Gilmore Andrew, King Louise
Wellcome Centre for Cell-Matrix Research, Faculty of Biology, Medicine and Health, Manchester Academic Health Science Centre, University of Manchester, Manchester, UK.
F1000Res. 2019 Oct 24;8. doi: 10.12688/f1000research.18872.1. eCollection 2019.
Apoptosis is a highly conserved programme for removing damaged and unwanted cells. Apoptosis in most cells is coordinated on mitochondria by the Bcl-2 family of proteins. The balance between pro- and anti-apoptotic Bcl-2 family proteins sets a threshold for mitochondrial apoptosis, a balance that is altered during cancer progression. Consequently, avoidance of cell death is an established cancer hallmark. Although there is a general perception that tumour cells are more resistant to apoptosis than their normal counterparts, the realities of cell death regulation in cancer are more nuanced. In this review we discuss how a profound understanding of this control has led to new therapeutic approaches, including the new class of BH3-mimetics, which directly target apoptosis as a vulnerability in cancer. We discuss recent findings that highlight the current limitations in our understanding of apoptosis and how these novel therapeutics work.
细胞凋亡是一种高度保守的程序,用于清除受损和不需要的细胞。大多数细胞中的细胞凋亡由Bcl-2蛋白家族在线粒体上进行协调。促凋亡和抗凋亡Bcl-2家族蛋白之间的平衡设定了线粒体凋亡的阈值,这种平衡在癌症进展过程中会发生改变。因此,避免细胞死亡是一种既定的癌症标志。尽管人们普遍认为肿瘤细胞比正常细胞对细胞凋亡更具抗性,但癌症中细胞死亡调控的实际情况更为细微。在本综述中,我们讨论了对这种调控的深入理解如何带来了新的治疗方法,包括新型的BH3模拟物,它们直接将细胞凋亡作为癌症的一个脆弱点进行靶向治疗。我们讨论了最近的研究发现,这些发现突出了我们目前对细胞凋亡理解的局限性以及这些新型疗法的作用机制。