Mesenchymal Stem Cells Promote Pancreatic Tumor Growth by Inducing Alternative Polarization of Macrophages
Pancreatic cancer is characterized by an extensive desmoplastic stroma, the functional relevance of which is poorly understood. Activated fibroblasts are a prevalent component of the stroma, and traditionally, these cells have been considered as a homogenous population derived from pancreatic stella...
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Series: | Neoplasia: An International Journal for Oncology Research |
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doaj-2302dae203264d8ea457f1a9f45934cc2020-11-24T22:56:47ZengElsevierNeoplasia: An International Journal for Oncology Research1476-55861522-80022016-03-0118314215110.1016/j.neo.2016.01.005Mesenchymal Stem Cells Promote Pancreatic Tumor Growth by Inducing Alternative Polarization of MacrophagesEsha Mathew0Arthur L. Brannon1AnnaChiara Del Vecchio2Paloma E. Garcia3Morgan K. Penny4Kevin T. Kane5Alekya Vinta6Ronald J. Buckanovich7Marina Pasca di Magliano8Cellular and Molecular Biology Program, University of Michigan, Ann Arbor, MI, 48109Cellular and Molecular Biology Program, University of Michigan, Ann Arbor, MI, 48109Department of Surgery, University of Michigan, Ann Arbor, MI, 48109Program in Pathology, University of Michigan, Ann Arbor, MI, 48109Program in Cancer Biology, University of Michigan, Ann Arbor, MI, 48109Department of Surgery, University of Michigan, Ann Arbor, MI, 48109Department of Surgery, University of Michigan, Ann Arbor, MI, 48109Cellular and Molecular Biology Program, University of Michigan, Ann Arbor, MI, 48109Cellular and Molecular Biology Program, University of Michigan, Ann Arbor, MI, 48109Pancreatic cancer is characterized by an extensive desmoplastic stroma, the functional relevance of which is poorly understood. Activated fibroblasts are a prevalent component of the stroma, and traditionally, these cells have been considered as a homogenous population derived from pancreatic stellate cells. In this study, we highlight a previously unappreciated heterogeneity of the fibroblast population within the stroma. In particular, a subset of stromal fibroblasts has characteristics of mesenchymal stem cells (MSCs). MSCs are present in the normal pancreas as well as in the carcinomatous pancreas (CA-MSCs). Here, we determine that CA-MSCs have increased tumor-promoting function compared with MSCs in normal pancreas. This ability to promote tumor growth is associated with CA-MSCs’ unique ability to promote alternative macrophage polarization. Thus, our study identifies a previously uncharacterized cell population within the stroma and sheds light on tumor-promoting interactions between different components of the stroma. Significance: Targeting the stroma is emerging as a new paradigm in pancreatic cancer; however, efforts to that effect are hampered by our limited understanding of the nature and function of stromal components. Here, we uncover previously unappreciated heterogeneity within the stroma and identify interactions among stromal components that promote tumor growth and could be targeted therapeutically.http://www.sciencedirect.com/science/article/pii/S1476558616000154 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Esha Mathew Arthur L. Brannon AnnaChiara Del Vecchio Paloma E. Garcia Morgan K. Penny Kevin T. Kane Alekya Vinta Ronald J. Buckanovich Marina Pasca di Magliano |
spellingShingle |
Esha Mathew Arthur L. Brannon AnnaChiara Del Vecchio Paloma E. Garcia Morgan K. Penny Kevin T. Kane Alekya Vinta Ronald J. Buckanovich Marina Pasca di Magliano Mesenchymal Stem Cells Promote Pancreatic Tumor Growth by Inducing Alternative Polarization of Macrophages Neoplasia: An International Journal for Oncology Research |
author_facet |
Esha Mathew Arthur L. Brannon AnnaChiara Del Vecchio Paloma E. Garcia Morgan K. Penny Kevin T. Kane Alekya Vinta Ronald J. Buckanovich Marina Pasca di Magliano |
author_sort |
Esha Mathew |
title |
Mesenchymal Stem Cells Promote Pancreatic Tumor Growth by Inducing Alternative Polarization of Macrophages |
title_short |
Mesenchymal Stem Cells Promote Pancreatic Tumor Growth by Inducing Alternative Polarization of Macrophages |
title_full |
Mesenchymal Stem Cells Promote Pancreatic Tumor Growth by Inducing Alternative Polarization of Macrophages |
title_fullStr |
Mesenchymal Stem Cells Promote Pancreatic Tumor Growth by Inducing Alternative Polarization of Macrophages |
title_full_unstemmed |
Mesenchymal Stem Cells Promote Pancreatic Tumor Growth by Inducing Alternative Polarization of Macrophages |
title_sort |
mesenchymal stem cells promote pancreatic tumor growth by inducing alternative polarization of macrophages |
publisher |
Elsevier |
series |
Neoplasia: An International Journal for Oncology Research |
issn |
1476-5586 1522-8002 |
publishDate |
2016-03-01 |
description |
Pancreatic cancer is characterized by an extensive desmoplastic stroma, the functional relevance of which is poorly understood. Activated fibroblasts are a prevalent component of the stroma, and traditionally, these cells have been considered as a homogenous population derived from pancreatic stellate cells. In this study, we highlight a previously unappreciated heterogeneity of the fibroblast population within the stroma. In particular, a subset of stromal fibroblasts has characteristics of mesenchymal stem cells (MSCs). MSCs are present in the normal pancreas as well as in the carcinomatous pancreas (CA-MSCs). Here, we determine that CA-MSCs have increased tumor-promoting function compared with MSCs in normal pancreas. This ability to promote tumor growth is associated with CA-MSCs’ unique ability to promote alternative macrophage polarization. Thus, our study identifies a previously uncharacterized cell population within the stroma and sheds light on tumor-promoting interactions between different components of the stroma.
Significance: Targeting the stroma is emerging as a new paradigm in pancreatic cancer; however, efforts to that effect are hampered by our limited understanding of the nature and function of stromal components. Here, we uncover previously unappreciated heterogeneity within the stroma and identify interactions among stromal components that promote tumor growth and could be targeted therapeutically. |
url |
http://www.sciencedirect.com/science/article/pii/S1476558616000154 |
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