Targeting Protein-Protein Interactions in Hematologic Malignancies

被引:1
作者
Cierpicki, Tomasz [1 ]
Grembecka, Jolanta [1 ]
机构
[1] Univ Michigan, Dept Pathol, Ann Arbor, MI 48109 USA
基金
美国国家卫生研究院;
关键词
protein-protein interactions; drug discovery; hematologic malignancies; targeted therapies; ACUTE MYELOID-LEUKEMIA; CHRONIC LYMPHOCYTIC-LEUKEMIA; SMALL-MOLECULE INHIBITORS; MENIN-MLL INTERACTION; X-LINKED INHIBITOR; APOPTOSIS PROTEINS; BCL-2; INHIBITION; STRUCTURAL BASIS; PHASE-I; THERAPEUTIC TARGET;
D O I
10.1146/annurev-pathmechdis-031521-033231
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
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.
引用
收藏
页码:275 / 301
页数:27
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