Cierpicki Tomasz, Grembecka Jolanta
Department of Pathology, University of Michigan, Ann Arbor, Michigan, USA; email:
Annu Rev Pathol. 2025 Jan;20(1):275-301. doi: 10.1146/annurev-pathmechdis-031521-033231.
Over the last two decades, there have been extensive efforts to develop small-molecule inhibitors of protein-protein interactions (PPIs) as novel therapeutics for cancer, including hematologic malignancies. Despite the numerous challenges associated with developing PPI inhibitors, a significant number of them have advanced to clinical studies in hematologic patients in recent years. The US Food and Drug Administration approval of the very first PPI inhibitor, venetoclax, demonstrated the real clinical value of blocking protein-protein interfaces. In this review, we discuss the most successful examples of PPI inhibitors that have reached clinical studies in patients with hematologic malignancies. We also describe the challenges of blocking PPIs with small molecules, clinical resistance to such compounds, and the lessons learned from the development of successful PPI inhibitors. Overall, this review highlights the remarkable success and substantial promise of blocking PPIs in hematologic malignancies.
在过去二十年中,人们付出了巨大努力来开发蛋白质-蛋白质相互作用(PPI)的小分子抑制剂,将其作为癌症(包括血液系统恶性肿瘤)的新型治疗药物。尽管开发PPI抑制剂面临诸多挑战,但近年来仍有相当数量的此类抑制剂进入了血液系统疾病患者的临床研究阶段。美国食品药品监督管理局批准的首个PPI抑制剂维奈克拉,证明了阻断蛋白质-蛋白质界面的实际临床价值。在本综述中,我们讨论了在血液系统恶性肿瘤患者中已进入临床研究的最成功的PPI抑制剂实例。我们还描述了用小分子阻断PPI的挑战、对此类化合物的临床耐药性,以及从成功开发PPI抑制剂中吸取的经验教训。总体而言,本综述突出了在血液系统恶性肿瘤中阻断PPI所取得的显著成功和巨大前景。