摘要
背景:骨肉瘤被认为是最常见的原发性骨恶性肿瘤。肺转移是导致死亡的主要原因,也是预测阴性患者预后的最一致的因素。n骨肉瘤。第三代含氮双膦酸盐,如唑来膦酸,已被证明能减少骨转移引起的骨溶解,并具有高度的选择性定位。并保留在骨中,从而使它们成为治疗骨转移的有吸引力的药物。研究表明,唑来膦酸对骨肉瘤细胞具有多种抗肿瘤作用。在体外,包括抗增殖、抗血管生成和免疫调节作用。唑来膦酸对骨肉瘤Ⅰ期原发肿瘤生长和肺转移的影响存在争议,限制了其临床应用。 目的:综述唑来膦酸对骨肉瘤原发肿瘤负担和肺转移的影响。同时,我们还分析了佐菌素的临床疗效。单用立膦酸联合化疗药物治疗骨肉瘤。 结论:唑来膦酸在体外对骨肉瘤具有不同的抗肿瘤作用,但其体内效应仍存在争议。CLA需要进一步的临床和临床研究。研究唑来膦酸治疗骨肉瘤的疗效。
关键词: 双膦酸盐,骨溶解,骨肉瘤,肺转移,唑来膦酸,骨。
图形摘要
Current Drug Targets
Title:Zoledronic Acid: Pleiotropic Anti-Tumor Mechanism and Therapeutic Outlook for Osteosarcoma
Volume: 19 Issue: 5
关键词: 双膦酸盐,骨溶解,骨肉瘤,肺转移,唑来膦酸,骨。
摘要: Background: Osteosarcoma is considered the most frequent primary bone malignancy. Lung metastasis is the leading cause of death and the most consistent factor for predicting negative patient outcome in osteosarcoma. Third-generation nitrogen-containing bisphosphonates, such as zoledronic acid, have been shown to reduce osteolysis induced by bone metastasis and exhibit highly selective localization and retention in bone, thus making them attractive agents in the treatment of bone metastasis. Studies have shown that zoledronic acid exerts pleiotropic anti-tumor effects against osteosarcoma cells in vitro, including anti-proliferative, anti-angiogenic, and immunomodulatory effects. However, the efficacy of zoledronic acid against primary tumor growth and pulmonary metastasis of osteosarcoma is controversial, which has limited its clinical application.
Objective: The present review summarizes the controversial effects of zoledronic acid on primary tumor burden and pulmonary metastases in osteosarcoma. We also analyze the clinical effectiveness of zoledronic acid alone and in combination with chemotherapeutic drugs for the treatment of osteosarcoma.
Conclusion: Zoledronic acid exhibits diverse anti-tumor effects in osteosarcoma in vitro, however, the in vivo effect is still controversial. Further preclinical and clinical studies are needed to clarify the effects of zoledronic acid in osteosarcoma.
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Zoledronic Acid: Pleiotropic Anti-Tumor Mechanism and Therapeutic Outlook for Osteosarcoma, Current Drug Targets 2018; 19 (5) . https://dx.doi.org/10.2174/1573399811666150615145409
DOI https://dx.doi.org/10.2174/1573399811666150615145409 |
Print ISSN 1389-4501 |
Publisher Name Bentham Science Publisher |
Online ISSN 1873-5592 |
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