Senescent Cells in Cancer Therapy: Friends or Foes?

被引:265
|
作者
Wang, Boshi [1 ]
Kohli, Jaskaren [1 ]
Demaria, Marco [1 ]
机构
[1] Univ Med Ctr Groningen, European Res Inst Biol Ageing ERIBA, NL-9713 AV Groningen, Netherlands
来源
TRENDS IN CANCER | 2020年 / 6卷 / 10期
关键词
EPITHELIAL-MESENCHYMAL TRANSITION; HISTONE DEACETYLASE INHIBITORS; CELLULAR SENESCENCE; SECRETORY PHENOTYPE; GROWTH ARREST; BREAST-CANCER; TUMOR-CELLS; DNA-DAMAGE; PREMATURE SENESCENCE; STROMAL SENESCENCE;
D O I
10.1016/j.trecan.2020.05.004
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Several cancer interventions induce DNA damage and promote senescence in cancer and nonmalignant cells. Senescent cells secrete a collection of proinflammatory factors collectively termed the senescence-associated secretory phenotype (SASP). SASP factors are able to potentiate various aspects of tumorigenesis, including proliferation, metastasis, and immunosuppression. Moreover, the accumulation and persistence of therapy-induced senescent cells can promote tissue dysfunction and the early onset of various age-related symptoms in treated cancer patients. Here, we review in detail the mechanisms by which cellular senescence contributes to cancer development and the side effects of cancer therapies. We also review how pharmacological interventions to eliminate senescent cells or inhibit SASP production can mitigate these negative effects and propose therapeutic strategies based on the age of the patient.
引用
收藏
页码:838 / 857
页数:20
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