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Purinergic Signaling in Pancreas—From Physiology to Therapeutic Strategies in Pancreatic Cancer

The purinergic signaling has an important role in regulating pancreatic exocrine secretion. The exocrine pancreas is also a site of one of the most serious cancer forms, the pancreatic ductal adenocarcinoma (PDAC). Here, we explore how the network of purinergic and adenosine receptors, as well as ec...

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Detalles Bibliográficos
Autores principales: Novak, Ivana, Yu, Haoran, Magni, Lara, Deshar, Ganga
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7699721/
https://www.ncbi.nlm.nih.gov/pubmed/33233631
http://dx.doi.org/10.3390/ijms21228781
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author Novak, Ivana
Yu, Haoran
Magni, Lara
Deshar, Ganga
author_facet Novak, Ivana
Yu, Haoran
Magni, Lara
Deshar, Ganga
author_sort Novak, Ivana
collection PubMed
description The purinergic signaling has an important role in regulating pancreatic exocrine secretion. The exocrine pancreas is also a site of one of the most serious cancer forms, the pancreatic ductal adenocarcinoma (PDAC). Here, we explore how the network of purinergic and adenosine receptors, as well as ecto-nucleotidases regulate normal pancreatic cells and various cells within the pancreatic tumor microenvironment. In particular, we focus on the P2X7 receptor, P2Y(2) and P2Y(12) receptors, as well as A(2) receptors and ecto-nucleotidases CD39 and CD73. Recent studies indicate that targeting one or more of these candidates could present new therapeutic approaches to treat pancreatic cancer. In pancreatic cancer, as much as possible of normal pancreatic function should be preserved, and therefore physiology of purinergic signaling in pancreas needs to be considered.
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spelling pubmed-76997212020-11-29 Purinergic Signaling in Pancreas—From Physiology to Therapeutic Strategies in Pancreatic Cancer Novak, Ivana Yu, Haoran Magni, Lara Deshar, Ganga Int J Mol Sci Review The purinergic signaling has an important role in regulating pancreatic exocrine secretion. The exocrine pancreas is also a site of one of the most serious cancer forms, the pancreatic ductal adenocarcinoma (PDAC). Here, we explore how the network of purinergic and adenosine receptors, as well as ecto-nucleotidases regulate normal pancreatic cells and various cells within the pancreatic tumor microenvironment. In particular, we focus on the P2X7 receptor, P2Y(2) and P2Y(12) receptors, as well as A(2) receptors and ecto-nucleotidases CD39 and CD73. Recent studies indicate that targeting one or more of these candidates could present new therapeutic approaches to treat pancreatic cancer. In pancreatic cancer, as much as possible of normal pancreatic function should be preserved, and therefore physiology of purinergic signaling in pancreas needs to be considered. MDPI 2020-11-20 /pmc/articles/PMC7699721/ /pubmed/33233631 http://dx.doi.org/10.3390/ijms21228781 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
Novak, Ivana
Yu, Haoran
Magni, Lara
Deshar, Ganga
Purinergic Signaling in Pancreas—From Physiology to Therapeutic Strategies in Pancreatic Cancer
title Purinergic Signaling in Pancreas—From Physiology to Therapeutic Strategies in Pancreatic Cancer
title_full Purinergic Signaling in Pancreas—From Physiology to Therapeutic Strategies in Pancreatic Cancer
title_fullStr Purinergic Signaling in Pancreas—From Physiology to Therapeutic Strategies in Pancreatic Cancer
title_full_unstemmed Purinergic Signaling in Pancreas—From Physiology to Therapeutic Strategies in Pancreatic Cancer
title_short Purinergic Signaling in Pancreas—From Physiology to Therapeutic Strategies in Pancreatic Cancer
title_sort purinergic signaling in pancreas—from physiology to therapeutic strategies in pancreatic cancer
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7699721/
https://www.ncbi.nlm.nih.gov/pubmed/33233631
http://dx.doi.org/10.3390/ijms21228781
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