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Conflicting Roles of Connexin43 in Tumor Invasion and Growth in the Central Nervous System

The tumor microenvironment is known to have increased levels of cytokines and metabolites, such as glutamate, due to their release from the surrounding cells. A normal cell around the tumor that responds to the inflammatory environment is likely to be subsequently altered. We discuss how these abnor...

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Autores principales: Uzu, Miaki, Sin, Wun Chey, Shimizu, Ayaka, Sato, Hiromi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5979343/
https://www.ncbi.nlm.nih.gov/pubmed/29641478
http://dx.doi.org/10.3390/ijms19041159
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author Uzu, Miaki
Sin, Wun Chey
Shimizu, Ayaka
Sato, Hiromi
author_facet Uzu, Miaki
Sin, Wun Chey
Shimizu, Ayaka
Sato, Hiromi
author_sort Uzu, Miaki
collection PubMed
description The tumor microenvironment is known to have increased levels of cytokines and metabolites, such as glutamate, due to their release from the surrounding cells. A normal cell around the tumor that responds to the inflammatory environment is likely to be subsequently altered. We discuss how these abnormalities will support tumor survival via the actions of gap junctions (GJs) and hemichannels (HCs) which are composed of hexamer of connexin43 (Cx43) protein. In particular, we discuss how GJ intercellular communication (GJIC) in glioma cells, the primary brain tumor, is a regulatory factor and its attenuation leads to tumor invasion. In contrast, the astrocytes, which are normal cells around the glioma, are “hijacked” by tumor cells, either by receiving the transmission of malignant substances from the cancer cells via GJIC, or perhaps via astrocytic HC activity through the paracrine signaling which enable the delivery of these substances to the distal astrocytes. This astrocytic signaling would promote tumor expansion in the brain. In addition, brain metastasis from peripheral tissues has also been known to be facilitated by GJs formed between cerebral vascular endothelial cells and cancer cells. Astrocytes and microglia are generally thought to eliminate cancer cells at the blood–brain barrier. In contrast, some reports suggest they facilitate tumor progression as tumor cells take advantage of the normal functions of astrocytes that support the survival of the neurons by exchanging nutrients and metabolites. In summary, GJIC is essential for the normal physiological function of growth and allowing the diffusion of physiological substances. Therefore, whether GJIC is cancer promoting or suppressing may be dependent on what permeates through GJs, when it is active, and to which cells. The nature of GJs, which has been ambiguous in brain tumor progression, needs to be revisited and understood together with new findings on Cx proteins and HC activities.
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spelling pubmed-59793432018-06-10 Conflicting Roles of Connexin43 in Tumor Invasion and Growth in the Central Nervous System Uzu, Miaki Sin, Wun Chey Shimizu, Ayaka Sato, Hiromi Int J Mol Sci Review The tumor microenvironment is known to have increased levels of cytokines and metabolites, such as glutamate, due to their release from the surrounding cells. A normal cell around the tumor that responds to the inflammatory environment is likely to be subsequently altered. We discuss how these abnormalities will support tumor survival via the actions of gap junctions (GJs) and hemichannels (HCs) which are composed of hexamer of connexin43 (Cx43) protein. In particular, we discuss how GJ intercellular communication (GJIC) in glioma cells, the primary brain tumor, is a regulatory factor and its attenuation leads to tumor invasion. In contrast, the astrocytes, which are normal cells around the glioma, are “hijacked” by tumor cells, either by receiving the transmission of malignant substances from the cancer cells via GJIC, or perhaps via astrocytic HC activity through the paracrine signaling which enable the delivery of these substances to the distal astrocytes. This astrocytic signaling would promote tumor expansion in the brain. In addition, brain metastasis from peripheral tissues has also been known to be facilitated by GJs formed between cerebral vascular endothelial cells and cancer cells. Astrocytes and microglia are generally thought to eliminate cancer cells at the blood–brain barrier. In contrast, some reports suggest they facilitate tumor progression as tumor cells take advantage of the normal functions of astrocytes that support the survival of the neurons by exchanging nutrients and metabolites. In summary, GJIC is essential for the normal physiological function of growth and allowing the diffusion of physiological substances. Therefore, whether GJIC is cancer promoting or suppressing may be dependent on what permeates through GJs, when it is active, and to which cells. The nature of GJs, which has been ambiguous in brain tumor progression, needs to be revisited and understood together with new findings on Cx proteins and HC activities. MDPI 2018-04-11 /pmc/articles/PMC5979343/ /pubmed/29641478 http://dx.doi.org/10.3390/ijms19041159 Text en © 2018 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
Uzu, Miaki
Sin, Wun Chey
Shimizu, Ayaka
Sato, Hiromi
Conflicting Roles of Connexin43 in Tumor Invasion and Growth in the Central Nervous System
title Conflicting Roles of Connexin43 in Tumor Invasion and Growth in the Central Nervous System
title_full Conflicting Roles of Connexin43 in Tumor Invasion and Growth in the Central Nervous System
title_fullStr Conflicting Roles of Connexin43 in Tumor Invasion and Growth in the Central Nervous System
title_full_unstemmed Conflicting Roles of Connexin43 in Tumor Invasion and Growth in the Central Nervous System
title_short Conflicting Roles of Connexin43 in Tumor Invasion and Growth in the Central Nervous System
title_sort conflicting roles of connexin43 in tumor invasion and growth in the central nervous system
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5979343/
https://www.ncbi.nlm.nih.gov/pubmed/29641478
http://dx.doi.org/10.3390/ijms19041159
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