Radioprotective Effects of Dermatan Sulfate in a Preclinical Model of Oral Mucositis—Targeting Inflammation, Hypoxia and Junction Proteins without Stimulating Proliferation
Oral mucositis is the most frequently occurring early side effect of head-and-neck cancer radiotherapy. Systemic dermatan sulfate (DS) treatment revealed a significant radioprotective potential in a preclinical model of oral mucositis. This study was initiated to elucidate the mechanistic effects of...
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doaj-fe19e4da626a4c209ffda15846b9823d2020-11-25T00:39:58ZengMDPI AGInternational Journal of Molecular Sciences1422-00672018-06-01196168410.3390/ijms19061684ijms19061684Radioprotective Effects of Dermatan Sulfate in a Preclinical Model of Oral Mucositis—Targeting Inflammation, Hypoxia and Junction Proteins without Stimulating ProliferationSylvia Gruber0Marlene Arnold1Nilsu Cini2Victoria Gernedl3Sabine Hetzendorfer4Lisa-Marie Kowald5Peter Kuess6Julia Mayer7Susanne Morava8Stephanie Pfaffinger9Andreas Rohorzka10Wolfgang Dörr11Christian Doppler Laboratory for Medical Radiation Research for Radiation Oncology, Medical University/AKH Vienna, 1090 Vienna, AustriaDepartment of Radiation Oncology, Applied and Translational Radiobiology, Medical University Vienna, 1090 Vienna, AustriaDepartment of Radiation Oncology, Kartal Dr. Lutfi Kırdar Training and Research Hospital, Health Science University, 34722 Istanbul, TurkeyDepartment of Radiation Oncology, Applied and Translational Radiobiology, Medical University Vienna, 1090 Vienna, AustriaDepartment of Radiation Oncology, Applied and Translational Radiobiology, Medical University Vienna, 1090 Vienna, AustriaDepartment of Radiation Oncology, Applied and Translational Radiobiology, Medical University Vienna, 1090 Vienna, AustriaChristian Doppler Laboratory for Medical Radiation Research for Radiation Oncology, Medical University/AKH Vienna, 1090 Vienna, AustriaDepartment of Radiation Oncology, Applied and Translational Radiobiology, Medical University Vienna, 1090 Vienna, AustriaDepartment of Radiation Oncology, Applied and Translational Radiobiology, Medical University Vienna, 1090 Vienna, AustriaDepartment of Radiation Oncology, Applied and Translational Radiobiology, Medical University Vienna, 1090 Vienna, AustriaDepartment of Radiation Oncology, Applied and Translational Radiobiology, Medical University Vienna, 1090 Vienna, AustriaDepartment of Radiation Oncology, Applied and Translational Radiobiology, Medical University Vienna, 1090 Vienna, AustriaOral mucositis is the most frequently occurring early side effect of head-and-neck cancer radiotherapy. Systemic dermatan sulfate (DS) treatment revealed a significant radioprotective potential in a preclinical model of oral mucositis. This study was initiated to elucidate the mechanistic effects of DS in the same model. Irradiation comprised daily fractionated irradiation (5 × 3 Gy/week) over two weeks, either alone (IR) or in combination with daily dermatan sulfate treatment of 4 mg/kg (IR + DS). Groups of mice (n = 5) were sacrificed every second day over the course of 14 days in both experimental arms, their tongues excised and evaluated. The response to irradiation with and without DS was analyzed on a morphological (cell numbers, epithelial thickness) as well as on a functional (proliferation and expression of inflammation, hypoxia and epithelial junction markers) level. The mucoprotective activity of DS can be attributed to a combination of various effects, comprising increased expression of epithelial junctions, reduced inflammation and reduced hypoxia. No DS-mediated effect on proliferation was observed. DS demonstrated a significant mucositis-ameliorating activity and could provide a promising strategy for mucositis treatment, based on targeting specific, radiation-induced, mucositis-associated signaling without stimulating proliferation.http://www.mdpi.com/1422-0067/19/6/1684oral mucositismouse modeldermatan sulfatefractionationinflammationhypoxiacellular junctions |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Sylvia Gruber Marlene Arnold Nilsu Cini Victoria Gernedl Sabine Hetzendorfer Lisa-Marie Kowald Peter Kuess Julia Mayer Susanne Morava Stephanie Pfaffinger Andreas Rohorzka Wolfgang Dörr |
spellingShingle |
Sylvia Gruber Marlene Arnold Nilsu Cini Victoria Gernedl Sabine Hetzendorfer Lisa-Marie Kowald Peter Kuess Julia Mayer Susanne Morava Stephanie Pfaffinger Andreas Rohorzka Wolfgang Dörr Radioprotective Effects of Dermatan Sulfate in a Preclinical Model of Oral Mucositis—Targeting Inflammation, Hypoxia and Junction Proteins without Stimulating Proliferation International Journal of Molecular Sciences oral mucositis mouse model dermatan sulfate fractionation inflammation hypoxia cellular junctions |
author_facet |
Sylvia Gruber Marlene Arnold Nilsu Cini Victoria Gernedl Sabine Hetzendorfer Lisa-Marie Kowald Peter Kuess Julia Mayer Susanne Morava Stephanie Pfaffinger Andreas Rohorzka Wolfgang Dörr |
author_sort |
Sylvia Gruber |
title |
Radioprotective Effects of Dermatan Sulfate in a Preclinical Model of Oral Mucositis—Targeting Inflammation, Hypoxia and Junction Proteins without Stimulating Proliferation |
title_short |
Radioprotective Effects of Dermatan Sulfate in a Preclinical Model of Oral Mucositis—Targeting Inflammation, Hypoxia and Junction Proteins without Stimulating Proliferation |
title_full |
Radioprotective Effects of Dermatan Sulfate in a Preclinical Model of Oral Mucositis—Targeting Inflammation, Hypoxia and Junction Proteins without Stimulating Proliferation |
title_fullStr |
Radioprotective Effects of Dermatan Sulfate in a Preclinical Model of Oral Mucositis—Targeting Inflammation, Hypoxia and Junction Proteins without Stimulating Proliferation |
title_full_unstemmed |
Radioprotective Effects of Dermatan Sulfate in a Preclinical Model of Oral Mucositis—Targeting Inflammation, Hypoxia and Junction Proteins without Stimulating Proliferation |
title_sort |
radioprotective effects of dermatan sulfate in a preclinical model of oral mucositis—targeting inflammation, hypoxia and junction proteins without stimulating proliferation |
publisher |
MDPI AG |
series |
International Journal of Molecular Sciences |
issn |
1422-0067 |
publishDate |
2018-06-01 |
description |
Oral mucositis is the most frequently occurring early side effect of head-and-neck cancer radiotherapy. Systemic dermatan sulfate (DS) treatment revealed a significant radioprotective potential in a preclinical model of oral mucositis. This study was initiated to elucidate the mechanistic effects of DS in the same model. Irradiation comprised daily fractionated irradiation (5 × 3 Gy/week) over two weeks, either alone (IR) or in combination with daily dermatan sulfate treatment of 4 mg/kg (IR + DS). Groups of mice (n = 5) were sacrificed every second day over the course of 14 days in both experimental arms, their tongues excised and evaluated. The response to irradiation with and without DS was analyzed on a morphological (cell numbers, epithelial thickness) as well as on a functional (proliferation and expression of inflammation, hypoxia and epithelial junction markers) level. The mucoprotective activity of DS can be attributed to a combination of various effects, comprising increased expression of epithelial junctions, reduced inflammation and reduced hypoxia. No DS-mediated effect on proliferation was observed. DS demonstrated a significant mucositis-ameliorating activity and could provide a promising strategy for mucositis treatment, based on targeting specific, radiation-induced, mucositis-associated signaling without stimulating proliferation. |
topic |
oral mucositis mouse model dermatan sulfate fractionation inflammation hypoxia cellular junctions |
url |
http://www.mdpi.com/1422-0067/19/6/1684 |
work_keys_str_mv |
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