基因组不稳定性
衰老
细胞生物学
细胞衰老
生物
遗传学
基因
DNA损伤
DNA
表型
作者
Haebeen Choi,Chanhee Kang
出处
期刊:FEBS Journal
[Wiley]
日期:2024-04-22
卷期号:291 (10): 2091-2093
摘要
Cellular immortalization is a complex process that requires multiple genetic alterations to overcome restricting barriers, including senescence. Not surprisingly, many of these alterations are associated with cancer; two tumor suppressor pathways, the cellular tumor antigen p53 and p16‐Retinoblastoma (RB) pathways, are the best‐characterized examples, but their mutations alone are known to be insufficient to drive full immortalization. En et al. identified a role for the lamin B receptor (LBR) in promoting cellular proliferation and immortalization in p53‐ and RB‐deficient cells by maintaining their genome integrity and suppressing senescence. Thus, modulation of LBR could be exploited to treat cancer and potentially also to promote cell rejuvenation.
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