Barthet Valentin J A, Lowe Scott W
Cancer Biology and Genetics Program, Sloan Kettering Institute, Memorial Sloan Kettering Cancer Center, New York, New York 10065, USA.
Cancer Biology and Genetics Program, Sloan Kettering Institute, Memorial Sloan Kettering Cancer Center, New York, New York 10065, USA;
Genes Dev. 2025 Aug 1;39(15-16):910-913. doi: 10.1101/gad.353134.125.
Cellular senescence plays a dual role in tissue biology by promoting tumor suppression and wound healing when transient but driving inflammation, fibrosis, and age-related disease when persistent. The growing recognition that senescent cell clearance can reverse these pathologies has catalyzed efforts to develop therapeutics that preferentially kill senescent cells (also known as "senolytics"). However, clinical translation from bench to bedside remains challenging due to senescent state heterogeneity, limited biomarkers, off-target toxicities, and the frailty of aged patients. Small molecule senolytics, although promising, often lack defined mechanisms of action and pose safety concerns that may constrain their use in older adults. Emerging precision approaches, including those that exploit surface markers and leverage engineered immune therapies, offer a rational and potentially more selective path forward. Here we highlight recent advances in senescence profiling and targeted clearance strategies, emphasizing the need for therapies designed with both biological complexity and the needs of aging populations in mind.
短暂存在时可促进肿瘤抑制和伤口愈合,但持续存在时会引发炎症、纤维化和与年龄相关的疾病。越来越多的人认识到清除衰老细胞可以逆转这些病理状况,这促使人们努力开发优先杀死衰老细胞的疗法(也称为“衰老细胞溶解剂”)。然而,由于衰老状态的异质性、有限的生物标志物、脱靶毒性以及老年患者的虚弱状况,从实验室到临床的转化仍然具有挑战性。小分子衰老细胞溶解剂虽然前景广阔,但往往缺乏明确的作用机制,并且存在安全问题,这可能会限制它们在老年人中的使用。新兴的精准方法,包括那些利用表面标志物和利用工程化免疫疗法的方法,提供了一条合理且可能更具选择性的前进道路。在这里,我们重点介绍衰老分析和靶向清除策略的最新进展,强调需要在设计疗法时兼顾生物学复杂性和老年人群的需求。