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Calcium-sensing receptor in colorectal inflammation and cancer: Current insights and future perspectives
The extracellular calcium-sensing receptor (CaSR) is best known for its action in the parathyroid gland and kidneys where it controls body calcium homeostasis. However, the CaSR has different roles in the gastrointestinal tract, where it is ubiquitously expressed. In the colon, the CaSR is involved...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Baishideng Publishing Group Inc
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6158479/ https://www.ncbi.nlm.nih.gov/pubmed/30271078 http://dx.doi.org/10.3748/wjg.v24.i36.4119 |
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author | Iamartino, Luca Elajnaf, Taha Kallay, Enikö Schepelmann, Martin |
author_facet | Iamartino, Luca Elajnaf, Taha Kallay, Enikö Schepelmann, Martin |
author_sort | Iamartino, Luca |
collection | PubMed |
description | The extracellular calcium-sensing receptor (CaSR) is best known for its action in the parathyroid gland and kidneys where it controls body calcium homeostasis. However, the CaSR has different roles in the gastrointestinal tract, where it is ubiquitously expressed. In the colon, the CaSR is involved in controlling multiple mechanisms, including fluid transport, inflammation, cell proliferation and differentiation. Although the expression pattern and functions of the CaSR in the colonic microenvironment are far from being completely understood, evidence has been accumulating that the CaSR might play a protective role against both colonic inflammation and colorectal cancer. For example, CaSR agonists such as dipeptides have been suggested to reduce colonic inflammation, while dietary calcium was shown to reduce the risk of colorectal cancer. CaSR expression is lost in colonic malignancies, indicating that the CaSR is a biomarker for colonic cancer progression. This dual anti-inflammatory and anti-tumourigenic role of the CaSR makes it especially interesting in colitis-associated colorectal cancer. In this review, we describe the clinical and experimental evidence for the role of the CaSR in colonic inflammation and colorectal cancer, the intracellular signalling pathways which are putatively involved in these actions, and the possibilities to exploit these actions of the CaSR for future therapies of colonic inflammation and cancer. |
format | Online Article Text |
id | pubmed-6158479 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Baishideng Publishing Group Inc |
record_format | MEDLINE/PubMed |
spelling | pubmed-61584792018-09-29 Calcium-sensing receptor in colorectal inflammation and cancer: Current insights and future perspectives Iamartino, Luca Elajnaf, Taha Kallay, Enikö Schepelmann, Martin World J Gastroenterol Review The extracellular calcium-sensing receptor (CaSR) is best known for its action in the parathyroid gland and kidneys where it controls body calcium homeostasis. However, the CaSR has different roles in the gastrointestinal tract, where it is ubiquitously expressed. In the colon, the CaSR is involved in controlling multiple mechanisms, including fluid transport, inflammation, cell proliferation and differentiation. Although the expression pattern and functions of the CaSR in the colonic microenvironment are far from being completely understood, evidence has been accumulating that the CaSR might play a protective role against both colonic inflammation and colorectal cancer. For example, CaSR agonists such as dipeptides have been suggested to reduce colonic inflammation, while dietary calcium was shown to reduce the risk of colorectal cancer. CaSR expression is lost in colonic malignancies, indicating that the CaSR is a biomarker for colonic cancer progression. This dual anti-inflammatory and anti-tumourigenic role of the CaSR makes it especially interesting in colitis-associated colorectal cancer. In this review, we describe the clinical and experimental evidence for the role of the CaSR in colonic inflammation and colorectal cancer, the intracellular signalling pathways which are putatively involved in these actions, and the possibilities to exploit these actions of the CaSR for future therapies of colonic inflammation and cancer. Baishideng Publishing Group Inc 2018-09-28 2018-09-28 /pmc/articles/PMC6158479/ /pubmed/30271078 http://dx.doi.org/10.3748/wjg.v24.i36.4119 Text en ©The Author(s) 2018. 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 | Review Iamartino, Luca Elajnaf, Taha Kallay, Enikö Schepelmann, Martin Calcium-sensing receptor in colorectal inflammation and cancer: Current insights and future perspectives |
title | Calcium-sensing receptor in colorectal inflammation and cancer: Current insights and future perspectives |
title_full | Calcium-sensing receptor in colorectal inflammation and cancer: Current insights and future perspectives |
title_fullStr | Calcium-sensing receptor in colorectal inflammation and cancer: Current insights and future perspectives |
title_full_unstemmed | Calcium-sensing receptor in colorectal inflammation and cancer: Current insights and future perspectives |
title_short | Calcium-sensing receptor in colorectal inflammation and cancer: Current insights and future perspectives |
title_sort | calcium-sensing receptor in colorectal inflammation and cancer: current insights and future perspectives |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6158479/ https://www.ncbi.nlm.nih.gov/pubmed/30271078 http://dx.doi.org/10.3748/wjg.v24.i36.4119 |
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