Factors released by the tumor far microenvironment are decisive for pancreatic adenocarcinoma development and progression

The REG3β protein was identified more than 2 decades ago, but its role in PDAC development was only recently reported. In Pancreatic Ductal Adenocarcinoma (PDAC), REG3β protein is expressed and released by the far microenvironment, which is situated out of the tumor, at the periphery of the tumor ma...

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Main Authors: Juan L. Iovanna, Daniel Closa
Format: Article
Language:English
Published: Taylor & Francis Group 2017-11-01
Series:OncoImmunology
Subjects:
Online Access:http://dx.doi.org/10.1080/2162402X.2017.1358840
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spelling doaj-052f96b0a719495390fa6016c295bf522020-11-25T03:03:03ZengTaylor & Francis GroupOncoImmunology2162-402X2017-11-0161110.1080/2162402X.2017.13588401358840Factors released by the tumor far microenvironment are decisive for pancreatic adenocarcinoma development and progressionJuan L. Iovanna0Daniel Closa1INSERM U1068, CNRS UMR 7258, Aix-Marseille Université and Institut Paoli-Calmettes, Parc Scientifique et Technologique de LuminyInstitut d'Investigacions Biomèdiques de Barcelona-Consejo Superior de Investigaciones científicas (IIBB-CSIC), Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS)The REG3β protein was identified more than 2 decades ago, but its role in PDAC development was only recently reported. In Pancreatic Ductal Adenocarcinoma (PDAC), REG3β protein is expressed and released by the far microenvironment, which is situated out of the tumor, at the periphery of the tumor mass, and is part of the healthy peri-tumoral region. This compartment is completely unrelated to the classical microenvironment that corresponds to the intra-tumoral stoma. Clinically relevant, the far microenvironment, and the factors released by it, could be novel and original therapeutic targets for treating patients with a PDAC. In this way we recently demonstrated that REG3β is an essential soluble factor necessary for PDAC development which is able to stimulate several simultaneous pro-tumoral mechanisms. We also find that secreted REG3β boosts interactions between epithelial cells and immune cells by activating the CXCL12/CXCR4 signaling cascade, which facilitates tumor escape through evasion of immune surveillance, and promotes metastasis. In addition, REG3β interfere the intercellular communication inside the tumor mediated by extracellular vesicles, resulting in relevant changes in macrophage phenotype or tumor cell migration. Therefore, we are proposing to call as near microenvironment to the classical microenvironment that is constituted by fibroblasts, inflammatory cells and fibers and located into the tumor, and as far microenvironment, which is constituted by the parenchymal non transformed cells located at the periphery of the tumor mass.http://dx.doi.org/10.1080/2162402X.2017.1358840pancreas cancerreg3betamicroenvironmentperi-tumoral regionpancreatitis
collection DOAJ
language English
format Article
sources DOAJ
author Juan L. Iovanna
Daniel Closa
spellingShingle Juan L. Iovanna
Daniel Closa
Factors released by the tumor far microenvironment are decisive for pancreatic adenocarcinoma development and progression
OncoImmunology
pancreas cancer
reg3beta
microenvironment
peri-tumoral region
pancreatitis
author_facet Juan L. Iovanna
Daniel Closa
author_sort Juan L. Iovanna
title Factors released by the tumor far microenvironment are decisive for pancreatic adenocarcinoma development and progression
title_short Factors released by the tumor far microenvironment are decisive for pancreatic adenocarcinoma development and progression
title_full Factors released by the tumor far microenvironment are decisive for pancreatic adenocarcinoma development and progression
title_fullStr Factors released by the tumor far microenvironment are decisive for pancreatic adenocarcinoma development and progression
title_full_unstemmed Factors released by the tumor far microenvironment are decisive for pancreatic adenocarcinoma development and progression
title_sort factors released by the tumor far microenvironment are decisive for pancreatic adenocarcinoma development and progression
publisher Taylor & Francis Group
series OncoImmunology
issn 2162-402X
publishDate 2017-11-01
description The REG3β protein was identified more than 2 decades ago, but its role in PDAC development was only recently reported. In Pancreatic Ductal Adenocarcinoma (PDAC), REG3β protein is expressed and released by the far microenvironment, which is situated out of the tumor, at the periphery of the tumor mass, and is part of the healthy peri-tumoral region. This compartment is completely unrelated to the classical microenvironment that corresponds to the intra-tumoral stoma. Clinically relevant, the far microenvironment, and the factors released by it, could be novel and original therapeutic targets for treating patients with a PDAC. In this way we recently demonstrated that REG3β is an essential soluble factor necessary for PDAC development which is able to stimulate several simultaneous pro-tumoral mechanisms. We also find that secreted REG3β boosts interactions between epithelial cells and immune cells by activating the CXCL12/CXCR4 signaling cascade, which facilitates tumor escape through evasion of immune surveillance, and promotes metastasis. In addition, REG3β interfere the intercellular communication inside the tumor mediated by extracellular vesicles, resulting in relevant changes in macrophage phenotype or tumor cell migration. Therefore, we are proposing to call as near microenvironment to the classical microenvironment that is constituted by fibroblasts, inflammatory cells and fibers and located into the tumor, and as far microenvironment, which is constituted by the parenchymal non transformed cells located at the periphery of the tumor mass.
topic pancreas cancer
reg3beta
microenvironment
peri-tumoral region
pancreatitis
url http://dx.doi.org/10.1080/2162402X.2017.1358840
work_keys_str_mv AT juanliovanna factorsreleasedbythetumorfarmicroenvironmentaredecisiveforpancreaticadenocarcinomadevelopmentandprogression
AT danielclosa factorsreleasedbythetumorfarmicroenvironmentaredecisiveforpancreaticadenocarcinomadevelopmentandprogression
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