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The role of CXCL12 axis in pancreatic cancer: New biomarkers and potential targets
INTRODUCTION: Chemokines are small, secreted peptides involved in the mediation of the immune cell recruitment. Chemokines have been implicated in several diseases including autoimmune diseases, viral infections and also played a critical role in the genesis and development of several malignant tumo...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10076769/ https://www.ncbi.nlm.nih.gov/pubmed/37035150 http://dx.doi.org/10.3389/fonc.2023.1154581 |
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author | Roberto, Michela Arrivi, Giulia Di Civita, Mattia Alberto Barchiesi, Giacomo Pilozzi, Emanuela Marchetti, Paolo Santini, Daniele Mazzuca, Federica Tomao, Silverio |
author_facet | Roberto, Michela Arrivi, Giulia Di Civita, Mattia Alberto Barchiesi, Giacomo Pilozzi, Emanuela Marchetti, Paolo Santini, Daniele Mazzuca, Federica Tomao, Silverio |
author_sort | Roberto, Michela |
collection | PubMed |
description | INTRODUCTION: Chemokines are small, secreted peptides involved in the mediation of the immune cell recruitment. Chemokines have been implicated in several diseases including autoimmune diseases, viral infections and also played a critical role in the genesis and development of several malignant tumors. CXCL12 is a homeostatic CXC chemokine involved in the process of proliferation, and tumor spread. Pancreatic ductal adenocarcinoma (PDAC) is one of the most aggressive tumors, that is still lacking effective therapies and with a dramatically poor prognosis. METHOD: We conducted a scientific literature search on Pubmed and Google Scholar including retrospective, prospective studies and reviews focused on the current research elucidating the emerging role of CXCL12 and its receptors CXCR4 – CXCR7 in the pathogenesis of pancreatic cancer. RESULTS: Considering the mechanism of immunomodulation of the CXCL12-CXCR4-CXCR7 axis, as well as the potential interaction with the microenvironment in the PDAC, several combined therapeutic approaches have been studied and developed, to overcome the “cold” immunological setting of PDAC, like combining CXCL12 axis inhibitors with anti PD-1/PDL1 drugs. CONCLUSION: Understanding the role of this chemokine’s axis in disease initiation and progression may provide the basis for developing new potential biomarkers as well as therapeutic targets for related pancreatic cancers. |
format | Online Article Text |
id | pubmed-10076769 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-100767692023-04-07 The role of CXCL12 axis in pancreatic cancer: New biomarkers and potential targets Roberto, Michela Arrivi, Giulia Di Civita, Mattia Alberto Barchiesi, Giacomo Pilozzi, Emanuela Marchetti, Paolo Santini, Daniele Mazzuca, Federica Tomao, Silverio Front Oncol Oncology INTRODUCTION: Chemokines are small, secreted peptides involved in the mediation of the immune cell recruitment. Chemokines have been implicated in several diseases including autoimmune diseases, viral infections and also played a critical role in the genesis and development of several malignant tumors. CXCL12 is a homeostatic CXC chemokine involved in the process of proliferation, and tumor spread. Pancreatic ductal adenocarcinoma (PDAC) is one of the most aggressive tumors, that is still lacking effective therapies and with a dramatically poor prognosis. METHOD: We conducted a scientific literature search on Pubmed and Google Scholar including retrospective, prospective studies and reviews focused on the current research elucidating the emerging role of CXCL12 and its receptors CXCR4 – CXCR7 in the pathogenesis of pancreatic cancer. RESULTS: Considering the mechanism of immunomodulation of the CXCL12-CXCR4-CXCR7 axis, as well as the potential interaction with the microenvironment in the PDAC, several combined therapeutic approaches have been studied and developed, to overcome the “cold” immunological setting of PDAC, like combining CXCL12 axis inhibitors with anti PD-1/PDL1 drugs. CONCLUSION: Understanding the role of this chemokine’s axis in disease initiation and progression may provide the basis for developing new potential biomarkers as well as therapeutic targets for related pancreatic cancers. Frontiers Media S.A. 2023-03-23 /pmc/articles/PMC10076769/ /pubmed/37035150 http://dx.doi.org/10.3389/fonc.2023.1154581 Text en Copyright © 2023 Roberto, Arrivi, Di Civita, Barchiesi, Pilozzi, Marchetti, Santini, Mazzuca and Tomao https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Oncology Roberto, Michela Arrivi, Giulia Di Civita, Mattia Alberto Barchiesi, Giacomo Pilozzi, Emanuela Marchetti, Paolo Santini, Daniele Mazzuca, Federica Tomao, Silverio The role of CXCL12 axis in pancreatic cancer: New biomarkers and potential targets |
title | The role of CXCL12 axis in pancreatic cancer: New biomarkers and potential targets |
title_full | The role of CXCL12 axis in pancreatic cancer: New biomarkers and potential targets |
title_fullStr | The role of CXCL12 axis in pancreatic cancer: New biomarkers and potential targets |
title_full_unstemmed | The role of CXCL12 axis in pancreatic cancer: New biomarkers and potential targets |
title_short | The role of CXCL12 axis in pancreatic cancer: New biomarkers and potential targets |
title_sort | role of cxcl12 axis in pancreatic cancer: new biomarkers and potential targets |
topic | Oncology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10076769/ https://www.ncbi.nlm.nih.gov/pubmed/37035150 http://dx.doi.org/10.3389/fonc.2023.1154581 |
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