Department of Leukemia, The University of Texas MD Anderson Cancer Center, 1515 Holcombe Blvd., Unit 428, Houston, TX, 77030, USA.
Drugs. 2019 Aug;79(12):1287-1304. doi: 10.1007/s40265-019-01163-4.
Apoptosis, the process of programmed cell death, occurs normally during development and aging. Members of the B-cell lymphoma 2 (BCL2) family of proteins are central regulators of apoptosis, and resistance to apoptosis is one of the hallmarks of cancer. Targeting the apoptotic pathway via BCL2 inhibitors has been considered a promising treatment strategy in the past decade. Initial efforts with small molecule BH3 mimetics such as ABT-737 and ABT-263 (navitoclax) pioneered the development of the first-in-class Food and Drug Administration (FDA)-approved oral BCL2 inhibitor, venetoclax. Venetoclax was approved for the treatment of chronic lymphocytic leukemia and acute myeloid leukemia, and is now being studied in a number of hematologic malignancies. Several other inhibitors targeting different BCL2 family members are now in early stages of development.
细胞凋亡是一种程序性细胞死亡的过程,正常发生于发育和衰老过程中。B 细胞淋巴瘤 2(BCL2)家族蛋白是细胞凋亡的核心调节因子,而对细胞凋亡的抵抗是癌症的一个标志。在过去十年中,通过 BCL2 抑制剂靶向细胞凋亡途径被认为是一种有前途的治疗策略。最初使用小分子 BH3 模拟物,如 ABT-737 和 ABT-263(navitoclax),开创了首个 FDA 批准的口服 BCL2 抑制剂 venetoclax 的发展。Venetoclax 被批准用于治疗慢性淋巴细胞白血病和急性髓细胞白血病,目前正在许多血液恶性肿瘤中进行研究。目前还有几种针对不同 BCL2 家族成员的其他抑制剂处于早期开发阶段。