Telomere Length Regulation Unit, Children's Medical Research Institute, Faculty of Medicine and Health, University of Sydney, Westmead, NSW, Australia.
Nat Rev Cancer. 2022 Sep;22(9):515-532. doi: 10.1038/s41568-022-00490-1. Epub 2022 Jul 5.
Cancer cells establish replicative immortality by activating a telomere-maintenance mechanism (TMM), be it telomerase or the alternative lengthening of telomeres (ALT) pathway. Targeting telomere maintenance represents an intriguing opportunity to treat the vast majority of all cancer types. Whilst telomerase inhibitors have historically been heralded as promising anticancer agents, the reality has been more challenging, and there are currently no therapeutic options for cancer types that use ALT despite their aggressive nature and poor prognosis. In this Review, we discuss the mechanistic differences between telomere maintenance by telomerase and ALT, the current methods used to detect each mechanism, the utility of these tests for clinical diagnosis, and recent developments in the therapeutic strategies being employed to target both telomerase and ALT. We present notable developments in repurposing established therapeutic agents and new avenues that are emerging to target cancer types according to which TMM they employ. These opportunities extend beyond inhibition of telomere maintenance, by finding and exploiting inherent weaknesses in the telomeres themselves to trigger rapid cellular effects that lead to cell death.
癌细胞通过激活端粒维持机制 (TMM) 来建立复制性永生,无论是端粒酶还是端粒的替代性延长 (ALT) 途径。针对端粒维持的治疗方法为治疗绝大多数癌症类型提供了诱人的机会。虽然端粒酶抑制剂一直被认为是很有前途的抗癌药物,但现实却更加具有挑战性,目前尚无针对使用 ALT 的癌症类型的治疗选择,尽管它们具有侵袭性和预后不良。在这篇综述中,我们讨论了端粒酶和 ALT 维持端粒的机制差异、目前用于检测每种机制的方法、这些检测方法在临床诊断中的应用,以及针对端粒酶和 ALT 所采用的治疗策略的最新进展。我们介绍了重新利用现有治疗剂的显著进展以及根据它们所采用的 TMM 出现的新途径,这些机会不仅限于抑制端粒维持,还可以通过发现和利用端粒本身的固有弱点来触发导致细胞死亡的快速细胞效应。