Medication-Related Osteonecrosis of the Jaw: A Systematic Review and a Bioinformatic Analysis

被引:2
作者
Laputkova, Galina [1 ]
Talian, Ivan [1 ]
Schwartzova, Vladimira [2 ,3 ]
机构
[1] Univ P J Safarik, Fac Med, Dept Med & Clin Biophys, Trieda SNP 1, Kosice 04011, Slovakia
[2] Univ P J Safarik, Fac Med, Clin Stomatol & Maxillofacial Surg, Kosice 04190, Slovakia
[3] Louis Pasteur Univ Hosp, Kosice 04190, Slovakia
关键词
osteonecrosis; systematic review; computational biology; BISPHOSPHONATE-RELATED OSTEONECROSIS; CELLS PREDICT OSTEONECROSIS; INDUCED AVASCULAR NECROSIS; SURGEONS POSITION PAPER; T-CELLS; AMERICAN ASSOCIATION; BONE TURNOVER; ANGIOGENESIS; CYTOSCAPE; MECHANISM;
D O I
10.3390/ijms242316745
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The objective was to evaluate the current evidence regarding the etiology of medication-related osteonecrosis of the jaw (MRONJ). This study systematically reviewed the literature by searching PubMed, Web of Science, and ProQuest databases for genes, proteins, and microRNAs associated with MRONJ from the earliest records through April 2023. Conference abstracts, letters, review articles, non-human studies, and non-English publications were excluded. Twelve studies meeting the inclusion criteria involving exposure of human oral mucosa, blood, serum, saliva, or adjacent bone or periodontium to anti-resorptive or anti-angiogenic agents were analyzed. The Cochrane Collaboration risk assessment tool was used to assess the quality of the studies. A total of 824 differentially expressed genes/proteins (DEGs) and 22 microRNAs were extracted for further bioinformatic analysis using Cytoscape, STRING, BiNGO, cytoHubba, MCODE, and ReactomeFI software packages and web-based platforms: DIANA mirPath, OmicsNet, and miRNet tools. The analysis yielded an interactome consisting of 17 hub genes and hsa-mir-16-1, hsa-mir-21, hsa-mir-23a, hsa-mir-145, hsa-mir-186, hsa-mir-221, and hsa-mir-424. A dominance of cytokine pathways was observed in both the cluster of hub DEGs and the interactome of hub genes with dysregulated miRNAs. In conclusion, a panel of genes, miRNAs, and related pathways were found, which is a step toward understanding the complexity of the disease.
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页数:20
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