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Comprehensive profiling of plasma and exosomal microRNAs in medication-related osteonecrosis of the jaw
Sujin Oh1, Minjae Park2, Hyun Hwang3
1Department of Laboratory Medicine, Seoul National University College of Medicine, Seoul, Republic of Korea.
Abstract:
The role of circulating microRNAs (miRNAs) in the pathophysiology of medication-related osteonecrosis of the jaw (MRONJ) remains to be elucidated. This study investigated the expression of plasma miRNAs in patients with MRONJ compared to healthy individuals. 16 patients with MRONJ and 15 healthy controls participated in this case-control study, which was conducted in three consecutive phases. As a pilot study, miRNA profiling was performed using quantitative real-time reverse transcriptase PCR (qPCR) array plates targeting 754 miRNAs in a subset of plasma samples. In the subsequent phases, individual qPCR assays validated the array results using plasma samples from the full cohort (second phase) and plasma-derived exosomes (third phase). The qPCR arrays revealed differential miRNA profiles between the MRONJ and control groups. We selected miR-153-3p, miR-1180-3p, miR-483-5p, miR-511-5p, miR-628-3p, miR-486-5p, miR-92b-5p, miR-16-3p, miR-23a-3p, and miR-23a-5p for additional assays. The expression of miR-483-5p, miR-92-5p, and miR-486-5p was elevated in patients with MRONJ compared to controls, whereas miR-628-3p was downregulated (q < 0.01). All four miRNAs consistently exhibited differences in expression in plasma-derived exosomes between MRONJ patients and controls. We identified four miRNAs that could serve as potential biomarkers for MRONJ: miR-483-5p, miR-92-5p, miR-628-3p, and miR-486-5p. These biomarkers may reflect key pathways in MRONJ pathogenesis and could be used to guide patient risk stratification and future therapeutic interventions for MRONJ.
Insights
Circulating microRNAs (miRNAs) show promise as biomarkers for medication-related osteonecrosis of the jaw (MRONJ). Four specific miRNAs (miR-483-5p, miR-92-5p, miR-628-3p, miR-486-5p) were identified in plasma and exosomes, potentially aiding MRONJ diagnosis and treatment.
Area of Science:
- Biochemistry
- Genetics
- Oncology
Background:
- Medication-related osteonecrosis of the jaw (MRONJ) is a serious adverse effect of certain medications.
- The underlying pathophysiology of MRONJ, particularly the role of circulating microRNAs (miRNAs), is not fully understood.
Purpose of the Study:
- To investigate plasma miRNA expression profiles in patients with MRONJ compared to healthy controls.
- To identify potential miRNA biomarkers for MRONJ diagnosis and risk stratification.
Main Methods:
- A case-control study involving 16 MRONJ patients and 15 healthy controls.
- Quantitative real-time reverse transcriptase PCR (qPCR) arrays to profile 754 miRNAs in plasma.
- Individual qPCR assays to validate array results in the full cohort and plasma-derived exosomes.
Main Results:
- Differential miRNA expression profiles were observed between MRONJ patients and controls.
- miR-483-5p, miR-92-5p, and miR-486-5p were upregulated, while miR-628-3p was downregulated in MRONJ patients.
- These four miRNAs showed consistent expression differences in both plasma and exosomes, confirming their potential as MRONJ biomarkers.
Conclusions:
- Four specific miRNAs (miR-483-5p, miR-92-5p, miR-628-3p, miR-486-5p) were identified as potential plasma biomarkers for MRONJ.
- These biomarkers may reflect key pathogenic pathways in MRONJ.
- The identified miRNAs could aid in patient risk stratification and guide future therapeutic interventions for MRONJ.
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