Department of Cellular and Molecular Pharmacology & Experimental Therapeutics, Medical University of South Carolina, Charleston, South Carolina, USA.
Adv Cancer Res. 2015;127:191-226. doi: 10.1016/bs.acr.2015.03.002. Epub 2015 Apr 11.
The debut of the proteasome inhibitor bortezomib (Btz; Velcade®) radically and immediately improved the treatment of multiple myeloma (MM), an incurable malignancy of the plasma cell. Therapeutic resistance is unavoidable, however, and represents a major obstacle to maximizing the clinical potential of the drug. To address this challenge, studies have been conducted to uncover the molecular mechanisms driving Btz resistance and to discover new targeted therapeutic strategies and combinations that restore Btz activity. This review discusses the literature describing molecular adaptations that confer Btz resistance with a primary disease focus on MM. Also discussed are the most recent advances in therapeutic strategies that overcome resistance, approaches that include redox-modulating agents, murine double minute 2 inhibitors, therapeutic monoclonal antibodies, and new epigenetic-targeted drugs like bromodomain and extra terminal domain inhibitors.
蛋白酶体抑制剂硼替佐米(Btz;万珂®)的问世,彻底改变并即刻改善了多发性骨髓瘤(MM)这种不可治愈的浆细胞瘤的治疗效果。然而,治疗耐药性是不可避免的,它是最大限度发挥该药物临床潜力的主要障碍。为了应对这一挑战,已经开展了多项研究,旨在揭示驱动硼替佐米耐药的分子机制,并发现新的靶向治疗策略和联合治疗方案,以恢复硼替佐米的活性。本综述讨论了描述多发性骨髓瘤中硼替佐米耐药相关分子适应性的文献,同时还讨论了克服耐药性的最新治疗策略进展,这些策略包括氧化还原调节剂、鼠双微体 2 抑制剂、治疗性单克隆抗体以及新的表观遗传靶向药物,如溴结构域和末端外结构域抑制剂。