Giudice Amerigo, Antonelli Alessandro, Chiarella Emanuela, Baudi Francesco, Barni Tullio, Di Vito Anna
Department of Health Sciences, University Magna Graecia of Catanzaro, 88100 Catanzaro, Italy.
Department of Experimental and Clinical Medicine, University Magna Graecia of Catanzaro, 88100 Catanzaro, Italy.
Pharmaceuticals (Basel). 2020 Nov 25;13(12):423. doi: 10.3390/ph13120423.
Bisphosphonates-related osteonecrosis of the jaw (BRONJ) was firstly reported by Marx in 2003. Since 2014, the term medication-related osteonecrosis of the jaw (MRONJ) is recommended by the American Association of Oral and Maxillofacial Surgeons (AAOMS). Development of MRONJ has been associated to the assumption of bisphosphonates but many MRONJ-promoting factors have been identified. A strong involvement of immunity components has been suggested. Therapeutic intervention includes surgical and non-surgical treatments, as well as regenerative medicine procedures for the replacement of the lost tissues. The literature confirms that the combination of mesenchymal stem cells (MSCs), biomaterials and local biomolecules can support the regeneration/repair of different structures. In this review, we report the major open topics in the pathogenesis of MRONJ. Then, we introduce the oral tissues recognized as sources of MSCs, summing up in functional terms what is known about the exosomes release in physiological and pathological conditions.
双膦酸盐相关颌骨坏死(BRONJ)于2003年由马克思首次报道。自2014年起,美国口腔颌面外科医师协会(AAOMS)推荐使用药物相关颌骨坏死(MRONJ)这一术语。MRONJ的发生与双膦酸盐的使用有关,但已确定许多促进MRONJ的因素。有人提出免疫成分有重要作用。治疗干预包括手术和非手术治疗,以及用于替代缺失组织的再生医学程序。文献证实,间充质干细胞(MSCs)、生物材料和局部生物分子的组合可支持不同结构的再生/修复。在本综述中,我们报告了MRONJ发病机制中的主要未解决问题。然后,我们介绍被认为是MSCs来源的口腔组织,从功能角度总结在生理和病理条件下关于外泌体释放的已知情况。