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Role of Muscarinic Acetylcholine Signaling in Gastrointestinal Cancers

In the tumor microenvironment, various stromal and immune cells accumulate and interact with cancer cells to contribute to tumor progression. Among stromal players, nerves have recently been recognized as key regulators of tumor growth. More neurotransmitters, such as catecholamines and acetylcholin...

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Detalles Bibliográficos
Autores principales: Konishi, Mitsuru, Hayakawa, Yoku, Koike, Kazuhiko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6783861/
https://www.ncbi.nlm.nih.gov/pubmed/31405140
http://dx.doi.org/10.3390/biomedicines7030058
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author Konishi, Mitsuru
Hayakawa, Yoku
Koike, Kazuhiko
author_facet Konishi, Mitsuru
Hayakawa, Yoku
Koike, Kazuhiko
author_sort Konishi, Mitsuru
collection PubMed
description In the tumor microenvironment, various stromal and immune cells accumulate and interact with cancer cells to contribute to tumor progression. Among stromal players, nerves have recently been recognized as key regulators of tumor growth. More neurotransmitters, such as catecholamines and acetylcholine (ACh), are present in tumors, as the cells that secrete neurotransmitters accumulate by the release of neurotrophic factors from cancer cells. In this short review, we focus on the role of nerve signaling in gastrointestinal (GI) cancers. Given that muscarinic acetylcholine receptor signaling seems to be a dominant regulator of GI stem cells and cancers, we review the function and mechanism of the muscarinic ACh pathway as a regulator of GI cancer progression. Accumulating evidence suggests that ACh, which is secreted from nerves and tuft cells, stimulates GI epithelial stem cells and contributes to cancer progression via muscarinic receptors.
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spelling pubmed-67838612019-10-16 Role of Muscarinic Acetylcholine Signaling in Gastrointestinal Cancers Konishi, Mitsuru Hayakawa, Yoku Koike, Kazuhiko Biomedicines Review In the tumor microenvironment, various stromal and immune cells accumulate and interact with cancer cells to contribute to tumor progression. Among stromal players, nerves have recently been recognized as key regulators of tumor growth. More neurotransmitters, such as catecholamines and acetylcholine (ACh), are present in tumors, as the cells that secrete neurotransmitters accumulate by the release of neurotrophic factors from cancer cells. In this short review, we focus on the role of nerve signaling in gastrointestinal (GI) cancers. Given that muscarinic acetylcholine receptor signaling seems to be a dominant regulator of GI stem cells and cancers, we review the function and mechanism of the muscarinic ACh pathway as a regulator of GI cancer progression. Accumulating evidence suggests that ACh, which is secreted from nerves and tuft cells, stimulates GI epithelial stem cells and contributes to cancer progression via muscarinic receptors. MDPI 2019-08-10 /pmc/articles/PMC6783861/ /pubmed/31405140 http://dx.doi.org/10.3390/biomedicines7030058 Text en © 2019 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
Konishi, Mitsuru
Hayakawa, Yoku
Koike, Kazuhiko
Role of Muscarinic Acetylcholine Signaling in Gastrointestinal Cancers
title Role of Muscarinic Acetylcholine Signaling in Gastrointestinal Cancers
title_full Role of Muscarinic Acetylcholine Signaling in Gastrointestinal Cancers
title_fullStr Role of Muscarinic Acetylcholine Signaling in Gastrointestinal Cancers
title_full_unstemmed Role of Muscarinic Acetylcholine Signaling in Gastrointestinal Cancers
title_short Role of Muscarinic Acetylcholine Signaling in Gastrointestinal Cancers
title_sort role of muscarinic acetylcholine signaling in gastrointestinal cancers
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6783861/
https://www.ncbi.nlm.nih.gov/pubmed/31405140
http://dx.doi.org/10.3390/biomedicines7030058
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