Reed John C, Pellecchia Maurizio
Burnham Institute, 10901 N Torrey Pines Rd, La Jolla, CA 92037, USA.
Blood. 2005 Jul 15;106(2):408-18. doi: 10.1182/blood-2004-07-2761. Epub 2005 Mar 29.
Apoptosis is an intrinsic cell death program that plays critical roles in tissue homeostasis, especially in organs where high rates of daily cell production are offset by rapid cell turnover. The hematopoietic system provides numerous examples attesting to the importance of cell death mechanisms for achieving homeostatic control. Much has been learned about the mechanisms of apoptosis of lymphoid and hematopoietic cells since the seminal observation in 1980 that glucocorticoids induce DNA fragmentation and apoptosis of thymocytes and the demonstration in 1990 that depriving colony-stimulating factors from factor-dependent hematopoietic cells causes programmed cell death. From an understanding of the core components of the apoptosis machinery at the molecular and structural levels, many potential new therapies for leukemia and lymphoma are emerging. In this review, we introduce some of the drug discovery targets thus far identified within the core apoptotic machinery and describe some of the progress to date toward translating our growing knowledge about these targets into new therapies for cancer and leukemia.
细胞凋亡是一种内在的细胞死亡程序,在组织稳态中发挥关键作用,尤其是在那些每日高细胞生成率被快速细胞更新所抵消的器官中。造血系统提供了许多例子,证明细胞死亡机制对于实现稳态控制的重要性。自1980年糖皮质激素诱导胸腺细胞DNA片段化和细胞凋亡的开创性观察以及1990年从依赖因子的造血细胞中去除集落刺激因子导致程序性细胞死亡的证明以来,人们对淋巴细胞和造血细胞凋亡的机制已经有了很多了解。从分子和结构水平上对凋亡机制核心成分的理解出发,许多针对白血病和淋巴瘤的潜在新疗法正在涌现。在这篇综述中,我们介绍了迄今为止在核心凋亡机制中确定的一些药物发现靶点,并描述了迄今为止在将我们对这些靶点的不断增长的认识转化为癌症和白血病新疗法方面取得的一些进展。