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巨噬细胞与药物相关性颌骨坏死(MRONJ):一篇全面的简短综述

Macrophage Involvement in Medication-Related Osteonecrosis of the Jaw (MRONJ): A Comprehensive, Short Review.

作者信息

Gkouveris Ioannis, Soundia Akrivoula, Gouveris Panagiotis, Zouki Dionysia, Hadaya Danny, Tetradis Sotirios

机构信息

Division of Diagnostic and Surgical Sciences, UCLA School of Dentistry, Los Angeles, CA 90095, USA.

Second Department of Medical Oncology, Agios Savvas Cancer Hospital, 11522 Athens, Greece.

出版信息

Cancers (Basel). 2022 Jan 10;14(2):330. doi: 10.3390/cancers14020330.

Abstract

Antiresorptive agents such as bisphosphonates (BP) and denosumab are commonly prescribed for the management of primary bone malignancy, bone metastasis, osteoporosis, Paget disease, or other bone disorders. Medication-related osteonecrosis of the Jaws (MRONJ) is a rare but significant complication of antiresorptive medications. Duration, dose, and antiresorptive potency as well as concomitant diseases, additional medications, and local factors affect MRONJ incidence and severity. MRONJ pathophysiology is still poorly understood. Nevertheless, decreased bone resorption due to osteoclastic inhibition along with trauma, infection/inflammation, or blood supply inhibition are considered synergistic factors for disease development. In addition, previous data research examined the effects of antiresorptive medication on immune system components and introduced potential alterations on immune response as novel elements in MRONJ pathogenesis. Considering that macrophages are the first cells in the nonspecific immune response, it is not surprising that these multifaceted players attracted increased attention in MRONJ research recently. This current review attempted to elucidate the effects of antiresorptive medications on several aspects of macrophage activity in relation to the complex inflammatory microenvironment of MRONJ. Collectively, unravelling the mode of action and extent of macrophages' potential contribution in MRONJ occurrence will provide novel insight in disease pathogenesis and potentially identify intrinsic therapeutic targets.

摘要

抗吸收药物,如双膦酸盐(BP)和地诺单抗,常用于治疗原发性骨恶性肿瘤、骨转移、骨质疏松症、佩吉特病或其他骨疾病。药物相关性颌骨坏死(MRONJ)是抗吸收药物罕见但严重的并发症。用药持续时间、剂量、抗吸收效力以及伴随疾病、其他药物和局部因素都会影响MRONJ的发生率和严重程度。MRONJ的病理生理学仍知之甚少。然而,破骨细胞抑制导致的骨吸收减少,以及创伤、感染/炎症或血液供应抑制,被认为是疾病发展的协同因素。此外,以往的数据研究考察了抗吸收药物对免疫系统成分的影响,并将免疫反应的潜在改变作为MRONJ发病机制中的新因素。鉴于巨噬细胞是非特异性免疫反应中的首要细胞,这些多面角色最近在MRONJ研究中受到越来越多的关注也就不足为奇了。本综述试图阐明抗吸收药物在MRONJ复杂炎症微环境中对巨噬细胞活性多个方面的影响。总体而言,揭示巨噬细胞在MRONJ发生中的作用方式和潜在贡献程度,将为疾病发病机制提供新的见解,并有可能确定内在的治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b29/8773732/37fd45e53a5c/cancers-14-00330-g001.jpg

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