Senescent cells in cancer therapy: why and how to remove them

Cancer Lett. 2021 Nov 1:520:68-79. doi: 10.1016/j.canlet.2021.07.002. Epub 2021 Jul 5.

Abstract

Cellular senescence is a stress response that imposes a growth arrest on cancer and nonmalignant cells during cancer therapy. By secreting a plethora of proinflammatory factors collectively termed the senescence-associated secretory phenotype (SASP), therapy-induced senescent cells can promote tumorigenesis. Moreover, the SASP from senescent cells is also able to drive therapy resistance and mediate many adverse effects of cancer therapy. Because senescent cell production often occurs during cancer therapy, it is important to carefully consider these potential detrimental effects. Senotherapy, which refers to selective removal of senescent cells, has been proposed as a promising adjuvant approach to eliminate the adverse effects of senescent cells. Thus, in this review we summarize in detail the mechanisms by which senescent cells contribute to tumorigenesis and therapeutic resistance. Also, we thoroughly discuss the potential strategies regarding how to effectively circumvent the undesirable effects of therapy-induced senescent cells.

Keywords: Cancer therapy; Cellular senescence; SASP; Senolysis; Senotherapy.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Carcinogenesis / genetics*
  • Cellular Senescence / genetics*
  • Humans
  • Neoplasms / genetics*
  • Neoplasms / pathology
  • Senescence-Associated Secretory Phenotype / genetics