Radiation induces changes in toll-like receptors of the uterine cervix of the rat.

Radiotherapy is an important therapeutic approach against cervical cancer but associated with adverse effects including vaginal fibrosis and dyspareunia. We here assessed the immunological and oxidative responses to cervical irradiation in an animal model for radiation-induced cervicitis. Rats were...

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Main Authors: Marie Francoise Mukanyangezi, Lucie Podmolíková, Wurood Al Hydad, Gunnar Tobin, Daniel Giglio
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2019-01-01
Series:PLoS ONE
Online Access:https://doi.org/10.1371/journal.pone.0215250
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spelling doaj-fd23703f4a86450f89d36614fbaf26882021-03-03T21:55:58ZengPublic Library of Science (PLoS)PLoS ONE1932-62032019-01-01144e021525010.1371/journal.pone.0215250Radiation induces changes in toll-like receptors of the uterine cervix of the rat.Marie Francoise MukanyangeziLucie PodmolíkováWurood Al HydadGunnar TobinDaniel GiglioRadiotherapy is an important therapeutic approach against cervical cancer but associated with adverse effects including vaginal fibrosis and dyspareunia. We here assessed the immunological and oxidative responses to cervical irradiation in an animal model for radiation-induced cervicitis. Rats were sedated and either exposed to 20 Gy of ionising radiation given by a linear accelerator or only sedated (controls) and euthanized 1-14 days later. The expressions of toll-like receptors (TLRs) and coupled intracellular pathways in the cervix were assessed with immunohistofluorescence and western blot. Expression of cytokines were analysed with the Bio-Plex Suspension Array System (Bio-Rad). We showed that TLRs 2-9 were expressed in the rat cervix and cervical irradiation induced up-regulation of TLR5, TRIF and NF-κB. In the irradiated cervical epithelium, TLR5 and TRIF were increased in concert with an up-regulation of oxidative stress (8-OHdG) and antioxidant enzymes (SOD-1 and catalase). G-CSF, M-CSF, IL-10, IL- 17A, IL-18 and RANTES expressions in the cervix decreased two weeks after cervical irradiation. In conclusion, the rat uterine cervix expresses the TLRs 2-9. Cervical irradiation induces immunological changes and oxidative stress, which could have importance in the development of adverse effects to radiotherapy.https://doi.org/10.1371/journal.pone.0215250
collection DOAJ
language English
format Article
sources DOAJ
author Marie Francoise Mukanyangezi
Lucie Podmolíková
Wurood Al Hydad
Gunnar Tobin
Daniel Giglio
spellingShingle Marie Francoise Mukanyangezi
Lucie Podmolíková
Wurood Al Hydad
Gunnar Tobin
Daniel Giglio
Radiation induces changes in toll-like receptors of the uterine cervix of the rat.
PLoS ONE
author_facet Marie Francoise Mukanyangezi
Lucie Podmolíková
Wurood Al Hydad
Gunnar Tobin
Daniel Giglio
author_sort Marie Francoise Mukanyangezi
title Radiation induces changes in toll-like receptors of the uterine cervix of the rat.
title_short Radiation induces changes in toll-like receptors of the uterine cervix of the rat.
title_full Radiation induces changes in toll-like receptors of the uterine cervix of the rat.
title_fullStr Radiation induces changes in toll-like receptors of the uterine cervix of the rat.
title_full_unstemmed Radiation induces changes in toll-like receptors of the uterine cervix of the rat.
title_sort radiation induces changes in toll-like receptors of the uterine cervix of the rat.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2019-01-01
description Radiotherapy is an important therapeutic approach against cervical cancer but associated with adverse effects including vaginal fibrosis and dyspareunia. We here assessed the immunological and oxidative responses to cervical irradiation in an animal model for radiation-induced cervicitis. Rats were sedated and either exposed to 20 Gy of ionising radiation given by a linear accelerator or only sedated (controls) and euthanized 1-14 days later. The expressions of toll-like receptors (TLRs) and coupled intracellular pathways in the cervix were assessed with immunohistofluorescence and western blot. Expression of cytokines were analysed with the Bio-Plex Suspension Array System (Bio-Rad). We showed that TLRs 2-9 were expressed in the rat cervix and cervical irradiation induced up-regulation of TLR5, TRIF and NF-κB. In the irradiated cervical epithelium, TLR5 and TRIF were increased in concert with an up-regulation of oxidative stress (8-OHdG) and antioxidant enzymes (SOD-1 and catalase). G-CSF, M-CSF, IL-10, IL- 17A, IL-18 and RANTES expressions in the cervix decreased two weeks after cervical irradiation. In conclusion, the rat uterine cervix expresses the TLRs 2-9. Cervical irradiation induces immunological changes and oxidative stress, which could have importance in the development of adverse effects to radiotherapy.
url https://doi.org/10.1371/journal.pone.0215250
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