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Radiotherapy of the Hepatocellular Carcinoma in Mice Has a Time-Of-Day-Dependent Impact on the Mouse Hippocampus

Chronic liver diseases including hepatocellular carcinoma (HCC) create a state of chronic inflammation that affects the brain via the liver–brain axis leading to an alteration of neurotransmission and cognition. However, little is known about the effects of HCC on the hippocampus, the key brain regi...

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Autores principales: Yassine, Mona, Hassan, Soha A., Sommer, Simon, Yücel, Lea Aylin, Bellert, Hanna, Hallenberger, Johanna, Sohn, Dennis, Korf, Horst-Werner, von Gall, Charlotte, Ali, Amira A. H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9818790/
https://www.ncbi.nlm.nih.gov/pubmed/36611854
http://dx.doi.org/10.3390/cells12010061
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author Yassine, Mona
Hassan, Soha A.
Sommer, Simon
Yücel, Lea Aylin
Bellert, Hanna
Hallenberger, Johanna
Sohn, Dennis
Korf, Horst-Werner
von Gall, Charlotte
Ali, Amira A. H.
author_facet Yassine, Mona
Hassan, Soha A.
Sommer, Simon
Yücel, Lea Aylin
Bellert, Hanna
Hallenberger, Johanna
Sohn, Dennis
Korf, Horst-Werner
von Gall, Charlotte
Ali, Amira A. H.
author_sort Yassine, Mona
collection PubMed
description Chronic liver diseases including hepatocellular carcinoma (HCC) create a state of chronic inflammation that affects the brain via the liver–brain axis leading to an alteration of neurotransmission and cognition. However, little is known about the effects of HCC on the hippocampus, the key brain region for learning and memory. Moreover, radiotherapy used to treat HCC has severe side effects that impair patients’ life quality. Thus, designing optimal strategies, such as chronotherapy, to enhance the efficacy and reduce the side effects of HCC treatment is critically important. We addressed the effects of HCC and the timed administration of radiotherapy in mice on the expression of pro-inflammatory cytokines, clock genes, markers for glial activation, oxidative stress, neuronal activity and proliferation in the hippocampal neurogenic niche. Our data showed that HCC induced the upregulation of genes encoding for pro-inflammatory cytokines, altered clock gene expressions and reduced proliferation in the hippocampus. Radiotherapy, in particular when applied during the light/inactive phase enhanced all these effects in addition to glial activation, increased oxidative stress, decreased neuronal activity and increased levels of phospho(p)-ERK. Our results suggested an interaction of the circadian molecular clockwork and the brain’s innate immune system as key players in liver–brain crosstalk in HCC and that radiotherapy when applied during the light/inactive phase induced the most profound alterations in the hippocampus.
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spelling pubmed-98187902023-01-07 Radiotherapy of the Hepatocellular Carcinoma in Mice Has a Time-Of-Day-Dependent Impact on the Mouse Hippocampus Yassine, Mona Hassan, Soha A. Sommer, Simon Yücel, Lea Aylin Bellert, Hanna Hallenberger, Johanna Sohn, Dennis Korf, Horst-Werner von Gall, Charlotte Ali, Amira A. H. Cells Article Chronic liver diseases including hepatocellular carcinoma (HCC) create a state of chronic inflammation that affects the brain via the liver–brain axis leading to an alteration of neurotransmission and cognition. However, little is known about the effects of HCC on the hippocampus, the key brain region for learning and memory. Moreover, radiotherapy used to treat HCC has severe side effects that impair patients’ life quality. Thus, designing optimal strategies, such as chronotherapy, to enhance the efficacy and reduce the side effects of HCC treatment is critically important. We addressed the effects of HCC and the timed administration of radiotherapy in mice on the expression of pro-inflammatory cytokines, clock genes, markers for glial activation, oxidative stress, neuronal activity and proliferation in the hippocampal neurogenic niche. Our data showed that HCC induced the upregulation of genes encoding for pro-inflammatory cytokines, altered clock gene expressions and reduced proliferation in the hippocampus. Radiotherapy, in particular when applied during the light/inactive phase enhanced all these effects in addition to glial activation, increased oxidative stress, decreased neuronal activity and increased levels of phospho(p)-ERK. Our results suggested an interaction of the circadian molecular clockwork and the brain’s innate immune system as key players in liver–brain crosstalk in HCC and that radiotherapy when applied during the light/inactive phase induced the most profound alterations in the hippocampus. MDPI 2022-12-23 /pmc/articles/PMC9818790/ /pubmed/36611854 http://dx.doi.org/10.3390/cells12010061 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Yassine, Mona
Hassan, Soha A.
Sommer, Simon
Yücel, Lea Aylin
Bellert, Hanna
Hallenberger, Johanna
Sohn, Dennis
Korf, Horst-Werner
von Gall, Charlotte
Ali, Amira A. H.
Radiotherapy of the Hepatocellular Carcinoma in Mice Has a Time-Of-Day-Dependent Impact on the Mouse Hippocampus
title Radiotherapy of the Hepatocellular Carcinoma in Mice Has a Time-Of-Day-Dependent Impact on the Mouse Hippocampus
title_full Radiotherapy of the Hepatocellular Carcinoma in Mice Has a Time-Of-Day-Dependent Impact on the Mouse Hippocampus
title_fullStr Radiotherapy of the Hepatocellular Carcinoma in Mice Has a Time-Of-Day-Dependent Impact on the Mouse Hippocampus
title_full_unstemmed Radiotherapy of the Hepatocellular Carcinoma in Mice Has a Time-Of-Day-Dependent Impact on the Mouse Hippocampus
title_short Radiotherapy of the Hepatocellular Carcinoma in Mice Has a Time-Of-Day-Dependent Impact on the Mouse Hippocampus
title_sort radiotherapy of the hepatocellular carcinoma in mice has a time-of-day-dependent impact on the mouse hippocampus
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9818790/
https://www.ncbi.nlm.nih.gov/pubmed/36611854
http://dx.doi.org/10.3390/cells12010061
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