II University of Naples, Department of Biochemistry and Biophysics, Via S. M. Costantinopoli 16, 80138 Naples, Italy.
Expert Opin Pharmacother. 2010 Jan;11(1):141-54. doi: 10.1517/14656560903485664.
Therapy with zoledronic acid (ZOL) is a standard for patients with malignant bone disease. However, the antitumor effects of ZOL are demonstrated only in the preclinical setting and, therefore, they require pharmacological and molecular optimization. ZOL blocks protein isoprenylation, a pleiotropic and basic biochemical process within the cells regulating the activity of several proteins involved in survival and proliferating pathways.
The present review will cover different areas of research from pharmacology to cell biology and molecular biology regarding both direct and indirect anticancer effects of ZOL in humans. The challenge in demonstrating the clinical activity of ZOL is mainly based on its pharmacokinetic properties, which are discussed in detail.
New data about the modes to overcome the limitations of ZOL and the following therapeutic strategies to implement its anticancer activity are described: i) development of pharmacological combinations; ii) finding of new molecular targets of ZOL; and iii) development of new pharmacological formulations of ZOL.
In conclusion, ZOL has still underestimated anticancer properties that require further investigation in both preclinical and clinical settings.
唑来膦酸(zoledronic acid,ZOL)治疗是恶性骨病患者的标准治疗方法。然而,zoledronic acid 的抗肿瘤作用仅在临床前研究中得到证实,因此需要进行药理学和分子优化。zoledronic acid 可阻断蛋白异戊烯化,这是细胞内一种多效且基本的生化过程,可调节参与存活和增殖途径的几种蛋白的活性。
本篇综述涵盖了从药理学到细胞生物学和分子生物学等不同研究领域,涉及 zoledronic acid 对人类的直接和间接抗癌作用。本文详细讨论了证明 zoledronic acid 临床活性的主要挑战,即其药代动力学特性。
为克服 zoledronic acid 的局限性并实施其抗癌活性,提出了以下治疗策略:i)开发药理学联合疗法;ii)寻找 zoledronic acid 的新分子靶点;iii)开发 zoledronic acid 的新药理制剂。
zoledronic acid 仍具有被低估的抗癌特性,需要在临床前和临床环境中进一步研究。