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Crosstalk between Tumor and Stromal Cells in Pancreatic Ductal Adenocarcinoma

Pancreatic ductal adenocarcinoma (PDAC) remains a lethal cancer. The poor prognosis calls for a more detailed understanding of disease biology in order to pave the way for the development of effective therapies. Typically, the pancreatic tumor is composed of a minority of malignant cells within an e...

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Detalles Bibliográficos
Autores principales: Sperb, Nadine, Tsesmelis, Miltiadis, Wirth, Thomas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7432853/
https://www.ncbi.nlm.nih.gov/pubmed/32752017
http://dx.doi.org/10.3390/ijms21155486
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author Sperb, Nadine
Tsesmelis, Miltiadis
Wirth, Thomas
author_facet Sperb, Nadine
Tsesmelis, Miltiadis
Wirth, Thomas
author_sort Sperb, Nadine
collection PubMed
description Pancreatic ductal adenocarcinoma (PDAC) remains a lethal cancer. The poor prognosis calls for a more detailed understanding of disease biology in order to pave the way for the development of effective therapies. Typically, the pancreatic tumor is composed of a minority of malignant cells within an excessive tumor microenvironment (TME) consisting of extracellular matrix (ECM), fibroblasts, immune cells, and endothelial cells. Research conducted in recent years has particularly focused on cancer-associated fibroblasts (CAFs) which represent the most prominent cellular component of the desmoplastic stroma. Here, we review the complex crosstalk between CAFs, tumor cells, and other components of the TME, and illustrate how these interactions drive disease progression. We also discuss the emerging field of CAF heterogeneity, their tumor-supportive versus tumor-suppressive capacity, and the consequences for designing stroma-targeted therapies in the future.
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spelling pubmed-74328532020-08-27 Crosstalk between Tumor and Stromal Cells in Pancreatic Ductal Adenocarcinoma Sperb, Nadine Tsesmelis, Miltiadis Wirth, Thomas Int J Mol Sci Review Pancreatic ductal adenocarcinoma (PDAC) remains a lethal cancer. The poor prognosis calls for a more detailed understanding of disease biology in order to pave the way for the development of effective therapies. Typically, the pancreatic tumor is composed of a minority of malignant cells within an excessive tumor microenvironment (TME) consisting of extracellular matrix (ECM), fibroblasts, immune cells, and endothelial cells. Research conducted in recent years has particularly focused on cancer-associated fibroblasts (CAFs) which represent the most prominent cellular component of the desmoplastic stroma. Here, we review the complex crosstalk between CAFs, tumor cells, and other components of the TME, and illustrate how these interactions drive disease progression. We also discuss the emerging field of CAF heterogeneity, their tumor-supportive versus tumor-suppressive capacity, and the consequences for designing stroma-targeted therapies in the future. MDPI 2020-07-31 /pmc/articles/PMC7432853/ /pubmed/32752017 http://dx.doi.org/10.3390/ijms21155486 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
Sperb, Nadine
Tsesmelis, Miltiadis
Wirth, Thomas
Crosstalk between Tumor and Stromal Cells in Pancreatic Ductal Adenocarcinoma
title Crosstalk between Tumor and Stromal Cells in Pancreatic Ductal Adenocarcinoma
title_full Crosstalk between Tumor and Stromal Cells in Pancreatic Ductal Adenocarcinoma
title_fullStr Crosstalk between Tumor and Stromal Cells in Pancreatic Ductal Adenocarcinoma
title_full_unstemmed Crosstalk between Tumor and Stromal Cells in Pancreatic Ductal Adenocarcinoma
title_short Crosstalk between Tumor and Stromal Cells in Pancreatic Ductal Adenocarcinoma
title_sort crosstalk between tumor and stromal cells in pancreatic ductal adenocarcinoma
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7432853/
https://www.ncbi.nlm.nih.gov/pubmed/32752017
http://dx.doi.org/10.3390/ijms21155486
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