Chin Kok-Yong, Ekeuku Sophia Ogechi, Trias Anne
Department of Pharmacology, Faculty of Medicine, Universiti Kebangsaan Malaysia, Cheras, Malaysia.
American River Nutrition, Hadley, MA, United States.
Front Pharmacol. 2022 May 4;13:878556. doi: 10.3389/fphar.2022.878556. eCollection 2022.
Medication-related osteonecrosis of the jaw (ONJ) is a rare but significant adverse side effect of antiresorptive drugs. Bisphosphonate-related ONJ (BRONJ) is the most prevalent condition due to the extensive use of the drug in cancer and osteoporosis treatment. Nitrogen-containing bisphosphonates suppress osteoclastic resorption by inhibiting farnesyl pyrophosphate synthase in the mevalonate pathway, leading to deficiency of the substrate for GTPase prenylation. The bone remodelling process is uncoupled, subsequently impairing bone healing and causing ONJ. Targeted administration of geranylgeraniol (GGOH) represents a promising approach to mitigate BRONJ because GGOH is a substrate for GTPase prenylation. In the current review, the effects of GGOH on osteoclasts, osteoblasts and other related cells of the jaw are summarised. We also present and appraise the current evidence of GGOH in managing BRONJ in animal models. Lastly, several considerations of using GGOH in the clinical management of BRONJ are highlighted. As a conclusion, GGOH is a promising topical agent to manage BRONJ, pending more research on an effective delivery system and validation from a clinical trial.
药物相关性颌骨坏死(ONJ)是抗吸收药物罕见但严重的不良副作用。由于双膦酸盐类药物在癌症和骨质疏松症治疗中的广泛应用,双膦酸盐相关性ONJ(BRONJ)是最常见的情况。含氮双膦酸盐通过抑制甲羟戊酸途径中的法尼基焦磷酸合酶来抑制破骨细胞的吸收,导致GTPase异戊二烯化底物的缺乏。骨重塑过程失调,随后损害骨愈合并导致ONJ。香叶基香叶醇(GGOH)的靶向给药是减轻BRONJ的一种有前景的方法,因为GGOH是GTPase异戊二烯化的底物。在本综述中,总结了GGOH对破骨细胞、成骨细胞和颌骨其他相关细胞的影响。我们还展示并评估了GGOH在动物模型中治疗BRONJ的现有证据。最后,强调了在BRONJ临床管理中使用GGOH的几点考虑。总之,在对有效递送系统进行更多研究并通过临床试验验证之前,GGOH是治疗BRONJ的一种有前景的局部用药。