Department of Lymphoma and Myeloma, The University of Texas MD Anderson Cancer Center, 1515 Holcombe Boulevard, Unit 429, Houston, Texas 77030-4009, USA.
Department of Experimental Therapeutics, The University of Texas MD Anderson Cancer Center, 1515 Holcombe Boulevard, Unit 429, Houston, Texas 77030-4009, USA.
Nat Rev Clin Oncol. 2017 Jul;14(7):417-433. doi: 10.1038/nrclinonc.2016.206. Epub 2017 Jan 24.
The ubiquitin proteasome pathway was discovered in the 1980s to be a central component of the cellular protein-degradation machinery with essential functions in homeostasis, which include preventing the accumulation of misfolded or deleterious proteins. Cancer cells produce proteins that promote both cell survival and proliferation, and/or inhibit mechanisms of cell death. This notion set the stage for preclinical testing of proteasome inhibitors as a means to shift this fine equilibrium towards cell death. Since the late 1990s, clinical trials have been conducted for a variety of malignancies, leading to regulatory approvals of proteasome inhibitors to treat multiple myeloma and mantle-cell lymphoma. First-generation and second-generation proteasome inhibitors can elicit deep initial responses in patients with myeloma, for whom these drugs have dramatically improved outcomes, but relapses are frequent and acquired resistance to treatment eventually emerges. In addition, promising preclinical data obtained with proteasome inhibitors in models of solid tumours have not been confirmed in the clinic, indicating the importance of primary resistance. Investigation of the mechanisms of resistance is, therefore, essential to further maximize the utility of this class of drugs in the era of personalized medicine. Herein, we discuss the advances and challenges resulting from the introduction of proteasome inhibitors into the clinic.
泛素蛋白酶体途径是在 20 世纪 80 年代被发现的,它是细胞内蛋白质降解机制的核心组成部分,在维持体内平衡方面具有重要功能,包括防止错误折叠或有害蛋白质的积累。癌细胞会产生促进细胞存活和增殖的蛋白质,和/或抑制细胞死亡的机制。这一概念为蛋白酶体抑制剂的临床前测试奠定了基础,以期将这种微妙的平衡转向细胞死亡。自 20 世纪 90 年代末以来,已经针对各种恶性肿瘤开展了临床试验,导致蛋白酶体抑制剂获得监管批准,用于治疗多发性骨髓瘤和套细胞淋巴瘤。第一代和第二代蛋白酶体抑制剂可以在骨髓瘤患者中引发深度初始反应,这些药物显著改善了患者的预后,但复发频繁,最终会出现获得性耐药。此外,在实体瘤模型中用蛋白酶体抑制剂获得的有前途的临床前数据并未在临床上得到证实,这表明原发性耐药的重要性。因此,研究耐药机制对于在个性化医疗时代进一步最大限度地利用这类药物至关重要。本文讨论了蛋白酶体抑制剂在临床应用中取得的进展和面临的挑战。