Research Institute for Medicines (iMed.ULisboa), Faculty of Pharmacy, Universidade de Lisboa, 1649-003 Lisboa, Portugal.
Center for Neuroscience and Cell Biology (CNC), Center for Innovative Biomedicine and Biotechnology (CIBB), Laboratory of Pharmaceutical Chemistry, Faculty of Pharmacy, University of Coimbra, 3004-504 Coimbra, Portugal.
Molecules. 2022 Mar 28;27(7):2201. doi: 10.3390/molecules27072201.
Proteasome inhibitors have shown relevant clinical activity in several hematological malignancies, namely in multiple myeloma and mantle cell lymphoma, improving patient outcomes such as survival and quality of life, when compared with other therapies. However, initial response to the therapy is a challenge as most patients show an innate resistance to proteasome inhibitors, and those that respond to the therapy usually develop late relapses suggesting the development of acquired resistance. The mechanisms of resistance to proteasome inhibition are still controversial and scarce in the literature. In this review, we discuss the development of proteasome inhibitors and the mechanisms of innate and acquired resistance to their activity-a major challenge in preclinical and clinical therapeutics. An improved understanding of these mechanisms is crucial to guiding the design of new and more effective drugs to tackle these devastating diseases. In addition, we provide a comprehensive overview of proteasome inhibitors used in combination with other chemotherapeutic agents, as this is a key strategy to combat resistance.
蛋白酶体抑制剂在多种血液系统恶性肿瘤中表现出相关的临床活性,特别是在多发性骨髓瘤和套细胞淋巴瘤中,与其他治疗方法相比,提高了患者的生存率和生活质量等预后。然而,由于大多数患者对蛋白酶体抑制剂具有先天耐药性,而那些对治疗有反应的患者通常会出现晚期复发,表明存在获得性耐药性,因此对治疗的初始反应是一个挑战。蛋白酶体抑制耐药的机制在文献中仍存在争议且很少。在这篇综述中,我们讨论了蛋白酶体抑制剂的发展以及对其活性产生先天和获得性耐药的机制——这是临床前和临床治疗中的一个主要挑战。更好地理解这些机制对于指导设计新的、更有效的药物来治疗这些毁灭性疾病至关重要。此外,我们还全面概述了与其他化疗药物联合使用的蛋白酶体抑制剂,因为这是对抗耐药性的关键策略。