4.6 Article

Senotherapeutics in Cancer and HIV

期刊

CELLS
卷 11, 期 7, 页码 -

出版社

MDPI
DOI: 10.3390/cells11071222

关键词

senescence; senotherapy; cancer; HIV; senolytic; senostatic; SASP

资金

  1. Ministerio de Ciencia, Innovacion y Universidades (MCIU) Plan Estatal de I+D+I 2018, a la Agencia Estatal de Investigacion (AEI) y al Fondo Europeo de Desarrollo Regional (MCIU/AEI/FEDER) [RTI2018-097455-B-I00]
  2. AEI-MICIU/FEDER [RED2018-102723-T]
  3. CIBER de Cancer [CB16/12/00275]
  4. FEDER from Regional Development European Funds (European Union)
  5. Consejeria de Salud [PI-0397-2017]
  6. 2018 competitive research projects call within the scope of PAIDI 2020 [P18-RT-2501]
  7. European Regional Development Fund (ERDF) from the Regional Ministry of Economic Transformation, Industry, Knowledge and Universities
  8. Fundacion AECC
  9. Fundacion Eugenio Rodriguez Pascual
  10. Ministerio de Ciencia, Innovacion y Universidades (MCIU) Plan Estatal de I+D+I 2018, a la Agencia Estatal de Investigacion (AEI) y al Fondo Europeo de Desarrollo Regional (MCIU/AEI/FEDER, UE)

向作者/读者索取更多资源

Cellular senescence plays a beneficial role in embryogenesis and maintaining normal adult organisms, but chronic activation of senescence can lead to age-related diseases, HIV, and cancer. Senescent cells share common phenotypes, including cell division arrest, abnormal shape, increased size, high granularity, apoptosis resistance, defective metabolism, and chromatin alterations. Developing senotherapeutics that selectively target senescent cells is important for treating aging-related disorders and acting as antitumor drugs in cancer.
Cellular senescence is a stress-response mechanism that contributes to homeostasis maintenance, playing a beneficial role during embryogenesis and in normal adult organisms. In contrast, chronic senescence activation may be responsible for other events such as age-related disorders, HIV and cancer development. Cellular senescence activation can be triggered by different insults. Regardless of the inducer, there are several phenotypes generally shared among senescent cells: cell division arrest, an aberrant shape, increased size, high granularity because of increased numbers of lysosomes and vacuoles, apoptosis resistance, defective metabolism and some chromatin alterations. Senescent cells constitute an important area for research due to their contributions to the pathogenesis of different diseases such as frailty, sarcopenia and aging-related diseases, including cancer and HIV infection, which show an accelerated aging. Hence, a new pharmacological category of treatments called senotherapeutics is under development. This group includes senolytic drugs that selectively attack senescent cells and senostatic drugs that suppress SASP factor delivery, inhibiting senescent cell development. These new drugs can have positive therapeutic effects on aging-related disorders and act in cancer as antitumor drugs, avoiding the undesired effects of senescent cells such as those from SASP. Here, we review senotherapeutics and how they might affect cancer and HIV disease, two very different aging-related diseases, and review some compounds acting as senolytics in clinical trials.

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