Senescence and the SASP: many therapeutic avenues

被引:936
作者
Birch, Jodie [1 ,2 ]
Gil, Jesus [1 ,2 ]
机构
[1] MRC London Inst Med Sci LMS, London W12 0NN, England
[2] Imperial Coll London, Fac Med, Inst Clin Sci, London W12 0NN, England
基金
英国医学研究理事会;
关键词
senescence; SASP; inflammation; cancer; aging; disease; senolytics; senomorphics; therapeutics; CELLULAR SENESCENCE; SECRETORY PHENOTYPE; LIVER-CANCER; CELLS; CHROMATIN; CLEARANCE; MTOR; INFLAMMATION; SURVEILLANCE; CHEMOTHERAPY;
D O I
10.1101/gad.343129.120
中图分类号
Q2 [细胞生物学];
学科分类号
071013 [干细胞生物学];
摘要
Cellular senescence is a stress response that elicits a permanent cell cycle arrest and triggers profound phenotypic changes such as the production of a bioactive secretome, referred to as the senescence-associated secretory phenotype (SASP). Acute senescence induction protects against cancer and limits fibrosis, but lingering senescent cells drive age-related disorders. Thus, targeting senescent cells to delay aging and limit dysfunction, known as "senotherapy," is gaining momentum. While drugs that selectively kill senescent cells, termed "senolytics" are a major focus, SASP-centered approaches are emerging as alternatives to target senescence-associated diseases. Here, we summarize the regulation and functions of the SASP and highlight the therapeutic potential of SASP modulation as complimentary or an alternative to current senolytic approaches.
引用
收藏
页码:1565 / 1576
页数:12
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