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Intraglandular mesenchymal stem cell treatment induces changes in the salivary proteome of irradiated patients

BACKGROUND: Hyposalivation and xerostomia (dry mouth), are the leading site-effects to treatment of head and neck cancer. Currently, there are no effective therapies to alleviate radiation-induced hyposalivation. Adipose tissue-derived mesenchymal stem/stromal cells (AT-MSCs) have shown potential fo...

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Autores principales: Lynggaard, Charlotte Duch, Jersie-Christensen, Rosa, Juhl, Morten, Jensen, Siri Beier, Grønhøj, Christian, Melchiors, Jacob, Jacobsen, Søren, Møller-Hansen, Michael, Herly, Mikkel, Ekblond, Annette, Kastrup, Jens, Fischer-Nielsen, Anne, Belstrøm, Daniel, von Buchwald, Christian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9735277/
https://www.ncbi.nlm.nih.gov/pubmed/36496530
http://dx.doi.org/10.1038/s43856-022-00223-3
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author Lynggaard, Charlotte Duch
Jersie-Christensen, Rosa
Juhl, Morten
Jensen, Siri Beier
Grønhøj, Christian
Melchiors, Jacob
Jacobsen, Søren
Møller-Hansen, Michael
Herly, Mikkel
Ekblond, Annette
Kastrup, Jens
Fischer-Nielsen, Anne
Belstrøm, Daniel
von Buchwald, Christian
author_facet Lynggaard, Charlotte Duch
Jersie-Christensen, Rosa
Juhl, Morten
Jensen, Siri Beier
Grønhøj, Christian
Melchiors, Jacob
Jacobsen, Søren
Møller-Hansen, Michael
Herly, Mikkel
Ekblond, Annette
Kastrup, Jens
Fischer-Nielsen, Anne
Belstrøm, Daniel
von Buchwald, Christian
author_sort Lynggaard, Charlotte Duch
collection PubMed
description BACKGROUND: Hyposalivation and xerostomia (dry mouth), are the leading site-effects to treatment of head and neck cancer. Currently, there are no effective therapies to alleviate radiation-induced hyposalivation. Adipose tissue-derived mesenchymal stem/stromal cells (AT-MSCs) have shown potential for restoring salivary gland function. However, the mode of action is unknown. The purpose of the present study was therefore to characterize the effect of AT-MSC therapy on the salivary proteome in previously irradiated head and neck cancer patients. METHODS: Whole saliva was collected from patients with radiation-induced salivary gland hypofunction (n = 8) at baseline, and 120 days after AT-MSC treatment, and from healthy controls (n = 10). The salivary proteome was characterized with mass spectrometry based proteomics, and data was compared within the AT-MSC group (baseline versus day 120) and between AT-MSC group and healthy controls. Significance levels between groups were determined by using double-sided t-test, and visualized by means of principal component analysis, volcano plots and cluster analysis. RESULTS: Here we show that 140 human proteins are significantly differentially expressed in saliva from patients with radiation-induced hypofunction versus healthy controls. AT-MSC treatment induce a significant impact on the salivary proteome, as 99 proteins are differentially expressed at baseline vs. 120 days after treatment. However, AT-MSC treatment does not restore healthy conditions, as 212 proteins are significantly differentially expressed in saliva 120 days after AT-MSCs treatment, as compared to healthy controls. CONCLUSION: The results indicate an increase in proteins related to tissue regeneration in AT-MSCs treated patients. Our study demonstrates the impact of AT-MSCs on the salivary proteome, thereby providing insight into the potential mode of action of this novel treatment approach.
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spelling pubmed-97352772022-12-12 Intraglandular mesenchymal stem cell treatment induces changes in the salivary proteome of irradiated patients Lynggaard, Charlotte Duch Jersie-Christensen, Rosa Juhl, Morten Jensen, Siri Beier Grønhøj, Christian Melchiors, Jacob Jacobsen, Søren Møller-Hansen, Michael Herly, Mikkel Ekblond, Annette Kastrup, Jens Fischer-Nielsen, Anne Belstrøm, Daniel von Buchwald, Christian Commun Med (Lond) Article BACKGROUND: Hyposalivation and xerostomia (dry mouth), are the leading site-effects to treatment of head and neck cancer. Currently, there are no effective therapies to alleviate radiation-induced hyposalivation. Adipose tissue-derived mesenchymal stem/stromal cells (AT-MSCs) have shown potential for restoring salivary gland function. However, the mode of action is unknown. The purpose of the present study was therefore to characterize the effect of AT-MSC therapy on the salivary proteome in previously irradiated head and neck cancer patients. METHODS: Whole saliva was collected from patients with radiation-induced salivary gland hypofunction (n = 8) at baseline, and 120 days after AT-MSC treatment, and from healthy controls (n = 10). The salivary proteome was characterized with mass spectrometry based proteomics, and data was compared within the AT-MSC group (baseline versus day 120) and between AT-MSC group and healthy controls. Significance levels between groups were determined by using double-sided t-test, and visualized by means of principal component analysis, volcano plots and cluster analysis. RESULTS: Here we show that 140 human proteins are significantly differentially expressed in saliva from patients with radiation-induced hypofunction versus healthy controls. AT-MSC treatment induce a significant impact on the salivary proteome, as 99 proteins are differentially expressed at baseline vs. 120 days after treatment. However, AT-MSC treatment does not restore healthy conditions, as 212 proteins are significantly differentially expressed in saliva 120 days after AT-MSCs treatment, as compared to healthy controls. CONCLUSION: The results indicate an increase in proteins related to tissue regeneration in AT-MSCs treated patients. Our study demonstrates the impact of AT-MSCs on the salivary proteome, thereby providing insight into the potential mode of action of this novel treatment approach. Nature Publishing Group UK 2022-12-10 /pmc/articles/PMC9735277/ /pubmed/36496530 http://dx.doi.org/10.1038/s43856-022-00223-3 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Lynggaard, Charlotte Duch
Jersie-Christensen, Rosa
Juhl, Morten
Jensen, Siri Beier
Grønhøj, Christian
Melchiors, Jacob
Jacobsen, Søren
Møller-Hansen, Michael
Herly, Mikkel
Ekblond, Annette
Kastrup, Jens
Fischer-Nielsen, Anne
Belstrøm, Daniel
von Buchwald, Christian
Intraglandular mesenchymal stem cell treatment induces changes in the salivary proteome of irradiated patients
title Intraglandular mesenchymal stem cell treatment induces changes in the salivary proteome of irradiated patients
title_full Intraglandular mesenchymal stem cell treatment induces changes in the salivary proteome of irradiated patients
title_fullStr Intraglandular mesenchymal stem cell treatment induces changes in the salivary proteome of irradiated patients
title_full_unstemmed Intraglandular mesenchymal stem cell treatment induces changes in the salivary proteome of irradiated patients
title_short Intraglandular mesenchymal stem cell treatment induces changes in the salivary proteome of irradiated patients
title_sort intraglandular mesenchymal stem cell treatment induces changes in the salivary proteome of irradiated patients
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9735277/
https://www.ncbi.nlm.nih.gov/pubmed/36496530
http://dx.doi.org/10.1038/s43856-022-00223-3
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