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Co-expression of caspase-3 or caspase-8 with galanin in the human stomach section affected by carcinoma
Neoplastic process may cause distinct changes in the morphology, i.e. size and number of the neurons of the neuronal plexuses forming the enteric nervous system (ENS) of the human intestine. Moreover, it was also reported that these changes were not directly associated with apoptosis. Thus, the main...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6153556/ https://www.ncbi.nlm.nih.gov/pubmed/30019295 http://dx.doi.org/10.1007/s10495-018-1470-y |
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author | Kozłowska, Anna Kozera, Piotr Majewski, Mariusz Godlewski, Janusz |
author_facet | Kozłowska, Anna Kozera, Piotr Majewski, Mariusz Godlewski, Janusz |
author_sort | Kozłowska, Anna |
collection | PubMed |
description | Neoplastic process may cause distinct changes in the morphology, i.e. size and number of the neurons of the neuronal plexuses forming the enteric nervous system (ENS) of the human intestine. Moreover, it was also reported that these changes were not directly associated with apoptosis. Thus, the main aim of this study was to determine the atrophic changes of myenteric plexuses (MPs) in the vicinity of cancer invasion and the potential reason which may be responsible for these changes if they occur. Tissue samples from the stomach were collected from ten patients which undergo organ resection due to cancer diagnosis. Samples were taken from the margin of cancer invasion and from a macroscopically-unchanged part of the stomach wall. Triple-immunofluorescence staining of the 10-µm-thick cryostat sections was used to visualize the co-expression of caspase-3 (CASP3) or caspase-8 (CASP8) with galanin (GAL) in the MPs of ENS. Microscopic observations of MPs located closely to gastric cancer invasion showed that they were significantly smaller than plexuses located distally. The percentage of neurons containing CASP3 within MPs located close to cancer-affected regions of the stomach was higher, while containing CASP8 was lower compared to the unchanged regions. Additionally, elevated high expression of CASP3 or CASP8 in the neurons from MPs was accompanied by a decreased expression of GAL. To our knowledge, this is the first report describing the decomposition of MPs within cancer-affected human stomach wall and the possible role of apoptosis in this process. |
format | Online Article Text |
id | pubmed-6153556 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-61535562018-10-09 Co-expression of caspase-3 or caspase-8 with galanin in the human stomach section affected by carcinoma Kozłowska, Anna Kozera, Piotr Majewski, Mariusz Godlewski, Janusz Apoptosis Article Neoplastic process may cause distinct changes in the morphology, i.e. size and number of the neurons of the neuronal plexuses forming the enteric nervous system (ENS) of the human intestine. Moreover, it was also reported that these changes were not directly associated with apoptosis. Thus, the main aim of this study was to determine the atrophic changes of myenteric plexuses (MPs) in the vicinity of cancer invasion and the potential reason which may be responsible for these changes if they occur. Tissue samples from the stomach were collected from ten patients which undergo organ resection due to cancer diagnosis. Samples were taken from the margin of cancer invasion and from a macroscopically-unchanged part of the stomach wall. Triple-immunofluorescence staining of the 10-µm-thick cryostat sections was used to visualize the co-expression of caspase-3 (CASP3) or caspase-8 (CASP8) with galanin (GAL) in the MPs of ENS. Microscopic observations of MPs located closely to gastric cancer invasion showed that they were significantly smaller than plexuses located distally. The percentage of neurons containing CASP3 within MPs located close to cancer-affected regions of the stomach was higher, while containing CASP8 was lower compared to the unchanged regions. Additionally, elevated high expression of CASP3 or CASP8 in the neurons from MPs was accompanied by a decreased expression of GAL. To our knowledge, this is the first report describing the decomposition of MPs within cancer-affected human stomach wall and the possible role of apoptosis in this process. Springer US 2018-07-17 2018 /pmc/articles/PMC6153556/ /pubmed/30019295 http://dx.doi.org/10.1007/s10495-018-1470-y Text en © The Author(s) 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Article Kozłowska, Anna Kozera, Piotr Majewski, Mariusz Godlewski, Janusz Co-expression of caspase-3 or caspase-8 with galanin in the human stomach section affected by carcinoma |
title | Co-expression of caspase-3 or caspase-8 with galanin in the human stomach section affected by carcinoma |
title_full | Co-expression of caspase-3 or caspase-8 with galanin in the human stomach section affected by carcinoma |
title_fullStr | Co-expression of caspase-3 or caspase-8 with galanin in the human stomach section affected by carcinoma |
title_full_unstemmed | Co-expression of caspase-3 or caspase-8 with galanin in the human stomach section affected by carcinoma |
title_short | Co-expression of caspase-3 or caspase-8 with galanin in the human stomach section affected by carcinoma |
title_sort | co-expression of caspase-3 or caspase-8 with galanin in the human stomach section affected by carcinoma |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6153556/ https://www.ncbi.nlm.nih.gov/pubmed/30019295 http://dx.doi.org/10.1007/s10495-018-1470-y |
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