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Radiation‐induced oral mucositis hamster model using a linear accelerator enhances clinical relevance of preclinical studies for treatment strategy investigation

Translational animal models for oral mucositis (OM) are necessary to simulate and assess the bioclinical effects and response in humans. These models should simulate high levels of radiation exposure that leads to oxidative stress and inflammatory‐initiated tissue changes. Hamster models have been e...

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Autores principales: Jordan, Carolyn T., Bradford, Emily M., Cheek, Dennis C., Kudrimoti, Mahesh, Miller, Craig S., Smith, Molly H., Hilt, J. Zach, Dziubla, Thomas D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7954840/
https://www.ncbi.nlm.nih.gov/pubmed/33738436
http://dx.doi.org/10.1002/ame2.12148
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author Jordan, Carolyn T.
Bradford, Emily M.
Cheek, Dennis C.
Kudrimoti, Mahesh
Miller, Craig S.
Smith, Molly H.
Hilt, J. Zach
Dziubla, Thomas D.
author_facet Jordan, Carolyn T.
Bradford, Emily M.
Cheek, Dennis C.
Kudrimoti, Mahesh
Miller, Craig S.
Smith, Molly H.
Hilt, J. Zach
Dziubla, Thomas D.
author_sort Jordan, Carolyn T.
collection PubMed
description Translational animal models for oral mucositis (OM) are necessary to simulate and assess the bioclinical effects and response in humans. These models should simulate high levels of radiation exposure that leads to oxidative stress and inflammatory‐initiated tissue changes. Hamster models have been extensively studied to observe pathological effects of radiation exposure and help in the development of effective treatments. To successfully evaluate the potential for treatment regimens with consistency and relevance, a radiation‐induced OM hamster model was developed using a clinical linear accelerator utilized by cancer patients daily. The dose exposure to the isolated, everted cheek pouch of a hamster, as well as the progression of injury, pro‐inflammatory marker, histological, and elasticity analyses of the buccal pouch were conducted to verify replicability and reproducibility of the injury model. The findings from this model demonstrated its ability to consistently induce injury and resolution over 28 days using an acute dose of 60 Gy. This model was developed to enhance clinical relevance when evaluating potential efficacious treatments and can now be utilized in efficacy studies to better evaluate developed therapeutics in a preclinical model that is easy to translate to clinical studies..
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spelling pubmed-79548402021-03-17 Radiation‐induced oral mucositis hamster model using a linear accelerator enhances clinical relevance of preclinical studies for treatment strategy investigation Jordan, Carolyn T. Bradford, Emily M. Cheek, Dennis C. Kudrimoti, Mahesh Miller, Craig S. Smith, Molly H. Hilt, J. Zach Dziubla, Thomas D. Animal Model Exp Med Short Communication Translational animal models for oral mucositis (OM) are necessary to simulate and assess the bioclinical effects and response in humans. These models should simulate high levels of radiation exposure that leads to oxidative stress and inflammatory‐initiated tissue changes. Hamster models have been extensively studied to observe pathological effects of radiation exposure and help in the development of effective treatments. To successfully evaluate the potential for treatment regimens with consistency and relevance, a radiation‐induced OM hamster model was developed using a clinical linear accelerator utilized by cancer patients daily. The dose exposure to the isolated, everted cheek pouch of a hamster, as well as the progression of injury, pro‐inflammatory marker, histological, and elasticity analyses of the buccal pouch were conducted to verify replicability and reproducibility of the injury model. The findings from this model demonstrated its ability to consistently induce injury and resolution over 28 days using an acute dose of 60 Gy. This model was developed to enhance clinical relevance when evaluating potential efficacious treatments and can now be utilized in efficacy studies to better evaluate developed therapeutics in a preclinical model that is easy to translate to clinical studies.. John Wiley and Sons Inc. 2021-01-26 /pmc/articles/PMC7954840/ /pubmed/33738436 http://dx.doi.org/10.1002/ame2.12148 Text en © 2021 The Authors. Animal Models and Experimental Medicine published by John Wiley & Sons Australia, Ltd on behalf of The Chinese Association for Laboratory Animal Sciences This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Short Communication
Jordan, Carolyn T.
Bradford, Emily M.
Cheek, Dennis C.
Kudrimoti, Mahesh
Miller, Craig S.
Smith, Molly H.
Hilt, J. Zach
Dziubla, Thomas D.
Radiation‐induced oral mucositis hamster model using a linear accelerator enhances clinical relevance of preclinical studies for treatment strategy investigation
title Radiation‐induced oral mucositis hamster model using a linear accelerator enhances clinical relevance of preclinical studies for treatment strategy investigation
title_full Radiation‐induced oral mucositis hamster model using a linear accelerator enhances clinical relevance of preclinical studies for treatment strategy investigation
title_fullStr Radiation‐induced oral mucositis hamster model using a linear accelerator enhances clinical relevance of preclinical studies for treatment strategy investigation
title_full_unstemmed Radiation‐induced oral mucositis hamster model using a linear accelerator enhances clinical relevance of preclinical studies for treatment strategy investigation
title_short Radiation‐induced oral mucositis hamster model using a linear accelerator enhances clinical relevance of preclinical studies for treatment strategy investigation
title_sort radiation‐induced oral mucositis hamster model using a linear accelerator enhances clinical relevance of preclinical studies for treatment strategy investigation
topic Short Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7954840/
https://www.ncbi.nlm.nih.gov/pubmed/33738436
http://dx.doi.org/10.1002/ame2.12148
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