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Preclinical models of medication-related osteonecrosis of the jaw (MRONJ)
J I Aguirre1, E J Castillo1, D B Kimmel1
1Department of Physiological Sciences, University of Florida (UF), Gainesville, FL, United States of America.
Abstract:
Medication-related osteonecrosis of the jaw (MRONJ) is a potentially severe adverse event affecting patients with cancer and patients with osteoporosis who have been treated with powerful antiresorptives (pARs) or angiogenesis inhibitors (AgIs). pARs, including nitrogen-containing bisphosphonates (N-BPs; e.g., zoledronic acid, alendronate) and anti-RANKL antibodies (e.g., denosumab), are used to manage bone metastases in patients with cancer or to prevent fragility fractures in patients with osteoporosis. Though significant advances have been made in understanding MRONJ, its pathophysiology is still not fully elucidated. Multiple species have been used in preclinical MRONJ research, including the rat, mouse, rice rat, rabbit, dog, sheep, and pig. Animal research has contributed immensely to advancing the MRONJ field, particularly, but not limited to, in developing models and investigating risk factors that were first observed in humans. MRONJ models have been developed using clinically relevant doses of systemic risk factors, like N-BPs, anti-RANKL antibodies, or AgIs. Specific local oral risk factors first noted in humans, including tooth extraction and inflammatory dental disease (e.g., periodontitis, periapical infection, etc.), were then added. Research in rodents, particularly the rat, and, to some extent, the mouse, across multiple laboratories, has contributed to establishing multiple relevant and complementary preclinical models. Models in larger species produced accurate clinical and histopathologic outcomes suggesting a potential role for confirming specific crucial findings from rodent research. We view the current state of animal models for MRONJ as good. The rodent models are now reliable enough to produce large numbers of MRONJ cases that could be applied in experiments testing treatment modalities. The course of MRONJ, including stage 0 MRONJ, is characterized well enough that basic studies of the molecular or enzyme-level findings in different MRONJ stages are possible. This review provides a current overview of the existing models of MRONJ, their more significant features and findings, and important instances of their application in preclinical research.
Insights
Medication-related osteonecrosis of the jaw (MRONJ) research utilizes various animal models, primarily rodents, to study risk factors and develop treatments. These models are crucial for advancing our understanding and management of MRONJ in patients.
Area of Science:
- Oral and Maxillofacial Surgery
- Oncology
- Pharmacology
Background:
- Medication-related osteonecrosis of the jaw (MRONJ) is a severe adverse event linked to antiresorptives and angiogenesis inhibitors.
- Understanding MRONJ pathophysiology remains incomplete despite significant research.
- Patients with cancer and osteoporosis are particularly at risk.
Purpose of the Study:
- To review existing animal models for Medication-related osteonecrosis of the jaw (MRONJ).
- To highlight key features, findings, and applications of these preclinical models.
- To assess the current state and reliability of MRONJ animal research.
Main Methods:
- Review of preclinical research utilizing various animal species (rat, mouse, rabbit, dog, sheep, pig).
- Development of MRONJ models incorporating systemic risk factors (N-BPs, anti-RANKL, AgIs) and local oral factors.
- Analysis of findings from rodent and larger animal models.
Main Results:
- Rodent models (rat, mouse) are reliable for generating MRONJ cases and studying risk factors.
- Larger animal models provide accurate clinical and histopathologic outcomes, confirming rodent findings.
- Current animal models adequately characterize MRONJ progression, enabling molecular and enzymatic studies.
Conclusions:
- Animal models, especially rodents, are well-established and reliable for MRONJ research.
- These models are essential for investigating risk factors, understanding pathophysiology, and testing treatments.
- The current state of MRONJ animal models is robust, supporting further preclinical investigations.
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