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.

Bone
|September 14, 2021
PubMed

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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