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Tumor reactive stroma in cholangiocarcinoma: The fuel behind cancer aggressiveness
Cholangiocarcinoma (CCA) is a highly aggressive epithelial malignancy still carrying a dismal prognosis, owing to early lymph node metastatic dissemination and striking resistance to conventional chemotherapy. Although mechanisms underpinning CCA progression are still a conundrum, it is now increasi...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Baishideng Publishing Group Inc
2017
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5368623/ https://www.ncbi.nlm.nih.gov/pubmed/28396716 http://dx.doi.org/10.4254/wjh.v9.i9.455 |
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author | Brivio, Simone Cadamuro, Massimiliano Strazzabosco, Mario Fabris, Luca |
author_facet | Brivio, Simone Cadamuro, Massimiliano Strazzabosco, Mario Fabris, Luca |
author_sort | Brivio, Simone |
collection | PubMed |
description | Cholangiocarcinoma (CCA) is a highly aggressive epithelial malignancy still carrying a dismal prognosis, owing to early lymph node metastatic dissemination and striking resistance to conventional chemotherapy. Although mechanisms underpinning CCA progression are still a conundrum, it is now increasingly recognized that the desmoplastic microenvironment developing in conjunction with biliary carcinogenesis, recently renamed tumor reactive stroma (TRS), behaves as a paramount tumor-promoting driver. Indeed, once being recruited, activated and dangerously co-opted by neoplastic cells, the cellular components of the TRS (myofibroblasts, macrophages, endothelial cells and mesenchymal stem cells) continuously rekindle malignancy by secreting a huge variety of soluble factors (cyto/chemokines, growth factors, morphogens and proteinases). Furthermore, these factors are long-term stored within an abnormally remodeled extracellular matrix (ECM), which in turn can deleteriously mold cancer cell behavior. In this review, we will highlight evidence for the active role played by reactive stromal cells (as well as by the TRS-associated ECM) in CCA progression, including an overview of the most relevant TRS-derived signals possibly fueling CCA cell aggressiveness. Hopefully, a deeper knowledge of the paracrine communications reciprocally exchanged between cancer and stromal cells will steer the development of innovative, combinatorial therapies, which can finally hinder the progression of CCA, as well as of other cancer types with abundant TRS, such as pancreatic and breast carcinomas. |
format | Online Article Text |
id | pubmed-5368623 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Baishideng Publishing Group Inc |
record_format | MEDLINE/PubMed |
spelling | pubmed-53686232017-04-10 Tumor reactive stroma in cholangiocarcinoma: The fuel behind cancer aggressiveness Brivio, Simone Cadamuro, Massimiliano Strazzabosco, Mario Fabris, Luca World J Hepatol Editorial Cholangiocarcinoma (CCA) is a highly aggressive epithelial malignancy still carrying a dismal prognosis, owing to early lymph node metastatic dissemination and striking resistance to conventional chemotherapy. Although mechanisms underpinning CCA progression are still a conundrum, it is now increasingly recognized that the desmoplastic microenvironment developing in conjunction with biliary carcinogenesis, recently renamed tumor reactive stroma (TRS), behaves as a paramount tumor-promoting driver. Indeed, once being recruited, activated and dangerously co-opted by neoplastic cells, the cellular components of the TRS (myofibroblasts, macrophages, endothelial cells and mesenchymal stem cells) continuously rekindle malignancy by secreting a huge variety of soluble factors (cyto/chemokines, growth factors, morphogens and proteinases). Furthermore, these factors are long-term stored within an abnormally remodeled extracellular matrix (ECM), which in turn can deleteriously mold cancer cell behavior. In this review, we will highlight evidence for the active role played by reactive stromal cells (as well as by the TRS-associated ECM) in CCA progression, including an overview of the most relevant TRS-derived signals possibly fueling CCA cell aggressiveness. Hopefully, a deeper knowledge of the paracrine communications reciprocally exchanged between cancer and stromal cells will steer the development of innovative, combinatorial therapies, which can finally hinder the progression of CCA, as well as of other cancer types with abundant TRS, such as pancreatic and breast carcinomas. Baishideng Publishing Group Inc 2017-03-28 2017-03-28 /pmc/articles/PMC5368623/ /pubmed/28396716 http://dx.doi.org/10.4254/wjh.v9.i9.455 Text en ©The Author(s) 2017. Published by Baishideng Publishing Group Inc. All rights reserved. http://creativecommons.org/licenses/by-nc/4.0/ This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. |
spellingShingle | Editorial Brivio, Simone Cadamuro, Massimiliano Strazzabosco, Mario Fabris, Luca Tumor reactive stroma in cholangiocarcinoma: The fuel behind cancer aggressiveness |
title | Tumor reactive stroma in cholangiocarcinoma: The fuel behind cancer aggressiveness |
title_full | Tumor reactive stroma in cholangiocarcinoma: The fuel behind cancer aggressiveness |
title_fullStr | Tumor reactive stroma in cholangiocarcinoma: The fuel behind cancer aggressiveness |
title_full_unstemmed | Tumor reactive stroma in cholangiocarcinoma: The fuel behind cancer aggressiveness |
title_short | Tumor reactive stroma in cholangiocarcinoma: The fuel behind cancer aggressiveness |
title_sort | tumor reactive stroma in cholangiocarcinoma: the fuel behind cancer aggressiveness |
topic | Editorial |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5368623/ https://www.ncbi.nlm.nih.gov/pubmed/28396716 http://dx.doi.org/10.4254/wjh.v9.i9.455 |
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