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Establishment and assessment of rodent models of medication-related osteonecrosis of the jaw (MRONJ)

Medication-related osteonecrosis of the jaw (MRONJ) is primarily associated with administering antiresorptive or antiangiogenic drugs. Despite significant research on MRONJ, its pathogenesis and effective treatments are still not fully understood. Animal models can be used to simulate the pathophysi...

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Autores principales: Yan, Ran, Jiang, Ruixue, Hu, Longwei, Deng, Yuwei, Wen, Jin, Jiang, Xinquan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9365764/
https://www.ncbi.nlm.nih.gov/pubmed/35948539
http://dx.doi.org/10.1038/s41368-022-00182-4
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author Yan, Ran
Jiang, Ruixue
Hu, Longwei
Deng, Yuwei
Wen, Jin
Jiang, Xinquan
author_facet Yan, Ran
Jiang, Ruixue
Hu, Longwei
Deng, Yuwei
Wen, Jin
Jiang, Xinquan
author_sort Yan, Ran
collection PubMed
description Medication-related osteonecrosis of the jaw (MRONJ) is primarily associated with administering antiresorptive or antiangiogenic drugs. Despite significant research on MRONJ, its pathogenesis and effective treatments are still not fully understood. Animal models can be used to simulate the pathophysiological features of MRONJ, serving as standardized in vivo experimental platforms to explore the pathogenesis and therapies of MRONJ. Rodent models exhibit excellent effectiveness and high reproducibility in mimicking human MRONJ, but classical methods cannot achieve a complete replica of the pathogenesis of MRONJ. Modified rodent models have been reported with improvements for better mimicking of MRONJ onset in clinic. This review summarizes representative classical and modified rodent models of MRONJ created through various combinations of systemic drug induction and local stimulation and discusses their effectiveness and efficiency. Currently, there is a lack of a unified assessment system for MRONJ models, which hinders a standard definition of MRONJ-like lesions in rodents. Therefore, this review comprehensively summarizes assessment systems based on published peer-review articles, including new approaches in gross observation, histological assessments, radiographic assessments, and serological assessments. This review can serve as a reference for model establishment and evaluation in future preclinical studies on MRONJ.
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spelling pubmed-93657642022-08-12 Establishment and assessment of rodent models of medication-related osteonecrosis of the jaw (MRONJ) Yan, Ran Jiang, Ruixue Hu, Longwei Deng, Yuwei Wen, Jin Jiang, Xinquan Int J Oral Sci Review Article Medication-related osteonecrosis of the jaw (MRONJ) is primarily associated with administering antiresorptive or antiangiogenic drugs. Despite significant research on MRONJ, its pathogenesis and effective treatments are still not fully understood. Animal models can be used to simulate the pathophysiological features of MRONJ, serving as standardized in vivo experimental platforms to explore the pathogenesis and therapies of MRONJ. Rodent models exhibit excellent effectiveness and high reproducibility in mimicking human MRONJ, but classical methods cannot achieve a complete replica of the pathogenesis of MRONJ. Modified rodent models have been reported with improvements for better mimicking of MRONJ onset in clinic. This review summarizes representative classical and modified rodent models of MRONJ created through various combinations of systemic drug induction and local stimulation and discusses their effectiveness and efficiency. Currently, there is a lack of a unified assessment system for MRONJ models, which hinders a standard definition of MRONJ-like lesions in rodents. Therefore, this review comprehensively summarizes assessment systems based on published peer-review articles, including new approaches in gross observation, histological assessments, radiographic assessments, and serological assessments. This review can serve as a reference for model establishment and evaluation in future preclinical studies on MRONJ. Nature Publishing Group UK 2022-08-10 /pmc/articles/PMC9365764/ /pubmed/35948539 http://dx.doi.org/10.1038/s41368-022-00182-4 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 Review Article
Yan, Ran
Jiang, Ruixue
Hu, Longwei
Deng, Yuwei
Wen, Jin
Jiang, Xinquan
Establishment and assessment of rodent models of medication-related osteonecrosis of the jaw (MRONJ)
title Establishment and assessment of rodent models of medication-related osteonecrosis of the jaw (MRONJ)
title_full Establishment and assessment of rodent models of medication-related osteonecrosis of the jaw (MRONJ)
title_fullStr Establishment and assessment of rodent models of medication-related osteonecrosis of the jaw (MRONJ)
title_full_unstemmed Establishment and assessment of rodent models of medication-related osteonecrosis of the jaw (MRONJ)
title_short Establishment and assessment of rodent models of medication-related osteonecrosis of the jaw (MRONJ)
title_sort establishment and assessment of rodent models of medication-related osteonecrosis of the jaw (mronj)
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9365764/
https://www.ncbi.nlm.nih.gov/pubmed/35948539
http://dx.doi.org/10.1038/s41368-022-00182-4
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