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Pancreatic Fibroblast Heterogeneity: From Development to Cancer
Pancreatic ductal adenocarcinoma (PDA) is characterized by an extensive fibroinflammatory microenvironment that accumulates from the onset of disease progression. Cancer-associated fibroblasts (CAFs) are a prominent cellular component of the stroma, but their role during carcinogenesis remains contr...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7698149/ https://www.ncbi.nlm.nih.gov/pubmed/33198201 http://dx.doi.org/10.3390/cells9112464 |
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author | Garcia, Paloma E. Scales, Michael K. Allen, Benjamin L. Pasca di Magliano, Marina |
author_facet | Garcia, Paloma E. Scales, Michael K. Allen, Benjamin L. Pasca di Magliano, Marina |
author_sort | Garcia, Paloma E. |
collection | PubMed |
description | Pancreatic ductal adenocarcinoma (PDA) is characterized by an extensive fibroinflammatory microenvironment that accumulates from the onset of disease progression. Cancer-associated fibroblasts (CAFs) are a prominent cellular component of the stroma, but their role during carcinogenesis remains controversial, with both tumor-supporting and tumor-restraining functions reported in different studies. One explanation for these contradictory findings is the heterogeneous nature of the fibroblast populations, and the different roles each subset might play in carcinogenesis. Here, we review the current literature on the origin and function of pancreatic fibroblasts, from the developing organ to the healthy adult pancreas, and throughout the initiation and progression of PDA. We also discuss clinical approaches to targeting fibroblasts in PDA. |
format | Online Article Text |
id | pubmed-7698149 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-76981492020-11-29 Pancreatic Fibroblast Heterogeneity: From Development to Cancer Garcia, Paloma E. Scales, Michael K. Allen, Benjamin L. Pasca di Magliano, Marina Cells Review Pancreatic ductal adenocarcinoma (PDA) is characterized by an extensive fibroinflammatory microenvironment that accumulates from the onset of disease progression. Cancer-associated fibroblasts (CAFs) are a prominent cellular component of the stroma, but their role during carcinogenesis remains controversial, with both tumor-supporting and tumor-restraining functions reported in different studies. One explanation for these contradictory findings is the heterogeneous nature of the fibroblast populations, and the different roles each subset might play in carcinogenesis. Here, we review the current literature on the origin and function of pancreatic fibroblasts, from the developing organ to the healthy adult pancreas, and throughout the initiation and progression of PDA. We also discuss clinical approaches to targeting fibroblasts in PDA. MDPI 2020-11-12 /pmc/articles/PMC7698149/ /pubmed/33198201 http://dx.doi.org/10.3390/cells9112464 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Garcia, Paloma E. Scales, Michael K. Allen, Benjamin L. Pasca di Magliano, Marina Pancreatic Fibroblast Heterogeneity: From Development to Cancer |
title | Pancreatic Fibroblast Heterogeneity: From Development to Cancer |
title_full | Pancreatic Fibroblast Heterogeneity: From Development to Cancer |
title_fullStr | Pancreatic Fibroblast Heterogeneity: From Development to Cancer |
title_full_unstemmed | Pancreatic Fibroblast Heterogeneity: From Development to Cancer |
title_short | Pancreatic Fibroblast Heterogeneity: From Development to Cancer |
title_sort | pancreatic fibroblast heterogeneity: from development to cancer |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7698149/ https://www.ncbi.nlm.nih.gov/pubmed/33198201 http://dx.doi.org/10.3390/cells9112464 |
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