| Literature DB >> 32482536 |
Boshi Wang1, Jaskaren Kohli1, Marco Demaria2.
Abstract
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.Entities:
Keywords: SASP; cancer therapy; cellular senescence; pro-tumorigenesis; senotherapy
Year: 2020 PMID: 32482536 DOI: 10.1016/j.trecan.2020.05.004
Source DB: PubMed Journal: Trends Cancer ISSN: 2405-8025