[1] Guo YX, Zhang JY, Wang DC, et al. Analysis of pathological characteristics of medication-related osteonecrosis of the jaw and discussion of clinical treatment strategies based on the pathological analysis results [J]. Beijing Da Xue Xue Bao Yi Xue Ban, 2022, 54(6):1190-1195. [2] Huang N, Wang P, Gong P, et al. The progress in reconstruction of mandibular defect caused by osteoradionecrosis [J]. J Oncol, 2023, 2023:1440889. [3] 何悦,陈珩,安金刚,等.药物相关性颌骨坏死临床诊疗专家共识[J].中国口腔颌面外科杂志,2023,21(4): 313-325. [4] Sharma S, Shankar R, Ravi Kiran BS, et al. A narrative review of osteonecrosis of the jaw: What a clinician should know [J]. Cureus, 2023, 15(12):e51183. [5] Agarwal R, Freeman TE, Li MM, et al. Outcomes with culture-directed antibiotics following microvascular free tissue reconstruction for osteonecrosis of the jaw [J]. Oral Oncol, 2022, 130:105878. [6] Fijardo M, Kwan JYY, Bissey PA, et al. The clinical manifestations and molecular pathogenesis of radiation fibrosis [J]. EBioMedicine, 2024, 103:105089. [7] Leong KX, Yang W, Sharma D, et al. Ultrasound-stimulated microbubbles enhanced vascular disruption in fractionated radiotherapy-treated tumours via ASMase activation [J]. Dis Model Mech, 2023, 16(6):dmm049531. [8] Huang F, Cai FY, Michael S, et al. Peroxisome disruption alters lipid metabolism and potentiates antitumor response with MAPK-targeted therapy in melanoma [J]. J Clin Invest, 2023, 133(20): e166644. [9] Xu J, He J, Zhou YL, et al. Von Willebrand factor promotes radiation-induced intestinal injury (RⅢ) development and its cleavage enzyme rhADAMTS13 protects against RⅢ by reducing inflammation and oxidative stress [J]. Free Radical Biology and Medicine, 2024, 210:1-12. [10] Tu W, Feng Y, Lai Q, et al. Metabolic profiling implicates a critical role of cyclooxygenase-2-mediated arachidonic acid metabolism in radiation-induced esophageal injury in rats [J]. Radiat Res, 2022, 197(5):480-490. [11] Alrowis R, Aldawood A, Alotaibi M, et al. Medication-related osteonecrosis of the jaw (MRONJ): A review of pathophysiology, risk factors, preventive measures and treatment strategies [J]. Saudi Dent J, 2022, 34(3):202-210. [12] Gulcu A, Akkaya O. Investigation of the antiangiogenic properties of zoledronic acid by using chorioallantoic membrane model [J]. Dose Response, 2022, 20(2):15593258221093410. [13] Shen X, Zhu W, Zhang P, et al. Macrophage miR-149-5p induction is a key driver and therapeutic target for BRONJ [J]. JCI Insight, 2022, 7(16):e159865. [14] Otto M, Weigel J, Ziebart T, et al. Significance of bisphosphonates on angiogenesis in vivo and their effect under geranyl-geraniol addition- could it alter the treatment of bisphosphonate-associated necrosis of the jaw? [J]. Oral Maxillofac Surg, 2023, 27(2):263-268. [15] Gao SY, Lin RB, Huang SH, et al. PDGF-BB exhibited therapeutic effects on rat model of bisphosphonate-related osteonecrosis of the jaw by enhancing angiogenesis and osteogenesis [J]. Bone, 2021, 144:115117. [16] Zhao D, Cui W, Liu M, et al. Tetrahedral framework nucleic acid promotes the treatment of bisphosphonate-related osteonecrosis of the jaws by promoting angiogenesis and M2 polarization [J]. ACS Appl Mater Interfaces, 2020, 12(40):44508-44522. [17] Lee KH, Kim SH, Kim CH, et al. Identifying genetic variants underlying medication-induced osteonecrosis of the jaw in cancer and osteoporosis: a case control study [J]. J Transl Med, 2019, 17(1): 381. [18] He L, Lu H, Ji X, et al. Stimulatory G-protein α subunit modulates endothelial cell permeability through regulation of plasmalemma vesicle-associated protein [J]. Front Pharmacol, 2022, 13:941064. [19] Chionh F, Gebski V, Al-Obaidi SJ, et al. VEGF-A, VEGFR1 and VEGFR2 single nucleotide polymorphisms and outcomes from the AGITG MAX trial of capecitabine, bevacizumab and mitomycin C in metastatic colorectal cancer [J]. Sci Rep, 2022, 12(1): 1238. [20] Ueda N, Imada M, Kato Y, et al. Bevacizumab-associated implant presence-triggered osteonecrosis: A case report and literature review [J]. J Oral Implantol, 2022, 48(4):325-331. [21] Hofmann E, Eggers B, Heim N, et al. Bevacizumab and sunitinib mediate osteogenic and pro-inflammatory molecular changes in primary human alveolar osteoblasts in vitro [J]. Odontology, 2022, 110(4):634-647. [22] Anita A, Mark D, Michael H, et al. Emerging antiresorptive medications and their potential implications for dental surgeries [J]. J Am Dent Assoc, 2022, 153(7):649-658. [23] Thomas JG, Ouanounou A. Medication-related osteonecrosis of the jaw: a narrative review of risk factors, diagnosis, and management [J]. Front Oral Maxillofac Med, 2022, 5:31. [24] 游丽娜,姜坤,宋琳婧,等.舒尼替尼致重度骨髓抑制及下颌骨坏死1例[J].医药导报, 2023, 42(2):279-280. [25] Hardeep SA,Thomas AW, Sasirekha P, et al. Medication-induced osteonecrosis of the jaw: a review of cases from the Food and Drug Administration Adverse Event Reporting System (FAERS) [J]. BMC Pharmacol Toxicol, 2023, 24(1):15. [26] Salomé M, Thierry T, Angélique B, et al. Osteonecrosis of the jaw with axitinib: A case report [J]. Therapie, 2023, 78:764-766. [27] 孙国文,田美.药物相关性颌骨坏死不同阶段治疗方法述评[J].口腔颌面外科杂志, 2022, 32(3):135-143. [28] Wang F, Wei SN, Zhang ZX, et al. Osimertinib: Another medication related to osteonecrosis of the jaws? A case report and literature review [J]. Front Pharmacol, 2022, 13:947947. [29] Jung S, Kim J, Park JH, et al. A 5-year retrospective cohort study of denosumab induced medication related osteonecrosis of the jaw in osteoporosis patients [J]. Sci Rep, 2022, 12(1):8641. [30] Hayano H, Kuroshima S, Sasaki M, et al. Distinct immunopathology in the early stages between different antiresorptives-related osteonecrosis of the jaw-like lesions in mice [J]. Bone, 2020, 135:115308. [31] Kaibuchi N, Iwata T, Yamato M, et al. Multipotent mesenchymal stromal cell sheet therapy for bisphosphonate-related osteonecrosis of the jaw in a rat model [J]. Acta Biomater, 2016, 42:400-410. [32] Yang G, Kim YN, Kim H, et al. Effect of human umbilical cord matrix-derived mesenchymal stem cells on bisphosphonate-related osteonecrosis of the jaw [J]. Tissue Eng Regen Med, 2021, 18(6):975-988. [33] Kuroshima S, Sasaki M, Nakajima K, et al. Transplantation of noncultured stromal vascular fraction cells of adipose tissue ameliorates osteonecrosis of the jaw-like lesions in mice [J]. J Bone Miner Res, 2018, 33(1):154-166. [34] Watanabe J, Sakai K, Urata Y, et al. Extracellular vesicles of stem cells to prevent BRONJ [J]. J Dent Res, 2020, 99(5):552-560. [35] Kuroshima S, Nakajima K, Sasaki M, et al. Systemic administration of quality- and quantity-controlled PBMNCs reduces bisphosphonate-related osteonecrosis of jaw-like lesions in mice [J]. Stem Cell Res Ther, 2019, 10(1):209. [36] Sadat-Ali M, Almasoud NA, Hegazi TM, et al. Treatment of bisphosphonate induced osteonecrosis of jaw in rats using an angiogenesis factor (A-Heal) and ABMDO (Autologous Bone Marrow Derived Osteoblasts) [J]. Saudi Dent J, 2022, 34(2):100-106. [37] Su Z, Li J, Bai X, et al. Borate bioactive glass prevents zoledronate-induced osteonecrosis of the jaw by restoring osteogenesis and angiogenesis [J]. Oral Dis, 2020, 26(8):1706-1717. [38] Zhao D, Xiao D, Liu M, et al. Tetrahedral framework nucleic acid carrying angiogenic peptide prevents bisphosphonate-related osteonecrosis of the jaw by promoting angiogenesis [J]. Int J Oral Sci, 2022, 14(1):23. [39] Bouland CL, Javadian R, Gilis S, et al. Treatment of medication-related osteonecrosis of the jaw with cell therapy [J]. Front Cell Dev Biol, 2024, 12:1338376. [40] Liu XN, Zhang PL, Gu Y, et al. Type H vessels: functions in bone development and diseases [J]. Front Cell Dev Biol, 2023, 11:1236545. |