–derived MSCs co-injected with Lewis lung carcinoma...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Neoplasia Press
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4547406/ https://www.ncbi.nlm.nih.gov/pubmed/26297433 http://dx.doi.org/10.1016/j.neo.2015.07.002 |
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author | Carnet, Oriane Lecomte, Julie Masset, Anne Primac, Irina Durré, Tania Maertens, Ludovic Detry, Benoit Blacher, Silvia Gilles, Christine Péqueux, Christel Paupert, Jenny Foidart, Jean-Michel Jerusalem, Guy Cataldo, Didier Noel, Agnès |
author_facet | Carnet, Oriane Lecomte, Julie Masset, Anne Primac, Irina Durré, Tania Maertens, Ludovic Detry, Benoit Blacher, Silvia Gilles, Christine Péqueux, Christel Paupert, Jenny Foidart, Jean-Michel Jerusalem, Guy Cataldo, Didier Noel, Agnès |
author_sort | Carnet, Oriane |
collection | PubMed |
description | Solid tumors comprise cancer cells and different supportive stromal cells, including mesenchymal stem cells (MSCs), which have recently been shown to enhance tumor growth and metastasis. We provide new mechanistic insights into how bone marrow (BM)–derived MSCs co-injected with Lewis lung carcinoma cells promote tumor growth and metastasis in mice. The proinvasive effect of BM-MSCs exerted on tumor cells relies on an unprecedented juxtacrine action of BM-MSC, leading to the trans-shedding of amphiregulin (AREG) from the tumor cell membrane by tumor necrosis factor-α–converting enzyme carried by the BM-MSC plasma membrane. The released soluble AREG activates cancer cells and promotes their invasiveness. This novel concept is supported by the exploitation of different 2D and 3D culture systems and by pharmacological approaches using a tumor necrosis factor-α–converting enzyme inhibitor and AREG-blocking antibodies. Altogether, we here assign a new function to BM-MSC in tumor progression and establish an uncovered link between AREG and BM-MSC. |
format | Online Article Text |
id | pubmed-4547406 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Neoplasia Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-45474062015-09-03 Mesenchymal Stem Cells Shed Amphiregulin at the Surface of Lung Carcinoma Cells in a Juxtacrine Manner()() Carnet, Oriane Lecomte, Julie Masset, Anne Primac, Irina Durré, Tania Maertens, Ludovic Detry, Benoit Blacher, Silvia Gilles, Christine Péqueux, Christel Paupert, Jenny Foidart, Jean-Michel Jerusalem, Guy Cataldo, Didier Noel, Agnès Neoplasia Article Solid tumors comprise cancer cells and different supportive stromal cells, including mesenchymal stem cells (MSCs), which have recently been shown to enhance tumor growth and metastasis. We provide new mechanistic insights into how bone marrow (BM)–derived MSCs co-injected with Lewis lung carcinoma cells promote tumor growth and metastasis in mice. The proinvasive effect of BM-MSCs exerted on tumor cells relies on an unprecedented juxtacrine action of BM-MSC, leading to the trans-shedding of amphiregulin (AREG) from the tumor cell membrane by tumor necrosis factor-α–converting enzyme carried by the BM-MSC plasma membrane. The released soluble AREG activates cancer cells and promotes their invasiveness. This novel concept is supported by the exploitation of different 2D and 3D culture systems and by pharmacological approaches using a tumor necrosis factor-α–converting enzyme inhibitor and AREG-blocking antibodies. Altogether, we here assign a new function to BM-MSC in tumor progression and establish an uncovered link between AREG and BM-MSC. Neoplasia Press 2015-08-18 /pmc/articles/PMC4547406/ /pubmed/26297433 http://dx.doi.org/10.1016/j.neo.2015.07.002 Text en © 2015 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Carnet, Oriane Lecomte, Julie Masset, Anne Primac, Irina Durré, Tania Maertens, Ludovic Detry, Benoit Blacher, Silvia Gilles, Christine Péqueux, Christel Paupert, Jenny Foidart, Jean-Michel Jerusalem, Guy Cataldo, Didier Noel, Agnès Mesenchymal Stem Cells Shed Amphiregulin at the Surface of Lung Carcinoma Cells in a Juxtacrine Manner()() |
title | Mesenchymal Stem Cells Shed Amphiregulin at the Surface of Lung Carcinoma Cells in a Juxtacrine Manner()() |
title_full | Mesenchymal Stem Cells Shed Amphiregulin at the Surface of Lung Carcinoma Cells in a Juxtacrine Manner()() |
title_fullStr | Mesenchymal Stem Cells Shed Amphiregulin at the Surface of Lung Carcinoma Cells in a Juxtacrine Manner()() |
title_full_unstemmed | Mesenchymal Stem Cells Shed Amphiregulin at the Surface of Lung Carcinoma Cells in a Juxtacrine Manner()() |
title_short | Mesenchymal Stem Cells Shed Amphiregulin at the Surface of Lung Carcinoma Cells in a Juxtacrine Manner()() |
title_sort | mesenchymal stem cells shed amphiregulin at the surface of lung carcinoma cells in a juxtacrine manner()() |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4547406/ https://www.ncbi.nlm.nih.gov/pubmed/26297433 http://dx.doi.org/10.1016/j.neo.2015.07.002 |
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