The Campbell Family Cancer Research Institute, Ontario Cancer Institute, University Health Network, Toronto, Ontario, Canada.
Curr Opin Cell Biol. 2009 Dec;21(6):871-7. doi: 10.1016/j.ceb.2009.09.004. Epub 2009 Oct 12.
Programmed cell death (apoptosis) is crucial for embryogenesis and tissue homeostasis. Deregulated apoptosis leads to immunodeficiency, autoimmune disorders or cancer. The two main routes to apoptosis are the extrinsic and intrinsic (mitochondrial) pathways. Both involve caspase activation that leads to the cleavage of multiple intracellular substrates [1,9]. This review highlights recent advances in our understanding of the intrinsic pathway. We describe how BCL-2-family members preserve or disrupt mitochondrial integrity, the contribution of BH3-only proteins to this process, and the importance of cytotoxic factors released by the mitochondria. The growing evidence that the intrinsic pathway is crucial for tumourigenesis makes this an intriguing field. In particular, the finding that BCL-2 homologues are inhibited by BH3-only proteins may have future therapeutic applications.
程序性细胞死亡(凋亡)对于胚胎发生和组织稳态至关重要。凋亡失调会导致免疫缺陷、自身免疫性疾病或癌症。凋亡的两个主要途径是外在途径和内在途径(线粒体途径)。两者都涉及半胱天冬酶的激活,导致多种细胞内底物的切割[1,9]。这篇综述强调了我们对内在途径的理解的最新进展。我们描述了 BCL-2 家族成员如何维持或破坏线粒体完整性,BH3 仅蛋白在此过程中的贡献,以及线粒体释放的细胞毒性因子的重要性。越来越多的证据表明内在途径对于肿瘤发生至关重要,这使得这一领域非常有趣。特别是发现 BCL-2 同源物被 BH3 仅蛋白抑制可能具有未来的治疗应用。