SENESCENCE Senescence in tumours: evidence from mice and humans

被引:842
作者
Collado, Manuel [1 ]
Serrano, Manuel [1 ]
机构
[1] Spanish Natl Canc Res Ctr CNIO, Tumour Suppress Grp, E-28029 Madrid, Spain
基金
欧洲研究理事会;
关键词
ONCOGENE-INDUCED SENESCENCE; P53-DEPENDENT CELLULAR SENESCENCE; IN-VIVO; DNA-DAMAGE; DEVELOPMENTAL DEFECTS; TELOMERE DYSFUNCTION; INDUCE SENESCENCE; CANCER-THERAPY; RAS ONCOGENE; MOUSE MODEL;
D O I
10.1038/nrc2772
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The importance of cellular senescence, which is a stress response that stably blocks proliferation, is increasingly being recognized. Senescence is prevalent in pre-malignant tumours, and progression to malignancy requires evading senescence. Malignant tumours, however, may still undergo senescence owing to interventions that restore tumour suppressor function or inactivate oncogenes. Senescent tumour cells can be cleared by immune cells, which may result in efficient tumour regression. Standard chemotherapy also has the potential to induce senescence, which may partly underlie its therapeutic activity. Although these concepts are well supported in mouse models, translating them to clinical oncology remains a challenge.
引用
收藏
页码:51 / 57
页数:7
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